Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 55164 |
|---|---|
| ensemblid | ENSG00000144736.14 |
| hgncid | 25543 |
| symbol | SHQ1 |
| name | SHQ1, H/ACA ribonucleoprotein assembly factor |
| refseq_nuc | NM_018130.3 |
| refseq_prot | NP_060600.2 |
| ensembl_nuc | ENST00000325599.13 |
| ensembl_prot | ENSP00000315182.8 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 72749277 |
| end | 72848445 |
| strand | - |
| ver | v1.2 |
| region | chr3:72749277-72848445 |
| region5000 | chr3:72744277-72853445 |
| regionname0 | SHQ1_chr3_72749277_72848445 |
| regionname5000 | SHQ1_chr3_72744277_72853445 |
| 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 | 577 | 131 | 24 | 26 | 59 | 4 | 16 | 46 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0002 | 0/0 | 577 | 65 | 41 | 11 | 10 | 2 | 1 | 5 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0003 | 0/0 | 577 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0004 | 0/0 | 577 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0005 | 0/0 | 577 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0006 | 0/0 | 577 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0007 | 0/0 | 577 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0008 | 0/0 | 577 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0009 | 0/0 | 577 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0010 | 0/0 | 577 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0011 | 0/0 | 577 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1734 | 131 | 24 | 26 | 59 | 4 | 16 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| c0002 | 0/0 | 1734 | 63 | 39 | 11 | 10 | 2 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| c0003 | 0/0 | 1734 | 10 | 10 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| c0004 | 0/0 | 1734 | 3 | 0 | 2 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| c0005 | 0/0 | 1734 | 3 | 3 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| c0006 | 0/0 | 1734 | 3 | 3 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| c0007 | 0/0 | 1734 | 2 | 2 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| c0008 | 0/0 | 1734 | 2 | 2 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| c0009 | 0/0 | 1734 | 2 | 2 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| c0010 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| c0011 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| c0012 | 0/0 | 1734 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| 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 | 1113 | 201 | 72 | 39 | 65 | 6 | 17 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| t0002 | 0/0 | 1108 | 5 | 5 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| t0003 | 0/0 | 1113 | 5 | 0 | 0 | 5 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| t0004 | 0/0 | 1113 | 4 | 4 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| t0005 | 0/0 | 1113 | 3 | 3 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| t0006 | 0/0 | 1113 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| t0007 | 0/0 | 1113 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| t0008 | 0/0 | 1113 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| t0009 | 0/0 | 1113 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0152 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0176 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1734 | 131 | 24 | 26 | 59 | 4 | 16 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0002c0002 | 0/0 | 1734 | 63 | 39 | 11 | 10 | 2 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0002c0008 | 0/0 | 1734 | 2 | 2 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0003c0003 | 0/0 | 1734 | 10 | 10 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0004c0004 | 0/0 | 1734 | 3 | 0 | 2 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0005c0005 | 0/0 | 1734 | 3 | 3 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0006c0006 | 0/0 | 1734 | 3 | 3 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0007c0009 | 0/0 | 1734 | 2 | 2 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0008c0007 | 0/0 | 1734 | 2 | 2 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0009c0011 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0010c0012 | 0/0 | 1734 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0011c0010 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2846 | 121 | 21 | 25 | 54 | 4 | 15 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0001c0001t0002 | 0/0 | 2841 | 3 | 3 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0001c0001t0003 | 0/0 | 2846 | 5 | 0 | 0 | 5 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0001c0001t0007 | 0/0 | 2846 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0001c0001t0009 | 0/0 | 2846 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0002c0002t0001 | 0/0 | 2846 | 54 | 30 | 11 | 10 | 2 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0002c0002t0004 | 0/0 | 2846 | 4 | 4 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0002c0002t0005 | 0/0 | 2846 | 3 | 3 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0002c0002t0006 | 0/0 | 2846 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0002c0002t0008 | 0/0 | 2846 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0002c0008t0001 | 0/0 | 2846 | 2 | 2 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0003c0003t0001 | 0/0 | 2846 | 10 | 10 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0004c0004t0001 | 0/0 | 2846 | 3 | 0 | 2 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0005c0005t0001 | 0/0 | 2846 | 3 | 3 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0006c0006t0001 | 0/0 | 2846 | 3 | 3 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0007c0009t0002 | 0/0 | 2841 | 2 | 2 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0008c0007t0001 | 0/0 | 2846 | 2 | 2 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0009c0011t0001 | 0/0 | 2846 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0010c0012t0001 | 0/0 | 2846 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| a0011c0010t0001 | 0/0 | 2846 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | copy fasta | chr3 | 72744277 | 72853445 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0152 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0176 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0007g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0001c0001t0009g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0004g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0006g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0002t0008g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0008t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0002c0008t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0003c0003t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0003c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0003c0003t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0003c0003t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0003c0003t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0003c0003t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0003c0003t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0003c0003t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0003c0003t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0003c0003t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0004c0004t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0004c0004t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0004c0004t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0005c0005t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0005c0005t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0005c0005t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0006c0006t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0006c0006t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0006c0006t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0007c0009t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0007c0009t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0008c0007t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0008c0007t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0009c0011t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0010c0012t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| a0011c0010t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | GBR | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | GBR | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0128 | EUR | GBR | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | GBR | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | CHS | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0126 | EAS | CHS | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG00642 | hp2 | a0004 | c0004 | t0001 | g0111 | AMR | PUR | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG00735 | hp2 | a0010 | c0012 | t0001 | g0124 | AMR | PUR | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG00741 | hp2 | a0004 | c0004 | t0001 | g0110 | AMR | PUR | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0118 | AMR | PUR | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG01109 | hp1 | a0001 | c0001 | t0007 | g0092 | AMR | PUR | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0134 | AMR | PUR | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | PUR | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0013 | AMR | CLM | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0127 | AMR | CLM | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0138 | AMR | CLM | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG01884 | hp1 | a0002 | c0002 | t0005 | g0026 | AFR | ACB | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0201 | AFR | ACB | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0113 | AFR | ACB | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG01891 | hp2 | a0006 | c0006 | t0001 | g0130 | AFR | ACB | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0137 | AMR | PEL | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0144 | AMR | PEL | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | KHV | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | KHV | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0139 | AFR | ACB | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0203 | AFR | ACB | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0132 | EAS | KHV | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0146 | AMR | PEL | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CDX | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CDX | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02257 | hp2 | a0003 | c0003 | t0001 | g0214 | AFR | ACB | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0014 | AFR | ACB | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02451 | hp1 | a0002 | c0002 | t0004 | g0005 | AFR | ACB | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0012 | AFR | GWD | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02615 | hp1 | a0008 | c0007 | t0001 | g0208 | AFR | GWD | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02622 | hp1 | a0005 | c0005 | t0001 | g0117 | AFR | GWD | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02630 | hp1 | a0003 | c0003 | t0001 | g0216 | AFR | GWD | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0198 | AFR | GWD | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02683 | hp1 | a0004 | c0004 | t0001 | g0112 | SAS | PJL | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02717 | hp1 | a0008 | c0007 | t0001 | g0207 | AFR | GWD | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | GWD | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02735 | hp2 | a0001 | c0001 | t0009 | g0107 | SAS | PJL | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0202 | AFR | GWD | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02809 | hp2 | a0002 | c0002 | t0004 | g0006 | AFR | GWD | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02818 | hp1 | a0003 | c0003 | t0001 | g0217 | AFR | GWD | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02886 | hp1 | a0005 | c0005 | t0001 | g0189 | AFR | GWD | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0199 | AFR | GWD | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0197 | AFR | GWD | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0136 | AFR | GWD | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02896 | hp2 | a0003 | c0003 | t0001 | g0219 | AFR | GWD | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02897 | hp1 | a0003 | c0003 | t0001 | g0218 | AFR | GWD | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0120 | AFR | GWD | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02965 | hp1 | a0003 | c0003 | t0001 | g0213 | AFR | ESN | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02965 | hp2 | a0003 | c0003 | t0001 | g0215 | AFR | ESN | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02970 | hp1 | a0003 | c0003 | t0001 | g0211 | AFR | ESN | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02970 | hp2 | a0002 | c0002 | t0004 | g0004 | AFR | ESN | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0200 | AFR | ESN | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | GWD | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0021 | AFR | GWD | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | MSL | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG03098 | hp2 | a0002 | c0002 | t0005 | g0025 | AFR | MSL | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG03130 | hp1 | a0003 | c0003 | t0001 | g0212 | AFR | ESN | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG03130 | hp2 | a0005 | c0005 | t0001 | g0135 | AFR | ESN | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG03139 | hp1 | a0002 | c0002 | t0006 | g0002 | AFR | ESN | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG03139 | hp2 | a0009 | c0011 | t0001 | g0051 | AFR | ESN | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0192 | AFR | MSL | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | MSL | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG03225 | hp2 | a0003 | c0003 | t0001 | g0210 | AFR | MSL | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0115 | AFR | MSL | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG03453 | hp2 | a0007 | c0009 | t0002 | g0221 | AFR | MSL | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG03486 | hp1 | a0006 | c0006 | t0001 | g0131 | AFR | MSL | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG03486 | hp2 | a0007 | c0009 | t0002 | g0220 | AFR | MSL | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0024 | AFR | ESN | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0191 | AFR | ESN | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG03540 | hp1 | a0002 | c0008 | t0001 | g0022 | AFR | GWD | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | BEB | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | STU | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0133 | SAS | STU | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | STU | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | STU | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | STU | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | STU | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | YRI | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0011 | AFR | YRI | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18906 | hp1 | a0002 | c0002 | t0004 | g0003 | AFR | YRI | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0123 | AFR | YRI | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18972 | hp2 | a0011 | c0010 | t0001 | g0007 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | LWK | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0143 | AFR | LWK | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | YRI | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0116 | AFR | YRI | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0205 | AFR | ASW | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0196 | AFR | ASW | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0169 | EUR | TSI | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0145 | EUR | TSI | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0129 | AMR | CLM | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02109 | hp2 | a0006 | c0006 | t0001 | g0125 | AFR | ACB | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02486 | hp1 | a0002 | c0002 | t0008 | g0206 | AFR | ACB | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | ACB | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02559 | hp1 | a0002 | c0002 | t0005 | g0027 | AFR | ACB | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG02559 | hp2 | a0002 | c0008 | t0001 | g0008 | AFR | ACB | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0204 | AFR | MSL | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | USA | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0023 | AFR | USA | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | USA | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | USA | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | LWK | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0209 | AFR | LWK | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0152 | REF | REF | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0176 | REF | REF | SHQ1_chr3_72744277_72853445 | SHQ1 | chr3 | 72744277 | 72853445 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:72750397
|
C | T | 1 | a0005 | 3 | HG02622.hp1 HG02886.hp1 HG03130.hp2 |
missense_variant | MODERATE | c.1621G>A | p.Glu541Lys | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 11/11 | 1726/2846 | 1621/1734 | 541/577 | chr3 | 72750397 | ||
| chr3:72750502
|
C | T | 1 | a0010 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.1516G>A | p.Asp506Asn | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 11/11 | 1621/2846 | 1516/1734 | 506/577 | chr3 | 72750502 | ||
| chr3:72750552
|
C | T | 7 | a0002a0003a0004others(4): Show | 87 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(84): Show |
missense_variant | MODERATE | c.1466G>A | p.Ser489Asn | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 11/11 | 1571/2846 | 1466/1734 | 489/577 | chr3 | 72750552 | ||
| chr3:72792964
|
A | G | 1 | a0009 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.1133T>C | p.Leu378Pro | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/11 | 1238/2846 | 1133/1734 | 378/577 | chr3 | 72792964 | ||
| chr3:72832463
|
T | C | 2 | a0006a0010 | 4 | HG00735.hp2 HG01891.hp2 HG02109.hp2 others(1): Show |
missense_variant | MODERATE | c.505A>G | p.Ile169Val | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/11 | 610/2846 | 505/1734 | 169/577 | chr3 | 72832463 | ||
| chr3:72841130
|
C | T | 2 | a0007a0008 | 4 | HG02615.hp1 HG02717.hp1 HG03453.hp2 others(1): Show |
missense_variant | MODERATE | c.401G>A | p.Cys134Tyr | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/11 | 506/2846 | 401/1734 | 134/577 | chr3 | 72841130 | ||
| chr3:72842396
|
A | C | 1 | a0004 | 3 | HG00642.hp2 HG00741.hp2 HG02683.hp1 |
missense_variant | MODERATE | c.215T>G | p.Phe72Cys | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 3/11 | 320/2846 | 215/1734 | 72/577 | chr3 | 72842396 | ||
| chr3:72848259
|
C | T | 1 | a0011 | 1 | NA18972.hp2 | missense_variant | MODERATE | c.82G>A | p.Glu28Lys | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/11 | 187/2846 | 82/1734 | 28/577 | chr3 | 72848259 | ||
| chr3:72848316
|
T | C | 2 | a0003a0007 | 12 | HG02257.hp2 HG02630.hp1 HG02818.hp1 others(9): Show |
missense_variant | MODERATE | c.25A>G | p.Ser9Gly | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/11 | 130/2846 | 25/1734 | 9/577 | chr3 | 72848316 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:72812680
|
A | G | 1 | a0007c0009 | 2 | HG03453.hp2 HG03486.hp2 |
synonymous_variant | LOW | c.1051T>C | p.Leu351Leu | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/11 | 1156/2846 | 1051/1734 | 351/577 | chr3 | 72812680 | ||
| chr3:72842349
|
G | A | 1 | a0002c0008 | 2 | HG02559.hp2 HG03540.hp1 |
synonymous_variant | LOW | c.262C>T | p.Leu88Leu | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 3/11 | 367/2846 | 262/1734 | 88/577 | chr3 | 72842349 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:72749502
|
T | C | 1 | a0002c0002t0005 | 3 | HG01884.hp1 HG02559.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*782A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 11/11 | 782 | chr3 | 72749502 | |||||
| chr3:72749537
|
A | G | 1 | a0002c0002t0004 | 4 | HG02451.hp1 HG02809.hp2 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*747T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 11/11 | 747 | chr3 | 72749537 | |||||
| chr3:72749667
|
A | G | 1 | a0002c0002t0008 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*617T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 11/11 | 617 | chr3 | 72749667 | |||||
| chr3:72749677
|
CTAAAA | C | 2 | a0001c0001t0002a0007c0009t0002 | 5 | HG02486.hp2 HG02723.hp1 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*602_*606delTTTTA | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 11/11 | 602 | chr3 | 72749677 | |||||
| chr3:72750029
|
T | G | 1 | a0001c0001t0009 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*255A>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 11/11 | 255 | chr3 | 72750029 | |||||
| chr3:72750106
|
G | A | 1 | a0001c0001t0003 | 5 | NA18953.hp1 NA18962.hp2 NA18988.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*178C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 11/11 | 178 | chr3 | 72750106 | |||||
| chr3:72750248
|
C | T | 1 | a0001c0001t0007 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*36G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 11/11 | 36 | chr3 | 72750248 | |||||
| chr3:72848364
|
G | T | 2 | a0002c0002t0004a0002c0002t0006 | 5 | HG02451.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-24C>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/11 | 24 | chr3 | 72848364 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:72751004
|
A | C | 6 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(3): Show | 6 | HG02486.hp1 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1182-168T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751004 | ||||||
| chr3:72751274
|
C | T | 2 | a0002c0002t0001g0121a0002c0002t0001g0142 | 2 | HG02027.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.1182-438G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751274 | ||||||
| chr3:72751313
|
G | C | 2 | a0002c0002t0001g0023a0002c0002t0001g0024 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1182-477C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751313 | ||||||
| chr3:72751314
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1182-478C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751314 | ||||||
| chr3:72751317
|
G | C | 1 | a0001c0001t0001g0174 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1182-481C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751317 | ||||||
| chr3:72751317
|
G | T | 32 | a0001c0001t0001g0085a0002c0002t0001g0010a0002c0002t0001g0011others(29): Show | 32 | HG01175.hp2 HG01243.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.1182-481C>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751317 | ||||||
| chr3:72751318
|
G | A | 3 | a0002c0002t0001g0203a0008c0007t0001g0207a0008c0007t0001g0208 | 3 | HG02055.hp2 HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1182-482C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751318 | ||||||
| chr3:72751332
|
A | G | 2 | a0004c0004t0001g0110a0004c0004t0001g0111 | 2 | HG00642.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.1182-496T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751332 | ||||||
| chr3:72751351
|
T | A | 1 | a0002c0002t0001g0196 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1182-515A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751351 | ||||||
| chr3:72751363
|
T | C | 3 | a0002c0002t0005g0025a0002c0002t0005g0026a0002c0002t0005g0027 | 3 | HG01884.hp1 HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1182-527A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751363 | ||||||
| chr3:72751411
|
T | A | 3 | a0002c0002t0005g0025a0002c0002t0005g0026a0002c0002t0005g0027 | 3 | HG01884.hp1 HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1182-575A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751411 | ||||||
| chr3:72751412
|
C | A | 44 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(41): Show | 44 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1182-576G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751412 | ||||||
| chr3:72751473
|
CAT | C | 3 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0077 | 3 | HG01123.hp2 HG02738.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1182-639_1182-638d others(4): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751473 | ||||||
| chr3:72751476
|
A | ATG | 24 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0031others(21): Show | 24 | HG01081.hp2 HG01175.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.1182-642_1182-641d others(4): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751476 | ||||||
| chr3:72751476
|
A | ATGTG | 5 | a0001c0001t0001g0090a0001c0001t0001g0153a0001c0001t0001g0184others(2): Show | 5 | HG01993.hp1 HG02040.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.1182-644_1182-641d others(6): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751476 | ||||||
| chr3:72751476
|
A | ATGTGTG | 5 | a0001c0001t0001g0082a0001c0001t0001g0094a0001c0001t0001g0183others(2): Show | 5 | HG00099.hp1 HG00741.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1182-646_1182-641d others(8): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751476 | ||||||
| chr3:72751476
|
A | G | 5 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0063others(2): Show | 5 | HG02109.hp1 HG02723.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1182-640T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751476 | ||||||
| chr3:72751494
|
G | GTACATAT others(5): Show |
1 | a0002c0002t0005g0027 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1182-659_1182-658i others(14): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751494 | ||||||
| chr3:72751494
|
G | GTACATAT others(13): Show |
1 | a0002c0002t0005g0025 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1182-659_1182-658i others(22): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751494 | ||||||
| chr3:72751496
|
G | A | 3 | a0002c0002t0005g0025a0002c0002t0005g0026a0002c0002t0005g0027 | 3 | HG01884.hp1 HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1182-660C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751496 | ||||||
| chr3:72751496
|
G | GTACATA | 3 | a0002c0002t0001g0113a0002c0002t0001g0114a0002c0002t0001g0142 | 3 | HG01891.hp1 HG02027.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.1182-661_1182-660i others(8): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751496 | ||||||
| chr3:72751496
|
G | GTACATAT others(1): Show |
3 | a0002c0002t0001g0133a0002c0002t0001g0137a0002c0002t0001g0204 | 3 | HG01952.hp2 HG03471.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1182-661_1182-660i others(10): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751496 | ||||||
| chr3:72751496
|
G | GTACATAT others(3): Show |
9 | a0002c0002t0001g0080a0002c0002t0001g0118a0002c0002t0001g0123others(6): Show | 9 | HG01081.hp1 HG01257.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1182-661_1182-660i others(12): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751496 | ||||||
| chr3:72751496
|
G | GTACATAT others(5): Show |
13 | a0002c0002t0001g0116a0002c0002t0001g0119a0002c0002t0001g0127others(10): Show | 13 | HG00140.hp1 HG00438.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.1182-661_1182-660i others(14): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751496 | ||||||
| chr3:72751496
|
G | GTACATAT others(7): Show |
12 | a0002c0002t0001g0115a0002c0002t0001g0120a0002c0002t0001g0121others(9): Show | 12 | HG00558.hp1 HG00735.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1182-661_1182-660i others(16): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751496 | ||||||
| chr3:72751497
|
T | C | 1 | a0002c0002t0005g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1182-661A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751497 | ||||||
| chr3:72751498
|
G | A | 44 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(41): Show | 44 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1182-662C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751498 | ||||||
| chr3:72751499
|
T | C | 1 | a0006c0006t0001g0131 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1182-663A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751499 | ||||||
| chr3:72751500
|
G | A | 44 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(41): Show | 44 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1182-664C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751500 | ||||||
| chr3:72751502
|
G | A | 48 | a0002c0002t0001g0021a0002c0002t0001g0080a0002c0002t0001g0113others(45): Show | 48 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.1182-666C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751502 | ||||||
| chr3:72751502
|
G | GTATATAT others(5): Show |
1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1182-667_1182-666i others(14): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751502 | ||||||
| chr3:72751504
|
G | A | 49 | a0002c0002t0001g0021a0002c0002t0001g0080a0002c0002t0001g0113others(46): Show | 49 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1182-668C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751504 | ||||||
| chr3:72751504
|
G | GTATATAT others(13): Show |
1 | a0002c0002t0001g0010 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1182-669_1182-668i others(22): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751504 | ||||||
| chr3:72751506
|
G | A | 50 | a0002c0002t0001g0010a0002c0002t0001g0021a0002c0002t0001g0080others(47): Show | 50 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.1182-670C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751506 | ||||||
| chr3:72751506
|
GTGTA | G | 3 | a0001c0001t0001g0057a0001c0001t0001g0148a0001c0001t0001g0180 | 3 | HG00673.hp2 HG01993.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1182-674_1182-671d others(6): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751506 | ||||||
| chr3:72751508
|
G | A | 50 | a0002c0002t0001g0010a0002c0002t0001g0021a0002c0002t0001g0080others(47): Show | 50 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.1182-672C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751508 | ||||||
| chr3:72751508
|
G | GTGTA | 5 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(2): Show | 5 | HG02572.hp1 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1182-673_1182-672i others(6): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751508 | ||||||
| chr3:72751508
|
G | GTGTATAT others(3): Show |
1 | a0002c0002t0001g0013 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1182-673_1182-672i others(12): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751508 | ||||||
| chr3:72751508
|
G | GTGTATAT others(7): Show |
1 | a0002c0002t0004g0006 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1182-673_1182-672i others(16): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751508 | ||||||
| chr3:72751508
|
G | GTGTATAT others(11): Show |
4 | a0002c0002t0001g0201a0003c0003t0001g0211a0003c0003t0001g0212others(1): Show | 4 | HG01884.hp2 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1182-673_1182-672i others(20): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751508 | ||||||
| chr3:72751508
|
G | GTGTATAT others(13): Show |
2 | a0003c0003t0001g0218a0003c0003t0001g0219 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1182-673_1182-672i others(22): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751508 | ||||||
| chr3:72751508
|
G | GTGTATAT others(15): Show |
2 | a0003c0003t0001g0213a0003c0003t0001g0215 | 2 | HG02965.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1182-673_1182-672i others(24): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751508 | ||||||
| chr3:72751508
|
G | GTGTATAT others(17): Show |
1 | a0003c0003t0001g0214 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1182-673_1182-672i others(26): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751508 | ||||||
| chr3:72751508
|
G | GTGTGTAT others(3): Show |
1 | a0002c0002t0001g0011 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1182-673_1182-672i others(12): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751508 | ||||||
| chr3:72751508
|
G | GTGTGTAT others(5): Show |
4 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0004g0003others(1): Show | 4 | HG02970.hp2 HG03516.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1182-673_1182-672i others(14): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751508 | ||||||
| chr3:72751508
|
G | GTGTGTAT others(9): Show |
2 | a0002c0002t0004g0005a0003c0003t0001g0210 | 2 | HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1182-673_1182-672i others(18): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751508 | ||||||
| chr3:72751508
|
G | GTGTGTAT others(11): Show |
3 | a0002c0002t0001g0200a0002c0002t0006g0002a0003c0003t0001g0216 | 3 | HG02630.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1182-673_1182-672i others(20): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751508 | ||||||
| chr3:72751508
|
G | GTGTGTGT others(5): Show |
1 | a0002c0002t0001g0203 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1182-673_1182-672i others(14): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751508 | ||||||
| chr3:72751508
|
G | GTGTGTGT others(11): Show |
2 | a0002c0002t0001g0192a0002c0002t0001g0197 | 2 | HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1182-673_1182-672i others(20): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751508 | ||||||
| chr3:72751508
|
G | GTGTGTGT others(13): Show |
1 | a0002c0002t0001g0191 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1182-673_1182-672i others(22): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751508 | ||||||
| chr3:72751508
|
G | GTGTGTGT others(17): Show |
1 | a0002c0002t0001g0018 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1182-673_1182-672i others(26): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751508 | ||||||
| chr3:72751508
|
G | GTGTGTGT others(19): Show |
1 | a0002c0002t0001g0015 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1182-673_1182-672i others(28): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751508 | ||||||
| chr3:72751508
|
G | GTGTGTGT others(21): Show |
1 | a0002c0002t0001g0016 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1182-673_1182-672i others(30): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751508 | ||||||
| chr3:72751508
|
G | GTGTGTGT others(21): Show |
2 | a0002c0002t0001g0014a0002c0002t0001g0017 | 2 | HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1182-673_1182-672i others(30): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751508 | ||||||
| chr3:72751508
|
GTA | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0059others(2): Show | 6 | HG02683.hp2 NA18945.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.1182-674_1182-673d others(4): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751508 | ||||||
| chr3:72751510
|
A | G | 101 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.1182-674T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751510 | ||||||
| chr3:72751512
|
A | G | 3 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0070 | 3 | HG03471.hp2 NA18944.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1182-676T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751512 | ||||||
| chr3:72751529
|
T | C | 9 | a0001c0001t0001g0036a0001c0001t0001g0088a0001c0001t0001g0102others(6): Show | 9 | HG02486.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1182-693A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751529 | ||||||
| chr3:72751529
|
T | TACACAC | 3 | a0002c0002t0001g0191a0002c0002t0001g0192a0002c0002t0001g0197 | 3 | HG02895.hp1 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1182-694_1182-693i others(8): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751529 | ||||||
| chr3:72751529
|
T | TATATATA others(7): Show |
1 | a0006c0006t0001g0131 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1182-694_1182-693i others(16): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751529 | ||||||
| chr3:72751529
|
T | TATATATA others(15): Show |
2 | a0008c0007t0001g0207a0008c0007t0001g0208 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1182-694_1182-693i others(24): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751529 | ||||||
| chr3:72751531
|
C | T | 38 | a0002c0002t0001g0010a0002c0002t0001g0011a0002c0002t0001g0012others(35): Show | 38 | HG01175.hp2 HG01243.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.1182-695G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751531 | ||||||
| chr3:72751533
|
T | C | 41 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(38): Show | 41 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1182-697A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751533 | ||||||
| chr3:72751535
|
T | C | 12 | a0002c0002t0005g0025a0002c0002t0005g0027a0003c0003t0001g0210others(9): Show | 12 | HG02257.hp2 HG02559.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1182-699A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751535 | ||||||
| chr3:72751535
|
T | TATATATA others(3): Show |
1 | a0002c0002t0005g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1182-700_1182-699i others(12): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751535 | ||||||
| chr3:72751537
|
C | T | 10 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0202others(7): Show | 10 | HG02055.hp2 HG02451.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1182-701G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751537 | ||||||
| chr3:72751539
|
T | C | 72 | a0002c0002t0001g0010a0002c0002t0001g0011a0002c0002t0001g0012others(69): Show | 72 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.1182-703A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751539 | ||||||
| chr3:72751539
|
T | TATATATA others(7): Show |
1 | a0002c0008t0001g0008 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1182-704_1182-703i others(16): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751539 | ||||||
| chr3:72751612
|
C | G | 2 | a0002c0002t0001g0023a0002c0002t0001g0024 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1182-776G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751612 | ||||||
| chr3:72751682
|
T | C | 1 | a0002c0002t0006g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1182-846A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751682 | ||||||
| chr3:72751728
|
A | AT | 37 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(34): Show | 37 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.1182-893dupA | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751728 | ||||||
| chr3:72751787
|
A | G | 3 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0203 | 3 | HG02055.hp2 HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1182-951T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751787 | ||||||
| chr3:72751840
|
G | A | 2 | a0001c0001t0001g0076a0001c0001t0001g0165 | 2 | HG01952.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1182-1004C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72751840 | ||||||
| chr3:72752063
|
G | A | 44 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(41): Show | 44 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1182-1227C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72752063 | ||||||
| chr3:72752388
|
C | T | 2 | a0002c0002t0001g0204a0002c0002t0001g0205 | 2 | HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1182-1552G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72752388 | ||||||
| chr3:72752395
|
T | C | 10 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(7): Show | 10 | HG02486.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1182-1559A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72752395 | ||||||
| chr3:72752454
|
T | C | 42 | a0001c0001t0001g0054a0002c0002t0001g0080a0002c0002t0001g0113others(39): Show | 42 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1182-1618A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72752454 | ||||||
| chr3:72752501
|
T | C | 4 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0004g0005others(1): Show | 4 | HG02451.hp1 HG02809.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1182-1665A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72752501 | ||||||
| chr3:72753484
|
AC | A | 3 | a0002c0002t0005g0025a0002c0002t0005g0026a0002c0002t0005g0027 | 3 | HG01884.hp1 HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1182-2649delG | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72753484 | ||||||
| chr3:72753573
|
G | C | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1182-2737C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72753573 | ||||||
| chr3:72753587
|
A | G | 1 | a0001c0001t0001g0036 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1182-2751T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72753587 | ||||||
| chr3:72753660
|
G | A | 5 | a0002c0002t0001g0011a0002c0002t0001g0012a0002c0002t0001g0013others(2): Show | 5 | HG01255.hp1 HG01884.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1182-2824C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72753660 | ||||||
| chr3:72753947
|
G | A | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1182-3111C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72753947 | ||||||
| chr3:72754243
|
C | T | 2 | a0001c0001t0001g0073a0002c0002t0001g0192 | 2 | HG02056.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1182-3407G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72754243 | ||||||
| chr3:72754260
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0060 | 3 | NA18945.hp2 NA18983.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1182-3424G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72754260 | ||||||
| chr3:72754272
|
G | A | 1 | a0001c0001t0002g0190 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1182-3436C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72754272 | ||||||
| chr3:72754356
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1182-3520T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72754356 | ||||||
| chr3:72754375
|
TTTC | T | 3 | a0002c0002t0005g0025a0002c0002t0005g0026a0002c0002t0005g0027 | 3 | HG01884.hp1 HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1182-3542_1182-354 others(7): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72754375 | ||||||
| chr3:72754384
|
C | CT | 10 | a0001c0001t0001g0097a0001c0001t0001g0102a0001c0001t0001g0103others(7): Show | 10 | HG02486.hp1 HG02572.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1182-3549dupA | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72754384 | ||||||
| chr3:72754384
|
CTTTT | C | 6 | a0002c0002t0001g0196a0002c0002t0001g0198a0002c0002t0001g0199others(3): Show | 6 | HG02559.hp2 HG02630.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1182-3552_1182-354 others(8): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72754384 | ||||||
| chr3:72754439
|
C | T | 97 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(94): Show | 97 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.1182-3603G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72754439 | ||||||
| chr3:72754500
|
G | A | 9 | a0001c0001t0001g0042a0001c0001t0001g0070a0001c0001t0001g0073others(6): Show | 9 | HG00673.hp1 HG00741.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.1182-3664C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72754500 | ||||||
| chr3:72754543
|
G | A | 2 | a0002c0002t0001g0023a0002c0002t0001g0024 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1182-3707C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72754543 | ||||||
| chr3:72754572
|
G | T | 2 | a0002c0002t0001g0023a0002c0002t0001g0024 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1182-3736C>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72754572 | ||||||
| chr3:72754607
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1182-3771G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72754607 | ||||||
| chr3:72754710
|
T | C | 1 | a0002c0002t0001g0137 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1182-3874A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72754710 | ||||||
| chr3:72754713
|
T | C | 2 | a0002c0002t0001g0139a0006c0006t0001g0130 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1182-3877A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72754713 | ||||||
| chr3:72754861
|
T | C | 3 | a0002c0002t0001g0209a0007c0009t0002g0220a0007c0009t0002g0221 | 3 | HG03453.hp2 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1182-4025A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72754861 | ||||||
| chr3:72755016
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1182-4180G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72755016 | ||||||
| chr3:72755071
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1182-4235C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72755071 | ||||||
| chr3:72755135
|
A | G | 1 | a0002c0002t0005g0027 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1182-4299T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72755135 | ||||||
| chr3:72755163
|
C | G | 4 | a0002c0002t0001g0192a0002c0002t0001g0197a0008c0007t0001g0207others(1): Show | 4 | HG02615.hp1 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1182-4327G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72755163 | ||||||
| chr3:72755242
|
T | TGATG | 2 | a0004c0004t0001g0110a0004c0004t0001g0111 | 2 | HG00642.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.1182-4410_1182-440 others(8): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72755242 | ||||||
| chr3:72755242
|
TGATGGAT others(33): Show |
T | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1182-4446_1182-440 others(44): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72755242 | ||||||
| chr3:72755274
|
A | AGATG | 5 | a0001c0001t0001g0086a0002c0002t0001g0192a0002c0002t0001g0197others(2): Show | 5 | HG02615.hp1 HG02622.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1182-4442_1182-443 others(8): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72755274 | ||||||
| chr3:72755274
|
A | AGATGGAT others(1): Show |
6 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(3): Show | 6 | HG02486.hp1 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1182-4446_1182-443 others(12): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72755274 | ||||||
| chr3:72755328
|
CAGAT | C | 3 | a0002c0002t0001g0119a0002c0002t0001g0122a0002c0002t0001g0126 | 3 | HG00438.hp1 HG00558.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1182-4496_1182-449 others(8): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72755328 | ||||||
| chr3:72755336
|
T | C | 1 | a0002c0002t0001g0191 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1182-4500A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72755336 | ||||||
| chr3:72755883
|
C | A | 42 | a0001c0001t0001g0054a0002c0002t0001g0080a0002c0002t0001g0113others(39): Show | 42 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1182-5047G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72755883 | ||||||
| chr3:72756165
|
T | G | 95 | a0001c0001t0001g0054a0001c0001t0001g0102a0001c0001t0001g0103others(92): Show | 95 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.1182-5329A>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72756165 | ||||||
| chr3:72756185
|
C | T | 2 | a0001c0001t0002g0194a0001c0001t0002g0195 | 2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1182-5349G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72756185 | ||||||
| chr3:72756400
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1182-5564G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72756400 | ||||||
| chr3:72756436
|
C | A | 2 | a0002c0002t0001g0115a0002c0002t0001g0116 | 2 | HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1182-5600G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72756436 | ||||||
| chr3:72756436
|
C | T | 42 | a0001c0001t0001g0054a0002c0002t0001g0080a0002c0002t0001g0113others(39): Show | 42 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1182-5600G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72756436 | ||||||
| chr3:72756555
|
A | G | 15 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0004g0005others(12): Show | 15 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.1182-5719T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72756555 | ||||||
| chr3:72756582
|
T | C | 45 | a0001c0001t0001g0054a0002c0002t0001g0080a0002c0002t0001g0113others(42): Show | 45 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1182-5746A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72756582 | ||||||
| chr3:72756604
|
G | A | 1 | a0002c0002t0005g0027 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1182-5768C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72756604 | ||||||
| chr3:72756636
|
T | C | 50 | a0001c0001t0001g0054a0002c0002t0001g0080a0002c0002t0001g0113others(47): Show | 50 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.1182-5800A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72756636 | ||||||
| chr3:72756638
|
G | A | 42 | a0001c0001t0001g0054a0002c0002t0001g0080a0002c0002t0001g0113others(39): Show | 42 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1182-5802C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72756638 | ||||||
| chr3:72756691
|
T | C | 2 | a0001c0001t0001g0050a0001c0001t0001g0074 | 2 | HG02683.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1182-5855A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72756691 | ||||||
| chr3:72756704
|
A | G | 5 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1182-5868T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72756704 | ||||||
| chr3:72756728
|
A | G | 3 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0202 | 3 | HG02630.hp2 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1182-5892T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72756728 | ||||||
| chr3:72756756
|
G | A | 1 | a0002c0002t0001g0127 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1182-5920C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72756756 | ||||||
| chr3:72756757
|
T | A | 1 | a0002c0002t0001g0127 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1182-5921A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72756757 | ||||||
| chr3:72756932
|
A | G | 42 | a0001c0001t0001g0054a0002c0002t0001g0080a0002c0002t0001g0113others(39): Show | 42 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1182-6096T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72756932 | ||||||
| chr3:72756963
|
G | A | 1 | a0003c0003t0001g0216 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1182-6127C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72756963 | ||||||
| chr3:72757137
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1182-6301T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72757137 | ||||||
| chr3:72757154
|
C | A | 4 | a0002c0002t0001g0118a0002c0002t0001g0128a0002c0002t0001g0129others(1): Show | 4 | HG00140.hp1 HG01081.hp1 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.1182-6318G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72757154 | ||||||
| chr3:72757201
|
T | C | 1 | a0002c0002t0001g0138 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1182-6365A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72757201 | ||||||
| chr3:72757381
|
C | CT | 44 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0054others(41): Show | 44 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1182-6546dupA | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72757381 | ||||||
| chr3:72757471
|
A | G | 84 | a0001c0001t0001g0054a0002c0002t0001g0010a0002c0002t0001g0011others(81): Show | 84 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.1182-6635T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72757471 | ||||||
| chr3:72757483
|
T | TGGCCTCA others(10): Show |
83 | a0001c0001t0001g0054a0002c0002t0001g0010a0002c0002t0001g0011others(80): Show | 83 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.1182-6664_1182-664 others(21): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72757483 | ||||||
| chr3:72757662
|
T | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0177 | 2 | HG03654.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1182-6826A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72757662 | ||||||
| chr3:72757816
|
C | G | 1 | a0001c0001t0001g0031 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1182-6980G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72757816 | ||||||
| chr3:72758067
|
C | T | 1 | a0002c0002t0001g0196 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1182-7231G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72758067 | ||||||
| chr3:72758139
|
T | C | 1 | a0002c0002t0001g0202 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1182-7303A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72758139 | ||||||
| chr3:72758173
|
T | C | 6 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(3): Show | 6 | HG02486.hp1 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1182-7337A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72758173 | ||||||
| chr3:72758320
|
A | G | 32 | a0002c0002t0001g0010a0002c0002t0001g0011a0002c0002t0001g0012others(29): Show | 32 | HG01175.hp2 HG01243.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.1182-7484T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72758320 | ||||||
| chr3:72758567
|
C | CT | 12 | a0001c0001t0001g0057a0001c0001t0001g0076a0001c0001t0001g0104others(9): Show | 12 | HG00673.hp2 HG01952.hp1 HG02148.hp1 others(9): Show |
intron_variant | MODIFIER | c.1182-7732dupA | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72758567 | ||||||
| chr3:72758567
|
C | CTT | 26 | a0002c0002t0001g0010a0002c0002t0001g0011a0002c0002t0001g0012others(23): Show | 26 | HG01175.hp2 HG01243.hp2 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.1182-7733_1182-773 others(6): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72758567 | ||||||
| chr3:72758585
|
T | C | 1 | a0002c0002t0001g0137 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1182-7749A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72758585 | ||||||
| chr3:72758610
|
C | CAAT | 42 | a0001c0001t0001g0054a0002c0002t0001g0080a0002c0002t0001g0113others(39): Show | 42 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1182-7775_1182-777 others(7): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72758610 | ||||||
| chr3:72758801
|
T | C | 2 | a0001c0001t0001g0055a0001c0001t0009g0107 | 2 | HG02735.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1182-7965A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72758801 | ||||||
| chr3:72758862
|
T | C | 27 | a0002c0002t0001g0010a0002c0002t0001g0011a0002c0002t0001g0012others(24): Show | 27 | HG01175.hp2 HG01243.hp2 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.1182-8026A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72758862 | ||||||
| chr3:72759021
|
G | T | 8 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0202others(5): Show | 8 | HG01884.hp1 HG02559.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1182-8185C>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72759021 | ||||||
| chr3:72759094
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1182-8258A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72759094 | ||||||
| chr3:72759135
|
G | A | 1 | a0002c0002t0001g0023 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1182-8299C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72759135 | ||||||
| chr3:72759209
|
T | C | 5 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0202others(2): Show | 5 | HG02559.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1182-8373A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72759209 | ||||||
| chr3:72759234
|
G | T | 8 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0202others(5): Show | 8 | HG01884.hp1 HG02559.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1182-8398C>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72759234 | ||||||
| chr3:72759243
|
G | A | 1 | a0002c0002t0006g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1182-8407C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72759243 | ||||||
| chr3:72759443
|
C | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0056 | 3 | HG02451.hp2 HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1182-8607G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72759443 | ||||||
| chr3:72759465
|
C | G | 1 | a0002c0002t0006g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1182-8629G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72759465 | ||||||
| chr3:72759466
|
G | T | 1 | a0002c0002t0006g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1182-8630C>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72759466 | ||||||
| chr3:72759467
|
G | C | 1 | a0002c0002t0006g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1182-8631C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72759467 | ||||||
| chr3:72759469
|
T | G | 1 | a0002c0002t0006g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1182-8633A>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72759469 | ||||||
| chr3:72759470
|
C | G | 1 | a0002c0002t0006g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1182-8634G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72759470 | ||||||
| chr3:72759488
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1182-8652G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72759488 | ||||||
| chr3:72759507
|
A | G | 1 | a0002c0002t0005g0025 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1182-8671T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72759507 | ||||||
| chr3:72759623
|
G | A | 8 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0202others(5): Show | 8 | HG01884.hp1 HG02559.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1182-8787C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72759623 | ||||||
| chr3:72759637
|
G | A | 1 | a0002c0008t0001g0008 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1182-8801C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72759637 | ||||||
| chr3:72760153
|
A | T | 1 | a0003c0003t0001g0217 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1182-9317T>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72760153 | ||||||
| chr3:72760161
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1182-9325G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72760161 | ||||||
| chr3:72760320
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1182-9484G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72760320 | ||||||
| chr3:72760386
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1182-9550T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72760386 | ||||||
| chr3:72760440
|
A | G | 83 | a0001c0001t0001g0054a0002c0002t0001g0010a0002c0002t0001g0011others(80): Show | 83 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.1182-9604T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72760440 | ||||||
| chr3:72760459
|
A | C | 42 | a0001c0001t0001g0054a0002c0002t0001g0080a0002c0002t0001g0113others(39): Show | 42 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1182-9623T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72760459 | ||||||
| chr3:72760672
|
T | C | 50 | a0001c0001t0001g0054a0002c0002t0001g0080a0002c0002t0001g0113others(47): Show | 50 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.1182-9836A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72760672 | ||||||
| chr3:72760742
|
G | C | 5 | a0002c0002t0001g0011a0002c0002t0001g0012a0002c0002t0001g0013others(2): Show | 5 | HG01255.hp1 HG01884.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1182-9906C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72760742 | ||||||
| chr3:72760863
|
C | A | 10 | a0003c0003t0001g0210a0003c0003t0001g0211a0003c0003t0001g0212others(7): Show | 10 | HG02257.hp2 HG02630.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1182-10027G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72760863 | ||||||
| chr3:72761168
|
T | A | 1 | a0001c0001t0001g0160 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1182-10332A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72761168 | ||||||
| chr3:72761203
|
G | C | 8 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0202others(5): Show | 8 | HG01884.hp1 HG02559.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1182-10367C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72761203 | ||||||
| chr3:72761306
|
G | A | 3 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0203 | 3 | HG02055.hp2 HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1182-10470C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72761306 | ||||||
| chr3:72761351
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1182-10515A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72761351 | ||||||
| chr3:72761409
|
C | T | 8 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0202others(5): Show | 8 | HG01884.hp1 HG02559.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1182-10573G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72761409 | ||||||
| chr3:72761681
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1182-10845T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72761681 | ||||||
| chr3:72761780
|
AT | A | 10 | a0003c0003t0001g0210a0003c0003t0001g0211a0003c0003t0001g0212others(7): Show | 10 | HG02257.hp2 HG02630.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1182-10945delA | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72761780 | ||||||
| chr3:72761897
|
T | C | 1 | a0002c0002t0001g0010 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1182-11061A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72761897 | ||||||
| chr3:72761913
|
C | T | 1 | a0002c0002t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1182-11077G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72761913 | ||||||
| chr3:72761926
|
G | T | 1 | a0002c0002t0001g0196 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1182-11090C>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72761926 | ||||||
| chr3:72761933
|
T | C | 1 | a0002c0002t0001g0203 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1182-11097A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72761933 | ||||||
| chr3:72761964
|
C | A | 1 | a0003c0003t0001g0216 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1182-11128G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72761964 | ||||||
| chr3:72762047
|
A | G | 3 | a0001c0001t0001g0052a0001c0001t0001g0159a0001c0001t0001g0164 | 3 | HG01256.hp1 HG01433.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1182-11211T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72762047 | ||||||
| chr3:72762091
|
A | C | 1 | a0002c0002t0001g0202 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1182-11255T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72762091 | ||||||
| chr3:72762387
|
C | T | 26 | a0002c0002t0001g0010a0002c0002t0001g0011a0002c0002t0001g0012others(23): Show | 26 | HG01175.hp2 HG01243.hp2 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.1182-11551G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72762387 | ||||||
| chr3:72762560
|
G | A | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1182-11724C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72762560 | ||||||
| chr3:72762573
|
G | A | 4 | a0006c0006t0001g0125a0006c0006t0001g0130a0006c0006t0001g0131others(1): Show | 4 | HG00735.hp2 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1182-11737C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72762573 | ||||||
| chr3:72762638
|
A | G | 8 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0202others(5): Show | 8 | HG01884.hp1 HG02559.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1182-11802T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72762638 | ||||||
| chr3:72762676
|
C | T | 41 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(38): Show | 41 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1182-11840G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72762676 | ||||||
| chr3:72762681
|
G | GT | 8 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0202others(5): Show | 8 | HG01884.hp1 HG02559.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1182-11846dupA | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72762681 | ||||||
| chr3:72762715
|
C | T | 1 | a0002c0002t0006g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1182-11879G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72762715 | ||||||
| chr3:72762874
|
C | T | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1182-12038G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72762874 | ||||||
| chr3:72762945
|
G | GATTATAG others(2): Show |
49 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(46): Show | 49 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1182-12110_1182-12 others(15): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72762945 | ||||||
| chr3:72762957
|
A | C | 8 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0202others(5): Show | 8 | HG01884.hp1 HG02559.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1182-12121T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72762957 | ||||||
| chr3:72763022
|
TAC | T | 24 | a0001c0001t0001g0032a0001c0001t0001g0069a0001c0001t0001g0072others(21): Show | 24 | HG00735.hp1 HG00738.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.1182-12188_1182-12 others(8): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763022 | ||||||
| chr3:72763022
|
TACAC | T | 64 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037others(61): Show | 64 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1182-12190_1182-12 others(10): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763022 | ||||||
| chr3:72763022
|
TACACAC | T | 25 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0030others(22): Show | 25 | HG00099.hp2 HG01346.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.1182-12192_1182-12 others(12): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763022 | ||||||
| chr3:72763022
|
TACACACA others(1): Show |
T | 13 | a0001c0001t0001g0040a0001c0001t0001g0151a0001c0001t0003g0033others(10): Show | 13 | HG01081.hp2 HG01884.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1182-12194_1182-12 others(14): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763022 | ||||||
| chr3:72763035
|
A | G | 1 | a0002c0002t0001g0114 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1182-12199T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763035 | ||||||
| chr3:72763046
|
CACACACA others(11): Show |
C | 1 | a0002c0002t0001g0133 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1182-12228_1182-12 others(24): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763046 | ||||||
| chr3:72763048
|
C | T | 1 | a0002c0008t0001g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1182-12212G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763048 | ||||||
| chr3:72763050
|
CACACACA others(9): Show |
C | 1 | a0001c0001t0002g0190 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1182-12230_1182-12 others(22): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763050 | ||||||
| chr3:72763052
|
C | T | 32 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(29): Show | 32 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1182-12216G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763052 | ||||||
| chr3:72763054
|
C | T | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1182-12218G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763054 | ||||||
| chr3:72763054
|
CACACACA others(5): Show |
C | 1 | a0002c0008t0001g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1182-12230_1182-12 others(18): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763054 | ||||||
| chr3:72763056
|
C | CAT | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1182-12221_1182-12 others(8): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763056 | ||||||
| chr3:72763056
|
C | T | 32 | a0002c0002t0001g0010a0002c0002t0001g0011a0002c0002t0001g0012others(29): Show | 32 | HG00735.hp2 HG01109.hp2 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.1182-12220G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763056 | ||||||
| chr3:72763056
|
CACACACA others(3): Show |
C | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0056 | 3 | HG02451.hp2 HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1182-12230_1182-12 others(16): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763056 | ||||||
| chr3:72763058
|
C | T | 4 | a0003c0003t0001g0210a0003c0003t0001g0214a0003c0003t0001g0215others(1): Show | 4 | HG02257.hp2 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1182-12222G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763058 | ||||||
| chr3:72763058
|
CACACAG | C | 33 | a0001c0001t0001g0180a0002c0002t0001g0080a0002c0002t0001g0113others(30): Show | 33 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.1182-12228_1182-12 others(12): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763058 | ||||||
| chr3:72763060
|
C | T | 7 | a0002c0002t0001g0023a0002c0002t0001g0024a0003c0003t0001g0211others(4): Show | 7 | HG02630.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1182-12224G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763060 | ||||||
| chr3:72763060
|
CACAG | C | 7 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0048others(4): Show | 8 | HG01256.hp1 HG02165.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.1182-12228_1182-12 others(10): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763060 | ||||||
| chr3:72763061
|
A | T | 1 | a0002c0002t0001g0192 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1182-12225T>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763061 | ||||||
| chr3:72763062
|
C | CACACTG | 2 | a0002c0002t0001g0023a0002c0002t0001g0024 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1182-12227_1182-12 others(12): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763062 | ||||||
| chr3:72763062
|
C | G | 13 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(10): Show | 13 | HG00558.hp2 HG01993.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1182-12226G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763062 | ||||||
| chr3:72763062
|
CAG | C | 12 | a0002c0002t0001g0115a0002c0002t0001g0116a0002c0002t0001g0120others(9): Show | 12 | HG00735.hp2 HG01109.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1182-12228_1182-12 others(8): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763062 | ||||||
| chr3:72763063
|
A | ACACT | 2 | a0008c0007t0001g0207a0008c0007t0001g0208 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1182-12228_1182-12 others(10): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763063 | ||||||
| chr3:72763063
|
A | T | 26 | a0002c0002t0001g0010a0002c0002t0001g0011a0002c0002t0001g0012others(23): Show | 26 | HG01175.hp2 HG01243.hp2 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.1182-12227T>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763063 | ||||||
| chr3:72763064
|
G | C | 5 | a0003c0003t0001g0211a0003c0003t0001g0213a0003c0003t0001g0216others(2): Show | 5 | HG02630.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1182-12228C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763064 | ||||||
| chr3:72763065
|
A | T | 41 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(38): Show | 41 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1182-12229T>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763065 | ||||||
| chr3:72763066
|
G | C | 9 | a0003c0003t0001g0210a0003c0003t0001g0211a0003c0003t0001g0213others(6): Show | 9 | HG02257.hp2 HG02630.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1182-12230C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763066 | ||||||
| chr3:72763067
|
A | T | 1 | a0002c0008t0001g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1182-12231T>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763067 | ||||||
| chr3:72763203
|
G | A | 8 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0202others(5): Show | 8 | HG01884.hp1 HG02559.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1182-12367C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763203 | ||||||
| chr3:72763336
|
G | A | 1 | a0003c0003t0001g0216 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1182-12500C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763336 | ||||||
| chr3:72763393
|
G | A | 5 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0004g0005others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1182-12557C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763393 | ||||||
| chr3:72763511
|
G | A | 3 | a0002c0002t0001g0191a0002c0002t0001g0192a0002c0002t0001g0197 | 3 | HG02895.hp1 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1182-12675C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763511 | ||||||
| chr3:72763538
|
G | A | 8 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0202others(5): Show | 8 | HG01884.hp1 HG02559.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1182-12702C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763538 | ||||||
| chr3:72763595
|
C | T | 124 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(121): Show | 124 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.1182-12759G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763595 | ||||||
| chr3:72763806
|
C | G | 1 | a0001c0001t0001g0154 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1182-12970G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72763806 | ||||||
| chr3:72764010
|
GA | G | 12 | a0001c0001t0001g0070a0002c0002t0008g0206a0003c0003t0001g0210others(9): Show | 12 | HG02257.hp2 HG02486.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1182-13175delT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72764010 | ||||||
| chr3:72764160
|
CCT | C | 9 | a0002c0002t0001g0021a0002c0002t0001g0198a0002c0002t0001g0199others(6): Show | 9 | HG01884.hp1 HG02559.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1182-13326_1182-13 others(8): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72764160 | ||||||
| chr3:72764183
|
C | A | 4 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0004g0005others(1): Show | 4 | HG02451.hp1 HG02809.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1182-13347G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72764183 | ||||||
| chr3:72764431
|
G | C | 82 | a0002c0002t0001g0010a0002c0002t0001g0011a0002c0002t0001g0012others(79): Show | 82 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.1182-13595C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72764431 | ||||||
| chr3:72764436
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1182-13600A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72764436 | ||||||
| chr3:72764495
|
C | T | 1 | a0002c0002t0001g0128 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1182-13659G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72764495 | ||||||
| chr3:72764669
|
C | T | 1 | a0003c0003t0001g0213 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1182-13833G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72764669 | ||||||
| chr3:72764797
|
C | G | 9 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0202others(6): Show | 9 | HG01884.hp1 HG02559.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1182-13961G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72764797 | ||||||
| chr3:72764862
|
T | C | 10 | a0002c0002t0001g0011a0002c0002t0001g0012a0002c0002t0001g0013others(7): Show | 10 | HG01243.hp2 HG01255.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1182-14026A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72764862 | ||||||
| chr3:72765428
|
A | AT | 27 | a0002c0002t0001g0010a0002c0002t0001g0011a0002c0002t0001g0012others(24): Show | 27 | HG01175.hp2 HG01243.hp2 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.1182-14593dupA | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765428 | ||||||
| chr3:72765428
|
AT | A | 45 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0108others(42): Show | 45 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1182-14593delA | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765428 | ||||||
| chr3:72765530
|
C | CAT | 2 | a0001c0001t0002g0194a0001c0001t0002g0195 | 2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1182-14696_1182-14 others(8): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765530 | ||||||
| chr3:72765530
|
C | CATACATA others(19): Show |
1 | a0008c0007t0001g0208 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1182-14695_1182-14 others(32): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765530 | ||||||
| chr3:72765530
|
C | CATACATA others(21): Show |
1 | a0008c0007t0001g0207 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1182-14695_1182-14 others(34): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765530 | ||||||
| chr3:72765530
|
C | CATATATA others(17): Show |
3 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105 | 3 | HG02615.hp2 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1182-14718_1182-14 others(30): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765530 | ||||||
| chr3:72765530
|
C | CATATATA others(21): Show |
1 | a0001c0001t0001g0106 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1182-14722_1182-14 others(34): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765530 | ||||||
| chr3:72765530
|
C | CATATATA others(27): Show |
1 | a0002c0002t0008g0206 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1182-14695_1182-14 others(40): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765530 | ||||||
| chr3:72765530
|
CAT | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0019others(73): Show | 77 | HG00140.hp2 HG00438.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.1182-14696_1182-14 others(8): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765530 | ||||||
| chr3:72765532
|
T | C | 2 | a0002c0002t0001g0023a0002c0002t0001g0024 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1182-14696A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765532 | ||||||
| chr3:72765550
|
TA | T | 3 | a0002c0002t0001g0114a0002c0002t0001g0137a0006c0006t0001g0130 | 3 | HG01891.hp2 HG01952.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.1182-14715delT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765550 | ||||||
| chr3:72765551
|
A | T | 1 | a0010c0012t0001g0124 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1182-14715T>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765551 | ||||||
| chr3:72765552
|
TA | T | 21 | a0002c0002t0001g0080a0002c0002t0001g0119a0002c0002t0001g0121others(18): Show | 21 | HG00438.hp1 HG00558.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1182-14717delT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765552 | ||||||
| chr3:72765553
|
A | AT | 4 | a0002c0002t0001g0142a0005c0005t0001g0117a0005c0005t0001g0135others(1): Show | 4 | HG02027.hp2 HG02622.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1182-14718dupA | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765553 | ||||||
| chr3:72765553
|
A | T | 7 | a0002c0002t0001g0011a0002c0002t0001g0114a0002c0002t0001g0137others(4): Show | 7 | HG00735.hp2 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1182-14717T>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765553 | ||||||
| chr3:72765554
|
TA | T | 10 | a0002c0002t0001g0113a0002c0002t0001g0118a0002c0002t0001g0127others(7): Show | 10 | HG00140.hp1 HG00642.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.1182-14719delT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765554 | ||||||
| chr3:72765554
|
TATA | T | 8 | a0001c0001t0001g0042a0001c0001t0001g0070a0001c0001t0001g0079others(5): Show | 8 | HG00673.hp1 HG00741.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1182-14721_1182-14 others(9): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765554 | ||||||
| chr3:72765555
|
A | T | 35 | a0001c0001t0001g0057a0002c0002t0001g0011a0002c0002t0001g0080others(32): Show | 35 | HG00438.hp1 HG00558.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.1182-14719T>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765555 | ||||||
| chr3:72765556
|
TA | T | 4 | a0001c0001t0001g0048a0001c0001t0001g0178a0004c0004t0001g0112others(1): Show | 4 | HG00558.hp2 HG02683.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.1182-14721delT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765556 | ||||||
| chr3:72765557
|
A | ATATATAT others(36): Show |
1 | a0002c0002t0001g0013 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1182-14722_1182-14 others(49): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765557 | ||||||
| chr3:72765557
|
A | ATATATAT others(34): Show |
1 | a0002c0002t0001g0201 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1182-14722_1182-14 others(47): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765557 | ||||||
| chr3:72765557
|
A | ATATATAT others(31): Show |
1 | a0002c0002t0004g0006 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1182-14722_1182-14 others(44): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765557 | ||||||
| chr3:72765557
|
A | ATATATAT others(32): Show |
1 | a0002c0002t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1182-14722_1182-14 others(45): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765557 | ||||||
| chr3:72765557
|
A | ATATATAT others(27): Show |
1 | a0002c0002t0001g0200 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1182-14722_1182-14 others(40): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765557 | ||||||
| chr3:72765557
|
A | ATATATAT others(33): Show |
1 | a0002c0002t0004g0005 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1182-14722_1182-14 others(46): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765557 | ||||||
| chr3:72765557
|
A | ATATATAT others(35): Show |
1 | a0002c0002t0004g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1182-14722_1182-14 others(48): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765557 | ||||||
| chr3:72765557
|
A | ATATATAT others(17): Show |
1 | a0002c0002t0006g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1182-14722_1182-14 others(30): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765557 | ||||||
| chr3:72765557
|
A | ATATATAT others(30): Show |
1 | a0002c0002t0004g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1182-14722_1182-14 others(43): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765557 | ||||||
| chr3:72765557
|
A | ATATATAT others(8): Show |
1 | a0002c0002t0001g0197 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1182-14722_1182-14 others(21): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765557 | ||||||
| chr3:72765557
|
A | ATATATAT others(7): Show |
1 | a0002c0002t0001g0010 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1182-14722_1182-14 others(20): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765557 | ||||||
| chr3:72765557
|
A | ATATATAT others(3): Show |
1 | a0002c0002t0001g0191 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1182-14722_1182-14 others(16): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765557 | ||||||
| chr3:72765557
|
A | ATATATAT others(10): Show |
1 | a0002c0002t0001g0018 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1182-14722_1182-14 others(23): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765557 | ||||||
| chr3:72765557
|
A | ATATATAT others(3): Show |
1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1182-14722_1182-14 others(16): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765557 | ||||||
| chr3:72765557
|
A | ATATATAT others(4): Show |
1 | a0002c0002t0001g0023 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1182-14722_1182-14 others(17): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765557 | ||||||
| chr3:72765557
|
A | ATATATAT others(8): Show |
1 | a0002c0002t0001g0192 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1182-14722_1182-14 others(21): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765557 | ||||||
| chr3:72765557
|
A | ATATATTT others(6): Show |
4 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(1): Show | 4 | HG02258.hp1 HG03098.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1182-14722_1182-14 others(19): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765557 | ||||||
| chr3:72765557
|
A | T | 66 | a0001c0001t0001g0054a0001c0001t0001g0057a0001c0001t0001g0073others(63): Show | 66 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1182-14721T>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765557 | ||||||
| chr3:72765557
|
ATT | A | 25 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(22): Show | 25 | HG00099.hp1 HG02056.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1182-14723_1182-14 others(8): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765557 | ||||||
| chr3:72765558
|
T | TA | 2 | a0001c0001t0001g0039a0002c0002t0001g0021 | 2 | HG03041.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.1182-14723_1182-14 others(7): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765558 | ||||||
| chr3:72765558
|
T | TATATATA others(12): Show |
1 | a0001c0001t0001g0102 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1182-14723_1182-14 others(25): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765558 | ||||||
| chr3:72765559
|
T | A | 9 | a0001c0001t0001g0058a0001c0001t0001g0104a0001c0001t0001g0106others(6): Show | 9 | HG01433.hp2 HG02486.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1182-14723A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765559 | ||||||
| chr3:72765560
|
T | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0081 | 2 | NA18944.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.1182-14724A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765560 | ||||||
| chr3:72765561
|
T | A | 9 | a0001c0001t0001g0046a0001c0001t0001g0104a0001c0001t0001g0184others(6): Show | 9 | HG02486.hp2 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1182-14725A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765561 | ||||||
| chr3:72765563
|
T | A | 1 | a0001c0001t0002g0190 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1182-14727A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765563 | ||||||
| chr3:72765578
|
C | T | 41 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(38): Show | 41 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1182-14742G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765578 | ||||||
| chr3:72765941
|
A | C | 1 | a0003c0003t0001g0213 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1182-15105T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72765941 | ||||||
| chr3:72766056
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1182-15220G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72766056 | ||||||
| chr3:72766103
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1182-15267G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72766103 | ||||||
| chr3:72766197
|
T | C | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1182-15361A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72766197 | ||||||
| chr3:72766284
|
C | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0068a0001c0001t0001g0075 | 3 | HG02165.hp2 NA18982.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1182-15448G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72766284 | ||||||
| chr3:72766603
|
T | C | 10 | a0002c0002t0001g0011a0002c0002t0001g0012a0002c0002t0001g0013others(7): Show | 10 | HG01243.hp2 HG01255.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1182-15767A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72766603 | ||||||
| chr3:72766874
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0109 | 2 | NA18951.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1182-16038C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72766874 | ||||||
| chr3:72767056
|
C | G | 1 | a0001c0001t0001g0067 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1182-16220G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72767056 | ||||||
| chr3:72767083
|
G | C | 1 | a0001c0001t0001g0043 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1182-16247C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72767083 | ||||||
| chr3:72767161
|
T | C | 5 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0202others(2): Show | 5 | HG02559.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1182-16325A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72767161 | ||||||
| chr3:72767323
|
G | A | 4 | a0002c0002t0001g0120a0002c0002t0001g0123a0002c0002t0001g0134others(1): Show | 4 | HG01109.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1182-16487C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72767323 | ||||||
| chr3:72767337
|
C | T | 41 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(38): Show | 41 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1182-16501G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72767337 | ||||||
| chr3:72767440
|
G | C | 1 | a0002c0002t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1182-16604C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72767440 | ||||||
| chr3:72767876
|
T | C | 1 | a0001c0001t0002g0190 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1182-17040A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72767876 | ||||||
| chr3:72767906
|
C | T | 1 | a0002c0002t0001g0010 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1182-17070G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72767906 | ||||||
| chr3:72767968
|
C | T | 1 | a0002c0002t0006g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1182-17132G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72767968 | ||||||
| chr3:72768056
|
A | AAGCAGGG others(9): Show |
1 | a0002c0002t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1182-17236_1182-17 others(22): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72768056 | ||||||
| chr3:72768129
|
A | G | 4 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0004g0005others(1): Show | 4 | HG02451.hp1 HG02809.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1182-17293T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72768129 | ||||||
| chr3:72768422
|
C | T | 10 | a0003c0003t0001g0210a0003c0003t0001g0211a0003c0003t0001g0212others(7): Show | 10 | HG02257.hp2 HG02630.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1182-17586G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72768422 | ||||||
| chr3:72768461
|
T | C | 10 | a0002c0002t0001g0011a0002c0002t0001g0012a0002c0002t0001g0013others(7): Show | 10 | HG01243.hp2 HG01255.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1182-17625A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72768461 | ||||||
| chr3:72768470
|
T | G | 1 | a0001c0001t0001g0158 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1182-17634A>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72768470 | ||||||
| chr3:72768491
|
A | G | 6 | a0002c0002t0001g0115a0002c0002t0001g0116a0002c0002t0001g0120others(3): Show | 6 | HG01109.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1182-17655T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72768491 | ||||||
| chr3:72768613
|
T | C | 1 | a0006c0006t0001g0130 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1182-17777A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72768613 | ||||||
| chr3:72768697
|
G | A | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1182-17861C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72768697 | ||||||
| chr3:72768893
|
A | G | 6 | a0002c0002t0001g0196a0002c0002t0001g0198a0002c0002t0001g0199others(3): Show | 6 | HG02559.hp2 HG02630.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1182-18057T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72768893 | ||||||
| chr3:72768903
|
G | A | 1 | a0002c0002t0006g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1182-18067C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72768903 | ||||||
| chr3:72768911
|
C | T | 5 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0202others(2): Show | 5 | HG02559.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1182-18075G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72768911 | ||||||
| chr3:72768990
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1182-18154G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72768990 | ||||||
| chr3:72769014
|
A | C | 75 | a0001c0001t0001g0054a0002c0002t0001g0010a0002c0002t0001g0011others(72): Show | 75 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.1182-18178T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72769014 | ||||||
| chr3:72769394
|
C | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0087 | 2 | HG02056.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.1182-18558G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72769394 | ||||||
| chr3:72769482
|
A | G | 1 | a0001c0001t0001g0032 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1182-18646T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72769482 | ||||||
| chr3:72769495
|
C | T | 10 | a0003c0003t0001g0210a0003c0003t0001g0211a0003c0003t0001g0212others(7): Show | 10 | HG02257.hp2 HG02630.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1182-18659G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72769495 | ||||||
| chr3:72769623
|
A | C | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1182-18787T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72769623 | ||||||
| chr3:72769675
|
T | C | 1 | a0002c0002t0005g0027 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1182-18839A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72769675 | ||||||
| chr3:72769733
|
T | A | 1 | a0001c0001t0001g0181 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1182-18897A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72769733 | ||||||
| chr3:72769745
|
A | C | 1 | a0002c0002t0001g0202 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1182-18909T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72769745 | ||||||
| chr3:72769751
|
T | A | 88 | a0001c0001t0001g0054a0001c0001t0001g0102a0001c0001t0001g0103others(85): Show | 88 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.1182-18915A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72769751 | ||||||
| chr3:72769845
|
C | T | 10 | a0003c0003t0001g0210a0003c0003t0001g0211a0003c0003t0001g0212others(7): Show | 10 | HG02257.hp2 HG02630.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1182-19009G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72769845 | ||||||
| chr3:72770260
|
A | C | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1182-19424T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72770260 | ||||||
| chr3:72770302
|
A | C | 84 | a0001c0001t0001g0054a0002c0002t0001g0010a0002c0002t0001g0011others(81): Show | 84 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.1182-19466T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72770302 | ||||||
| chr3:72770521
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1182-19685A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72770521 | ||||||
| chr3:72770526
|
C | T | 3 | a0001c0001t0001g0036a0001c0001t0001g0088a0001c0001t0001g0161 | 3 | NA18957.hp2 NA19058.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1182-19690G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72770526 | ||||||
| chr3:72770622
|
T | C | 1 | a0002c0002t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1182-19786A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72770622 | ||||||
| chr3:72770733
|
T | C | 1 | a0002c0002t0001g0011 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1182-19897A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72770733 | ||||||
| chr3:72770780
|
A | G | 1 | a0002c0002t0001g0010 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1182-19944T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72770780 | ||||||
| chr3:72770864
|
C | T | 1 | a0001c0001t0002g0190 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1182-20028G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72770864 | ||||||
| chr3:72770878
|
T | C | 1 | a0002c0002t0001g0203 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1182-20042A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72770878 | ||||||
| chr3:72770944
|
T | A | 2 | a0008c0007t0001g0207a0008c0007t0001g0208 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1182-20108A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72770944 | ||||||
| chr3:72770979
|
A | G | 12 | a0002c0002t0001g0011a0002c0002t0001g0012a0002c0002t0001g0013others(9): Show | 12 | HG01243.hp2 HG01255.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1182-20143T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72770979 | ||||||
| chr3:72771029
|
T | A | 1 | a0002c0008t0001g0008 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1182-20193A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72771029 | ||||||
| chr3:72771157
|
C | G | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1182-20321G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72771157 | ||||||
| chr3:72771352
|
A | C | 95 | a0001c0001t0001g0054a0001c0001t0001g0102a0001c0001t0001g0103others(92): Show | 95 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.1182-20516T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72771352 | ||||||
| chr3:72771703
|
G | C | 3 | a0001c0001t0002g0190a0001c0001t0002g0194a0001c0001t0002g0195 | 3 | HG02486.hp2 HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1182-20867C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72771703 | ||||||
| chr3:72771715
|
G | C | 5 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0173others(2): Show | 5 | NA18944.hp1 NA18964.hp1 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.1182-20879C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72771715 | ||||||
| chr3:72772003
|
A | AG | 12 | a0002c0002t0001g0011a0002c0002t0001g0012a0002c0002t0001g0013others(9): Show | 12 | HG01243.hp2 HG01255.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1181+20912dupC | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72772003 | ||||||
| chr3:72772010
|
A | G | 5 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1181+20906T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72772010 | ||||||
| chr3:72772216
|
C | T | 1 | a0002c0002t0005g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1181+20700G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72772216 | ||||||
| chr3:72772396
|
C | A | 1 | a0002c0002t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1181+20520G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72772396 | ||||||
| chr3:72772445
|
A | G | 2 | a0002c0002t0001g0023a0002c0002t0001g0024 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1181+20471T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72772445 | ||||||
| chr3:72772448
|
GTCAGATG others(5): Show |
G | 1 | a0002c0002t0001g0017 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1181+20456_1181+20 others(18): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72772448 | ||||||
| chr3:72772463
|
A | G | 1 | a0002c0002t0001g0017 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1181+20453T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72772463 | ||||||
| chr3:72772465
|
C | G | 1 | a0002c0002t0001g0017 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1181+20451G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72772465 | ||||||
| chr3:72772466
|
T | A | 1 | a0002c0002t0001g0017 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1181+20450A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72772466 | ||||||
| chr3:72772539
|
C | G | 1 | a0001c0001t0001g0159 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1181+20377G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72772539 | ||||||
| chr3:72772557
|
T | C | 42 | a0001c0001t0001g0054a0002c0002t0001g0080a0002c0002t0001g0113others(39): Show | 42 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1181+20359A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72772557 | ||||||
| chr3:72773024
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1181+19892T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72773024 | ||||||
| chr3:72773221
|
T | C | 3 | a0002c0002t0005g0025a0002c0002t0005g0026a0002c0002t0005g0027 | 3 | HG01884.hp1 HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1181+19695A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72773221 | ||||||
| chr3:72773228
|
C | T | 1 | a0002c0002t0005g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1181+19688G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72773228 | ||||||
| chr3:72773272
|
G | T | 1 | a0001c0001t0001g0054 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1181+19644C>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72773272 | ||||||
| chr3:72773299
|
T | C | 2 | a0002c0002t0001g0023a0002c0002t0001g0024 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1181+19617A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72773299 | ||||||
| chr3:72773477
|
A | G | 10 | a0002c0002t0001g0011a0002c0002t0001g0012a0002c0002t0001g0013others(7): Show | 10 | HG01243.hp2 HG01255.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1181+19439T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72773477 | ||||||
| chr3:72773494
|
A | AAAAAAAA others(3): Show |
4 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0004g0006others(1): Show | 4 | HG02809.hp2 HG02970.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1181+19421_1181+19 others(16): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72773494 | ||||||
| chr3:72773559
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1181+19357A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72773559 | ||||||
| chr3:72773711
|
T | C | 1 | a0002c0002t0001g0129 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1181+19205A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72773711 | ||||||
| chr3:72773770
|
A | G | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1181+19146T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72773770 | ||||||
| chr3:72773830
|
C | T | 4 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0004g0005others(1): Show | 4 | HG02451.hp1 HG02809.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1181+19086G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72773830 | ||||||
| chr3:72773890
|
A | G | 1 | a0002c0002t0001g0122 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1181+19026T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72773890 | ||||||
| chr3:72773937
|
T | C | 1 | a0002c0002t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1181+18979A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72773937 | ||||||
| chr3:72774112
|
G | A | 1 | a0002c0002t0001g0203 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1181+18804C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72774112 | ||||||
| chr3:72774396
|
T | TAAGAATA others(318): Show |
1 | a0002c0002t0001g0198 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1181+18519_1181+18 others(331): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72774396 | ||||||
| chr3:72774396
|
T | TAAGAATA others(320): Show |
1 | a0002c0008t0001g0008 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1181+18519_1181+18 others(333): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72774396 | ||||||
| chr3:72774396
|
T | TAAGAATA others(326): Show |
1 | a0002c0008t0001g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1181+18519_1181+18 others(339): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72774396 | ||||||
| chr3:72774396
|
T | TAAGAATA others(328): Show |
1 | a0002c0002t0001g0202 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1181+18519_1181+18 others(341): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72774396 | ||||||
| chr3:72774396
|
T | TAAGAATA others(335): Show |
1 | a0002c0002t0001g0199 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1181+18519_1181+18 others(348): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72774396 | ||||||
| chr3:72774428
|
C | T | 1 | a0002c0002t0001g0133 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1181+18488G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72774428 | ||||||
| chr3:72774429
|
A | G | 1 | a0001c0001t0002g0190 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1181+18487T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72774429 | ||||||
| chr3:72774463
|
T | C | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1181+18453A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72774463 | ||||||
| chr3:72774598
|
T | C | 10 | a0003c0003t0001g0210a0003c0003t0001g0211a0003c0003t0001g0212others(7): Show | 10 | HG02257.hp2 HG02630.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+18318A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72774598 | ||||||
| chr3:72774608
|
A | C | 3 | a0002c0002t0001g0191a0002c0002t0001g0192a0002c0002t0001g0197 | 3 | HG02895.hp1 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1181+18308T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72774608 | ||||||
| chr3:72774754
|
G | C | 1 | a0001c0001t0001g0072 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1181+18162C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72774754 | ||||||
| chr3:72774825
|
G | A | 10 | a0003c0003t0001g0210a0003c0003t0001g0211a0003c0003t0001g0212others(7): Show | 10 | HG02257.hp2 HG02630.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+18091C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72774825 | ||||||
| chr3:72775012
|
A | G | 90 | a0001c0001t0001g0054a0001c0001t0001g0102a0001c0001t0001g0103others(87): Show | 90 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.1181+17904T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72775012 | ||||||
| chr3:72775093
|
C | T | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1181+17823G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72775093 | ||||||
| chr3:72775109
|
C | T | 43 | a0001c0001t0001g0054a0002c0002t0001g0080a0002c0002t0001g0113others(40): Show | 43 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.1181+17807G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72775109 | ||||||
| chr3:72775415
|
T | C | 1 | a0001c0001t0003g0038 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1181+17501A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72775415 | ||||||
| chr3:72775459
|
C | CT | 20 | a0001c0001t0001g0068a0001c0001t0001g0077a0001c0001t0001g0102others(17): Show | 20 | HG00438.hp1 HG01123.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.1181+17456dupA | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72775459 | ||||||
| chr3:72775459
|
C | CTT | 7 | a0002c0002t0001g0021a0002c0002t0004g0003a0002c0002t0004g0004others(4): Show | 7 | HG02451.hp1 HG02809.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1181+17455_1181+17 others(8): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72775459 | ||||||
| chr3:72775459
|
CT | C | 6 | a0001c0001t0001g0009a0001c0001t0001g0083a0001c0001t0001g0084others(3): Show | 6 | HG00099.hp2 HG01346.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1181+17456delA | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72775459 | ||||||
| chr3:72775631
|
C | T | 3 | a0002c0002t0005g0025a0002c0002t0005g0026a0002c0002t0005g0027 | 3 | HG01884.hp1 HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1181+17285G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72775631 | ||||||
| chr3:72775768
|
C | T | 2 | a0003c0003t0001g0218a0003c0003t0001g0219 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1181+17148G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72775768 | ||||||
| chr3:72775817
|
A | G | 1 | a0001c0001t0001g0155 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1181+17099T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72775817 | ||||||
| chr3:72775860
|
C | T | 76 | a0001c0001t0001g0054a0002c0002t0001g0010a0002c0002t0001g0011others(73): Show | 76 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.1181+17056G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72775860 | ||||||
| chr3:72775997
|
C | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0070a0001c0001t0001g0073 | 3 | HG02056.hp1 NA18998.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1181+16919G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72775997 | ||||||
| chr3:72776100
|
C | T | 1 | a0002c0002t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1181+16816G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72776100 | ||||||
| chr3:72776687
|
TAA | T | 5 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0004g0005others(2): Show | 5 | HG02451.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1181+16227_1181+16 others(8): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72776687 | ||||||
| chr3:72776850
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0060a0002c0002t0001g0191 | 4 | HG03516.hp2 NA18945.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.1181+16066C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72776850 | ||||||
| chr3:72776913
|
T | C | 4 | a0002c0002t0001g0196a0002c0002t0005g0025a0002c0002t0005g0026others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1181+16003A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72776913 | ||||||
| chr3:72776967
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1181+15949G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72776967 | ||||||
| chr3:72777002
|
T | C | 1 | a0002c0002t0005g0027 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1181+15914A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72777002 | ||||||
| chr3:72777035
|
T | C | 6 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(3): Show | 6 | HG02486.hp1 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1181+15881A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72777035 | ||||||
| chr3:72777058
|
G | C | 1 | a0001c0001t0002g0195 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1181+15858C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72777058 | ||||||
| chr3:72777342
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1181+15574T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72777342 | ||||||
| chr3:72777356
|
A | G | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1181+15560T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72777356 | ||||||
| chr3:72777382
|
A | T | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1181+15534T>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72777382 | ||||||
| chr3:72777388
|
T | C | 3 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0202 | 3 | HG02630.hp2 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1181+15528A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72777388 | ||||||
| chr3:72777398
|
T | C | 3 | a0002c0002t0005g0025a0002c0002t0005g0026a0002c0002t0005g0027 | 3 | HG01884.hp1 HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1181+15518A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72777398 | ||||||
| chr3:72777451
|
C | T | 5 | a0002c0002t0001g0011a0002c0002t0001g0012a0002c0002t0001g0013others(2): Show | 5 | HG01255.hp1 HG01884.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1181+15465G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72777451 | ||||||
| chr3:72777750
|
T | C | 83 | a0002c0002t0001g0010a0002c0002t0001g0011a0002c0002t0001g0012others(80): Show | 83 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.1181+15166A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72777750 | ||||||
| chr3:72777866
|
T | C | 1 | a0002c0002t0001g0010 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1181+15050A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72777866 | ||||||
| chr3:72777964
|
C | T | 82 | a0002c0002t0001g0010a0002c0002t0001g0011a0002c0002t0001g0012others(79): Show | 82 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.1181+14952G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72777964 | ||||||
| chr3:72777966
|
T | C | 4 | a0001c0001t0001g0050a0001c0001t0001g0055a0001c0001t0001g0074others(1): Show | 4 | HG02683.hp2 HG02735.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1181+14950A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72777966 | ||||||
| chr3:72778074
|
A | C | 1 | a0002c0002t0004g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1181+14842T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72778074 | ||||||
| chr3:72778242
|
T | C | 55 | a0002c0002t0001g0021a0002c0002t0001g0080a0002c0002t0001g0113others(52): Show | 55 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.1181+14674A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72778242 | ||||||
| chr3:72778274
|
A | C | 1 | a0002c0002t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1181+14642T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72778274 | ||||||
| chr3:72778341
|
C | T | 1 | a0002c0008t0001g0008 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1181+14575G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72778341 | ||||||
| chr3:72778403
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1181+14513G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72778403 | ||||||
| chr3:72778450
|
AAAAAGAA others(3): Show |
A | 2 | a0001c0001t0002g0194a0001c0001t0002g0195 | 2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1181+14456_1181+14 others(16): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72778450 | ||||||
| chr3:72778456
|
A | AAAAGAAA others(7): Show |
2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1181+14446_1181+14 others(20): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72778456 | ||||||
| chr3:72778526
|
CTTTCA | C | 3 | a0001c0001t0001g0163a0001c0001t0001g0178a0001c0001t0001g0179 | 3 | HG00558.hp2 HG02165.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1181+14385_1181+14 others(11): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72778526 | ||||||
| chr3:72778625
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1181+14291T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72778625 | ||||||
| chr3:72778675
|
T | C | 1 | a0002c0002t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1181+14241A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72778675 | ||||||
| chr3:72778810
|
G | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0081 | 2 | NA18962.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1181+14106C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72778810 | ||||||
| chr3:72778836
|
T | C | 44 | a0001c0001t0001g0096a0002c0002t0001g0023a0002c0002t0001g0024others(41): Show | 44 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1181+14080A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72778836 | ||||||
| chr3:72779000
|
T | C | 52 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(49): Show | 52 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.1181+13916A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72779000 | ||||||
| chr3:72779093
|
A | G | 1 | a0002c0002t0001g0191 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1181+13823T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72779093 | ||||||
| chr3:72779272
|
G | A | 10 | a0003c0003t0001g0210a0003c0003t0001g0211a0003c0003t0001g0212others(7): Show | 10 | HG02257.hp2 HG02630.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+13644C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72779272 | ||||||
| chr3:72779274
|
C | A | 10 | a0002c0002t0001g0196a0002c0002t0001g0209a0002c0002t0004g0003others(7): Show | 10 | HG01884.hp1 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+13642G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72779274 | ||||||
| chr3:72779502
|
G | A | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1181+13414C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72779502 | ||||||
| chr3:72779670
|
A | G | 19 | a0002c0002t0001g0010a0002c0002t0001g0011a0002c0002t0001g0012others(16): Show | 19 | HG01175.hp2 HG01243.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.1181+13246T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72779670 | ||||||
| chr3:72779949
|
A | G | 41 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(38): Show | 41 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1181+12967T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72779949 | ||||||
| chr3:72779972
|
T | C | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1181+12944A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72779972 | ||||||
| chr3:72780042
|
C | A | 4 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(1): Show | 4 | NA18967.hp2 NA18979.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1181+12874G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72780042 | ||||||
| chr3:72780399
|
G | A | 1 | a0002c0002t0001g0203 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1181+12517C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72780399 | ||||||
| chr3:72780563
|
G | C | 1 | a0001c0001t0001g0064 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1181+12353C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72780563 | ||||||
| chr3:72780718
|
A | G | 83 | a0002c0002t0001g0010a0002c0002t0001g0011a0002c0002t0001g0012others(80): Show | 83 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.1181+12198T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72780718 | ||||||
| chr3:72780907
|
A | G | 51 | a0002c0002t0001g0011a0002c0002t0001g0012a0002c0002t0001g0013others(48): Show | 51 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.1181+12009T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72780907 | ||||||
| chr3:72780936
|
T | G | 41 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(38): Show | 41 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1181+11980A>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72780936 | ||||||
| chr3:72780962
|
C | A | 1 | a0002c0002t0001g0113 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1181+11954G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72780962 | ||||||
| chr3:72781206
|
C | T | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1181+11710G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72781206 | ||||||
| chr3:72781207
|
G | A | 11 | a0002c0002t0001g0021a0002c0002t0001g0196a0002c0002t0001g0209others(8): Show | 11 | HG01884.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1181+11709C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72781207 | ||||||
| chr3:72781210
|
C | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0068a0001c0001t0001g0075 | 3 | HG02165.hp2 NA18982.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1181+11706G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72781210 | ||||||
| chr3:72781248
|
G | T | 1 | a0009c0011t0001g0051 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1181+11668C>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72781248 | ||||||
| chr3:72781344
|
C | G | 3 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0203 | 3 | HG02055.hp2 HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1181+11572G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72781344 | ||||||
| chr3:72781351
|
C | T | 27 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(24): Show | 27 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.1181+11565G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72781351 | ||||||
| chr3:72781526
|
T | C | 6 | a0001c0001t0001g0035a0001c0001t0001g0068a0001c0001t0001g0075others(3): Show | 6 | HG02165.hp2 NA18944.hp1 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.1181+11390A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72781526 | ||||||
| chr3:72781530
|
A | G | 1 | a0006c0006t0001g0131 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1181+11386T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72781530 | ||||||
| chr3:72781531
|
T | G | 3 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0203 | 3 | HG02055.hp2 HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1181+11385A>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72781531 | ||||||
| chr3:72781784
|
T | C | 41 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(38): Show | 41 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1181+11132A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72781784 | ||||||
| chr3:72781899
|
A | G | 1 | a0002c0002t0008g0206 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1181+11017T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72781899 | ||||||
| chr3:72781946
|
G | GA | 3 | a0001c0001t0002g0190a0001c0001t0002g0194a0001c0001t0002g0195 | 3 | HG02486.hp2 HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1181+10969dupT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72781946 | ||||||
| chr3:72782247
|
T | G | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1181+10669A>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72782247 | ||||||
| chr3:72782472
|
G | A | 11 | a0002c0002t0001g0021a0002c0002t0001g0196a0002c0002t0001g0209others(8): Show | 11 | HG01884.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1181+10444C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72782472 | ||||||
| chr3:72782672
|
G | A | 3 | a0001c0001t0002g0190a0001c0001t0002g0194a0001c0001t0002g0195 | 3 | HG02486.hp2 HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1181+10244C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72782672 | ||||||
| chr3:72782766
|
T | C | 2 | a0001c0001t0001g0057a0001c0001t0001g0160 | 2 | HG00673.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.1181+10150A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72782766 | ||||||
| chr3:72782794
|
T | C | 1 | a0003c0003t0001g0217 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1181+10122A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72782794 | ||||||
| chr3:72782925
|
C | T | 33 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(30): Show | 33 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.1181+9991G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72782925 | ||||||
| chr3:72783359
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1181+9557A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72783359 | ||||||
| chr3:72783363
|
CT | C | 65 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0083others(62): Show | 65 | HG00140.hp1 HG00642.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.1181+9552delA | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72783363 | ||||||
| chr3:72783363
|
CTT | C | 5 | a0001c0001t0001g0086a0001c0001t0002g0195a0002c0002t0001g0120others(2): Show | 5 | HG02622.hp2 HG02818.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1181+9551_1181+955 others(6): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72783363 | ||||||
| chr3:72783363
|
CTTTTTT | C | 8 | a0003c0003t0001g0210a0003c0003t0001g0211a0003c0003t0001g0213others(5): Show | 8 | HG02257.hp2 HG02630.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1181+9547_1181+955 others(10): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72783363 | ||||||
| chr3:72783383
|
G | T | 3 | a0002c0002t0001g0011a0002c0002t0001g0012a0002c0002t0001g0013 | 3 | HG01255.hp1 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1181+9533C>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72783383 | ||||||
| chr3:72783489
|
T | C | 21 | a0002c0002t0001g0010a0002c0002t0001g0011a0002c0002t0001g0012others(18): Show | 21 | HG01175.hp2 HG01243.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.1181+9427A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72783489 | ||||||
| chr3:72783515
|
T | C | 1 | a0002c0002t0001g0196 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1181+9401A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72783515 | ||||||
| chr3:72783620
|
T | G | 2 | a0001c0001t0001g0043a0001c0001t0001g0045 | 2 | HG02723.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1181+9296A>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72783620 | ||||||
| chr3:72783830
|
T | C | 8 | a0001c0001t0001g0153a0001c0001t0001g0183a0001c0001t0001g0184others(5): Show | 8 | HG02040.hp2 HG02071.hp2 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.1181+9086A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72783830 | ||||||
| chr3:72784136
|
TA | T | 35 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0080others(32): Show | 35 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.1181+8779delT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72784136 | ||||||
| chr3:72784165
|
TA | T | 38 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0080others(35): Show | 38 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.1181+8750delT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72784165 | ||||||
| chr3:72784183
|
C | A | 1 | a0002c0002t0001g0010 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1181+8733G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72784183 | ||||||
| chr3:72784331
|
T | C | 1 | a0001c0001t0001g0103 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1181+8585A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72784331 | ||||||
| chr3:72784365
|
G | A | 5 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0200others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1181+8551C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72784365 | ||||||
| chr3:72784378
|
G | A | 1 | a0002c0002t0001g0010 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1181+8538C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72784378 | ||||||
| chr3:72784544
|
T | C | 2 | a0001c0001t0001g0069a0001c0001t0001g0078 | 2 | HG00738.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1181+8372A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72784544 | ||||||
| chr3:72784641
|
C | T | 6 | a0002c0002t0001g0115a0002c0002t0001g0116a0002c0002t0001g0120others(3): Show | 6 | HG01109.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1181+8275G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72784641 | ||||||
| chr3:72784738
|
T | C | 19 | a0002c0002t0001g0010a0002c0002t0001g0011a0002c0002t0001g0012others(16): Show | 19 | HG01175.hp2 HG01243.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.1181+8178A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72784738 | ||||||
| chr3:72784818
|
G | A | 3 | a0002c0002t0001g0191a0002c0002t0001g0192a0002c0002t0001g0197 | 3 | HG02895.hp1 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1181+8098C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72784818 | ||||||
| chr3:72785295
|
A | C | 12 | a0002c0002t0001g0011a0002c0002t0001g0012a0002c0002t0001g0013others(9): Show | 12 | HG01243.hp2 HG01255.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1181+7621T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72785295 | ||||||
| chr3:72785370
|
G | A | 1 | a0002c0002t0001g0203 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1181+7546C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72785370 | ||||||
| chr3:72785412
|
G | A | 11 | a0002c0002t0001g0010a0003c0003t0001g0210a0003c0003t0001g0211others(8): Show | 11 | HG01175.hp2 HG02257.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1181+7504C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72785412 | ||||||
| chr3:72785568
|
A | G | 8 | a0002c0002t0001g0011a0002c0002t0001g0012a0002c0002t0001g0013others(5): Show | 8 | HG01243.hp2 HG01255.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1181+7348T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72785568 | ||||||
| chr3:72785712
|
C | G | 2 | a0001c0001t0001g0030a0001c0001t0001g0062 | 2 | NA18983.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1181+7204G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72785712 | ||||||
| chr3:72786146
|
A | T | 1 | a0002c0002t0001g0121 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1181+6770T>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72786146 | ||||||
| chr3:72786227
|
C | A | 4 | a0002c0002t0001g0118a0002c0002t0001g0128a0002c0002t0001g0129others(1): Show | 4 | HG00140.hp1 HG01081.hp1 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.1181+6689G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72786227 | ||||||
| chr3:72786479
|
G | A | 70 | a0002c0002t0001g0010a0002c0002t0001g0011a0002c0002t0001g0012others(67): Show | 70 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1181+6437C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72786479 | ||||||
| chr3:72786655
|
T | C | 1 | a0002c0002t0001g0203 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1181+6261A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72786655 | ||||||
| chr3:72786669
|
C | G | 1 | a0002c0002t0001g0010 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1181+6247G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72786669 | ||||||
| chr3:72786694
|
C | T | 18 | a0002c0002t0001g0010a0002c0002t0001g0198a0002c0002t0001g0199others(15): Show | 18 | HG01175.hp2 HG01884.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1181+6222G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72786694 | ||||||
| chr3:72786807
|
T | A | 1 | a0002c0002t0001g0203 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1181+6109A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72786807 | ||||||
| chr3:72786863
|
A | G | 1 | a0002c0002t0001g0010 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1181+6053T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72786863 | ||||||
| chr3:72786864
|
T | C | 1 | a0002c0002t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1181+6052A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72786864 | ||||||
| chr3:72786968
|
C | T | 33 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(30): Show | 33 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.1181+5948G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72786968 | ||||||
| chr3:72786984
|
T | G | 1 | a0001c0001t0001g0180 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1181+5932A>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72786984 | ||||||
| chr3:72787059
|
C | G | 1 | a0001c0001t0001g0093 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1181+5857G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72787059 | ||||||
| chr3:72787073
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1181+5843C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72787073 | ||||||
| chr3:72787250
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1181+5666G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72787250 | ||||||
| chr3:72787666
|
A | G | 1 | a0001c0001t0001g0044 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1181+5250T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72787666 | ||||||
| chr3:72787756
|
T | TGAGGA | 7 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0200others(4): Show | 7 | HG01884.hp2 HG02559.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1181+5159_1181+516 others(9): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72787756 | ||||||
| chr3:72787763
|
G | A | 1 | a0002c0008t0001g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1181+5153C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72787763 | ||||||
| chr3:72787947
|
C | G | 1 | a0002c0002t0001g0199 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1181+4969G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72787947 | ||||||
| chr3:72788086
|
T | G | 41 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(38): Show | 41 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1181+4830A>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72788086 | ||||||
| chr3:72788170
|
C | T | 10 | a0003c0003t0001g0210a0003c0003t0001g0211a0003c0003t0001g0212others(7): Show | 10 | HG02257.hp2 HG02630.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+4746G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72788170 | ||||||
| chr3:72788178
|
G | A | 1 | a0006c0006t0001g0130 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1181+4738C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72788178 | ||||||
| chr3:72788179
|
T | C | 1 | a0002c0002t0001g0204 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1181+4737A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72788179 | ||||||
| chr3:72788205
|
C | T | 1 | a0002c0002t0001g0196 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1181+4711G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72788205 | ||||||
| chr3:72788206
|
G | A | 3 | a0002c0002t0001g0191a0002c0002t0001g0192a0002c0002t0001g0197 | 3 | HG02895.hp1 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1181+4710C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72788206 | ||||||
| chr3:72788221
|
G | T | 1 | a0002c0002t0008g0206 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1181+4695C>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72788221 | ||||||
| chr3:72788236
|
T | G | 1 | a0001c0001t0001g0106 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1181+4680A>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72788236 | ||||||
| chr3:72788253
|
C | T | 2 | a0001c0001t0002g0194a0001c0001t0002g0195 | 2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1181+4663G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72788253 | ||||||
| chr3:72788262
|
T | C | 43 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(40): Show | 43 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.1181+4654A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72788262 | ||||||
| chr3:72788263
|
G | A | 2 | a0002c0002t0001g0120a0002c0002t0001g0136 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1181+4653C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72788263 | ||||||
| chr3:72788286
|
G | A | 1 | a0002c0002t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1181+4630C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72788286 | ||||||
| chr3:72788301
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1181+4615A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72788301 | ||||||
| chr3:72788308
|
C | T | 4 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0004g0005others(1): Show | 4 | HG02451.hp1 HG02809.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1181+4608G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72788308 | ||||||
| chr3:72788389
|
A | G | 1 | a0002c0002t0008g0206 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1181+4527T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72788389 | ||||||
| chr3:72788402
|
C | T | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1181+4514G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72788402 | ||||||
| chr3:72788407
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1181+4509G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72788407 | ||||||
| chr3:72788466
|
G | A | 3 | a0002c0002t0001g0011a0002c0002t0001g0012a0002c0002t0001g0013 | 3 | HG01255.hp1 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1181+4450C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72788466 | ||||||
| chr3:72788512
|
C | G | 1 | a0001c0001t0001g0101 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1181+4404G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72788512 | ||||||
| chr3:72788562
|
A | AC | 16 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0043others(13): Show | 16 | HG00642.hp1 HG00735.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1181+4353dupG | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72788562 | ||||||
| chr3:72788622
|
T | C | 1 | a0001c0001t0001g0030 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1181+4294A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72788622 | ||||||
| chr3:72788773
|
C | T | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1181+4143G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72788773 | ||||||
| chr3:72788931
|
C | T | 4 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(1): Show | 4 | NA18967.hp2 NA18979.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1181+3985G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72788931 | ||||||
| chr3:72789026
|
A | G | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1181+3890T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72789026 | ||||||
| chr3:72789098
|
A | G | 1 | a0002c0002t0001g0010 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1181+3818T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72789098 | ||||||
| chr3:72789145
|
T | TA | 2 | a0002c0002t0005g0025a0002c0002t0005g0027 | 2 | HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1181+3770dupT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72789145 | ||||||
| chr3:72789168
|
T | C | 2 | a0002c0002t0001g0144a0002c0002t0001g0146 | 2 | HG01978.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1181+3748A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72789168 | ||||||
| chr3:72789400
|
C | T | 73 | a0002c0002t0001g0010a0002c0002t0001g0011a0002c0002t0001g0012others(70): Show | 73 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.1181+3516G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72789400 | ||||||
| chr3:72789433
|
TGGAAGCC others(3): Show |
T | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1181+3473_1181+348 others(14): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72789433 | ||||||
| chr3:72789600
|
T | A | 8 | a0002c0002t0001g0011a0002c0002t0001g0012a0002c0002t0001g0013others(5): Show | 8 | HG01243.hp2 HG01255.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1181+3316A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72789600 | ||||||
| chr3:72789605
|
C | A | 55 | a0002c0002t0001g0011a0002c0002t0001g0012a0002c0002t0001g0013others(52): Show | 55 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.1181+3311G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72789605 | ||||||
| chr3:72789833
|
CAG | C | 5 | a0003c0003t0001g0210a0003c0003t0001g0211a0003c0003t0001g0214others(2): Show | 5 | HG02257.hp2 HG02630.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1181+3081_1181+308 others(6): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72789833 | ||||||
| chr3:72789933
|
A | G | 1 | a0002c0002t0001g0203 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1181+2983T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72789933 | ||||||
| chr3:72789969
|
C | T | 2 | a0008c0007t0001g0207a0008c0007t0001g0208 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1181+2947G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72789969 | ||||||
| chr3:72789992
|
A | G | 1 | a0002c0008t0001g0008 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1181+2924T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72789992 | ||||||
| chr3:72790034
|
A | G | 1 | a0002c0002t0005g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1181+2882T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72790034 | ||||||
| chr3:72790134
|
T | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0048others(1): Show | 5 | NA18945.hp2 NA18972.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.1181+2782A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72790134 | ||||||
| chr3:72790158
|
GGCCAGGA | G | 3 | a0002c0002t0005g0025a0002c0002t0005g0026a0002c0002t0005g0027 | 3 | HG01884.hp1 HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1181+2751_1181+275 others(11): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72790158 | ||||||
| chr3:72790398
|
C | T | 1 | a0003c0003t0001g0212 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1181+2518G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72790398 | ||||||
| chr3:72790471
|
T | C | 1 | a0002c0002t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1181+2445A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72790471 | ||||||
| chr3:72790599
|
T | C | 1 | a0003c0003t0001g0213 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1181+2317A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72790599 | ||||||
| chr3:72790681
|
A | G | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1181+2235T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72790681 | ||||||
| chr3:72790910
|
C | T | 9 | a0001c0001t0001g0049a0001c0001t0001g0052a0001c0001t0001g0067others(6): Show | 9 | HG01071.hp1 HG01109.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1181+2006G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72790910 | ||||||
| chr3:72791055
|
T | A | 89 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(86): Show | 89 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.1181+1861A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72791055 | ||||||
| chr3:72791114
|
G | A | 2 | a0002c0002t0001g0023a0002c0002t0001g0024 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1181+1802C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72791114 | ||||||
| chr3:72791366
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1181+1550G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72791366 | ||||||
| chr3:72791491
|
T | C | 2 | a0002c0002t0001g0204a0002c0002t0001g0205 | 2 | HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1181+1425A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72791491 | ||||||
| chr3:72791602
|
G | A | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1181+1314C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72791602 | ||||||
| chr3:72791701
|
C | T | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1181+1215G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72791701 | ||||||
| chr3:72791721
|
G | GT | 7 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0200others(4): Show | 7 | HG01884.hp2 HG02559.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1181+1194dupA | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72791721 | ||||||
| chr3:72791726
|
T | G | 33 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(30): Show | 33 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.1181+1190A>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72791726 | ||||||
| chr3:72791937
|
C | T | 3 | a0002c0002t0001g0191a0002c0002t0001g0192a0002c0002t0001g0197 | 3 | HG02895.hp1 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1181+979G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72791937 | ||||||
| chr3:72791972
|
G | A | 1 | a0002c0002t0001g0196 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1181+944C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72791972 | ||||||
| chr3:72792106
|
T | G | 3 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0203 | 3 | HG02055.hp2 HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1181+810A>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72792106 | ||||||
| chr3:72792306
|
G | C | 5 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0004g0005others(2): Show | 5 | HG02451.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1181+610C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72792306 | ||||||
| chr3:72792407
|
C | A | 1 | a0001c0001t0001g0097 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1181+509G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72792407 | ||||||
| chr3:72792552
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1181+364C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72792552 | ||||||
| chr3:72792657
|
C | A | 1 | a0002c0002t0001g0203 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1181+259G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72792657 | ||||||
| chr3:72792657
|
C | T | 2 | a0001c0001t0002g0194a0001c0001t0002g0195 | 2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1181+259G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72792657 | ||||||
| chr3:72792761
|
G | A | 9 | a0002c0002t0001g0011a0002c0002t0001g0012a0002c0002t0001g0013others(6): Show | 9 | HG01243.hp2 HG01255.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1181+155C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72792761 | ||||||
| chr3:72792784
|
C | CA | 49 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0001g0041others(46): Show | 49 | HG00642.hp1 HG00642.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.1181+131dupT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72792784 | ||||||
| chr3:72792784
|
C | CAA | 10 | a0001c0001t0001g0042a0001c0001t0001g0103a0002c0002t0001g0023others(7): Show | 10 | HG00741.hp2 HG02486.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+130_1181+131d others(4): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72792784 | ||||||
| chr3:72792784
|
CA | C | 18 | a0001c0001t0009g0107a0002c0002t0001g0011a0002c0002t0001g0012others(15): Show | 18 | HG01255.hp1 HG01256.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1181+131delT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72792784 | ||||||
| chr3:72792892
|
G | A | 10 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0004g0005others(7): Show | 10 | HG01884.hp1 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1181+24C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 10/10 | chr3 | 72792892 | ||||||
| chr3:72793143
|
C | A | 18 | a0002c0002t0001g0010a0002c0002t0001g0198a0002c0002t0001g0199others(15): Show | 18 | HG01175.hp2 HG01884.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1061-107G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72793143 | ||||||
| chr3:72793461
|
C | T | 19 | a0001c0001t0001g0088a0001c0001t0001g0153a0001c0001t0001g0155others(16): Show | 19 | HG00558.hp2 HG02040.hp2 HG02071.hp2 others(16): Show |
intron_variant | MODIFIER | c.1061-425G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72793461 | ||||||
| chr3:72793474
|
T | G | 6 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(3): Show | 6 | HG02486.hp1 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1061-438A>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72793474 | ||||||
| chr3:72793486
|
G | A | 1 | a0002c0002t0006g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1061-450C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72793486 | ||||||
| chr3:72793507
|
G | GA | 5 | a0001c0001t0001g0073a0001c0001t0001g0188a0002c0002t0004g0003others(2): Show | 5 | HG01175.hp1 HG02056.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1061-472dupT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72793507 | ||||||
| chr3:72793539
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1061-503A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72793539 | ||||||
| chr3:72793575
|
T | C | 8 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0004g0005others(5): Show | 8 | HG01884.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1061-539A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72793575 | ||||||
| chr3:72793673
|
T | C | 1 | a0002c0002t0001g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1061-637A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72793673 | ||||||
| chr3:72793852
|
AGAAATAA others(3): Show |
A | 1 | a0001c0001t0001g0076 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1061-826_1061-817d others(12): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72793852 | ||||||
| chr3:72793929
|
G | A | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1061-893C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72793929 | ||||||
| chr3:72794017
|
CATG | C | 3 | a0002c0002t0001g0011a0002c0002t0001g0012a0002c0002t0001g0013 | 3 | HG01255.hp1 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1061-984_1061-982d others(5): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72794017 | ||||||
| chr3:72794024
|
T | C | 1 | a0002c0002t0001g0196 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1061-988A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72794024 | ||||||
| chr3:72794035
|
T | G | 3 | a0001c0001t0001g0160a0007c0009t0002g0220a0007c0009t0002g0221 | 3 | HG03453.hp2 HG03486.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.1061-999A>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72794035 | ||||||
| chr3:72794151
|
A | C | 1 | a0002c0002t0001g0137 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1061-1115T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72794151 | ||||||
| chr3:72794230
|
T | C | 1 | a0002c0002t0001g0010 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1061-1194A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72794230 | ||||||
| chr3:72794384
|
G | A | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1061-1348C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72794384 | ||||||
| chr3:72794394
|
G | C | 1 | a0001c0001t0001g0094 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1061-1358C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72794394 | ||||||
| chr3:72794409
|
G | A | 11 | a0002c0002t0001g0010a0003c0003t0001g0210a0003c0003t0001g0211others(8): Show | 11 | HG01175.hp2 HG02257.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1061-1373C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72794409 | ||||||
| chr3:72794422
|
A | G | 2 | a0001c0001t0001g0029a0001c0001t0001g0087 | 2 | HG02056.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.1061-1386T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72794422 | ||||||
| chr3:72794484
|
G | A | 9 | a0002c0002t0001g0080a0002c0002t0001g0114a0002c0002t0001g0119others(6): Show | 9 | HG00438.hp1 HG00558.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.1061-1448C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72794484 | ||||||
| chr3:72794492
|
C | A | 1 | a0001c0001t0001g0044 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1061-1456G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72794492 | ||||||
| chr3:72794553
|
T | A | 11 | a0002c0002t0001g0010a0003c0003t0001g0210a0003c0003t0001g0211others(8): Show | 11 | HG01175.hp2 HG02257.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1061-1517A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72794553 | ||||||
| chr3:72794607
|
T | A | 1 | a0002c0002t0001g0010 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1061-1571A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72794607 | ||||||
| chr3:72794607
|
T | C | 6 | a0002c0002t0001g0115a0002c0002t0001g0116a0002c0002t0001g0120others(3): Show | 6 | HG01109.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1061-1571A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72794607 | ||||||
| chr3:72794640
|
C | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0070a0001c0001t0001g0073 | 3 | HG02056.hp1 NA18998.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1061-1604G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72794640 | ||||||
| chr3:72794643
|
C | T | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1061-1607G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72794643 | ||||||
| chr3:72794748
|
C | T | 4 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0004g0005others(1): Show | 4 | HG02451.hp1 HG02809.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1061-1712G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72794748 | ||||||
| chr3:72794749
|
A | G | 1 | a0001c0001t0001g0072 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1061-1713T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72794749 | ||||||
| chr3:72794773
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1061-1737A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72794773 | ||||||
| chr3:72794830
|
G | A | 1 | a0001c0001t0003g0171 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1061-1794C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72794830 | ||||||
| chr3:72794943
|
G | A | 3 | a0001c0001t0001g0069a0001c0001t0001g0078a0001c0001t0001g0091 | 3 | HG00140.hp2 HG00738.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1061-1907C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72794943 | ||||||
| chr3:72795634
|
G | A | 33 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(30): Show | 33 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.1061-2598C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72795634 | ||||||
| chr3:72795660
|
C | G | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1061-2624G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72795660 | ||||||
| chr3:72795976
|
G | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0062 | 2 | NA18983.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1061-2940C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72795976 | ||||||
| chr3:72796041
|
T | G | 11 | a0002c0002t0001g0010a0003c0003t0001g0210a0003c0003t0001g0211others(8): Show | 11 | HG01175.hp2 HG02257.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1061-3005A>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72796041 | ||||||
| chr3:72796059
|
C | G | 3 | a0002c0002t0005g0025a0002c0002t0005g0026a0002c0002t0005g0027 | 3 | HG01884.hp1 HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1061-3023G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72796059 | ||||||
| chr3:72796101
|
C | CA | 18 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(15): Show | 18 | HG00140.hp2 HG00738.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.1061-3066dupT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72796101 | ||||||
| chr3:72796101
|
CA | C | 20 | a0001c0001t0001g0029a0001c0001t0001g0075a0001c0001t0001g0097others(17): Show | 20 | HG01256.hp1 HG02257.hp2 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.1061-3066delT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72796101 | ||||||
| chr3:72796101
|
CAAAAAAA others(3): Show |
C | 1 | a0002c0002t0001g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1061-3075_1061-306 others(14): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72796101 | ||||||
| chr3:72796101
|
CAAAAAAA others(5): Show |
C | 5 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0200others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1061-3077_1061-306 others(16): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72796101 | ||||||
| chr3:72796182
|
T | A | 1 | a0001c0001t0001g0056 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1061-3146A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72796182 | ||||||
| chr3:72796218
|
T | C | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1061-3182A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72796218 | ||||||
| chr3:72796239
|
C | A | 1 | a0001c0001t0001g0090 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1061-3203G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72796239 | ||||||
| chr3:72796259
|
C | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0085 | 2 | HG03654.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1061-3223G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72796259 | ||||||
| chr3:72796579
|
G | C | 1 | a0004c0004t0001g0112 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1061-3543C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72796579 | ||||||
| chr3:72796725
|
C | T | 7 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0200others(4): Show | 7 | HG01884.hp2 HG02559.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1061-3689G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72796725 | ||||||
| chr3:72796928
|
T | TA | 55 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0030others(52): Show | 55 | HG00558.hp1 HG01243.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.1061-3893dupT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72796928 | ||||||
| chr3:72796928
|
T | TAA | 35 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(32): Show | 35 | HG00140.hp1 HG00438.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.1061-3894_1061-389 others(6): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72796928 | ||||||
| chr3:72796928
|
TA | T | 10 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0091others(7): Show | 10 | HG00140.hp2 HG02257.hp1 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.1061-3893delT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72796928 | ||||||
| chr3:72796928
|
TAAAAAA | T | 5 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0004g0005others(2): Show | 5 | HG02451.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1061-3898_1061-389 others(10): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72796928 | ||||||
| chr3:72797112
|
G | T | 8 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0004g0005others(5): Show | 8 | HG01884.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1061-4076C>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72797112 | ||||||
| chr3:72797129
|
G | T | 1 | a0002c0002t0001g0196 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1061-4093C>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72797129 | ||||||
| chr3:72797365
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1061-4329G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72797365 | ||||||
| chr3:72797504
|
AC | A | 4 | a0001c0001t0001g0050a0001c0001t0001g0055a0001c0001t0001g0074others(1): Show | 4 | HG02683.hp2 HG02735.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1061-4469delG | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72797504 | ||||||
| chr3:72797736
|
G | T | 1 | a0001c0001t0001g0158 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1061-4700C>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72797736 | ||||||
| chr3:72797808
|
G | A | 2 | a0002c0002t0001g0192a0002c0002t0001g0197 | 2 | HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1061-4772C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72797808 | ||||||
| chr3:72797892
|
C | CT | 42 | a0001c0001t0001g0065a0002c0002t0001g0080a0002c0002t0001g0113others(39): Show | 42 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1061-4857dupA | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72797892 | ||||||
| chr3:72797928
|
T | G | 1 | a0001c0001t0001g0090 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1061-4892A>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72797928 | ||||||
| chr3:72798066
|
G | A | 4 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0004g0005others(1): Show | 4 | HG02451.hp1 HG02809.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1061-5030C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72798066 | ||||||
| chr3:72798209
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1061-5173G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72798209 | ||||||
| chr3:72798267
|
C | T | 5 | a0001c0001t0001g0009a0001c0001t0001g0083a0001c0001t0001g0084others(2): Show | 5 | HG00099.hp2 HG01346.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1061-5231G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72798267 | ||||||
| chr3:72798333
|
C | T | 1 | a0002c0002t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1061-5297G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72798333 | ||||||
| chr3:72798349
|
C | T | 1 | a0002c0002t0006g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1061-5313G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72798349 | ||||||
| chr3:72798368
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1061-5332A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72798368 | ||||||
| chr3:72798391
|
A | G | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1061-5355T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72798391 | ||||||
| chr3:72798460
|
C | G | 2 | a0008c0007t0001g0207a0008c0007t0001g0208 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1061-5424G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72798460 | ||||||
| chr3:72798656
|
A | G | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0056 | 3 | HG02451.hp2 HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1061-5620T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72798656 | ||||||
| chr3:72798878
|
T | C | 1 | a0002c0002t0001g0140 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1061-5842A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72798878 | ||||||
| chr3:72799005
|
C | T | 1 | a0002c0008t0001g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1061-5969G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72799005 | ||||||
| chr3:72799053
|
G | A | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1061-6017C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72799053 | ||||||
| chr3:72799053
|
G | T | 1 | a0001c0001t0002g0190 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1061-6017C>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72799053 | ||||||
| chr3:72799067
|
T | C | 4 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0004g0005others(1): Show | 4 | HG02451.hp1 HG02809.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1061-6031A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72799067 | ||||||
| chr3:72799165
|
A | T | 2 | a0001c0001t0002g0194a0001c0001t0002g0195 | 2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1061-6129T>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72799165 | ||||||
| chr3:72799166
|
T | A | 2 | a0001c0001t0001g0058a0002c0002t0001g0137 | 2 | HG01952.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1061-6130A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72799166 | ||||||
| chr3:72799277
|
A | G | 1 | a0002c0002t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1061-6241T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72799277 | ||||||
| chr3:72799364
|
A | G | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1061-6328T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72799364 | ||||||
| chr3:72799420
|
T | C | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1061-6384A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72799420 | ||||||
| chr3:72799479
|
G | A | 4 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0004g0005others(1): Show | 4 | HG02451.hp1 HG02809.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1061-6443C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72799479 | ||||||
| chr3:72799571
|
T | C | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1061-6535A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72799571 | ||||||
| chr3:72799579
|
G | A | 3 | a0002c0002t0001g0191a0002c0002t0001g0192a0002c0002t0001g0197 | 3 | HG02895.hp1 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1061-6543C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72799579 | ||||||
| chr3:72799676
|
T | C | 28 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0049others(25): Show | 28 | HG00140.hp2 HG00438.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.1061-6640A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72799676 | ||||||
| chr3:72799699
|
C | T | 6 | a0002c0002t0001g0115a0002c0002t0001g0116a0002c0002t0001g0120others(3): Show | 6 | HG01109.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1061-6663G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72799699 | ||||||
| chr3:72799823
|
C | T | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1061-6787G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72799823 | ||||||
| chr3:72799825
|
A | C | 1 | a0001c0001t0001g0086 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1061-6789T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72799825 | ||||||
| chr3:72799970
|
C | T | 5 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1061-6934G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72799970 | ||||||
| chr3:72800027
|
A | G | 1 | a0001c0001t0001g0152 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1061-6991T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72800027 | ||||||
| chr3:72800149
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1061-7113G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72800149 | ||||||
| chr3:72800220
|
T | G | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1061-7184A>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72800220 | ||||||
| chr3:72800330
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1061-7294T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72800330 | ||||||
| chr3:72800396
|
T | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0162 | 2 | NA19056.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1061-7360A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72800396 | ||||||
| chr3:72800406
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1061-7370G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72800406 | ||||||
| chr3:72800463
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1061-7427C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72800463 | ||||||
| chr3:72800541
|
A | G | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1061-7505T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72800541 | ||||||
| chr3:72800589
|
C | T | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1061-7553G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72800589 | ||||||
| chr3:72800655
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1061-7619G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72800655 | ||||||
| chr3:72801141
|
TA | T | 128 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(125): Show | 128 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.1061-8106delT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72801141 | ||||||
| chr3:72801214
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1061-8178A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72801214 | ||||||
| chr3:72801372
|
C | T | 10 | a0003c0003t0001g0210a0003c0003t0001g0211a0003c0003t0001g0212others(7): Show | 10 | HG02257.hp2 HG02630.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1061-8336G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72801372 | ||||||
| chr3:72801475
|
G | C | 1 | a0002c0002t0001g0133 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1061-8439C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72801475 | ||||||
| chr3:72801703
|
T | C | 2 | a0002c0002t0001g0144a0002c0002t0001g0146 | 2 | HG01978.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1061-8667A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72801703 | ||||||
| chr3:72801944
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1061-8908C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72801944 | ||||||
| chr3:72802101
|
T | A | 1 | a0002c0002t0001g0203 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1061-9065A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72802101 | ||||||
| chr3:72802233
|
C | A | 2 | a0002c0002t0001g0023a0002c0002t0001g0024 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1061-9197G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72802233 | ||||||
| chr3:72802290
|
T | A | 47 | a0002c0002t0001g0010a0002c0002t0001g0011a0002c0002t0001g0012others(44): Show | 47 | HG01175.hp2 HG01243.hp2 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.1061-9254A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72802290 | ||||||
| chr3:72802532
|
C | T | 10 | a0003c0003t0001g0210a0003c0003t0001g0211a0003c0003t0001g0212others(7): Show | 10 | HG02257.hp2 HG02630.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1061-9496G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72802532 | ||||||
| chr3:72802613
|
T | C | 7 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0200others(4): Show | 7 | HG01884.hp2 HG02559.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1061-9577A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72802613 | ||||||
| chr3:72802653
|
C | T | 1 | a0002c0002t0006g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1061-9617G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72802653 | ||||||
| chr3:72802904
|
T | A | 10 | a0003c0003t0001g0210a0003c0003t0001g0211a0003c0003t0001g0212others(7): Show | 10 | HG02257.hp2 HG02630.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1060+9767A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72802904 | ||||||
| chr3:72802905
|
A | T | 5 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060+9766T>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72802905 | ||||||
| chr3:72802921
|
A | G | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1060+9750T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72802921 | ||||||
| chr3:72803124
|
T | C | 1 | a0002c0002t0001g0146 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1060+9547A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72803124 | ||||||
| chr3:72803314
|
G | A | 1 | a0001c0001t0009g0107 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1060+9357C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72803314 | ||||||
| chr3:72803329
|
T | C | 28 | a0002c0002t0001g0010a0002c0002t0001g0011a0002c0002t0001g0012others(25): Show | 28 | HG01175.hp2 HG01243.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.1060+9342A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72803329 | ||||||
| chr3:72803492
|
C | A | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1060+9179G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72803492 | ||||||
| chr3:72803721
|
C | T | 1 | a0001c0001t0001g0029 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1060+8950G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72803721 | ||||||
| chr3:72803900
|
G | C | 1 | a0002c0002t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1060+8771C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72803900 | ||||||
| chr3:72804012
|
G | A | 2 | a0002c0002t0001g0023a0002c0002t0001g0024 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1060+8659C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72804012 | ||||||
| chr3:72804073
|
C | T | 4 | a0002c0002t0005g0025a0002c0002t0005g0026a0002c0002t0005g0027others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1060+8598G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72804073 | ||||||
| chr3:72804094
|
A | T | 1 | a0002c0002t0001g0196 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1060+8577T>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72804094 | ||||||
| chr3:72804426
|
C | A | 1 | a0002c0002t0001g0080 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1060+8245G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72804426 | ||||||
| chr3:72804618
|
G | A | 1 | a0002c0002t0001g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1060+8053C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72804618 | ||||||
| chr3:72804635
|
C | G | 2 | a0008c0007t0001g0207a0008c0007t0001g0208 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1060+8036G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72804635 | ||||||
| chr3:72804730
|
C | T | 1 | a0002c0002t0001g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1060+7941G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72804730 | ||||||
| chr3:72804735
|
C | A | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1060+7936G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72804735 | ||||||
| chr3:72804737
|
A | G | 3 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0203 | 3 | HG02055.hp2 HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1060+7934T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72804737 | ||||||
| chr3:72804897
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1060+7774A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72804897 | ||||||
| chr3:72805035
|
A | G | 19 | a0002c0002t0001g0010a0002c0002t0001g0011a0002c0002t0001g0012others(16): Show | 19 | HG01175.hp2 HG01243.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.1060+7636T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72805035 | ||||||
| chr3:72805099
|
T | C | 1 | a0001c0001t0001g0075 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1060+7572A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72805099 | ||||||
| chr3:72805678
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1060+6993T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72805678 | ||||||
| chr3:72805709
|
C | A | 2 | a0002c0002t0001g0023a0002c0002t0001g0024 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1060+6962G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72805709 | ||||||
| chr3:72805905
|
T | C | 2 | a0001c0001t0001g0049a0001c0001t0007g0092 | 2 | HG01109.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1060+6766A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72805905 | ||||||
| chr3:72805953
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1060+6718G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72805953 | ||||||
| chr3:72806003
|
ATGACTAG others(4): Show |
A | 3 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0203 | 3 | HG02055.hp2 HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1060+6657_1060+666 others(15): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72806003 | ||||||
| chr3:72806012
|
A | G | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1060+6659T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72806012 | ||||||
| chr3:72806067
|
A | C | 8 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0004g0005others(5): Show | 8 | HG01884.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1060+6604T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72806067 | ||||||
| chr3:72806067
|
A | G | 81 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(78): Show | 81 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.1060+6604T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72806067 | ||||||
| chr3:72806084
|
C | T | 6 | a0002c0002t0001g0115a0002c0002t0001g0116a0002c0002t0001g0120others(3): Show | 6 | HG01109.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1060+6587G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72806084 | ||||||
| chr3:72806325
|
T | C | 1 | a0002c0002t0001g0192 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1060+6346A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72806325 | ||||||
| chr3:72806676
|
C | T | 2 | a0001c0001t0001g0166a0011c0010t0001g0007 | 2 | NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.1060+5995G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72806676 | ||||||
| chr3:72806856
|
T | C | 1 | a0002c0002t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1060+5815A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72806856 | ||||||
| chr3:72806986
|
A | C | 5 | a0003c0003t0001g0210a0003c0003t0001g0211a0003c0003t0001g0214others(2): Show | 5 | HG02257.hp2 HG02630.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1060+5685T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72806986 | ||||||
| chr3:72807133
|
T | A | 1 | a0001c0001t0001g0098 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1060+5538A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72807133 | ||||||
| chr3:72807176
|
A | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0162 | 2 | NA19056.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1060+5495T>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72807176 | ||||||
| chr3:72807340
|
T | C | 3 | a0002c0002t0001g0191a0002c0002t0001g0192a0002c0002t0001g0197 | 3 | HG02895.hp1 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1060+5331A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72807340 | ||||||
| chr3:72807389
|
T | C | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1060+5282A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72807389 | ||||||
| chr3:72807400
|
T | C | 41 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(38): Show | 41 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1060+5271A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72807400 | ||||||
| chr3:72807554
|
G | A | 1 | a0002c0002t0001g0010 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1060+5117C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72807554 | ||||||
| chr3:72807691
|
C | T | 4 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(1): Show | 4 | NA18967.hp2 NA18979.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1060+4980G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72807691 | ||||||
| chr3:72807765
|
A | T | 2 | a0001c0001t0001g0166a0011c0010t0001g0007 | 2 | NA18964.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.1060+4906T>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72807765 | ||||||
| chr3:72808527
|
T | C | 3 | a0002c0002t0005g0025a0002c0002t0005g0026a0002c0002t0005g0027 | 3 | HG01884.hp1 HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1060+4144A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72808527 | ||||||
| chr3:72808541
|
C | T | 1 | a0001c0001t0002g0190 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1060+4130G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72808541 | ||||||
| chr3:72808594
|
T | G | 4 | a0002c0002t0001g0021a0002c0002t0001g0023a0002c0002t0001g0024others(1): Show | 4 | HG02055.hp2 HG03041.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1060+4077A>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72808594 | ||||||
| chr3:72808751
|
G | A | 3 | a0002c0002t0001g0200a0002c0002t0001g0201a0002c0002t0001g0202 | 3 | HG01884.hp2 HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1060+3920C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72808751 | ||||||
| chr3:72808755
|
GTAT | G | 8 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(5): Show | 8 | HG02109.hp1 HG02723.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1060+3913_1060+391 others(7): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72808755 | ||||||
| chr3:72808757
|
A | G | 7 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0200others(4): Show | 7 | HG01884.hp2 HG02559.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1060+3914T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72808757 | ||||||
| chr3:72808971
|
A | G | 15 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(12): Show | 15 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1060+3700T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72808971 | ||||||
| chr3:72808984
|
G | A | 1 | a0002c0002t0001g0145 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1060+3687C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72808984 | ||||||
| chr3:72809022
|
G | T | 1 | a0001c0001t0001g0042 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1060+3649C>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72809022 | ||||||
| chr3:72809032
|
G | C | 1 | a0002c0002t0001g0132 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1060+3639C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72809032 | ||||||
| chr3:72809063
|
C | T | 1 | a0002c0002t0001g0196 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1060+3608G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72809063 | ||||||
| chr3:72809070
|
T | TGGAAATT others(299): Show |
2 | a0008c0007t0001g0207a0008c0007t0001g0208 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1060+3600_1060+360 others(310): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72809070 | ||||||
| chr3:72809146
|
C | A | 1 | a0002c0002t0001g0203 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1060+3525G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72809146 | ||||||
| chr3:72809479
|
C | G | 77 | a0002c0002t0001g0010a0002c0002t0001g0011a0002c0002t0001g0012others(74): Show | 77 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.1060+3192G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72809479 | ||||||
| chr3:72809505
|
A | T | 2 | a0002c0002t0001g0023a0002c0002t0001g0024 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1060+3166T>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72809505 | ||||||
| chr3:72809754
|
T | C | 2 | a0002c0002t0005g0025a0002c0002t0005g0027 | 2 | HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1060+2917A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72809754 | ||||||
| chr3:72809877
|
T | C | 1 | a0002c0002t0008g0206 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1060+2794A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72809877 | ||||||
| chr3:72809877
|
T | G | 1 | a0001c0001t0001g0031 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1060+2794A>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72809877 | ||||||
| chr3:72809922
|
G | C | 1 | a0003c0003t0001g0217 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1060+2749C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72809922 | ||||||
| chr3:72810086
|
T | C | 6 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(3): Show | 6 | HG02486.hp1 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1060+2585A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72810086 | ||||||
| chr3:72810392
|
A | T | 1 | a0002c0002t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1060+2279T>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72810392 | ||||||
| chr3:72810402
|
T | C | 1 | a0002c0002t0001g0015 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1060+2269A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72810402 | ||||||
| chr3:72810466
|
G | A | 1 | a0002c0002t0008g0206 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1060+2205C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72810466 | ||||||
| chr3:72810610
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1060+2061T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72810610 | ||||||
| chr3:72810743
|
C | A | 1 | a0002c0002t0001g0010 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1060+1928G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72810743 | ||||||
| chr3:72810806
|
G | C | 1 | a0002c0002t0008g0206 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1060+1865C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72810806 | ||||||
| chr3:72810968
|
TTTC | T | 3 | a0005c0005t0001g0117a0005c0005t0001g0135a0005c0005t0001g0189 | 3 | HG02622.hp1 HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1060+1700_1060+170 others(7): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72810968 | ||||||
| chr3:72811023
|
A | G | 1 | a0003c0003t0001g0216 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1060+1648T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72811023 | ||||||
| chr3:72811172
|
TGTGA | T | 2 | a0008c0007t0001g0207a0008c0007t0001g0208 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1060+1495_1060+149 others(8): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72811172 | ||||||
| chr3:72811174
|
TGAGTGA | T | 8 | a0001c0001t0001g0155a0001c0001t0001g0166a0001c0001t0001g0167others(5): Show | 8 | HG02129.hp1 NA18944.hp1 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.1060+1491_1060+149 others(10): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72811174 | ||||||
| chr3:72811283
|
C | T | 1 | a0002c0002t0001g0197 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1060+1388G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72811283 | ||||||
| chr3:72811672
|
C | G | 1 | a0002c0002t0005g0027 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1060+999G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72811672 | ||||||
| chr3:72811717
|
G | A | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1060+954C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72811717 | ||||||
| chr3:72811931
|
A | T | 1 | a0002c0002t0001g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1060+740T>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72811931 | ||||||
| chr3:72812004
|
G | T | 1 | a0002c0002t0004g0006 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1060+667C>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72812004 | ||||||
| chr3:72812273
|
T | A | 1 | a0002c0002t0001g0191 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1060+398A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72812273 | ||||||
| chr3:72812369
|
T | C | 1 | a0002c0002t0001g0132 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1060+302A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72812369 | ||||||
| chr3:72812415
|
C | A | 1 | a0007c0009t0002g0220 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1060+256G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72812415 | ||||||
| chr3:72812473
|
A | G | 5 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060+198T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72812473 | ||||||
| chr3:72812582
|
T | C | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1060+89A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72812582 | ||||||
| chr3:72812659
|
G | A | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1060+12C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 9/10 | chr3 | 72812659 | ||||||
| chr3:72812951
|
T | C | 1 | a0001c0001t0001g0031 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.937-157A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 8/10 | chr3 | 72812951 | ||||||
| chr3:72812969
|
T | G | 1 | a0002c0002t0001g0134 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.937-175A>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 8/10 | chr3 | 72812969 | ||||||
| chr3:72813124
|
A | G | 3 | a0002c0002t0005g0025a0002c0002t0005g0026a0002c0002t0005g0027 | 3 | HG01884.hp1 HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.937-330T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 8/10 | chr3 | 72813124 | ||||||
| chr3:72813224
|
T | C | 2 | a0002c0008t0001g0008a0002c0008t0001g0022 | 2 | HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.937-430A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 8/10 | chr3 | 72813224 | ||||||
| chr3:72813465
|
C | CA | 55 | a0001c0001t0001g0048a0001c0001t0001g0054a0001c0001t0001g0057others(52): Show | 55 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.937-672dupT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 8/10 | chr3 | 72813465 | ||||||
| chr3:72813527
|
A | C | 4 | a0002c0002t0001g0203a0002c0002t0001g0209a0002c0008t0001g0008others(1): Show | 4 | HG02055.hp2 HG02559.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.937-733T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 8/10 | chr3 | 72813527 | ||||||
| chr3:72813532
|
G | A | 2 | a0002c0002t0001g0192a0002c0002t0001g0197 | 2 | HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.937-738C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 8/10 | chr3 | 72813532 | ||||||
| chr3:72813548
|
G | C | 1 | a0001c0001t0001g0031 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.937-754C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 8/10 | chr3 | 72813548 | ||||||
| chr3:72813604
|
C | A | 129 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(126): Show | 129 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.937-810G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 8/10 | chr3 | 72813604 | ||||||
| chr3:72813622
|
G | A | 2 | a0002c0002t0001g0023a0002c0002t0001g0024 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.937-828C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 8/10 | chr3 | 72813622 | ||||||
| chr3:72813760
|
C | CA | 31 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0047others(28): Show | 31 | HG00642.hp1 HG00741.hp2 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.937-967dupT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 8/10 | chr3 | 72813760 | ||||||
| chr3:72813830
|
C | CT | 61 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0030others(58): Show | 61 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.937-1037dupA | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 8/10 | chr3 | 72813830 | ||||||
| chr3:72813830
|
C | CTT | 6 | a0001c0001t0001g0103a0001c0001t0003g0033a0002c0002t0001g0119others(3): Show | 6 | HG00438.hp1 HG00741.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.937-1038_937-1037d others(4): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 8/10 | chr3 | 72813830 | ||||||
| chr3:72813830
|
CT | C | 16 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(13): Show | 16 | HG01884.hp2 HG02055.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.937-1037delA | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 8/10 | chr3 | 72813830 | ||||||
| chr3:72813887
|
T | C | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.937-1093A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 8/10 | chr3 | 72813887 | ||||||
| chr3:72813926
|
T | A | 1 | a0002c0002t0006g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.937-1132A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 8/10 | chr3 | 72813926 | ||||||
| chr3:72814058
|
A | C | 41 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(38): Show | 41 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.937-1264T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 8/10 | chr3 | 72814058 | ||||||
| chr3:72814163
|
G | A | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.936+1187C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 8/10 | chr3 | 72814163 | ||||||
| chr3:72814203
|
G | A | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.936+1147C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 8/10 | chr3 | 72814203 | ||||||
| chr3:72814283
|
C | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0070a0001c0001t0001g0073 | 3 | HG02056.hp1 NA18998.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.936+1067G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 8/10 | chr3 | 72814283 | ||||||
| chr3:72814353
|
T | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0019others(175): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.936+997A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 8/10 | chr3 | 72814353 | ||||||
| chr3:72814415
|
G | C | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.936+935C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 8/10 | chr3 | 72814415 | ||||||
| chr3:72814430
|
C | A | 3 | a0002c0002t0001g0191a0002c0002t0001g0192a0002c0002t0001g0197 | 3 | HG02895.hp1 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.936+920G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 8/10 | chr3 | 72814430 | ||||||
| chr3:72814440
|
G | T | 1 | a0002c0002t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.936+910C>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 8/10 | chr3 | 72814440 | ||||||
| chr3:72814952
|
A | G | 2 | a0002c0002t0001g0198a0002c0002t0001g0199 | 2 | HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.936+398T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 8/10 | chr3 | 72814952 | ||||||
| chr3:72815010
|
C | T | 41 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(38): Show | 41 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.936+340G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 8/10 | chr3 | 72815010 | ||||||
| chr3:72815122
|
C | T | 8 | a0002c0002t0001g0137a0005c0005t0001g0117a0005c0005t0001g0135others(5): Show | 8 | HG00735.hp2 HG01891.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.936+228G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 8/10 | chr3 | 72815122 | ||||||
| chr3:72815125
|
T | C | 8 | a0002c0002t0001g0011a0002c0002t0001g0012a0002c0002t0001g0013others(5): Show | 8 | HG01243.hp2 HG01255.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.936+225A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 8/10 | chr3 | 72815125 | ||||||
| chr3:72815275
|
C | A | 3 | a0002c0002t0005g0025a0002c0002t0005g0026a0002c0002t0005g0027 | 3 | HG01884.hp1 HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.936+75G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 8/10 | chr3 | 72815275 | ||||||
| chr3:72815459
|
T | C | 8 | a0002c0002t0001g0137a0005c0005t0001g0117a0005c0005t0001g0135others(5): Show | 8 | HG00735.hp2 HG01891.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.883-56A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 7/10 | chr3 | 72815459 | ||||||
| chr3:72815599
|
G | T | 1 | a0002c0002t0001g0196 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.883-196C>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 7/10 | chr3 | 72815599 | ||||||
| chr3:72815624
|
T | A | 1 | a0002c0002t0006g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.883-221A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 7/10 | chr3 | 72815624 | ||||||
| chr3:72815724
|
TAA | T | 2 | a0002c0002t0001g0023a0002c0002t0001g0024 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.883-323_883-322del others(2): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 7/10 | chr3 | 72815724 | ||||||
| chr3:72815727
|
G | C | 3 | a0002c0002t0001g0011a0002c0002t0001g0012a0002c0002t0001g0013 | 3 | HG01255.hp1 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.883-324C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 7/10 | chr3 | 72815727 | ||||||
| chr3:72815975
|
A | G | 41 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(38): Show | 41 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.883-572T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 7/10 | chr3 | 72815975 | ||||||
| chr3:72816032
|
C | T | 7 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(4): Show | 7 | HG00735.hp1 HG01255.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.883-629G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 7/10 | chr3 | 72816032 | ||||||
| chr3:72816093
|
A | T | 1 | a0001c0001t0001g0148 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.883-690T>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 7/10 | chr3 | 72816093 | ||||||
| chr3:72816113
|
T | C | 220 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0019others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.883-710A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 7/10 | chr3 | 72816113 | ||||||
| chr3:72816629
|
A | C | 1 | a0002c0002t0001g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.882+601T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 7/10 | chr3 | 72816629 | ||||||
| chr3:72816704
|
GAT | G | 4 | a0002c0002t0005g0025a0002c0002t0005g0026a0002c0002t0005g0027others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+524_882+525del others(2): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 7/10 | chr3 | 72816704 | ||||||
| chr3:72816707
|
A | G | 1 | a0001c0001t0002g0190 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.882+523T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 7/10 | chr3 | 72816707 | ||||||
| chr3:72816879
|
T | C | 41 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(38): Show | 41 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.882+351A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 7/10 | chr3 | 72816879 | ||||||
| chr3:72816922
|
T | G | 41 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(38): Show | 41 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.882+308A>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 7/10 | chr3 | 72816922 | ||||||
| chr3:72817215
|
C | T | 10 | a0003c0003t0001g0210a0003c0003t0001g0211a0003c0003t0001g0212others(7): Show | 10 | HG02257.hp2 HG02630.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.882+15G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 7/10 | chr3 | 72817215 | ||||||
| chr3:72817396
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.728-12G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72817396 | ||||||
| chr3:72817723
|
G | A | 5 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-339C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72817723 | ||||||
| chr3:72817729
|
A | C | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.728-345T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72817729 | ||||||
| chr3:72817846
|
T | C | 10 | a0003c0003t0001g0210a0003c0003t0001g0211a0003c0003t0001g0212others(7): Show | 10 | HG02257.hp2 HG02630.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.728-462A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72817846 | ||||||
| chr3:72817905
|
T | G | 1 | a0002c0002t0001g0196 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.728-521A>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72817905 | ||||||
| chr3:72817940
|
G | A | 41 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(38): Show | 41 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.728-556C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72817940 | ||||||
| chr3:72818210
|
T | A | 2 | a0002c0002t0001g0023a0002c0002t0001g0024 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.728-826A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72818210 | ||||||
| chr3:72818315
|
T | G | 2 | a0001c0001t0001g0071a0001c0001t0001g0082 | 2 | HG00099.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.728-931A>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72818315 | ||||||
| chr3:72818376
|
T | C | 1 | a0002c0002t0001g0114 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.728-992A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72818376 | ||||||
| chr3:72818628
|
A | G | 41 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(38): Show | 41 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.728-1244T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72818628 | ||||||
| chr3:72818679
|
C | T | 2 | a0002c0002t0001g0023a0002c0002t0001g0024 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.728-1295G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72818679 | ||||||
| chr3:72818798
|
G | C | 41 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(38): Show | 41 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.728-1414C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72818798 | ||||||
| chr3:72818877
|
C | T | 18 | a0002c0002t0001g0011a0002c0002t0001g0012a0002c0002t0001g0013others(15): Show | 18 | HG01243.hp2 HG01255.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.728-1493G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72818877 | ||||||
| chr3:72818882
|
A | C | 3 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0170 | 3 | HG02027.hp1 HG02129.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.728-1498T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72818882 | ||||||
| chr3:72818942
|
T | C | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.728-1558A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72818942 | ||||||
| chr3:72819083
|
T | C | 97 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(94): Show | 97 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.728-1699A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72819083 | ||||||
| chr3:72819122
|
T | A | 1 | a0001c0001t0002g0195 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.728-1738A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72819122 | ||||||
| chr3:72819169
|
T | C | 3 | a0002c0002t0005g0025a0002c0002t0005g0026a0002c0002t0005g0027 | 3 | HG01884.hp1 HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.728-1785A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72819169 | ||||||
| chr3:72819379
|
A | G | 1 | a0002c0002t0006g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.728-1995T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72819379 | ||||||
| chr3:72819408
|
T | C | 9 | a0002c0002t0001g0080a0002c0002t0001g0114a0002c0002t0001g0119others(6): Show | 9 | HG00438.hp1 HG00558.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.728-2024A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72819408 | ||||||
| chr3:72819515
|
G | C | 41 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(38): Show | 41 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.728-2131C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72819515 | ||||||
| chr3:72819727
|
T | C | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.728-2343A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72819727 | ||||||
| chr3:72819877
|
C | T | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.728-2493G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72819877 | ||||||
| chr3:72820229
|
C | G | 1 | a0002c0002t0008g0206 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.728-2845G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72820229 | ||||||
| chr3:72820229
|
C | T | 2 | a0002c0008t0001g0008a0002c0008t0001g0022 | 2 | HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.728-2845G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72820229 | ||||||
| chr3:72820256
|
C | G | 31 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0029others(28): Show | 31 | HG01978.hp2 HG02056.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.728-2872G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72820256 | ||||||
| chr3:72820315
|
T | C | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.728-2931A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72820315 | ||||||
| chr3:72820484
|
C | T | 4 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0004g0005others(1): Show | 4 | HG02451.hp1 HG02809.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.728-3100G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72820484 | ||||||
| chr3:72820565
|
G | A | 4 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0004g0005others(1): Show | 4 | HG02451.hp1 HG02809.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.728-3181C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72820565 | ||||||
| chr3:72820932
|
C | T | 4 | a0002c0002t0005g0025a0002c0002t0005g0026a0002c0002t0005g0027others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.727+3492G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72820932 | ||||||
| chr3:72821013
|
T | C | 18 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0042others(15): Show | 19 | HG00673.hp1 HG00741.hp1 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.727+3411A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72821013 | ||||||
| chr3:72821075
|
G | T | 2 | a0002c0002t0001g0144a0002c0002t0001g0146 | 2 | HG01978.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.727+3349C>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72821075 | ||||||
| chr3:72821091
|
A | T | 41 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(38): Show | 41 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.727+3333T>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72821091 | ||||||
| chr3:72821130
|
G | T | 4 | a0002c0002t0005g0025a0002c0002t0005g0026a0002c0002t0005g0027others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.727+3294C>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72821130 | ||||||
| chr3:72821200
|
T | C | 41 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(38): Show | 41 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.727+3224A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72821200 | ||||||
| chr3:72821263
|
T | C | 2 | a0008c0007t0001g0207a0008c0007t0001g0208 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.727+3161A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72821263 | ||||||
| chr3:72821357
|
G | A | 1 | a0002c0002t0001g0114 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.727+3067C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72821357 | ||||||
| chr3:72821625
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.727+2799G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72821625 | ||||||
| chr3:72821740
|
G | A | 2 | a0002c0002t0001g0204a0002c0002t0001g0205 | 2 | HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.727+2684C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72821740 | ||||||
| chr3:72821761
|
G | C | 2 | a0002c0002t0001g0023a0002c0002t0001g0024 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.727+2663C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72821761 | ||||||
| chr3:72821988
|
C | T | 1 | a0002c0002t0001g0204 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.727+2436G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72821988 | ||||||
| chr3:72822214
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.727+2210G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72822214 | ||||||
| chr3:72822240
|
G | A | 1 | a0001c0001t0001g0039 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.727+2184C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72822240 | ||||||
| chr3:72822301
|
A | T | 1 | a0002c0002t0001g0203 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.727+2123T>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72822301 | ||||||
| chr3:72822376
|
G | A | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.727+2048C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72822376 | ||||||
| chr3:72822404
|
T | C | 1 | a0002c0002t0001g0203 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.727+2020A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72822404 | ||||||
| chr3:72822486
|
T | C | 1 | a0001c0001t0007g0092 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.727+1938A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72822486 | ||||||
| chr3:72822514
|
C | A | 1 | a0003c0003t0001g0212 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.727+1910G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72822514 | ||||||
| chr3:72822581
|
C | T | 2 | a0008c0007t0001g0207a0008c0007t0001g0208 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.727+1843G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72822581 | ||||||
| chr3:72822603
|
C | T | 18 | a0002c0002t0001g0011a0002c0002t0001g0012a0002c0002t0001g0013others(15): Show | 18 | HG01243.hp2 HG01255.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.727+1821G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72822603 | ||||||
| chr3:72822622
|
C | T | 76 | a0002c0002t0001g0010a0002c0002t0001g0011a0002c0002t0001g0012others(73): Show | 76 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.727+1802G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72822622 | ||||||
| chr3:72822708
|
G | A | 4 | a0002c0002t0005g0025a0002c0002t0005g0026a0002c0002t0005g0027others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.727+1716C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72822708 | ||||||
| chr3:72822724
|
A | T | 3 | a0002c0002t0001g0191a0002c0002t0001g0192a0002c0002t0001g0197 | 3 | HG02895.hp1 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.727+1700T>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72822724 | ||||||
| chr3:72822776
|
A | T | 16 | a0001c0001t0001g0001a0001c0001t0001g0042a0001c0001t0001g0044others(13): Show | 17 | HG00673.hp1 HG00741.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.727+1648T>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72822776 | ||||||
| chr3:72822842
|
T | A | 1 | a0001c0001t0001g0058 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.727+1582A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72822842 | ||||||
| chr3:72822876
|
G | A | 1 | a0002c0002t0006g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.727+1548C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72822876 | ||||||
| chr3:72822877
|
C | T | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.727+1547G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72822877 | ||||||
| chr3:72822881
|
A | G | 1 | a0001c0001t0001g0060 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.727+1543T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72822881 | ||||||
| chr3:72823054
|
T | C | 4 | a0007c0009t0002g0220a0007c0009t0002g0221a0008c0007t0001g0207others(1): Show | 4 | HG02615.hp1 HG02717.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.727+1370A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72823054 | ||||||
| chr3:72823127
|
C | T | 1 | a0001c0001t0001g0059 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.727+1297G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72823127 | ||||||
| chr3:72823148
|
C | CAA | 5 | a0002c0002t0001g0014a0002c0002t0001g0015a0002c0002t0001g0016others(2): Show | 5 | HG01243.hp2 HG02258.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.727+1274_727+1275d others(4): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72823148 | ||||||
| chr3:72823148
|
CA | C | 46 | a0001c0001t0001g0072a0001c0001t0001g0164a0001c0001t0001g0187others(43): Show | 46 | HG00140.hp1 HG00558.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.727+1275delT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72823148 | ||||||
| chr3:72823305
|
T | C | 2 | a0008c0007t0001g0207a0008c0007t0001g0208 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.727+1119A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72823305 | ||||||
| chr3:72823311
|
G | C | 2 | a0002c0002t0001g0023a0002c0002t0001g0024 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.727+1113C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72823311 | ||||||
| chr3:72823416
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.727+1008G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72823416 | ||||||
| chr3:72823442
|
A | C | 1 | a0001c0001t0001g0060 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.727+982T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72823442 | ||||||
| chr3:72823596
|
T | C | 3 | a0001c0001t0001g0154a0002c0008t0001g0008a0002c0008t0001g0022 | 3 | HG02148.hp1 HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.727+828A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72823596 | ||||||
| chr3:72823684
|
T | C | 3 | a0002c0002t0001g0191a0002c0002t0001g0192a0002c0002t0001g0197 | 3 | HG02895.hp1 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.727+740A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72823684 | ||||||
| chr3:72823701
|
G | A | 74 | a0001c0001t0001g0149a0002c0002t0001g0011a0002c0002t0001g0012others(71): Show | 74 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.727+723C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72823701 | ||||||
| chr3:72823720
|
T | C | 2 | a0008c0007t0001g0207a0008c0007t0001g0208 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.727+704A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72823720 | ||||||
| chr3:72823722
|
T | C | 1 | a0003c0003t0001g0213 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.727+702A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72823722 | ||||||
| chr3:72823974
|
A | G | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.727+450T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72823974 | ||||||
| chr3:72824064
|
A | C | 8 | a0002c0002t0001g0011a0002c0002t0001g0012a0002c0002t0001g0013others(5): Show | 8 | HG01243.hp2 HG01255.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.727+360T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72824064 | ||||||
| chr3:72824252
|
C | T | 1 | a0002c0008t0001g0008 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.727+172G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 6/10 | chr3 | 72824252 | ||||||
| chr3:72824571
|
G | T | 1 | a0002c0002t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.600-20C>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72824571 | ||||||
| chr3:72824578
|
C | G | 5 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0083others(2): Show | 5 | HG00099.hp2 HG01346.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.600-27G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72824578 | ||||||
| chr3:72824658
|
A | G | 41 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(38): Show | 41 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.600-107T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72824658 | ||||||
| chr3:72824787
|
C | CT | 7 | a0002c0002t0001g0120a0002c0002t0001g0139a0002c0002t0001g0191others(4): Show | 7 | HG02055.hp1 HG02615.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.600-237dupA | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72824787 | ||||||
| chr3:72824787
|
C | CTT | 49 | a0002c0002t0001g0011a0002c0002t0001g0012a0002c0002t0001g0013others(46): Show | 49 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.600-238_600-237dup others(2): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72824787 | ||||||
| chr3:72824787
|
CT | C | 43 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0032others(40): Show | 43 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.600-237delA | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72824787 | ||||||
| chr3:72824803
|
T | A | 3 | a0003c0003t0001g0213a0003c0003t0001g0215a0003c0003t0001g0219 | 3 | HG02896.hp2 HG02965.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.600-252A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72824803 | ||||||
| chr3:72824803
|
T | TA | 7 | a0003c0003t0001g0210a0003c0003t0001g0211a0003c0003t0001g0212others(4): Show | 7 | HG02257.hp2 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.600-253dupT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72824803 | ||||||
| chr3:72824845
|
C | G | 1 | a0002c0002t0001g0122 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.600-294G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72824845 | ||||||
| chr3:72824858
|
G | A | 1 | a0002c0002t0001g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.600-307C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72824858 | ||||||
| chr3:72825184
|
G | A | 11 | a0002c0002t0001g0010a0003c0003t0001g0210a0003c0003t0001g0211others(8): Show | 11 | HG01175.hp2 HG02257.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.600-633C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72825184 | ||||||
| chr3:72825361
|
T | TAC | 30 | a0001c0001t0001g0009a0001c0001t0001g0042a0001c0001t0001g0046others(27): Show | 30 | HG00099.hp2 HG00438.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.600-812_600-811dup others(2): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72825361 | ||||||
| chr3:72825361
|
T | TACAC | 21 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0036others(18): Show | 21 | HG01884.hp2 HG01978.hp2 HG02622.hp2 others(18): Show |
intron_variant | MODIFIER | c.600-814_600-811dup others(4): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72825361 | ||||||
| chr3:72825361
|
T | TACACAC | 13 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0001g0087others(10): Show | 13 | HG01255.hp1 HG02055.hp2 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.600-816_600-811dup others(6): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72825361 | ||||||
| chr3:72825361
|
T | TACACACA others(1): Show |
9 | a0001c0001t0001g0039a0001c0001t0001g0058a0002c0002t0001g0014others(6): Show | 9 | HG01243.hp2 HG02258.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.600-818_600-811dup others(8): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72825361 | ||||||
| chr3:72825361
|
T | TACACACA others(3): Show |
3 | a0002c0002t0001g0015a0003c0003t0001g0214a0003c0003t0001g0218 | 3 | HG02257.hp2 HG02897.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.600-820_600-811dup others(10): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72825361 | ||||||
| chr3:72825361
|
T | TACACACA others(5): Show |
1 | a0002c0002t0001g0196 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.600-822_600-811dup others(12): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72825361 | ||||||
| chr3:72825361
|
T | TACACACA others(7): Show |
1 | a0003c0003t0001g0216 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.600-824_600-811dup others(14): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72825361 | ||||||
| chr3:72825361
|
T | TACACACA others(9): Show |
2 | a0003c0003t0001g0210a0003c0003t0001g0211 | 2 | HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.600-826_600-811dup others(16): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72825361 | ||||||
| chr3:72825361
|
T | TACACACA others(11): Show |
1 | a0003c0003t0001g0215 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.600-828_600-811dup others(18): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72825361 | ||||||
| chr3:72825361
|
T | TACACACA others(15): Show |
1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.600-832_600-811dup others(22): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72825361 | ||||||
| chr3:72825361
|
TAC | T | 30 | a0001c0001t0001g0076a0002c0002t0001g0113a0002c0002t0001g0114others(27): Show | 30 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.600-812_600-811del others(2): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72825361 | ||||||
| chr3:72825361
|
TACAC | T | 8 | a0001c0001t0001g0047a0001c0001t0001g0099a0002c0002t0001g0115others(5): Show | 8 | HG00735.hp1 HG01109.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.600-814_600-811del others(4): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72825361 | ||||||
| chr3:72825361
|
TACACAC | T | 2 | a0002c0002t0001g0140a0002c0002t0001g0141 | 2 | NA18969.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.600-816_600-811del others(6): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72825361 | ||||||
| chr3:72825361
|
TACACACA others(3): Show |
T | 1 | a0002c0002t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.600-820_600-811del others(10): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72825361 | ||||||
| chr3:72825399
|
C | CACACACA others(4): Show |
1 | a0003c0003t0001g0219 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.600-849_600-848ins others(11): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72825399 | ||||||
| chr3:72825402
|
T | C | 1 | a0002c0002t0001g0016 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.600-851A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72825402 | ||||||
| chr3:72825411
|
T | C | 1 | a0002c0002t0001g0196 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.600-860A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72825411 | ||||||
| chr3:72825611
|
C | T | 1 | a0002c0002t0008g0206 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.600-1060G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72825611 | ||||||
| chr3:72825628
|
T | G | 2 | a0002c0002t0001g0140a0002c0002t0001g0141 | 2 | NA18969.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.600-1077A>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72825628 | ||||||
| chr3:72825709
|
A | G | 2 | a0002c0002t0001g0204a0002c0002t0001g0205 | 2 | HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.600-1158T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72825709 | ||||||
| chr3:72825912
|
C | T | 1 | a0002c0002t0001g0203 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.600-1361G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72825912 | ||||||
| chr3:72826052
|
C | T | 1 | a0002c0002t0001g0127 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.600-1501G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72826052 | ||||||
| chr3:72826232
|
G | A | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.600-1681C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72826232 | ||||||
| chr3:72826246
|
G | C | 1 | a0001c0001t0001g0180 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.600-1695C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72826246 | ||||||
| chr3:72826299
|
A | C | 2 | a0002c0002t0001g0023a0002c0002t0001g0024 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.600-1748T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72826299 | ||||||
| chr3:72826483
|
C | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0175 | 2 | HG01433.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.600-1932G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72826483 | ||||||
| chr3:72826774
|
G | C | 1 | a0001c0001t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.600-2223C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72826774 | ||||||
| chr3:72826924
|
T | A | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.600-2373A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72826924 | ||||||
| chr3:72827020
|
G | C | 1 | a0003c0003t0001g0216 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.600-2469C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72827020 | ||||||
| chr3:72827064
|
C | T | 2 | a0002c0002t0001g0023a0002c0002t0001g0024 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.600-2513G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72827064 | ||||||
| chr3:72827086
|
T | A | 79 | a0002c0002t0001g0010a0002c0002t0001g0011a0002c0002t0001g0012others(76): Show | 79 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.600-2535A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72827086 | ||||||
| chr3:72827265
|
G | C | 1 | a0002c0002t0001g0017 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.600-2714C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72827265 | ||||||
| chr3:72827310
|
C | G | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.600-2759G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72827310 | ||||||
| chr3:72827431
|
T | C | 8 | a0002c0002t0001g0011a0002c0002t0001g0012a0002c0002t0001g0013others(5): Show | 8 | HG01243.hp2 HG01255.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.600-2880A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72827431 | ||||||
| chr3:72827461
|
T | G | 1 | a0002c0002t0001g0203 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.600-2910A>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72827461 | ||||||
| chr3:72827467
|
C | T | 2 | a0002c0002t0001g0023a0002c0002t0001g0024 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.600-2916G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72827467 | ||||||
| chr3:72827470
|
A | G | 1 | a0003c0003t0001g0217 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.600-2919T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72827470 | ||||||
| chr3:72827668
|
C | T | 12 | a0001c0001t0002g0190a0001c0001t0002g0194a0001c0001t0002g0195others(9): Show | 12 | HG01243.hp2 HG01255.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.600-3117G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72827668 | ||||||
| chr3:72827669
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.600-3118C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72827669 | ||||||
| chr3:72827707
|
A | C | 2 | a0008c0007t0001g0207a0008c0007t0001g0208 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.600-3156T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72827707 | ||||||
| chr3:72827753
|
C | CT | 42 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0188others(39): Show | 42 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.600-3203dupA | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72827753 | ||||||
| chr3:72827753
|
CT | C | 7 | a0001c0001t0001g0084a0001c0001t0001g0183a0002c0002t0001g0014others(4): Show | 7 | HG00099.hp2 HG01243.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.600-3203delA | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72827753 | ||||||
| chr3:72827779
|
G | C | 41 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(38): Show | 41 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.600-3228C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72827779 | ||||||
| chr3:72827815
|
C | T | 3 | a0002c0002t0005g0025a0002c0002t0005g0026a0002c0002t0005g0027 | 3 | HG01884.hp1 HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.600-3264G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72827815 | ||||||
| chr3:72827834
|
A | G | 12 | a0002c0002t0001g0011a0002c0002t0001g0012a0002c0002t0001g0013others(9): Show | 12 | HG01243.hp2 HG01255.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.600-3283T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72827834 | ||||||
| chr3:72827856
|
G | A | 1 | a0002c0002t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.600-3305C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72827856 | ||||||
| chr3:72828021
|
T | A | 3 | a0002c0002t0001g0191a0002c0002t0001g0192a0002c0002t0001g0197 | 3 | HG02895.hp1 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.600-3470A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72828021 | ||||||
| chr3:72828050
|
C | T | 1 | a0002c0002t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.600-3499G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72828050 | ||||||
| chr3:72828052
|
C | T | 1 | a0002c0002t0001g0010 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.600-3501G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72828052 | ||||||
| chr3:72828184
|
T | C | 12 | a0002c0002t0001g0011a0002c0002t0001g0012a0002c0002t0001g0013others(9): Show | 12 | HG01243.hp2 HG01255.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.600-3633A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72828184 | ||||||
| chr3:72828304
|
TGAGCCTA others(9): Show |
T | 3 | a0002c0002t0001g0119a0002c0002t0001g0122a0002c0002t0001g0126 | 3 | HG00438.hp1 HG00558.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.600-3769_600-3754d others(18): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72828304 | ||||||
| chr3:72828335
|
A | G | 2 | a0002c0002t0001g0140a0002c0002t0001g0141 | 2 | NA18969.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.600-3784T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72828335 | ||||||
| chr3:72828454
|
G | A | 41 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(38): Show | 41 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.600-3903C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72828454 | ||||||
| chr3:72828615
|
AC | A | 4 | a0007c0009t0002g0220a0007c0009t0002g0221a0008c0007t0001g0207others(1): Show | 4 | HG02615.hp1 HG02717.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.599+3753delG | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72828615 | ||||||
| chr3:72828620
|
G | A | 1 | a0006c0006t0001g0131 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.599+3749C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72828620 | ||||||
| chr3:72828650
|
G | A | 4 | a0002c0002t0001g0137a0005c0005t0001g0117a0005c0005t0001g0135others(1): Show | 4 | HG01952.hp2 HG02622.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.599+3719C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72828650 | ||||||
| chr3:72828673
|
C | T | 1 | a0002c0002t0001g0198 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.599+3696G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72828673 | ||||||
| chr3:72828793
|
A | G | 1 | a0005c0005t0001g0117 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.599+3576T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72828793 | ||||||
| chr3:72829049
|
A | C | 2 | a0002c0002t0001g0192a0002c0002t0001g0197 | 2 | HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.599+3320T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72829049 | ||||||
| chr3:72829083
|
T | C | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.599+3286A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72829083 | ||||||
| chr3:72829134
|
C | T | 4 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0164others(1): Show | 4 | HG01081.hp2 HG01256.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.599+3235G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72829134 | ||||||
| chr3:72829177
|
T | C | 4 | a0002c0002t0001g0191a0002c0002t0001g0192a0002c0002t0001g0196others(1): Show | 4 | HG02895.hp1 HG03209.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.599+3192A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72829177 | ||||||
| chr3:72829335
|
T | G | 2 | a0002c0002t0001g0023a0002c0002t0001g0024 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.599+3034A>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72829335 | ||||||
| chr3:72829389
|
A | G | 1 | a0002c0002t0001g0196 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.599+2980T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72829389 | ||||||
| chr3:72829481
|
T | C | 41 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(38): Show | 41 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.599+2888A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72829481 | ||||||
| chr3:72829584
|
G | C | 1 | a0002c0002t0001g0080 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.599+2785C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72829584 | ||||||
| chr3:72829608
|
G | A | 11 | a0002c0002t0001g0010a0003c0003t0001g0210a0003c0003t0001g0211others(8): Show | 11 | HG01175.hp2 HG02257.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.599+2761C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72829608 | ||||||
| chr3:72829733
|
C | T | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.599+2636G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72829733 | ||||||
| chr3:72829744
|
A | G | 4 | a0007c0009t0002g0220a0007c0009t0002g0221a0008c0007t0001g0207others(1): Show | 4 | HG02615.hp1 HG02717.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.599+2625T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72829744 | ||||||
| chr3:72829948
|
G | A | 83 | a0001c0001t0001g0019a0001c0001t0001g0020a0002c0002t0001g0010others(80): Show | 83 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.599+2421C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72829948 | ||||||
| chr3:72829969
|
A | G | 8 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0004g0005others(5): Show | 8 | HG01884.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.599+2400T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72829969 | ||||||
| chr3:72830033
|
G | A | 1 | a0002c0002t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.599+2336C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72830033 | ||||||
| chr3:72830055
|
C | G | 1 | a0001c0001t0001g0159 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.599+2314G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72830055 | ||||||
| chr3:72830071
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.599+2298A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72830071 | ||||||
| chr3:72830112
|
C | CA | 19 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0063others(16): Show | 19 | HG01255.hp1 HG02109.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.599+2256dupT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72830112 | ||||||
| chr3:72830112
|
CA | C | 6 | a0001c0001t0001g0094a0002c0002t0004g0003a0002c0002t0004g0004others(3): Show | 6 | HG00741.hp1 HG02451.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.599+2256delT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72830112 | ||||||
| chr3:72830374
|
TATACA | T | 3 | a0002c0002t0005g0025a0002c0002t0005g0026a0002c0002t0005g0027 | 3 | HG01884.hp1 HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.599+1990_599+1994d others(7): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72830374 | ||||||
| chr3:72830402
|
A | T | 3 | a0002c0002t0005g0025a0002c0002t0005g0026a0002c0002t0005g0027 | 3 | HG01884.hp1 HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.599+1967T>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72830402 | ||||||
| chr3:72830467
|
T | C | 1 | a0002c0002t0001g0203 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.599+1902A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72830467 | ||||||
| chr3:72830519
|
T | TA | 8 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0004g0005others(5): Show | 8 | HG01884.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.599+1849dupT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72830519 | ||||||
| chr3:72830608
|
TATAA | T | 2 | a0002c0002t0001g0023a0002c0002t0001g0024 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.599+1757_599+1760d others(6): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72830608 | ||||||
| chr3:72830614
|
T | C | 14 | a0001c0001t0001g0019a0001c0001t0001g0020a0002c0002t0001g0011others(11): Show | 14 | HG01243.hp2 HG01255.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.599+1755A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72830614 | ||||||
| chr3:72830621
|
T | TAGTA | 4 | a0007c0009t0002g0220a0007c0009t0002g0221a0008c0007t0001g0207others(1): Show | 4 | HG02615.hp1 HG02717.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.599+1744_599+1747d others(6): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72830621 | ||||||
| chr3:72830718
|
A | G | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.599+1651T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72830718 | ||||||
| chr3:72830756
|
T | C | 1 | a0002c0008t0001g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.599+1613A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72830756 | ||||||
| chr3:72831319
|
T | C | 10 | a0001c0001t0001g0019a0001c0001t0001g0020a0002c0002t0001g0011others(7): Show | 10 | HG01243.hp2 HG01255.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.599+1050A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72831319 | ||||||
| chr3:72831423
|
C | A | 1 | a0002c0002t0001g0010 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.599+946G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72831423 | ||||||
| chr3:72831508
|
C | T | 1 | a0002c0002t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.599+861G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72831508 | ||||||
| chr3:72831649
|
C | T | 4 | a0007c0009t0002g0220a0007c0009t0002g0221a0008c0007t0001g0207others(1): Show | 4 | HG02615.hp1 HG02717.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.599+720G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72831649 | ||||||
| chr3:72831847
|
A | C | 14 | a0001c0001t0001g0019a0001c0001t0001g0020a0002c0002t0001g0011others(11): Show | 14 | HG01243.hp2 HG01255.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.599+522T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72831847 | ||||||
| chr3:72831959
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.599+410A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72831959 | ||||||
| chr3:72832044
|
A | G | 4 | a0007c0009t0002g0220a0007c0009t0002g0221a0008c0007t0001g0207others(1): Show | 4 | HG02615.hp1 HG02717.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.599+325T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 5/10 | chr3 | 72832044 | ||||||
| chr3:72832537
|
A | G | 1 | a0002c0002t0001g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.487-56T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72832537 | ||||||
| chr3:72832665
|
T | A | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.487-184A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72832665 | ||||||
| chr3:72832848
|
T | C | 2 | a0002c0008t0001g0008a0002c0008t0001g0022 | 2 | HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.487-367A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72832848 | ||||||
| chr3:72832878
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.487-397C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72832878 | ||||||
| chr3:72832986
|
T | C | 2 | a0002c0002t0005g0025a0002c0002t0005g0027 | 2 | HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.487-505A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72832986 | ||||||
| chr3:72833057
|
G | A | 3 | a0002c0002t0005g0025a0002c0002t0005g0026a0002c0002t0005g0027 | 3 | HG01884.hp1 HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.487-576C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833057 | ||||||
| chr3:72833091
|
T | C | 3 | a0002c0002t0001g0203a0002c0008t0001g0008a0002c0008t0001g0022 | 3 | HG02055.hp2 HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.487-610A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833091 | ||||||
| chr3:72833339
|
G | A | 2 | a0008c0007t0001g0207a0008c0007t0001g0208 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.487-858C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833339 | ||||||
| chr3:72833359
|
T | G | 2 | a0008c0007t0001g0207a0008c0007t0001g0208 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.487-878A>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833359 | ||||||
| chr3:72833399
|
C | A | 5 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0004g0005others(2): Show | 5 | HG02451.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.487-918G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833399 | ||||||
| chr3:72833410
|
T | C | 81 | a0001c0001t0001g0019a0001c0001t0001g0020a0002c0002t0001g0010others(78): Show | 81 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.487-929A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833410 | ||||||
| chr3:72833415
|
T | C | 1 | a0001c0001t0001g0009 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.487-934A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833415 | ||||||
| chr3:72833419
|
C | T | 1 | a0002c0002t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.487-938G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833419 | ||||||
| chr3:72833444
|
TGATA | T | 5 | a0002c0002t0001g0012a0002c0002t0001g0017a0002c0002t0001g0132others(2): Show | 5 | HG02071.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.487-967_487-964del others(4): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833444 | ||||||
| chr3:72833444
|
TGATAGAT others(1): Show |
T | 22 | a0001c0001t0001g0019a0001c0001t0001g0020a0002c0002t0001g0013others(19): Show | 22 | HG00140.hp1 HG00558.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.487-971_487-964del others(8): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833444 | ||||||
| chr3:72833444
|
TGATAGAT others(5): Show |
T | 16 | a0002c0002t0001g0011a0002c0002t0001g0014a0002c0002t0001g0015others(13): Show | 16 | HG00735.hp2 HG01978.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.487-975_487-964del others(12): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833444 | ||||||
| chr3:72833444
|
TGATAGAT others(9): Show |
T | 9 | a0002c0002t0001g0021a0002c0002t0001g0119a0002c0002t0001g0120others(6): Show | 9 | HG00438.hp1 HG01109.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.487-979_487-964del others(16): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833444 | ||||||
| chr3:72833444
|
TGATAGAT others(13): Show |
T | 2 | a0001c0001t0002g0190a0003c0003t0001g0217 | 2 | HG02486.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.487-983_487-964del others(20): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833444 | ||||||
| chr3:72833444
|
TGATAGAT others(17): Show |
T | 1 | a0002c0002t0001g0133 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.487-987_487-964del others(24): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833444 | ||||||
| chr3:72833444
|
TGATAGAT others(21): Show |
T | 9 | a0002c0002t0001g0113a0002c0002t0004g0003a0002c0002t0004g0004others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.487-991_487-964del others(28): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833444 | ||||||
| chr3:72833479
|
TAGATAGA others(17): Show |
T | 4 | a0002c0002t0001g0023a0002c0002t0001g0024a0008c0007t0001g0207others(1): Show | 4 | HG02615.hp1 HG02717.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.487-1022_487-999de others(25): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833479 | ||||||
| chr3:72833483
|
TAGATAGA others(13): Show |
T | 3 | a0003c0003t0001g0210a0003c0003t0001g0211a0003c0003t0001g0216 | 3 | HG02630.hp1 HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.487-1022_487-1003d others(22): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833483 | ||||||
| chr3:72833483
|
TAGATAGA others(17): Show |
T | 3 | a0001c0001t0001g0088a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | HG01433.hp2 NA18957.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.487-1026_487-1003d others(26): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833483 | ||||||
| chr3:72833487
|
TAGATAGA others(9): Show |
T | 10 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0174others(7): Show | 10 | HG00738.hp2 HG01175.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.487-1022_487-1007d others(18): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833487 | ||||||
| chr3:72833487
|
TAGATAGA others(13): Show |
T | 17 | a0001c0001t0001g0029a0001c0001t0001g0035a0001c0001t0001g0047others(14): Show | 17 | HG00140.hp2 HG00738.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.487-1026_487-1007d others(22): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833487 | ||||||
| chr3:72833491
|
T | C | 1 | a0001c0001t0003g0033 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.487-1010A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833491 | ||||||
| chr3:72833491
|
TAGATAGA others(5): Show |
T | 20 | a0001c0001t0001g0001a0001c0001t0001g0041a0001c0001t0001g0059others(17): Show | 21 | HG00438.hp2 HG01081.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.487-1022_487-1011d others(14): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833491 | ||||||
| chr3:72833491
|
TAGATAGA others(9): Show |
T | 37 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(34): Show | 37 | HG00099.hp1 HG00558.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.487-1026_487-1011d others(18): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833491 | ||||||
| chr3:72833491
|
TAGATAGA others(13): Show |
T | 4 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0063others(1): Show | 4 | HG02976.hp2 HG03209.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.487-1030_487-1011d others(22): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833491 | ||||||
| chr3:72833495
|
T | C | 4 | a0001c0001t0001g0043a0001c0001t0003g0033a0002c0002t0001g0143others(1): Show | 4 | HG02723.hp2 HG03540.hp1 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.487-1014A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833495 | ||||||
| chr3:72833495
|
TAGATAGA others(1): Show |
T | 5 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0001g0084others(2): Show | 5 | HG00099.hp2 NA18945.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.487-1022_487-1015d others(10): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833495 | ||||||
| chr3:72833495
|
TAGATAGA others(5): Show |
T | 23 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0040others(20): Show | 23 | HG00642.hp1 HG01255.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.487-1026_487-1015d others(14): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833495 | ||||||
| chr3:72833495
|
TAGATAGA others(9): Show |
T | 3 | a0001c0001t0001g0009a0001c0001t0001g0065a0001c0001t0001g0085 | 3 | HG02109.hp1 HG03654.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.487-1030_487-1015d others(18): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833495 | ||||||
| chr3:72833499
|
T | C | 8 | a0001c0001t0001g0044a0001c0001t0001g0096a0001c0001t0001g0151others(5): Show | 8 | HG01081.hp2 HG01175.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.487-1018A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833499 | ||||||
| chr3:72833499
|
TAGAC | T | 4 | a0001c0001t0001g0058a0001c0001t0001g0095a0001c0001t0001g0185others(1): Show | 4 | HG01257.hp2 HG03540.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.487-1022_487-1019d others(6): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833499 | ||||||
| chr3:72833499
|
TAGACAGA others(1): Show |
T | 11 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(8): Show | 11 | HG00673.hp1 HG00673.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.487-1026_487-1019d others(10): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833499 | ||||||
| chr3:72833499
|
TAGACAGA others(5): Show |
T | 1 | a0001c0001t0001g0066 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.487-1030_487-1019d others(14): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833499 | ||||||
| chr3:72833503
|
C | T | 4 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0188others(1): Show | 4 | HG01175.hp1 HG02723.hp2 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.487-1022G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833503 | ||||||
| chr3:72833504
|
A | G | 2 | a0001c0001t0001g0043a0001c0001t0003g0033 | 2 | HG02723.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.487-1023T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833504 | ||||||
| chr3:72833506
|
A | G | 2 | a0001c0001t0002g0194a0001c0001t0002g0195 | 2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.487-1025T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833506 | ||||||
| chr3:72833506
|
AC | A | 2 | a0001c0001t0001g0043a0001c0001t0003g0033 | 2 | HG02723.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.487-1026delG | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833506 | ||||||
| chr3:72833507
|
C | T | 9 | a0001c0001t0001g0044a0001c0001t0001g0058a0001c0001t0001g0095others(6): Show | 9 | HG01081.hp2 HG01175.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.487-1026G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833507 | ||||||
| chr3:72833508
|
A | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0188 | 2 | HG01175.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.487-1027T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833508 | ||||||
| chr3:72833508
|
A | T | 2 | a0001c0001t0001g0043a0001c0001t0003g0033 | 2 | HG02723.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.487-1027T>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833508 | ||||||
| chr3:72833510
|
ACAGAC | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0188 | 2 | HG01175.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.487-1034_487-1030d others(7): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833510 | ||||||
| chr3:72833511
|
C | T | 6 | a0001c0001t0001g0043a0001c0001t0001g0096a0001c0001t0001g0150others(3): Show | 6 | HG01081.hp2 HG01346.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.487-1030G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833511 | ||||||
| chr3:72833512
|
A | G | 3 | a0001c0001t0001g0096a0001c0001t0001g0150a0001c0001t0001g0151 | 3 | HG01081.hp2 HG01346.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.487-1031T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833512 | ||||||
| chr3:72833514
|
AC | A | 3 | a0001c0001t0001g0096a0001c0001t0001g0150a0001c0001t0001g0151 | 3 | HG01081.hp2 HG01346.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.487-1034delG | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833514 | ||||||
| chr3:72833515
|
C | T | 5 | a0001c0001t0001g0042a0001c0001t0001g0180a0001c0001t0001g0181others(2): Show | 5 | HG02129.hp1 HG03516.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.487-1034G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833515 | ||||||
| chr3:72833516
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.487-1035T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833516 | ||||||
| chr3:72833516
|
A | T | 5 | a0001c0001t0001g0044a0001c0001t0001g0096a0001c0001t0001g0150others(2): Show | 5 | HG01081.hp2 HG01175.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.487-1035T>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833516 | ||||||
| chr3:72833519
|
T | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0085 | 2 | HG03654.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.487-1038A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833519 | ||||||
| chr3:72833520
|
A | G | 1 | a0001c0001t0001g0042 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.487-1039T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833520 | ||||||
| chr3:72833522
|
ATGG | A | 5 | a0001c0001t0001g0044a0001c0001t0001g0096a0001c0001t0001g0150others(2): Show | 5 | HG01081.hp2 HG01175.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.487-1044_487-1042d others(5): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833522 | ||||||
| chr3:72833523
|
TGGATGAT others(4): Show |
T | 2 | a0001c0001t0001g0043a0001c0001t0003g0033 | 2 | HG02723.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.487-1053_487-1043d others(13): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833523 | ||||||
| chr3:72833524
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.487-1043C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833524 | ||||||
| chr3:72833526
|
A | AC | 2 | a0001c0001t0001g0042a0001c0001t0001g0180 | 2 | HG04115.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.487-1046_487-1045i others(3): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833526 | ||||||
| chr3:72833526
|
A | C | 5 | a0001c0001t0001g0044a0001c0001t0001g0096a0001c0001t0001g0150others(2): Show | 5 | HG01081.hp2 HG01175.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.487-1045T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833526 | ||||||
| chr3:72833527
|
T | A | 7 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0096others(4): Show | 7 | HG01081.hp2 HG01175.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.487-1046A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833527 | ||||||
| chr3:72833534
|
C | CAGAT | 59 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0031others(56): Show | 60 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.487-1057_487-1054d others(6): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833534 | ||||||
| chr3:72833534
|
C | CAGATAGA others(1): Show |
4 | a0001c0001t0001g0020a0001c0001t0001g0090a0001c0001t0002g0194others(1): Show | 4 | HG01993.hp1 HG02055.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.487-1061_487-1054d others(10): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833534 | ||||||
| chr3:72833534
|
C | T | 8 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0095others(5): Show | 8 | HG01081.hp2 HG01175.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.487-1053G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833534 | ||||||
| chr3:72833534
|
CAGAT | C | 8 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(5): Show | 8 | HG00438.hp2 HG01071.hp2 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.487-1057_487-1054d others(6): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833534 | ||||||
| chr3:72833534
|
CAGATAGA others(1): Show |
C | 16 | a0002c0002t0001g0010a0002c0002t0001g0021a0002c0002t0001g0192others(13): Show | 16 | HG01175.hp2 HG02257.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.487-1061_487-1054d others(10): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833534 | ||||||
| chr3:72833534
|
CAGATAGA others(5): Show |
C | 48 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(45): Show | 48 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.487-1065_487-1054d others(14): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833534 | ||||||
| chr3:72833534
|
CAGATAGA others(9): Show |
C | 3 | a0002c0002t0001g0144a0002c0002t0001g0145a0002c0002t0001g0146 | 3 | HG01978.hp1 HG02148.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.487-1069_487-1054d others(18): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833534 | ||||||
| chr3:72833534
|
CAGATAGA others(13): Show |
C | 1 | a0002c0008t0001g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.487-1073_487-1054d others(22): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833534 | ||||||
| chr3:72833565
|
ATAGAT | A | 2 | a0002c0002t0001g0023a0002c0002t0001g0024 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.487-1089_487-1085d others(7): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833565 | ||||||
| chr3:72833572
|
G | T | 2 | a0002c0002t0001g0023a0002c0002t0001g0024 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.487-1091C>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833572 | ||||||
| chr3:72833573
|
A | T | 2 | a0002c0002t0001g0023a0002c0002t0001g0024 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.487-1092T>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833573 | ||||||
| chr3:72833574
|
A | T | 2 | a0002c0002t0001g0023a0002c0002t0001g0024 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.487-1093T>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833574 | ||||||
| chr3:72833582
|
G | A | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.487-1101C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833582 | ||||||
| chr3:72833627
|
A | C | 41 | a0002c0002t0001g0080a0002c0002t0001g0113a0002c0002t0001g0114others(38): Show | 41 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.487-1146T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833627 | ||||||
| chr3:72833632
|
C | T | 2 | a0002c0008t0001g0008a0002c0008t0001g0022 | 2 | HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.487-1151G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833632 | ||||||
| chr3:72833660
|
T | C | 1 | a0002c0002t0001g0203 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.487-1179A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833660 | ||||||
| chr3:72833682
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.487-1201T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72833682 | ||||||
| chr3:72834034
|
T | C | 5 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0004g0005others(2): Show | 5 | HG02451.hp1 HG02809.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.487-1553A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72834034 | ||||||
| chr3:72834067
|
T | C | 1 | a0002c0002t0001g0137 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.487-1586A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72834067 | ||||||
| chr3:72834079
|
T | C | 1 | a0002c0002t0001g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.487-1598A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72834079 | ||||||
| chr3:72834157
|
T | C | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.487-1676A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72834157 | ||||||
| chr3:72834258
|
G | A | 84 | a0001c0001t0001g0019a0001c0001t0001g0020a0002c0002t0001g0010others(81): Show | 84 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.487-1777C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72834258 | ||||||
| chr3:72834833
|
C | T | 1 | a0002c0002t0006g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.487-2352G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72834833 | ||||||
| chr3:72834847
|
T | C | 8 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0004g0005others(5): Show | 8 | HG01884.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.487-2366A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72834847 | ||||||
| chr3:72834894
|
A | G | 11 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0001g0036others(8): Show | 11 | HG01978.hp2 HG02056.hp2 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.487-2413T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72834894 | ||||||
| chr3:72834906
|
C | T | 1 | a0002c0002t0004g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.487-2425G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72834906 | ||||||
| chr3:72835028
|
T | C | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.487-2547A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72835028 | ||||||
| chr3:72835034
|
A | G | 5 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0200others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.487-2553T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72835034 | ||||||
| chr3:72835083
|
T | G | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.487-2602A>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72835083 | ||||||
| chr3:72835106
|
C | CT | 9 | a0001c0001t0001g0035a0002c0002t0001g0012a0002c0002t0001g0198others(6): Show | 9 | HG01884.hp2 HG02165.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.487-2626dupA | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72835106 | ||||||
| chr3:72835106
|
C | CTT | 9 | a0002c0002t0001g0199a0002c0002t0004g0003a0002c0002t0004g0004others(6): Show | 9 | HG01884.hp1 HG02451.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.487-2627_487-2626d others(4): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72835106 | ||||||
| chr3:72835106
|
CT | C | 7 | a0001c0001t0001g0081a0001c0001t0001g0086a0001c0001t0001g0109others(4): Show | 7 | HG00558.hp2 HG02622.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.487-2626delA | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72835106 | ||||||
| chr3:72835181
|
T | C | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.487-2700A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72835181 | ||||||
| chr3:72835260
|
T | G | 2 | a0008c0007t0001g0207a0008c0007t0001g0208 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.487-2779A>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72835260 | ||||||
| chr3:72835281
|
G | T | 2 | a0008c0007t0001g0207a0008c0007t0001g0208 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.487-2800C>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72835281 | ||||||
| chr3:72835344
|
G | A | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.487-2863C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72835344 | ||||||
| chr3:72835384
|
C | G | 1 | a0001c0001t0001g0181 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.487-2903G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72835384 | ||||||
| chr3:72835590
|
C | T | 1 | a0002c0002t0001g0137 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.487-3109G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72835590 | ||||||
| chr3:72835691
|
C | T | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.487-3210G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72835691 | ||||||
| chr3:72835744
|
A | G | 2 | a0008c0007t0001g0207a0008c0007t0001g0208 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.487-3263T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72835744 | ||||||
| chr3:72835813
|
G | A | 2 | a0008c0007t0001g0207a0008c0007t0001g0208 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.487-3332C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72835813 | ||||||
| chr3:72835896
|
T | C | 1 | a0002c0002t0001g0191 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.487-3415A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72835896 | ||||||
| chr3:72836118
|
A | G | 10 | a0001c0001t0001g0019a0001c0001t0001g0020a0002c0002t0001g0011others(7): Show | 10 | HG01243.hp2 HG01255.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.487-3637T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72836118 | ||||||
| chr3:72836221
|
G | A | 1 | a0002c0002t0001g0137 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.487-3740C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72836221 | ||||||
| chr3:72836224
|
T | A | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.487-3743A>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72836224 | ||||||
| chr3:72836347
|
G | C | 39 | a0001c0001t0001g0082a0002c0002t0001g0113a0002c0002t0001g0114others(36): Show | 39 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.487-3866C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72836347 | ||||||
| chr3:72836684
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.487-4203C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72836684 | ||||||
| chr3:72836848
|
T | C | 1 | a0002c0002t0001g0134 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.486+4197A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72836848 | ||||||
| chr3:72836910
|
G | C | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.486+4135C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72836910 | ||||||
| chr3:72837424
|
C | T | 3 | a0002c0002t0001g0011a0002c0002t0001g0012a0002c0002t0001g0013 | 3 | HG01255.hp1 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.486+3621G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72837424 | ||||||
| chr3:72837458
|
T | C | 1 | a0002c0002t0006g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.486+3587A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72837458 | ||||||
| chr3:72837571
|
A | G | 40 | a0002c0002t0001g0113a0002c0002t0001g0114a0002c0002t0001g0115others(37): Show | 40 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.486+3474T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72837571 | ||||||
| chr3:72837814
|
A | G | 40 | a0002c0002t0001g0113a0002c0002t0001g0114a0002c0002t0001g0115others(37): Show | 40 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.486+3231T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72837814 | ||||||
| chr3:72837929
|
C | G | 4 | a0007c0009t0002g0220a0007c0009t0002g0221a0008c0007t0001g0207others(1): Show | 4 | HG02615.hp1 HG02717.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.486+3116G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72837929 | ||||||
| chr3:72837947
|
G | C | 1 | a0001c0001t0001g0180 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.486+3098C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72837947 | ||||||
| chr3:72837957
|
G | C | 1 | a0002c0002t0001g0205 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.486+3088C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72837957 | ||||||
| chr3:72837963
|
T | TAA | 83 | a0001c0001t0001g0019a0001c0001t0001g0020a0002c0002t0001g0010others(80): Show | 83 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.486+3080_486+3081d others(4): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72837963 | ||||||
| chr3:72838005
|
C | A | 14 | a0001c0001t0001g0019a0001c0001t0001g0020a0002c0002t0001g0011others(11): Show | 14 | HG01243.hp2 HG01255.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.486+3040G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72838005 | ||||||
| chr3:72838045
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.486+3000A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72838045 | ||||||
| chr3:72838086
|
T | C | 1 | a0005c0005t0001g0135 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.486+2959A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72838086 | ||||||
| chr3:72838575
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.486+2470G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72838575 | ||||||
| chr3:72838858
|
T | C | 3 | a0002c0002t0001g0191a0002c0002t0001g0192a0002c0002t0001g0197 | 3 | HG02895.hp1 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.486+2187A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72838858 | ||||||
| chr3:72838951
|
T | TA | 12 | a0001c0001t0001g0009a0001c0001t0001g0083a0001c0001t0001g0084others(9): Show | 12 | HG00099.hp2 HG01346.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.486+2093dupT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72838951 | ||||||
| chr3:72838951
|
TA | T | 15 | a0002c0002t0001g0011a0002c0002t0001g0191a0002c0002t0005g0025others(12): Show | 15 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.486+2093delT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72838951 | ||||||
| chr3:72839089
|
G | C | 1 | a0002c0002t0006g0002 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.486+1956C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72839089 | ||||||
| chr3:72839197
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.486+1848T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72839197 | ||||||
| chr3:72839265
|
T | C | 5 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(2): Show | 5 | HG02572.hp1 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.486+1780A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72839265 | ||||||
| chr3:72839539
|
C | T | 40 | a0002c0002t0001g0113a0002c0002t0001g0114a0002c0002t0001g0115others(37): Show | 40 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.486+1506G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72839539 | ||||||
| chr3:72839708
|
G | A | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.486+1337C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72839708 | ||||||
| chr3:72839721
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.486+1324A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72839721 | ||||||
| chr3:72839836
|
C | A | 2 | a0002c0008t0001g0008a0002c0008t0001g0022 | 2 | HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.486+1209G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72839836 | ||||||
| chr3:72839936
|
A | G | 1 | a0002c0002t0001g0198 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.486+1109T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72839936 | ||||||
| chr3:72839996
|
G | A | 1 | a0002c0002t0001g0196 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486+1049C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72839996 | ||||||
| chr3:72840037
|
C | T | 1 | a0002c0002t0001g0114 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.486+1008G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72840037 | ||||||
| chr3:72840124
|
C | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0028others(81): Show | 85 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.486+921G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72840124 | ||||||
| chr3:72840223
|
G | GCCTGGGC others(2): Show |
10 | a0001c0001t0001g0019a0001c0001t0001g0020a0002c0002t0001g0011others(7): Show | 10 | HG01243.hp2 HG01255.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.486+821_486+822ins others(9): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72840223 | ||||||
| chr3:72840226
|
A | G | 10 | a0001c0001t0001g0019a0001c0001t0001g0020a0002c0002t0001g0011others(7): Show | 10 | HG01243.hp2 HG01255.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.486+819T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72840226 | ||||||
| chr3:72840229
|
T | C | 10 | a0001c0001t0001g0019a0001c0001t0001g0020a0002c0002t0001g0011others(7): Show | 10 | HG01243.hp2 HG01255.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.486+816A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72840229 | ||||||
| chr3:72840237
|
T | C | 10 | a0001c0001t0001g0019a0001c0001t0001g0020a0002c0002t0001g0011others(7): Show | 10 | HG01243.hp2 HG01255.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.486+808A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72840237 | ||||||
| chr3:72840240
|
CT | C | 10 | a0001c0001t0001g0019a0001c0001t0001g0020a0002c0002t0001g0011others(7): Show | 10 | HG01243.hp2 HG01255.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.486+804delA | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72840240 | ||||||
| chr3:72840242
|
T | TA | 5 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0094others(2): Show | 5 | HG00735.hp1 HG00741.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.486+802dupT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72840242 | ||||||
| chr3:72840242
|
TA | T | 15 | a0001c0001t0001g0108a0001c0001t0001g0148a0001c0001t0003g0033others(12): Show | 15 | HG01884.hp2 HG01993.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.486+802delT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72840242 | ||||||
| chr3:72840242
|
TAA | T | 62 | a0002c0002t0001g0010a0002c0002t0001g0021a0002c0002t0001g0113others(59): Show | 62 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.486+801_486+802del others(2): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72840242 | ||||||
| chr3:72840243
|
A | C | 10 | a0001c0001t0001g0019a0001c0001t0001g0020a0002c0002t0001g0011others(7): Show | 10 | HG01243.hp2 HG01255.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.486+802T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72840243 | ||||||
| chr3:72840265
|
A | G | 10 | a0001c0001t0001g0019a0001c0001t0001g0020a0002c0002t0001g0011others(7): Show | 10 | HG01243.hp2 HG01255.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.486+780T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72840265 | ||||||
| chr3:72840399
|
T | C | 1 | a0002c0002t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.486+646A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72840399 | ||||||
| chr3:72840504
|
C | T | 1 | a0002c0002t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.486+541G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72840504 | ||||||
| chr3:72840505
|
G | A | 1 | a0002c0002t0001g0137 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.486+540C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72840505 | ||||||
| chr3:72840560
|
CA | C | 78 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0032others(75): Show | 78 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.486+484delT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72840560 | ||||||
| chr3:72840576
|
A | G | 4 | a0007c0009t0002g0220a0007c0009t0002g0221a0008c0007t0001g0207others(1): Show | 4 | HG02615.hp1 HG02717.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.486+469T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72840576 | ||||||
| chr3:72840684
|
G | C | 2 | a0008c0007t0001g0207a0008c0007t0001g0208 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.486+361C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72840684 | ||||||
| chr3:72840717
|
C | T | 3 | a0002c0002t0001g0011a0002c0002t0001g0012a0002c0002t0001g0013 | 3 | HG01255.hp1 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.486+328G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72840717 | ||||||
| chr3:72840793
|
T | C | 1 | a0002c0002t0001g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.486+252A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 4/10 | chr3 | 72840793 | ||||||
| chr3:72841331
|
T | C | 5 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0200others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.332-132A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 3/10 | chr3 | 72841331 | ||||||
| chr3:72841479
|
C | T | 5 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0200others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.332-280G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 3/10 | chr3 | 72841479 | ||||||
| chr3:72841512
|
T | C | 1 | a0002c0002t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.332-313A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 3/10 | chr3 | 72841512 | ||||||
| chr3:72841627
|
C | T | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.332-428G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 3/10 | chr3 | 72841627 | ||||||
| chr3:72841783
|
T | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0028others(94): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.331+497A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 3/10 | chr3 | 72841783 | ||||||
| chr3:72841808
|
C | T | 1 | a0002c0002t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.331+472G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 3/10 | chr3 | 72841808 | ||||||
| chr3:72841902
|
G | A | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.331+378C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 3/10 | chr3 | 72841902 | ||||||
| chr3:72841934
|
C | T | 10 | a0003c0003t0001g0210a0003c0003t0001g0211a0003c0003t0001g0212others(7): Show | 10 | HG02257.hp2 HG02630.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.331+346G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 3/10 | chr3 | 72841934 | ||||||
| chr3:72842002
|
C | A | 1 | a0002c0002t0001g0203 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.331+278G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 3/10 | chr3 | 72842002 | ||||||
| chr3:72842014
|
G | T | 1 | a0002c0002t0001g0113 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.331+266C>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 3/10 | chr3 | 72842014 | ||||||
| chr3:72842506
|
A | C | 1 | a0001c0001t0001g0031 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.209-104T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72842506 | ||||||
| chr3:72842531
|
C | G | 2 | a0002c0002t0001g0023a0002c0002t0001g0024 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.209-129G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72842531 | ||||||
| chr3:72842563
|
T | C | 2 | a0002c0002t0001g0140a0002c0002t0001g0141 | 2 | NA18969.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.209-161A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72842563 | ||||||
| chr3:72842585
|
A | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0019others(134): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.209-183T>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72842585 | ||||||
| chr3:72842614
|
T | C | 5 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(2): Show | 5 | HG02071.hp2 NA18967.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-212A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72842614 | ||||||
| chr3:72842669
|
A | G | 10 | a0001c0001t0001g0019a0001c0001t0001g0020a0002c0002t0001g0011others(7): Show | 10 | HG01243.hp2 HG01255.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.209-267T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72842669 | ||||||
| chr3:72842673
|
T | C | 119 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0028others(116): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.209-271A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72842673 | ||||||
| chr3:72842700
|
C | A | 2 | a0002c0002t0001g0023a0002c0002t0001g0024 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.209-298G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72842700 | ||||||
| chr3:72842711
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.209-309A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72842711 | ||||||
| chr3:72842771
|
T | C | 8 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0004g0005others(5): Show | 8 | HG01884.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.209-369A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72842771 | ||||||
| chr3:72842777
|
T | C | 2 | a0002c0008t0001g0008a0002c0008t0001g0022 | 2 | HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.209-375A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72842777 | ||||||
| chr3:72842834
|
G | A | 10 | a0001c0001t0001g0019a0001c0001t0001g0020a0002c0002t0001g0011others(7): Show | 10 | HG01243.hp2 HG01255.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.209-432C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72842834 | ||||||
| chr3:72842838
|
G | C | 1 | a0002c0002t0001g0010 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.209-436C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72842838 | ||||||
| chr3:72842843
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.209-441T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72842843 | ||||||
| chr3:72842876
|
C | T | 2 | a0008c0007t0001g0207a0008c0007t0001g0208 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.209-474G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72842876 | ||||||
| chr3:72842879
|
T | C | 1 | a0002c0002t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.209-477A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72842879 | ||||||
| chr3:72842968
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.209-566A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72842968 | ||||||
| chr3:72843031
|
C | T | 1 | a0002c0002t0001g0196 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.209-629G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72843031 | ||||||
| chr3:72843076
|
C | CA | 10 | a0001c0001t0001g0091a0001c0001t0001g0100a0001c0001t0001g0188others(7): Show | 10 | HG00140.hp2 HG01109.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.209-675dupT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72843076 | ||||||
| chr3:72843076
|
C | CAA | 5 | a0002c0002t0004g0003a0002c0002t0004g0004a0002c0002t0004g0005others(2): Show | 5 | HG02451.hp1 HG02559.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.209-676_209-675dup others(2): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72843076 | ||||||
| chr3:72843210
|
T | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0028others(94): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.209-808A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72843210 | ||||||
| chr3:72843380
|
G | C | 10 | a0001c0001t0001g0019a0001c0001t0001g0020a0002c0002t0001g0011others(7): Show | 10 | HG01243.hp2 HG01255.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.209-978C>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72843380 | ||||||
| chr3:72843403
|
A | G | 2 | a0007c0009t0002g0220a0007c0009t0002g0221 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.208+956T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72843403 | ||||||
| chr3:72843443
|
C | G | 1 | a0002c0002t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.208+916G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72843443 | ||||||
| chr3:72843635
|
C | A | 2 | a0002c0002t0001g0023a0002c0002t0001g0024 | 2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.208+724G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72843635 | ||||||
| chr3:72843688
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.208+671A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72843688 | ||||||
| chr3:72843752
|
C | CA | 11 | a0002c0002t0001g0010a0003c0003t0001g0210a0003c0003t0001g0211others(8): Show | 11 | HG01175.hp2 HG02257.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.208+606dupT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72843752 | ||||||
| chr3:72843834
|
G | T | 1 | a0001c0001t0001g0029 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.208+525C>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72843834 | ||||||
| chr3:72843837
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0028others(91): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.208+522C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72843837 | ||||||
| chr3:72843986
|
G | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0019others(134): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.208+373C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72843986 | ||||||
| chr3:72844160
|
T | C | 1 | a0002c0002t0001g0203 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.208+199A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72844160 | ||||||
| chr3:72844176
|
A | C | 1 | a0003c0003t0001g0217 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.208+183T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72844176 | ||||||
| chr3:72844176
|
A | T | 9 | a0003c0003t0001g0210a0003c0003t0001g0211a0003c0003t0001g0212others(6): Show | 9 | HG02257.hp2 HG02630.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.208+183T>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72844176 | ||||||
| chr3:72844203
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.208+156T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 2/10 | chr3 | 72844203 | ||||||
| chr3:72844693
|
C | T | 10 | a0003c0003t0001g0210a0003c0003t0001g0211a0003c0003t0001g0212others(7): Show | 10 | HG02257.hp2 HG02630.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.144-270G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72844693 | ||||||
| chr3:72844702
|
T | C | 1 | a0002c0002t0001g0196 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.144-279A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72844702 | ||||||
| chr3:72844965
|
C | G | 1 | a0002c0002t0001g0203 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.144-542G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72844965 | ||||||
| chr3:72845112
|
TA | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0028others(96): Show | 100 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.144-690delT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72845112 | ||||||
| chr3:72845233
|
T | C | 2 | a0003c0003t0001g0218a0003c0003t0001g0219 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.144-810A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72845233 | ||||||
| chr3:72845331
|
A | C | 5 | a0002c0002t0001g0021a0007c0009t0002g0220a0007c0009t0002g0221others(2): Show | 5 | HG02615.hp1 HG02717.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.144-908T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72845331 | ||||||
| chr3:72845412
|
A | G | 5 | a0002c0002t0001g0021a0007c0009t0002g0220a0007c0009t0002g0221others(2): Show | 5 | HG02615.hp1 HG02717.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.144-989T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72845412 | ||||||
| chr3:72845485
|
C | CA | 10 | a0001c0001t0001g0019a0001c0001t0001g0094a0002c0002t0001g0011others(7): Show | 10 | HG00741.hp1 HG01243.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.144-1063dupT | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72845485 | ||||||
| chr3:72845584
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.144-1161T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72845584 | ||||||
| chr3:72845599
|
T | C | 3 | a0002c0002t0001g0144a0002c0002t0001g0145a0002c0002t0001g0146 | 3 | HG01978.hp1 HG02148.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.144-1176A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72845599 | ||||||
| chr3:72845838
|
T | C | 1 | a0002c0002t0001g0197 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.144-1415A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72845838 | ||||||
| chr3:72846053
|
C | T | 1 | a0002c0002t0001g0021 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.144-1630G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72846053 | ||||||
| chr3:72846194
|
G | T | 58 | a0001c0001t0001g0019a0001c0001t0001g0020a0002c0002t0001g0011others(55): Show | 58 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.144-1771C>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72846194 | ||||||
| chr3:72846298
|
CT | C | 9 | a0001c0001t0001g0020a0001c0001t0001g0095a0001c0001t0001g0096others(6): Show | 9 | HG00735.hp1 HG01255.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.144-1876delA | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72846298 | ||||||
| chr3:72846317
|
G | A | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.143+1881C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72846317 | ||||||
| chr3:72846319
|
C | A | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.143+1879G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72846319 | ||||||
| chr3:72846534
|
G | A | 6 | a0002c0002t0001g0198a0002c0002t0001g0199a0002c0002t0001g0200others(3): Show | 6 | HG01884.hp2 HG02486.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.143+1664C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72846534 | ||||||
| chr3:72846550
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.143+1648C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72846550 | ||||||
| chr3:72846623
|
C | T | 1 | a0001c0001t0002g0190 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.143+1575G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72846623 | ||||||
| chr3:72846667
|
C | A | 95 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0028others(92): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.143+1531G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72846667 | ||||||
| chr3:72846891
|
T | C | 5 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(2): Show | 5 | HG02572.hp1 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.143+1307A>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72846891 | ||||||
| chr3:72847027
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | NA18951.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.143+1171G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72847027 | ||||||
| chr3:72847225
|
A | C | 10 | a0001c0001t0001g0019a0001c0001t0001g0020a0002c0002t0001g0011others(7): Show | 10 | HG01243.hp2 HG01255.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.143+973T>G | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72847225 | ||||||
| chr3:72847333
|
C | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0019others(133): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.143+865G>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72847333 | ||||||
| chr3:72847404
|
C | A | 3 | a0002c0002t0001g0209a0008c0007t0001g0207a0008c0007t0001g0208 | 3 | HG02615.hp1 HG02717.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.143+794G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72847404 | ||||||
| chr3:72847453
|
C | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0019others(129): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.143+745G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72847453 | ||||||
| chr3:72847456
|
CAA | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0019others(117): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.143+740_143+741del others(2): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72847456 | ||||||
| chr3:72847572
|
A | G | 1 | a0002c0002t0001g0010 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.143+626T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72847572 | ||||||
| chr3:72847590
|
C | A | 1 | a0005c0005t0001g0189 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.143+608G>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72847590 | ||||||
| chr3:72847590
|
CAG | C | 14 | a0001c0001t0001g0193a0001c0001t0002g0190a0001c0001t0002g0194others(11): Show | 14 | HG01884.hp2 HG02257.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.143+606_143+607del others(2): Show |
SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72847590 | ||||||
| chr3:72847641
|
A | G | 1 | a0001c0001t0001g0009 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.143+557T>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72847641 | ||||||
| chr3:72847691
|
G | A | 1 | a0002c0008t0001g0008 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.143+507C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72847691 | ||||||
| chr3:72847698
|
G | A | 1 | a0002c0002t0001g0203 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.143+500C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72847698 | ||||||
| chr3:72847729
|
T | G | 2 | a0002c0002t0001g0204a0002c0002t0001g0205 | 2 | HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.143+469A>C | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72847729 | ||||||
| chr3:72847845
|
G | T | 15 | a0002c0002t0001g0209a0003c0003t0001g0210a0003c0003t0001g0211others(12): Show | 15 | HG02257.hp2 HG02615.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.143+353C>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72847845 | ||||||
| chr3:72847863
|
G | T | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.143+335C>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72847863 | ||||||
| chr3:72847896
|
G | A | 1 | a0002c0002t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.143+302C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72847896 | ||||||
| chr3:72848062
|
G | A | 1 | a0002c0002t0008g0206 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.143+136C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72848062 | ||||||
| chr3:72848139
|
C | T | 1 | a0002c0008t0001g0008 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.143+59G>A | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72848139 | ||||||
| chr3:72848177
|
G | A | 3 | a0002c0002t0001g0209a0008c0007t0001g0207a0008c0007t0001g0208 | 3 | HG02615.hp1 HG02717.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.143+21C>T | SHQ1 | ENSG00000144736.14 | transcript | ENST00000325599.13 | protein_coding | 1/10 | chr3 | 72848177 |