Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 64374 |
|---|---|
| ensemblid | ENSG00000120725.13 |
| hgncid | 24624 |
| symbol | SIL1 |
| name | SIL1 nucleotide exchange factor |
| refseq_nuc | NM_022464.5 |
| refseq_prot | NP_071909.1 |
| ensembl_nuc | ENST00000394817.7 |
| ensembl_prot | ENSP00000378294.2 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 138946724 |
| end | 139198368 |
| strand | - |
| ver | v1.2 |
| region | chr5:138946724-139198368 |
| region5000 | chr5:138941724-139203368 |
| regionname0 | SIL1_chr5_138946724_139198368 |
| regionname5000 | SIL1_chr5_138941724_139203368 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 461 | 184 | 52 | 38 | 64 | 4 | 24 | 56 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0002 | 0/0 | 461 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0003 | 0/0 | 461 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0004 | 0/0 | 461 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0005 | 0/0 | 461 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0006 | 0/0 | 461 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0007 | 0/0 | 461 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0008 | 0/0 | 461 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0009 | 0/0 | 461 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| 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 | 1386 | 96 | 27 | 20 | 35 | 2 | 11 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| c0002 | 1/0 | 1386 | 84 | 23 | 17 | 28 | 2 | 13 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| c0003 | 0/0 | 1386 | 4 | 4 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| c0004 | 0/0 | 1386 | 3 | 3 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| c0005 | 0/0 | 1386 | 3 | 2 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| c0006 | 0/0 | 1386 | 2 | 2 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| c0007 | 0/0 | 1386 | 2 | 2 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| c0008 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| c0009 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| c0010 | 0/0 | 1386 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| c0011 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| c0012 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| c0013 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| 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 | 504 | 190 | 64 | 36 | 60 | 4 | 24 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| t0002 | 0/0 | 504 | 6 | 1 | 2 | 3 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| t0003 | 0/0 | 504 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| t0004 | 0/0 | 504 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| t0005 | 0/0 | 534 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| t0006 | 0/0 | 504 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| 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 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0125 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0154 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| 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 | 1386 | 96 | 27 | 20 | 35 | 2 | 11 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0001c0002 | 1/0 | 1386 | 84 | 23 | 17 | 28 | 2 | 13 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0001c0005 | 0/0 | 1386 | 3 | 2 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0001c0010 | 0/0 | 1386 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0002c0003 | 0/0 | 1386 | 4 | 4 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0002c0006 | 0/0 | 1386 | 2 | 2 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0003c0004 | 0/0 | 1386 | 3 | 3 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0004c0007 | 0/0 | 1386 | 2 | 2 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0005c0012 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0006c0009 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0007c0008 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0008c0011 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0009c0013 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1889 | 87 | 23 | 18 | 32 | 2 | 11 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0001c0001t0002 | 0/0 | 1889 | 6 | 1 | 2 | 3 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0001c0001t0003 | 0/0 | 1889 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0001c0001t0005 | 0/0 | 1919 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0001c0001t0006 | 0/0 | 1889 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0001c0002t0001 | 1/0 | 1889 | 83 | 23 | 17 | 27 | 2 | 13 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0001c0002t0004 | 0/0 | 1889 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0001c0005t0001 | 0/0 | 1889 | 3 | 2 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0001c0010t0001 | 0/0 | 1889 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0002c0003t0001 | 0/0 | 1889 | 4 | 4 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0002c0006t0001 | 0/0 | 1889 | 2 | 2 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0003c0004t0001 | 0/0 | 1889 | 3 | 3 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0004c0007t0001 | 0/0 | 1889 | 2 | 2 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0005c0012t0001 | 0/0 | 1889 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0006c0009t0001 | 0/0 | 1889 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0007c0008t0001 | 0/0 | 1889 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0008c0011t0001 | 0/0 | 1889 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| a0009c0013t0001 | 0/0 | 1889 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | copy fasta | chr5 | 138941724 | 139203368 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0154 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0003g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0001t0006g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0125 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0002t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0005t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0005t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0005t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0001c0010t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0002c0003t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0002c0003t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0002c0003t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0002c0003t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0002c0006t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0002c0006t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0003c0004t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0003c0004t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0003c0004t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0004c0007t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0004c0007t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0005c0012t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0006c0009t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0007c0008t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0008c0011t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| a0009c0013t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0155 | EUR | FIN | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0077 | EUR | FIN | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | CHS | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0142 | AMR | PUR | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0153 | AMR | PUR | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0070 | AMR | PUR | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0090 | AMR | PUR | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0072 | AMR | PUR | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0173 | AMR | PUR | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0190 | AMR | PUR | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01243 | hp1 | a0001 | c0005 | t0001 | g0007 | AMR | PUR | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | CLM | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0111 | AMR | CLM | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0112 | AMR | CLM | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0126 | AMR | CLM | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0038 | AMR | CLM | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0117 | AMR | CLM | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0128 | EUR | IBS | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | IBS | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0101 | AFR | ACB | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01891 | hp1 | a0002 | c0003 | t0001 | g0160 | AFR | ACB | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0068 | AFR | ACB | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0127 | AMR | PEL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0132 | AMR | PEL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0085 | AMR | PEL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0065 | AMR | PEL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0102 | AMR | PEL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0156 | EAS | KHV | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | KHV | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02083 | hp2 | a0001 | c0010 | t0001 | g0064 | EAS | KHV | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0084 | AFR | ACB | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0194 | AFR | ACB | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0118 | AFR | ACB | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0199 | AFR | ACB | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02280 | hp1 | a0007 | c0008 | t0001 | g0105 | AFR | ACB | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02280 | hp2 | a0003 | c0004 | t0001 | g0164 | AFR | ACB | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | ACB | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0146 | AFR | GWD | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0008 | SAS | PJL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02615 | hp1 | a0002 | c0006 | t0001 | g0103 | AFR | GWD | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0189 | AFR | GWD | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02622 | hp2 | a0005 | c0012 | t0001 | g0095 | AFR | GWD | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02630 | hp1 | a0004 | c0007 | t0001 | g0195 | AFR | GWD | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0188 | SAS | PJL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0182 | SAS | PJL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0184 | AFR | GWD | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0200 | AFR | GWD | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02723 | hp1 | a0002 | c0003 | t0001 | g0134 | AFR | GWD | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | GWD | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0183 | SAS | PJL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | GWD | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02895 | hp2 | a0002 | c0006 | t0001 | g0097 | AFR | GWD | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | ESN | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0144 | AFR | ESN | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0115 | SAS | PJL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0099 | AFR | GWD | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0192 | AFR | MSL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG03195 | hp1 | a0001 | c0005 | t0001 | g0011 | AFR | ESN | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG03195 | hp2 | a0008 | c0011 | t0001 | g0196 | AFR | ESN | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0113 | AFR | MSL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0028 | AFR | MSL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG03225 | hp2 | a0004 | c0007 | t0001 | g0158 | AFR | MSL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0100 | SAS | PJL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0104 | AFR | MSL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG03486 | hp1 | a0001 | c0005 | t0001 | g0091 | AFR | MSL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0025 | AFR | MSL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0143 | SAS | PJL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0136 | SAS | PJL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0187 | SAS | BEB | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0124 | SAS | BEB | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0175 | SAS | STU | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0073 | SAS | STU | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18522 | hp1 | a0002 | c0003 | t0001 | g0034 | AFR | YRI | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18522 | hp2 | a0003 | c0004 | t0001 | g0005 | AFR | YRI | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | LWK | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA19043 | hp2 | a0003 | c0004 | t0001 | g0138 | AFR | LWK | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA19060 | hp2 | a0001 | c0002 | t0004 | g0131 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0151 | AFR | YRI | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA19240 | hp2 | a0006 | c0009 | t0001 | g0157 | AFR | YRI | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ASW | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ASW | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0119 | SAS | GIH | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | GIH | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | ACB | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0176 | AFR | MSL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0185 | AFR | MSL | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | USA | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | USA | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA21309 | hp1 | a0002 | c0003 | t0001 | g0161 | AFR | LWK | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| NA21309 | hp2 | a0009 | c0013 | t0001 | g0045 | AFR | LWK | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0154 | REF | REF | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0125 | REF | REF | SIL1_chr5_138941724_139203368 | SIL1 | chr5 | 138941724 | 139203368 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:138947464
|
C | T | 1 | a0006 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.1039G>A | p.Glu347Lys | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 10/10 | 1149/1889 | 1039/1386 | 347/461 | chr5 | 138947464 | ||
| chr5:138951278
|
G | T | 1 | a0007 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.922C>A | p.Leu308Met | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 9/10 | 1032/1889 | 922/1386 | 308/461 | chr5 | 138951278 | ||
| chr5:139042679
|
T | G | 1 | a0002 | 6 | HG01891.hp1 HG02615.hp1 HG02723.hp1 others(3): Show |
missense_variant | MODERATE | c.394A>C | p.Lys132Gln | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/10 | 504/1889 | 394/1386 | 132/461 | chr5 | 139042679 | ||
| chr5:139121040
|
T | C | 1 | a0008 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.239A>G | p.Gln80Arg | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/10 | 349/1889 | 239/1386 | 80/461 | chr5 | 139121040 | ||
| chr5:139121064
|
G | A | 1 | a0005 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.215C>T | p.Pro72Leu | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/10 | 325/1889 | 215/1386 | 72/461 | chr5 | 139121064 | ||
| chr5:139121090
|
A | C | 1 | a0003 | 3 | HG02280.hp2 NA18522.hp2 NA19043.hp2 |
missense_variant | MODERATE | c.189T>G | p.Asp63Glu | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/10 | 299/1889 | 189/1386 | 63/461 | chr5 | 139121090 | ||
| chr5:139121127
|
G | A | 1 | a0004 | 2 | HG02630.hp1 HG03225.hp2 |
missense_variant | MODERATE | c.152C>T | p.Thr51Ile | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/10 | 262/1889 | 152/1386 | 51/461 | chr5 | 139121127 | ||
| chr5:139127749
|
T | C | 1 | a0009 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.95A>G | p.His32Arg | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/10 | 205/1889 | 95/1386 | 32/461 | chr5 | 139127749 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:138947342
|
C | T | 1 | a0001c0010 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.1161G>A | p.Ala387Ala | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 10/10 | 1271/1889 | 1161/1386 | 387/461 | chr5 | 138947342 | ||
| chr5:138951300
|
G | A | 1 | a0001c0005 | 3 | HG01243.hp1 HG03195.hp1 HG03486.hp1 |
synonymous_variant | LOW | c.900C>T | p.Phe300Phe | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 9/10 | 1010/1889 | 900/1386 | 300/461 | chr5 | 138951300 | ||
| chr5:139121126
|
T | C | 10 | a0001c0001a0001c0005a0001c0010others(7): Show | 113 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(110): Show |
synonymous_variant | LOW | c.153A>G | p.Thr51Thr | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/10 | 263/1889 | 153/1386 | 51/461 | chr5 | 139121126 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:138946744
|
A | G | 1 | a0001c0002t0004 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*373T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 10/10 | 373 | chr5 | 138946744 | |||||
| chr5:139127849
|
G | C | 1 | a0001c0001t0002 | 6 | HG01258.hp1 HG01258.hp2 HG02109.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-6C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/10 | 6 | chr5 | 139127849 | |||||
| chr5:139198321
|
C | CCGCGGCG others(23): Show |
1 | a0001c0001t0005 | 1 | HG02258.hp2 | 5_prime_UTR_variant | MODIFIER | c.-93_-64dupTTTGCGCA others(22): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/10 | 70479 | chr5 | 139198321 | |||||
| chr5:139198342
|
C | G | 1 | a0001c0001t0003 | 1 | HG02895.hp1 | 5_prime_UTR_variant | MODIFIER | c.-84G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/10 | 70499 | chr5 | 139198342 | |||||
| chr5:139198345
|
G | A | 1 | a0001c0001t0006 | 1 | HG02717.hp2 | 5_prime_UTR_variant | MODIFIER | c.-87C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/10 | 70502 | chr5 | 139198345 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:138947548
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1030-75G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 9/9 | chr5 | 138947548 | ||||||
| chr5:138947669
|
G | T | 4 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166others(1): Show | 4 | HG01109.hp2 HG01993.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1030-196C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 9/9 | chr5 | 138947669 | ||||||
| chr5:138947705
|
T | C | 28 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(25): Show | 28 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1030-232A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 9/9 | chr5 | 138947705 | ||||||
| chr5:138947918
|
C | T | 4 | a0001c0001t0001g0017a0001c0001t0001g0162a0001c0001t0001g0163others(1): Show | 4 | HG02109.hp2 HG02630.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1030-445G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 9/9 | chr5 | 138947918 | ||||||
| chr5:138948167
|
A | G | 3 | a0001c0001t0001g0023a0001c0001t0001g0094a0005c0012t0001g0095 | 3 | HG02257.hp2 HG02622.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1030-694T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 9/9 | chr5 | 138948167 | ||||||
| chr5:138948196
|
C | T | 1 | a0001c0002t0001g0108 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1030-723G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 9/9 | chr5 | 138948196 | ||||||
| chr5:138948395
|
T | C | 33 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(30): Show | 33 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1030-922A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 9/9 | chr5 | 138948395 | ||||||
| chr5:138948513
|
C | T | 2 | a0001c0001t0002g0029a0001c0001t0002g0093 | 2 | NA18961.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.1030-1040G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 9/9 | chr5 | 138948513 | ||||||
| chr5:138948636
|
AT | A | 199 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(196): Show | 199 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.1030-1164delA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 9/9 | chr5 | 138948636 | ||||||
| chr5:138949421
|
C | T | 1 | a0002c0003t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1029+1750G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 9/9 | chr5 | 138949421 | ||||||
| chr5:138949552
|
C | G | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1029+1619G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 9/9 | chr5 | 138949552 | ||||||
| chr5:138949553
|
G | A | 1 | a0001c0002t0001g0002 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1029+1618C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 9/9 | chr5 | 138949553 | ||||||
| chr5:138949741
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1029+1430C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 9/9 | chr5 | 138949741 | ||||||
| chr5:138949798
|
C | CA | 51 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0030others(48): Show | 51 | HG00323.hp2 HG00423.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.1029+1372dupT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 9/9 | chr5 | 138949798 | ||||||
| chr5:138949798
|
C | CAA | 6 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0081others(3): Show | 6 | HG00642.hp1 HG01346.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1029+1371_1029+137 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 9/9 | chr5 | 138949798 | ||||||
| chr5:138949798
|
CAAAAAAA | C | 36 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(33): Show | 36 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.1029+1366_1029+137 others(11): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 9/9 | chr5 | 138949798 | ||||||
| chr5:138949810
|
A | AG | 3 | a0004c0007t0001g0158a0004c0007t0001g0195a0008c0011t0001g0196 | 3 | HG02630.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1029+1360_1029+136 others(5): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 9/9 | chr5 | 138949810 | ||||||
| chr5:138949810
|
A | G | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1029+1361T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 9/9 | chr5 | 138949810 | ||||||
| chr5:138949812
|
AAAAAGAA others(10): Show |
A | 1 | a0001c0002t0001g0137 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1029+1342_1029+135 others(21): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 9/9 | chr5 | 138949812 | ||||||
| chr5:138950330
|
A | G | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1029+841T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 9/9 | chr5 | 138950330 | ||||||
| chr5:138950439
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1029+732G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 9/9 | chr5 | 138950439 | ||||||
| chr5:138950450
|
G | C | 33 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(30): Show | 33 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.1029+721C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 9/9 | chr5 | 138950450 | ||||||
| chr5:138950450
|
G | T | 4 | a0001c0001t0001g0017a0001c0001t0001g0162a0001c0001t0001g0163others(1): Show | 4 | HG02109.hp2 HG02630.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1029+721C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 9/9 | chr5 | 138950450 | ||||||
| chr5:138950525
|
C | T | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1029+646G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 9/9 | chr5 | 138950525 | ||||||
| chr5:138950669
|
A | G | 3 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0163 | 3 | HG01069.hp1 HG01071.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1029+502T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 9/9 | chr5 | 138950669 | ||||||
| chr5:138950924
|
C | T | 1 | a0001c0002t0001g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1029+247G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 9/9 | chr5 | 138950924 | ||||||
| chr5:138951082
|
C | T | 1 | a0001c0002t0001g0109 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1029+89G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 9/9 | chr5 | 138951082 | ||||||
| chr5:138951165
|
A | G | 2 | a0001c0001t0001g0163a0006c0009t0001g0157 | 2 | HG03453.hp2 NA19240.hp2 |
splice_region_variant&intron_variant | LOW | c.1029+6T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 9/9 | chr5 | 138951165 | ||||||
| chr5:138951374
|
G | T | 6 | a0001c0001t0001g0021a0001c0001t0001g0031a0001c0001t0001g0033others(3): Show | 6 | HG01243.hp2 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.865-39C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 8/9 | chr5 | 138951374 | ||||||
| chr5:138951441
|
C | T | 4 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166others(1): Show | 4 | HG01109.hp2 HG01993.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.865-106G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 8/9 | chr5 | 138951441 | ||||||
| chr5:138951529
|
A | G | 1 | a0002c0006t0001g0097 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.865-194T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 8/9 | chr5 | 138951529 | ||||||
| chr5:138951603
|
C | T | 1 | a0001c0002t0001g0004 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.864+185G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 8/9 | chr5 | 138951603 | ||||||
| chr5:138952550
|
C | A | 1 | a0001c0002t0001g0144 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.768-666G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138952550 | ||||||
| chr5:138952610
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.768-726G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138952610 | ||||||
| chr5:138952623
|
G | A | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.768-739C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138952623 | ||||||
| chr5:138952747
|
T | C | 1 | a0001c0002t0001g0142 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.768-863A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138952747 | ||||||
| chr5:138952841
|
G | A | 5 | a0001c0002t0001g0038a0001c0002t0001g0115a0001c0002t0001g0119others(2): Show | 5 | HG01496.hp1 HG03017.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.768-957C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138952841 | ||||||
| chr5:138952990
|
C | T | 6 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0054others(3): Show | 6 | NA18960.hp2 NA18964.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.768-1106G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138952990 | ||||||
| chr5:138953327
|
C | T | 1 | a0002c0006t0001g0097 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.768-1443G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138953327 | ||||||
| chr5:138953533
|
G | A | 12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(9): Show | 12 | NA18942.hp1 NA18946.hp2 NA18948.hp1 others(9): Show |
intron_variant | MODIFIER | c.768-1649C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138953533 | ||||||
| chr5:138953693
|
CA | C | 97 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(94): Show | 97 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.768-1810delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138953693 | ||||||
| chr5:138953694
|
A | C | 9 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0019others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.768-1810T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138953694 | ||||||
| chr5:138953871
|
C | T | 1 | a0001c0002t0001g0098 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.768-1987G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138953871 | ||||||
| chr5:138954047
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.768-2163T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138954047 | ||||||
| chr5:138954362
|
T | A | 16 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(13): Show | 16 | HG02055.hp2 HG02559.hp2 HG03041.hp1 others(13): Show |
intron_variant | MODIFIER | c.768-2478A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138954362 | ||||||
| chr5:138954455
|
C | A | 1 | a0001c0002t0001g0019 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.768-2571G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138954455 | ||||||
| chr5:138954680
|
C | T | 1 | a0001c0002t0001g0176 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.768-2796G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138954680 | ||||||
| chr5:138954681
|
G | A | 6 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0054others(3): Show | 6 | NA18960.hp2 NA18964.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.768-2797C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138954681 | ||||||
| chr5:138954790
|
C | G | 108 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(105): Show | 108 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(105): Show |
intron_variant | MODIFIER | c.768-2906G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138954790 | ||||||
| chr5:138954918
|
C | G | 109 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(106): Show | 109 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(106): Show |
intron_variant | MODIFIER | c.768-3034G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138954918 | ||||||
| chr5:138955037
|
GTATGGCA others(7): Show |
G | 5 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0019others(2): Show | 5 | HG02145.hp1 HG02615.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.768-3167_768-3154d others(16): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138955037 | ||||||
| chr5:138955174
|
C | G | 1 | a0001c0001t0001g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.768-3290G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138955174 | ||||||
| chr5:138955198
|
C | T | 1 | a0002c0003t0001g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.768-3314G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138955198 | ||||||
| chr5:138955331
|
A | C | 1 | a0002c0003t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.768-3447T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138955331 | ||||||
| chr5:138955611
|
G | A | 3 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0001t0001g0172 | 3 | HG01081.hp1 HG03710.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.768-3727C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138955611 | ||||||
| chr5:138955716
|
A | G | 103 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(100): Show | 103 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.768-3832T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138955716 | ||||||
| chr5:138955875
|
G | A | 1 | a0001c0002t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.768-3991C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138955875 | ||||||
| chr5:138956008
|
G | A | 1 | a0001c0002t0001g0126 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.768-4124C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138956008 | ||||||
| chr5:138956251
|
A | G | 1 | a0002c0003t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.768-4367T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138956251 | ||||||
| chr5:138956380
|
T | C | 1 | a0002c0003t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.768-4496A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138956380 | ||||||
| chr5:138956465
|
T | C | 29 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(26): Show | 29 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.768-4581A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138956465 | ||||||
| chr5:138956465
|
T | G | 19 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(16): Show | 19 | HG01243.hp1 HG02055.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.768-4581A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138956465 | ||||||
| chr5:138956637
|
G | T | 1 | a0001c0001t0001g0163 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.768-4753C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138956637 | ||||||
| chr5:138956644
|
A | G | 116 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(113): Show | 116 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(113): Show |
intron_variant | MODIFIER | c.768-4760T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138956644 | ||||||
| chr5:138956650
|
G | A | 1 | a0002c0003t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.768-4766C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138956650 | ||||||
| chr5:138956735
|
T | C | 5 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0019others(2): Show | 5 | HG02145.hp1 HG02615.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.768-4851A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138956735 | ||||||
| chr5:138956742
|
T | TA | 29 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(26): Show | 29 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.768-4859dupT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138956742 | ||||||
| chr5:138956742
|
T | TAA | 19 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(16): Show | 19 | HG01243.hp1 HG02055.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.768-4860_768-4859d others(4): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138956742 | ||||||
| chr5:138956742
|
TA | T | 5 | a0001c0001t0001g0055a0001c0001t0001g0077a0001c0001t0002g0140others(2): Show | 5 | HG00323.hp2 HG01975.hp2 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.768-4859delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138956742 | ||||||
| chr5:138956881
|
C | T | 1 | a0001c0002t0001g0135 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.768-4997G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138956881 | ||||||
| chr5:138957374
|
T | C | 13 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(10): Show | 13 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.768-5490A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138957374 | ||||||
| chr5:138957414
|
T | TA | 47 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(44): Show | 47 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.768-5531dupT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138957414 | ||||||
| chr5:138957414
|
T | TAA | 8 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0162others(5): Show | 8 | HG02055.hp2 HG02109.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.768-5532_768-5531d others(4): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138957414 | ||||||
| chr5:138957499
|
A | G | 1 | a0002c0003t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.768-5615T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138957499 | ||||||
| chr5:138957653
|
A | G | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.768-5769T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138957653 | ||||||
| chr5:138957920
|
CT | C | 15 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(12): Show | 15 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.768-6037delA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138957920 | ||||||
| chr5:138957955
|
G | A | 34 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(31): Show | 34 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.768-6071C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138957955 | ||||||
| chr5:138958119
|
C | T | 1 | a0002c0003t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.768-6235G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138958119 | ||||||
| chr5:138958655
|
G | A | 102 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(99): Show | 102 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.768-6771C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138958655 | ||||||
| chr5:138958833
|
G | A | 47 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(44): Show | 47 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.768-6949C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138958833 | ||||||
| chr5:138958879
|
A | G | 102 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(99): Show | 102 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.768-6995T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138958879 | ||||||
| chr5:138958964
|
A | G | 1 | a0001c0001t0001g0149 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.768-7080T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138958964 | ||||||
| chr5:138958986
|
C | T | 3 | a0001c0002t0001g0038a0001c0002t0001g0115a0001c0002t0001g0119 | 3 | HG01496.hp1 HG03017.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.768-7102G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138958986 | ||||||
| chr5:138959093
|
G | A | 3 | a0001c0002t0001g0073a0001c0002t0001g0124a0001c0002t0001g0182 | 3 | HG02698.hp2 HG03942.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.768-7209C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138959093 | ||||||
| chr5:138959743
|
C | A | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.768-7859G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138959743 | ||||||
| chr5:138959749
|
T | A | 47 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(44): Show | 47 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.768-7865A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138959749 | ||||||
| chr5:138959851
|
G | T | 1 | a0001c0002t0001g0098 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.768-7967C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138959851 | ||||||
| chr5:138959937
|
C | A | 13 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(10): Show | 13 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.768-8053G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138959937 | ||||||
| chr5:138960350
|
C | T | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.768-8466G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138960350 | ||||||
| chr5:138960413
|
C | CT | 21 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(18): Show | 21 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.768-8530dupA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138960413 | ||||||
| chr5:138960413
|
CT | C | 7 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0046others(4): Show | 7 | HG01516.hp2 HG01884.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.768-8530delA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138960413 | ||||||
| chr5:138960594
|
T | C | 47 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(44): Show | 47 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.768-8710A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138960594 | ||||||
| chr5:138960685
|
G | A | 5 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0019others(2): Show | 5 | HG02145.hp1 HG02615.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.768-8801C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138960685 | ||||||
| chr5:138960926
|
C | G | 110 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(107): Show | 110 | HG00323.hp2 HG00423.hp2 HG00735.hp1 others(107): Show |
intron_variant | MODIFIER | c.768-9042G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138960926 | ||||||
| chr5:138961007
|
C | T | 4 | a0001c0001t0001g0086a0001c0001t0001g0177a0001c0001t0001g0180others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.768-9123G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138961007 | ||||||
| chr5:138961043
|
T | C | 3 | a0002c0006t0001g0097a0004c0007t0001g0158a0004c0007t0001g0195 | 3 | HG02630.hp1 HG02895.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.768-9159A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138961043 | ||||||
| chr5:138961046
|
G | C | 3 | a0002c0006t0001g0097a0004c0007t0001g0158a0004c0007t0001g0195 | 3 | HG02630.hp1 HG02895.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.768-9162C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138961046 | ||||||
| chr5:138961184
|
C | G | 1 | a0006c0009t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.768-9300G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138961184 | ||||||
| chr5:138961218
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | NA19057.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.768-9334G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138961218 | ||||||
| chr5:138961397
|
T | C | 1 | a0001c0002t0001g0178 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.768-9513A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138961397 | ||||||
| chr5:138961694
|
G | A | 1 | a0001c0002t0001g0119 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.768-9810C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138961694 | ||||||
| chr5:138961952
|
C | CT | 52 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0020others(49): Show | 52 | HG00323.hp2 HG00423.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.768-10069dupA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138961952 | ||||||
| chr5:138961952
|
CT | C | 22 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0032others(19): Show | 22 | HG01070.hp2 HG01496.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.768-10069delA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138961952 | ||||||
| chr5:138962066
|
G | C | 1 | a0006c0009t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.768-10182C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138962066 | ||||||
| chr5:138962111
|
C | CT | 5 | a0001c0001t0001g0086a0001c0001t0001g0177a0001c0001t0001g0180others(2): Show | 5 | HG02055.hp2 HG02559.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.768-10228dupA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138962111 | ||||||
| chr5:138962216
|
C | T | 1 | a0001c0002t0001g0098 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.768-10332G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138962216 | ||||||
| chr5:138962303
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.768-10419G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138962303 | ||||||
| chr5:138962304
|
A | T | 1 | a0001c0001t0001g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.768-10420T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138962304 | ||||||
| chr5:138962607
|
T | C | 5 | a0001c0001t0001g0003a0001c0001t0001g0107a0001c0001t0001g0129others(2): Show | 5 | NA18959.hp2 NA18963.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.768-10723A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138962607 | ||||||
| chr5:138962707
|
C | T | 62 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0020others(59): Show | 62 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.768-10823G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138962707 | ||||||
| chr5:138963034
|
C | T | 2 | a0001c0001t0001g0067a0001c0001t0001g0074 | 2 | HG01934.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.768-11150G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138963034 | ||||||
| chr5:138963173
|
T | C | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.768-11289A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138963173 | ||||||
| chr5:138963563
|
G | A | 3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0005g0199 | 3 | HG00323.hp2 HG00735.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.768-11679C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138963563 | ||||||
| chr5:138963758
|
G | C | 1 | a0001c0002t0001g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.768-11874C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138963758 | ||||||
| chr5:138963796
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0107a0001c0001t0001g0129others(2): Show | 5 | NA18959.hp2 NA18963.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.768-11912C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138963796 | ||||||
| chr5:138963797
|
C | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0107a0001c0001t0001g0129others(2): Show | 5 | NA18959.hp2 NA18963.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.768-11913G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138963797 | ||||||
| chr5:138963806
|
A | G | 1 | a0002c0003t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.768-11922T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138963806 | ||||||
| chr5:138963851
|
C | G | 1 | a0001c0002t0004g0131 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.768-11967G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138963851 | ||||||
| chr5:138963941
|
G | A | 99 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(96): Show | 99 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.768-12057C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138963941 | ||||||
| chr5:138964146
|
A | G | 58 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0030others(55): Show | 58 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.768-12262T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138964146 | ||||||
| chr5:138964325
|
C | T | 1 | a0001c0002t0001g0119 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.768-12441G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138964325 | ||||||
| chr5:138964380
|
A | G | 1 | a0006c0009t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.768-12496T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138964380 | ||||||
| chr5:138964588
|
C | T | 1 | a0001c0001t0001g0014 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.768-12704G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138964588 | ||||||
| chr5:138964719
|
T | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0096 | 2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.768-12835A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138964719 | ||||||
| chr5:138964722
|
C | G | 2 | a0002c0003t0001g0034a0002c0003t0001g0161 | 2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.768-12838G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138964722 | ||||||
| chr5:138964744
|
G | A | 1 | a0002c0003t0001g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.768-12860C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138964744 | ||||||
| chr5:138964994
|
A | G | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.768-13110T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138964994 | ||||||
| chr5:138965375
|
T | G | 4 | a0001c0001t0001g0086a0001c0001t0001g0177a0001c0001t0001g0180others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.768-13491A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138965375 | ||||||
| chr5:138965593
|
C | G | 1 | a0004c0007t0001g0158 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.768-13709G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138965593 | ||||||
| chr5:138965793
|
T | C | 1 | a0002c0006t0001g0097 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.768-13909A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138965793 | ||||||
| chr5:138965797
|
A | G | 7 | a0001c0001t0001g0017a0001c0001t0001g0088a0001c0001t0001g0133others(4): Show | 7 | HG01109.hp2 HG01993.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.768-13913T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138965797 | ||||||
| chr5:138965859
|
G | A | 1 | a0001c0002t0001g0002 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.768-13975C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138965859 | ||||||
| chr5:138965910
|
C | T | 108 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(105): Show | 108 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(105): Show |
intron_variant | MODIFIER | c.768-14026G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138965910 | ||||||
| chr5:138966024
|
C | T | 3 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0185 | 3 | HG02451.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.768-14140G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138966024 | ||||||
| chr5:138966085
|
C | T | 1 | a0001c0001t0006g0200 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.768-14201G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138966085 | ||||||
| chr5:138966139
|
A | G | 109 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(106): Show | 109 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(106): Show |
intron_variant | MODIFIER | c.768-14255T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138966139 | ||||||
| chr5:138966167
|
C | T | 17 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(14): Show | 17 | HG01109.hp2 HG01243.hp1 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.768-14283G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138966167 | ||||||
| chr5:138966188
|
G | A | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.768-14304C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138966188 | ||||||
| chr5:138966198
|
G | T | 5 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0104others(2): Show | 5 | HG02451.hp1 HG03195.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.768-14314C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138966198 | ||||||
| chr5:138966641
|
C | T | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.768-14757G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138966641 | ||||||
| chr5:138966754
|
A | T | 1 | a0001c0002t0001g0139 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.768-14870T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138966754 | ||||||
| chr5:138966982
|
C | G | 3 | a0001c0002t0001g0065a0001c0002t0001g0085a0001c0002t0001g0102 | 3 | HG01975.hp1 HG01981.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.768-15098G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138966982 | ||||||
| chr5:138967077
|
C | T | 3 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0185 | 3 | HG02451.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.768-15193G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138967077 | ||||||
| chr5:138967276
|
G | A | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.768-15392C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138967276 | ||||||
| chr5:138967292
|
G | A | 5 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0019others(2): Show | 5 | HG02145.hp1 HG02615.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.768-15408C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138967292 | ||||||
| chr5:138967304
|
A | G | 9 | a0001c0001t0001g0017a0001c0001t0001g0088a0001c0001t0001g0133others(6): Show | 9 | HG01109.hp2 HG01993.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.768-15420T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138967304 | ||||||
| chr5:138967325
|
T | C | 1 | a0001c0010t0001g0064 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.768-15441A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138967325 | ||||||
| chr5:138967572
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.768-15688A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138967572 | ||||||
| chr5:138967619
|
T | A | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.768-15735A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138967619 | ||||||
| chr5:138967682
|
C | T | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.768-15798G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138967682 | ||||||
| chr5:138967712
|
G | A | 2 | a0004c0007t0001g0158a0004c0007t0001g0195 | 2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.768-15828C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138967712 | ||||||
| chr5:138967985
|
T | C | 3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0005g0199 | 3 | HG00323.hp2 HG00735.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.768-16101A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138967985 | ||||||
| chr5:138968059
|
C | T | 1 | a0002c0003t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.768-16175G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138968059 | ||||||
| chr5:138968065
|
C | A | 1 | a0002c0003t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.768-16181G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138968065 | ||||||
| chr5:138968095
|
G | A | 1 | a0001c0001t0001g0014 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.768-16211C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138968095 | ||||||
| chr5:138968126
|
G | T | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.768-16242C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138968126 | ||||||
| chr5:138968456
|
C | T | 2 | a0001c0001t0001g0149a0006c0009t0001g0157 | 2 | NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.768-16572G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138968456 | ||||||
| chr5:138969069
|
C | T | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.768-17185G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138969069 | ||||||
| chr5:138969285
|
G | C | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.768-17401C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138969285 | ||||||
| chr5:138969306
|
C | A | 2 | a0002c0003t0001g0134a0008c0011t0001g0196 | 2 | HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.768-17422G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138969306 | ||||||
| chr5:138969399
|
C | T | 1 | a0001c0002t0001g0068 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.768-17515G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138969399 | ||||||
| chr5:138969520
|
T | A | 5 | a0001c0001t0001g0016a0001c0002t0001g0184a0003c0004t0001g0005others(2): Show | 5 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.768-17636A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138969520 | ||||||
| chr5:138969525
|
G | C | 5 | a0001c0001t0001g0016a0001c0002t0001g0184a0003c0004t0001g0005others(2): Show | 5 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.768-17641C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138969525 | ||||||
| chr5:138969650
|
C | T | 1 | a0001c0002t0001g0084 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.768-17766G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138969650 | ||||||
| chr5:138969813
|
C | T | 47 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(44): Show | 47 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.768-17929G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138969813 | ||||||
| chr5:138969856
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.768-17972G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138969856 | ||||||
| chr5:138969891
|
C | T | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG00323.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.768-18007G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138969891 | ||||||
| chr5:138970071
|
T | G | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.768-18187A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138970071 | ||||||
| chr5:138970099
|
C | T | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.768-18215G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138970099 | ||||||
| chr5:138970125
|
G | A | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.768-18241C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138970125 | ||||||
| chr5:138970176
|
T | C | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.768-18292A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138970176 | ||||||
| chr5:138970229
|
G | A | 1 | a0001c0002t0001g0175 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.768-18345C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138970229 | ||||||
| chr5:138970354
|
G | A | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.768-18470C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138970354 | ||||||
| chr5:138970768
|
G | A | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.768-18884C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138970768 | ||||||
| chr5:138970773
|
G | A | 3 | a0002c0003t0001g0034a0002c0003t0001g0161a0007c0008t0001g0105 | 3 | HG02280.hp1 NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.768-18889C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138970773 | ||||||
| chr5:138970913
|
C | CA | 13 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(10): Show | 13 | NA18942.hp1 NA18946.hp2 NA18948.hp1 others(10): Show |
intron_variant | MODIFIER | c.768-19030dupT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138970913 | ||||||
| chr5:138971043
|
C | A | 3 | a0002c0003t0001g0034a0002c0003t0001g0161a0007c0008t0001g0105 | 3 | HG02280.hp1 NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.768-19159G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138971043 | ||||||
| chr5:138971380
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.768-19496T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138971380 | ||||||
| chr5:138971617
|
A | G | 62 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0017others(59): Show | 62 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.768-19733T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138971617 | ||||||
| chr5:138971690
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.768-19806T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138971690 | ||||||
| chr5:138971958
|
C | T | 1 | a0001c0002t0001g0002 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.768-20074G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138971958 | ||||||
| chr5:138972390
|
T | A | 1 | a0002c0003t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.768-20506A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138972390 | ||||||
| chr5:138972524
|
T | C | 5 | a0001c0001t0001g0016a0001c0002t0001g0184a0003c0004t0001g0005others(2): Show | 5 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.768-20640A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138972524 | ||||||
| chr5:138972623
|
G | A | 2 | a0004c0007t0001g0158a0004c0007t0001g0195 | 2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.768-20739C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138972623 | ||||||
| chr5:138972716
|
C | T | 1 | a0006c0009t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.768-20832G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138972716 | ||||||
| chr5:138972777
|
C | T | 61 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0030others(58): Show | 61 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.768-20893G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138972777 | ||||||
| chr5:138973201
|
T | TA | 60 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0030others(57): Show | 60 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.768-21318dupT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138973201 | ||||||
| chr5:138973201
|
T | TAA | 6 | a0001c0001t0001g0059a0001c0001t0001g0062a0001c0001t0001g0080others(3): Show | 6 | HG02723.hp1 HG03942.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.768-21319_768-2131 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138973201 | ||||||
| chr5:138973201
|
TA | T | 12 | a0001c0001t0001g0042a0001c0001t0001g0088a0001c0001t0001g0133others(9): Show | 12 | HG00642.hp2 HG01109.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.768-21318delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138973201 | ||||||
| chr5:138973588
|
T | C | 5 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0019others(2): Show | 5 | HG02145.hp1 HG02615.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.768-21704A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138973588 | ||||||
| chr5:138973618
|
C | T | 56 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0030others(53): Show | 56 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.768-21734G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138973618 | ||||||
| chr5:138973701
|
C | T | 1 | a0001c0002t0001g0142 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.768-21817G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138973701 | ||||||
| chr5:138973716
|
C | T | 63 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0030others(60): Show | 63 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.768-21832G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138973716 | ||||||
| chr5:138973930
|
T | G | 1 | a0002c0003t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.768-22046A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138973930 | ||||||
| chr5:138974176
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.768-22292G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138974176 | ||||||
| chr5:138974193
|
C | T | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.768-22309G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138974193 | ||||||
| chr5:138974490
|
T | C | 2 | a0001c0002t0001g0008a0001c0002t0001g0183 | 2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.768-22606A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138974490 | ||||||
| chr5:138974667
|
G | A | 1 | a0002c0003t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.768-22783C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138974667 | ||||||
| chr5:138974681
|
G | A | 12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(9): Show | 12 | NA18942.hp1 NA18946.hp2 NA18948.hp1 others(9): Show |
intron_variant | MODIFIER | c.768-22797C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138974681 | ||||||
| chr5:138974847
|
T | C | 5 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0019others(2): Show | 5 | HG02145.hp1 HG02615.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.768-22963A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138974847 | ||||||
| chr5:138974852
|
A | G | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.768-22968T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138974852 | ||||||
| chr5:138974888
|
T | C | 1 | a0001c0002t0001g0010 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.768-23004A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138974888 | ||||||
| chr5:138974964
|
A | G | 1 | a0001c0002t0001g0104 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.768-23080T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138974964 | ||||||
| chr5:138975001
|
A | C | 1 | a0001c0002t0001g0104 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.768-23117T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138975001 | ||||||
| chr5:138975115
|
T | C | 1 | a0002c0003t0001g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.768-23231A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138975115 | ||||||
| chr5:138975185
|
G | C | 1 | a0001c0001t0001g0012 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.768-23301C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138975185 | ||||||
| chr5:138975583
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.768-23699G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138975583 | ||||||
| chr5:138975621
|
A | T | 4 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0142others(1): Show | 4 | HG00642.hp2 HG01261.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.768-23737T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138975621 | ||||||
| chr5:138976053
|
A | G | 55 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0030others(52): Show | 55 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.768-24169T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138976053 | ||||||
| chr5:138976142
|
C | T | 9 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.768-24258G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138976142 | ||||||
| chr5:138976159
|
C | T | 2 | a0002c0003t0001g0034a0002c0003t0001g0161 | 2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.768-24275G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138976159 | ||||||
| chr5:138976200
|
C | T | 1 | a0001c0002t0001g0109 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.768-24316G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138976200 | ||||||
| chr5:138976310
|
C | CT | 14 | a0001c0001t0001g0021a0001c0001t0001g0031a0001c0001t0001g0033others(11): Show | 14 | HG01069.hp2 HG01243.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.768-24427dupA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138976310 | ||||||
| chr5:138976310
|
CT | C | 22 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(19): Show | 22 | HG01943.hp2 HG01975.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.768-24427delA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138976310 | ||||||
| chr5:138976312
|
T | C | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.768-24428A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138976312 | ||||||
| chr5:138976575
|
A | G | 2 | a0002c0003t0001g0034a0002c0003t0001g0161 | 2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.768-24691T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138976575 | ||||||
| chr5:138976593
|
A | G | 192 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(189): Show | 192 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.768-24709T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138976593 | ||||||
| chr5:138977138
|
A | C | 1 | a0001c0002t0001g0120 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.768-25254T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138977138 | ||||||
| chr5:138977340
|
A | C | 4 | a0001c0001t0001g0017a0001c0001t0001g0162a0001c0001t0001g0163others(1): Show | 4 | HG02109.hp2 HG02630.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.768-25456T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138977340 | ||||||
| chr5:138977457
|
A | G | 61 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0030others(58): Show | 61 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.768-25573T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138977457 | ||||||
| chr5:138977475
|
T | C | 1 | a0002c0003t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.768-25591A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138977475 | ||||||
| chr5:138977856
|
G | A | 1 | a0001c0002t0001g0153 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.768-25972C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138977856 | ||||||
| chr5:138978417
|
C | T | 59 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0030others(56): Show | 59 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.768-26533G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138978417 | ||||||
| chr5:138978580
|
A | G | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.768-26696T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138978580 | ||||||
| chr5:138978728
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.768-26844C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138978728 | ||||||
| chr5:138978840
|
A | C | 2 | a0002c0003t0001g0034a0002c0003t0001g0161 | 2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.768-26956T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138978840 | ||||||
| chr5:138978852
|
T | A | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.768-26968A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138978852 | ||||||
| chr5:138979063
|
A | T | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.768-27179T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138979063 | ||||||
| chr5:138979068
|
T | A | 17 | a0001c0001t0001g0017a0001c0001t0001g0056a0001c0001t0001g0060others(14): Show | 17 | HG01074.hp2 HG02083.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.768-27184A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138979068 | ||||||
| chr5:138979073
|
TA | T | 17 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0021others(14): Show | 17 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.768-27190delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138979073 | ||||||
| chr5:138979074
|
A | T | 6 | a0001c0002t0001g0117a0001c0002t0001g0118a0001c0002t0001g0146others(3): Show | 6 | HG01496.hp2 HG02258.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.768-27190T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138979074 | ||||||
| chr5:138979097
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.768-27213G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138979097 | ||||||
| chr5:138979158
|
G | A | 5 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0019others(2): Show | 5 | HG02145.hp1 HG02615.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.768-27274C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138979158 | ||||||
| chr5:138979309
|
C | T | 11 | a0001c0002t0001g0065a0001c0002t0001g0070a0001c0002t0001g0073others(8): Show | 11 | HG00423.hp1 HG01069.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.768-27425G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138979309 | ||||||
| chr5:138979563
|
G | A | 2 | a0002c0003t0001g0034a0002c0003t0001g0161 | 2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.768-27679C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138979563 | ||||||
| chr5:138979572
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.768-27688G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138979572 | ||||||
| chr5:138979607
|
G | A | 1 | a0001c0002t0001g0198 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.768-27723C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138979607 | ||||||
| chr5:138979669
|
A | C | 1 | a0001c0002t0001g0176 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.768-27785T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138979669 | ||||||
| chr5:138979801
|
A | G | 2 | a0002c0003t0001g0134a0008c0011t0001g0196 | 2 | HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.768-27917T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138979801 | ||||||
| chr5:138980115
|
A | G | 5 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0019others(2): Show | 5 | HG02145.hp1 HG02615.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.768-28231T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138980115 | ||||||
| chr5:138980246
|
TAAG | T | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.768-28365_768-2836 others(7): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138980246 | ||||||
| chr5:138980298
|
T | A | 1 | a0001c0002t0001g0132 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.768-28414A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138980298 | ||||||
| chr5:138980579
|
G | A | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.768-28695C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138980579 | ||||||
| chr5:138980632
|
T | C | 1 | a0001c0001t0002g0018 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.768-28748A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138980632 | ||||||
| chr5:138980909
|
A | G | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.768-29025T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138980909 | ||||||
| chr5:138980977
|
G | A | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.768-29093C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138980977 | ||||||
| chr5:138981145
|
G | A | 1 | a0001c0002t0001g0004 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.768-29261C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138981145 | ||||||
| chr5:138981169
|
C | T | 4 | a0001c0001t0001g0017a0001c0001t0001g0162a0001c0001t0001g0163others(1): Show | 4 | HG02109.hp2 HG02630.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.768-29285G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138981169 | ||||||
| chr5:138981213
|
CA | C | 102 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(99): Show | 102 | HG00323.hp1 HG00423.hp1 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.768-29330delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138981213 | ||||||
| chr5:138981213
|
CAA | C | 23 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(20): Show | 23 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.768-29331_768-2933 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138981213 | ||||||
| chr5:138981213
|
CAAA | C | 60 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0021others(57): Show | 60 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.768-29332_768-2933 others(7): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138981213 | ||||||
| chr5:138981348
|
A | G | 7 | a0001c0001t0001g0017a0001c0001t0001g0088a0001c0001t0001g0133others(4): Show | 7 | HG01109.hp2 HG01993.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.768-29464T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138981348 | ||||||
| chr5:138981536
|
C | T | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.768-29652G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138981536 | ||||||
| chr5:138981811
|
C | T | 28 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(25): Show | 28 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.768-29927G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138981811 | ||||||
| chr5:138981840
|
T | TC | 5 | a0001c0002t0001g0068a0001c0002t0001g0072a0001c0002t0001g0173others(2): Show | 5 | HG01074.hp1 HG01081.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.768-29957_768-2995 others(5): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138981840 | ||||||
| chr5:138981876
|
A | G | 1 | a0001c0002t0001g0139 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.768-29992T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138981876 | ||||||
| chr5:138982216
|
A | G | 1 | a0001c0001t0001g0041 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.768-30332T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138982216 | ||||||
| chr5:138982301
|
C | T | 13 | a0001c0002t0001g0038a0001c0002t0001g0068a0001c0002t0001g0111others(10): Show | 13 | HG00642.hp2 HG00735.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.768-30417G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138982301 | ||||||
| chr5:138982469
|
G | A | 15 | a0001c0002t0001g0038a0001c0002t0001g0068a0001c0002t0001g0072others(12): Show | 15 | HG00642.hp2 HG01074.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.768-30585C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138982469 | ||||||
| chr5:138982523
|
T | G | 1 | a0001c0001t0001g0063 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.768-30639A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138982523 | ||||||
| chr5:138983077
|
A | T | 1 | a0001c0001t0001g0079 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.768-31193T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138983077 | ||||||
| chr5:138983198
|
CA | C | 107 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0015others(104): Show | 107 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.768-31315delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138983198 | ||||||
| chr5:138983198
|
CAA | C | 11 | a0001c0001t0001g0024a0001c0001t0001g0096a0001c0002t0001g0026others(8): Show | 11 | HG02280.hp1 HG02451.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.768-31316_768-3131 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138983198 | ||||||
| chr5:138983198
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0027 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.768-31329_768-3131 others(19): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138983198 | ||||||
| chr5:138983199
|
A | C | 2 | a0001c0005t0001g0011a0001c0005t0001g0091 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.768-31315T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138983199 | ||||||
| chr5:138983369
|
G | A | 2 | a0001c0002t0001g0113a0001c0002t0001g0144 | 2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.768-31485C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138983369 | ||||||
| chr5:138983423
|
G | A | 1 | a0003c0004t0001g0005 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.768-31539C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138983423 | ||||||
| chr5:138983425
|
G | A | 1 | a0001c0002t0001g0155 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.768-31541C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138983425 | ||||||
| chr5:138983852
|
CT | C | 95 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.768-31969delA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138983852 | ||||||
| chr5:138984126
|
G | T | 75 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(72): Show | 75 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.768-32242C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138984126 | ||||||
| chr5:138984269
|
C | T | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.768-32385G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138984269 | ||||||
| chr5:138984332
|
G | GT | 77 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(74): Show | 77 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.768-32449dupA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138984332 | ||||||
| chr5:138984354
|
G | GT | 14 | a0001c0001t0001g0051a0001c0001t0001g0154a0001c0001t0002g0029others(11): Show | 14 | HG00423.hp2 HG02145.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.768-32471dupA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138984354 | ||||||
| chr5:138984481
|
C | G | 2 | a0001c0001t0001g0149a0006c0009t0001g0157 | 2 | NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.768-32597G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138984481 | ||||||
| chr5:138985096
|
G | A | 1 | a0001c0001t0001g0050 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.768-33212C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138985096 | ||||||
| chr5:138985120
|
C | T | 74 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(71): Show | 74 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.768-33236G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138985120 | ||||||
| chr5:138985182
|
T | A | 3 | a0001c0001t0001g0054a0001c0001t0001g0080a0001c0001t0001g0174 | 3 | NA18964.hp2 NA18965.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.768-33298A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138985182 | ||||||
| chr5:138985416
|
T | G | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.768-33532A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138985416 | ||||||
| chr5:138985431
|
G | A | 6 | a0001c0002t0001g0118a0001c0002t0001g0146a0001c0002t0001g0151others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.768-33547C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138985431 | ||||||
| chr5:138985704
|
C | G | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.768-33820G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138985704 | ||||||
| chr5:138985877
|
A | G | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.768-33993T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138985877 | ||||||
| chr5:138986186
|
C | A | 1 | a0001c0002t0001g0123 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.768-34302G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138986186 | ||||||
| chr5:138986286
|
G | A | 4 | a0001c0001t0001g0086a0001c0001t0001g0177a0001c0001t0001g0180others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.768-34402C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138986286 | ||||||
| chr5:138986500
|
G | A | 4 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0019others(1): Show | 4 | HG02145.hp1 HG02723.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.768-34616C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138986500 | ||||||
| chr5:138986550
|
C | G | 6 | a0002c0003t0001g0034a0002c0003t0001g0134a0002c0003t0001g0160others(3): Show | 6 | HG01891.hp1 HG02615.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.767+34621G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138986550 | ||||||
| chr5:138986850
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.767+34321A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138986850 | ||||||
| chr5:138987017
|
T | C | 1 | a0001c0001t0001g0169 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.767+34154A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138987017 | ||||||
| chr5:138987082
|
A | ATTATT | 71 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(68): Show | 71 | HG00423.hp1 HG01069.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.767+34084_767+3408 others(9): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138987082 | ||||||
| chr5:138987082
|
A | ATTATTTT others(3): Show |
21 | a0001c0001t0001g0042a0001c0001t0001g0149a0001c0001t0002g0140others(18): Show | 21 | HG00735.hp2 HG01070.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.767+34079_767+3408 others(14): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138987082 | ||||||
| chr5:138987082
|
A | ATTATTTT others(8): Show |
2 | a0005c0012t0001g0095a0006c0009t0001g0157 | 2 | HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.767+34074_767+3408 others(19): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138987082 | ||||||
| chr5:138987082
|
ATTATT | A | 18 | a0001c0001t0001g0057a0001c0001t0001g0086a0001c0001t0001g0088others(15): Show | 18 | HG00642.hp2 HG01109.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.767+34084_767+3408 others(9): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138987082 | ||||||
| chr5:138987082
|
ATTATTTT others(8): Show |
A | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.767+34074_767+3408 others(19): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138987082 | ||||||
| chr5:138987276
|
C | T | 1 | a0001c0002t0001g0073 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.767+33895G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138987276 | ||||||
| chr5:138987336
|
C | G | 92 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(89): Show | 92 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.767+33835G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138987336 | ||||||
| chr5:138987349
|
T | C | 1 | a0004c0007t0001g0158 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.767+33822A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138987349 | ||||||
| chr5:138987603
|
A | T | 20 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(17): Show | 20 | HG01884.hp1 HG02055.hp2 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.767+33568T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138987603 | ||||||
| chr5:138987690
|
T | C | 99 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(96): Show | 99 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.767+33481A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138987690 | ||||||
| chr5:138987731
|
CA | C | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.767+33439delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138987731 | ||||||
| chr5:138987911
|
A | G | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.767+33260T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138987911 | ||||||
| chr5:138988125
|
G | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG01070.hp1 HG01071.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.767+33046C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138988125 | ||||||
| chr5:138988182
|
C | T | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.767+32989G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138988182 | ||||||
| chr5:138988237
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.767+32934G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138988237 | ||||||
| chr5:138988259
|
C | T | 1 | a0005c0012t0001g0095 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.767+32912G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138988259 | ||||||
| chr5:138988602
|
T | C | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0171 | 3 | NA18948.hp1 NA18983.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.767+32569A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138988602 | ||||||
| chr5:138988619
|
T | C | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.767+32552A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138988619 | ||||||
| chr5:138988925
|
G | T | 2 | a0002c0003t0001g0034a0002c0003t0001g0161 | 2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.767+32246C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138988925 | ||||||
| chr5:138989005
|
T | C | 2 | a0004c0007t0001g0158a0004c0007t0001g0195 | 2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.767+32166A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138989005 | ||||||
| chr5:138989017
|
A | G | 99 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(96): Show | 99 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.767+32154T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138989017 | ||||||
| chr5:138989064
|
C | G | 1 | a0001c0002t0001g0115 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.767+32107G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138989064 | ||||||
| chr5:138989182
|
A | C | 1 | a0001c0001t0002g0167 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.767+31989T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138989182 | ||||||
| chr5:138989416
|
G | C | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.767+31755C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138989416 | ||||||
| chr5:138989644
|
A | G | 2 | a0001c0002t0001g0113a0001c0002t0001g0144 | 2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.767+31527T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138989644 | ||||||
| chr5:138989664
|
T | C | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.767+31507A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138989664 | ||||||
| chr5:138989755
|
G | A | 1 | a0001c0002t0001g0141 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.767+31416C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138989755 | ||||||
| chr5:138990090
|
C | T | 12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(9): Show | 12 | NA18942.hp1 NA18946.hp2 NA18948.hp1 others(9): Show |
intron_variant | MODIFIER | c.767+31081G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138990090 | ||||||
| chr5:138990164
|
C | G | 1 | a0001c0001t0001g0003 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.767+31007G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138990164 | ||||||
| chr5:138990188
|
G | A | 1 | a0001c0002t0001g0146 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.767+30983C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138990188 | ||||||
| chr5:138990738
|
T | G | 2 | a0001c0001t0001g0162a0001c0002t0001g0028 | 2 | HG02109.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.767+30433A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138990738 | ||||||
| chr5:138990798
|
C | T | 2 | a0001c0001t0001g0162a0001c0002t0001g0028 | 2 | HG02109.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.767+30373G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138990798 | ||||||
| chr5:138990931
|
G | A | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.767+30240C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138990931 | ||||||
| chr5:138991049
|
T | C | 1 | a0002c0003t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.767+30122A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138991049 | ||||||
| chr5:138991232
|
G | C | 1 | a0001c0002t0001g0100 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.767+29939C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138991232 | ||||||
| chr5:138991373
|
T | C | 3 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0084 | 3 | HG02145.hp1 HG02723.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.767+29798A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138991373 | ||||||
| chr5:138991470
|
T | C | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.767+29701A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138991470 | ||||||
| chr5:138991772
|
A | C | 1 | a0002c0006t0001g0097 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.767+29399T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138991772 | ||||||
| chr5:138991911
|
T | C | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.767+29260A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138991911 | ||||||
| chr5:138992609
|
A | C | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.767+28562T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138992609 | ||||||
| chr5:138993078
|
T | C | 2 | a0004c0007t0001g0158a0004c0007t0001g0195 | 2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.767+28093A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138993078 | ||||||
| chr5:138993169
|
C | T | 4 | a0001c0001t0001g0086a0001c0001t0001g0177a0001c0001t0001g0180others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.767+28002G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138993169 | ||||||
| chr5:138993224
|
C | T | 2 | a0001c0002t0001g0099a0001c0002t0001g0101 | 2 | HG01884.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.767+27947G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138993224 | ||||||
| chr5:138993378
|
T | C | 1 | a0001c0002t0001g0120 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.767+27793A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138993378 | ||||||
| chr5:138993430
|
A | G | 99 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(96): Show | 99 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.767+27741T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138993430 | ||||||
| chr5:138993554
|
G | A | 12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(9): Show | 12 | NA18942.hp1 NA18946.hp2 NA18948.hp1 others(9): Show |
intron_variant | MODIFIER | c.767+27617C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138993554 | ||||||
| chr5:138994447
|
T | C | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.767+26724A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138994447 | ||||||
| chr5:138994626
|
G | A | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(3): Show | 6 | HG02257.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.767+26545C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138994626 | ||||||
| chr5:138994643
|
C | A | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.767+26528G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138994643 | ||||||
| chr5:138994744
|
G | T | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.767+26427C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138994744 | ||||||
| chr5:138994753
|
A | G | 9 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.767+26418T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138994753 | ||||||
| chr5:138994840
|
T | C | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.767+26331A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138994840 | ||||||
| chr5:138995250
|
C | CT | 96 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(93): Show | 96 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.767+25920dupA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138995250 | ||||||
| chr5:138995372
|
GT | G | 4 | a0001c0001t0001g0086a0001c0001t0001g0177a0001c0001t0001g0180others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.767+25798delA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138995372 | ||||||
| chr5:138995620
|
C | T | 1 | a0002c0003t0001g0034 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.767+25551G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138995620 | ||||||
| chr5:138995636
|
G | A | 1 | a0001c0002t0001g0176 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.767+25535C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138995636 | ||||||
| chr5:138995737
|
T | C | 1 | a0001c0002t0001g0187 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.767+25434A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138995737 | ||||||
| chr5:138996163
|
C | A | 1 | a0001c0002t0001g0189 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.767+25008G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138996163 | ||||||
| chr5:138996255
|
T | A | 1 | a0001c0002t0001g0068 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.767+24916A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138996255 | ||||||
| chr5:138996355
|
C | T | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.767+24816G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138996355 | ||||||
| chr5:138996513
|
A | AT | 49 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0022others(46): Show | 49 | HG00423.hp1 HG01069.hp1 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.767+24657dupA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138996513 | ||||||
| chr5:138996513
|
A | ATT | 9 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0027others(6): Show | 9 | HG01071.hp1 HG01993.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.767+24656_767+2465 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138996513 | ||||||
| chr5:138996513
|
AT | A | 15 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(12): Show | 15 | HG01069.hp2 HG02257.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.767+24657delA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138996513 | ||||||
| chr5:138996667
|
G | A | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.767+24504C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138996667 | ||||||
| chr5:138996676
|
C | A | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.767+24495G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138996676 | ||||||
| chr5:138996676
|
C | T | 2 | a0002c0003t0001g0134a0002c0003t0001g0160 | 2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.767+24495G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138996676 | ||||||
| chr5:138996732
|
A | G | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.767+24439T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138996732 | ||||||
| chr5:138996777
|
C | T | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.767+24394G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138996777 | ||||||
| chr5:138996913
|
G | C | 1 | a0002c0003t0001g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.767+24258C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138996913 | ||||||
| chr5:138997347
|
G | A | 2 | a0001c0001t0001g0162a0001c0002t0001g0028 | 2 | HG02109.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.767+23824C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138997347 | ||||||
| chr5:138997441
|
G | A | 6 | a0002c0003t0001g0034a0002c0003t0001g0134a0002c0003t0001g0160others(3): Show | 6 | HG01891.hp1 HG02615.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.767+23730C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138997441 | ||||||
| chr5:138997472
|
G | A | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.767+23699C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138997472 | ||||||
| chr5:138997524
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.767+23647A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138997524 | ||||||
| chr5:138997704
|
G | A | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.767+23467C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138997704 | ||||||
| chr5:138997791
|
T | C | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.767+23380A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138997791 | ||||||
| chr5:138997975
|
T | C | 95 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.767+23196A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138997975 | ||||||
| chr5:138998095
|
G | A | 81 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(78): Show | 81 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.767+23076C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138998095 | ||||||
| chr5:138998116
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.767+23055A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138998116 | ||||||
| chr5:138998137
|
C | T | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(3): Show | 6 | HG02257.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.767+23034G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138998137 | ||||||
| chr5:138998320
|
A | G | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.767+22851T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138998320 | ||||||
| chr5:138998380
|
C | A | 75 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(72): Show | 75 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.767+22791G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138998380 | ||||||
| chr5:138998550
|
C | T | 23 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(20): Show | 23 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.767+22621G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138998550 | ||||||
| chr5:138998852
|
C | CT | 11 | a0001c0001t0001g0015a0001c0001t0001g0088a0001c0001t0001g0133others(8): Show | 11 | HG00423.hp1 HG01109.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.767+22318dupA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138998852 | ||||||
| chr5:138998852
|
CT | C | 5 | a0001c0001t0001g0013a0001c0001t0001g0037a0001c0001t0001g0149others(2): Show | 5 | HG00323.hp1 NA18981.hp2 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.767+22318delA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138998852 | ||||||
| chr5:138998852
|
CTTT | C | 86 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(83): Show | 86 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.767+22316_767+2231 others(7): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138998852 | ||||||
| chr5:138998881
|
A | C | 2 | a0001c0002t0001g0006a0001c0002t0001g0010 | 2 | HG02723.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.767+22290T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138998881 | ||||||
| chr5:138999014
|
G | A | 1 | a0001c0002t0001g0100 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.767+22157C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138999014 | ||||||
| chr5:138999209
|
C | A | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.767+21962G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138999209 | ||||||
| chr5:138999317
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.767+21854C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138999317 | ||||||
| chr5:138999669
|
T | C | 3 | a0001c0001t0001g0054a0001c0001t0001g0080a0001c0001t0001g0174 | 3 | NA18964.hp2 NA18965.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.767+21502A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138999669 | ||||||
| chr5:138999723
|
C | T | 3 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0001t0001g0172 | 3 | HG01081.hp1 HG03710.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.767+21448G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 138999723 | ||||||
| chr5:139000115
|
C | G | 1 | a0001c0002t0001g0150 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.767+21056G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139000115 | ||||||
| chr5:139000236
|
T | C | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.767+20935A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139000236 | ||||||
| chr5:139000448
|
A | C | 1 | a0001c0001t0001g0061 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.767+20723T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139000448 | ||||||
| chr5:139000683
|
T | C | 1 | a0001c0001t0001g0013 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.767+20488A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139000683 | ||||||
| chr5:139000889
|
C | A | 1 | a0001c0001t0001g0009 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.767+20282G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139000889 | ||||||
| chr5:139001081
|
T | G | 6 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0001t0001g0088others(3): Show | 6 | HG01081.hp1 HG01109.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.767+20090A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139001081 | ||||||
| chr5:139001083
|
G | T | 7 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0162others(4): Show | 7 | HG01109.hp2 HG01993.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.767+20088C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139001083 | ||||||
| chr5:139001130
|
CA | C | 6 | a0002c0003t0001g0034a0002c0003t0001g0134a0002c0003t0001g0160others(3): Show | 6 | HG01891.hp1 HG02615.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.767+20040delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139001130 | ||||||
| chr5:139001628
|
C | T | 1 | a0001c0002t0001g0143 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.767+19543G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139001628 | ||||||
| chr5:139001828
|
C | A | 1 | a0001c0001t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.767+19343G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139001828 | ||||||
| chr5:139001962
|
G | A | 3 | a0001c0002t0001g0038a0001c0002t0001g0115a0001c0002t0001g0119 | 3 | HG01496.hp1 HG03017.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.767+19209C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139001962 | ||||||
| chr5:139002008
|
C | T | 98 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(95): Show | 98 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.767+19163G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139002008 | ||||||
| chr5:139002163
|
T | C | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.767+19008A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139002163 | ||||||
| chr5:139002165
|
A | G | 99 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(96): Show | 99 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.767+19006T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139002165 | ||||||
| chr5:139002271
|
T | A | 99 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(96): Show | 99 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.767+18900A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139002271 | ||||||
| chr5:139002475
|
T | A | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.767+18696A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139002475 | ||||||
| chr5:139003174
|
G | C | 1 | a0001c0001t0001g0047 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.767+17997C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139003174 | ||||||
| chr5:139003514
|
T | C | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.767+17657A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139003514 | ||||||
| chr5:139003725
|
T | C | 1 | a0001c0002t0001g0104 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.767+17446A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139003725 | ||||||
| chr5:139003842
|
T | G | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.767+17329A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139003842 | ||||||
| chr5:139004368
|
G | A | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.767+16803C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139004368 | ||||||
| chr5:139004433
|
G | T | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.767+16738C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139004433 | ||||||
| chr5:139004547
|
T | A | 2 | a0004c0007t0001g0158a0004c0007t0001g0195 | 2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.767+16624A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139004547 | ||||||
| chr5:139004658
|
G | C | 1 | a0001c0005t0001g0091 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.767+16513C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139004658 | ||||||
| chr5:139004760
|
G | A | 192 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(189): Show | 192 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.767+16411C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139004760 | ||||||
| chr5:139004846
|
A | T | 1 | a0001c0002t0001g0156 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.767+16325T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139004846 | ||||||
| chr5:139004877
|
T | A | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.767+16294A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139004877 | ||||||
| chr5:139005205
|
T | C | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.767+15966A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139005205 | ||||||
| chr5:139005246
|
G | C | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.767+15925C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139005246 | ||||||
| chr5:139005247
|
TAAAA | T | 75 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(72): Show | 75 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.767+15920_767+1592 others(8): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139005247 | ||||||
| chr5:139005287
|
T | C | 98 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(95): Show | 98 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.767+15884A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139005287 | ||||||
| chr5:139005357
|
T | A | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.767+15814A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139005357 | ||||||
| chr5:139005412
|
A | G | 1 | a0001c0002t0001g0104 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.767+15759T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139005412 | ||||||
| chr5:139005433
|
T | G | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.767+15738A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139005433 | ||||||
| chr5:139005454
|
CT | C | 14 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(11): Show | 14 | HG01975.hp2 HG01981.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.767+15716delA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139005454 | ||||||
| chr5:139005464
|
T | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0197 | 2 | HG00423.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.767+15707A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139005464 | ||||||
| chr5:139005547
|
G | A | 75 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(72): Show | 75 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.767+15624C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139005547 | ||||||
| chr5:139005559
|
A | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(93): Show | 96 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.767+15612T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139005559 | ||||||
| chr5:139005567
|
G | A | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.767+15604C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139005567 | ||||||
| chr5:139005601
|
C | G | 1 | a0001c0001t0001g0062 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.767+15570G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139005601 | ||||||
| chr5:139005609
|
C | G | 1 | a0001c0001t0001g0149 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.767+15562G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139005609 | ||||||
| chr5:139005722
|
G | A | 11 | a0001c0001t0002g0165a0001c0001t0002g0167a0001c0002t0001g0004others(8): Show | 11 | HG01258.hp1 HG02109.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.767+15449C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139005722 | ||||||
| chr5:139005758
|
C | T | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.767+15413G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139005758 | ||||||
| chr5:139005875
|
C | T | 1 | a0001c0002t0001g0123 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.767+15296G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139005875 | ||||||
| chr5:139005905
|
A | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.767+15266T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139005905 | ||||||
| chr5:139005917
|
A | G | 98 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(95): Show | 98 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.767+15254T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139005917 | ||||||
| chr5:139005950
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.767+15221A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139005950 | ||||||
| chr5:139005952
|
A | C | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.767+15219T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139005952 | ||||||
| chr5:139005966
|
C | G | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.767+15205G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139005966 | ||||||
| chr5:139006081
|
T | C | 4 | a0001c0002t0001g0110a0001c0002t0001g0136a0001c0002t0001g0141others(1): Show | 4 | HG00323.hp1 HG03710.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.767+15090A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139006081 | ||||||
| chr5:139006219
|
T | C | 2 | a0001c0001t0001g0046a0001c0001t0001g0168 | 2 | HG01346.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.767+14952A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139006219 | ||||||
| chr5:139006279
|
C | T | 1 | a0001c0002t0001g0142 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.767+14892G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139006279 | ||||||
| chr5:139006378
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.767+14793C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139006378 | ||||||
| chr5:139006511
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.767+14660C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139006511 | ||||||
| chr5:139006530
|
C | T | 2 | a0002c0006t0001g0097a0002c0006t0001g0103 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.767+14641G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139006530 | ||||||
| chr5:139006592
|
A | C | 6 | a0002c0003t0001g0034a0002c0003t0001g0134a0002c0003t0001g0160others(3): Show | 6 | HG01891.hp1 HG02615.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.767+14579T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139006592 | ||||||
| chr5:139006628
|
A | G | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.767+14543T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139006628 | ||||||
| chr5:139006777
|
C | T | 1 | a0002c0003t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.767+14394G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139006777 | ||||||
| chr5:139006842
|
A | T | 3 | a0001c0002t0001g0073a0001c0002t0001g0124a0001c0002t0001g0182 | 3 | HG02698.hp2 HG03942.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.767+14329T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139006842 | ||||||
| chr5:139007067
|
T | C | 98 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(95): Show | 98 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.767+14104A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139007067 | ||||||
| chr5:139007076
|
T | G | 1 | a0001c0002t0001g0175 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.767+14095A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139007076 | ||||||
| chr5:139007093
|
C | T | 1 | a0002c0003t0001g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.767+14078G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139007093 | ||||||
| chr5:139007142
|
G | C | 1 | a0002c0003t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.767+14029C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139007142 | ||||||
| chr5:139007145
|
T | G | 2 | a0001c0001t0001g0056a0001c0002t0001g0084 | 2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.767+14026A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139007145 | ||||||
| chr5:139007177
|
T | A | 97 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(94): Show | 97 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.767+13994A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139007177 | ||||||
| chr5:139007261
|
T | C | 1 | a0001c0001t0001g0059 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.767+13910A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139007261 | ||||||
| chr5:139007263
|
T | C | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.767+13908A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139007263 | ||||||
| chr5:139007269
|
G | A | 1 | a0006c0009t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.767+13902C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139007269 | ||||||
| chr5:139007369
|
A | G | 2 | a0003c0004t0001g0005a0003c0004t0001g0164 | 2 | HG02280.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.767+13802T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139007369 | ||||||
| chr5:139007384
|
T | C | 92 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(89): Show | 92 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.767+13787A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139007384 | ||||||
| chr5:139007399
|
T | C | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.767+13772A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139007399 | ||||||
| chr5:139007458
|
T | C | 98 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(95): Show | 98 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.767+13713A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139007458 | ||||||
| chr5:139007655
|
G | C | 1 | a0001c0002t0001g0117 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.767+13516C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139007655 | ||||||
| chr5:139007665
|
C | T | 92 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(89): Show | 92 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.767+13506G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139007665 | ||||||
| chr5:139007850
|
G | A | 2 | a0001c0002t0001g0114a0001c0002t0001g0122 | 2 | HG00423.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.767+13321C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139007850 | ||||||
| chr5:139007876
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.767+13295T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139007876 | ||||||
| chr5:139007884
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.767+13287A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139007884 | ||||||
| chr5:139008116
|
T | C | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.767+13055A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139008116 | ||||||
| chr5:139008138
|
C | A | 4 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0019others(1): Show | 4 | HG02145.hp1 HG02723.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.767+13033G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139008138 | ||||||
| chr5:139008139
|
T | G | 4 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0019others(1): Show | 4 | HG02145.hp1 HG02723.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.767+13032A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139008139 | ||||||
| chr5:139008157
|
A | C | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.767+13014T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139008157 | ||||||
| chr5:139008218
|
A | G | 1 | a0001c0002t0001g0136 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.767+12953T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139008218 | ||||||
| chr5:139008470
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.767+12701C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139008470 | ||||||
| chr5:139008477
|
A | T | 98 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(95): Show | 98 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.767+12694T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139008477 | ||||||
| chr5:139008636
|
C | T | 4 | a0001c0001t0001g0086a0001c0001t0001g0177a0001c0001t0001g0180others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.767+12535G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139008636 | ||||||
| chr5:139008637
|
G | A | 2 | a0001c0002t0001g0108a0001c0002t0001g0145 | 2 | NA18983.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.767+12534C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139008637 | ||||||
| chr5:139008751
|
C | T | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.767+12420G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139008751 | ||||||
| chr5:139008805
|
G | C | 2 | a0004c0007t0001g0158a0004c0007t0001g0195 | 2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.767+12366C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139008805 | ||||||
| chr5:139008812
|
C | T | 1 | a0001c0002t0001g0070 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.767+12359G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139008812 | ||||||
| chr5:139008902
|
T | C | 1 | a0001c0001t0001g0069 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.767+12269A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139008902 | ||||||
| chr5:139009050
|
T | G | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.767+12121A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139009050 | ||||||
| chr5:139009220
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.767+11951G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139009220 | ||||||
| chr5:139009267
|
A | C | 2 | a0001c0002t0001g0114a0001c0002t0001g0122 | 2 | HG00423.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.767+11904T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139009267 | ||||||
| chr5:139009423
|
C | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0107a0001c0001t0001g0152others(1): Show | 4 | NA18959.hp2 NA18963.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.767+11748G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139009423 | ||||||
| chr5:139009456
|
A | G | 1 | a0001c0010t0001g0064 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.767+11715T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139009456 | ||||||
| chr5:139009463
|
T | C | 2 | a0001c0001t0002g0029a0001c0001t0002g0093 | 2 | NA18961.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.767+11708A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139009463 | ||||||
| chr5:139009568
|
T | C | 1 | a0001c0001t0003g0001 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.767+11603A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139009568 | ||||||
| chr5:139009592
|
G | A | 1 | a0001c0002t0001g0132 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.767+11579C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139009592 | ||||||
| chr5:139009601
|
T | C | 1 | a0002c0003t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.767+11570A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139009601 | ||||||
| chr5:139010435
|
G | C | 2 | a0001c0001t0001g0046a0001c0001t0001g0168 | 2 | HG01346.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.767+10736C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139010435 | ||||||
| chr5:139010526
|
G | A | 1 | a0001c0002t0001g0153 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.767+10645C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139010526 | ||||||
| chr5:139010535
|
C | T | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.767+10636G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139010535 | ||||||
| chr5:139010817
|
G | C | 24 | a0001c0002t0001g0065a0001c0002t0001g0070a0001c0002t0001g0073others(21): Show | 24 | HG00423.hp1 HG00735.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.767+10354C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139010817 | ||||||
| chr5:139010903
|
C | T | 1 | a0001c0002t0001g0153 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.767+10268G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139010903 | ||||||
| chr5:139011061
|
C | A | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.767+10110G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139011061 | ||||||
| chr5:139011092
|
C | T | 2 | a0001c0001t0001g0149a0006c0009t0001g0157 | 2 | NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.767+10079G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139011092 | ||||||
| chr5:139011098
|
T | G | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.767+10073A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139011098 | ||||||
| chr5:139011102
|
A | T | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.767+10069T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139011102 | ||||||
| chr5:139011131
|
A | G | 2 | a0001c0001t0002g0165a0001c0001t0002g0167 | 2 | HG01258.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.767+10040T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139011131 | ||||||
| chr5:139011233
|
C | T | 1 | a0001c0001t0001g0013 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.767+9938G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139011233 | ||||||
| chr5:139011234
|
G | A | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.767+9937C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139011234 | ||||||
| chr5:139011246
|
T | G | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.767+9925A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139011246 | ||||||
| chr5:139011272
|
C | T | 1 | a0001c0002t0001g0132 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.767+9899G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139011272 | ||||||
| chr5:139011276
|
C | T | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.767+9895G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139011276 | ||||||
| chr5:139011283
|
C | G | 1 | a0001c0001t0001g0027 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.767+9888G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139011283 | ||||||
| chr5:139011324
|
C | G | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.767+9847G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139011324 | ||||||
| chr5:139011575
|
C | A | 1 | a0004c0007t0001g0158 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.767+9596G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139011575 | ||||||
| chr5:139011829
|
A | G | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.767+9342T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139011829 | ||||||
| chr5:139012541
|
C | T | 1 | a0004c0007t0001g0158 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.767+8630G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139012541 | ||||||
| chr5:139012722
|
C | T | 1 | a0001c0002t0001g0187 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.767+8449G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139012722 | ||||||
| chr5:139013185
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.767+7986A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139013185 | ||||||
| chr5:139013331
|
C | T | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.767+7840G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139013331 | ||||||
| chr5:139013475
|
G | A | 72 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(69): Show | 72 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.767+7696C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139013475 | ||||||
| chr5:139013584
|
TA | T | 91 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(88): Show | 91 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(88): Show |
intron_variant | MODIFIER | c.767+7586delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139013584 | ||||||
| chr5:139013710
|
G | T | 3 | a0001c0005t0001g0007a0001c0005t0001g0011a0001c0005t0001g0091 | 3 | HG01243.hp1 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.767+7461C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139013710 | ||||||
| chr5:139013771
|
G | A | 1 | a0001c0001t0002g0093 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.767+7400C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139013771 | ||||||
| chr5:139014367
|
CA | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(93): Show | 96 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.767+6803delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139014367 | ||||||
| chr5:139014479
|
AG | A | 3 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0083 | 3 | HG01069.hp1 HG01071.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.767+6691delC | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139014479 | ||||||
| chr5:139014687
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.767+6484A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139014687 | ||||||
| chr5:139014942
|
C | T | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.767+6229G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139014942 | ||||||
| chr5:139015164
|
G | C | 1 | a0001c0002t0001g0148 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.767+6007C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139015164 | ||||||
| chr5:139015515
|
C | T | 1 | a0001c0002t0001g0010 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.767+5656G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139015515 | ||||||
| chr5:139015700
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.767+5471C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139015700 | ||||||
| chr5:139015891
|
T | C | 11 | a0001c0002t0001g0065a0001c0002t0001g0070a0001c0002t0001g0073others(8): Show | 11 | HG00423.hp1 HG01069.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.767+5280A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139015891 | ||||||
| chr5:139016061
|
G | A | 1 | a0001c0002t0001g0186 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.767+5110C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139016061 | ||||||
| chr5:139016313
|
T | G | 1 | a0001c0001t0001g0013 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.767+4858A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139016313 | ||||||
| chr5:139016670
|
G | C | 11 | a0001c0002t0001g0065a0001c0002t0001g0070a0001c0002t0001g0073others(8): Show | 11 | HG00423.hp1 HG01069.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.767+4501C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139016670 | ||||||
| chr5:139016715
|
AAGTACTC others(18): Show |
A | 3 | a0001c0002t0001g0073a0001c0002t0001g0124a0001c0002t0001g0182 | 3 | HG02698.hp2 HG03942.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.767+4431_767+4455d others(27): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139016715 | ||||||
| chr5:139016722
|
C | A | 4 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0019others(1): Show | 4 | HG02145.hp1 HG02723.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.767+4449G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139016722 | ||||||
| chr5:139016859
|
T | C | 1 | a0001c0002t0001g0038 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.767+4312A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139016859 | ||||||
| chr5:139016866
|
T | C | 124 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(121): Show | 124 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(121): Show |
intron_variant | MODIFIER | c.767+4305A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139016866 | ||||||
| chr5:139016974
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.767+4197C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139016974 | ||||||
| chr5:139017087
|
C | A | 94 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(91): Show | 94 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.767+4084G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139017087 | ||||||
| chr5:139017748
|
C | G | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.767+3423G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139017748 | ||||||
| chr5:139017901
|
G | A | 1 | a0001c0002t0001g0108 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.767+3270C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139017901 | ||||||
| chr5:139018040
|
G | A | 1 | a0006c0009t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.767+3131C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139018040 | ||||||
| chr5:139018338
|
A | G | 99 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(96): Show | 99 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.767+2833T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139018338 | ||||||
| chr5:139018386
|
G | A | 95 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.767+2785C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139018386 | ||||||
| chr5:139018534
|
G | A | 1 | a0002c0003t0001g0034 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.767+2637C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139018534 | ||||||
| chr5:139018590
|
C | CA | 9 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0021others(6): Show | 9 | HG00423.hp1 HG02145.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.767+2580dupT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139018590 | ||||||
| chr5:139018590
|
C | CAA | 22 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0022others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.767+2579_767+2580d others(4): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139018590 | ||||||
| chr5:139018590
|
CA | C | 50 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(47): Show | 50 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.767+2580delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139018590 | ||||||
| chr5:139018979
|
G | C | 1 | a0001c0001t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.767+2192C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139018979 | ||||||
| chr5:139019143
|
G | A | 3 | a0003c0004t0001g0005a0003c0004t0001g0138a0003c0004t0001g0164 | 3 | HG02280.hp2 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.767+2028C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139019143 | ||||||
| chr5:139019501
|
TA | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0174 | 2 | NA18965.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.767+1669delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139019501 | ||||||
| chr5:139019622
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.767+1549G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139019622 | ||||||
| chr5:139019660
|
G | A | 1 | a0001c0005t0001g0011 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.767+1511C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139019660 | ||||||
| chr5:139019756
|
C | T | 198 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(195): Show | 198 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.767+1415G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139019756 | ||||||
| chr5:139019923
|
CT | C | 55 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(52): Show | 55 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.767+1247delA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139019923 | ||||||
| chr5:139020182
|
G | A | 94 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(91): Show | 94 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.767+989C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139020182 | ||||||
| chr5:139020274
|
G | T | 98 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(95): Show | 98 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.767+897C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139020274 | ||||||
| chr5:139020718
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.767+453C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139020718 | ||||||
| chr5:139020976
|
CAG | C | 2 | a0001c0002t0001g0099a0001c0002t0001g0101 | 2 | HG01884.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.767+193_767+194del others(2): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139020976 | ||||||
| chr5:139021067
|
G | A | 94 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(91): Show | 94 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.767+104C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139021067 | ||||||
| chr5:139021086
|
C | A | 126 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(123): Show | 126 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(123): Show |
intron_variant | MODIFIER | c.767+85G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139021086 | ||||||
| chr5:139021164
|
T | C | 1 | a0001c0002t0001g0182 | 1 | HG02698.hp2 | splice_region_variant&intron_variant | LOW | c.767+7A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 7/9 | chr5 | 139021164 | ||||||
| chr5:139021404
|
T | G | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.646-112A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139021404 | ||||||
| chr5:139021522
|
A | G | 126 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(123): Show | 126 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(123): Show |
intron_variant | MODIFIER | c.646-230T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139021522 | ||||||
| chr5:139021776
|
C | T | 2 | a0001c0002t0001g0006a0001c0002t0001g0010 | 2 | HG02723.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.646-484G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139021776 | ||||||
| chr5:139021777
|
G | A | 1 | a0001c0002t0001g0146 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.646-485C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139021777 | ||||||
| chr5:139021853
|
C | A | 1 | a0001c0001t0001g0149 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.646-561G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139021853 | ||||||
| chr5:139021886
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.646-594T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139021886 | ||||||
| chr5:139021889
|
G | A | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.646-597C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139021889 | ||||||
| chr5:139021926
|
G | C | 1 | a0001c0002t0001g0104 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.646-634C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139021926 | ||||||
| chr5:139021993
|
T | C | 10 | a0001c0002t0001g0106a0001c0002t0001g0130a0001c0002t0001g0135others(7): Show | 10 | HG00735.hp2 HG02071.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.646-701A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139021993 | ||||||
| chr5:139022073
|
C | T | 1 | a0001c0002t0001g0108 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.646-781G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139022073 | ||||||
| chr5:139022088
|
C | T | 1 | a0001c0002t0001g0065 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.646-796G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139022088 | ||||||
| chr5:139022135
|
C | T | 1 | a0001c0002t0001g0127 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.646-843G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139022135 | ||||||
| chr5:139022204
|
G | A | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.646-912C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139022204 | ||||||
| chr5:139022569
|
G | C | 2 | a0004c0007t0001g0158a0004c0007t0001g0195 | 2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.646-1277C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139022569 | ||||||
| chr5:139022659
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.646-1367C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139022659 | ||||||
| chr5:139022830
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.646-1538C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139022830 | ||||||
| chr5:139023400
|
G | GT | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.646-2109_646-2108i others(3): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139023400 | ||||||
| chr5:139023402
|
A | C | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.646-2110T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139023402 | ||||||
| chr5:139023403
|
A | C | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.646-2111T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139023403 | ||||||
| chr5:139023404
|
A | C | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.646-2112T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139023404 | ||||||
| chr5:139023405
|
G | T | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.646-2113C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139023405 | ||||||
| chr5:139023406
|
A | G | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.646-2114T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139023406 | ||||||
| chr5:139023407
|
A | C | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.646-2115T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139023407 | ||||||
| chr5:139023408
|
G | T | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.646-2116C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139023408 | ||||||
| chr5:139023409
|
C | T | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.646-2117G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139023409 | ||||||
| chr5:139023410
|
A | C | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.646-2118T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139023410 | ||||||
| chr5:139023483
|
C | T | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.646-2191G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139023483 | ||||||
| chr5:139023494
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.646-2202C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139023494 | ||||||
| chr5:139023499
|
T | G | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.646-2207A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139023499 | ||||||
| chr5:139023712
|
T | C | 1 | a0001c0002t0001g0155 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.646-2420A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139023712 | ||||||
| chr5:139024374
|
C | G | 1 | a0001c0001t0001g0027 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.645+2427G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139024374 | ||||||
| chr5:139024399
|
G | A | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.645+2402C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139024399 | ||||||
| chr5:139024824
|
C | A | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.645+1977G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139024824 | ||||||
| chr5:139024889
|
T | C | 55 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(52): Show | 55 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.645+1912A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139024889 | ||||||
| chr5:139025172
|
CTTGAT | C | 6 | a0002c0003t0001g0034a0002c0003t0001g0134a0002c0003t0001g0160others(3): Show | 6 | HG01891.hp1 HG02615.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.645+1624_645+1628d others(7): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139025172 | ||||||
| chr5:139025446
|
C | T | 94 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(91): Show | 94 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.645+1355G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139025446 | ||||||
| chr5:139025492
|
G | A | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.645+1309C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139025492 | ||||||
| chr5:139025669
|
G | A | 98 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(95): Show | 98 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.645+1132C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139025669 | ||||||
| chr5:139026040
|
A | G | 1 | a0001c0001t0002g0093 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.645+761T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139026040 | ||||||
| chr5:139026495
|
C | G | 6 | a0002c0003t0001g0034a0002c0003t0001g0134a0002c0003t0001g0160others(3): Show | 6 | HG01891.hp1 HG02615.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.645+306G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139026495 | ||||||
| chr5:139026558
|
G | C | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.645+243C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139026558 | ||||||
| chr5:139026594
|
C | T | 95 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.645+207G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139026594 | ||||||
| chr5:139026767
|
A | G | 3 | a0001c0001t0001g0159a0001c0002t0001g0099a0001c0002t0001g0101 | 3 | HG01884.hp1 HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.645+34T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 6/9 | chr5 | 139026767 | ||||||
| chr5:139026998
|
G | A | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | splice_region_variant&intron_variant | LOW | c.454-6C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139026998 | ||||||
| chr5:139027128
|
A | C | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.454-136T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139027128 | ||||||
| chr5:139027479
|
A | G | 5 | a0001c0001t0001g0049a0001c0001t0001g0053a0001c0001t0001g0058others(2): Show | 5 | NA18945.hp2 NA18968.hp2 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.454-487T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139027479 | ||||||
| chr5:139027554
|
T | C | 2 | a0002c0003t0001g0034a0002c0003t0001g0161 | 2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.454-562A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139027554 | ||||||
| chr5:139028066
|
A | G | 2 | a0004c0007t0001g0158a0004c0007t0001g0195 | 2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.454-1074T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139028066 | ||||||
| chr5:139028109
|
A | G | 1 | a0002c0003t0001g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.454-1117T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139028109 | ||||||
| chr5:139028162
|
A | C | 95 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.454-1170T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139028162 | ||||||
| chr5:139028187
|
CAAG | C | 2 | a0002c0003t0001g0134a0002c0003t0001g0160 | 2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.454-1198_454-1196d others(5): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139028187 | ||||||
| chr5:139028342
|
A | G | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.454-1350T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139028342 | ||||||
| chr5:139028355
|
G | A | 94 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(91): Show | 94 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.454-1363C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139028355 | ||||||
| chr5:139028391
|
G | A | 55 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(52): Show | 55 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.454-1399C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139028391 | ||||||
| chr5:139028462
|
C | T | 1 | a0001c0002t0001g0065 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.454-1470G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139028462 | ||||||
| chr5:139028495
|
C | CACAAA | 7 | a0001c0002t0001g0070a0001c0002t0001g0084a0001c0002t0001g0116others(4): Show | 7 | HG01069.hp2 HG02145.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.454-1508_454-1504d others(7): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139028495 | ||||||
| chr5:139028495
|
CACAAA | C | 29 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0177others(26): Show | 29 | HG00642.hp2 HG01074.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.454-1508_454-1504d others(7): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139028495 | ||||||
| chr5:139028495
|
CACAAAAC others(3): Show |
C | 29 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(26): Show | 29 | HG01346.hp1 HG01891.hp1 HG02258.hp1 others(26): Show |
intron_variant | MODIFIER | c.454-1513_454-1504d others(12): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139028495 | ||||||
| chr5:139028495
|
CACAAAAC others(8): Show |
C | 86 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(83): Show | 86 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.454-1518_454-1504d others(17): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139028495 | ||||||
| chr5:139028495
|
CACAAAAC others(13): Show |
C | 1 | a0002c0006t0001g0103 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.454-1523_454-1504d others(22): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139028495 | ||||||
| chr5:139028705
|
T | C | 55 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(52): Show | 55 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.454-1713A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139028705 | ||||||
| chr5:139028993
|
G | A | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.454-2001C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139028993 | ||||||
| chr5:139029009
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(93): Show | 96 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.454-2017A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139029009 | ||||||
| chr5:139029122
|
A | T | 1 | a0001c0001t0001g0048 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.454-2130T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139029122 | ||||||
| chr5:139029576
|
G | A | 1 | a0001c0002t0001g0100 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.454-2584C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139029576 | ||||||
| chr5:139029601
|
A | C | 1 | a0001c0001t0001g0166 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.454-2609T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139029601 | ||||||
| chr5:139029801
|
G | T | 98 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(95): Show | 98 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.454-2809C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139029801 | ||||||
| chr5:139030037
|
C | T | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.454-3045G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139030037 | ||||||
| chr5:139030202
|
C | T | 1 | a0003c0004t0001g0005 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.454-3210G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139030202 | ||||||
| chr5:139030658
|
T | G | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.454-3666A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139030658 | ||||||
| chr5:139030658
|
T | TG | 6 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0031others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.454-3667dupC | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139030658 | ||||||
| chr5:139030705
|
C | T | 1 | a0001c0001t0005g0199 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.454-3713G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139030705 | ||||||
| chr5:139030794
|
G | A | 1 | a0001c0002t0001g0104 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.454-3802C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139030794 | ||||||
| chr5:139030829
|
C | T | 11 | a0001c0001t0002g0165a0001c0001t0002g0167a0001c0002t0001g0004others(8): Show | 11 | HG01258.hp1 HG02109.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.454-3837G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139030829 | ||||||
| chr5:139030850
|
C | G | 126 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(123): Show | 126 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(123): Show |
intron_variant | MODIFIER | c.454-3858G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139030850 | ||||||
| chr5:139030919
|
C | T | 2 | a0002c0006t0001g0097a0002c0006t0001g0103 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.454-3927G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139030919 | ||||||
| chr5:139031376
|
T | G | 1 | a0001c0001t0001g0015 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.454-4384A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139031376 | ||||||
| chr5:139031609
|
T | C | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.454-4617A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139031609 | ||||||
| chr5:139031718
|
G | A | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.454-4726C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139031718 | ||||||
| chr5:139032355
|
G | A | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.454-5363C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139032355 | ||||||
| chr5:139032482
|
G | A | 2 | a0004c0007t0001g0158a0004c0007t0001g0195 | 2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.454-5490C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139032482 | ||||||
| chr5:139032741
|
G | A | 1 | a0001c0002t0001g0110 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.454-5749C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139032741 | ||||||
| chr5:139033024
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.454-6032G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139033024 | ||||||
| chr5:139033477
|
C | A | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.454-6485G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139033477 | ||||||
| chr5:139033575
|
T | A | 1 | a0001c0001t0001g0163 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.454-6583A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139033575 | ||||||
| chr5:139033880
|
G | A | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.454-6888C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139033880 | ||||||
| chr5:139034913
|
A | G | 4 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0019others(1): Show | 4 | HG02145.hp1 HG02723.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.453+7707T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139034913 | ||||||
| chr5:139035152
|
C | G | 1 | a0001c0002t0001g0175 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.453+7468G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139035152 | ||||||
| chr5:139035427
|
G | A | 96 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(93): Show | 96 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.453+7193C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139035427 | ||||||
| chr5:139035642
|
C | CT | 45 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0021others(42): Show | 45 | HG01069.hp1 HG01243.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.453+6977dupA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139035642 | ||||||
| chr5:139035642
|
C | CTT | 18 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(15): Show | 18 | HG01109.hp2 HG01993.hp1 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.453+6976_453+6977d others(4): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139035642 | ||||||
| chr5:139035642
|
CT | C | 7 | a0001c0001t0001g0049a0001c0001t0001g0071a0001c0001t0001g0197others(4): Show | 7 | HG01069.hp2 HG02071.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.453+6977delA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139035642 | ||||||
| chr5:139035676
|
C | G | 99 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(96): Show | 99 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.453+6944G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139035676 | ||||||
| chr5:139035688
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.453+6932G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139035688 | ||||||
| chr5:139035789
|
C | T | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.453+6831G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139035789 | ||||||
| chr5:139035793
|
C | T | 1 | a0001c0002t0001g0178 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.453+6827G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139035793 | ||||||
| chr5:139035923
|
A | G | 2 | a0001c0002t0001g0113a0001c0002t0001g0144 | 2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.453+6697T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139035923 | ||||||
| chr5:139036113
|
G | T | 2 | a0001c0002t0001g0148a0001c0002t0001g0178 | 2 | NA18961.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.453+6507C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139036113 | ||||||
| chr5:139036210
|
C | T | 52 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(49): Show | 52 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.453+6410G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139036210 | ||||||
| chr5:139036291
|
AG | A | 2 | a0001c0001t0001g0147a0001c0001t0006g0200 | 2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.453+6328delC | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139036291 | ||||||
| chr5:139036452
|
C | T | 2 | a0001c0002t0001g0114a0001c0002t0001g0122 | 2 | HG00423.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.453+6168G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139036452 | ||||||
| chr5:139036656
|
C | T | 95 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.453+5964G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139036656 | ||||||
| chr5:139036745
|
C | T | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.453+5875G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139036745 | ||||||
| chr5:139036991
|
G | A | 2 | a0001c0001t0002g0029a0001c0001t0002g0093 | 2 | NA18961.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.453+5629C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139036991 | ||||||
| chr5:139036994
|
TATCCTTT others(4): Show |
T | 52 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(49): Show | 52 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.453+5615_453+5625d others(13): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139036994 | ||||||
| chr5:139037076
|
C | T | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.453+5544G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139037076 | ||||||
| chr5:139037100
|
C | T | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.453+5520G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139037100 | ||||||
| chr5:139037106
|
T | TAAAATTC others(1092): Show |
2 | a0001c0001t0001g0023a0001c0001t0001g0094 | 2 | HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.453+5513_453+5514i others(1101): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139037106 | ||||||
| chr5:139037106
|
T | TAAAATTC others(1109): Show |
1 | a0001c0001t0001g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.453+5513_453+5514i others(1118): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139037106 | ||||||
| chr5:139037106
|
T | TAAAATTC others(1125): Show |
1 | a0005c0012t0001g0095 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.453+5513_453+5514i others(1134): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139037106 | ||||||
| chr5:139037106
|
T | TAAAATTC others(1127): Show |
1 | a0001c0001t0001g0032 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.453+5513_453+5514i others(1136): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139037106 | ||||||
| chr5:139037106
|
T | TAAAATTC others(1130): Show |
1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.453+5513_453+5514i others(1139): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139037106 | ||||||
| chr5:139037114
|
T | C | 19 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(16): Show | 19 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.453+5506A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139037114 | ||||||
| chr5:139037138
|
CCAG | C | 6 | a0002c0003t0001g0034a0002c0003t0001g0134a0002c0003t0001g0160others(3): Show | 6 | HG01891.hp1 HG02615.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.453+5479_453+5481d others(5): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139037138 | ||||||
| chr5:139037161
|
A | C | 1 | a0001c0002t0001g0178 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.453+5459T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139037161 | ||||||
| chr5:139037714
|
G | T | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.453+4906C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139037714 | ||||||
| chr5:139037766
|
A | G | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.453+4854T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139037766 | ||||||
| chr5:139037787
|
A | T | 1 | a0001c0002t0001g0178 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.453+4833T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139037787 | ||||||
| chr5:139038038
|
A | G | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.453+4582T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139038038 | ||||||
| chr5:139038304
|
G | A | 3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0005g0199 | 3 | HG00323.hp2 HG00735.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.453+4316C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139038304 | ||||||
| chr5:139038434
|
T | G | 1 | a0001c0002t0001g0178 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.453+4186A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139038434 | ||||||
| chr5:139038552
|
T | A | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(3): Show | 6 | HG02257.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.453+4068A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139038552 | ||||||
| chr5:139038621
|
A | G | 52 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(49): Show | 52 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.453+3999T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139038621 | ||||||
| chr5:139038663
|
C | T | 2 | a0002c0006t0001g0097a0002c0006t0001g0103 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.453+3957G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139038663 | ||||||
| chr5:139038736
|
T | C | 1 | a0001c0002t0001g0068 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.453+3884A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139038736 | ||||||
| chr5:139038739
|
C | T | 95 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.453+3881G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139038739 | ||||||
| chr5:139038816
|
G | A | 1 | a0001c0002t0001g0137 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.453+3804C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139038816 | ||||||
| chr5:139039102
|
T | A | 1 | a0001c0002t0001g0137 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.453+3518A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139039102 | ||||||
| chr5:139039210
|
C | T | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.453+3410G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139039210 | ||||||
| chr5:139039247
|
G | A | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.453+3373C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139039247 | ||||||
| chr5:139039987
|
T | C | 1 | a0002c0003t0001g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.453+2633A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139039987 | ||||||
| chr5:139039998
|
G | A | 94 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(91): Show | 94 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.453+2622C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139039998 | ||||||
| chr5:139040066
|
AG | A | 95 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.453+2553delC | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139040066 | ||||||
| chr5:139040433
|
A | T | 1 | a0001c0001t0001g0181 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.453+2187T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139040433 | ||||||
| chr5:139040459
|
T | C | 3 | a0001c0001t0002g0029a0001c0001t0002g0093a0001c0001t0002g0140 | 3 | NA18948.hp2 NA18961.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.453+2161A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139040459 | ||||||
| chr5:139040484
|
C | CT | 11 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0057others(8): Show | 11 | HG01074.hp2 HG02083.hp2 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.453+2135dupA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139040484 | ||||||
| chr5:139040484
|
C | CTT | 6 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0169others(3): Show | 6 | HG01891.hp1 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.453+2134_453+2135d others(4): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139040484 | ||||||
| chr5:139040490
|
TC | T | 29 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(26): Show | 29 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.453+2129delG | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139040490 | ||||||
| chr5:139040491
|
C | T | 65 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0023others(62): Show | 65 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.453+2129G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139040491 | ||||||
| chr5:139040498
|
C | T | 94 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(91): Show | 94 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.453+2122G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139040498 | ||||||
| chr5:139040498
|
CT | C | 95 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(92): Show | 95 | HG00323.hp1 HG00423.hp1 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.453+2121delA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139040498 | ||||||
| chr5:139040515
|
T | G | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.453+2105A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139040515 | ||||||
| chr5:139040688
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.453+1932C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139040688 | ||||||
| chr5:139041002
|
C | T | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.453+1618G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139041002 | ||||||
| chr5:139041193
|
C | T | 1 | a0002c0003t0001g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.453+1427G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139041193 | ||||||
| chr5:139041370
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.453+1250A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139041370 | ||||||
| chr5:139041427
|
A | G | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.453+1193T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139041427 | ||||||
| chr5:139041520
|
A | G | 10 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0036others(7): Show | 10 | NA18942.hp1 NA18946.hp2 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.453+1100T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139041520 | ||||||
| chr5:139041530
|
A | G | 98 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(95): Show | 98 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.453+1090T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139041530 | ||||||
| chr5:139041659
|
C | T | 2 | a0002c0006t0001g0097a0002c0006t0001g0103 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.453+961G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139041659 | ||||||
| chr5:139041718
|
C | T | 1 | a0002c0003t0001g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.453+902G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139041718 | ||||||
| chr5:139041818
|
C | CA | 6 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0061others(3): Show | 6 | HG01261.hp1 HG01934.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.453+801dupT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139041818 | ||||||
| chr5:139041818
|
CA | C | 20 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(17): Show | 20 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.453+801delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139041818 | ||||||
| chr5:139041821
|
A | C | 1 | a0001c0002t0001g0143 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.453+799T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139041821 | ||||||
| chr5:139041822
|
A | C | 7 | a0001c0001t0002g0165a0001c0001t0002g0167a0001c0002t0001g0098others(4): Show | 7 | HG01258.hp1 HG02109.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.453+798T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139041822 | ||||||
| chr5:139041824
|
A | C | 1 | a0001c0005t0001g0007 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.453+796T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139041824 | ||||||
| chr5:139041834
|
C | A | 1 | a0001c0002t0001g0113 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.453+786G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139041834 | ||||||
| chr5:139041861
|
G | C | 52 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(49): Show | 52 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.453+759C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139041861 | ||||||
| chr5:139042065
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.453+555G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139042065 | ||||||
| chr5:139042153
|
C | A | 1 | a0001c0001t0006g0200 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.453+467G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 5/9 | chr5 | 139042153 | ||||||
| chr5:139042829
|
T | C | 2 | a0002c0003t0001g0034a0002c0003t0001g0161 | 2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.354-110A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139042829 | ||||||
| chr5:139043240
|
A | G | 6 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0081others(3): Show | 6 | HG00642.hp1 HG01346.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.354-521T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139043240 | ||||||
| chr5:139043458
|
C | T | 1 | a0001c0002t0001g0137 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.354-739G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139043458 | ||||||
| chr5:139043974
|
T | C | 1 | a0003c0004t0001g0164 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.354-1255A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139043974 | ||||||
| chr5:139044072
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.354-1353C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139044072 | ||||||
| chr5:139044135
|
A | T | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.354-1416T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139044135 | ||||||
| chr5:139044309
|
TAAGTATT others(16): Show |
T | 1 | a0001c0002t0001g0179 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.354-1613_354-1591d others(25): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139044309 | ||||||
| chr5:139044593
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.354-1874G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139044593 | ||||||
| chr5:139044645
|
A | G | 1 | a0001c0002t0001g0198 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.354-1926T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139044645 | ||||||
| chr5:139044791
|
G | T | 95 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.354-2072C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139044791 | ||||||
| chr5:139044800
|
C | T | 52 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(49): Show | 52 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.354-2081G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139044800 | ||||||
| chr5:139045103
|
T | C | 12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(9): Show | 12 | NA18942.hp1 NA18946.hp2 NA18948.hp1 others(9): Show |
intron_variant | MODIFIER | c.354-2384A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139045103 | ||||||
| chr5:139045146
|
C | T | 22 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.354-2427G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139045146 | ||||||
| chr5:139046084
|
T | G | 2 | a0001c0002t0001g0085a0001c0002t0001g0102 | 2 | HG01975.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.354-3365A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139046084 | ||||||
| chr5:139046268
|
A | G | 1 | a0001c0002t0001g0145 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.354-3549T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139046268 | ||||||
| chr5:139046284
|
G | A | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.354-3565C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139046284 | ||||||
| chr5:139046321
|
C | T | 3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0005g0199 | 3 | HG00323.hp2 HG00735.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.354-3602G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139046321 | ||||||
| chr5:139046332
|
G | GA | 75 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(72): Show | 75 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.354-3614dupT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139046332 | ||||||
| chr5:139046493
|
A | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(93): Show | 96 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.354-3774T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139046493 | ||||||
| chr5:139046679
|
A | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(93): Show | 96 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.354-3960T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139046679 | ||||||
| chr5:139046920
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.353+4018A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139046920 | ||||||
| chr5:139047063
|
G | T | 3 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0142 | 3 | HG00642.hp2 HG01261.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.353+3875C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139047063 | ||||||
| chr5:139047452
|
T | C | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.353+3486A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139047452 | ||||||
| chr5:139047678
|
G | T | 1 | a0001c0002t0001g0192 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.353+3260C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139047678 | ||||||
| chr5:139047680
|
A | G | 1 | a0001c0002t0001g0192 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.353+3258T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139047680 | ||||||
| chr5:139048157
|
T | C | 21 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(18): Show | 21 | HG01243.hp1 HG02055.hp2 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.353+2781A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139048157 | ||||||
| chr5:139048347
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.353+2591C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139048347 | ||||||
| chr5:139048369
|
G | GT | 29 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0086others(26): Show | 29 | HG01069.hp2 HG01109.hp2 HG01516.hp1 others(26): Show |
intron_variant | MODIFIER | c.353+2568dupA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139048369 | ||||||
| chr5:139048369
|
GT | G | 45 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0044others(42): Show | 45 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.353+2568delA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139048369 | ||||||
| chr5:139048381
|
T | G | 27 | a0001c0002t0001g0038a0001c0002t0001g0068a0001c0002t0001g0072others(24): Show | 27 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.353+2557A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139048381 | ||||||
| chr5:139048383
|
T | G | 1 | a0001c0001t0003g0001 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.353+2555A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139048383 | ||||||
| chr5:139048639
|
G | C | 1 | a0001c0001t0002g0140 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.353+2299C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139048639 | ||||||
| chr5:139048758
|
A | G | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.353+2180T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139048758 | ||||||
| chr5:139048849
|
G | C | 3 | a0001c0005t0001g0007a0001c0005t0001g0011a0001c0005t0001g0091 | 3 | HG01243.hp1 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.353+2089C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139048849 | ||||||
| chr5:139049127
|
T | A | 1 | a0004c0007t0001g0195 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.353+1811A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139049127 | ||||||
| chr5:139049198
|
A | G | 1 | a0002c0003t0001g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.353+1740T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139049198 | ||||||
| chr5:139049303
|
T | G | 95 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.353+1635A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139049303 | ||||||
| chr5:139049374
|
A | T | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.353+1564T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139049374 | ||||||
| chr5:139049472
|
C | T | 6 | a0002c0003t0001g0034a0002c0003t0001g0134a0002c0003t0001g0160others(3): Show | 6 | HG01891.hp1 HG02615.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.353+1466G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139049472 | ||||||
| chr5:139049710
|
T | A | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.353+1228A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139049710 | ||||||
| chr5:139049793
|
T | TA | 5 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0074others(2): Show | 5 | HG01361.hp2 HG01934.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.353+1144dupT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139049793 | ||||||
| chr5:139049918
|
G | A | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.353+1020C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139049918 | ||||||
| chr5:139049956
|
T | C | 1 | a0001c0002t0001g0119 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.353+982A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139049956 | ||||||
| chr5:139049995
|
A | C | 1 | a0001c0001t0001g0181 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.353+943T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139049995 | ||||||
| chr5:139050107
|
C | T | 98 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(95): Show | 98 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.353+831G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139050107 | ||||||
| chr5:139050117
|
A | AT | 52 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(49): Show | 52 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.353+820dupA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139050117 | ||||||
| chr5:139050435
|
C | A | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.353+503G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139050435 | ||||||
| chr5:139050435
|
C | T | 2 | a0002c0006t0001g0097a0002c0006t0001g0103 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.353+503G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139050435 | ||||||
| chr5:139050715
|
C | T | 1 | a0009c0013t0001g0045 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.353+223G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 4/9 | chr5 | 139050715 | ||||||
| chr5:139051131
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.245-85A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139051131 | ||||||
| chr5:139051170
|
C | A | 94 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(91): Show | 94 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.245-124G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139051170 | ||||||
| chr5:139051183
|
A | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0081 | 2 | HG02738.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.245-137T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139051183 | ||||||
| chr5:139051260
|
C | T | 16 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(13): Show | 16 | HG02055.hp2 HG02559.hp2 HG03041.hp1 others(13): Show |
intron_variant | MODIFIER | c.245-214G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139051260 | ||||||
| chr5:139051261
|
G | A | 1 | a0001c0005t0001g0011 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.245-215C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139051261 | ||||||
| chr5:139051294
|
A | G | 1 | a0001c0002t0001g0143 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.245-248T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139051294 | ||||||
| chr5:139051457
|
T | G | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.245-411A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139051457 | ||||||
| chr5:139051460
|
T | C | 98 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(95): Show | 98 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.245-414A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139051460 | ||||||
| chr5:139051638
|
G | A | 1 | a0002c0003t0001g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.245-592C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139051638 | ||||||
| chr5:139051873
|
A | C | 1 | a0001c0005t0001g0091 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.245-827T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139051873 | ||||||
| chr5:139052048
|
T | C | 52 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(49): Show | 52 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.245-1002A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139052048 | ||||||
| chr5:139052220
|
C | CCAGT | 98 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(95): Show | 98 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.245-1178_245-1175d others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139052220 | ||||||
| chr5:139052563
|
A | T | 1 | a0001c0002t0001g0019 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.245-1517T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139052563 | ||||||
| chr5:139052738
|
G | A | 1 | a0001c0002t0001g0185 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.245-1692C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139052738 | ||||||
| chr5:139052769
|
G | A | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.245-1723C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139052769 | ||||||
| chr5:139052772
|
T | A | 1 | a0001c0002t0004g0131 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.245-1726A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139052772 | ||||||
| chr5:139053179
|
A | T | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.245-2133T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139053179 | ||||||
| chr5:139053261
|
C | T | 1 | a0001c0002t0001g0004 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.245-2215G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139053261 | ||||||
| chr5:139053291
|
C | A | 2 | a0001c0002t0001g0008a0001c0002t0001g0183 | 2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.245-2245G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139053291 | ||||||
| chr5:139053461
|
G | A | 2 | a0001c0001t0001g0076a0001c0002t0001g0141 | 2 | HG00735.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.245-2415C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139053461 | ||||||
| chr5:139053872
|
C | T | 95 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.245-2826G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139053872 | ||||||
| chr5:139053913
|
A | G | 95 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.245-2867T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139053913 | ||||||
| chr5:139054038
|
T | A | 1 | a0001c0002t0001g0148 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.245-2992A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139054038 | ||||||
| chr5:139054215
|
G | C | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.245-3169C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139054215 | ||||||
| chr5:139054231
|
C | T | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.245-3185G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139054231 | ||||||
| chr5:139054287
|
T | G | 1 | a0001c0002t0001g0100 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.245-3241A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139054287 | ||||||
| chr5:139054575
|
G | T | 5 | a0002c0003t0001g0034a0002c0003t0001g0134a0002c0003t0001g0161others(2): Show | 5 | HG02615.hp1 HG02723.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.245-3529C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139054575 | ||||||
| chr5:139054629
|
C | T | 95 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.245-3583G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139054629 | ||||||
| chr5:139054707
|
G | A | 1 | a0001c0001t0006g0200 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.245-3661C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139054707 | ||||||
| chr5:139054942
|
A | C | 95 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.245-3896T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139054942 | ||||||
| chr5:139054975
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.245-3929C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139054975 | ||||||
| chr5:139055047
|
A | G | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.245-4001T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139055047 | ||||||
| chr5:139055057
|
C | G | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.245-4011G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139055057 | ||||||
| chr5:139055165
|
C | G | 95 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.245-4119G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139055165 | ||||||
| chr5:139055237
|
T | C | 1 | a0001c0002t0001g0104 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.245-4191A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139055237 | ||||||
| chr5:139055383
|
T | C | 98 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(95): Show | 98 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.245-4337A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139055383 | ||||||
| chr5:139055405
|
C | G | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.245-4359G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139055405 | ||||||
| chr5:139055589
|
ACTCTCC | A | 44 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(41): Show | 44 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.245-4549_245-4544d others(8): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139055589 | ||||||
| chr5:139055589
|
ACTCTCCC others(5): Show |
A | 51 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(48): Show | 51 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.245-4555_245-4544d others(14): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139055589 | ||||||
| chr5:139055622
|
C | CTCTCCCC others(1): Show |
93 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(90): Show | 93 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.245-4577_245-4576i others(10): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139055622 | ||||||
| chr5:139055622
|
C | T | 2 | a0001c0001t0001g0047a0008c0011t0001g0196 | 2 | HG02683.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.245-4576G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139055622 | ||||||
| chr5:139055630
|
C | T | 2 | a0002c0006t0001g0097a0002c0006t0001g0103 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.245-4584G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139055630 | ||||||
| chr5:139055635
|
CCCCTCTC others(16): Show |
C | 1 | a0001c0001t0001g0047 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.245-4612_245-4590d others(25): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139055635 | ||||||
| chr5:139055643
|
CCTCTCCC others(8): Show |
C | 2 | a0002c0006t0001g0097a0002c0006t0001g0103 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.245-4612_245-4598d others(17): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139055643 | ||||||
| chr5:139055702
|
G | A | 1 | a0001c0002t0001g0019 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.245-4656C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139055702 | ||||||
| chr5:139055710
|
T | C | 95 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.245-4664A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139055710 | ||||||
| chr5:139055780
|
C | T | 94 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(91): Show | 94 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.245-4734G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139055780 | ||||||
| chr5:139055796
|
G | C | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.245-4750C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139055796 | ||||||
| chr5:139055805
|
CGATT | C | 95 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.245-4763_245-4760d others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139055805 | ||||||
| chr5:139055810
|
G | A | 95 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.245-4764C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139055810 | ||||||
| chr5:139055818
|
G | A | 6 | a0002c0003t0001g0034a0002c0003t0001g0134a0002c0003t0001g0160others(3): Show | 6 | HG01891.hp1 HG02615.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.245-4772C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139055818 | ||||||
| chr5:139055827
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.245-4781G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139055827 | ||||||
| chr5:139055828
|
G | A | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.245-4782C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139055828 | ||||||
| chr5:139055870
|
A | G | 95 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.245-4824T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139055870 | ||||||
| chr5:139055907
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.245-4861C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139055907 | ||||||
| chr5:139055933
|
G | A | 1 | a0001c0002t0001g0123 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.245-4887C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139055933 | ||||||
| chr5:139056039
|
C | A | 15 | a0001c0002t0001g0038a0001c0002t0001g0068a0001c0002t0001g0072others(12): Show | 15 | HG00642.hp2 HG01074.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.245-4993G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056039 | ||||||
| chr5:139056091
|
A | AC | 10 | a0001c0001t0001g0027a0001c0001t0001g0061a0001c0001t0001g0166others(7): Show | 10 | HG00735.hp2 HG01109.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.245-5046dupG | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056091 | ||||||
| chr5:139056099
|
T | C | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.245-5053A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056099 | ||||||
| chr5:139056100
|
G | A | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.245-5054C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056100 | ||||||
| chr5:139056101
|
G | A | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.245-5055C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056101 | ||||||
| chr5:139056229
|
C | T | 95 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.245-5183G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056229 | ||||||
| chr5:139056243
|
C | T | 95 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.245-5197G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056243 | ||||||
| chr5:139056339
|
G | A | 8 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0039others(5): Show | 8 | NA18942.hp1 NA18946.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.245-5293C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056339 | ||||||
| chr5:139056404
|
C | T | 2 | a0001c0001t0001g0162a0001c0002t0001g0028 | 2 | HG02109.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.245-5358G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056404 | ||||||
| chr5:139056416
|
G | T | 1 | a0001c0001t0002g0140 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.245-5370C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056416 | ||||||
| chr5:139056420
|
A | C | 1 | a0001c0001t0001g0174 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.245-5374T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056420 | ||||||
| chr5:139056429
|
G | A | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.245-5383C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056429 | ||||||
| chr5:139056443
|
C | T | 1 | a0001c0002t0001g0156 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.245-5397G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056443 | ||||||
| chr5:139056463
|
G | A | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.245-5417C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056463 | ||||||
| chr5:139056473
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.245-5427C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056473 | ||||||
| chr5:139056488
|
C | T | 1 | a0001c0002t0001g0099 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.245-5442G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056488 | ||||||
| chr5:139056489
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.245-5443C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056489 | ||||||
| chr5:139056514
|
C | T | 95 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.245-5468G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056514 | ||||||
| chr5:139056518
|
AGGCCAGC others(42): Show |
A | 1 | a0001c0002t0001g0184 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.245-5521_245-5473d others(51): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056518 | ||||||
| chr5:139056535
|
C | T | 6 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.245-5489G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056535 | ||||||
| chr5:139056563
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.245-5517G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056563 | ||||||
| chr5:139056567
|
CGGCCAGC others(91): Show |
C | 1 | a0001c0002t0001g0192 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.245-5619_245-5522d others(100): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056567 | ||||||
| chr5:139056581
|
G | A | 1 | a0001c0002t0001g0068 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.245-5535C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056581 | ||||||
| chr5:139056584
|
CGGGAGGG others(42): Show |
C | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.245-5587_245-5539d others(51): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056584 | ||||||
| chr5:139056585
|
G | A | 83 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(80): Show | 83 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.245-5539C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056585 | ||||||
| chr5:139056595
|
T | G | 1 | a0001c0002t0001g0070 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.245-5549A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056595 | ||||||
| chr5:139056634
|
AGGAGGGA others(42): Show |
A | 6 | a0002c0003t0001g0034a0002c0003t0001g0134a0002c0003t0001g0160others(3): Show | 6 | HG01891.hp1 HG02615.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.245-5637_245-5589d others(51): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056634 | ||||||
| chr5:139056665
|
T | C | 92 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(89): Show | 92 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.245-5619A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056665 | ||||||
| chr5:139056673
|
C | T | 1 | a0001c0001t0002g0018 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.245-5627G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056673 | ||||||
| chr5:139056699
|
C | G | 1 | a0001c0001t0001g0052 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.245-5653G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056699 | ||||||
| chr5:139056706
|
C | CCCCCGCC others(10): Show |
1 | a0001c0001t0001g0081 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.245-5661_245-5660i others(19): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056706 | ||||||
| chr5:139056722
|
C | T | 95 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.245-5676G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056722 | ||||||
| chr5:139056759
|
C | T | 1 | a0002c0003t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.245-5713G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056759 | ||||||
| chr5:139056793
|
G | A | 55 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(52): Show | 55 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.245-5747C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056793 | ||||||
| chr5:139056839
|
G | A | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.245-5793C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056839 | ||||||
| chr5:139056844
|
A | G | 4 | a0001c0001t0002g0029a0001c0001t0002g0093a0002c0003t0001g0034others(1): Show | 4 | NA18522.hp1 NA18961.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.245-5798T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056844 | ||||||
| chr5:139056845
|
T | G | 4 | a0001c0001t0002g0029a0001c0001t0002g0093a0002c0003t0001g0034others(1): Show | 4 | NA18522.hp1 NA18961.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.245-5799A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056845 | ||||||
| chr5:139056869
|
A | C | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.245-5823T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056869 | ||||||
| chr5:139056979
|
ATTC | A | 2 | a0002c0003t0001g0034a0002c0003t0001g0161 | 2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.245-5936_245-5934d others(5): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139056979 | ||||||
| chr5:139057075
|
A | C | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.245-6029T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139057075 | ||||||
| chr5:139057187
|
C | T | 1 | a0001c0002t0001g0132 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.245-6141G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139057187 | ||||||
| chr5:139057193
|
A | G | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.245-6147T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139057193 | ||||||
| chr5:139057216
|
A | G | 1 | a0001c0002t0001g0137 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.245-6170T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139057216 | ||||||
| chr5:139057314
|
T | TTAAAAAA others(1): Show |
2 | a0001c0001t0001g0027a0001c0001t0001g0096 | 2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.245-6269_245-6268i others(10): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139057314 | ||||||
| chr5:139057314
|
T | TTAAAAAA others(2): Show |
3 | a0001c0001t0001g0050a0001c0001t0001g0088a0001c0001t0001g0133 | 3 | HG01993.hp1 NA18960.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.245-6269_245-6268i others(11): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139057314 | ||||||
| chr5:139057314
|
T | TTAAAAAA others(3): Show |
1 | a0001c0001t0001g0166 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.245-6269_245-6268i others(12): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139057314 | ||||||
| chr5:139057314
|
T | TTAAAAAA others(4): Show |
1 | a0002c0003t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.245-6269_245-6268i others(13): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139057314 | ||||||
| chr5:139057314
|
T | TTAAAAAA others(5): Show |
1 | a0001c0001t0001g0032 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.245-6269_245-6268i others(14): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139057314 | ||||||
| chr5:139057314
|
T | TTAAAAAA others(7): Show |
1 | a0001c0001t0003g0001 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.245-6269_245-6268i others(16): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139057314 | ||||||
| chr5:139057314
|
T | TTAAAAAA others(8): Show |
18 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(15): Show | 18 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.245-6269_245-6268i others(17): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139057314 | ||||||
| chr5:139057314
|
T | TTAAAAAA others(9): Show |
12 | a0001c0001t0001g0035a0001c0001t0001g0049a0001c0001t0001g0054others(9): Show | 12 | HG00323.hp2 HG01081.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.245-6269_245-6268i others(18): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139057314 | ||||||
| chr5:139057314
|
T | TTAAAAAA others(10): Show |
21 | a0001c0001t0001g0009a0001c0001t0001g0047a0001c0001t0001g0048others(18): Show | 21 | HG00735.hp1 HG01074.hp2 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.245-6269_245-6268i others(19): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139057314 | ||||||
| chr5:139057314
|
T | TTAAAAAA others(11): Show |
21 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0044others(18): Show | 21 | HG00423.hp2 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.245-6269_245-6268i others(20): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139057314 | ||||||
| chr5:139057314
|
T | TTAAAAAA others(12): Show |
6 | a0001c0001t0001g0024a0001c0001t0001g0046a0001c0001t0001g0191others(3): Show | 6 | HG01516.hp2 HG02622.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.245-6269_245-6268i others(21): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139057314 | ||||||
| chr5:139057314
|
T | TTAAAAAA others(13): Show |
5 | a0001c0001t0001g0023a0001c0001t0001g0089a0001c0001t0001g0094others(2): Show | 5 | HG00642.hp1 HG01346.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.245-6269_245-6268i others(22): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139057314 | ||||||
| chr5:139057314
|
T | TTAAAAAA others(14): Show |
2 | a0001c0002t0001g0185a0002c0003t0001g0160 | 2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.245-6269_245-6268i others(23): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139057314 | ||||||
| chr5:139057324
|
A | G | 1 | a0001c0002t0001g0114 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.245-6278T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139057324 | ||||||
| chr5:139057329
|
G | A | 77 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0023others(74): Show | 77 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.245-6283C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139057329 | ||||||
| chr5:139057572
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.245-6526C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139057572 | ||||||
| chr5:139057636
|
C | T | 1 | a0002c0003t0001g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.245-6590G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139057636 | ||||||
| chr5:139057640
|
T | C | 98 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(95): Show | 98 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.245-6594A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139057640 | ||||||
| chr5:139057866
|
C | A | 1 | a0001c0001t0006g0200 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.245-6820G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139057866 | ||||||
| chr5:139057992
|
T | C | 10 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0092others(7): Show | 10 | HG01884.hp2 HG02280.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.245-6946A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139057992 | ||||||
| chr5:139058032
|
T | C | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.245-6986A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139058032 | ||||||
| chr5:139058056
|
A | C | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.245-7010T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139058056 | ||||||
| chr5:139058057
|
G | A | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.245-7011C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139058057 | ||||||
| chr5:139058078
|
C | A | 3 | a0001c0001t0002g0029a0001c0001t0002g0093a0001c0001t0002g0140 | 3 | NA18948.hp2 NA18961.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.245-7032G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139058078 | ||||||
| chr5:139058283
|
C | T | 2 | a0002c0003t0001g0134a0002c0003t0001g0160 | 2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.245-7237G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139058283 | ||||||
| chr5:139058573
|
G | T | 94 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(91): Show | 94 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.245-7527C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139058573 | ||||||
| chr5:139058915
|
A | C | 98 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(95): Show | 98 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.245-7869T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139058915 | ||||||
| chr5:139058964
|
A | ATGTGTGT others(7): Show |
1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.245-7919_245-7918i others(16): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139058964 | ||||||
| chr5:139058964
|
A | ATGTGTGT others(9): Show |
2 | a0001c0001t0001g0059a0001c0001t0001g0071 | 2 | HG02132.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.245-7919_245-7918i others(18): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139058964 | ||||||
| chr5:139058970
|
A | ATGTGTGT others(5): Show |
6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(3): Show | 6 | HG02257.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.245-7936_245-7925d others(14): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139058970 | ||||||
| chr5:139058970
|
A | ATGTGTGT others(7): Show |
23 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(20): Show | 23 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.245-7938_245-7925d others(16): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139058970 | ||||||
| chr5:139058970
|
A | ATGTGTGT others(9): Show |
51 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(48): Show | 51 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.245-7940_245-7925d others(18): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139058970 | ||||||
| chr5:139058970
|
A | ATGTGTGT others(11): Show |
6 | a0001c0001t0001g0044a0001c0001t0001g0062a0001c0001t0001g0168others(3): Show | 6 | HG01346.hp1 HG02630.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.245-7925_245-7924i others(20): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139058970 | ||||||
| chr5:139058970
|
A | ATGTGTGT others(13): Show |
6 | a0001c0001t0001g0030a0001c0001t0001g0088a0001c0001t0001g0133others(3): Show | 6 | HG01109.hp2 HG01891.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.245-7925_245-7924i others(22): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139058970 | ||||||
| chr5:139058970
|
A | ATGTGTGT others(15): Show |
1 | a0002c0006t0001g0103 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.245-7925_245-7924i others(24): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139058970 | ||||||
| chr5:139058970
|
A | ATGTGTGT others(17): Show |
2 | a0002c0003t0001g0034a0002c0003t0001g0161 | 2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.245-7925_245-7924i others(26): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139058970 | ||||||
| chr5:139058970
|
A | G | 3 | a0001c0001t0001g0059a0001c0001t0001g0071a0008c0011t0001g0196 | 3 | HG02132.hp2 HG03195.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.245-7924T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139058970 | ||||||
| chr5:139059293
|
A | G | 5 | a0001c0001t0001g0049a0001c0001t0001g0053a0001c0001t0001g0058others(2): Show | 5 | NA18945.hp2 NA18968.hp2 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.245-8247T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139059293 | ||||||
| chr5:139059341
|
T | C | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0003c0004t0001g0005others(2): Show | 5 | HG02280.hp2 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.245-8295A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139059341 | ||||||
| chr5:139059379
|
C | T | 95 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.245-8333G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139059379 | ||||||
| chr5:139059467
|
A | T | 95 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.245-8421T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139059467 | ||||||
| chr5:139059868
|
G | A | 1 | a0001c0002t0001g0122 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.245-8822C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139059868 | ||||||
| chr5:139059928
|
T | G | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.245-8882A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139059928 | ||||||
| chr5:139060279
|
T | G | 3 | a0001c0001t0001g0159a0001c0002t0001g0099a0001c0002t0001g0101 | 3 | HG01884.hp1 HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.245-9233A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139060279 | ||||||
| chr5:139060296
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.245-9250A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139060296 | ||||||
| chr5:139060317
|
G | GTGTT | 165 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(162): Show | 165 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.245-9275_245-9272d others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139060317 | ||||||
| chr5:139060523
|
AT | A | 11 | a0001c0001t0001g0055a0001c0002t0001g0006a0001c0002t0001g0010others(8): Show | 11 | HG01496.hp2 HG01516.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.245-9478delA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139060523 | ||||||
| chr5:139060588
|
T | G | 52 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(49): Show | 52 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.245-9542A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139060588 | ||||||
| chr5:139060612
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.245-9566A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139060612 | ||||||
| chr5:139060827
|
A | G | 165 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(162): Show | 165 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.245-9781T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139060827 | ||||||
| chr5:139061245
|
G | A | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.245-10199C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139061245 | ||||||
| chr5:139061276
|
C | T | 94 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(91): Show | 94 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.245-10230G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139061276 | ||||||
| chr5:139061388
|
T | C | 3 | a0001c0002t0001g0073a0001c0002t0001g0124a0001c0002t0001g0182 | 3 | HG02698.hp2 HG03942.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.245-10342A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139061388 | ||||||
| chr5:139061411
|
T | C | 100 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(97): Show | 100 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.245-10365A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139061411 | ||||||
| chr5:139061492
|
G | A | 2 | a0001c0002t0001g0113a0001c0002t0001g0144 | 2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.245-10446C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139061492 | ||||||
| chr5:139061600
|
G | A | 97 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(94): Show | 97 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.245-10554C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139061600 | ||||||
| chr5:139061836
|
G | T | 39 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(36): Show | 39 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.245-10790C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139061836 | ||||||
| chr5:139062250
|
T | A | 1 | a0001c0002t0001g0117 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.245-11204A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139062250 | ||||||
| chr5:139062368
|
T | C | 1 | a0006c0009t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.245-11322A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139062368 | ||||||
| chr5:139062415
|
A | C | 190 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(187): Show | 190 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.245-11369T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139062415 | ||||||
| chr5:139062416
|
C | T | 39 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(36): Show | 39 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.245-11370G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139062416 | ||||||
| chr5:139062438
|
G | T | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.245-11392C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139062438 | ||||||
| chr5:139062483
|
G | A | 55 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(52): Show | 55 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.245-11437C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139062483 | ||||||
| chr5:139062533
|
G | C | 39 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(36): Show | 39 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.245-11487C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139062533 | ||||||
| chr5:139062807
|
C | A | 1 | a0001c0002t0001g0187 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.245-11761G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139062807 | ||||||
| chr5:139063112
|
T | C | 1 | a0001c0001t0001g0016 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.245-12066A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139063112 | ||||||
| chr5:139063279
|
T | C | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.245-12233A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139063279 | ||||||
| chr5:139063309
|
C | T | 39 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(36): Show | 39 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.245-12263G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139063309 | ||||||
| chr5:139063426
|
T | C | 2 | a0002c0003t0001g0034a0002c0003t0001g0161 | 2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.245-12380A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139063426 | ||||||
| chr5:139063888
|
G | T | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.245-12842C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139063888 | ||||||
| chr5:139063959
|
T | C | 2 | a0001c0002t0001g0008a0001c0002t0001g0183 | 2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.245-12913A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139063959 | ||||||
| chr5:139064407
|
G | A | 4 | a0001c0002t0001g0135a0001c0002t0001g0148a0001c0002t0001g0153others(1): Show | 4 | HG00735.hp2 NA18961.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.245-13361C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139064407 | ||||||
| chr5:139064489
|
T | C | 2 | a0002c0006t0001g0097a0002c0006t0001g0103 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.245-13443A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139064489 | ||||||
| chr5:139064563
|
T | C | 3 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0084 | 3 | HG02145.hp1 HG02723.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.245-13517A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139064563 | ||||||
| chr5:139064648
|
T | C | 39 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(36): Show | 39 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.245-13602A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139064648 | ||||||
| chr5:139064708
|
C | A | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.245-13662G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139064708 | ||||||
| chr5:139064727
|
A | G | 1 | a0001c0002t0001g0127 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.245-13681T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139064727 | ||||||
| chr5:139065001
|
G | A | 4 | a0002c0003t0001g0134a0002c0003t0001g0160a0002c0006t0001g0097others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.245-13955C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139065001 | ||||||
| chr5:139065189
|
G | A | 1 | a0001c0002t0001g0100 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.245-14143C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139065189 | ||||||
| chr5:139065201
|
TG | T | 2 | a0004c0007t0001g0158a0004c0007t0001g0195 | 2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.245-14156delC | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139065201 | ||||||
| chr5:139065507
|
C | T | 25 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(22): Show | 25 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.245-14461G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139065507 | ||||||
| chr5:139065537
|
A | G | 1 | a0001c0002t0001g0193 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.245-14491T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139065537 | ||||||
| chr5:139065663
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0168 | 2 | HG01346.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.245-14617G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139065663 | ||||||
| chr5:139066084
|
C | T | 22 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.245-15038G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139066084 | ||||||
| chr5:139066489
|
A | G | 1 | a0001c0001t0001g0012 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.245-15443T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139066489 | ||||||
| chr5:139066503
|
G | A | 2 | a0001c0001t0002g0165a0001c0001t0002g0167 | 2 | HG01258.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.245-15457C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139066503 | ||||||
| chr5:139066750
|
C | G | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.245-15704G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139066750 | ||||||
| chr5:139067428
|
C | G | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.245-16382G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139067428 | ||||||
| chr5:139067487
|
C | T | 6 | a0001c0001t0002g0165a0001c0001t0002g0167a0001c0002t0001g0004others(3): Show | 6 | HG01258.hp1 HG02109.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.245-16441G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139067487 | ||||||
| chr5:139067628
|
G | T | 105 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(102): Show | 105 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(102): Show |
intron_variant | MODIFIER | c.245-16582C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139067628 | ||||||
| chr5:139067863
|
T | C | 1 | a0001c0002t0001g0145 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.245-16817A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139067863 | ||||||
| chr5:139068001
|
T | C | 1 | a0001c0002t0001g0019 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.245-16955A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139068001 | ||||||
| chr5:139068399
|
C | A | 55 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(52): Show | 55 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.245-17353G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139068399 | ||||||
| chr5:139068472
|
G | A | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.245-17426C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139068472 | ||||||
| chr5:139068655
|
G | GA | 6 | a0001c0001t0001g0163a0001c0001t0001g0177a0001c0002t0001g0028others(3): Show | 6 | HG02055.hp2 HG03041.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.245-17610dupT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139068655 | ||||||
| chr5:139068655
|
GA | G | 25 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(22): Show | 25 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.245-17610delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139068655 | ||||||
| chr5:139068673
|
AAG | A | 53 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(50): Show | 53 | HG00423.hp2 HG00642.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.245-17629_245-1762 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139068673 | ||||||
| chr5:139068779
|
T | C | 3 | a0001c0002t0001g0073a0001c0002t0001g0124a0001c0002t0001g0182 | 3 | HG02698.hp2 HG03942.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.245-17733A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139068779 | ||||||
| chr5:139069094
|
C | T | 2 | a0001c0002t0001g0099a0001c0002t0001g0101 | 2 | HG01884.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.245-18048G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139069094 | ||||||
| chr5:139069161
|
A | C | 1 | a0001c0002t0001g0132 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.245-18115T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139069161 | ||||||
| chr5:139069206
|
T | C | 56 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(53): Show | 56 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.245-18160A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139069206 | ||||||
| chr5:139069215
|
G | A | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.245-18169C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139069215 | ||||||
| chr5:139069225
|
T | C | 1 | a0002c0003t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.245-18179A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139069225 | ||||||
| chr5:139069466
|
GAAGA | G | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.245-18424_245-1842 others(8): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139069466 | ||||||
| chr5:139069846
|
G | A | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.245-18800C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139069846 | ||||||
| chr5:139069975
|
A | G | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.245-18929T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139069975 | ||||||
| chr5:139070022
|
C | G | 7 | a0001c0002t0001g0117a0001c0002t0001g0118a0001c0002t0001g0146others(4): Show | 7 | HG01496.hp2 HG02258.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.245-18976G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139070022 | ||||||
| chr5:139070305
|
G | A | 93 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(90): Show | 93 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.245-19259C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139070305 | ||||||
| chr5:139070336
|
C | G | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.245-19290G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139070336 | ||||||
| chr5:139070389
|
C | T | 93 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(90): Show | 93 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.245-19343G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139070389 | ||||||
| chr5:139070486
|
G | A | 1 | a0001c0002t0001g0100 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.245-19440C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139070486 | ||||||
| chr5:139070611
|
G | A | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.245-19565C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139070611 | ||||||
| chr5:139070690
|
T | A | 55 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(52): Show | 55 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.245-19644A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139070690 | ||||||
| chr5:139070830
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.245-19784A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139070830 | ||||||
| chr5:139071188
|
TAAG | T | 92 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(89): Show | 92 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.245-20145_245-2014 others(7): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139071188 | ||||||
| chr5:139071213
|
A | G | 191 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(188): Show | 191 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.245-20167T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139071213 | ||||||
| chr5:139071505
|
T | G | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.245-20459A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139071505 | ||||||
| chr5:139071666
|
A | AT | 7 | a0001c0001t0001g0014a0001c0002t0001g0006a0001c0002t0001g0087others(4): Show | 7 | HG02615.hp1 HG02723.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.245-20621dupA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139071666 | ||||||
| chr5:139071666
|
AT | A | 11 | a0001c0001t0001g0044a0001c0001t0002g0165a0001c0001t0002g0167others(8): Show | 11 | HG01258.hp1 HG02109.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.245-20621delA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139071666 | ||||||
| chr5:139071666
|
ATT | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(54): Show | 57 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.245-20622_245-2062 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139071666 | ||||||
| chr5:139072188
|
G | A | 22 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.245-21142C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139072188 | ||||||
| chr5:139072255
|
A | G | 2 | a0001c0002t0001g0008a0001c0002t0001g0183 | 2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.245-21209T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139072255 | ||||||
| chr5:139072361
|
G | T | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.245-21315C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139072361 | ||||||
| chr5:139072626
|
G | A | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.245-21580C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139072626 | ||||||
| chr5:139072838
|
A | C | 2 | a0001c0001t0001g0030a0001c0001t0001g0159 | 2 | HG02145.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.245-21792T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139072838 | ||||||
| chr5:139072874
|
C | A | 1 | a0001c0002t0001g0117 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.245-21828G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139072874 | ||||||
| chr5:139072879
|
T | C | 55 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(52): Show | 55 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.245-21833A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139072879 | ||||||
| chr5:139072968
|
C | T | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.245-21922G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139072968 | ||||||
| chr5:139073013
|
C | T | 1 | a0002c0006t0001g0103 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.245-21967G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139073013 | ||||||
| chr5:139073079
|
A | C | 1 | a0001c0002t0001g0070 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.245-22033T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139073079 | ||||||
| chr5:139073096
|
C | T | 1 | a0001c0002t0001g0072 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.245-22050G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139073096 | ||||||
| chr5:139073262
|
A | C | 1 | a0002c0003t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.245-22216T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139073262 | ||||||
| chr5:139073267
|
G | A | 93 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(90): Show | 93 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.245-22221C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139073267 | ||||||
| chr5:139073318
|
G | T | 93 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(90): Show | 93 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.245-22272C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139073318 | ||||||
| chr5:139073404
|
A | G | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.245-22358T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139073404 | ||||||
| chr5:139073530
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.245-22484G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139073530 | ||||||
| chr5:139073565
|
T | A | 4 | a0002c0003t0001g0134a0002c0003t0001g0160a0002c0006t0001g0097others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.245-22519A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139073565 | ||||||
| chr5:139073832
|
G | A | 1 | a0001c0002t0001g0178 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.245-22786C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139073832 | ||||||
| chr5:139074002
|
G | C | 1 | a0001c0001t0001g0032 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.245-22956C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139074002 | ||||||
| chr5:139074170
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.245-23124G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139074170 | ||||||
| chr5:139074407
|
T | G | 95 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.245-23361A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139074407 | ||||||
| chr5:139074468
|
A | G | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.245-23422T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139074468 | ||||||
| chr5:139074513
|
T | G | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.245-23467A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139074513 | ||||||
| chr5:139074585
|
A | G | 1 | a0001c0001t0001g0052 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.245-23539T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139074585 | ||||||
| chr5:139074813
|
T | C | 1 | a0001c0002t0001g0141 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.245-23767A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139074813 | ||||||
| chr5:139074816
|
CTCTG | C | 52 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(49): Show | 52 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.245-23774_245-2377 others(8): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139074816 | ||||||
| chr5:139075113
|
G | A | 1 | a0001c0002t0001g0112 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.245-24067C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139075113 | ||||||
| chr5:139075233
|
G | A | 52 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(49): Show | 52 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.245-24187C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139075233 | ||||||
| chr5:139075277
|
G | A | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.245-24231C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139075277 | ||||||
| chr5:139075621
|
G | A | 1 | a0001c0002t0001g0124 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.245-24575C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139075621 | ||||||
| chr5:139075713
|
G | A | 1 | a0001c0001t0002g0018 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.245-24667C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139075713 | ||||||
| chr5:139075744
|
T | C | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.245-24698A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139075744 | ||||||
| chr5:139076397
|
C | T | 1 | a0003c0004t0001g0005 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.245-25351G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139076397 | ||||||
| chr5:139076629
|
A | G | 1 | a0001c0002t0001g0123 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.245-25583T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139076629 | ||||||
| chr5:139076704
|
C | T | 42 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(39): Show | 42 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.245-25658G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139076704 | ||||||
| chr5:139076905
|
C | T | 31 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(28): Show | 31 | HG01243.hp1 HG01258.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.245-25859G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139076905 | ||||||
| chr5:139076992
|
C | T | 1 | a0001c0002t0001g0119 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.245-25946G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139076992 | ||||||
| chr5:139077090
|
T | C | 101 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(98): Show | 101 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.245-26044A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139077090 | ||||||
| chr5:139077214
|
C | T | 1 | a0001c0002t0001g0087 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.245-26168G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139077214 | ||||||
| chr5:139077241
|
C | G | 1 | a0001c0002t0001g0137 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.245-26195G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139077241 | ||||||
| chr5:139077364
|
T | C | 122 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(119): Show | 122 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(119): Show |
intron_variant | MODIFIER | c.245-26318A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139077364 | ||||||
| chr5:139077814
|
CT | C | 41 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(38): Show | 41 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.245-26769delA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139077814 | ||||||
| chr5:139077893
|
C | T | 1 | a0001c0002t0001g0070 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.245-26847G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139077893 | ||||||
| chr5:139078046
|
T | C | 59 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(56): Show | 59 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.245-27000A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139078046 | ||||||
| chr5:139078290
|
A | T | 5 | a0001c0001t0001g0023a0001c0001t0001g0086a0001c0001t0001g0177others(2): Show | 5 | HG02055.hp2 HG02257.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.245-27244T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139078290 | ||||||
| chr5:139078300
|
T | G | 1 | a0001c0002t0001g0176 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.245-27254A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139078300 | ||||||
| chr5:139078491
|
G | A | 76 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0023others(73): Show | 76 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.245-27445C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139078491 | ||||||
| chr5:139078548
|
A | AG | 3 | a0001c0001t0001g0054a0001c0001t0001g0080a0001c0001t0001g0174 | 3 | NA18964.hp2 NA18965.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.245-27503dupC | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139078548 | ||||||
| chr5:139078675
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.245-27629G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139078675 | ||||||
| chr5:139078695
|
G | C | 2 | a0001c0002t0001g0113a0001c0002t0001g0144 | 2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.245-27649C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139078695 | ||||||
| chr5:139078908
|
T | C | 4 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028others(1): Show | 4 | HG02109.hp2 HG03195.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.245-27862A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139078908 | ||||||
| chr5:139078910
|
G | T | 1 | a0001c0001t0001g0030 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.245-27864C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139078910 | ||||||
| chr5:139079011
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.245-27965G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139079011 | ||||||
| chr5:139079167
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.245-28121T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139079167 | ||||||
| chr5:139079257
|
TG | T | 6 | a0001c0002t0001g0098a0001c0002t0001g0108a0001c0002t0001g0109others(3): Show | 6 | NA18946.hp1 NA19003.hp2 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.245-28212delC | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139079257 | ||||||
| chr5:139079438
|
C | G | 2 | a0003c0004t0001g0005a0003c0004t0001g0164 | 2 | HG02280.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.245-28392G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139079438 | ||||||
| chr5:139080099
|
A | G | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.245-29053T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139080099 | ||||||
| chr5:139080116
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.245-29070A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139080116 | ||||||
| chr5:139080304
|
G | A | 1 | a0002c0003t0001g0034 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.245-29258C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139080304 | ||||||
| chr5:139080543
|
T | A | 1 | a0001c0005t0001g0091 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.245-29497A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139080543 | ||||||
| chr5:139080902
|
C | T | 3 | a0001c0001t0002g0029a0001c0001t0002g0093a0001c0001t0002g0140 | 3 | NA18948.hp2 NA18961.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.245-29856G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139080902 | ||||||
| chr5:139081092
|
C | A | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.245-30046G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139081092 | ||||||
| chr5:139081114
|
A | G | 1 | a0001c0002t0001g0143 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.245-30068T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139081114 | ||||||
| chr5:139081365
|
G | T | 102 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(99): Show | 102 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.245-30319C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139081365 | ||||||
| chr5:139081657
|
T | C | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.245-30611A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139081657 | ||||||
| chr5:139081742
|
G | A | 1 | a0001c0002t0001g0176 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.245-30696C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139081742 | ||||||
| chr5:139081842
|
G | A | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.245-30796C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139081842 | ||||||
| chr5:139081868
|
G | T | 1 | a0001c0001t0002g0165 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.245-30822C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139081868 | ||||||
| chr5:139082057
|
A | G | 56 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(53): Show | 56 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.245-31011T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139082057 | ||||||
| chr5:139082137
|
T | C | 1 | a0001c0001t0001g0013 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.245-31091A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139082137 | ||||||
| chr5:139082150
|
G | T | 39 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(36): Show | 39 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.245-31104C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139082150 | ||||||
| chr5:139082256
|
A | G | 1 | a0001c0010t0001g0064 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.245-31210T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139082256 | ||||||
| chr5:139082500
|
T | C | 6 | a0001c0001t0001g0086a0001c0001t0001g0177a0001c0001t0001g0180others(3): Show | 6 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.245-31454A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139082500 | ||||||
| chr5:139082506
|
T | C | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.245-31460A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139082506 | ||||||
| chr5:139082665
|
G | T | 1 | a0001c0002t0001g0173 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.245-31619C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139082665 | ||||||
| chr5:139082807
|
G | A | 1 | a0001c0002t0001g0143 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.245-31761C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139082807 | ||||||
| chr5:139083135
|
T | A | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.245-32089A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139083135 | ||||||
| chr5:139083184
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.245-32138G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139083184 | ||||||
| chr5:139083197
|
G | A | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.245-32151C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139083197 | ||||||
| chr5:139083336
|
C | T | 15 | a0001c0001t0001g0159a0001c0001t0002g0165a0001c0001t0002g0167others(12): Show | 15 | HG01243.hp1 HG01258.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.245-32290G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139083336 | ||||||
| chr5:139083473
|
GTCT | G | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.245-32430_245-3242 others(7): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139083473 | ||||||
| chr5:139083506
|
C | T | 11 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(8): Show | 11 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.245-32460G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139083506 | ||||||
| chr5:139083605
|
A | G | 29 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(26): Show | 29 | HG01243.hp1 HG01258.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.245-32559T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139083605 | ||||||
| chr5:139083647
|
G | A | 1 | a0001c0002t0001g0132 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.245-32601C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139083647 | ||||||
| chr5:139083664
|
T | C | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.245-32618A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139083664 | ||||||
| chr5:139083805
|
T | C | 52 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(49): Show | 52 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.245-32759A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139083805 | ||||||
| chr5:139083907
|
A | T | 2 | a0001c0005t0001g0007a0001c0005t0001g0011 | 2 | HG01243.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.245-32861T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139083907 | ||||||
| chr5:139083908
|
G | A | 1 | a0001c0001t0003g0001 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.245-32862C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139083908 | ||||||
| chr5:139083930
|
A | C | 2 | a0001c0005t0001g0007a0001c0005t0001g0011 | 2 | HG01243.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.245-32884T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139083930 | ||||||
| chr5:139083952
|
G | A | 1 | a0001c0002t0001g0179 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.245-32906C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139083952 | ||||||
| chr5:139083978
|
A | T | 2 | a0001c0002t0001g0099a0001c0002t0001g0101 | 2 | HG01884.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.245-32932T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139083978 | ||||||
| chr5:139083992
|
G | A | 102 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(99): Show | 102 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.245-32946C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139083992 | ||||||
| chr5:139084383
|
C | T | 102 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(99): Show | 102 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.245-33337G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139084383 | ||||||
| chr5:139084614
|
T | C | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.245-33568A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139084614 | ||||||
| chr5:139084663
|
T | C | 1 | a0002c0003t0001g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.245-33617A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139084663 | ||||||
| chr5:139084667
|
G | A | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0002g0029others(3): Show | 6 | HG01884.hp2 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.245-33621C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139084667 | ||||||
| chr5:139084796
|
T | A | 85 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0023others(82): Show | 85 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.245-33750A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139084796 | ||||||
| chr5:139084806
|
A | T | 2 | a0001c0001t0001g0056a0001c0001t0001g0058 | 2 | HG06807.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.245-33760T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139084806 | ||||||
| chr5:139085018
|
C | A | 12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(9): Show | 12 | NA18942.hp1 NA18946.hp2 NA18948.hp1 others(9): Show |
intron_variant | MODIFIER | c.245-33972G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139085018 | ||||||
| chr5:139085096
|
C | A | 46 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(43): Show | 46 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.245-34050G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139085096 | ||||||
| chr5:139085271
|
C | T | 105 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(102): Show | 105 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(102): Show |
intron_variant | MODIFIER | c.245-34225G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139085271 | ||||||
| chr5:139085294
|
G | A | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.245-34248C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139085294 | ||||||
| chr5:139085491
|
A | G | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.245-34445T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139085491 | ||||||
| chr5:139085563
|
G | T | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.245-34517C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139085563 | ||||||
| chr5:139085716
|
G | C | 69 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0030others(66): Show | 69 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.245-34670C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139085716 | ||||||
| chr5:139086108
|
GA | G | 71 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0030others(68): Show | 71 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.244+34926delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139086108 | ||||||
| chr5:139086108
|
GAA | G | 34 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(31): Show | 34 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.244+34925_244+3492 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139086108 | ||||||
| chr5:139086266
|
G | A | 4 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0019others(1): Show | 4 | HG02145.hp1 HG02723.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+34769C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139086266 | ||||||
| chr5:139086270
|
TA | T | 7 | a0001c0001t0001g0092a0001c0002t0001g0113a0001c0002t0001g0130others(4): Show | 7 | HG02451.hp2 HG02970.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.244+34764delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139086270 | ||||||
| chr5:139086286
|
A | AAAG | 49 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(46): Show | 49 | HG00323.hp2 HG00423.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.244+34746_244+3474 others(7): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139086286 | ||||||
| chr5:139086286
|
A | AAG | 11 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(8): Show | 11 | HG01891.hp1 HG01943.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.244+34748_244+3474 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139086286 | ||||||
| chr5:139086286
|
A | AG | 5 | a0001c0001t0001g0030a0002c0003t0001g0134a0002c0006t0001g0097others(2): Show | 5 | HG02145.hp2 HG02280.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.244+34748_244+3474 others(5): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139086286 | ||||||
| chr5:139086286
|
A | G | 4 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0133others(1): Show | 4 | HG00642.hp1 HG01109.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+34749T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139086286 | ||||||
| chr5:139086302
|
A | C | 1 | a0001c0002t0001g0087 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.244+34733T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139086302 | ||||||
| chr5:139086472
|
C | A | 2 | a0002c0006t0001g0097a0002c0006t0001g0103 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.244+34563G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139086472 | ||||||
| chr5:139086538
|
A | C | 2 | a0002c0006t0001g0097a0002c0006t0001g0103 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.244+34497T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139086538 | ||||||
| chr5:139086646
|
C | T | 1 | a0001c0002t0001g0099 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.244+34389G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139086646 | ||||||
| chr5:139086758
|
G | C | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.244+34277C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139086758 | ||||||
| chr5:139086999
|
A | T | 1 | a0001c0001t0001g0035 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.244+34036T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139086999 | ||||||
| chr5:139087449
|
C | T | 2 | a0001c0005t0001g0091a0008c0011t0001g0196 | 2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.244+33586G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139087449 | ||||||
| chr5:139087636
|
A | G | 4 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0019others(1): Show | 4 | HG02145.hp1 HG02723.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+33399T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139087636 | ||||||
| chr5:139087904
|
T | C | 1 | a0001c0002t0001g0142 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.244+33131A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139087904 | ||||||
| chr5:139088029
|
A | AC | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.244+33005dupG | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139088029 | ||||||
| chr5:139088346
|
T | G | 1 | a0001c0002t0001g0038 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.244+32689A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139088346 | ||||||
| chr5:139088508
|
G | C | 10 | a0001c0001t0002g0165a0001c0001t0002g0167a0001c0002t0001g0004others(7): Show | 10 | HG01258.hp1 HG02109.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.244+32527C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139088508 | ||||||
| chr5:139088589
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.244+32446T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139088589 | ||||||
| chr5:139088748
|
A | G | 113 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(110): Show | 113 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(110): Show |
intron_variant | MODIFIER | c.244+32287T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139088748 | ||||||
| chr5:139089044
|
C | G | 1 | a0001c0002t0001g0111 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.244+31991G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139089044 | ||||||
| chr5:139089337
|
C | T | 22 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(19): Show | 22 | HG01258.hp1 HG01884.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.244+31698G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139089337 | ||||||
| chr5:139089532
|
T | TA | 57 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(54): Show | 57 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.244+31502dupT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139089532 | ||||||
| chr5:139089543
|
TAA | T | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.244+31490_244+3149 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139089543 | ||||||
| chr5:139089634
|
A | G | 2 | a0002c0006t0001g0097a0002c0006t0001g0103 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.244+31401T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139089634 | ||||||
| chr5:139090012
|
T | G | 5 | a0001c0001t0002g0165a0001c0001t0002g0167a0001c0002t0001g0004others(2): Show | 5 | HG01258.hp1 HG02109.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.244+31023A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139090012 | ||||||
| chr5:139090083
|
T | G | 19 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(16): Show | 19 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.244+30952A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139090083 | ||||||
| chr5:139090108
|
C | T | 1 | a0001c0002t0001g0072 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.244+30927G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139090108 | ||||||
| chr5:139090354
|
C | A | 1 | a0001c0002t0001g0106 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.244+30681G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139090354 | ||||||
| chr5:139090484
|
T | C | 55 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(52): Show | 55 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.244+30551A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139090484 | ||||||
| chr5:139090642
|
C | T | 2 | a0003c0004t0001g0005a0003c0004t0001g0164 | 2 | HG02280.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.244+30393G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139090642 | ||||||
| chr5:139091130
|
T | C | 2 | a0001c0002t0001g0006a0001c0002t0001g0010 | 2 | HG02723.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.244+29905A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139091130 | ||||||
| chr5:139091322
|
G | A | 1 | a0001c0001t0001g0154 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.244+29713C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139091322 | ||||||
| chr5:139091851
|
G | A | 2 | a0002c0006t0001g0097a0002c0006t0001g0103 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.244+29184C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139091851 | ||||||
| chr5:139091981
|
C | T | 2 | a0001c0005t0001g0091a0008c0011t0001g0196 | 2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.244+29054G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139091981 | ||||||
| chr5:139092186
|
C | G | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.244+28849G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139092186 | ||||||
| chr5:139092555
|
G | A | 3 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0185 | 3 | HG02451.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.244+28480C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139092555 | ||||||
| chr5:139092645
|
G | A | 4 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0019others(1): Show | 4 | HG02145.hp1 HG02723.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+28390C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139092645 | ||||||
| chr5:139092693
|
T | C | 1 | a0001c0001t0003g0001 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.244+28342A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139092693 | ||||||
| chr5:139092732
|
C | T | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.244+28303G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139092732 | ||||||
| chr5:139092953
|
A | G | 13 | a0001c0001t0001g0030a0001c0001t0001g0086a0001c0001t0001g0159others(10): Show | 13 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.244+28082T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139092953 | ||||||
| chr5:139092975
|
C | T | 22 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(19): Show | 22 | HG01258.hp1 HG01884.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.244+28060G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139092975 | ||||||
| chr5:139093100
|
A | G | 70 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0030others(67): Show | 70 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.244+27935T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139093100 | ||||||
| chr5:139093365
|
T | G | 4 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0019others(1): Show | 4 | HG02145.hp1 HG02723.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+27670A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139093365 | ||||||
| chr5:139093412
|
G | A | 2 | a0001c0002t0001g0099a0001c0002t0001g0101 | 2 | HG01884.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.244+27623C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139093412 | ||||||
| chr5:139093459
|
T | A | 1 | a0001c0001t0001g0047 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.244+27576A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139093459 | ||||||
| chr5:139093736
|
T | C | 4 | a0001c0001t0001g0086a0001c0001t0001g0177a0001c0001t0001g0180others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+27299A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139093736 | ||||||
| chr5:139093802
|
A | C | 8 | a0001c0001t0001g0086a0001c0001t0001g0177a0001c0001t0001g0180others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.244+27233T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139093802 | ||||||
| chr5:139093820
|
A | G | 3 | a0001c0002t0001g0065a0001c0002t0001g0085a0001c0002t0001g0102 | 3 | HG01975.hp1 HG01981.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.244+27215T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139093820 | ||||||
| chr5:139093855
|
A | G | 1 | a0001c0002t0001g0153 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.244+27180T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139093855 | ||||||
| chr5:139094073
|
T | C | 1 | a0001c0002t0001g0184 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.244+26962A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139094073 | ||||||
| chr5:139094569
|
G | T | 1 | a0001c0002t0001g0115 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.244+26466C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139094569 | ||||||
| chr5:139094626
|
G | A | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.244+26409C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139094626 | ||||||
| chr5:139094906
|
C | T | 2 | a0001c0005t0001g0091a0008c0011t0001g0196 | 2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.244+26129G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139094906 | ||||||
| chr5:139095265
|
C | CT | 9 | a0001c0001t0001g0033a0001c0001t0001g0086a0001c0001t0001g0149others(6): Show | 9 | HG01243.hp2 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.244+25769dupA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139095265 | ||||||
| chr5:139095265
|
C | CTT | 5 | a0001c0001t0001g0030a0001c0001t0001g0159a0002c0006t0001g0097others(2): Show | 5 | HG02145.hp2 HG02280.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.244+25768_244+2576 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139095265 | ||||||
| chr5:139095265
|
CT | C | 19 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0032others(16): Show | 19 | HG01069.hp2 HG01109.hp2 HG01993.hp1 others(16): Show |
intron_variant | MODIFIER | c.244+25769delA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139095265 | ||||||
| chr5:139095265
|
CTT | C | 11 | a0001c0001t0002g0165a0001c0001t0002g0167a0001c0002t0001g0004others(8): Show | 11 | HG01258.hp1 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.244+25768_244+2576 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139095265 | ||||||
| chr5:139095266
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.244+25769A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139095266 | ||||||
| chr5:139095315
|
G | A | 52 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(49): Show | 52 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.244+25720C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139095315 | ||||||
| chr5:139095319
|
G | A | 95 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0023others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.244+25716C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139095319 | ||||||
| chr5:139095476
|
G | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(54): Show | 57 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.244+25559C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139095476 | ||||||
| chr5:139095768
|
C | T | 57 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(54): Show | 57 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.244+25267G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139095768 | ||||||
| chr5:139095863
|
G | T | 18 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(15): Show | 18 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.244+25172C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139095863 | ||||||
| chr5:139096757
|
G | A | 125 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(122): Show | 125 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(122): Show |
intron_variant | MODIFIER | c.244+24278C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139096757 | ||||||
| chr5:139096824
|
G | A | 1 | a0001c0002t0001g0185 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.244+24211C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139096824 | ||||||
| chr5:139096961
|
C | T | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.244+24074G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139096961 | ||||||
| chr5:139097070
|
G | C | 57 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(54): Show | 57 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.244+23965C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139097070 | ||||||
| chr5:139097218
|
C | T | 12 | a0001c0001t0002g0165a0001c0001t0002g0167a0001c0002t0001g0004others(9): Show | 12 | HG01258.hp1 HG01884.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.244+23817G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139097218 | ||||||
| chr5:139097241
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.244+23794C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139097241 | ||||||
| chr5:139097485
|
CT | C | 46 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(43): Show | 46 | HG00323.hp2 HG00735.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.244+23549delA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139097485 | ||||||
| chr5:139097608
|
G | T | 36 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(33): Show | 36 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.244+23427C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139097608 | ||||||
| chr5:139097766
|
G | A | 4 | a0001c0002t0001g0118a0001c0002t0001g0146a0001c0002t0001g0151others(1): Show | 4 | HG02258.hp1 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+23269C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139097766 | ||||||
| chr5:139098156
|
A | G | 12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(9): Show | 12 | NA18942.hp1 NA18946.hp2 NA18948.hp1 others(9): Show |
intron_variant | MODIFIER | c.244+22879T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139098156 | ||||||
| chr5:139098285
|
T | C | 1 | a0001c0002t0001g0002 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.244+22750A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139098285 | ||||||
| chr5:139098309
|
T | C | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.244+22726A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139098309 | ||||||
| chr5:139098530
|
TG | T | 7 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.244+22504delC | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139098530 | ||||||
| chr5:139098558
|
A | G | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.244+22477T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139098558 | ||||||
| chr5:139098680
|
C | A | 1 | a0002c0003t0001g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.244+22355G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139098680 | ||||||
| chr5:139098809
|
C | CT | 11 | a0001c0001t0001g0027a0001c0001t0001g0177a0001c0002t0001g0065others(8): Show | 11 | HG00735.hp2 HG01981.hp2 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.244+22225dupA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139098809 | ||||||
| chr5:139098809
|
C | CTT | 5 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0053others(2): Show | 5 | HG01258.hp2 HG01516.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.244+22224_244+2222 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139098809 | ||||||
| chr5:139098809
|
C | CTTT | 43 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0044others(40): Show | 43 | HG00323.hp2 HG00642.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.244+22223_244+2222 others(7): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139098809 | ||||||
| chr5:139098809
|
CT | C | 11 | a0001c0001t0001g0092a0001c0001t0001g0180a0001c0001t0002g0140others(8): Show | 11 | HG01891.hp1 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.244+22225delA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139098809 | ||||||
| chr5:139098809
|
CTT | C | 5 | a0001c0001t0001g0030a0001c0001t0001g0159a0001c0001t0001g0162others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.244+22224_244+2222 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139098809 | ||||||
| chr5:139098809
|
CTTTTT | C | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.244+22221_244+2222 others(9): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139098809 | ||||||
| chr5:139098809
|
CTTTTTT | C | 12 | a0001c0001t0002g0165a0001c0001t0002g0167a0001c0002t0001g0004others(9): Show | 12 | HG01258.hp1 HG01884.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.244+22220_244+2222 others(10): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139098809 | ||||||
| chr5:139098809
|
CTTTTTTT others(1): Show |
C | 14 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(11): Show | 14 | NA18522.hp1 NA18942.hp1 NA18946.hp2 others(11): Show |
intron_variant | MODIFIER | c.244+22218_244+2222 others(12): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139098809 | ||||||
| chr5:139098809
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.244+22216_244+2222 others(14): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139098809 | ||||||
| chr5:139098847
|
C | T | 1 | a0001c0002t0001g0127 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.244+22188G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139098847 | ||||||
| chr5:139099188
|
A | T | 1 | a0006c0009t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.244+21847T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139099188 | ||||||
| chr5:139099354
|
T | C | 2 | a0004c0007t0001g0158a0004c0007t0001g0195 | 2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.244+21681A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139099354 | ||||||
| chr5:139099614
|
A | G | 52 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(49): Show | 52 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.244+21421T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139099614 | ||||||
| chr5:139099715
|
T | C | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.244+21320A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139099715 | ||||||
| chr5:139099809
|
T | C | 2 | a0001c0001t0001g0044a0001c0001t0001g0081 | 2 | HG02738.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.244+21226A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139099809 | ||||||
| chr5:139099908
|
C | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0159 | 2 | HG02145.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.244+21127G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139099908 | ||||||
| chr5:139099944
|
A | G | 9 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.244+21091T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139099944 | ||||||
| chr5:139100681
|
T | C | 13 | a0001c0001t0001g0030a0001c0001t0001g0086a0001c0001t0001g0159others(10): Show | 13 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.244+20354A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139100681 | ||||||
| chr5:139100703
|
C | T | 36 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(33): Show | 36 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.244+20332G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139100703 | ||||||
| chr5:139100764
|
T | C | 2 | a0001c0002t0001g0025a0001c0002t0001g0026 | 2 | HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.244+20271A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139100764 | ||||||
| chr5:139101074
|
T | C | 1 | a0001c0002t0001g0176 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.244+19961A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139101074 | ||||||
| chr5:139101127
|
G | A | 6 | a0001c0001t0002g0165a0001c0001t0002g0167a0001c0002t0001g0004others(3): Show | 6 | HG01258.hp1 HG02109.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.244+19908C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139101127 | ||||||
| chr5:139101176
|
A | G | 57 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(54): Show | 57 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.244+19859T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139101176 | ||||||
| chr5:139101227
|
C | T | 13 | a0001c0001t0001g0030a0001c0001t0001g0086a0001c0001t0001g0159others(10): Show | 13 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.244+19808G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139101227 | ||||||
| chr5:139101242
|
A | G | 1 | a0001c0002t0001g0130 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.244+19793T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139101242 | ||||||
| chr5:139101278
|
C | T | 3 | a0003c0004t0001g0005a0003c0004t0001g0138a0003c0004t0001g0164 | 3 | HG02280.hp2 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.244+19757G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139101278 | ||||||
| chr5:139101608
|
T | C | 13 | a0001c0001t0001g0030a0001c0001t0001g0086a0001c0001t0001g0159others(10): Show | 13 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.244+19427A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139101608 | ||||||
| chr5:139101790
|
G | A | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.244+19245C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139101790 | ||||||
| chr5:139102007
|
T | C | 95 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0023others(92): Show | 95 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.244+19028A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139102007 | ||||||
| chr5:139102033
|
T | C | 13 | a0001c0001t0001g0030a0001c0001t0001g0086a0001c0001t0001g0159others(10): Show | 13 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.244+19002A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139102033 | ||||||
| chr5:139102398
|
T | TTTG | 3 | a0003c0004t0001g0005a0003c0004t0001g0138a0003c0004t0001g0164 | 3 | HG02280.hp2 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.244+18634_244+1863 others(7): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139102398 | ||||||
| chr5:139102484
|
CAA | C | 11 | a0001c0001t0001g0030a0001c0001t0001g0086a0001c0001t0001g0159others(8): Show | 11 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.244+18549_244+1855 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139102484 | ||||||
| chr5:139102484
|
CAAA | C | 5 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028others(2): Show | 5 | HG02109.hp2 HG02630.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.244+18548_244+1855 others(7): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139102484 | ||||||
| chr5:139102496
|
AAAAAAGA others(1): Show |
A | 75 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0023others(72): Show | 75 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.244+18531_244+1853 others(12): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139102496 | ||||||
| chr5:139102708
|
CT | C | 83 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0022others(80): Show | 83 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.244+18326delA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139102708 | ||||||
| chr5:139102736
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.244+18299C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139102736 | ||||||
| chr5:139102806
|
C | G | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.244+18229G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139102806 | ||||||
| chr5:139102862
|
G | C | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.244+18173C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139102862 | ||||||
| chr5:139103167
|
G | T | 1 | a0001c0002t0001g0142 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.244+17868C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139103167 | ||||||
| chr5:139103868
|
CT | C | 13 | a0001c0001t0001g0030a0001c0001t0001g0086a0001c0001t0001g0159others(10): Show | 13 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.244+17166delA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139103868 | ||||||
| chr5:139103935
|
T | C | 45 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(42): Show | 45 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.244+17100A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139103935 | ||||||
| chr5:139103992
|
T | A | 1 | a0001c0002t0001g0132 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.244+17043A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139103992 | ||||||
| chr5:139103993
|
C | T | 1 | a0001c0002t0001g0132 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.244+17042G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139103993 | ||||||
| chr5:139104110
|
C | T | 2 | a0002c0006t0001g0097a0002c0006t0001g0103 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.244+16925G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139104110 | ||||||
| chr5:139104112
|
G | A | 57 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(54): Show | 57 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.244+16923C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139104112 | ||||||
| chr5:139104229
|
A | G | 1 | a0001c0001t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.244+16806T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139104229 | ||||||
| chr5:139104231
|
C | A | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0002t0001g0028 | 3 | HG02109.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.244+16804G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139104231 | ||||||
| chr5:139104311
|
TGAA | T | 2 | a0004c0007t0001g0158a0004c0007t0001g0195 | 2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.244+16721_244+1672 others(7): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139104311 | ||||||
| chr5:139104669
|
G | A | 2 | a0001c0005t0001g0091a0008c0011t0001g0196 | 2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.244+16366C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139104669 | ||||||
| chr5:139105045
|
C | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0159a0001c0005t0001g0091others(1): Show | 4 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.244+15990G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139105045 | ||||||
| chr5:139105056
|
G | A | 1 | a0001c0002t0001g0150 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.244+15979C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139105056 | ||||||
| chr5:139105638
|
C | G | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG02109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.244+15397G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139105638 | ||||||
| chr5:139105714
|
C | T | 2 | a0002c0006t0001g0097a0002c0006t0001g0103 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.244+15321G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139105714 | ||||||
| chr5:139105807
|
A | C | 1 | a0001c0002t0001g0099 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.244+15228T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139105807 | ||||||
| chr5:139105890
|
T | C | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.244+15145A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139105890 | ||||||
| chr5:139105960
|
C | T | 2 | a0001c0002t0001g0099a0001c0002t0001g0101 | 2 | HG01884.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.244+15075G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139105960 | ||||||
| chr5:139106128
|
C | T | 1 | a0001c0002t0001g0019 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.244+14907G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139106128 | ||||||
| chr5:139106609
|
T | C | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.244+14426A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139106609 | ||||||
| chr5:139106633
|
A | T | 57 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(54): Show | 57 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.244+14402T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139106633 | ||||||
| chr5:139106815
|
C | T | 103 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(100): Show | 103 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.244+14220G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139106815 | ||||||
| chr5:139106866
|
C | T | 3 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0001t0001g0172 | 3 | HG01081.hp1 HG03710.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.244+14169G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139106866 | ||||||
| chr5:139107217
|
C | T | 1 | a0001c0002t0001g0104 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.244+13818G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139107217 | ||||||
| chr5:139107465
|
C | A | 52 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(49): Show | 52 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.244+13570G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139107465 | ||||||
| chr5:139107820
|
T | G | 1 | a0001c0001t0001g0163 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.244+13215A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139107820 | ||||||
| chr5:139107821
|
T | A | 1 | a0001c0001t0001g0163 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.244+13214A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139107821 | ||||||
| chr5:139107822
|
C | A | 1 | a0001c0001t0001g0163 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.244+13213G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139107822 | ||||||
| chr5:139108481
|
G | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(54): Show | 57 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.244+12554C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139108481 | ||||||
| chr5:139108542
|
G | A | 3 | a0003c0004t0001g0005a0003c0004t0001g0138a0003c0004t0001g0164 | 3 | HG02280.hp2 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.244+12493C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139108542 | ||||||
| chr5:139108695
|
C | T | 26 | a0001c0001t0001g0030a0001c0001t0001g0086a0001c0001t0001g0177others(23): Show | 26 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.244+12340G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139108695 | ||||||
| chr5:139108906
|
G | GA | 91 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0020others(88): Show | 91 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(88): Show |
intron_variant | MODIFIER | c.244+12128dupT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139108906 | ||||||
| chr5:139109188
|
A | G | 26 | a0001c0001t0001g0030a0001c0001t0001g0086a0001c0001t0001g0177others(23): Show | 26 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.244+11847T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139109188 | ||||||
| chr5:139109237
|
A | G | 84 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0030others(81): Show | 84 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.244+11798T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139109237 | ||||||
| chr5:139109396
|
C | T | 1 | a0001c0002t0001g0087 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.244+11639G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139109396 | ||||||
| chr5:139109457
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.244+11578C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139109457 | ||||||
| chr5:139109695
|
T | TA | 33 | a0001c0001t0001g0047a0001c0001t0001g0079a0001c0001t0002g0093others(30): Show | 33 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.244+11339dupT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139109695 | ||||||
| chr5:139109695
|
TA | T | 26 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(23): Show | 26 | HG01109.hp2 HG01243.hp1 HG01993.hp1 others(23): Show |
intron_variant | MODIFIER | c.244+11339delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139109695 | ||||||
| chr5:139109695
|
TAA | T | 21 | a0001c0001t0001g0030a0001c0001t0001g0086a0001c0001t0001g0177others(18): Show | 21 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.244+11338_244+1133 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139109695 | ||||||
| chr5:139109780
|
C | CT | 10 | a0001c0002t0001g0072a0001c0002t0001g0098a0001c0002t0001g0108others(7): Show | 10 | HG01074.hp1 HG01081.hp2 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.244+11254dupA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139109780 | ||||||
| chr5:139109780
|
CT | C | 78 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0030others(75): Show | 78 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.244+11254delA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139109780 | ||||||
| chr5:139110163
|
T | A | 1 | a0001c0002t0001g0113 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.244+10872A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139110163 | ||||||
| chr5:139110281
|
C | A | 10 | a0001c0001t0001g0030a0001c0001t0001g0086a0001c0001t0001g0177others(7): Show | 10 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.244+10754G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139110281 | ||||||
| chr5:139110385
|
T | C | 55 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(52): Show | 55 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.244+10650A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139110385 | ||||||
| chr5:139110580
|
A | G | 5 | a0001c0001t0001g0049a0001c0001t0001g0053a0001c0001t0001g0058others(2): Show | 5 | NA18945.hp2 NA18968.hp2 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.244+10455T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139110580 | ||||||
| chr5:139110753
|
G | C | 1 | a0002c0003t0001g0034 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.244+10282C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139110753 | ||||||
| chr5:139110828
|
A | G | 2 | a0001c0001t0001g0067a0001c0001t0001g0074 | 2 | HG01934.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.244+10207T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139110828 | ||||||
| chr5:139110926
|
C | G | 2 | a0001c0001t0001g0056a0001c0001t0001g0063 | 2 | HG03654.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.244+10109G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139110926 | ||||||
| chr5:139111017
|
G | T | 1 | a0001c0001t0001g0069 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.244+10018C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139111017 | ||||||
| chr5:139111127
|
A | C | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.244+9908T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139111127 | ||||||
| chr5:139111330
|
T | A | 1 | a0001c0002t0001g0179 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.244+9705A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139111330 | ||||||
| chr5:139111602
|
G | A | 1 | a0001c0002t0001g0179 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.244+9433C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139111602 | ||||||
| chr5:139111657
|
T | C | 3 | a0003c0004t0001g0005a0003c0004t0001g0138a0003c0004t0001g0164 | 3 | HG02280.hp2 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.244+9378A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139111657 | ||||||
| chr5:139111811
|
C | A | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.244+9224G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139111811 | ||||||
| chr5:139111884
|
T | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(54): Show | 57 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.244+9151A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139111884 | ||||||
| chr5:139111893
|
G | T | 5 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0028others(2): Show | 5 | HG02451.hp1 HG03225.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.244+9142C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139111893 | ||||||
| chr5:139111898
|
A | G | 5 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0028others(2): Show | 5 | HG02451.hp1 HG03225.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.244+9137T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139111898 | ||||||
| chr5:139111973
|
C | T | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG02109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.244+9062G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139111973 | ||||||
| chr5:139111991
|
C | T | 1 | a0001c0002t0001g0117 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.244+9044G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139111991 | ||||||
| chr5:139112078
|
C | G | 45 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(42): Show | 45 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.244+8957G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139112078 | ||||||
| chr5:139112090
|
G | A | 2 | a0001c0002t0001g0099a0001c0002t0001g0101 | 2 | HG01884.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.244+8945C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139112090 | ||||||
| chr5:139112274
|
G | A | 102 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(99): Show | 102 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.244+8761C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139112274 | ||||||
| chr5:139112337
|
G | A | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.244+8698C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139112337 | ||||||
| chr5:139112414
|
G | A | 61 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(58): Show | 61 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.244+8621C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139112414 | ||||||
| chr5:139112424
|
C | T | 57 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(54): Show | 57 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.244+8611G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139112424 | ||||||
| chr5:139112449
|
G | A | 1 | a0001c0002t0001g0136 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.244+8586C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139112449 | ||||||
| chr5:139112475
|
G | A | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.244+8560C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139112475 | ||||||
| chr5:139112623
|
G | A | 11 | a0001c0001t0001g0030a0001c0001t0001g0086a0001c0001t0001g0177others(8): Show | 11 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.244+8412C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139112623 | ||||||
| chr5:139112648
|
G | A | 9 | a0001c0001t0001g0086a0001c0001t0001g0177a0001c0001t0001g0180others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.244+8387C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139112648 | ||||||
| chr5:139112692
|
CGCCCGGC others(33): Show |
C | 1 | a0001c0001t0001g0052 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.244+8303_244+8342d others(42): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139112692 | ||||||
| chr5:139112798
|
C | T | 1 | a0001c0002t0001g0135 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.244+8237G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139112798 | ||||||
| chr5:139112839
|
A | G | 1 | a0001c0002t0001g0002 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.244+8196T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139112839 | ||||||
| chr5:139112851
|
C | T | 103 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(100): Show | 103 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.244+8184G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139112851 | ||||||
| chr5:139112867
|
G | A | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.244+8168C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139112867 | ||||||
| chr5:139112937
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.244+8098A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139112937 | ||||||
| chr5:139113097
|
AGCATGCT others(9): Show |
A | 1 | a0001c0001t0002g0018 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.244+7922_244+7937d others(18): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139113097 | ||||||
| chr5:139113106
|
G | C | 1 | a0001c0002t0001g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.244+7929C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139113106 | ||||||
| chr5:139113157
|
T | C | 52 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(49): Show | 52 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.244+7878A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139113157 | ||||||
| chr5:139113196
|
A | G | 3 | a0001c0002t0001g0124a0001c0002t0001g0175a0001c0002t0001g0182 | 3 | HG02698.hp2 HG03942.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.244+7839T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139113196 | ||||||
| chr5:139113252
|
T | A | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.244+7783A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139113252 | ||||||
| chr5:139113317
|
A | T | 45 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(42): Show | 45 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.244+7718T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139113317 | ||||||
| chr5:139113321
|
A | T | 48 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(45): Show | 48 | HG00423.hp2 HG01069.hp1 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.244+7714T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139113321 | ||||||
| chr5:139113325
|
A | T | 103 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(100): Show | 103 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.244+7710T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139113325 | ||||||
| chr5:139113327
|
AT | A | 94 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(91): Show | 94 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.244+7707delA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139113327 | ||||||
| chr5:139113329
|
TTA | T | 3 | a0001c0001t0001g0159a0002c0003t0001g0034a0002c0003t0001g0161 | 3 | HG02976.hp1 NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.244+7704_244+7705d others(4): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139113329 | ||||||
| chr5:139113330
|
T | A | 7 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0162others(4): Show | 7 | HG01109.hp2 HG01993.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.244+7705A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139113330 | ||||||
| chr5:139113631
|
T | C | 1 | a0001c0002t0001g0126 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.244+7404A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139113631 | ||||||
| chr5:139113697
|
C | T | 1 | a0001c0002t0001g0145 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.244+7338G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139113697 | ||||||
| chr5:139113934
|
T | C | 1 | a0001c0002t0001g0004 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.244+7101A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139113934 | ||||||
| chr5:139114560
|
G | A | 26 | a0001c0001t0001g0030a0001c0001t0001g0086a0001c0001t0001g0177others(23): Show | 26 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.244+6475C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139114560 | ||||||
| chr5:139114873
|
CA | C | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG02109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.244+6161delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139114873 | ||||||
| chr5:139114960
|
G | A | 1 | a0001c0001t0002g0018 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.244+6075C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139114960 | ||||||
| chr5:139115037
|
G | T | 1 | a0001c0002t0001g0068 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.244+5998C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139115037 | ||||||
| chr5:139115135
|
CAGGG | C | 2 | a0001c0002t0001g0008a0001c0002t0001g0183 | 2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.244+5896_244+5899d others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139115135 | ||||||
| chr5:139115147
|
G | A | 18 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(15): Show | 18 | HG01243.hp1 HG02976.hp1 HG03195.hp1 others(15): Show |
intron_variant | MODIFIER | c.244+5888C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139115147 | ||||||
| chr5:139115257
|
T | C | 9 | a0001c0001t0001g0086a0001c0001t0001g0177a0001c0001t0001g0180others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.244+5778A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139115257 | ||||||
| chr5:139115302
|
T | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0071 | 2 | HG02132.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.244+5733A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139115302 | ||||||
| chr5:139115468
|
T | G | 2 | a0001c0002t0001g0113a0001c0002t0001g0144 | 2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.244+5567A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139115468 | ||||||
| chr5:139115596
|
A | G | 30 | a0001c0001t0001g0030a0001c0001t0001g0086a0001c0001t0001g0088others(27): Show | 30 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.244+5439T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139115596 | ||||||
| chr5:139115621
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.244+5414G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139115621 | ||||||
| chr5:139115626
|
G | A | 52 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(49): Show | 52 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.244+5409C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139115626 | ||||||
| chr5:139115704
|
C | T | 1 | a0001c0001t0001g0050 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.244+5331G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139115704 | ||||||
| chr5:139115901
|
G | C | 2 | a0001c0001t0001g0035a0001c0001t0001g0055 | 2 | HG01975.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.244+5134C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139115901 | ||||||
| chr5:139115941
|
T | G | 1 | a0001c0002t0001g0132 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.244+5094A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139115941 | ||||||
| chr5:139116022
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.244+5013G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139116022 | ||||||
| chr5:139116198
|
A | C | 1 | a0001c0002t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.244+4837T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139116198 | ||||||
| chr5:139116221
|
G | A | 2 | a0001c0002t0001g0008a0001c0002t0001g0183 | 2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.244+4814C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139116221 | ||||||
| chr5:139116491
|
A | T | 9 | a0001c0001t0001g0086a0001c0001t0001g0177a0001c0001t0001g0180others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.244+4544T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139116491 | ||||||
| chr5:139116536
|
C | G | 99 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(96): Show | 99 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.244+4499G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139116536 | ||||||
| chr5:139116848
|
G | T | 1 | a0002c0006t0001g0103 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.244+4187C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139116848 | ||||||
| chr5:139116918
|
C | G | 1 | a0001c0002t0001g0114 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.244+4117G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139116918 | ||||||
| chr5:139117415
|
G | A | 27 | a0001c0001t0001g0030a0001c0001t0001g0086a0001c0001t0001g0177others(24): Show | 27 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.244+3620C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139117415 | ||||||
| chr5:139117464
|
C | T | 10 | a0001c0001t0001g0030a0001c0001t0001g0086a0001c0001t0001g0177others(7): Show | 10 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.244+3571G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139117464 | ||||||
| chr5:139118155
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.244+2880C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139118155 | ||||||
| chr5:139118503
|
G | A | 127 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(124): Show | 127 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(124): Show |
intron_variant | MODIFIER | c.244+2532C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139118503 | ||||||
| chr5:139119315
|
G | A | 4 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0019others(1): Show | 4 | HG02145.hp1 HG02723.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+1720C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139119315 | ||||||
| chr5:139120688
|
G | A | 1 | a0001c0002t0001g0084 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.244+347C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139120688 | ||||||
| chr5:139120726
|
A | G | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.244+309T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139120726 | ||||||
| chr5:139120915
|
T | C | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG02109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.244+120A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139120915 | ||||||
| chr5:139120964
|
C | T | 1 | a0001c0002t0001g0087 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.244+71G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139120964 | ||||||
| chr5:139120978
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.244+57C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 3/9 | chr5 | 139120978 | ||||||
| chr5:139121219
|
A | C | 1 | a0001c0002t0001g0100 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.106-46T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139121219 | ||||||
| chr5:139121227
|
A | G | 13 | a0001c0001t0001g0030a0001c0001t0001g0086a0001c0001t0001g0088others(10): Show | 13 | HG01109.hp2 HG01891.hp1 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.106-54T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139121227 | ||||||
| chr5:139121305
|
G | A | 52 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(49): Show | 52 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.106-132C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139121305 | ||||||
| chr5:139121673
|
A | C | 1 | a0001c0001t0001g0056 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.106-500T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139121673 | ||||||
| chr5:139121741
|
G | A | 1 | a0001c0002t0001g0143 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.106-568C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139121741 | ||||||
| chr5:139122081
|
G | A | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.106-908C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139122081 | ||||||
| chr5:139122091
|
CA | C | 3 | a0001c0001t0001g0088a0001c0001t0001g0133a0001c0001t0001g0166 | 3 | HG01109.hp2 HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.106-919delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139122091 | ||||||
| chr5:139122185
|
C | A | 44 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(41): Show | 44 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.106-1012G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139122185 | ||||||
| chr5:139122533
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.106-1360A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139122533 | ||||||
| chr5:139122624
|
T | A | 1 | a0001c0002t0001g0112 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.106-1451A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139122624 | ||||||
| chr5:139122836
|
T | G | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.106-1663A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139122836 | ||||||
| chr5:139122879
|
C | T | 45 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(42): Show | 45 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.106-1706G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139122879 | ||||||
| chr5:139122895
|
G | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(54): Show | 57 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.106-1722C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139122895 | ||||||
| chr5:139122944
|
A | C | 45 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(42): Show | 45 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.106-1771T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139122944 | ||||||
| chr5:139122967
|
T | C | 1 | a0001c0002t0001g0087 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.106-1794A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139122967 | ||||||
| chr5:139123013
|
ATAGT | A | 6 | a0001c0001t0002g0018a0001c0001t0002g0029a0001c0001t0002g0093others(3): Show | 6 | HG01258.hp1 HG01258.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.106-1844_106-1841d others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139123013 | ||||||
| chr5:139123164
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.106-1991C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139123164 | ||||||
| chr5:139123307
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG02109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.106-2134C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139123307 | ||||||
| chr5:139123380
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.106-2207G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139123380 | ||||||
| chr5:139123419
|
A | G | 57 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(54): Show | 57 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.106-2246T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139123419 | ||||||
| chr5:139123682
|
A | C | 4 | a0001c0001t0001g0086a0001c0001t0001g0177a0001c0001t0001g0180others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-2509T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139123682 | ||||||
| chr5:139123801
|
G | T | 1 | a0001c0001t0001g0030 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.106-2628C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139123801 | ||||||
| chr5:139124080
|
G | A | 45 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(42): Show | 45 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.106-2907C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139124080 | ||||||
| chr5:139124187
|
T | A | 1 | a0001c0001t0001g0030 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.106-3014A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139124187 | ||||||
| chr5:139124199
|
G | A | 1 | a0001c0002t0001g0002 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.106-3026C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139124199 | ||||||
| chr5:139124225
|
C | T | 1 | a0001c0002t0001g0120 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.106-3052G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139124225 | ||||||
| chr5:139124393
|
T | C | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.106-3220A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139124393 | ||||||
| chr5:139124456
|
A | T | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.105+3283T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139124456 | ||||||
| chr5:139124853
|
T | C | 1 | a0002c0003t0001g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.105+2886A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139124853 | ||||||
| chr5:139125011
|
C | T | 1 | a0001c0001t0001g0050 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.105+2728G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139125011 | ||||||
| chr5:139125054
|
C | T | 3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0005g0199 | 3 | HG00323.hp2 HG00735.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.105+2685G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139125054 | ||||||
| chr5:139125514
|
T | C | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.105+2225A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139125514 | ||||||
| chr5:139125858
|
C | T | 119 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(116): Show | 119 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(116): Show |
intron_variant | MODIFIER | c.105+1881G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139125858 | ||||||
| chr5:139125892
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.105+1847T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139125892 | ||||||
| chr5:139126076
|
T | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.105+1663A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139126076 | ||||||
| chr5:139126392
|
A | G | 3 | a0001c0002t0001g0124a0001c0002t0001g0175a0001c0002t0001g0182 | 3 | HG02698.hp2 HG03942.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.105+1347T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139126392 | ||||||
| chr5:139126591
|
G | T | 2 | a0001c0001t0001g0059a0001c0001t0001g0071 | 2 | HG02132.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.105+1148C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139126591 | ||||||
| chr5:139126605
|
T | C | 13 | a0001c0001t0001g0030a0001c0001t0001g0086a0001c0001t0001g0088others(10): Show | 13 | HG01109.hp2 HG01891.hp1 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.105+1134A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139126605 | ||||||
| chr5:139126671
|
G | C | 2 | a0001c0001t0001g0088a0001c0001t0001g0133 | 2 | HG01993.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.105+1068C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139126671 | ||||||
| chr5:139126714
|
T | A | 1 | a0001c0002t0001g0120 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.105+1025A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139126714 | ||||||
| chr5:139126764
|
C | T | 5 | a0001c0001t0001g0149a0001c0001t0001g0159a0002c0003t0001g0034others(2): Show | 5 | HG02976.hp1 NA18522.hp1 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+975G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139126764 | ||||||
| chr5:139127042
|
G | A | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.105+697C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139127042 | ||||||
| chr5:139127101
|
G | A | 1 | a0001c0002t0001g0139 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.105+638C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139127101 | ||||||
| chr5:139127502
|
TATC | T | 37 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(34): Show | 37 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.105+234_105+236del others(3): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 2/9 | chr5 | 139127502 | ||||||
| chr5:139128298
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-10-445A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139128298 | ||||||
| chr5:139128547
|
G | A | 16 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0006others(13): Show | 16 | HG01884.hp1 HG01884.hp2 HG02132.hp1 others(13): Show |
intron_variant | MODIFIER | c.-10-694C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139128547 | ||||||
| chr5:139128651
|
CA | C | 59 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(56): Show | 59 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.-10-799delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139128651 | ||||||
| chr5:139128693
|
C | T | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-10-840G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139128693 | ||||||
| chr5:139128784
|
C | T | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-10-931G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139128784 | ||||||
| chr5:139128824
|
G | A | 16 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0006others(13): Show | 16 | HG01884.hp1 HG01884.hp2 HG02132.hp1 others(13): Show |
intron_variant | MODIFIER | c.-10-971C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139128824 | ||||||
| chr5:139129088
|
G | A | 1 | a0001c0001t0001g0012 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-10-1235C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139129088 | ||||||
| chr5:139129659
|
G | A | 1 | a0001c0002t0001g0175 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-10-1806C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139129659 | ||||||
| chr5:139129804
|
C | T | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10-1951G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139129804 | ||||||
| chr5:139130162
|
C | T | 113 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(110): Show | 113 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(110): Show |
intron_variant | MODIFIER | c.-10-2309G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139130162 | ||||||
| chr5:139130298
|
A | T | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-10-2445T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139130298 | ||||||
| chr5:139130361
|
T | C | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10-2508A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139130361 | ||||||
| chr5:139130446
|
A | G | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-10-2593T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139130446 | ||||||
| chr5:139130498
|
T | C | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-10-2645A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139130498 | ||||||
| chr5:139130997
|
G | A | 4 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0019others(1): Show | 4 | HG02145.hp1 HG02723.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-3144C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139130997 | ||||||
| chr5:139131067
|
C | G | 51 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(48): Show | 51 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.-10-3214G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139131067 | ||||||
| chr5:139131071
|
A | G | 9 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10-3218T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139131071 | ||||||
| chr5:139131340
|
T | G | 1 | a0001c0002t0001g0004 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-10-3487A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139131340 | ||||||
| chr5:139131494
|
C | T | 2 | a0001c0002t0001g0114a0001c0002t0001g0122 | 2 | HG00423.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.-10-3641G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139131494 | ||||||
| chr5:139131539
|
G | A | 1 | a0001c0002t0001g0113 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-10-3686C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139131539 | ||||||
| chr5:139131603
|
C | G | 62 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(59): Show | 62 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.-10-3750G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139131603 | ||||||
| chr5:139131617
|
C | A | 1 | a0001c0001t0006g0200 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-10-3764G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139131617 | ||||||
| chr5:139131803
|
C | T | 4 | a0001c0001t0001g0086a0001c0001t0001g0177a0001c0001t0001g0180others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-3950G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139131803 | ||||||
| chr5:139131930
|
A | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0107a0001c0001t0001g0129others(2): Show | 5 | NA18959.hp2 NA18963.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-4077T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139131930 | ||||||
| chr5:139132169
|
G | T | 1 | a0002c0003t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-10-4316C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139132169 | ||||||
| chr5:139132173
|
T | C | 2 | a0001c0002t0001g0114a0001c0002t0001g0122 | 2 | HG00423.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.-10-4320A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139132173 | ||||||
| chr5:139132635
|
C | T | 1 | a0001c0002t0001g0192 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-10-4782G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139132635 | ||||||
| chr5:139132655
|
C | T | 91 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0030others(88): Show | 91 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(88): Show |
intron_variant | MODIFIER | c.-10-4802G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139132655 | ||||||
| chr5:139132712
|
C | T | 1 | a0001c0002t0001g0143 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-10-4859G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139132712 | ||||||
| chr5:139132780
|
T | G | 17 | a0001c0001t0001g0030a0001c0001t0001g0086a0001c0001t0001g0088others(14): Show | 17 | HG01109.hp2 HG01891.hp1 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.-10-4927A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139132780 | ||||||
| chr5:139133042
|
C | A | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10-5189G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139133042 | ||||||
| chr5:139133063
|
CA | C | 191 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(188): Show | 191 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.-10-5211delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139133063 | ||||||
| chr5:139133870
|
C | A | 11 | a0001c0001t0001g0035a0001c0001t0001g0055a0001c0001t0001g0061others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.-10-6017G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139133870 | ||||||
| chr5:139133988
|
CTT | C | 2 | a0001c0001t0002g0165a0001c0001t0002g0167 | 2 | HG01258.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-10-6137_-10-6136d others(4): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139133988 | ||||||
| chr5:139134446
|
T | C | 2 | a0001c0002t0001g0008a0001c0002t0001g0183 | 2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-10-6593A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139134446 | ||||||
| chr5:139134495
|
C | T | 9 | a0001c0001t0001g0086a0001c0001t0001g0177a0001c0001t0001g0180others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10-6642G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139134495 | ||||||
| chr5:139134665
|
G | A | 1 | a0002c0003t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-10-6812C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139134665 | ||||||
| chr5:139134952
|
G | A | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-10-7099C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139134952 | ||||||
| chr5:139135100
|
G | A | 61 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(58): Show | 61 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.-10-7247C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139135100 | ||||||
| chr5:139135641
|
C | T | 122 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(119): Show | 122 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(119): Show |
intron_variant | MODIFIER | c.-10-7788G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139135641 | ||||||
| chr5:139135709
|
C | CA | 24 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(21): Show | 24 | HG01891.hp1 HG01934.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.-10-7857dupT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139135709 | ||||||
| chr5:139135709
|
CA | C | 55 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0036others(52): Show | 55 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.-10-7857delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139135709 | ||||||
| chr5:139135757
|
T | C | 3 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0084 | 3 | HG02145.hp1 HG02723.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-10-7904A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139135757 | ||||||
| chr5:139135823
|
G | C | 9 | a0001c0001t0001g0086a0001c0001t0001g0177a0001c0001t0001g0180others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10-7970C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139135823 | ||||||
| chr5:139135891
|
C | A | 1 | a0002c0003t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-10-8038G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139135891 | ||||||
| chr5:139136015
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-10-8162G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139136015 | ||||||
| chr5:139136396
|
A | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0066 | 2 | HG01261.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.-10-8543T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139136396 | ||||||
| chr5:139136428
|
G | A | 2 | a0001c0001t0002g0165a0001c0001t0002g0167 | 2 | HG01258.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-10-8575C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139136428 | ||||||
| chr5:139136756
|
G | A | 1 | a0001c0001t0002g0018 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-10-8903C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139136756 | ||||||
| chr5:139136870
|
C | T | 2 | a0001c0002t0001g0113a0001c0002t0001g0144 | 2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-10-9017G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139136870 | ||||||
| chr5:139136888
|
C | A | 1 | a0001c0001t0001g0017 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-10-9035G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139136888 | ||||||
| chr5:139137090
|
C | T | 2 | a0001c0001t0002g0029a0001c0001t0002g0093 | 2 | NA18961.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.-10-9237G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139137090 | ||||||
| chr5:139137369
|
T | C | 1 | a0001c0005t0001g0011 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-10-9516A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139137369 | ||||||
| chr5:139137388
|
C | CA | 199 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(196): Show | 199 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.-10-9536dupT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139137388 | ||||||
| chr5:139137684
|
C | T | 3 | a0001c0001t0001g0024a0001c0001t0001g0096a0001c0002t0001g0002 | 3 | HG01884.hp2 HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-10-9831G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139137684 | ||||||
| chr5:139137914
|
C | A | 1 | a0001c0001t0003g0001 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-10-10061G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139137914 | ||||||
| chr5:139138144
|
TAC | T | 118 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(115): Show | 118 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(115): Show |
intron_variant | MODIFIER | c.-10-10293_-10-1029 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139138144 | ||||||
| chr5:139138144
|
TACAC | T | 6 | a0001c0001t0001g0030a0001c0002t0001g0025a0001c0002t0001g0026others(3): Show | 6 | HG02145.hp2 HG02451.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-10295_-10-1029 others(8): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139138144 | ||||||
| chr5:139138196
|
C | T | 1 | a0001c0002t0001g0004 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-10-10343G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139138196 | ||||||
| chr5:139138210
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0170 | 2 | NA18945.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.-10-10357C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139138210 | ||||||
| chr5:139138228
|
G | A | 6 | a0001c0001t0001g0030a0001c0002t0001g0025a0001c0002t0001g0026others(3): Show | 6 | HG02145.hp2 HG02451.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-10375C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139138228 | ||||||
| chr5:139138403
|
G | A | 1 | a0001c0002t0001g0127 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-10-10550C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139138403 | ||||||
| chr5:139138463
|
C | T | 1 | a0001c0001t0003g0001 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-10-10610G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139138463 | ||||||
| chr5:139138464
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-10-10611C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139138464 | ||||||
| chr5:139138577
|
C | T | 2 | a0004c0007t0001g0158a0004c0007t0001g0195 | 2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-10-10724G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139138577 | ||||||
| chr5:139138734
|
G | T | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(3): Show | 6 | HG02257.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-10881C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139138734 | ||||||
| chr5:139138787
|
G | T | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-10-10934C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139138787 | ||||||
| chr5:139138917
|
T | A | 1 | a0001c0005t0001g0091 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-10-11064A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139138917 | ||||||
| chr5:139139099
|
G | A | 8 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0023others(5): Show | 8 | HG02257.hp2 HG02559.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10-11246C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139139099 | ||||||
| chr5:139139319
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-10-11466C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139139319 | ||||||
| chr5:139139712
|
C | T | 61 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(58): Show | 61 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.-10-11859G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139139712 | ||||||
| chr5:139139839
|
C | T | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-10-11986G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139139839 | ||||||
| chr5:139140037
|
G | A | 4 | a0001c0002t0001g0002a0001c0002t0001g0099a0001c0002t0001g0101others(1): Show | 4 | HG01884.hp1 HG01884.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-12184C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139140037 | ||||||
| chr5:139140099
|
G | C | 1 | a0001c0001t0001g0014 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-10-12246C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139140099 | ||||||
| chr5:139140548
|
G | A | 1 | a0002c0003t0001g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-10-12695C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139140548 | ||||||
| chr5:139140667
|
G | A | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-10-12814C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139140667 | ||||||
| chr5:139141192
|
C | T | 9 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10-13339G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139141192 | ||||||
| chr5:139141247
|
T | C | 5 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0028others(2): Show | 5 | HG02451.hp1 HG03225.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-13394A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139141247 | ||||||
| chr5:139141385
|
C | T | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-10-13532G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139141385 | ||||||
| chr5:139141482
|
C | CA | 9 | a0001c0001t0001g0074a0001c0001t0001g0149a0001c0001t0001g0159others(6): Show | 9 | HG01243.hp1 HG02083.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-13630dupT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139141482 | ||||||
| chr5:139141483
|
A | C | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-10-13630T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139141483 | ||||||
| chr5:139141498
|
A | T | 8 | a0001c0001t0001g0086a0001c0001t0001g0177a0001c0001t0001g0180others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10-13645T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139141498 | ||||||
| chr5:139141531
|
A | C | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-10-13678T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139141531 | ||||||
| chr5:139141827
|
T | C | 1 | a0001c0001t0001g0069 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-10-13974A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139141827 | ||||||
| chr5:139141892
|
T | G | 1 | a0001c0001t0001g0197 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-10-14039A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139141892 | ||||||
| chr5:139142090
|
C | T | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-10-14237G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139142090 | ||||||
| chr5:139142258
|
C | A | 4 | a0001c0002t0001g0002a0001c0002t0001g0099a0001c0002t0001g0101others(1): Show | 4 | HG01884.hp1 HG01884.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-14405G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139142258 | ||||||
| chr5:139142329
|
A | C | 1 | a0001c0001t0001g0089 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-10-14476T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139142329 | ||||||
| chr5:139142449
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-10-14596C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139142449 | ||||||
| chr5:139142479
|
G | A | 1 | a0001c0002t0001g0102 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-10-14626C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139142479 | ||||||
| chr5:139142538
|
A | G | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-10-14685T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139142538 | ||||||
| chr5:139142975
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-10-15122T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139142975 | ||||||
| chr5:139142997
|
T | C | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-10-15144A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139142997 | ||||||
| chr5:139143010
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-10-15157G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143010 | ||||||
| chr5:139143011
|
G | A | 24 | a0001c0001t0001g0030a0001c0001t0001g0086a0001c0001t0001g0088others(21): Show | 24 | HG01109.hp2 HG01891.hp1 HG01993.hp1 others(21): Show |
intron_variant | MODIFIER | c.-10-15158C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143011 | ||||||
| chr5:139143201
|
A | T | 1 | a0001c0001t0002g0018 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-10-15348T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143201 | ||||||
| chr5:139143250
|
CATATAT | C | 62 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(59): Show | 62 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.-10-15403_-10-1539 others(10): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143250 | ||||||
| chr5:139143258
|
A | C | 1 | a0001c0002t0001g0185 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-10-15405T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143258 | ||||||
| chr5:139143272
|
C | CATGTGTA others(3): Show |
1 | a0001c0002t0001g0185 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-10-15420_-10-1541 others(14): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143272 | ||||||
| chr5:139143300
|
C | CAT | 3 | a0001c0001t0001g0177a0001c0001t0001g0181a0001c0002t0001g0185 | 3 | HG02055.hp2 HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-10-15449_-10-1544 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143300 | ||||||
| chr5:139143304
|
T | C | 1 | a0001c0002t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-10-15451A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143304 | ||||||
| chr5:139143304
|
TATACACA others(3): Show |
T | 1 | a0001c0002t0001g0139 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-10-15461_-10-1545 others(14): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143304 | ||||||
| chr5:139143306
|
T | C | 2 | a0001c0002t0001g0099a0001c0002t0001g0101 | 2 | HG01884.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-10-15453A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143306 | ||||||
| chr5:139143306
|
T | TAC | 7 | a0001c0002t0001g0111a0001c0002t0001g0115a0001c0002t0001g0118others(4): Show | 7 | HG01261.hp2 HG02258.hp1 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10-15455_-10-1545 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143306 | ||||||
| chr5:139143306
|
T | TACAC | 2 | a0001c0002t0001g0068a0001c0002t0001g0120 | 2 | HG01891.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.-10-15457_-10-1545 others(8): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143306 | ||||||
| chr5:139143306
|
TAC | T | 6 | a0001c0001t0001g0030a0001c0002t0001g0100a0001c0002t0004g0131others(3): Show | 6 | HG01891.hp1 HG02145.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-15455_-10-1545 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143306 | ||||||
| chr5:139143306
|
TACAC | T | 6 | a0001c0001t0001g0168a0001c0002t0001g0114a0001c0002t0001g0116others(3): Show | 6 | HG00423.hp1 HG01346.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-15457_-10-1545 others(8): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143306 | ||||||
| chr5:139143306
|
TACACAC | T | 4 | a0001c0001t0001g0046a0001c0002t0001g0155a0001c0002t0001g0156others(1): Show | 4 | HG00323.hp1 HG01516.hp2 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-15459_-10-1545 others(10): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143306 | ||||||
| chr5:139143306
|
TACACACA others(1): Show |
T | 9 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0044others(6): Show | 9 | HG00642.hp1 HG02257.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-15461_-10-1545 others(12): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143306 | ||||||
| chr5:139143306
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0001g0171 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-10-15463_-10-1545 others(14): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143306 | ||||||
| chr5:139143306
|
TACACACA others(5): Show |
T | 27 | a0001c0001t0001g0003a0001c0001t0001g0036a0001c0001t0001g0037others(24): Show | 27 | HG00423.hp2 HG01981.hp2 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.-10-15465_-10-1545 others(16): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143306 | ||||||
| chr5:139143306
|
TACACACA others(7): Show |
T | 25 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0047others(22): Show | 25 | HG00323.hp2 HG00735.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.-10-15467_-10-1545 others(18): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143306 | ||||||
| chr5:139143306
|
TACACACA others(9): Show |
T | 2 | a0001c0001t0001g0063a0001c0001t0001g0079 | 2 | HG01943.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-10-15469_-10-1545 others(20): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143306 | ||||||
| chr5:139143308
|
C | T | 41 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(38): Show | 41 | HG01109.hp2 HG01258.hp1 HG01258.hp2 others(38): Show |
intron_variant | MODIFIER | c.-10-15455G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143308 | ||||||
| chr5:139143310
|
C | CACATGTG others(5): Show |
1 | a0001c0001t0001g0015 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-10-15458_-10-1545 others(16): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143310 | ||||||
| chr5:139143310
|
C | T | 4 | a0001c0001t0001g0030a0002c0003t0001g0134a0002c0003t0001g0160others(1): Show | 4 | HG01891.hp1 HG02145.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-15457G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143310 | ||||||
| chr5:139143312
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-10-15459G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143312 | ||||||
| chr5:139143314
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0046 | 2 | HG01516.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.-10-15461G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143314 | ||||||
| chr5:139143316
|
C | T | 10 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0032others(7): Show | 10 | HG00642.hp1 HG02257.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10-15463G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143316 | ||||||
| chr5:139143318
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0171 | 2 | NA19002.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.-10-15465G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143318 | ||||||
| chr5:139143320
|
C | T | 27 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0036others(24): Show | 27 | HG00423.hp2 HG01981.hp2 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.-10-15467G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143320 | ||||||
| chr5:139143322
|
C | T | 25 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0047others(22): Show | 25 | HG00323.hp2 HG00735.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.-10-15469G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143322 | ||||||
| chr5:139143324
|
C | T | 2 | a0001c0001t0001g0063a0001c0001t0001g0079 | 2 | HG01943.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-10-15471G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143324 | ||||||
| chr5:139143326
|
C | T | 2 | a0001c0002t0001g0006a0001c0002t0001g0010 | 2 | HG02723.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-10-15473G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143326 | ||||||
| chr5:139143328
|
C | T | 2 | a0001c0002t0001g0006a0001c0002t0001g0010 | 2 | HG02723.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-10-15475G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143328 | ||||||
| chr5:139143330
|
C | T | 2 | a0001c0002t0001g0006a0001c0002t0001g0010 | 2 | HG02723.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-10-15477G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143330 | ||||||
| chr5:139143330
|
CACACACA others(9): Show |
C | 7 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(4): Show | 7 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-15493_-10-1547 others(20): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143330 | ||||||
| chr5:139143332
|
C | T | 3 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0084 | 3 | HG02145.hp1 HG02723.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-10-15479G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143332 | ||||||
| chr5:139143332
|
CACACACA others(7): Show |
C | 1 | a0001c0001t0001g0147 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-10-15493_-10-1548 others(18): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143332 | ||||||
| chr5:139143334
|
C | T | 4 | a0001c0001t0001g0168a0001c0002t0001g0006a0001c0002t0001g0010others(1): Show | 4 | HG01346.hp1 HG02145.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-15481G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143334 | ||||||
| chr5:139143334
|
CACACACA others(5): Show |
C | 16 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(13): Show | 16 | HG01258.hp1 HG01258.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.-10-15493_-10-1548 others(16): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143334 | ||||||
| chr5:139143334
|
CACACACA others(7): Show |
C | 1 | a0001c0005t0001g0091 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-10-15495_-10-1548 others(18): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143334 | ||||||
| chr5:139143336
|
C | T | 6 | a0001c0001t0001g0046a0001c0001t0001g0168a0001c0002t0001g0006others(3): Show | 6 | HG01346.hp1 HG01516.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-15483G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143336 | ||||||
| chr5:139143336
|
CACACACA others(3): Show |
C | 3 | a0001c0002t0001g0113a0001c0002t0001g0137a0001c0002t0001g0144 | 3 | HG02970.hp1 HG03209.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-10-15493_-10-1548 others(14): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143336 | ||||||
| chr5:139143338
|
C | CATATATA others(3): Show |
1 | a0001c0002t0001g0004 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-10-15486_-10-1548 others(14): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143338 | ||||||
| chr5:139143338
|
C | CATATATA others(5): Show |
1 | a0001c0002t0001g0008 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-10-15486_-10-1548 others(16): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143338 | ||||||
| chr5:139143338
|
C | CATATATA others(7): Show |
1 | a0001c0002t0001g0183 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-10-15486_-10-1548 others(18): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143338 | ||||||
| chr5:139143338
|
C | CATATATA others(9): Show |
1 | a0001c0001t0001g0163 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-10-15486_-10-1548 others(20): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143338 | ||||||
| chr5:139143338
|
C | T | 11 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0081others(8): Show | 11 | HG00642.hp1 HG01346.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.-10-15485G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143338 | ||||||
| chr5:139143338
|
CACACACA others(3): Show |
C | 3 | a0001c0001t0001g0149a0001c0005t0001g0011a0006c0009t0001g0157 | 3 | HG03195.hp1 NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-10-15495_-10-1548 others(14): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143338 | ||||||
| chr5:139143340
|
C | CATATATA others(5): Show |
1 | a0001c0001t0001g0166 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-10-15488_-10-1548 others(16): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143340 | ||||||
| chr5:139143340
|
C | CATATATA others(13): Show |
1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-10-15488_-10-1548 others(24): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143340 | ||||||
| chr5:139143340
|
C | T | 16 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0081others(13): Show | 16 | HG00642.hp1 HG01346.hp1 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.-10-15487G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143340 | ||||||
| chr5:139143340
|
CACACATA others(1): Show |
C | 4 | a0001c0001t0001g0159a0001c0005t0001g0007a0002c0003t0001g0034others(1): Show | 4 | HG01243.hp1 HG02976.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-15495_-10-1548 others(12): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143340 | ||||||
| chr5:139143342
|
C | CATATATA others(5): Show |
2 | a0001c0001t0001g0133a0001c0001t0001g0162 | 2 | HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-10-15490_-10-1548 others(16): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143342 | ||||||
| chr5:139143342
|
C | T | 44 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0044others(41): Show | 44 | HG00423.hp2 HG00642.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.-10-15489G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143342 | ||||||
| chr5:139143342
|
CACAT | C | 4 | a0001c0002t0001g0038a0001c0002t0001g0098a0001c0002t0001g0151others(1): Show | 4 | HG01496.hp1 HG02622.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-15493_-10-1549 others(8): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143342 | ||||||
| chr5:139143344
|
C | CACACACA others(13): Show |
1 | a0001c0002t0001g0026 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-10-15492_-10-1549 others(24): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143344 | ||||||
| chr5:139143344
|
C | CACACACA others(11): Show |
1 | a0001c0002t0001g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-10-15492_-10-1549 others(22): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143344 | ||||||
| chr5:139143344
|
C | CACACATA others(11): Show |
1 | a0001c0002t0001g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-10-15492_-10-1549 others(22): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143344 | ||||||
| chr5:139143344
|
C | CACACATA others(13): Show |
1 | a0001c0002t0001g0104 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-10-15492_-10-1549 others(24): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143344 | ||||||
| chr5:139143344
|
C | CAT | 4 | a0001c0002t0001g0127a0001c0002t0001g0128a0001c0002t0001g0135others(1): Show | 4 | HG00642.hp2 HG01516.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-15493_-10-1549 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143344 | ||||||
| chr5:139143344
|
C | T | 76 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0036others(73): Show | 76 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.-10-15491G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143344 | ||||||
| chr5:139143344
|
CAT | C | 3 | a0001c0002t0001g0146a0001c0002t0001g0184a0001c0002t0001g0192 | 3 | HG02572.hp1 HG02717.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-10-15493_-10-1549 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143344 | ||||||
| chr5:139143346
|
T | C | 9 | a0001c0001t0001g0015a0001c0002t0001g0090a0001c0002t0001g0115others(6): Show | 9 | HG01070.hp2 HG01109.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-15493A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143346 | ||||||
| chr5:139143348
|
T | C | 1 | a0001c0002t0001g0118 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-10-15495A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143348 | ||||||
| chr5:139143536
|
A | C | 1 | a0001c0001t0001g0027 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-10-15683T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143536 | ||||||
| chr5:139143537
|
A | T | 2 | a0001c0002t0001g0099a0001c0002t0001g0101 | 2 | HG01884.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-10-15684T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143537 | ||||||
| chr5:139143592
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-10-15739C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143592 | ||||||
| chr5:139143688
|
G | T | 61 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(58): Show | 61 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.-10-15835C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143688 | ||||||
| chr5:139143761
|
A | T | 2 | a0001c0005t0001g0007a0001c0005t0001g0011 | 2 | HG01243.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-10-15908T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139143761 | ||||||
| chr5:139144044
|
C | T | 128 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(125): Show | 128 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(125): Show |
intron_variant | MODIFIER | c.-10-16191G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139144044 | ||||||
| chr5:139144198
|
C | A | 63 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(60): Show | 63 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.-10-16345G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139144198 | ||||||
| chr5:139144336
|
A | G | 63 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(60): Show | 63 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.-10-16483T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139144336 | ||||||
| chr5:139144600
|
G | T | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-10-16747C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139144600 | ||||||
| chr5:139144608
|
C | A | 24 | a0001c0001t0001g0030a0001c0001t0001g0086a0001c0001t0001g0088others(21): Show | 24 | HG01109.hp2 HG01891.hp1 HG01993.hp1 others(21): Show |
intron_variant | MODIFIER | c.-10-16755G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139144608 | ||||||
| chr5:139144715
|
A | T | 3 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0142 | 3 | HG00642.hp2 HG01261.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.-10-16862T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139144715 | ||||||
| chr5:139144717
|
A | C | 1 | a0001c0001t0001g0057 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-10-16864T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139144717 | ||||||
| chr5:139144940
|
C | T | 24 | a0001c0001t0001g0030a0001c0001t0001g0086a0001c0001t0001g0088others(21): Show | 24 | HG01109.hp2 HG01891.hp1 HG01993.hp1 others(21): Show |
intron_variant | MODIFIER | c.-10-17087G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139144940 | ||||||
| chr5:139145039
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-10-17186C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139145039 | ||||||
| chr5:139145399
|
C | T | 61 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(58): Show | 61 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.-10-17546G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139145399 | ||||||
| chr5:139145494
|
A | G | 1 | a0001c0001t0001g0013 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-10-17641T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139145494 | ||||||
| chr5:139145608
|
ATGTGGG | A | 64 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(61): Show | 64 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.-10-17761_-10-1775 others(10): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139145608 | ||||||
| chr5:139145619
|
GGTGTGGG others(17): Show |
G | 3 | a0001c0001t0001g0066a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG01070.hp1 HG01071.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.-10-17790_-10-1776 others(28): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139145619 | ||||||
| chr5:139145629
|
CGT | C | 6 | a0001c0002t0001g0073a0001c0002t0001g0090a0001c0002t0001g0128others(3): Show | 6 | HG00323.hp1 HG01070.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-17778_-10-1777 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139145629 | ||||||
| chr5:139145629
|
CGTGT | C | 7 | a0001c0002t0001g0085a0001c0002t0001g0100a0001c0002t0001g0135others(4): Show | 7 | HG00642.hp2 HG01109.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10-17780_-10-1777 others(8): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139145629 | ||||||
| chr5:139145629
|
CGTGTGT | C | 15 | a0001c0001t0001g0149a0001c0001t0002g0029a0001c0001t0002g0093others(12): Show | 15 | HG01074.hp1 HG01081.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.-10-17782_-10-1777 others(10): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139145629 | ||||||
| chr5:139145629
|
CGTGTGTG others(1): Show |
C | 37 | a0001c0001t0001g0027a0001c0001t0001g0092a0001c0001t0001g0159others(34): Show | 37 | HG00423.hp1 HG00735.hp2 HG01496.hp1 others(34): Show |
intron_variant | MODIFIER | c.-10-17784_-10-1777 others(12): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139145629 | ||||||
| chr5:139145629
|
CGTGTGTG others(3): Show |
C | 20 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0021others(17): Show | 20 | HG01069.hp2 HG01243.hp2 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-10-17786_-10-1777 others(14): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139145629 | ||||||
| chr5:139145629
|
CGTGTGTG others(5): Show |
C | 18 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0023others(15): Show | 18 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.-10-17788_-10-1777 others(16): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139145629 | ||||||
| chr5:139145629
|
CGTGTGTG others(7): Show |
C | 13 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0059others(10): Show | 13 | HG00323.hp2 HG00423.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.-10-17790_-10-1777 others(18): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139145629 | ||||||
| chr5:139145629
|
CGTGTGTG others(9): Show |
C | 49 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(46): Show | 49 | HG00642.hp1 HG01074.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.-10-17792_-10-1777 others(20): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139145629 | ||||||
| chr5:139145629
|
CGTGTGTG others(11): Show |
C | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | NA18981.hp2 NA18986.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-17794_-10-1777 others(22): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139145629 | ||||||
| chr5:139145629
|
CGTGTGTG others(13): Show |
C | 3 | a0001c0002t0001g0004a0001c0002t0001g0084a0001c0002t0001g0118 | 3 | HG02132.hp1 HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-10-17796_-10-1777 others(24): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139145629 | ||||||
| chr5:139145629
|
CGTGTGTG others(15): Show |
C | 5 | a0001c0002t0001g0006a0001c0002t0001g0008a0001c0002t0001g0010others(2): Show | 5 | HG02602.hp1 HG02723.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-17798_-10-1777 others(26): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139145629 | ||||||
| chr5:139145629
|
CGTGTGTG others(17): Show |
C | 17 | a0001c0001t0001g0030a0001c0001t0001g0086a0001c0001t0001g0088others(14): Show | 17 | HG01109.hp2 HG01891.hp1 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.-10-17800_-10-1777 others(28): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139145629 | ||||||
| chr5:139145629
|
CGTGTGTG others(27): Show |
C | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-10-17810_-10-1777 others(38): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139145629 | ||||||
| chr5:139145645
|
T | G | 3 | a0001c0001t0001g0066a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG01070.hp1 HG01071.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.-10-17792A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139145645 | ||||||
| chr5:139145647
|
T | C | 3 | a0001c0001t0001g0066a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG01070.hp1 HG01071.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.-10-17794A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139145647 | ||||||
| chr5:139145680
|
G | A | 2 | a0001c0005t0001g0007a0001c0005t0001g0011 | 2 | HG01243.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-10-17827C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139145680 | ||||||
| chr5:139145831
|
G | A | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-10-17978C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139145831 | ||||||
| chr5:139146155
|
A | G | 3 | a0001c0002t0001g0124a0001c0002t0001g0175a0001c0002t0001g0182 | 3 | HG02698.hp2 HG03942.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-10-18302T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139146155 | ||||||
| chr5:139146187
|
T | C | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-10-18334A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139146187 | ||||||
| chr5:139146765
|
A | G | 4 | a0001c0001t0001g0086a0001c0001t0001g0177a0001c0001t0001g0180others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-18912T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139146765 | ||||||
| chr5:139146817
|
G | T | 129 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(126): Show | 129 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(126): Show |
intron_variant | MODIFIER | c.-10-18964C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139146817 | ||||||
| chr5:139146993
|
C | T | 2 | a0004c0007t0001g0158a0004c0007t0001g0195 | 2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-10-19140G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139146993 | ||||||
| chr5:139147337
|
G | A | 126 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(123): Show | 126 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(123): Show |
intron_variant | MODIFIER | c.-10-19484C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139147337 | ||||||
| chr5:139147372
|
C | T | 1 | a0001c0002t0001g0150 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-10-19519G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139147372 | ||||||
| chr5:139147397
|
A | G | 2 | a0001c0001t0001g0036a0001c0001t0001g0039 | 2 | NA18964.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-10-19544T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139147397 | ||||||
| chr5:139147521
|
T | C | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-10-19668A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139147521 | ||||||
| chr5:139147573
|
A | G | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-10-19720T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139147573 | ||||||
| chr5:139147652
|
A | G | 3 | a0001c0001t0001g0054a0001c0001t0001g0080a0001c0001t0001g0174 | 3 | NA18964.hp2 NA18965.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.-10-19799T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139147652 | ||||||
| chr5:139147817
|
C | T | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-10-19964G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139147817 | ||||||
| chr5:139147876
|
C | T | 38 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(35): Show | 38 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.-10-20023G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139147876 | ||||||
| chr5:139147877
|
G | A | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-10-20024C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139147877 | ||||||
| chr5:139147966
|
C | T | 10 | a0001c0001t0001g0086a0001c0001t0001g0162a0001c0001t0001g0163others(7): Show | 10 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10-20113G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139147966 | ||||||
| chr5:139148092
|
A | G | 3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0005g0199 | 3 | HG00323.hp2 HG00735.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-10-20239T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139148092 | ||||||
| chr5:139148112
|
TA | T | 38 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(35): Show | 38 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.-10-20260delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139148112 | ||||||
| chr5:139148416
|
A | G | 54 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0036others(51): Show | 54 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.-10-20563T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139148416 | ||||||
| chr5:139148454
|
G | T | 2 | a0001c0002t0001g0006a0001c0002t0001g0010 | 2 | HG02723.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-10-20601C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139148454 | ||||||
| chr5:139148489
|
A | G | 1 | a0001c0002t0001g0070 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-10-20636T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139148489 | ||||||
| chr5:139148883
|
C | T | 2 | a0001c0002t0001g0137a0001c0002t0001g0145 | 2 | NA18983.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.-10-21030G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139148883 | ||||||
| chr5:139148997
|
A | C | 5 | a0001c0001t0001g0016a0001c0001t0001g0162a0001c0001t0001g0163others(2): Show | 5 | HG02109.hp2 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-21144T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139148997 | ||||||
| chr5:139149074
|
G | A | 63 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0030others(60): Show | 63 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.-10-21221C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139149074 | ||||||
| chr5:139149206
|
C | T | 3 | a0001c0001t0001g0197a0001c0002t0001g0141a0001c0002t0001g0155 | 3 | HG00323.hp1 HG02071.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.-10-21353G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139149206 | ||||||
| chr5:139149355
|
G | A | 4 | a0001c0002t0001g0090a0001c0002t0001g0126a0001c0002t0001g0127others(1): Show | 4 | HG01070.hp2 HG01109.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-21502C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139149355 | ||||||
| chr5:139149659
|
A | T | 97 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0024others(94): Show | 97 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.-10-21806T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139149659 | ||||||
| chr5:139150053
|
C | T | 1 | a0001c0002t0001g0019 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-10-22200G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139150053 | ||||||
| chr5:139150176
|
C | T | 84 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0036others(81): Show | 84 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.-10-22323G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139150176 | ||||||
| chr5:139150358
|
C | T | 1 | a0001c0002t0001g0116 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-10-22505G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139150358 | ||||||
| chr5:139150532
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-10-22679C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139150532 | ||||||
| chr5:139150535
|
G | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0174 | 2 | NA18965.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.-10-22682C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139150535 | ||||||
| chr5:139150601
|
T | C | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-10-22748A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139150601 | ||||||
| chr5:139150612
|
T | C | 1 | a0002c0006t0001g0103 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-10-22759A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139150612 | ||||||
| chr5:139150731
|
T | C | 1 | a0001c0002t0001g0175 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-10-22878A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139150731 | ||||||
| chr5:139150854
|
T | C | 75 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(72): Show | 75 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.-10-23001A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139150854 | ||||||
| chr5:139151024
|
G | A | 3 | a0001c0002t0001g0099a0001c0002t0001g0101a0001c0002t0001g0104 | 3 | HG01884.hp1 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-10-23171C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139151024 | ||||||
| chr5:139151025
|
G | A | 9 | a0001c0001t0001g0086a0001c0001t0001g0162a0001c0001t0001g0163others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10-23172C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139151025 | ||||||
| chr5:139151035
|
C | T | 75 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(72): Show | 75 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.-10-23182G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139151035 | ||||||
| chr5:139151173
|
C | T | 2 | a0001c0002t0001g0004a0001c0002t0001g0150 | 2 | HG02132.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.-10-23320G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139151173 | ||||||
| chr5:139151404
|
A | T | 9 | a0001c0001t0001g0086a0001c0001t0001g0162a0001c0001t0001g0163others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10-23551T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139151404 | ||||||
| chr5:139151444
|
A | C | 75 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(72): Show | 75 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.-10-23591T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139151444 | ||||||
| chr5:139151542
|
T | C | 8 | a0001c0001t0001g0009a0001c0002t0001g0006a0001c0002t0001g0008others(5): Show | 8 | HG01243.hp1 HG02145.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10-23689A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139151542 | ||||||
| chr5:139151564
|
A | G | 97 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(94): Show | 97 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.-10-23711T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139151564 | ||||||
| chr5:139151680
|
C | T | 3 | a0001c0001t0001g0086a0001c0001t0001g0180a0001c0001t0001g0181 | 3 | HG02559.hp2 HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-10-23827G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139151680 | ||||||
| chr5:139151681
|
G | A | 1 | a0001c0002t0001g0019 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-10-23828C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139151681 | ||||||
| chr5:139151794
|
G | A | 73 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(70): Show | 73 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.-10-23941C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139151794 | ||||||
| chr5:139152110
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-10-24257G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139152110 | ||||||
| chr5:139152143
|
T | C | 1 | a0001c0002t0001g0002 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-10-24290A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139152143 | ||||||
| chr5:139152282
|
T | C | 1 | a0002c0003t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-10-24429A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139152282 | ||||||
| chr5:139152761
|
T | C | 1 | a0001c0002t0001g0002 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-10-24908A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139152761 | ||||||
| chr5:139153063
|
C | T | 3 | a0001c0005t0001g0091a0004c0007t0001g0158a0004c0007t0001g0195 | 3 | HG02630.hp1 HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-10-25210G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139153063 | ||||||
| chr5:139153471
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-10-25618C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139153471 | ||||||
| chr5:139153649
|
G | A | 73 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(70): Show | 73 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.-10-25796C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139153649 | ||||||
| chr5:139153821
|
T | G | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG02109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-10-25968A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139153821 | ||||||
| chr5:139153995
|
G | C | 74 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(71): Show | 74 | HG00323.hp2 HG00423.hp2 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.-10-26142C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139153995 | ||||||
| chr5:139154061
|
C | T | 1 | a0002c0003t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-10-26208G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139154061 | ||||||
| chr5:139154230
|
TA | T | 72 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(69): Show | 72 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.-10-26378delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139154230 | ||||||
| chr5:139154840
|
T | C | 1 | a0006c0009t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-10-26987A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139154840 | ||||||
| chr5:139154913
|
A | G | 2 | a0001c0001t0002g0140a0001c0002t0001g0108 | 2 | NA18948.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.-10-27060T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139154913 | ||||||
| chr5:139155448
|
T | A | 1 | a0001c0010t0001g0064 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-10-27595A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139155448 | ||||||
| chr5:139155448
|
T | TGA | 3 | a0001c0001t0001g0027a0001c0002t0001g0006a0001c0002t0001g0010 | 3 | HG02055.hp1 HG02723.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-10-27597_-10-2759 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139155448 | ||||||
| chr5:139155448
|
T | TGAGA | 4 | a0001c0001t0001g0092a0001c0001t0002g0093a0001c0002t0001g0026others(1): Show | 4 | HG02451.hp1 HG02451.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-27599_-10-2759 others(8): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139155448 | ||||||
| chr5:139155448
|
T | TGAGAGAG others(3): Show |
1 | a0001c0001t0001g0163 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-10-27605_-10-2759 others(14): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139155448 | ||||||
| chr5:139155448
|
T | TGAGAGAG others(5): Show |
3 | a0001c0001t0001g0086a0001c0001t0001g0180a0001c0001t0001g0181 | 3 | HG02559.hp2 HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-10-27607_-10-2759 others(16): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139155448 | ||||||
| chr5:139155448
|
T | TGAGAGAG others(7): Show |
1 | a0001c0005t0001g0091 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-10-27609_-10-2759 others(18): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139155448 | ||||||
| chr5:139155448
|
T | TGAGAGAG others(9): Show |
3 | a0001c0001t0001g0043a0001c0002t0001g0065a0004c0007t0001g0195 | 3 | HG01981.hp2 HG02630.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.-10-27611_-10-2759 others(20): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139155448 | ||||||
| chr5:139155448
|
T | TGAGAGAG others(11): Show |
4 | a0001c0001t0001g0080a0001c0001t0001g0162a0002c0003t0001g0160others(1): Show | 4 | HG01891.hp1 HG02109.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-27613_-10-2759 others(22): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139155448 | ||||||
| chr5:139155448
|
T | TGAGAGAG others(13): Show |
6 | a0001c0001t0001g0054a0001c0001t0001g0069a0001c0001t0001g0174others(3): Show | 6 | HG01081.hp2 HG03041.hp2 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-27615_-10-2759 others(24): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139155448 | ||||||
| chr5:139155448
|
T | TGAGAGAG others(15): Show |
4 | a0001c0001t0001g0079a0001c0001t0001g0088a0001c0001t0001g0169others(1): Show | 4 | HG01891.hp2 HG01943.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-27617_-10-2759 others(26): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139155448 | ||||||
| chr5:139155448
|
T | TGAGAGAG others(17): Show |
9 | a0001c0001t0001g0035a0001c0001t0001g0050a0001c0001t0001g0053others(6): Show | 9 | HG01070.hp1 HG01071.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-27619_-10-2759 others(28): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139155448 | ||||||
| chr5:139155448
|
T | TGAGAGAG others(19): Show |
7 | a0001c0001t0001g0036a0001c0001t0001g0041a0001c0001t0001g0047others(4): Show | 7 | HG01109.hp2 HG01934.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-27621_-10-2759 others(30): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139155448 | ||||||
| chr5:139155448
|
T | TGAGAGAG others(21): Show |
13 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(10): Show | 13 | HG01361.hp2 HG01884.hp1 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.-10-27623_-10-2759 others(32): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139155448 | ||||||
| chr5:139155448
|
T | TGAGAGAG others(23): Show |
7 | a0001c0001t0001g0057a0001c0001t0001g0075a0001c0001t0001g0076others(4): Show | 7 | HG00735.hp1 HG01069.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10-27625_-10-2759 others(34): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139155448 | ||||||
| chr5:139155448
|
T | TGAGAGAG others(25): Show |
4 | a0001c0001t0001g0046a0001c0001t0001g0058a0001c0001t0001g0062others(1): Show | 4 | HG01516.hp2 HG03942.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-27596_-10-2759 others(36): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139155448 | ||||||
| chr5:139155448
|
T | TGAGAGAG others(27): Show |
6 | a0001c0001t0001g0051a0001c0001t0001g0059a0001c0001t0001g0061others(3): Show | 6 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-27596_-10-2759 others(38): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139155448 | ||||||
| chr5:139155448
|
T | TGAGAGAG others(29): Show |
2 | a0001c0001t0001g0168a0001c0001t0002g0165 | 2 | HG01346.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-10-27596_-10-2759 others(40): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139155448 | ||||||
| chr5:139155448
|
T | TGAGAGAG others(31): Show |
2 | a0001c0001t0001g0044a0001c0001t0001g0081 | 2 | HG02738.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-10-27596_-10-2759 others(42): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139155448 | ||||||
| chr5:139155448
|
T | TGAGAGAG others(33): Show |
2 | a0001c0001t0001g0052a0001c0002t0001g0038 | 2 | HG01496.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.-10-27596_-10-2759 others(44): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139155448 | ||||||
| chr5:139155501
|
A | T | 2 | a0001c0001t0001g0067a0001c0001t0001g0074 | 2 | HG01934.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.-10-27648T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139155501 | ||||||
| chr5:139155727
|
G | GT | 15 | a0001c0001t0001g0086a0001c0001t0001g0162a0001c0001t0001g0163others(12): Show | 15 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-10-27875dupA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139155727 | ||||||
| chr5:139155751
|
C | T | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-10-27898G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139155751 | ||||||
| chr5:139155841
|
C | CT | 76 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(73): Show | 76 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.-10-27989dupA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139155841 | ||||||
| chr5:139155886
|
G | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG01070.hp1 HG01071.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.-10-28033C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139155886 | ||||||
| chr5:139155990
|
G | A | 1 | a0002c0003t0001g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-10-28137C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139155990 | ||||||
| chr5:139156400
|
T | TA | 8 | a0001c0001t0001g0009a0001c0002t0001g0006a0001c0002t0001g0008others(5): Show | 8 | HG01243.hp1 HG02145.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10-28548dupT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139156400 | ||||||
| chr5:139156408
|
A | AAAG | 6 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0081others(3): Show | 6 | HG00642.hp1 HG01346.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-28558_-10-2855 others(7): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139156408 | ||||||
| chr5:139156408
|
A | AAG | 70 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(67): Show | 70 | HG00323.hp2 HG00423.hp2 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.-10-28556_-10-2855 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139156408 | ||||||
| chr5:139156535
|
C | G | 62 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(59): Show | 62 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.-10-28682G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139156535 | ||||||
| chr5:139157065
|
C | A | 1 | a0001c0001t0001g0057 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-10-29212G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139157065 | ||||||
| chr5:139157155
|
T | C | 76 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(73): Show | 76 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.-10-29302A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139157155 | ||||||
| chr5:139157210
|
A | G | 74 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(71): Show | 74 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.-10-29357T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139157210 | ||||||
| chr5:139157506
|
G | A | 1 | a0001c0005t0001g0091 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-10-29653C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139157506 | ||||||
| chr5:139157562
|
A | G | 1 | a0001c0002t0001g0019 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-10-29709T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139157562 | ||||||
| chr5:139157669
|
G | A | 1 | a0001c0002t0001g0085 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-10-29816C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139157669 | ||||||
| chr5:139157694
|
T | C | 7 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0039others(4): Show | 7 | NA18942.hp1 NA18946.hp2 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10-29841A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139157694 | ||||||
| chr5:139157712
|
T | C | 4 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0142others(1): Show | 4 | HG00642.hp2 HG01261.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-29859A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139157712 | ||||||
| chr5:139157848
|
G | A | 1 | a0001c0002t0001g0179 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-10-29995C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139157848 | ||||||
| chr5:139158006
|
G | A | 74 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(71): Show | 74 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.-10-30153C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139158006 | ||||||
| chr5:139158029
|
G | A | 1 | a0001c0002t0001g0128 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-10-30176C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139158029 | ||||||
| chr5:139158093
|
T | C | 61 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(58): Show | 61 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.-10-30240A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139158093 | ||||||
| chr5:139158244
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-10-30391T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139158244 | ||||||
| chr5:139158273
|
A | C | 76 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(73): Show | 76 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.-10-30420T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139158273 | ||||||
| chr5:139158543
|
C | T | 1 | a0001c0001t0001g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-10-30690G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139158543 | ||||||
| chr5:139158639
|
TG | T | 59 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(56): Show | 59 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.-10-30787delC | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139158639 | ||||||
| chr5:139158672
|
T | A | 124 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(121): Show | 124 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(121): Show |
intron_variant | MODIFIER | c.-10-30819A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139158672 | ||||||
| chr5:139158970
|
T | G | 1 | a0001c0001t0002g0093 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-10-31117A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139158970 | ||||||
| chr5:139159001
|
T | C | 75 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(72): Show | 75 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.-10-31148A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139159001 | ||||||
| chr5:139159071
|
G | A | 72 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(69): Show | 72 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.-10-31218C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139159071 | ||||||
| chr5:139159105
|
G | A | 125 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(122): Show | 125 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(122): Show |
intron_variant | MODIFIER | c.-10-31252C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139159105 | ||||||
| chr5:139159149
|
A | C | 25 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(22): Show | 25 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.-10-31296T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139159149 | ||||||
| chr5:139159599
|
T | C | 3 | a0001c0001t0002g0018a0001c0001t0002g0029a0001c0001t0002g0093 | 3 | HG01258.hp2 NA18961.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.-10-31746A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139159599 | ||||||
| chr5:139159723
|
C | T | 1 | a0001c0005t0001g0091 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-10-31870G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139159723 | ||||||
| chr5:139159839
|
G | A | 50 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(47): Show | 50 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.-10-31986C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139159839 | ||||||
| chr5:139160143
|
T | TCA | 55 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(52): Show | 55 | HG00423.hp1 HG00735.hp2 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.-10-32292_-10-3229 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139160143 | ||||||
| chr5:139160143
|
T | TCACA | 9 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0002t0001g0004others(6): Show | 9 | HG01975.hp1 HG01993.hp2 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-32294_-10-3229 others(8): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139160143 | ||||||
| chr5:139160143
|
T | TCACACA | 2 | a0001c0001t0001g0032a0001c0002t0001g0019 | 2 | HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-10-32296_-10-3229 others(10): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139160143 | ||||||
| chr5:139160143
|
TCA | T | 25 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(22): Show | 25 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.-10-32292_-10-3229 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139160143 | ||||||
| chr5:139160143
|
TCACA | T | 11 | a0001c0001t0001g0021a0001c0001t0001g0149a0001c0002t0001g0002others(8): Show | 11 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-10-32294_-10-3229 others(8): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139160143 | ||||||
| chr5:139160143
|
TCACACA | T | 4 | a0001c0001t0002g0018a0001c0001t0002g0029a0001c0001t0002g0093others(1): Show | 4 | HG01258.hp2 NA18961.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-32296_-10-3229 others(10): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139160143 | ||||||
| chr5:139160143
|
TCACACAC others(3): Show |
T | 59 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(56): Show | 59 | HG00323.hp2 HG00423.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.-10-32300_-10-3229 others(14): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139160143 | ||||||
| chr5:139160143
|
TCACACAC others(5): Show |
T | 1 | a0001c0001t0001g0088 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-10-32302_-10-3229 others(16): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139160143 | ||||||
| chr5:139160187
|
A | AC | 3 | a0001c0001t0001g0152a0001c0002t0001g0193a0001c0005t0001g0091 | 3 | HG03486.hp1 NA18959.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.-10-32335_-10-3233 others(5): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139160187 | ||||||
| chr5:139160188
|
A | C | 1 | a0001c0002t0001g0178 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-10-32335T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139160188 | ||||||
| chr5:139160189
|
A | C | 1 | a0001c0001t0001g0030 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-10-32336T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139160189 | ||||||
| chr5:139160210
|
G | A | 2 | a0002c0006t0001g0097a0002c0006t0001g0103 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-10-32357C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139160210 | ||||||
| chr5:139160971
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-10-33118G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139160971 | ||||||
| chr5:139161015
|
G | C | 1 | a0001c0001t0001g0162 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-10-33162C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139161015 | ||||||
| chr5:139161508
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-10-33655T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139161508 | ||||||
| chr5:139161707
|
C | T | 58 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(55): Show | 58 | HG00323.hp2 HG00423.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.-10-33854G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139161707 | ||||||
| chr5:139161830
|
T | C | 1 | a0001c0002t0001g0183 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-10-33977A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139161830 | ||||||
| chr5:139162683
|
C | G | 7 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(4): Show | 7 | HG02257.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-34830G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139162683 | ||||||
| chr5:139162716
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-10-34863A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139162716 | ||||||
| chr5:139163039
|
A | G | 64 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(61): Show | 64 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.-10-35186T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139163039 | ||||||
| chr5:139163118
|
G | A | 5 | a0001c0001t0001g0092a0002c0006t0001g0097a0002c0006t0001g0103others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11+35151C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139163118 | ||||||
| chr5:139163145
|
T | C | 1 | a0001c0002t0001g0119 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-11+35124A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139163145 | ||||||
| chr5:139163171
|
G | A | 1 | a0001c0002t0001g0190 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-11+35098C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139163171 | ||||||
| chr5:139163361
|
G | GT | 6 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0002t0001g0099others(3): Show | 6 | HG01069.hp1 HG01071.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+34907dupA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139163361 | ||||||
| chr5:139163401
|
G | A | 29 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(26): Show | 29 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.-11+34868C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139163401 | ||||||
| chr5:139163436
|
C | G | 36 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(33): Show | 36 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.-11+34833G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139163436 | ||||||
| chr5:139163527
|
G | A | 14 | a0001c0001t0001g0009a0001c0001t0001g0030a0001c0002t0001g0006others(11): Show | 14 | HG01243.hp1 HG02145.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.-11+34742C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139163527 | ||||||
| chr5:139163616
|
C | T | 1 | a0009c0013t0001g0045 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-11+34653G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139163616 | ||||||
| chr5:139164068
|
AAG | A | 7 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(4): Show | 7 | HG02976.hp1 NA18522.hp1 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11+34199_-11+3420 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139164068 | ||||||
| chr5:139164106
|
G | A | 1 | a0001c0002t0001g0126 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-11+34163C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139164106 | ||||||
| chr5:139164116
|
C | CA | 74 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0024others(71): Show | 74 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.-11+34152dupT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139164116 | ||||||
| chr5:139164116
|
C | CAA | 31 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(28): Show | 31 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.-11+34151_-11+3415 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139164116 | ||||||
| chr5:139164116
|
CA | C | 6 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0026others(3): Show | 6 | HG02451.hp1 HG02965.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+34152delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139164116 | ||||||
| chr5:139164510
|
T | C | 1 | a0001c0005t0001g0007 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-11+33759A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139164510 | ||||||
| chr5:139164641
|
A | G | 2 | a0001c0001t0001g0067a0001c0001t0001g0074 | 2 | HG01934.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.-11+33628T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139164641 | ||||||
| chr5:139164764
|
G | A | 1 | a0003c0004t0001g0164 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-11+33505C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139164764 | ||||||
| chr5:139165159
|
T | C | 75 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(72): Show | 75 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.-11+33110A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139165159 | ||||||
| chr5:139165159
|
T | G | 1 | a0001c0002t0001g0065 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-11+33110A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139165159 | ||||||
| chr5:139165627
|
G | A | 2 | a0001c0001t0002g0165a0001c0001t0002g0167 | 2 | HG01258.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-11+32642C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139165627 | ||||||
| chr5:139165633
|
A | T | 1 | a0001c0001t0001g0051 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-11+32636T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139165633 | ||||||
| chr5:139165805
|
A | G | 97 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(94): Show | 97 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.-11+32464T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139165805 | ||||||
| chr5:139165885
|
G | A | 74 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(71): Show | 74 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.-11+32384C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139165885 | ||||||
| chr5:139165931
|
G | A | 7 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(4): Show | 7 | HG02976.hp1 NA18522.hp1 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11+32338C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139165931 | ||||||
| chr5:139166191
|
A | C | 1 | a0001c0002t0001g0114 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-11+32078T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139166191 | ||||||
| chr5:139166238
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-11+32031A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139166238 | ||||||
| chr5:139166336
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-11+31933T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139166336 | ||||||
| chr5:139166481
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-11+31788C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139166481 | ||||||
| chr5:139166664
|
G | A | 1 | a0001c0002t0001g0002 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-11+31605C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139166664 | ||||||
| chr5:139166685
|
C | A | 59 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(56): Show | 59 | HG00323.hp2 HG00423.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.-11+31584G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139166685 | ||||||
| chr5:139166700
|
G | A | 75 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(72): Show | 75 | HG00323.hp2 HG00423.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.-11+31569C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139166700 | ||||||
| chr5:139166777
|
G | A | 1 | a0001c0001t0001g0015 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-11+31492C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139166777 | ||||||
| chr5:139166816
|
T | C | 1 | a0001c0002t0001g0087 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-11+31453A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139166816 | ||||||
| chr5:139166903
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-11+31366T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139166903 | ||||||
| chr5:139167059
|
G | A | 10 | a0001c0001t0001g0086a0001c0001t0001g0162a0001c0001t0001g0163others(7): Show | 10 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-11+31210C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139167059 | ||||||
| chr5:139167204
|
C | G | 4 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0084others(1): Show | 4 | HG02145.hp1 HG02723.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+31065G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139167204 | ||||||
| chr5:139167606
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-11+30663T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139167606 | ||||||
| chr5:139167700
|
G | A | 9 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0039others(6): Show | 9 | HG02132.hp2 NA18942.hp1 NA18946.hp2 others(6): Show |
intron_variant | MODIFIER | c.-11+30569C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139167700 | ||||||
| chr5:139167911
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-11+30358C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139167911 | ||||||
| chr5:139168476
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-11+29793C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139168476 | ||||||
| chr5:139168563
|
G | T | 87 | a0001c0001t0001g0009a0001c0001t0001g0030a0001c0001t0001g0035others(84): Show | 87 | HG00323.hp2 HG00423.hp2 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.-11+29706C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139168563 | ||||||
| chr5:139168622
|
CT | C | 96 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(93): Show | 96 | HG00323.hp2 HG00423.hp2 HG00735.hp1 others(93): Show |
intron_variant | MODIFIER | c.-11+29646delA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139168622 | ||||||
| chr5:139168889
|
G | C | 1 | a0001c0002t0001g0120 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-11+29380C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139168889 | ||||||
| chr5:139168928
|
C | T | 75 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(72): Show | 75 | HG00323.hp2 HG00423.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.-11+29341G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139168928 | ||||||
| chr5:139168943
|
T | C | 1 | a0001c0001t0001g0162 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-11+29326A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139168943 | ||||||
| chr5:139168957
|
C | CA | 25 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0039others(22): Show | 25 | HG01891.hp1 HG02109.hp2 HG02280.hp2 others(22): Show |
intron_variant | MODIFIER | c.-11+29311dupT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139168957 | ||||||
| chr5:139169450
|
G | A | 3 | a0001c0001t0001g0159a0002c0003t0001g0034a0002c0003t0001g0161 | 3 | HG02976.hp1 NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-11+28819C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139169450 | ||||||
| chr5:139169476
|
AT | A | 5 | a0001c0001t0001g0088a0001c0001t0002g0165a0001c0001t0002g0167others(2): Show | 5 | HG01258.hp1 HG01891.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11+28792delA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139169476 | ||||||
| chr5:139169476
|
ATT | A | 105 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(102): Show | 105 | HG00323.hp2 HG00423.hp2 HG00735.hp1 others(102): Show |
intron_variant | MODIFIER | c.-11+28791_-11+2879 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139169476 | ||||||
| chr5:139169585
|
G | A | 3 | a0001c0002t0001g0099a0001c0002t0001g0101a0001c0002t0001g0104 | 3 | HG01884.hp1 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-11+28684C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139169585 | ||||||
| chr5:139169817
|
TCCCTCTC | T | 4 | a0001c0001t0001g0154a0001c0001t0003g0001a0002c0006t0001g0097others(1): Show | 4 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+28445_-11+2845 others(11): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139169817 | ||||||
| chr5:139169845
|
C | CCTCTTT | 7 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0039others(4): Show | 7 | NA18942.hp1 NA18946.hp2 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11+28423_-11+2842 others(10): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139169845 | ||||||
| chr5:139169861
|
C | CCCTCTTT others(16): Show |
50 | a0001c0001t0001g0035a0001c0001t0001g0043a0001c0001t0001g0044others(47): Show | 50 | HG00323.hp2 HG00735.hp1 HG01069.hp2 others(47): Show |
intron_variant | MODIFIER | c.-11+28407_-11+2840 others(27): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139169861 | ||||||
| chr5:139169861
|
C | CCCTCTTT others(39): Show |
2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | HG00423.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-11+28407_-11+2840 others(50): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139169861 | ||||||
| chr5:139169861
|
C | G | 7 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0039others(4): Show | 7 | NA18942.hp1 NA18946.hp2 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11+28408G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139169861 | ||||||
| chr5:139169880
|
C | G | 4 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0028others(1): Show | 4 | HG02451.hp1 HG03225.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+28389G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139169880 | ||||||
| chr5:139169885
|
CCTCT | C | 3 | a0001c0001t0001g0159a0002c0003t0001g0034a0002c0003t0001g0161 | 3 | HG02976.hp1 NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-11+28380_-11+2838 others(8): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139169885 | ||||||
| chr5:139169958
|
G | A | 1 | a0001c0002t0001g0122 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-11+28311C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139169958 | ||||||
| chr5:139170013
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-11+28256G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139170013 | ||||||
| chr5:139170102
|
C | T | 2 | a0001c0002t0001g0072a0001c0002t0001g0173 | 2 | HG01074.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.-11+28167G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139170102 | ||||||
| chr5:139170199
|
C | T | 49 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(46): Show | 49 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.-11+28070G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139170199 | ||||||
| chr5:139170208
|
G | A | 1 | a0001c0005t0001g0091 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-11+28061C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139170208 | ||||||
| chr5:139170212
|
C | T | 1 | a0001c0002t0001g0100 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-11+28057G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139170212 | ||||||
| chr5:139170250
|
C | A | 14 | a0001c0001t0001g0009a0001c0001t0001g0030a0001c0002t0001g0006others(11): Show | 14 | HG01243.hp1 HG02145.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.-11+28019G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139170250 | ||||||
| chr5:139170290
|
C | A | 1 | a0001c0001t0001g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-11+27979G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139170290 | ||||||
| chr5:139170339
|
C | T | 3 | a0001c0001t0001g0159a0002c0003t0001g0034a0002c0003t0001g0161 | 3 | HG02976.hp1 NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-11+27930G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139170339 | ||||||
| chr5:139170549
|
C | T | 2 | a0001c0001t0001g0009a0001c0002t0001g0008 | 2 | HG02602.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.-11+27720G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139170549 | ||||||
| chr5:139170555
|
C | T | 1 | a0001c0002t0001g0090 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-11+27714G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139170555 | ||||||
| chr5:139170589
|
C | T | 14 | a0001c0001t0001g0009a0001c0001t0001g0030a0001c0002t0001g0006others(11): Show | 14 | HG01243.hp1 HG02145.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.-11+27680G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139170589 | ||||||
| chr5:139170606
|
G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0096 | 2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-11+27663C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139170606 | ||||||
| chr5:139170642
|
ATCTGAGA others(33): Show |
A | 4 | a0001c0002t0001g0099a0001c0002t0001g0101a0001c0002t0001g0104others(1): Show | 4 | HG01884.hp1 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+27587_-11+2762 others(44): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139170642 | ||||||
| chr5:139170706
|
G | A | 34 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(31): Show | 34 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.-11+27563C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139170706 | ||||||
| chr5:139170710
|
G | A | 1 | a0001c0002t0001g0123 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-11+27559C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139170710 | ||||||
| chr5:139170838
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-11+27431G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139170838 | ||||||
| chr5:139170844
|
G | A | 3 | a0001c0001t0001g0159a0002c0003t0001g0034a0002c0003t0001g0161 | 3 | HG02976.hp1 NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-11+27425C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139170844 | ||||||
| chr5:139170875
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-11+27394C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139170875 | ||||||
| chr5:139170889
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-11+27380C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139170889 | ||||||
| chr5:139170938
|
C | T | 49 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(46): Show | 49 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.-11+27331G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139170938 | ||||||
| chr5:139170987
|
C | T | 1 | a0002c0003t0001g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-11+27282G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139170987 | ||||||
| chr5:139171077
|
G | A | 3 | a0001c0001t0002g0018a0001c0001t0002g0029a0001c0001t0002g0093 | 3 | HG01258.hp2 NA18961.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.-11+27192C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139171077 | ||||||
| chr5:139171088
|
C | T | 1 | a0001c0002t0001g0110 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-11+27181G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139171088 | ||||||
| chr5:139171111
|
G | A | 1 | a0001c0002t0001g0002 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-11+27158C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139171111 | ||||||
| chr5:139171115
|
G | A | 49 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(46): Show | 49 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.-11+27154C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139171115 | ||||||
| chr5:139171127
|
G | A | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-11+27142C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139171127 | ||||||
| chr5:139171149
|
A | C | 1 | a0001c0005t0001g0091 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-11+27120T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139171149 | ||||||
| chr5:139171260
|
G | T | 2 | a0001c0001t0001g0177a0001c0002t0001g0176 | 2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-11+27009C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139171260 | ||||||
| chr5:139171304
|
A | G | 109 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00323.hp2 HG00423.hp2 HG00735.hp1 others(106): Show |
intron_variant | MODIFIER | c.-11+26965T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139171304 | ||||||
| chr5:139171503
|
C | T | 49 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(46): Show | 49 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.-11+26766G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139171503 | ||||||
| chr5:139171563
|
C | T | 58 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(55): Show | 58 | HG00323.hp2 HG00423.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.-11+26706G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139171563 | ||||||
| chr5:139171713
|
G | T | 3 | a0001c0001t0001g0159a0002c0003t0001g0034a0002c0003t0001g0161 | 3 | HG02976.hp1 NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-11+26556C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139171713 | ||||||
| chr5:139171722
|
TAAAAAAG others(3): Show |
T | 5 | a0001c0001t0001g0030a0001c0002t0001g0099a0001c0002t0001g0101others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+26537_-11+2654 others(14): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139171722 | ||||||
| chr5:139171744
|
A | T | 1 | a0001c0001t0001g0088 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-11+26525T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139171744 | ||||||
| chr5:139171748
|
T | G | 3 | a0001c0001t0001g0086a0001c0001t0001g0180a0001c0001t0001g0181 | 3 | HG02559.hp2 HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-11+26521A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139171748 | ||||||
| chr5:139171793
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-11+26476G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139171793 | ||||||
| chr5:139172207
|
A | G | 3 | a0001c0001t0001g0086a0001c0001t0001g0180a0001c0001t0001g0181 | 3 | HG02559.hp2 HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-11+26062T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139172207 | ||||||
| chr5:139172413
|
C | A | 1 | a0001c0002t0001g0110 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-11+25856G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139172413 | ||||||
| chr5:139172458
|
C | T | 2 | a0001c0001t0001g0177a0001c0002t0001g0176 | 2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-11+25811G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139172458 | ||||||
| chr5:139172589
|
C | T | 2 | a0001c0002t0001g0100a0008c0011t0001g0196 | 2 | HG03195.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-11+25680G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139172589 | ||||||
| chr5:139172631
|
C | CA | 76 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(73): Show | 76 | HG00323.hp2 HG00423.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.-11+25637dupT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139172631 | ||||||
| chr5:139172744
|
G | A | 1 | a0001c0005t0001g0091 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-11+25525C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139172744 | ||||||
| chr5:139172843
|
AGTGCTGA others(204): Show |
A | 1 | a0001c0001t0001g0133 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-11+25215_-11+2542 others(4): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139172843 | ||||||
| chr5:139172899
|
C | G | 4 | a0001c0002t0001g0006a0001c0002t0001g0010a0001c0002t0001g0084others(1): Show | 4 | HG02145.hp1 HG02723.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+25370G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139172899 | ||||||
| chr5:139172992
|
C | T | 1 | a0001c0002t0001g0113 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-11+25277G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139172992 | ||||||
| chr5:139173083
|
A | T | 49 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(46): Show | 49 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.-11+25186T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139173083 | ||||||
| chr5:139173300
|
C | T | 1 | a0001c0001t0001g0015 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-11+24969G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139173300 | ||||||
| chr5:139173465
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-11+24804C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139173465 | ||||||
| chr5:139173702
|
C | T | 49 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(46): Show | 49 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.-11+24567G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139173702 | ||||||
| chr5:139173790
|
C | CA | 8 | a0001c0001t0001g0081a0001c0001t0001g0088a0001c0002t0001g0099others(5): Show | 8 | HG01884.hp1 HG01934.hp2 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.-11+24478dupT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139173790 | ||||||
| chr5:139173790
|
C | CAA | 54 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(51): Show | 54 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.-11+24477_-11+2447 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139173790 | ||||||
| chr5:139173790
|
C | CAAA | 6 | a0001c0001t0001g0044a0001c0001t0001g0061a0001c0001t0001g0062others(3): Show | 6 | HG01069.hp2 HG01109.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+24476_-11+2447 others(7): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139173790 | ||||||
| chr5:139173790
|
CA | C | 36 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(33): Show | 36 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.-11+24478delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139173790 | ||||||
| chr5:139173790
|
CAA | C | 12 | a0001c0001t0001g0030a0001c0002t0001g0006a0001c0002t0001g0010others(9): Show | 12 | HG01243.hp1 HG02145.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-11+24477_-11+2447 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139173790 | ||||||
| chr5:139173816
|
G | T | 49 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(46): Show | 49 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.-11+24453C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139173816 | ||||||
| chr5:139173985
|
A | C | 1 | a0003c0004t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-11+24284T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139173985 | ||||||
| chr5:139174427
|
G | T | 3 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0142 | 3 | HG00642.hp2 HG01261.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.-11+23842C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139174427 | ||||||
| chr5:139174670
|
G | A | 1 | a0001c0002t0001g0128 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-11+23599C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139174670 | ||||||
| chr5:139174794
|
C | T | 49 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(46): Show | 49 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.-11+23475G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139174794 | ||||||
| chr5:139174799
|
A | G | 1 | a0001c0002t0001g0176 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-11+23470T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139174799 | ||||||
| chr5:139174937
|
CA | C | 56 | a0001c0001t0001g0035a0001c0001t0001g0039a0001c0001t0001g0043others(53): Show | 56 | HG00423.hp2 HG00642.hp1 HG01070.hp2 others(53): Show |
intron_variant | MODIFIER | c.-11+23331delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139174937 | ||||||
| chr5:139175282
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-11+22987G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139175282 | ||||||
| chr5:139175632
|
G | A | 1 | a0001c0001t0002g0140 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-11+22637C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139175632 | ||||||
| chr5:139175646
|
A | G | 1 | a0006c0009t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-11+22623T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139175646 | ||||||
| chr5:139175675
|
C | T | 1 | a0001c0002t0001g0148 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-11+22594G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139175675 | ||||||
| chr5:139175788
|
A | C | 189 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(186): Show | 189 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.-11+22481T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139175788 | ||||||
| chr5:139175834
|
A | G | 61 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(58): Show | 61 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.-11+22435T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139175834 | ||||||
| chr5:139175875
|
A | C | 1 | a0001c0002t0001g0151 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-11+22394T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139175875 | ||||||
| chr5:139175914
|
G | A | 1 | a0001c0001t0002g0018 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-11+22355C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139175914 | ||||||
| chr5:139176126
|
G | A | 1 | a0002c0003t0001g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-11+22143C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139176126 | ||||||
| chr5:139176347
|
G | A | 113 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(110): Show | 113 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(110): Show |
intron_variant | MODIFIER | c.-11+21922C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139176347 | ||||||
| chr5:139176521
|
T | C | 4 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0028others(1): Show | 4 | HG02451.hp1 HG03225.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+21748A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139176521 | ||||||
| chr5:139176867
|
G | A | 35 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(32): Show | 35 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.-11+21402C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139176867 | ||||||
| chr5:139176927
|
C | CT | 67 | a0001c0001t0001g0027a0001c0001t0001g0035a0001c0001t0001g0036others(64): Show | 67 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.-11+21341dupA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139176927 | ||||||
| chr5:139176927
|
C | CTT | 8 | a0001c0001t0001g0044a0001c0001t0001g0047a0001c0001t0001g0050others(5): Show | 8 | HG01109.hp2 HG01934.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11+21340_-11+2134 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139176927 | ||||||
| chr5:139176927
|
CT | C | 13 | a0001c0001t0001g0129a0001c0001t0001g0152a0001c0001t0001g0191others(10): Show | 13 | HG00735.hp2 HG01943.hp1 NA18942.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11+21341delA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139176927 | ||||||
| chr5:139177002
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-11+21267G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139177002 | ||||||
| chr5:139177341
|
G | T | 62 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(59): Show | 62 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.-11+20928C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139177341 | ||||||
| chr5:139178789
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-11+19480T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139178789 | ||||||
| chr5:139178928
|
A | G | 2 | a0001c0001t0001g0177a0001c0002t0001g0176 | 2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-11+19341T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139178928 | ||||||
| chr5:139179109
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-11+19160T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139179109 | ||||||
| chr5:139179376
|
A | T | 1 | a0001c0001t0001g0044 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-11+18893T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139179376 | ||||||
| chr5:139179655
|
G | A | 1 | a0001c0002t0001g0002 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-11+18614C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139179655 | ||||||
| chr5:139179896
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-11+18373T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139179896 | ||||||
| chr5:139180058
|
T | TA | 9 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0082others(6): Show | 9 | HG01070.hp1 HG01884.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.-11+18210dupT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139180058 | ||||||
| chr5:139180058
|
T | TAA | 58 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0039others(55): Show | 58 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.-11+18209_-11+1821 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139180058 | ||||||
| chr5:139180058
|
TA | T | 12 | a0001c0001t0001g0020a0001c0001t0001g0086a0001c0001t0001g0162others(9): Show | 12 | HG01071.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-11+18210delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139180058 | ||||||
| chr5:139180329
|
C | T | 22 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.-11+17940G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139180329 | ||||||
| chr5:139180330
|
G | A | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG00323.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.-11+17939C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139180330 | ||||||
| chr5:139180381
|
C | A | 1 | a0001c0001t0001g0078 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-11+17888G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139180381 | ||||||
| chr5:139180381
|
C | CA | 75 | a0001c0001t0001g0030a0001c0001t0001g0036a0001c0001t0001g0039others(72): Show | 75 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.-11+17887dupT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139180381 | ||||||
| chr5:139180381
|
C | CAA | 13 | a0001c0001t0001g0035a0001c0001t0001g0063a0001c0001t0001g0066others(10): Show | 13 | HG01109.hp2 HG01346.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11+17886_-11+1788 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139180381 | ||||||
| chr5:139180381
|
CA | C | 7 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0159others(4): Show | 7 | HG02976.hp1 HG03471.hp2 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11+17887delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139180381 | ||||||
| chr5:139181441
|
G | A | 3 | a0001c0001t0002g0018a0001c0001t0002g0029a0001c0001t0002g0093 | 3 | HG01258.hp2 NA18961.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.-11+16828C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139181441 | ||||||
| chr5:139181494
|
A | C | 3 | a0001c0001t0001g0086a0001c0001t0001g0180a0001c0001t0001g0181 | 3 | HG02559.hp2 HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-11+16775T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139181494 | ||||||
| chr5:139181546
|
A | G | 58 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(55): Show | 58 | HG00323.hp2 HG00423.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.-11+16723T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139181546 | ||||||
| chr5:139181796
|
C | T | 59 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(56): Show | 59 | HG00323.hp2 HG00423.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.-11+16473G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139181796 | ||||||
| chr5:139181843
|
T | C | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | NA18981.hp2 NA18986.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+16426A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139181843 | ||||||
| chr5:139181988
|
T | C | 3 | a0001c0002t0001g0099a0001c0002t0001g0101a0001c0002t0001g0104 | 3 | HG01884.hp1 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-11+16281A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139181988 | ||||||
| chr5:139182021
|
G | A | 7 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(4): Show | 7 | HG02976.hp1 NA18522.hp1 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11+16248C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139182021 | ||||||
| chr5:139182166
|
G | A | 1 | a0001c0010t0001g0064 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-11+16103C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139182166 | ||||||
| chr5:139182203
|
C | T | 5 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0081others(2): Show | 5 | HG01346.hp1 HG01516.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11+16066G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139182203 | ||||||
| chr5:139182235
|
C | T | 3 | a0001c0002t0001g0099a0001c0002t0001g0101a0001c0002t0001g0104 | 3 | HG01884.hp1 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-11+16034G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139182235 | ||||||
| chr5:139182516
|
C | A | 1 | a0001c0002t0001g0065 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-11+15753G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139182516 | ||||||
| chr5:139182663
|
A | C | 1 | a0001c0002t0001g0087 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-11+15606T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139182663 | ||||||
| chr5:139182801
|
T | C | 1 | a0001c0002t0001g0136 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-11+15468A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139182801 | ||||||
| chr5:139183126
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-11+15143C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139183126 | ||||||
| chr5:139183560
|
G | C | 1 | a0001c0002t0001g0139 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-11+14709C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139183560 | ||||||
| chr5:139183726
|
G | A | 4 | a0001c0002t0001g0137a0001c0002t0001g0139a0003c0004t0001g0138others(1): Show | 4 | HG02280.hp2 NA18945.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+14543C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139183726 | ||||||
| chr5:139184016
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-11+14253G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139184016 | ||||||
| chr5:139184036
|
T | C | 16 | a0001c0001t0001g0086a0001c0001t0001g0159a0001c0001t0001g0162others(13): Show | 16 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.-11+14233A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139184036 | ||||||
| chr5:139184235
|
T | G | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | NA18981.hp2 NA18986.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+14034A>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139184235 | ||||||
| chr5:139184482
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-11+13787G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139184482 | ||||||
| chr5:139185044
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-11+13225C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139185044 | ||||||
| chr5:139185154
|
G | A | 1 | a0001c0005t0001g0091 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-11+13115C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139185154 | ||||||
| chr5:139185231
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-11+13038A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139185231 | ||||||
| chr5:139185381
|
C | T | 58 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(55): Show | 58 | HG00323.hp2 HG00423.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.-11+12888G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139185381 | ||||||
| chr5:139185652
|
A | C | 4 | a0001c0001t0001g0107a0001c0001t0001g0191a0001c0002t0001g0150others(1): Show | 4 | NA18959.hp1 NA18963.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+12617T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139185652 | ||||||
| chr5:139186132
|
C | A | 3 | a0001c0001t0001g0086a0001c0001t0001g0180a0001c0001t0001g0181 | 3 | HG02559.hp2 HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-11+12137G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139186132 | ||||||
| chr5:139186202
|
C | T | 1 | a0001c0002t0001g0106 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-11+12067G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139186202 | ||||||
| chr5:139186259
|
C | A | 1 | a0001c0001t0001g0149 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-11+12010G>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139186259 | ||||||
| chr5:139186961
|
G | C | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-11+11308C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139186961 | ||||||
| chr5:139187033
|
C | G | 1 | a0001c0001t0002g0167 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-11+11236G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139187033 | ||||||
| chr5:139187165
|
G | C | 1 | a0001c0001t0001g0180 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-11+11104C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139187165 | ||||||
| chr5:139187517
|
T | TA | 78 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0036others(75): Show | 78 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.-11+10751dupT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139187517 | ||||||
| chr5:139187643
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-11+10626C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139187643 | ||||||
| chr5:139187656
|
C | CG | 79 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(76): Show | 79 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.-11+10612dupC | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139187656 | ||||||
| chr5:139187713
|
A | AAG | 98 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0024others(95): Show | 98 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.-11+10555_-11+1055 others(6): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139187713 | ||||||
| chr5:139187822
|
C | T | 7 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0039others(4): Show | 7 | NA18942.hp1 NA18946.hp2 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11+10447G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139187822 | ||||||
| chr5:139187939
|
A | G | 1 | a0007c0008t0001g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-11+10330T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139187939 | ||||||
| chr5:139188442
|
G | C | 1 | a0001c0002t0001g0144 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-11+9827C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139188442 | ||||||
| chr5:139188474
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-11+9795C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139188474 | ||||||
| chr5:139188987
|
A | C | 98 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0024others(95): Show | 98 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.-11+9282T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139188987 | ||||||
| chr5:139189243
|
C | T | 4 | a0001c0002t0001g0099a0001c0002t0001g0101a0001c0002t0001g0104others(1): Show | 4 | HG01884.hp1 HG03041.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+9026G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139189243 | ||||||
| chr5:139189437
|
C | G | 4 | a0001c0002t0001g0099a0001c0002t0001g0101a0001c0002t0001g0104others(1): Show | 4 | HG01884.hp1 HG03041.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+8832G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139189437 | ||||||
| chr5:139189439
|
G | C | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-11+8830C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139189439 | ||||||
| chr5:139189472
|
A | T | 2 | a0001c0001t0001g0177a0001c0002t0001g0176 | 2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-11+8797T>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139189472 | ||||||
| chr5:139190197
|
T | C | 1 | a0001c0002t0001g0141 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-11+8072A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139190197 | ||||||
| chr5:139190262
|
C | T | 3 | a0001c0002t0001g0038a0001c0002t0001g0068a0001c0002t0001g0070 | 3 | HG01069.hp2 HG01496.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.-11+8007G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139190262 | ||||||
| chr5:139190410
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-11+7859G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139190410 | ||||||
| chr5:139190436
|
G | A | 1 | a0001c0002t0001g0065 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-11+7833C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139190436 | ||||||
| chr5:139190629
|
C | G | 98 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0024others(95): Show | 98 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.-11+7640G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139190629 | ||||||
| chr5:139190667
|
G | C | 1 | a0001c0001t0001g0066 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-11+7602C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139190667 | ||||||
| chr5:139190896
|
C | T | 3 | a0001c0001t0001g0159a0002c0003t0001g0034a0002c0003t0001g0161 | 3 | HG02976.hp1 NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-11+7373G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139190896 | ||||||
| chr5:139190998
|
G | A | 2 | a0001c0001t0001g0154a0001c0005t0001g0007 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-11+7271C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139190998 | ||||||
| chr5:139191108
|
T | A | 1 | a0001c0001t0001g0088 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-11+7161A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139191108 | ||||||
| chr5:139191217
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-11+7052C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139191217 | ||||||
| chr5:139191221
|
C | CA | 12 | a0001c0001t0001g0159a0001c0001t0001g0191a0001c0002t0001g0087others(9): Show | 12 | HG00323.hp1 HG00642.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11+7047dupT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139191221 | ||||||
| chr5:139191221
|
CA | C | 42 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(39): Show | 42 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.-11+7047delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139191221 | ||||||
| chr5:139191221
|
CAA | C | 54 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(51): Show | 54 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.-11+7046_-11+7047d others(4): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139191221 | ||||||
| chr5:139191222
|
A | C | 1 | a0002c0003t0001g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-11+7047T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139191222 | ||||||
| chr5:139191365
|
T | C | 1 | a0001c0002t0001g0145 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-11+6904A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139191365 | ||||||
| chr5:139191610
|
C | G | 62 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(59): Show | 62 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.-11+6659G>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139191610 | ||||||
| chr5:139191619
|
TA | T | 21 | a0001c0001t0001g0009a0001c0001t0001g0030a0001c0001t0001g0037others(18): Show | 21 | HG01070.hp1 HG01109.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.-11+6649delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139191619 | ||||||
| chr5:139192074
|
C | CA | 89 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0021others(86): Show | 89 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+6194dupT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139192074 | ||||||
| chr5:139192074
|
C | CAA | 11 | a0001c0001t0001g0033a0001c0001t0001g0071a0001c0001t0001g0074others(8): Show | 11 | HG01069.hp2 HG01074.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.-11+6193_-11+6194d others(4): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139192074 | ||||||
| chr5:139192074
|
CA | C | 5 | a0001c0002t0001g0087a0001c0002t0001g0090a0001c0002t0001g0098others(2): Show | 5 | HG01070.hp2 HG02895.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+6194delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139192074 | ||||||
| chr5:139192223
|
C | CA | 9 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(6): Show | 9 | HG00323.hp2 HG00735.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.-11+6045dupT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139192223 | ||||||
| chr5:139192997
|
C | CA | 14 | a0001c0001t0001g0149a0001c0001t0001g0152a0001c0001t0001g0154others(11): Show | 14 | HG00735.hp2 HG01891.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.-11+5271dupT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139192997 | ||||||
| chr5:139192997
|
CA | C | 34 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(31): Show | 34 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.-11+5271delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139192997 | ||||||
| chr5:139192997
|
CAAAAAAA others(5): Show |
C | 61 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(58): Show | 61 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.-11+5260_-11+5271d others(14): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139192997 | ||||||
| chr5:139193013
|
A | C | 1 | a0001c0001t0001g0174 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-11+5256T>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139193013 | ||||||
| chr5:139193014
|
AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0001g0174 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-11+5241_-11+5254d others(16): Show |
SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139193014 | ||||||
| chr5:139193160
|
G | A | 1 | a0001c0002t0001g0194 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-11+5109C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139193160 | ||||||
| chr5:139193216
|
T | C | 12 | a0001c0001t0001g0086a0001c0001t0001g0159a0001c0001t0001g0162others(9): Show | 12 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-11+5053A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139193216 | ||||||
| chr5:139193292
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG02109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-11+4977C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139193292 | ||||||
| chr5:139193361
|
C | T | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-11+4908G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139193361 | ||||||
| chr5:139193424
|
T | C | 2 | a0001c0002t0001g0155a0001c0002t0001g0156 | 2 | HG00323.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.-11+4845A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139193424 | ||||||
| chr5:139193773
|
G | A | 1 | a0001c0001t0001g0003 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-11+4496C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139193773 | ||||||
| chr5:139194338
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-11+3931C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139194338 | ||||||
| chr5:139194481
|
G | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-11+3788C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139194481 | ||||||
| chr5:139194884
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-11+3385T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139194884 | ||||||
| chr5:139194930
|
C | CT | 12 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(9): Show | 12 | HG01243.hp1 HG01993.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11+3338dupA | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139194930 | ||||||
| chr5:139194935
|
T | C | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG02109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-11+3334A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139194935 | ||||||
| chr5:139194941
|
T | C | 12 | a0001c0001t0001g0086a0001c0001t0001g0159a0001c0001t0001g0162others(9): Show | 12 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-11+3328A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139194941 | ||||||
| chr5:139195184
|
A | G | 1 | a0001c0002t0001g0087 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-11+3085T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139195184 | ||||||
| chr5:139195221
|
C | T | 1 | a0001c0002t0001g0182 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-11+3048G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139195221 | ||||||
| chr5:139195428
|
G | A | 1 | a0003c0004t0001g0164 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-11+2841C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139195428 | ||||||
| chr5:139195515
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-11+2754C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139195515 | ||||||
| chr5:139195589
|
G | A | 60 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(57): Show | 60 | HG00323.hp2 HG00423.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.-11+2680C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139195589 | ||||||
| chr5:139195746
|
G | A | 1 | a0001c0002t0001g0175 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-11+2523C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139195746 | ||||||
| chr5:139195788
|
G | T | 3 | a0001c0001t0001g0086a0001c0001t0001g0180a0001c0001t0001g0181 | 3 | HG02559.hp2 HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-11+2481C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139195788 | ||||||
| chr5:139195878
|
T | C | 2 | a0001c0001t0001g0177a0001c0002t0001g0176 | 2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-11+2391A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139195878 | ||||||
| chr5:139195914
|
G | T | 1 | a0001c0002t0001g0085 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-11+2355C>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139195914 | ||||||
| chr5:139196030
|
A | G | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | NA18981.hp2 NA18986.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+2239T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139196030 | ||||||
| chr5:139196362
|
C | T | 8 | a0001c0001t0001g0009a0001c0002t0001g0006a0001c0002t0001g0008others(5): Show | 8 | HG01243.hp1 HG02145.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.-11+1907G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139196362 | ||||||
| chr5:139196500
|
T | C | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-11+1769A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139196500 | ||||||
| chr5:139196510
|
T | C | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-11+1759A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139196510 | ||||||
| chr5:139196932
|
G | C | 2 | a0001c0001t0001g0177a0001c0002t0001g0176 | 2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-11+1337C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139196932 | ||||||
| chr5:139197087
|
G | C | 1 | a0001c0002t0001g0178 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-11+1182C>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139197087 | ||||||
| chr5:139197120
|
T | C | 1 | a0001c0002t0001g0179 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-11+1149A>G | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139197120 | ||||||
| chr5:139197268
|
C | CA | 17 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0191others(14): Show | 17 | HG01109.hp1 HG02132.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-11+1000dupT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139197268 | ||||||
| chr5:139197268
|
CA | C | 82 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(79): Show | 82 | HG00323.hp2 HG00423.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.-11+1000delT | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139197268 | ||||||
| chr5:139197642
|
C | T | 2 | a0001c0001t0001g0003a0001c0002t0001g0004 | 2 | HG02132.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.-11+627G>A | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139197642 | ||||||
| chr5:139197697
|
A | G | 1 | a0001c0002t0001g0002 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-11+572T>C | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139197697 | ||||||
| chr5:139197711
|
G | A | 1 | a0008c0011t0001g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-11+558C>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139197711 | ||||||
| chr5:139197994
|
T | A | 2 | a0001c0001t0001g0197a0001c0002t0001g0198 | 2 | HG02071.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.-11+275A>T | SIL1 | ENSG00000120725.13 | transcript | ENST00000394817.7 | protein_coding | 1/9 | chr5 | 139197994 |