Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 549 |
|---|---|
| ensemblid | ENSG00000148090.12 |
| hgncid | 890 |
| symbol | AUH |
| name | AU RNA binding methylglutaconyl-CoA hydratase |
| refseq_nuc | NM_001698.3 |
| refseq_prot | NP_001689.1 |
| ensembl_nuc | ENST00000375731.9 |
| ensembl_prot | ENSP00000364883.5 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 91213823 |
| end | 91361918 |
| strand | - |
| ver | v1.2 |
| region | chr9:91213823-91361918 |
| region5000 | chr9:91208823-91366918 |
| regionname0 | AUH_chr9_91213823_91361918 |
| regionname5000 | AUH_chr9_91208823_91366918 |
| 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 | 339 | 351 | 77 | 59 | 170 | 6 | 37 | 132 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| a0002 | 0/0 | 339 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| a0003 | 0/0 | 339 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| a0004 | 0/0 | 339 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| a0005 | 0/0 | 339 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| 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 | 1020 | 317 | 61 | 52 | 163 | 6 | 33 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| c0002 | 0/0 | 1020 | 31 | 15 | 6 | 7 | 0 | 3 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| c0003 | 0/0 | 1020 | 3 | 3 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| c0004 | 0/0 | 1020 | 2 | 0 | 1 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| c0005 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| c0006 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| c0007 | 0/0 | 1020 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| c0008 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| c0009 | 0/0 | 1020 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| 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 | 555 | 352 | 77 | 60 | 169 | 6 | 38 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| t0002 | 0/0 | 555 | 4 | 4 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| t0003 | 0/0 | 555 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| t0004 | 0/0 | 555 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0122 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0162 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0344 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| 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 | 1020 | 317 | 61 | 52 | 163 | 6 | 33 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| a0001c0002 | 0/0 | 1020 | 31 | 15 | 6 | 7 | 0 | 3 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| a0001c0006 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| a0001c0007 | 0/0 | 1020 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| a0001c0009 | 0/0 | 1020 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| a0002c0003 | 0/0 | 1020 | 3 | 3 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| a0003c0004 | 0/0 | 1020 | 2 | 0 | 1 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| a0004c0008 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| a0005c0005 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1574 | 316 | 61 | 52 | 162 | 6 | 33 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| a0001c0001t0003 | 0/0 | 1574 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| a0001c0002t0001 | 0/0 | 1574 | 26 | 10 | 6 | 7 | 0 | 3 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| a0001c0002t0002 | 0/0 | 1574 | 4 | 4 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| a0001c0002t0004 | 0/0 | 1574 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| a0001c0006t0001 | 0/0 | 1574 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| a0001c0007t0001 | 0/0 | 1574 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| a0001c0009t0001 | 0/0 | 1574 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| a0002c0003t0001 | 0/0 | 1574 | 3 | 3 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| a0003c0004t0001 | 0/0 | 1574 | 2 | 0 | 1 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| a0004c0008t0001 | 0/0 | 1574 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| a0005c0005t0001 | 0/0 | 1574 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | copy fasta | chr9 | 91208823 | 91366918 |
| 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 | 0 | 0 | 2 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0122 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0162 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0002t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0002t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0002t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0002t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0002t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0002t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0002t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0006t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0007t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0001c0009t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0002c0003t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0002c0003t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0002c0003t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0003c0004t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0003c0004t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0004c0008t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| a0005c0005t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0159 | EUR | FIN | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0344 | EUR | FIN | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | CHS | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | CHS | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | CHS | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0341 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0270 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | CHS | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG00735 | hp1 | a0003 | c0004 | t0001 | g0199 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0267 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0016 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0271 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0345 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0269 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01433 | hp2 | a0001 | c0009 | t0001 | g0347 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PEL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | PEL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0265 | AMR | PEL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0328 | AMR | PEL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | KHV | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | KHV | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CDX | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CDX | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | CDX | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CDX | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | PEL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02451 | hp2 | a0002 | c0003 | t0001 | g0014 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0258 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0343 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0115 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0342 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0255 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02976 | hp2 | a0005 | c0005 | t0001 | g0012 | AFR | ESN | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0272 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0264 | AFR | MSL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | MSL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0257 | AFR | ESN | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0263 | AFR | MSL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0274 | AFR | MSL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03239 | hp2 | a0001 | c0007 | t0001 | g0225 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0256 | AFR | MSL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ESN | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0260 | AFR | ESN | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0275 | AFR | MSL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0273 | SAS | STU | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | STU | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03704 | hp2 | a0003 | c0004 | t0001 | g0198 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0324 | SAS | BEB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0346 | SAS | BEB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | BEB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | STU | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0302 | SAS | STU | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | STU | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | STU | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | STU | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0266 | SAS | STU | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | STU | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | STU | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18522 | hp1 | a0001 | c0002 | t0004 | g0276 | AFR | YRI | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | YRI | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CHB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | YRI | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0261 | AFR | YRI | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0338 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0336 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18987 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0339 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0337 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0259 | AFR | LWK | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19030 | hp2 | a0001 | c0006 | t0001 | g0291 | AFR | LWK | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19043 | hp1 | a0002 | c0003 | t0001 | g0015 | AFR | LWK | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | LWK | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA19240 | hp2 | a0004 | c0008 | t0001 | g0099 | AFR | YRI | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0248 | EUR | TSI | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | TSI | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0294 | EUR | TSI | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | TSI | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | GIH | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | GIH | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0152 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0262 | AFR | MSL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG03471 | hp2 | a0002 | c0003 | t0001 | g0013 | AFR | MSL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | USA | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | USA | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | USA | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | LWK | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0122 | REF | REF | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0162 | REF | REF | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:91220986
|
G | A | 1 | a0004 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.662C>T | p.Thr221Ile | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/10 | 691/1574 | 662/1020 | 221/339 | chr9 | 91220986 | ||
| chr9:91355920
|
T | C | 1 | a0003 | 2 | HG00735.hp1 HG03704.hp2 |
missense_variant | MODERATE | c.381A>G | p.Ile127Met | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/10 | 410/1574 | 381/1020 | 127/339 | chr9 | 91355920 | ||
| chr9:91361708
|
G | T | 1 | a0002 | 3 | HG02451.hp2 HG03471.hp2 NA19043.hp1 |
missense_variant | MODERATE | c.182C>A | p.Pro61His | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/10 | 211/1574 | 182/1020 | 61/339 | chr9 | 91361708 | ||
| chr9:91361813
|
C | T | 1 | a0005 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.77G>A | p.Cys26Tyr | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/10 | 106/1574 | 77/1020 | 26/339 | chr9 | 91361813 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:91216074
|
T | C | 1 | a0001c0006 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.927A>G | p.Glu309Glu | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 9/10 | 956/1574 | 927/1020 | 309/339 | chr9 | 91216074 | ||
| chr9:91220910
|
T | C | 1 | a0001c0007 | 1 | HG03239.hp2 | synonymous_variant | LOW | c.738A>G | p.Lys246Lys | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/10 | 767/1574 | 738/1020 | 246/339 | chr9 | 91220910 | ||
| chr9:91325340
|
T | G | 1 | a0001c0002 | 31 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(28): Show |
synonymous_variant | LOW | c.483A>C | p.Ile161Ile | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/10 | 512/1574 | 483/1020 | 161/339 | chr9 | 91325340 | ||
| chr9:91361848
|
G | A | 1 | a0001c0009 | 1 | HG01433.hp2 | synonymous_variant | LOW | c.42C>T | p.Ser14Ser | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/10 | 71/1574 | 42/1020 | 14/339 | chr9 | 91361848 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:91214148
|
T | C | 1 | a0001c0002t0004 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*200A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 10/10 | 200 | chr9 | 91214148 | |||||
| chr9:91214241
|
T | C | 1 | a0001c0002t0002 | 4 | HG02896.hp1 HG03139.hp1 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*107A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 10/10 | 107 | chr9 | 91214241 | |||||
| chr9:91214245
|
C | G | 1 | a0001c0001t0003 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*103G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 10/10 | 103 | chr9 | 91214245 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:91214528
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.943-103A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 9/9 | chr9 | 91214528 | ||||||
| chr9:91214646
|
GTTA | G | 10 | a0001c0001t0001g0120a0001c0001t0001g0277a0001c0001t0001g0278others(7): Show | 10 | HG02257.hp1 HG02818.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.943-224_943-222del others(3): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 9/9 | chr9 | 91214646 | ||||||
| chr9:91214931
|
C | A | 8 | a0001c0001t0001g0017a0001c0001t0001g0282a0001c0001t0001g0283others(5): Show | 8 | HG00597.hp2 HG00609.hp1 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.943-506G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 9/9 | chr9 | 91214931 | ||||||
| chr9:91215043
|
A | G | 34 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0066others(31): Show | 36 | HG00408.hp2 HG00609.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.943-618T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 9/9 | chr9 | 91215043 | ||||||
| chr9:91215071
|
C | G | 1 | a0001c0001t0001g0120 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.943-646G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 9/9 | chr9 | 91215071 | ||||||
| chr9:91215181
|
A | G | 2 | a0003c0004t0001g0198a0003c0004t0001g0199 | 2 | HG00735.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.943-756T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 9/9 | chr9 | 91215181 | ||||||
| chr9:91215359
|
T | C | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.942+700A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 9/9 | chr9 | 91215359 | ||||||
| chr9:91215391
|
G | C | 10 | a0001c0001t0001g0120a0001c0001t0001g0277a0001c0001t0001g0278others(7): Show | 10 | HG02257.hp1 HG02818.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.942+668C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 9/9 | chr9 | 91215391 | ||||||
| chr9:91215417
|
T | C | 1 | a0001c0001t0001g0030 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.942+642A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 9/9 | chr9 | 91215417 | ||||||
| chr9:91215664
|
C | T | 1 | a0001c0001t0001g0345 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.942+395G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 9/9 | chr9 | 91215664 | ||||||
| chr9:91215824
|
T | C | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.942+235A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 9/9 | chr9 | 91215824 | ||||||
| chr9:91215948
|
T | C | 1 | a0001c0001t0001g0030 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.942+111A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 9/9 | chr9 | 91215948 | ||||||
| chr9:91216162
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.895-56T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 8/9 | chr9 | 91216162 | ||||||
| chr9:91216362
|
G | C | 1 | a0001c0001t0001g0136 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.895-256C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 8/9 | chr9 | 91216362 | ||||||
| chr9:91216439
|
G | GAC | 53 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0058others(50): Show | 54 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.895-335_895-334dup others(2): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 8/9 | chr9 | 91216439 | ||||||
| chr9:91216439
|
G | GACAC | 32 | a0001c0001t0001g0008a0001c0001t0001g0067a0001c0001t0001g0068others(29): Show | 33 | HG00408.hp2 HG00609.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.895-337_895-334dup others(4): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 8/9 | chr9 | 91216439 | ||||||
| chr9:91216439
|
G | GACACAC | 7 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0066others(4): Show | 9 | HG01952.hp2 HG01978.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.895-339_895-334dup others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 8/9 | chr9 | 91216439 | ||||||
| chr9:91216439
|
GAC | G | 13 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(10): Show | 13 | HG02257.hp1 HG02818.hp2 HG02976.hp2 others(10): Show |
intron_variant | MODIFIER | c.895-335_895-334del others(2): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 8/9 | chr9 | 91216439 | ||||||
| chr9:91216439
|
GACACAC | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(78): Show | 83 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.895-339_895-334del others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 8/9 | chr9 | 91216439 | ||||||
| chr9:91216464
|
G | A | 2 | a0001c0001t0001g0297a0001c0001t0001g0323 | 2 | HG01081.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.895-358C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 8/9 | chr9 | 91216464 | ||||||
| chr9:91216528
|
A | T | 1 | a0001c0001t0001g0332 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.895-422T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 8/9 | chr9 | 91216528 | ||||||
| chr9:91216529
|
T | A | 1 | a0001c0001t0001g0332 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.895-423A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 8/9 | chr9 | 91216529 | ||||||
| chr9:91216530
|
A | T | 1 | a0001c0001t0001g0332 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.895-424T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 8/9 | chr9 | 91216530 | ||||||
| chr9:91216606
|
G | T | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | NA18950.hp1 NA18968.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.895-500C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 8/9 | chr9 | 91216606 | ||||||
| chr9:91216846
|
T | C | 12 | a0001c0001t0001g0017a0001c0001t0001g0280a0001c0001t0001g0281others(9): Show | 12 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.894+431A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 8/9 | chr9 | 91216846 | ||||||
| chr9:91216948
|
C | T | 10 | a0001c0001t0001g0120a0001c0001t0001g0277a0001c0001t0001g0278others(7): Show | 10 | HG02257.hp1 HG02818.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.894+329G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 8/9 | chr9 | 91216948 | ||||||
| chr9:91217369
|
T | A | 1 | a0001c0001t0001g0331 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.844-42A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91217369 | ||||||
| chr9:91217372
|
A | T | 1 | a0001c0001t0001g0204 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.844-45T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91217372 | ||||||
| chr9:91217582
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.844-255T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91217582 | ||||||
| chr9:91217625
|
C | G | 1 | a0001c0001t0001g0326 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.844-298G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91217625 | ||||||
| chr9:91217703
|
T | G | 4 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(1): Show | 4 | HG02257.hp1 HG02818.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.844-376A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91217703 | ||||||
| chr9:91217872
|
T | A | 1 | a0001c0001t0001g0326 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.844-545A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91217872 | ||||||
| chr9:91218038
|
A | T | 1 | a0001c0001t0001g0332 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.844-711T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91218038 | ||||||
| chr9:91218092
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.844-765A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91218092 | ||||||
| chr9:91218189
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.844-862A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91218189 | ||||||
| chr9:91218190
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0197 | 3 | HG02895.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.844-863A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91218190 | ||||||
| chr9:91218276
|
T | A | 49 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0058others(46): Show | 51 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.844-949A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91218276 | ||||||
| chr9:91218475
|
C | T | 1 | a0002c0003t0001g0013 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.844-1148G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91218475 | ||||||
| chr9:91218501
|
T | C | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.844-1174A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91218501 | ||||||
| chr9:91218561
|
G | A | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(111): Show | 118 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.844-1234C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91218561 | ||||||
| chr9:91218715
|
G | C | 1 | a0001c0001t0001g0231 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.844-1388C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91218715 | ||||||
| chr9:91218781
|
C | T | 7 | a0001c0002t0001g0115a0001c0002t0001g0152a0001c0002t0001g0258others(4): Show | 7 | HG02559.hp1 HG02572.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.844-1454G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91218781 | ||||||
| chr9:91218926
|
C | G | 2 | a0001c0001t0001g0139a0001c0001t0001g0331 | 2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.844-1599G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91218926 | ||||||
| chr9:91219076
|
G | A | 1 | a0001c0001t0001g0003 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.843+1729C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91219076 | ||||||
| chr9:91219143
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.843+1662G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91219143 | ||||||
| chr9:91219367
|
G | A | 62 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0096others(59): Show | 64 | HG00280.hp1 HG00642.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.843+1438C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91219367 | ||||||
| chr9:91219812
|
G | C | 1 | a0001c0001t0001g0113 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.843+993C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91219812 | ||||||
| chr9:91219899
|
A | G | 10 | a0001c0001t0001g0120a0001c0001t0001g0277a0001c0001t0001g0278others(7): Show | 10 | HG02257.hp1 HG02818.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.843+906T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91219899 | ||||||
| chr9:91219969
|
T | A | 1 | a0001c0001t0001g0233 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.843+836A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91219969 | ||||||
| chr9:91220092
|
T | C | 1 | a0001c0001t0001g0173 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.843+713A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91220092 | ||||||
| chr9:91220105
|
C | A | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.843+700G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91220105 | ||||||
| chr9:91220160
|
G | A | 76 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(73): Show | 80 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.843+645C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91220160 | ||||||
| chr9:91220187
|
T | C | 1 | a0004c0008t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.843+618A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91220187 | ||||||
| chr9:91220210
|
G | A | 76 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(73): Show | 80 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.843+595C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91220210 | ||||||
| chr9:91220573
|
A | G | 1 | a0001c0002t0001g0272 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.843+232T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91220573 | ||||||
| chr9:91220617
|
G | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.843+188C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91220617 | ||||||
| chr9:91220634
|
G | C | 2 | a0001c0001t0001g0240a0001c0001t0001g0243 | 2 | NA18968.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.843+171C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91220634 | ||||||
| chr9:91220640
|
T | C | 1 | a0001c0001t0001g0030 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.843+165A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91220640 | ||||||
| chr9:91220650
|
C | T | 116 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(113): Show | 119 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.843+155G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91220650 | ||||||
| chr9:91220676
|
A | C | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.843+129T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91220676 | ||||||
| chr9:91221117
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.656-125G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91221117 | ||||||
| chr9:91221255
|
A | C | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(144): Show | 152 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.656-263T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91221255 | ||||||
| chr9:91221281
|
C | A | 1 | a0001c0001t0001g0101 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.656-289G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91221281 | ||||||
| chr9:91221508
|
C | G | 1 | a0001c0002t0004g0276 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.656-516G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91221508 | ||||||
| chr9:91221509
|
A | T | 1 | a0001c0002t0001g0267 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.656-517T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91221509 | ||||||
| chr9:91221716
|
A | G | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-724T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91221716 | ||||||
| chr9:91221938
|
A | C | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172 | 3 | HG02451.hp1 HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.656-946T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91221938 | ||||||
| chr9:91222039
|
C | G | 1 | a0001c0001t0001g0057 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.656-1047G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91222039 | ||||||
| chr9:91222155
|
T | TA | 31 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0066others(28): Show | 32 | HG00408.hp2 HG00639.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.656-1164dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91222155 | ||||||
| chr9:91222156
|
A | T | 1 | a0001c0002t0001g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.656-1164T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91222156 | ||||||
| chr9:91222224
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.656-1232G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91222224 | ||||||
| chr9:91222415
|
T | C | 24 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(21): Show | 25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-1423A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91222415 | ||||||
| chr9:91222555
|
C | A | 2 | a0001c0001t0001g0242a0001c0001t0001g0245 | 2 | NA18978.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.656-1563G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91222555 | ||||||
| chr9:91222635
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0066 | 3 | HG02280.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.656-1643C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91222635 | ||||||
| chr9:91222878
|
T | A | 2 | a0001c0002t0001g0270a0001c0002t0001g0271 | 2 | HG00639.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.656-1886A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91222878 | ||||||
| chr9:91223165
|
A | T | 1 | a0001c0001t0001g0057 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.656-2173T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91223165 | ||||||
| chr9:91223183
|
T | C | 4 | a0001c0001t0001g0072a0001c0001t0001g0080a0001c0001t0001g0081others(1): Show | 4 | NA18957.hp1 NA19058.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.656-2191A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91223183 | ||||||
| chr9:91223224
|
C | A | 1 | a0001c0001t0001g0160 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.656-2232G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91223224 | ||||||
| chr9:91223225
|
G | A | 1 | a0001c0002t0001g0016 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.656-2233C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91223225 | ||||||
| chr9:91223245
|
G | A | 24 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(21): Show | 25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-2253C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91223245 | ||||||
| chr9:91223346
|
T | C | 1 | a0001c0001t0001g0326 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.656-2354A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91223346 | ||||||
| chr9:91223422
|
A | G | 25 | a0001c0001t0001g0071a0001c0002t0001g0011a0001c0002t0001g0016others(22): Show | 26 | HG00639.hp2 HG01106.hp2 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.656-2430T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91223422 | ||||||
| chr9:91223542
|
A | G | 67 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(64): Show | 68 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.656-2550T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91223542 | ||||||
| chr9:91223697
|
G | C | 26 | a0001c0001t0001g0071a0001c0002t0001g0011a0001c0002t0001g0016others(23): Show | 27 | HG00639.hp2 HG01106.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-2705C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91223697 | ||||||
| chr9:91223793
|
T | C | 1 | a0001c0001t0001g0074 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.656-2801A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91223793 | ||||||
| chr9:91223837
|
C | G | 21 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(18): Show | 22 | HG00408.hp2 HG00673.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.656-2845G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91223837 | ||||||
| chr9:91223838
|
T | C | 1 | a0001c0001t0001g0156 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.656-2846A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91223838 | ||||||
| chr9:91224345
|
T | C | 2 | a0001c0001t0001g0118a0001c0001t0001g0218 | 2 | HG01109.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.656-3353A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91224345 | ||||||
| chr9:91224373
|
A | T | 24 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(21): Show | 25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-3381T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91224373 | ||||||
| chr9:91224611
|
T | G | 1 | a0001c0001t0001g0208 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.656-3619A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91224611 | ||||||
| chr9:91224732
|
T | C | 1 | a0001c0001t0001g0302 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.656-3740A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91224732 | ||||||
| chr9:91225024
|
G | A | 4 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(1): Show | 4 | HG02257.hp1 HG02818.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.656-4032C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91225024 | ||||||
| chr9:91225085
|
C | T | 24 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(21): Show | 25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-4093G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91225085 | ||||||
| chr9:91225167
|
A | C | 1 | a0001c0001t0001g0226 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.656-4175T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91225167 | ||||||
| chr9:91225500
|
C | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(88): Show | 93 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.656-4508G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91225500 | ||||||
| chr9:91225545
|
T | A | 48 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0058others(45): Show | 50 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.656-4553A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91225545 | ||||||
| chr9:91225614
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0282a0001c0001t0001g0285 | 3 | HG00609.hp1 NA18954.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.656-4622C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91225614 | ||||||
| chr9:91225794
|
T | C | 1 | a0001c0001t0001g0156 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.656-4802A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91225794 | ||||||
| chr9:91225804
|
T | C | 24 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(21): Show | 25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-4812A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91225804 | ||||||
| chr9:91225812
|
T | C | 1 | a0001c0001t0001g0022 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.656-4820A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91225812 | ||||||
| chr9:91225950
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.656-4958A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91225950 | ||||||
| chr9:91225998
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.656-5006G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91225998 | ||||||
| chr9:91226000
|
G | A | 10 | a0001c0001t0001g0120a0001c0001t0001g0202a0001c0001t0001g0277others(7): Show | 10 | HG02257.hp1 HG02818.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.656-5008C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91226000 | ||||||
| chr9:91226096
|
T | G | 24 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(21): Show | 25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-5104A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91226096 | ||||||
| chr9:91226121
|
A | G | 25 | a0001c0001t0001g0071a0001c0002t0001g0011a0001c0002t0001g0016others(22): Show | 26 | HG00639.hp2 HG01106.hp2 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.656-5129T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91226121 | ||||||
| chr9:91226185
|
C | T | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-5193G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91226185 | ||||||
| chr9:91226210
|
CTGT | C | 3 | a0001c0001t0001g0280a0001c0001t0001g0289a0001c0002t0001g0268 | 3 | HG01109.hp2 HG03098.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.656-5221_656-5219d others(5): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91226210 | ||||||
| chr9:91226257
|
A | G | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-5265T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91226257 | ||||||
| chr9:91226276
|
C | T | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(280): Show | 293 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(290): Show |
intron_variant | MODIFIER | c.656-5284G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91226276 | ||||||
| chr9:91226327
|
T | C | 111 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(108): Show | 115 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.656-5335A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91226327 | ||||||
| chr9:91226434
|
G | T | 1 | a0001c0001t0001g0160 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.656-5442C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91226434 | ||||||
| chr9:91226493
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.656-5501G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91226493 | ||||||
| chr9:91226788
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.656-5796C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91226788 | ||||||
| chr9:91226828
|
T | A | 1 | a0001c0001t0001g0033 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.656-5836A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91226828 | ||||||
| chr9:91226917
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.656-5925C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91226917 | ||||||
| chr9:91226980
|
T | C | 1 | a0002c0003t0001g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.656-5988A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91226980 | ||||||
| chr9:91226989
|
G | A | 24 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(21): Show | 25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-5997C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91226989 | ||||||
| chr9:91227072
|
C | T | 346 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(343): Show | 357 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(354): Show |
intron_variant | MODIFIER | c.656-6080G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227072 | ||||||
| chr9:91227073
|
T | A | 6 | a0001c0001t0001g0017a0001c0001t0001g0282a0001c0001t0001g0283others(3): Show | 6 | HG00597.hp2 HG00609.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.656-6081A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227073 | ||||||
| chr9:91227106
|
G | C | 6 | a0001c0001t0001g0017a0001c0001t0001g0282a0001c0001t0001g0283others(3): Show | 6 | HG00597.hp2 HG00609.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.656-6114C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227106 | ||||||
| chr9:91227160
|
G | A | 35 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(32): Show | 36 | HG00408.hp2 HG00673.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.656-6168C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227160 | ||||||
| chr9:91227235
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.656-6243G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227235 | ||||||
| chr9:91227262
|
G | A | 41 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(38): Show | 41 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.656-6270C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227262 | ||||||
| chr9:91227262
|
G | C | 168 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(165): Show | 175 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(172): Show |
intron_variant | MODIFIER | c.656-6270C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227262 | ||||||
| chr9:91227308
|
G | A | 41 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(38): Show | 41 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.656-6316C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227308 | ||||||
| chr9:91227332
|
C | T | 4 | a0001c0001t0001g0219a0001c0001t0001g0228a0001c0001t0001g0249others(1): Show | 4 | HG02129.hp2 HG02165.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.656-6340G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227332 | ||||||
| chr9:91227385
|
T | C | 2 | a0001c0001t0001g0019a0001c0001t0001g0025 | 2 | HG02074.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.656-6393A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227385 | ||||||
| chr9:91227393
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.656-6401G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227393 | ||||||
| chr9:91227420
|
TG | T | 24 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(21): Show | 25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-6429delC | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227420 | ||||||
| chr9:91227460
|
A | G | 3 | a0001c0001t0001g0124a0001c0001t0001g0132a0001c0001t0001g0184 | 3 | HG01243.hp2 HG02559.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.656-6468T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227460 | ||||||
| chr9:91227545
|
TC | T | 24 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(21): Show | 25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-6554delG | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227545 | ||||||
| chr9:91227553
|
C | T | 24 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(21): Show | 25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-6561G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227553 | ||||||
| chr9:91227557
|
C | G | 24 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(21): Show | 25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-6565G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227557 | ||||||
| chr9:91227559
|
A | G | 24 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(21): Show | 25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-6567T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227559 | ||||||
| chr9:91227604
|
T | G | 1 | a0001c0002t0001g0268 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.656-6612A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227604 | ||||||
| chr9:91227662
|
C | G | 11 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(8): Show | 11 | HG00280.hp1 HG00642.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.656-6670G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227662 | ||||||
| chr9:91227677
|
T | C | 10 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(7): Show | 10 | HG02040.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.656-6685A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227677 | ||||||
| chr9:91227720
|
A | G | 8 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0060others(5): Show | 9 | HG03491.hp1 HG03492.hp1 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.656-6728T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227720 | ||||||
| chr9:91227721
|
T | C | 42 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0065others(39): Show | 44 | HG00544.hp1 HG00558.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.656-6729A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227721 | ||||||
| chr9:91227777
|
T | A | 1 | a0001c0002t0004g0276 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.656-6785A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227777 | ||||||
| chr9:91227904
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.656-6912G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227904 | ||||||
| chr9:91228106
|
T | G | 1 | a0001c0001t0001g0020 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.656-7114A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91228106 | ||||||
| chr9:91228205
|
C | T | 4 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(1): Show | 4 | HG02257.hp1 HG02818.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.656-7213G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91228205 | ||||||
| chr9:91228275
|
G | A | 1 | a0001c0001t0001g0326 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.656-7283C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91228275 | ||||||
| chr9:91228336
|
T | C | 1 | a0001c0001t0001g0312 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.656-7344A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91228336 | ||||||
| chr9:91228610
|
T | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(88): Show | 93 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.656-7618A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91228610 | ||||||
| chr9:91228692
|
G | A | 41 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0065others(38): Show | 43 | HG00544.hp1 HG00558.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.656-7700C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91228692 | ||||||
| chr9:91228766
|
T | C | 1 | a0001c0001t0001g0024 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.656-7774A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91228766 | ||||||
| chr9:91228864
|
T | C | 8 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0060others(5): Show | 9 | HG03491.hp1 HG03492.hp1 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.656-7872A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91228864 | ||||||
| chr9:91228940
|
A | C | 9 | a0001c0001t0001g0120a0001c0001t0001g0277a0001c0001t0001g0278others(6): Show | 9 | HG02257.hp1 HG02818.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.656-7948T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91228940 | ||||||
| chr9:91229012
|
G | GA | 26 | a0001c0001t0001g0071a0001c0002t0001g0011a0001c0002t0001g0016others(23): Show | 27 | HG00639.hp2 HG01106.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-8021dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91229012 | ||||||
| chr9:91229206
|
A | G | 1 | a0001c0002t0002g0257 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.656-8214T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91229206 | ||||||
| chr9:91229448
|
C | T | 42 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0065others(39): Show | 44 | HG00544.hp1 HG00558.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.656-8456G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91229448 | ||||||
| chr9:91229608
|
T | C | 3 | a0002c0003t0001g0013a0002c0003t0001g0014a0002c0003t0001g0015 | 3 | HG02451.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.656-8616A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91229608 | ||||||
| chr9:91229916
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(112): Show | 118 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.656-8924T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91229916 | ||||||
| chr9:91229965
|
C | A | 24 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(21): Show | 25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-8973G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91229965 | ||||||
| chr9:91230024
|
A | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0299a0001c0001t0001g0327others(1): Show | 5 | HG01952.hp2 HG01978.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.656-9032T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91230024 | ||||||
| chr9:91230051
|
C | T | 1 | a0001c0002t0001g0273 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.656-9059G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91230051 | ||||||
| chr9:91230069
|
C | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0042others(2): Show | 5 | NA18957.hp2 NA18969.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.656-9077G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91230069 | ||||||
| chr9:91230135
|
A | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.656-9143T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91230135 | ||||||
| chr9:91230203
|
G | A | 48 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0058others(45): Show | 50 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.656-9211C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91230203 | ||||||
| chr9:91230555
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.656-9563C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91230555 | ||||||
| chr9:91230571
|
G | A | 26 | a0001c0001t0001g0071a0001c0001t0001g0172a0001c0002t0001g0011others(23): Show | 27 | HG00639.hp2 HG01106.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-9579C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91230571 | ||||||
| chr9:91230585
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.656-9593G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91230585 | ||||||
| chr9:91230731
|
T | C | 1 | a0001c0002t0001g0262 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.656-9739A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91230731 | ||||||
| chr9:91230756
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.656-9764A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91230756 | ||||||
| chr9:91230819
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.656-9827C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91230819 | ||||||
| chr9:91230819
|
G | C | 1 | a0001c0001t0001g0220 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.656-9827C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91230819 | ||||||
| chr9:91230865
|
C | T | 24 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(21): Show | 25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-9873G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91230865 | ||||||
| chr9:91230881
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0299a0001c0001t0001g0327others(1): Show | 5 | HG01952.hp2 HG01978.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.656-9889G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91230881 | ||||||
| chr9:91230915
|
C | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(112): Show | 118 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.656-9923G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91230915 | ||||||
| chr9:91231046
|
C | G | 1 | a0001c0001t0001g0172 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.656-10054G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231046 | ||||||
| chr9:91231093
|
C | T | 4 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0181others(1): Show | 4 | HG01123.hp1 HG01261.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.656-10101G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231093 | ||||||
| chr9:91231106
|
T | G | 1 | a0001c0001t0001g0222 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.656-10114A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231106 | ||||||
| chr9:91231254
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.656-10262G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231254 | ||||||
| chr9:91231282
|
G | A | 1 | a0001c0002t0001g0337 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.656-10290C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231282 | ||||||
| chr9:91231291
|
G | A | 5 | a0001c0001t0001g0116a0001c0002t0001g0261a0001c0002t0001g0262others(2): Show | 5 | HG03098.hp1 HG03209.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.656-10299C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231291 | ||||||
| chr9:91231305
|
T | G | 3 | a0001c0001t0001g0310a0001c0001t0001g0314a0001c0001t0001g0315 | 3 | NA18941.hp2 NA18954.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.656-10313A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231305 | ||||||
| chr9:91231326
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.656-10334C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231326 | ||||||
| chr9:91231400
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0197 | 3 | HG02895.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.656-10408C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231400 | ||||||
| chr9:91231421
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.656-10429C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231421 | ||||||
| chr9:91231478
|
T | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(112): Show | 118 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.656-10486A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231478 | ||||||
| chr9:91231569
|
A | G | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-10577T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231569 | ||||||
| chr9:91231607
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.656-10615A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231607 | ||||||
| chr9:91231667
|
C | G | 24 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(21): Show | 25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-10675G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231667 | ||||||
| chr9:91231919
|
T | G | 26 | a0001c0001t0001g0071a0001c0002t0001g0011a0001c0002t0001g0016others(23): Show | 27 | HG00639.hp2 HG01106.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-10927A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231919 | ||||||
| chr9:91231963
|
C | G | 1 | a0001c0001t0001g0063 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.656-10971G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231963 | ||||||
| chr9:91231984
|
C | T | 1 | a0001c0001t0001g0335 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.656-10992G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231984 | ||||||
| chr9:91231984
|
CT | C | 24 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(21): Show | 25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-10993delA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231984 | ||||||
| chr9:91232128
|
T | C | 1 | a0001c0001t0001g0074 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.656-11136A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91232128 | ||||||
| chr9:91232290
|
T | C | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-11298A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91232290 | ||||||
| chr9:91232329
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.656-11337A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91232329 | ||||||
| chr9:91232499
|
C | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | NA18979.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.656-11507G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91232499 | ||||||
| chr9:91232584
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.656-11592G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91232584 | ||||||
| chr9:91232610
|
C | G | 1 | a0001c0001t0001g0279 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.656-11618G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91232610 | ||||||
| chr9:91232662
|
C | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0039 | 3 | NA18946.hp1 NA18948.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.656-11670G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91232662 | ||||||
| chr9:91232915
|
C | T | 1 | a0001c0001t0001g0309 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.656-11923G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91232915 | ||||||
| chr9:91232926
|
T | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(88): Show | 93 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.656-11934A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91232926 | ||||||
| chr9:91233086
|
C | A | 4 | a0001c0002t0001g0261a0001c0002t0001g0262a0001c0002t0001g0263others(1): Show | 4 | HG03098.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.656-12094G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91233086 | ||||||
| chr9:91233168
|
C | T | 1 | a0004c0008t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.656-12176G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91233168 | ||||||
| chr9:91233309
|
A | T | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(166): Show | 174 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.656-12317T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91233309 | ||||||
| chr9:91233555
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.656-12563C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91233555 | ||||||
| chr9:91233592
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.656-12600G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91233592 | ||||||
| chr9:91233617
|
G | T | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.656-12625C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91233617 | ||||||
| chr9:91233727
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.656-12735G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91233727 | ||||||
| chr9:91233781
|
C | T | 24 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(21): Show | 25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-12789G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91233781 | ||||||
| chr9:91233789
|
G | A | 24 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(21): Show | 25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-12797C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91233789 | ||||||
| chr9:91233793
|
A | G | 24 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(21): Show | 25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-12801T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91233793 | ||||||
| chr9:91233836
|
G | C | 54 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0017others(51): Show | 56 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.656-12844C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91233836 | ||||||
| chr9:91233906
|
C | G | 24 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(21): Show | 25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-12914G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91233906 | ||||||
| chr9:91233987
|
G | A | 26 | a0001c0001t0001g0071a0001c0002t0001g0011a0001c0002t0001g0016others(23): Show | 27 | HG00639.hp2 HG01106.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-12995C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91233987 | ||||||
| chr9:91234101
|
A | G | 10 | a0001c0001t0001g0120a0001c0001t0001g0277a0001c0001t0001g0278others(7): Show | 10 | HG02257.hp1 HG02818.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.656-13109T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91234101 | ||||||
| chr9:91234125
|
G | A | 24 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(21): Show | 25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-13133C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91234125 | ||||||
| chr9:91234253
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.656-13261G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91234253 | ||||||
| chr9:91234347
|
G | C | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-13355C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91234347 | ||||||
| chr9:91234532
|
C | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0141 | 2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.656-13540G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91234532 | ||||||
| chr9:91234614
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.656-13622G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91234614 | ||||||
| chr9:91234849
|
A | T | 1 | a0001c0001t0001g0125 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.656-13857T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91234849 | ||||||
| chr9:91235078
|
G | A | 1 | a0001c0001t0001g0039 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.656-14086C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91235078 | ||||||
| chr9:91235254
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.656-14262G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91235254 | ||||||
| chr9:91235482
|
T | G | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(279): Show | 292 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(289): Show |
intron_variant | MODIFIER | c.656-14490A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91235482 | ||||||
| chr9:91235591
|
A | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(78): Show | 83 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.656-14599T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91235591 | ||||||
| chr9:91235861
|
T | C | 31 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(28): Show | 32 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.656-14869A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91235861 | ||||||
| chr9:91236090
|
A | C | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-15098T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91236090 | ||||||
| chr9:91236092
|
G | A | 12 | a0001c0001t0001g0017a0001c0001t0001g0280a0001c0001t0001g0281others(9): Show | 12 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.656-15100C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91236092 | ||||||
| chr9:91236324
|
G | A | 1 | a0001c0002t0004g0276 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.656-15332C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91236324 | ||||||
| chr9:91236325
|
T | A | 2 | a0001c0001t0001g0294a0001c0001t0001g0301 | 2 | HG02738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.656-15333A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91236325 | ||||||
| chr9:91236420
|
A | G | 20 | a0001c0001t0001g0017a0001c0001t0001g0277a0001c0001t0001g0278others(17): Show | 20 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.656-15428T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91236420 | ||||||
| chr9:91236424
|
C | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.656-15432G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91236424 | ||||||
| chr9:91236912
|
C | G | 17 | a0001c0001t0001g0017a0001c0001t0001g0280a0001c0001t0001g0281others(14): Show | 17 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.656-15920G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91236912 | ||||||
| chr9:91236920
|
C | A | 1 | a0001c0001t0001g0035 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.656-15928G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91236920 | ||||||
| chr9:91237092
|
T | G | 25 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(22): Show | 26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.656-16100A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91237092 | ||||||
| chr9:91237286
|
G | A | 1 | a0001c0001t0001g0286 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.656-16294C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91237286 | ||||||
| chr9:91237476
|
A | T | 25 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(22): Show | 26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.656-16484T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91237476 | ||||||
| chr9:91237513
|
T | G | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-16521A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91237513 | ||||||
| chr9:91237559
|
T | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(99): Show | 104 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.656-16567A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91237559 | ||||||
| chr9:91237689
|
GT | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.656-16698delA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91237689 | ||||||
| chr9:91237690
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.656-16698A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91237690 | ||||||
| chr9:91238002
|
T | C | 1 | a0001c0001t0001g0122 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.656-17010A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91238002 | ||||||
| chr9:91238189
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.656-17197A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91238189 | ||||||
| chr9:91238229
|
T | G | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-17237A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91238229 | ||||||
| chr9:91238264
|
T | C | 25 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(22): Show | 26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.656-17272A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91238264 | ||||||
| chr9:91238351
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.656-17359G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91238351 | ||||||
| chr9:91238437
|
G | A | 25 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(22): Show | 26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.656-17445C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91238437 | ||||||
| chr9:91238518
|
G | A | 16 | a0001c0001t0001g0005a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.656-17526C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91238518 | ||||||
| chr9:91238570
|
A | G | 1 | a0001c0001t0001g0322 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.656-17578T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91238570 | ||||||
| chr9:91238571
|
T | C | 1 | a0001c0001t0001g0064 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.656-17579A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91238571 | ||||||
| chr9:91238581
|
A | G | 20 | a0001c0001t0001g0017a0001c0001t0001g0277a0001c0001t0001g0278others(17): Show | 20 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.656-17589T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91238581 | ||||||
| chr9:91238901
|
T | C | 1 | a0001c0001t0001g0094 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.656-17909A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91238901 | ||||||
| chr9:91238981
|
A | G | 25 | a0001c0001t0001g0071a0001c0002t0001g0011a0001c0002t0001g0016others(22): Show | 26 | HG00639.hp2 HG01106.hp2 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.656-17989T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91238981 | ||||||
| chr9:91239129
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.656-18137G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91239129 | ||||||
| chr9:91239156
|
G | GT | 30 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0097others(27): Show | 32 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.656-18165dupA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91239156 | ||||||
| chr9:91239156
|
G | GTT | 47 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0095others(44): Show | 47 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.656-18166_656-1816 others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91239156 | ||||||
| chr9:91239168
|
T | C | 40 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0060others(37): Show | 42 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.656-18176A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91239168 | ||||||
| chr9:91239168
|
T | TC | 41 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(38): Show | 41 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.656-18177_656-1817 others(5): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91239168 | ||||||
| chr9:91239176
|
A | G | 25 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(22): Show | 26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.656-18184T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91239176 | ||||||
| chr9:91239374
|
C | G | 25 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(22): Show | 26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.656-18382G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91239374 | ||||||
| chr9:91239441
|
T | C | 2 | a0001c0001t0001g0118a0001c0001t0001g0218 | 2 | HG01109.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.656-18449A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91239441 | ||||||
| chr9:91239743
|
A | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.656-18751T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91239743 | ||||||
| chr9:91239745
|
G | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.656-18753C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91239745 | ||||||
| chr9:91239755
|
A | ATG | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.656-18764_656-1876 others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91239755 | ||||||
| chr9:91239982
|
A | C | 1 | a0001c0001t0001g0129 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.656-18990T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91239982 | ||||||
| chr9:91240010
|
C | A | 1 | a0001c0001t0001g0244 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.656-19018G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91240010 | ||||||
| chr9:91240159
|
A | T | 297 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(294): Show | 307 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(304): Show |
intron_variant | MODIFIER | c.656-19167T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91240159 | ||||||
| chr9:91240218
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.656-19226A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91240218 | ||||||
| chr9:91240294
|
C | T | 25 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(22): Show | 26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.656-19302G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91240294 | ||||||
| chr9:91240403
|
C | T | 6 | a0001c0002t0001g0115a0001c0002t0001g0152a0001c0002t0002g0255others(3): Show | 6 | HG02559.hp1 HG02723.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.656-19411G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91240403 | ||||||
| chr9:91240418
|
C | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(124): Show | 130 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.656-19426G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91240418 | ||||||
| chr9:91240501
|
G | A | 1 | a0001c0002t0001g0272 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.656-19509C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91240501 | ||||||
| chr9:91240603
|
T | C | 12 | a0001c0001t0001g0017a0001c0001t0001g0280a0001c0001t0001g0281others(9): Show | 12 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.656-19611A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91240603 | ||||||
| chr9:91240637
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.656-19645T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91240637 | ||||||
| chr9:91240792
|
C | G | 6 | a0001c0001t0001g0322a0001c0001t0001g0341a0001c0001t0001g0342others(3): Show | 6 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.656-19800G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91240792 | ||||||
| chr9:91240927
|
T | C | 5 | a0001c0001t0001g0122a0001c0002t0001g0261a0001c0002t0001g0262others(2): Show | 5 | HG03098.hp1 HG03209.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.656-19935A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91240927 | ||||||
| chr9:91240988
|
G | A | 47 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0058others(44): Show | 49 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.656-19996C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91240988 | ||||||
| chr9:91241065
|
G | A | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-20073C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91241065 | ||||||
| chr9:91241224
|
A | G | 1 | a0001c0001t0001g0311 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.656-20232T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91241224 | ||||||
| chr9:91241235
|
T | G | 1 | a0001c0001t0001g0133 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.656-20243A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91241235 | ||||||
| chr9:91241268
|
G | A | 1 | a0001c0001t0001g0238 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.656-20276C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91241268 | ||||||
| chr9:91241334
|
T | C | 47 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0095others(44): Show | 47 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.656-20342A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91241334 | ||||||
| chr9:91241444
|
T | C | 1 | a0001c0002t0002g0257 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.656-20452A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91241444 | ||||||
| chr9:91241457
|
T | C | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(124): Show | 130 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.656-20465A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91241457 | ||||||
| chr9:91241466
|
T | C | 2 | a0001c0001t0001g0111a0001c0001t0001g0141 | 2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.656-20474A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91241466 | ||||||
| chr9:91241496
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.656-20504C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91241496 | ||||||
| chr9:91241568
|
T | C | 1 | a0001c0001t0001g0058 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.656-20576A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91241568 | ||||||
| chr9:91241570
|
T | C | 3 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0166 | 3 | HG02257.hp2 HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.656-20578A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91241570 | ||||||
| chr9:91242069
|
G | A | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-21077C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91242069 | ||||||
| chr9:91242136
|
G | T | 12 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0103others(9): Show | 12 | HG02040.hp1 HG02071.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.656-21144C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91242136 | ||||||
| chr9:91242404
|
C | A | 1 | a0001c0001t0001g0018 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.656-21412G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91242404 | ||||||
| chr9:91242474
|
A | T | 1 | a0001c0001t0001g0138 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.656-21482T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91242474 | ||||||
| chr9:91242507
|
G | A | 5 | a0001c0001t0001g0123a0001c0001t0001g0129a0001c0001t0001g0130others(2): Show | 5 | NA18945.hp1 NA18946.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.656-21515C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91242507 | ||||||
| chr9:91242534
|
T | C | 8 | a0001c0001t0001g0017a0001c0001t0001g0282a0001c0001t0001g0283others(5): Show | 8 | HG00597.hp2 HG00609.hp1 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.656-21542A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91242534 | ||||||
| chr9:91242615
|
C | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(99): Show | 104 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.656-21623G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91242615 | ||||||
| chr9:91242642
|
G | A | 1 | a0001c0001t0001g0030 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.656-21650C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91242642 | ||||||
| chr9:91243048
|
T | C | 1 | a0001c0001t0001g0104 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.656-22056A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91243048 | ||||||
| chr9:91243518
|
C | T | 4 | a0001c0002t0001g0261a0001c0002t0001g0262a0001c0002t0001g0263others(1): Show | 4 | HG03098.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.656-22526G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91243518 | ||||||
| chr9:91243547
|
T | C | 25 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(22): Show | 26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.656-22555A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91243547 | ||||||
| chr9:91243729
|
C | T | 16 | a0001c0001t0001g0005a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.656-22737G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91243729 | ||||||
| chr9:91243981
|
T | C | 4 | a0001c0001t0001g0298a0001c0001t0001g0303a0001c0001t0001g0304others(1): Show | 4 | NA18943.hp1 NA18969.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.656-22989A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91243981 | ||||||
| chr9:91243995
|
T | C | 1 | a0001c0001t0001g0343 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.656-23003A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91243995 | ||||||
| chr9:91244066
|
T | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.656-23074A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91244066 | ||||||
| chr9:91244204
|
T | G | 17 | a0001c0001t0001g0017a0001c0001t0001g0280a0001c0001t0001g0281others(14): Show | 17 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.656-23212A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91244204 | ||||||
| chr9:91244285
|
G | A | 1 | a0001c0001t0001g0207 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.656-23293C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91244285 | ||||||
| chr9:91244626
|
A | AAT | 20 | a0001c0001t0001g0017a0001c0001t0001g0277a0001c0001t0001g0278others(17): Show | 20 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.656-23635_656-2363 others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91244626 | ||||||
| chr9:91244758
|
A | G | 41 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(38): Show | 41 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.656-23766T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91244758 | ||||||
| chr9:91244851
|
G | A | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-23859C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91244851 | ||||||
| chr9:91245161
|
C | A | 4 | a0001c0001t0001g0298a0001c0001t0001g0303a0001c0001t0001g0304others(1): Show | 4 | NA18943.hp1 NA18969.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.656-24169G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91245161 | ||||||
| chr9:91245219
|
G | A | 1 | a0001c0002t0004g0276 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.656-24227C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91245219 | ||||||
| chr9:91245233
|
G | GC | 12 | a0001c0001t0001g0017a0001c0001t0001g0280a0001c0001t0001g0281others(9): Show | 12 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.656-24242dupG | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91245233 | ||||||
| chr9:91245523
|
G | C | 20 | a0001c0001t0001g0017a0001c0001t0001g0277a0001c0001t0001g0278others(17): Show | 20 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.656-24531C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91245523 | ||||||
| chr9:91245721
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.656-24729T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91245721 | ||||||
| chr9:91245896
|
T | G | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-24904A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91245896 | ||||||
| chr9:91245923
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.656-24931C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91245923 | ||||||
| chr9:91246089
|
CT | C | 35 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0227others(32): Show | 37 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.656-25098delA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91246089 | ||||||
| chr9:91246177
|
A | G | 2 | a0001c0001t0001g0002a0001c0001t0001g0066 | 3 | HG02280.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.656-25185T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91246177 | ||||||
| chr9:91246348
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.656-25356G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91246348 | ||||||
| chr9:91246533
|
G | A | 41 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(38): Show | 41 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.656-25541C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91246533 | ||||||
| chr9:91246652
|
T | C | 26 | a0001c0001t0001g0071a0001c0002t0001g0011a0001c0002t0001g0016others(23): Show | 27 | HG00639.hp2 HG01106.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-25660A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91246652 | ||||||
| chr9:91246659
|
A | G | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-25667T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91246659 | ||||||
| chr9:91246723
|
T | C | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-25731A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91246723 | ||||||
| chr9:91246753
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.656-25761A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91246753 | ||||||
| chr9:91246819
|
G | A | 22 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(19): Show | 22 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.656-25827C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91246819 | ||||||
| chr9:91246971
|
T | C | 3 | a0002c0003t0001g0013a0002c0003t0001g0014a0002c0003t0001g0015 | 3 | HG02451.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.656-25979A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91246971 | ||||||
| chr9:91246987
|
G | A | 12 | a0001c0001t0001g0017a0001c0001t0001g0280a0001c0001t0001g0281others(9): Show | 12 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.656-25995C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91246987 | ||||||
| chr9:91247245
|
C | G | 1 | a0001c0001t0001g0136 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.656-26253G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91247245 | ||||||
| chr9:91247258
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.656-26266A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91247258 | ||||||
| chr9:91247275
|
A | C | 25 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(22): Show | 26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.656-26283T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91247275 | ||||||
| chr9:91247822
|
G | A | 1 | a0001c0001t0001g0061 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.656-26830C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91247822 | ||||||
| chr9:91247882
|
G | C | 1 | a0001c0001t0001g0151 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.656-26890C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91247882 | ||||||
| chr9:91248016
|
G | A | 26 | a0001c0001t0001g0071a0001c0002t0001g0011a0001c0002t0001g0016others(23): Show | 27 | HG00639.hp2 HG01106.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-27024C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91248016 | ||||||
| chr9:91248462
|
A | C | 1 | a0001c0001t0001g0249 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.656-27470T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91248462 | ||||||
| chr9:91248530
|
G | A | 7 | a0001c0001t0001g0298a0001c0001t0001g0303a0001c0001t0001g0304others(4): Show | 7 | HG02135.hp1 NA18943.hp1 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.656-27538C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91248530 | ||||||
| chr9:91248600
|
C | G | 2 | a0001c0001t0001g0281a0001c0001t0001g0287 | 2 | HG02602.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.656-27608G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91248600 | ||||||
| chr9:91248625
|
GT | G | 14 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(11): Show | 14 | HG00408.hp2 NA18955.hp1 NA18956.hp2 others(11): Show |
intron_variant | MODIFIER | c.656-27634delA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91248625 | ||||||
| chr9:91248961
|
T | C | 16 | a0001c0001t0001g0005a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.656-27969A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91248961 | ||||||
| chr9:91248982
|
A | G | 1 | a0001c0001t0001g0320 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.656-27990T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91248982 | ||||||
| chr9:91249166
|
G | A | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-28174C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249166 | ||||||
| chr9:91249200
|
G | A | 12 | a0001c0001t0001g0017a0001c0001t0001g0280a0001c0001t0001g0281others(9): Show | 12 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.656-28208C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249200 | ||||||
| chr9:91249229
|
T | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(228): Show | 237 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.656-28237A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249229 | ||||||
| chr9:91249292
|
C | CA | 26 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0001g0114others(23): Show | 26 | HG00642.hp1 HG00735.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.656-28301dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249292 | ||||||
| chr9:91249292
|
C | CAA | 9 | a0001c0001t0001g0101a0001c0001t0001g0119a0001c0001t0001g0128others(6): Show | 9 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.656-28302_656-2830 others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249292 | ||||||
| chr9:91249292
|
CA | C | 41 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(38): Show | 44 | HG00408.hp1 HG00609.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.656-28301delT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249292 | ||||||
| chr9:91249292
|
CAA | C | 44 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0065others(41): Show | 46 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.656-28302_656-2830 others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249292 | ||||||
| chr9:91249292
|
CAAA | C | 46 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0067others(43): Show | 47 | HG00609.hp1 HG00673.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.656-28303_656-2830 others(7): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249292 | ||||||
| chr9:91249292
|
CAAAA | C | 10 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0069others(7): Show | 11 | HG00558.hp2 HG01175.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.656-28304_656-2830 others(8): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249292 | ||||||
| chr9:91249292
|
CAAAAA | C | 7 | a0001c0001t0001g0022a0001c0001t0001g0051a0001c0001t0001g0054others(4): Show | 7 | HG00639.hp2 HG01433.hp1 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.656-28305_656-2830 others(9): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249292 | ||||||
| chr9:91249292
|
CAAAAAA | C | 57 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(54): Show | 58 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.656-28306_656-2830 others(10): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249292 | ||||||
| chr9:91249292
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-28311_656-2830 others(15): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249292 | ||||||
| chr9:91249292
|
CAAAAAAA others(6): Show |
C | 3 | a0001c0001t0001g0092a0001c0001t0001g0232a0001c0001t0001g0233 | 3 | HG02630.hp1 NA18612.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.656-28313_656-2830 others(17): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249292 | ||||||
| chr9:91249297
|
A | AAAAAAAA others(7): Show |
12 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(9): Show | 12 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.656-28306_656-2830 others(18): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249297 | ||||||
| chr9:91249298
|
A | AAAAAAAA others(6): Show |
1 | a0001c0001t0001g0001 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.656-28307_656-2830 others(17): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249298 | ||||||
| chr9:91249298
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0001g0342 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.656-28307_656-2830 others(16): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249298 | ||||||
| chr9:91249478
|
C | CTT | 39 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0065others(36): Show | 41 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.656-28488_656-2848 others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249478 | ||||||
| chr9:91249490
|
T | C | 1 | a0005c0005t0001g0012 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.656-28498A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249490 | ||||||
| chr9:91249525
|
G | A | 25 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(22): Show | 26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.656-28533C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249525 | ||||||
| chr9:91249610
|
C | T | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(140): Show | 147 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.656-28618G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249610 | ||||||
| chr9:91249774
|
A | C | 1 | a0001c0001t0001g0103 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.656-28782T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249774 | ||||||
| chr9:91249809
|
AGACC | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(53): Show | 57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.656-28821_656-2881 others(8): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249809 | ||||||
| chr9:91249855
|
CA | C | 5 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(2): Show | 5 | HG00735.hp2 HG01433.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.656-28864delT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249855 | ||||||
| chr9:91249894
|
C | G | 1 | a0001c0001t0001g0182 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.656-28902G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249894 | ||||||
| chr9:91249960
|
T | C | 1 | a0001c0001t0001g0295 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.656-28968A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249960 | ||||||
| chr9:91250013
|
G | GA | 116 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0017others(113): Show | 119 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.656-29022dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91250013 | ||||||
| chr9:91250013
|
G | GAA | 28 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0066others(25): Show | 29 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.656-29023_656-2902 others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91250013 | ||||||
| chr9:91250077
|
G | GA | 56 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(53): Show | 57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.656-29086dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91250077 | ||||||
| chr9:91250158
|
G | C | 1 | a0001c0001t0001g0161 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.656-29166C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91250158 | ||||||
| chr9:91250189
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.656-29197C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91250189 | ||||||
| chr9:91250250
|
G | A | 26 | a0001c0001t0001g0071a0001c0002t0001g0011a0001c0002t0001g0016others(23): Show | 27 | HG00639.hp2 HG01106.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-29258C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91250250 | ||||||
| chr9:91250411
|
G | C | 1 | a0001c0001t0001g0136 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.656-29419C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91250411 | ||||||
| chr9:91250463
|
T | C | 1 | a0001c0001t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.656-29471A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91250463 | ||||||
| chr9:91250741
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.656-29749A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91250741 | ||||||
| chr9:91251055
|
C | T | 25 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(22): Show | 26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.656-30063G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91251055 | ||||||
| chr9:91251206
|
G | T | 20 | a0001c0001t0001g0017a0001c0001t0001g0277a0001c0001t0001g0278others(17): Show | 20 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.656-30214C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91251206 | ||||||
| chr9:91251348
|
C | T | 1 | a0001c0001t0001g0345 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.656-30356G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91251348 | ||||||
| chr9:91251528
|
C | T | 20 | a0001c0001t0001g0017a0001c0001t0001g0277a0001c0001t0001g0278others(17): Show | 20 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.656-30536G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91251528 | ||||||
| chr9:91251735
|
G | A | 47 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0095others(44): Show | 47 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.656-30743C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91251735 | ||||||
| chr9:91251753
|
A | G | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-30761T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91251753 | ||||||
| chr9:91251812
|
TGGTAAGG | T | 25 | a0001c0001t0001g0071a0001c0002t0001g0011a0001c0002t0001g0016others(22): Show | 26 | HG00639.hp2 HG01106.hp2 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.656-30827_656-3082 others(11): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91251812 | ||||||
| chr9:91252107
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.656-31115G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91252107 | ||||||
| chr9:91252211
|
T | C | 297 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(294): Show | 307 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(304): Show |
intron_variant | MODIFIER | c.656-31219A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91252211 | ||||||
| chr9:91252217
|
G | A | 26 | a0001c0001t0001g0071a0001c0002t0001g0011a0001c0002t0001g0016others(23): Show | 27 | HG00639.hp2 HG01106.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-31225C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91252217 | ||||||
| chr9:91252296
|
C | T | 11 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0001g0101others(8): Show | 11 | HG01243.hp1 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.656-31304G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91252296 | ||||||
| chr9:91252358
|
G | GA | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.656-31367dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91252358 | ||||||
| chr9:91252359
|
A | G | 1 | a0001c0002t0004g0276 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.656-31367T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91252359 | ||||||
| chr9:91252470
|
G | A | 26 | a0001c0001t0001g0071a0001c0002t0001g0011a0001c0002t0001g0016others(23): Show | 27 | HG00639.hp2 HG01106.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-31478C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91252470 | ||||||
| chr9:91252498
|
C | T | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-31506G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91252498 | ||||||
| chr9:91252901
|
C | T | 6 | a0001c0001t0001g0322a0001c0001t0001g0341a0001c0001t0001g0342others(3): Show | 6 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.656-31909G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91252901 | ||||||
| chr9:91253080
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.656-32088C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91253080 | ||||||
| chr9:91253095
|
A | G | 1 | a0001c0002t0002g0255 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.656-32103T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91253095 | ||||||
| chr9:91253117
|
G | C | 2 | a0001c0002t0001g0270a0001c0002t0001g0271 | 2 | HG00639.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.656-32125C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91253117 | ||||||
| chr9:91253158
|
G | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(53): Show | 57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.656-32166C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91253158 | ||||||
| chr9:91253203
|
A | C | 1 | a0001c0001t0001g0229 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.656-32211T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91253203 | ||||||
| chr9:91253473
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.656-32481T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91253473 | ||||||
| chr9:91253870
|
G | A | 2 | a0001c0001t0001g0329a0001c0001t0001g0330 | 2 | NA18980.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.656-32878C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91253870 | ||||||
| chr9:91253983
|
C | G | 1 | a0003c0004t0001g0199 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.656-32991G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91253983 | ||||||
| chr9:91254183
|
G | C | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-33191C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91254183 | ||||||
| chr9:91254265
|
A | G | 1 | a0001c0001t0001g0021 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.656-33273T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91254265 | ||||||
| chr9:91254297
|
C | A | 1 | a0004c0008t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.656-33305G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91254297 | ||||||
| chr9:91254380
|
A | G | 25 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(22): Show | 26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.656-33388T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91254380 | ||||||
| chr9:91254625
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.656-33633T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91254625 | ||||||
| chr9:91254838
|
T | C | 1 | a0001c0001t0001g0103 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.656-33846A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91254838 | ||||||
| chr9:91254845
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.656-33853A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91254845 | ||||||
| chr9:91254874
|
T | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | HG03491.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.656-33882A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91254874 | ||||||
| chr9:91254987
|
T | C | 2 | a0001c0002t0001g0270a0001c0002t0001g0271 | 2 | HG00639.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.656-33995A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91254987 | ||||||
| chr9:91255095
|
A | G | 1 | a0001c0001t0001g0251 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.656-34103T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91255095 | ||||||
| chr9:91255285
|
G | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.656-34293C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91255285 | ||||||
| chr9:91255361
|
G | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(229): Show | 238 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(235): Show |
intron_variant | MODIFIER | c.656-34369C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91255361 | ||||||
| chr9:91256002
|
ATTAAAT | A | 25 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(22): Show | 26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.656-35016_656-3501 others(10): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91256002 | ||||||
| chr9:91256008
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.656-35016A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91256008 | ||||||
| chr9:91256158
|
T | C | 1 | a0001c0001t0001g0344 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.656-35166A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91256158 | ||||||
| chr9:91256191
|
G | T | 25 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(22): Show | 26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.656-35199C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91256191 | ||||||
| chr9:91256207
|
T | C | 1 | a0001c0001t0001g0094 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.656-35215A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91256207 | ||||||
| chr9:91256895
|
G | A | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-35903C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91256895 | ||||||
| chr9:91256913
|
G | A | 25 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(22): Show | 26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.656-35921C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91256913 | ||||||
| chr9:91256950
|
T | C | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-35958A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91256950 | ||||||
| chr9:91257128
|
G | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.656-36136C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91257128 | ||||||
| chr9:91257251
|
T | G | 16 | a0001c0001t0001g0010a0001c0001t0001g0227a0001c0001t0001g0296others(13): Show | 17 | HG00544.hp1 HG00673.hp2 HG02165.hp2 others(14): Show |
intron_variant | MODIFIER | c.656-36259A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91257251 | ||||||
| chr9:91257438
|
G | A | 5 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0163others(2): Show | 5 | HG02257.hp2 HG02630.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.656-36446C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91257438 | ||||||
| chr9:91257659
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.656-36667C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91257659 | ||||||
| chr9:91257779
|
T | G | 4 | a0001c0002t0001g0261a0001c0002t0001g0262a0001c0002t0001g0263others(1): Show | 4 | HG03098.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.656-36787A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91257779 | ||||||
| chr9:91258295
|
G | A | 2 | a0001c0001t0001g0154a0001c0001t0001g0159 | 2 | HG00280.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.656-37303C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91258295 | ||||||
| chr9:91258304
|
C | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.656-37312G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91258304 | ||||||
| chr9:91258479
|
C | A | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-37487G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91258479 | ||||||
| chr9:91258481
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0196a0001c0001t0001g0197 | 4 | HG02895.hp1 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.656-37489G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91258481 | ||||||
| chr9:91258517
|
G | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+37504C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91258517 | ||||||
| chr9:91258672
|
A | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+37349T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91258672 | ||||||
| chr9:91258948
|
A | G | 3 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279 | 3 | HG02257.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.655+37073T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91258948 | ||||||
| chr9:91258972
|
T | A | 2 | a0001c0001t0001g0242a0001c0001t0001g0245 | 2 | NA18978.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.655+37049A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91258972 | ||||||
| chr9:91259179
|
A | C | 1 | a0001c0001t0001g0033 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.655+36842T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91259179 | ||||||
| chr9:91259201
|
A | T | 1 | a0001c0001t0001g0003 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.655+36820T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91259201 | ||||||
| chr9:91259245
|
T | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0196a0001c0001t0001g0197 | 4 | HG02895.hp1 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.655+36776A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91259245 | ||||||
| chr9:91259252
|
T | G | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+36769A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91259252 | ||||||
| chr9:91259284
|
T | G | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(109): Show | 115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.655+36737A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91259284 | ||||||
| chr9:91259305
|
C | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(109): Show | 115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.655+36716G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91259305 | ||||||
| chr9:91259375
|
T | TCTC | 31 | a0001c0001t0001g0071a0001c0002t0001g0011a0001c0002t0001g0016others(28): Show | 32 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.655+36643_655+3664 others(7): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91259375 | ||||||
| chr9:91259559
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.655+36462A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91259559 | ||||||
| chr9:91259750
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.655+36271G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91259750 | ||||||
| chr9:91259757
|
T | C | 41 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(38): Show | 41 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.655+36264A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91259757 | ||||||
| chr9:91259793
|
T | C | 4 | a0001c0002t0001g0261a0001c0002t0001g0262a0001c0002t0001g0263others(1): Show | 4 | HG03098.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.655+36228A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91259793 | ||||||
| chr9:91259809
|
T | G | 6 | a0001c0001t0001g0322a0001c0001t0001g0341a0001c0001t0001g0342others(3): Show | 6 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.655+36212A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91259809 | ||||||
| chr9:91259873
|
C | T | 2 | a0001c0001t0001g0098a0001c0001t0001g0100 | 2 | HG02895.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.655+36148G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91259873 | ||||||
| chr9:91259902
|
C | T | 25 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(22): Show | 26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.655+36119G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91259902 | ||||||
| chr9:91260095
|
T | G | 1 | a0001c0001t0001g0333 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.655+35926A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91260095 | ||||||
| chr9:91260226
|
A | G | 1 | a0005c0005t0001g0012 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.655+35795T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91260226 | ||||||
| chr9:91260400
|
CTTCT | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+35617_655+3562 others(8): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91260400 | ||||||
| chr9:91260554
|
G | A | 34 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0227others(31): Show | 36 | HG00544.hp1 HG00673.hp2 HG01496.hp1 others(33): Show |
intron_variant | MODIFIER | c.655+35467C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91260554 | ||||||
| chr9:91260570
|
T | C | 4 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0082others(1): Show | 4 | NA18959.hp1 NA18983.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.655+35451A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91260570 | ||||||
| chr9:91260594
|
A | G | 3 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279 | 3 | HG02257.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.655+35427T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91260594 | ||||||
| chr9:91260664
|
T | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+35357A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91260664 | ||||||
| chr9:91260765
|
G | T | 1 | a0001c0001t0001g0036 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.655+35256C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91260765 | ||||||
| chr9:91260847
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.655+35174C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91260847 | ||||||
| chr9:91261028
|
T | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+34993A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91261028 | ||||||
| chr9:91261039
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.655+34982A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91261039 | ||||||
| chr9:91261060
|
C | T | 285 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(282): Show | 294 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(291): Show |
intron_variant | MODIFIER | c.655+34961G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91261060 | ||||||
| chr9:91261153
|
C | A | 15 | a0001c0001t0001g0007a0001c0001t0001g0200a0001c0001t0001g0201others(12): Show | 16 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.655+34868G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91261153 | ||||||
| chr9:91261178
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.655+34843C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91261178 | ||||||
| chr9:91261189
|
T | C | 3 | a0001c0001t0001g0341a0001c0001t0001g0344a0001c0001t0001g0345 | 3 | HG00280.hp2 HG00639.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.655+34832A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91261189 | ||||||
| chr9:91261293
|
A | G | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(109): Show | 115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.655+34728T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91261293 | ||||||
| chr9:91261322
|
C | T | 3 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279 | 3 | HG02257.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.655+34699G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91261322 | ||||||
| chr9:91261612
|
T | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+34409A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91261612 | ||||||
| chr9:91261660
|
A | G | 1 | a0001c0001t0001g0288 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.655+34361T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91261660 | ||||||
| chr9:91261923
|
G | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0309others(1): Show | 4 | NA18948.hp1 NA19068.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.655+34098C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91261923 | ||||||
| chr9:91262389
|
C | T | 4 | a0001c0001t0001g0112a0001c0001t0001g0145a0001c0001t0001g0146others(1): Show | 4 | HG01243.hp1 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.655+33632G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91262389 | ||||||
| chr9:91262422
|
C | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+33599G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91262422 | ||||||
| chr9:91262424
|
C | A | 6 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0029others(3): Show | 6 | NA18960.hp2 NA18965.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.655+33597G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91262424 | ||||||
| chr9:91262695
|
T | C | 5 | a0001c0002t0001g0261a0001c0002t0001g0262a0001c0002t0001g0263others(2): Show | 5 | HG03098.hp1 HG03209.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.655+33326A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91262695 | ||||||
| chr9:91262701
|
T | C | 6 | a0001c0001t0001g0322a0001c0001t0001g0341a0001c0001t0001g0342others(3): Show | 6 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.655+33320A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91262701 | ||||||
| chr9:91262941
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.655+33080C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91262941 | ||||||
| chr9:91262960
|
G | A | 25 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(22): Show | 26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.655+33061C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91262960 | ||||||
| chr9:91262964
|
T | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.655+33057A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91262964 | ||||||
| chr9:91263064
|
T | C | 16 | a0001c0001t0001g0005a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.655+32957A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91263064 | ||||||
| chr9:91263105
|
C | T | 1 | a0001c0001t0001g0284 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.655+32916G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91263105 | ||||||
| chr9:91263121
|
G | C | 1 | a0001c0001t0001g0094 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.655+32900C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91263121 | ||||||
| chr9:91263177
|
T | C | 26 | a0001c0001t0001g0071a0001c0002t0001g0011a0001c0002t0001g0016others(23): Show | 27 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.655+32844A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91263177 | ||||||
| chr9:91263184
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.655+32837C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91263184 | ||||||
| chr9:91263211
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.655+32810A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91263211 | ||||||
| chr9:91263216
|
T | C | 3 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279 | 3 | HG02257.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.655+32805A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91263216 | ||||||
| chr9:91263349
|
A | C | 1 | a0001c0001t0001g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.655+32672T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91263349 | ||||||
| chr9:91263567
|
A | C | 1 | a0001c0001t0001g0302 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.655+32454T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91263567 | ||||||
| chr9:91263621
|
A | C | 2 | a0001c0002t0001g0274a0001c0002t0001g0275 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.655+32400T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91263621 | ||||||
| chr9:91263709
|
G | A | 31 | a0001c0001t0001g0071a0001c0002t0001g0011a0001c0002t0001g0016others(28): Show | 32 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.655+32312C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91263709 | ||||||
| chr9:91263941
|
T | C | 1 | a0001c0001t0001g0024 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.655+32080A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91263941 | ||||||
| chr9:91264108
|
T | C | 1 | a0001c0001t0001g0094 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.655+31913A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91264108 | ||||||
| chr9:91264234
|
T | C | 1 | a0001c0001t0001g0302 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.655+31787A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91264234 | ||||||
| chr9:91264270
|
T | C | 2 | a0001c0001t0001g0067a0001c0001t0001g0090 | 2 | HG01256.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.655+31751A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91264270 | ||||||
| chr9:91264624
|
T | C | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+31397A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91264624 | ||||||
| chr9:91264661
|
A | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(53): Show | 57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.655+31360T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91264661 | ||||||
| chr9:91264836
|
A | G | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+31185T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91264836 | ||||||
| chr9:91265085
|
A | AG | 3 | a0001c0001t0001g0006a0001c0001t0001g0196a0001c0001t0001g0197 | 4 | HG02895.hp1 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.655+30935dupC | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91265085 | ||||||
| chr9:91265146
|
G | A | 3 | a0001c0001t0001g0065a0001c0001t0001g0292a0001c0001t0001g0293 | 3 | HG01167.hp1 HG01169.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.655+30875C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91265146 | ||||||
| chr9:91265277
|
A | AT | 55 | a0001c0001t0001g0028a0001c0001t0001g0092a0001c0001t0001g0093others(52): Show | 55 | HG00280.hp2 HG00639.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.655+30743dupA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91265277 | ||||||
| chr9:91265277
|
AT | A | 25 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(22): Show | 26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.655+30743delA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91265277 | ||||||
| chr9:91265327
|
CTTCA | C | 31 | a0001c0001t0001g0071a0001c0002t0001g0011a0001c0002t0001g0016others(28): Show | 32 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.655+30690_655+3069 others(8): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91265327 | ||||||
| chr9:91265395
|
T | A | 30 | a0001c0001t0001g0071a0001c0002t0001g0011a0001c0002t0001g0016others(27): Show | 31 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.655+30626A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91265395 | ||||||
| chr9:91265524
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.655+30497C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91265524 | ||||||
| chr9:91265676
|
T | A | 25 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(22): Show | 26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.655+30345A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91265676 | ||||||
| chr9:91265705
|
A | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(53): Show | 57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.655+30316T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91265705 | ||||||
| chr9:91265925
|
C | A | 13 | a0001c0001t0001g0017a0001c0001t0001g0280a0001c0001t0001g0281others(10): Show | 13 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.655+30096G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91265925 | ||||||
| chr9:91266085
|
G | A | 1 | a0005c0005t0001g0012 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.655+29936C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266085 | ||||||
| chr9:91266088
|
C | G | 47 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0095others(44): Show | 47 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.655+29933G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266088 | ||||||
| chr9:91266102
|
C | A | 1 | a0005c0005t0001g0012 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.655+29919G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266102 | ||||||
| chr9:91266186
|
A | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+29835T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266186 | ||||||
| chr9:91266233
|
A | G | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(109): Show | 115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.655+29788T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266233 | ||||||
| chr9:91266276
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.655+29745G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266276 | ||||||
| chr9:91266277
|
G | A | 1 | a0002c0003t0001g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.655+29744C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266277 | ||||||
| chr9:91266287
|
G | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0141 | 2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.655+29734C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266287 | ||||||
| chr9:91266362
|
A | AAAAT | 3 | a0001c0001t0001g0155a0001c0001t0001g0182a0001c0001t0001g0248 | 3 | HG01261.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.655+29655_655+2965 others(8): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266362 | ||||||
| chr9:91266362
|
AAAAT | A | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(233): Show | 243 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(240): Show |
intron_variant | MODIFIER | c.655+29655_655+2965 others(8): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266362 | ||||||
| chr9:91266535
|
C | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(53): Show | 57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.655+29486G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266535 | ||||||
| chr9:91266616
|
C | T | 26 | a0001c0001t0001g0071a0001c0002t0001g0011a0001c0002t0001g0016others(23): Show | 27 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.655+29405G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266616 | ||||||
| chr9:91266617
|
A | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(53): Show | 57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.655+29404T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266617 | ||||||
| chr9:91266618
|
T | C | 1 | a0001c0001t0001g0318 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.655+29403A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266618 | ||||||
| chr9:91266949
|
C | T | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0194 | 3 | HG02622.hp1 HG02647.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.655+29072G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266949 | ||||||
| chr9:91266950
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.655+29071C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266950 | ||||||
| chr9:91266956
|
G | C | 1 | a0001c0001t0001g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.655+29065C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266956 | ||||||
| chr9:91266974
|
A | G | 299 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(296): Show | 309 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(306): Show |
intron_variant | MODIFIER | c.655+29047T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266974 | ||||||
| chr9:91267099
|
T | C | 16 | a0001c0001t0001g0005a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.655+28922A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91267099 | ||||||
| chr9:91267359
|
A | G | 19 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(16): Show | 19 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.655+28662T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91267359 | ||||||
| chr9:91267411
|
T | C | 16 | a0001c0001t0001g0005a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.655+28610A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91267411 | ||||||
| chr9:91267633
|
T | C | 25 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(22): Show | 26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.655+28388A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91267633 | ||||||
| chr9:91267704
|
G | C | 41 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(38): Show | 41 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.655+28317C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91267704 | ||||||
| chr9:91267877
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.655+28144A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91267877 | ||||||
| chr9:91267903
|
G | A | 31 | a0001c0001t0001g0071a0001c0002t0001g0011a0001c0002t0001g0016others(28): Show | 32 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.655+28118C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91267903 | ||||||
| chr9:91267936
|
T | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(53): Show | 57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.655+28085A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91267936 | ||||||
| chr9:91268173
|
C | T | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+27848G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91268173 | ||||||
| chr9:91268217
|
A | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(53): Show | 57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.655+27804T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91268217 | ||||||
| chr9:91268286
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.655+27735T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91268286 | ||||||
| chr9:91268423
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.655+27598G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91268423 | ||||||
| chr9:91268433
|
A | AT | 62 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(59): Show | 65 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.655+27587dupA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91268433 | ||||||
| chr9:91268446
|
T | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+27575A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91268446 | ||||||
| chr9:91268499
|
C | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0060others(5): Show | 9 | HG03491.hp1 HG03492.hp1 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.655+27522G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91268499 | ||||||
| chr9:91268516
|
G | A | 31 | a0001c0001t0001g0071a0001c0002t0001g0011a0001c0002t0001g0016others(28): Show | 32 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.655+27505C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91268516 | ||||||
| chr9:91268523
|
C | T | 12 | a0001c0001t0001g0017a0001c0001t0001g0280a0001c0001t0001g0281others(9): Show | 12 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.655+27498G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91268523 | ||||||
| chr9:91268838
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.655+27183C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91268838 | ||||||
| chr9:91268882
|
A | T | 47 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0095others(44): Show | 47 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.655+27139T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91268882 | ||||||
| chr9:91268987
|
CT | C | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(109): Show | 115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.655+27033delA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91268987 | ||||||
| chr9:91269011
|
C | T | 25 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(22): Show | 26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.655+27010G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91269011 | ||||||
| chr9:91269067
|
A | G | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(109): Show | 115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.655+26954T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91269067 | ||||||
| chr9:91269115
|
G | A | 3 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279 | 3 | HG02257.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.655+26906C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91269115 | ||||||
| chr9:91269189
|
C | G | 1 | a0001c0001t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.655+26832G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91269189 | ||||||
| chr9:91269193
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.655+26828G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91269193 | ||||||
| chr9:91269247
|
G | T | 1 | a0001c0002t0001g0265 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.655+26774C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91269247 | ||||||
| chr9:91269258
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.655+26763G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91269258 | ||||||
| chr9:91269340
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.655+26681A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91269340 | ||||||
| chr9:91269375
|
G | A | 1 | a0001c0002t0004g0276 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.655+26646C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91269375 | ||||||
| chr9:91269393
|
G | T | 1 | a0001c0001t0001g0189 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.655+26628C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91269393 | ||||||
| chr9:91269408
|
T | C | 40 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0065others(37): Show | 42 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.655+26613A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91269408 | ||||||
| chr9:91269493
|
G | A | 25 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(22): Show | 26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.655+26528C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91269493 | ||||||
| chr9:91269740
|
T | C | 2 | a0001c0001t0001g0045a0001c0001t0001g0340 | 2 | HG00621.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.655+26281A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91269740 | ||||||
| chr9:91269923
|
C | T | 26 | a0001c0001t0001g0071a0001c0002t0001g0011a0001c0002t0001g0016others(23): Show | 27 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.655+26098G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91269923 | ||||||
| chr9:91269944
|
C | T | 1 | a0001c0001t0001g0122 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.655+26077G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91269944 | ||||||
| chr9:91270059
|
T | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+25962A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91270059 | ||||||
| chr9:91270431
|
G | C | 1 | a0001c0001t0001g0084 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.655+25590C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91270431 | ||||||
| chr9:91270445
|
G | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0196a0001c0001t0001g0197 | 4 | HG02895.hp1 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.655+25576C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91270445 | ||||||
| chr9:91270516
|
T | A | 1 | a0001c0001t0001g0161 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.655+25505A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91270516 | ||||||
| chr9:91270691
|
C | T | 3 | a0001c0001t0001g0294a0001c0001t0001g0301a0001c0001t0001g0305 | 3 | HG01496.hp1 HG02738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.655+25330G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91270691 | ||||||
| chr9:91270708
|
G | A | 2 | a0001c0001t0001g0297a0001c0001t0001g0323 | 2 | HG01081.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.655+25313C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91270708 | ||||||
| chr9:91270768
|
T | C | 1 | a0001c0001t0001g0097 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.655+25253A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91270768 | ||||||
| chr9:91270840
|
C | T | 60 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(57): Show | 63 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.655+25181G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91270840 | ||||||
| chr9:91270873
|
A | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+25148T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91270873 | ||||||
| chr9:91270930
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.655+25091C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91270930 | ||||||
| chr9:91270945
|
A | G | 1 | a0001c0002t0001g0267 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.655+25076T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91270945 | ||||||
| chr9:91271029
|
T | C | 3 | a0002c0003t0001g0013a0002c0003t0001g0014a0002c0003t0001g0015 | 3 | HG02451.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.655+24992A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91271029 | ||||||
| chr9:91271252
|
C | T | 1 | a0001c0001t0001g0296 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.655+24769G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91271252 | ||||||
| chr9:91271552
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.655+24469C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91271552 | ||||||
| chr9:91271825
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.655+24196G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91271825 | ||||||
| chr9:91272067
|
G | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+23954C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91272067 | ||||||
| chr9:91272286
|
A | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(53): Show | 57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.655+23735T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91272286 | ||||||
| chr9:91272469
|
T | C | 60 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(57): Show | 63 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.655+23552A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91272469 | ||||||
| chr9:91272577
|
G | A | 1 | a0001c0001t0001g0308 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.655+23444C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91272577 | ||||||
| chr9:91272670
|
T | C | 15 | a0001c0001t0001g0007a0001c0001t0001g0200a0001c0001t0001g0201others(12): Show | 16 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.655+23351A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91272670 | ||||||
| chr9:91272857
|
C | A | 1 | a0001c0001t0001g0189 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.655+23164G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91272857 | ||||||
| chr9:91272906
|
A | G | 1 | a0001c0001t0001g0094 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.655+23115T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91272906 | ||||||
| chr9:91272990
|
G | T | 31 | a0001c0001t0001g0071a0001c0002t0001g0011a0001c0002t0001g0016others(28): Show | 32 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.655+23031C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91272990 | ||||||
| chr9:91273051
|
C | T | 3 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0166 | 3 | HG02257.hp2 HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.655+22970G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91273051 | ||||||
| chr9:91273232
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.655+22789C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91273232 | ||||||
| chr9:91273336
|
T | C | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+22685A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91273336 | ||||||
| chr9:91273386
|
G | GT | 31 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0095others(28): Show | 31 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.655+22634dupA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91273386 | ||||||
| chr9:91273963
|
G | A | 31 | a0001c0001t0001g0071a0001c0002t0001g0011a0001c0002t0001g0016others(28): Show | 32 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.655+22058C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91273963 | ||||||
| chr9:91273987
|
C | A | 3 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335 | 3 | NA18990.hp2 NA19005.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.655+22034G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91273987 | ||||||
| chr9:91274046
|
C | A | 16 | a0001c0001t0001g0005a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.655+21975G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91274046 | ||||||
| chr9:91274081
|
A | G | 1 | a0001c0002t0001g0261 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.655+21940T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91274081 | ||||||
| chr9:91274165
|
A | T | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+21856T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91274165 | ||||||
| chr9:91274390
|
A | G | 8 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0060others(5): Show | 9 | HG03491.hp1 HG03492.hp1 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.655+21631T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91274390 | ||||||
| chr9:91274392
|
A | G | 34 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0227others(31): Show | 36 | HG00544.hp1 HG00673.hp2 HG01496.hp1 others(33): Show |
intron_variant | MODIFIER | c.655+21629T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91274392 | ||||||
| chr9:91274612
|
A | C | 1 | a0001c0001t0001g0144 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.655+21409T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91274612 | ||||||
| chr9:91274886
|
G | A | 1 | a0001c0001t0001g0331 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.655+21135C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91274886 | ||||||
| chr9:91275041
|
T | A | 1 | a0001c0001t0001g0190 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.655+20980A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91275041 | ||||||
| chr9:91275075
|
C | T | 1 | a0001c0001t0001g0326 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.655+20946G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91275075 | ||||||
| chr9:91275284
|
C | A | 8 | a0001c0001t0001g0071a0001c0002t0001g0011a0001c0002t0001g0272others(5): Show | 9 | HG03017.hp1 HG03688.hp1 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.655+20737G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91275284 | ||||||
| chr9:91275335
|
C | T | 1 | a0001c0001t0001g0175 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.655+20686G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91275335 | ||||||
| chr9:91275390
|
A | G | 16 | a0001c0001t0001g0005a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.655+20631T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91275390 | ||||||
| chr9:91275447
|
T | C | 1 | a0001c0001t0001g0223 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.655+20574A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91275447 | ||||||
| chr9:91275560
|
A | G | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(233): Show | 243 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(240): Show |
intron_variant | MODIFIER | c.655+20461T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91275560 | ||||||
| chr9:91275585
|
T | C | 345 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(342): Show | 356 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(353): Show |
intron_variant | MODIFIER | c.655+20436A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91275585 | ||||||
| chr9:91275591
|
T | C | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(230): Show | 239 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(236): Show |
intron_variant | MODIFIER | c.655+20430A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91275591 | ||||||
| chr9:91275739
|
T | C | 31 | a0001c0001t0001g0071a0001c0002t0001g0011a0001c0002t0001g0016others(28): Show | 32 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.655+20282A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91275739 | ||||||
| chr9:91275799
|
A | C | 2 | a0001c0001t0001g0139a0001c0001t0001g0331 | 2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.655+20222T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91275799 | ||||||
| chr9:91275843
|
T | A | 1 | a0001c0002t0004g0276 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.655+20178A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91275843 | ||||||
| chr9:91276101
|
C | T | 25 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(22): Show | 26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.655+19920G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91276101 | ||||||
| chr9:91276265
|
C | A | 2 | a0001c0002t0001g0258a0001c0002t0001g0260 | 2 | HG02572.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.655+19756G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91276265 | ||||||
| chr9:91276303
|
C | T | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+19718G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91276303 | ||||||
| chr9:91276342
|
A | C | 47 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0095others(44): Show | 47 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.655+19679T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91276342 | ||||||
| chr9:91276383
|
A | G | 1 | a0001c0001t0001g0232 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.655+19638T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91276383 | ||||||
| chr9:91276414
|
CA | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(112): Show | 119 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.655+19606delT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91276414 | ||||||
| chr9:91276416
|
A | C | 1 | a0001c0001t0001g0346 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.655+19605T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91276416 | ||||||
| chr9:91276468
|
C | A | 6 | a0001c0001t0001g0322a0001c0001t0001g0341a0001c0001t0001g0342others(3): Show | 6 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.655+19553G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91276468 | ||||||
| chr9:91276544
|
A | G | 1 | a0001c0001t0001g0302 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.655+19477T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91276544 | ||||||
| chr9:91276567
|
G | T | 2 | a0001c0001t0001g0327a0001c0001t0001g0328 | 2 | HG01978.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.655+19454C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91276567 | ||||||
| chr9:91276574
|
G | T | 1 | a0001c0001t0001g0220 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.655+19447C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91276574 | ||||||
| chr9:91276664
|
T | C | 1 | a0001c0001t0001g0023 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.655+19357A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91276664 | ||||||
| chr9:91277226
|
T | C | 1 | a0001c0001t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.655+18795A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91277226 | ||||||
| chr9:91277281
|
A | T | 1 | a0001c0001t0001g0120 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.655+18740T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91277281 | ||||||
| chr9:91277474
|
G | GT | 41 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(38): Show | 41 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.655+18546dupA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91277474 | ||||||
| chr9:91277572
|
T | C | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+18449A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91277572 | ||||||
| chr9:91277757
|
T | G | 1 | a0001c0001t0001g0052 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.655+18264A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91277757 | ||||||
| chr9:91277801
|
A | T | 6 | a0001c0001t0001g0121a0001c0001t0001g0127a0001c0001t0001g0128others(3): Show | 6 | NA18940.hp1 NA18951.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.655+18220T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91277801 | ||||||
| chr9:91277927
|
C | A | 32 | a0001c0001t0001g0071a0001c0001t0001g0079a0001c0002t0001g0011others(29): Show | 33 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.655+18094G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91277927 | ||||||
| chr9:91278003
|
T | C | 1 | a0001c0001t0001g0219 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.655+18018A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91278003 | ||||||
| chr9:91278014
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.655+18007C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91278014 | ||||||
| chr9:91278103
|
T | A | 16 | a0001c0001t0001g0017a0001c0001t0001g0277a0001c0001t0001g0278others(13): Show | 16 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.655+17918A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91278103 | ||||||
| chr9:91278127
|
T | C | 1 | a0004c0008t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.655+17894A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91278127 | ||||||
| chr9:91278211
|
A | G | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+17810T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91278211 | ||||||
| chr9:91278327
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.655+17694T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91278327 | ||||||
| chr9:91278560
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.655+17461A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91278560 | ||||||
| chr9:91278561
|
A | G | 12 | a0001c0001t0001g0017a0001c0001t0001g0280a0001c0001t0001g0281others(9): Show | 12 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.655+17460T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91278561 | ||||||
| chr9:91278732
|
A | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+17289T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91278732 | ||||||
| chr9:91278807
|
T | C | 1 | a0003c0004t0001g0199 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.655+17214A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91278807 | ||||||
| chr9:91278824
|
G | A | 1 | a0001c0001t0001g0328 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.655+17197C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91278824 | ||||||
| chr9:91278877
|
T | C | 16 | a0001c0001t0001g0005a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.655+17144A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91278877 | ||||||
| chr9:91279119
|
TTAA | T | 25 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(22): Show | 26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.655+16899_655+1690 others(7): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91279119 | ||||||
| chr9:91279185
|
A | G | 1 | a0001c0002t0001g0267 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.655+16836T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91279185 | ||||||
| chr9:91279234
|
T | C | 1 | a0001c0001t0001g0030 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.655+16787A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91279234 | ||||||
| chr9:91279307
|
A | C | 1 | a0001c0001t0001g0052 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.655+16714T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91279307 | ||||||
| chr9:91279370
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.655+16651C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91279370 | ||||||
| chr9:91279382
|
A | G | 1 | a0001c0001t0001g0330 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.655+16639T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91279382 | ||||||
| chr9:91279466
|
T | C | 1 | a0001c0001t0001g0313 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.655+16555A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91279466 | ||||||
| chr9:91279662
|
G | A | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+16359C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91279662 | ||||||
| chr9:91279726
|
C | T | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+16295G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91279726 | ||||||
| chr9:91279736
|
G | A | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+16285C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91279736 | ||||||
| chr9:91280025
|
T | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(125): Show | 132 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.655+15996A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91280025 | ||||||
| chr9:91280077
|
C | G | 16 | a0001c0001t0001g0005a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.655+15944G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91280077 | ||||||
| chr9:91280178
|
T | G | 16 | a0001c0001t0001g0017a0001c0001t0001g0277a0001c0001t0001g0278others(13): Show | 16 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.655+15843A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91280178 | ||||||
| chr9:91280425
|
C | T | 285 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(282): Show | 294 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(291): Show |
intron_variant | MODIFIER | c.655+15596G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91280425 | ||||||
| chr9:91280473
|
C | A | 16 | a0001c0001t0001g0005a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.655+15548G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91280473 | ||||||
| chr9:91280506
|
A | G | 16 | a0001c0001t0001g0005a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.655+15515T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91280506 | ||||||
| chr9:91280513
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.655+15508A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91280513 | ||||||
| chr9:91281092
|
A | AT | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.655+14928dupA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91281092 | ||||||
| chr9:91281257
|
T | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0043 | 2 | HG02602.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.655+14764A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91281257 | ||||||
| chr9:91281322
|
GTTTT | G | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.655+14695_655+1469 others(8): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91281322 | ||||||
| chr9:91281732
|
T | C | 5 | a0001c0001t0001g0119a0001c0001t0001g0139a0001c0001t0001g0140others(2): Show | 5 | HG01168.hp1 HG01884.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.655+14289A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91281732 | ||||||
| chr9:91281852
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0196a0001c0001t0001g0197 | 4 | HG02895.hp1 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.655+14169G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91281852 | ||||||
| chr9:91281917
|
C | T | 1 | a0001c0001t0001g0211 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.655+14104G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91281917 | ||||||
| chr9:91281956
|
G | A | 1 | a0001c0002t0004g0276 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.655+14065C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91281956 | ||||||
| chr9:91281990
|
C | T | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(125): Show | 131 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.655+14031G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91281990 | ||||||
| chr9:91282007
|
A | G | 16 | a0001c0001t0001g0005a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.655+14014T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91282007 | ||||||
| chr9:91282024
|
A | C | 16 | a0001c0001t0001g0017a0001c0001t0001g0277a0001c0001t0001g0278others(13): Show | 16 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.655+13997T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91282024 | ||||||
| chr9:91282037
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.655+13984A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91282037 | ||||||
| chr9:91282104
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.655+13917G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91282104 | ||||||
| chr9:91282176
|
T | G | 1 | a0001c0001t0001g0164 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.655+13845A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91282176 | ||||||
| chr9:91282234
|
C | A | 1 | a0001c0001t0001g0335 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.655+13787G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91282234 | ||||||
| chr9:91282369
|
A | G | 2 | a0001c0001t0001g0060a0001c0001t0001g0062 | 2 | NA18947.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.655+13652T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91282369 | ||||||
| chr9:91282433
|
C | G | 1 | a0001c0001t0001g0005 | 2 | HG02615.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.655+13588G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91282433 | ||||||
| chr9:91282488
|
G | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+13533C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91282488 | ||||||
| chr9:91282647
|
G | A | 27 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(24): Show | 28 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.655+13374C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91282647 | ||||||
| chr9:91282782
|
T | C | 1 | a0005c0005t0001g0012 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.655+13239A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91282782 | ||||||
| chr9:91282790
|
T | A | 2 | a0001c0001t0001g0297a0001c0001t0001g0323 | 2 | HG01081.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.655+13231A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91282790 | ||||||
| chr9:91282849
|
C | T | 57 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(54): Show | 59 | HG00408.hp2 HG00558.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.655+13172G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91282849 | ||||||
| chr9:91282895
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.655+13126C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91282895 | ||||||
| chr9:91282945
|
T | C | 1 | a0001c0002t0001g0260 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.655+13076A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91282945 | ||||||
| chr9:91282977
|
C | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+13044G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91282977 | ||||||
| chr9:91283049
|
T | C | 1 | a0001c0001t0001g0167 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.655+12972A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91283049 | ||||||
| chr9:91283081
|
G | A | 1 | a0001c0001t0001g0310 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.655+12940C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91283081 | ||||||
| chr9:91283097
|
C | G | 1 | a0001c0001t0001g0131 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.655+12924G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91283097 | ||||||
| chr9:91283110
|
C | T | 2 | a0001c0001t0001g0280a0001c0001t0001g0289 | 2 | HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.655+12911G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91283110 | ||||||
| chr9:91283189
|
T | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+12832A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91283189 | ||||||
| chr9:91283312
|
CA | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0197 | 3 | HG02895.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.655+12708delT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91283312 | ||||||
| chr9:91283433
|
T | C | 1 | a0001c0001t0001g0071 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.655+12588A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91283433 | ||||||
| chr9:91283489
|
C | G | 25 | a0001c0002t0001g0011a0001c0002t0001g0016a0001c0002t0001g0115others(22): Show | 26 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.655+12532G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91283489 | ||||||
| chr9:91283508
|
G | C | 15 | a0001c0001t0001g0007a0001c0001t0001g0200a0001c0001t0001g0201others(12): Show | 16 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.655+12513C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91283508 | ||||||
| chr9:91283526
|
C | T | 3 | a0001c0001t0001g0122a0001c0001t0001g0135a0001c0001t0001g0193 | 3 | HG02738.hp2 NA20905.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.655+12495G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91283526 | ||||||
| chr9:91283590
|
A | G | 1 | a0001c0001t0001g0094 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.655+12431T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91283590 | ||||||
| chr9:91283624
|
C | T | 30 | a0001c0002t0001g0011a0001c0002t0001g0016a0001c0002t0001g0115others(27): Show | 31 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.655+12397G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91283624 | ||||||
| chr9:91283765
|
C | G | 1 | a0001c0001t0001g0109 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.655+12256G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91283765 | ||||||
| chr9:91283950
|
A | G | 1 | a0001c0001t0001g0088 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.655+12071T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91283950 | ||||||
| chr9:91283999
|
T | A | 3 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279 | 3 | HG02257.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.655+12022A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91283999 | ||||||
| chr9:91284074
|
C | T | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(125): Show | 131 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.655+11947G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91284074 | ||||||
| chr9:91284110
|
C | A | 1 | a0001c0001t0001g0335 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.655+11911G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91284110 | ||||||
| chr9:91284112
|
G | A | 1 | a0001c0001t0001g0335 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.655+11909C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91284112 | ||||||
| chr9:91284113
|
A | T | 1 | a0001c0001t0001g0335 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.655+11908T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91284113 | ||||||
| chr9:91284114
|
G | A | 1 | a0001c0001t0001g0335 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.655+11907C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91284114 | ||||||
| chr9:91284614
|
C | T | 27 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(24): Show | 28 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.655+11407G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91284614 | ||||||
| chr9:91284655
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.655+11366C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91284655 | ||||||
| chr9:91284802
|
G | A | 11 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0127others(8): Show | 11 | NA18940.hp1 NA18945.hp1 NA18946.hp2 others(8): Show |
intron_variant | MODIFIER | c.655+11219C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91284802 | ||||||
| chr9:91284837
|
T | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+11184A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91284837 | ||||||
| chr9:91284995
|
G | C | 1 | a0001c0001t0001g0172 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.655+11026C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91284995 | ||||||
| chr9:91285307
|
T | G | 1 | a0001c0001t0001g0061 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.655+10714A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91285307 | ||||||
| chr9:91285351
|
C | A | 1 | a0001c0001t0001g0163 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.655+10670G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91285351 | ||||||
| chr9:91285532
|
T | C | 41 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(38): Show | 41 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.655+10489A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91285532 | ||||||
| chr9:91285559
|
ACAGTATT others(7): Show |
A | 46 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0095others(43): Show | 46 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.655+10448_655+1046 others(18): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91285559 | ||||||
| chr9:91285573
|
G | A | 1 | a0001c0001t0001g0240 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.655+10448C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91285573 | ||||||
| chr9:91286247
|
C | T | 30 | a0001c0002t0001g0011a0001c0002t0001g0016a0001c0002t0001g0115others(27): Show | 31 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.655+9774G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91286247 | ||||||
| chr9:91286370
|
T | C | 1 | a0001c0001t0001g0054 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.655+9651A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91286370 | ||||||
| chr9:91286449
|
TG | T | 6 | a0001c0001t0001g0020a0001c0001t0001g0045a0001c0001t0001g0047others(3): Show | 6 | HG00597.hp1 HG00621.hp1 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.655+9571delC | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91286449 | ||||||
| chr9:91286720
|
T | TA | 76 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(73): Show | 79 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.655+9300dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91286720 | ||||||
| chr9:91286720
|
TA | T | 7 | a0001c0001t0001g0055a0001c0001t0001g0080a0001c0001t0001g0090others(4): Show | 7 | HG01256.hp1 HG01433.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.655+9300delT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91286720 | ||||||
| chr9:91286747
|
T | C | 1 | a0001c0001t0001g0246 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.655+9274A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91286747 | ||||||
| chr9:91286771
|
A | C | 4 | a0001c0001t0001g0117a0001c0001t0001g0277a0001c0001t0001g0278others(1): Show | 4 | HG02257.hp1 HG02818.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.655+9250T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91286771 | ||||||
| chr9:91286781
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.655+9240C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91286781 | ||||||
| chr9:91286783
|
G | A | 5 | a0001c0001t0001g0072a0001c0001t0001g0080a0001c0001t0001g0081others(2): Show | 5 | NA18957.hp1 NA19058.hp2 NA19064.hp2 others(2): Show |
intron_variant | MODIFIER | c.655+9238C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91286783 | ||||||
| chr9:91286786
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.655+9235A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91286786 | ||||||
| chr9:91286930
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.655+9091A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91286930 | ||||||
| chr9:91286993
|
CTTAAT | C | 3 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279 | 3 | HG02257.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.655+9023_655+9027d others(7): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91286993 | ||||||
| chr9:91287034
|
T | A | 1 | a0001c0001t0001g0335 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.655+8987A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91287034 | ||||||
| chr9:91287077
|
T | A | 1 | a0001c0001t0001g0160 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.655+8944A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91287077 | ||||||
| chr9:91287094
|
TA | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+8926delT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91287094 | ||||||
| chr9:91287474
|
A | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+8547T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91287474 | ||||||
| chr9:91287523
|
T | C | 1 | a0001c0001t0001g0294 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.655+8498A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91287523 | ||||||
| chr9:91287524
|
A | G | 16 | a0001c0001t0001g0005a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.655+8497T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91287524 | ||||||
| chr9:91287597
|
T | C | 13 | a0001c0001t0001g0003a0001c0001t0001g0118a0001c0001t0001g0214others(10): Show | 14 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.655+8424A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91287597 | ||||||
| chr9:91287837
|
G | A | 1 | a0001c0001t0001g0022 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.655+8184C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91287837 | ||||||
| chr9:91287929
|
A | G | 1 | a0001c0001t0001g0303 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.655+8092T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91287929 | ||||||
| chr9:91288035
|
T | C | 1 | a0001c0001t0001g0059 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.655+7986A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91288035 | ||||||
| chr9:91288216
|
C | T | 5 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(2): Show | 5 | HG00735.hp2 HG01433.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.655+7805G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91288216 | ||||||
| chr9:91288537
|
A | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0196a0001c0001t0001g0197 | 4 | HG02895.hp1 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.655+7484T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91288537 | ||||||
| chr9:91288756
|
A | G | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+7265T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91288756 | ||||||
| chr9:91288787
|
T | C | 12 | a0001c0001t0001g0017a0001c0001t0001g0280a0001c0001t0001g0281others(9): Show | 12 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.655+7234A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91288787 | ||||||
| chr9:91288887
|
A | G | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+7134T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91288887 | ||||||
| chr9:91289076
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.655+6945G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91289076 | ||||||
| chr9:91289083
|
A | T | 1 | a0001c0001t0001g0087 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.655+6938T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91289083 | ||||||
| chr9:91289514
|
A | G | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+6507T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91289514 | ||||||
| chr9:91289608
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.655+6413T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91289608 | ||||||
| chr9:91289772
|
ATCT | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.655+6246_655+6248d others(5): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91289772 | ||||||
| chr9:91289886
|
G | A | 6 | a0001c0001t0001g0322a0001c0001t0001g0341a0001c0001t0001g0342others(3): Show | 6 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.655+6135C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91289886 | ||||||
| chr9:91289892
|
G | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+6129C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91289892 | ||||||
| chr9:91289999
|
C | T | 3 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279 | 3 | HG02257.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.655+6022G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91289999 | ||||||
| chr9:91290186
|
CAGG | C | 47 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0095others(44): Show | 47 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.655+5832_655+5834d others(5): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91290186 | ||||||
| chr9:91290220
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.655+5801T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91290220 | ||||||
| chr9:91290336
|
A | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+5685T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91290336 | ||||||
| chr9:91290411
|
T | A | 1 | a0001c0001t0001g0340 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.655+5610A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91290411 | ||||||
| chr9:91290474
|
T | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.655+5547A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91290474 | ||||||
| chr9:91290762
|
C | T | 11 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(8): Show | 11 | HG00280.hp1 HG00642.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.655+5259G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91290762 | ||||||
| chr9:91290830
|
T | C | 16 | a0001c0001t0001g0005a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.655+5191A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91290830 | ||||||
| chr9:91290983
|
T | C | 15 | a0001c0001t0001g0005a0001c0001t0001g0170a0001c0001t0001g0171others(12): Show | 16 | HG02145.hp1 HG02451.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.655+5038A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91290983 | ||||||
| chr9:91291036
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.655+4985C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91291036 | ||||||
| chr9:91291262
|
C | T | 48 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(45): Show | 48 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.655+4759G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91291262 | ||||||
| chr9:91291311
|
G | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0153 | 3 | HG01168.hp2 HG01169.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.655+4710C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91291311 | ||||||
| chr9:91291598
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.655+4423T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91291598 | ||||||
| chr9:91291686
|
C | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.655+4335G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91291686 | ||||||
| chr9:91291906
|
G | C | 1 | a0001c0001t0001g0140 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.655+4115C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91291906 | ||||||
| chr9:91291922
|
CA | C | 70 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(67): Show | 71 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.655+4098delT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91291922 | ||||||
| chr9:91291922
|
CAA | C | 185 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(182): Show | 192 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.655+4097_655+4098d others(4): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91291922 | ||||||
| chr9:91291922
|
CAAA | C | 53 | a0001c0001t0001g0017a0001c0001t0001g0082a0001c0001t0001g0097others(50): Show | 54 | HG00597.hp2 HG00609.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.655+4096_655+4098d others(5): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91291922 | ||||||
| chr9:91292025
|
A | C | 1 | a0001c0002t0001g0339 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.655+3996T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91292025 | ||||||
| chr9:91292214
|
G | A | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | NA18954.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.655+3807C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91292214 | ||||||
| chr9:91292273
|
C | CT | 21 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(18): Show | 21 | HG00544.hp1 HG00673.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.655+3747dupA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91292273 | ||||||
| chr9:91292273
|
CT | C | 39 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0019others(36): Show | 40 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.655+3747delA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91292273 | ||||||
| chr9:91292298
|
C | T | 1 | a0001c0001t0001g0008 | 2 | NA18946.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.655+3723G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91292298 | ||||||
| chr9:91292360
|
T | C | 3 | a0002c0003t0001g0013a0002c0003t0001g0014a0002c0003t0001g0015 | 3 | HG02451.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.655+3661A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91292360 | ||||||
| chr9:91292384
|
T | C | 30 | a0001c0002t0001g0011a0001c0002t0001g0016a0001c0002t0001g0115others(27): Show | 31 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.655+3637A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91292384 | ||||||
| chr9:91292392
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.655+3629G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91292392 | ||||||
| chr9:91292414
|
G | A | 16 | a0001c0001t0001g0005a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.655+3607C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91292414 | ||||||
| chr9:91292564
|
A | C | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(109): Show | 115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.655+3457T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91292564 | ||||||
| chr9:91292664
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.655+3357G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91292664 | ||||||
| chr9:91292845
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.655+3176A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91292845 | ||||||
| chr9:91292889
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.655+3132G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91292889 | ||||||
| chr9:91292981
|
T | C | 6 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(3): Show | 6 | HG02132.hp1 NA18982.hp1 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.655+3040A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91292981 | ||||||
| chr9:91293110
|
G | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(141): Show | 148 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.655+2911C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91293110 | ||||||
| chr9:91293324
|
C | A | 1 | a0001c0001t0001g0217 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.655+2697G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91293324 | ||||||
| chr9:91293389
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.655+2632G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91293389 | ||||||
| chr9:91293744
|
T | C | 1 | a0001c0001t0001g0233 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.655+2277A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91293744 | ||||||
| chr9:91293972
|
T | C | 1 | a0001c0002t0001g0269 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.655+2049A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91293972 | ||||||
| chr9:91294275
|
C | T | 30 | a0001c0002t0001g0011a0001c0002t0001g0016a0001c0002t0001g0115others(27): Show | 31 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.655+1746G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91294275 | ||||||
| chr9:91294287
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.655+1734G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91294287 | ||||||
| chr9:91294304
|
C | T | 47 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0095others(44): Show | 47 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.655+1717G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91294304 | ||||||
| chr9:91294737
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.655+1284T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91294737 | ||||||
| chr9:91294801
|
C | T | 6 | a0001c0002t0001g0011a0001c0002t0001g0272a0001c0002t0001g0336others(3): Show | 7 | HG03017.hp1 NA18947.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.655+1220G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91294801 | ||||||
| chr9:91294853
|
C | T | 6 | a0001c0002t0001g0011a0001c0002t0001g0272a0001c0002t0001g0336others(3): Show | 7 | HG03017.hp1 NA18947.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.655+1168G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91294853 | ||||||
| chr9:91294896
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.655+1125C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91294896 | ||||||
| chr9:91294954
|
C | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(109): Show | 115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.655+1067G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91294954 | ||||||
| chr9:91294980
|
CAT | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0153 | 3 | HG01168.hp2 HG01169.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.655+1039_655+1040d others(4): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91294980 | ||||||
| chr9:91295048
|
G | A | 2 | a0001c0001t0001g0322a0001c0002t0001g0264 | 2 | HG02300.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.655+973C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91295048 | ||||||
| chr9:91295201
|
T | C | 1 | a0001c0001t0001g0094 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.655+820A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91295201 | ||||||
| chr9:91295539
|
C | T | 5 | a0001c0001t0001g0111a0001c0001t0001g0141a0002c0003t0001g0013others(2): Show | 5 | HG02451.hp2 HG02572.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.655+482G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91295539 | ||||||
| chr9:91295785
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.655+236G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91295785 | ||||||
| chr9:91295822
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.655+199G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91295822 | ||||||
| chr9:91295925
|
G | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.655+96C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91295925 | ||||||
| chr9:91296197
|
C | CTTTTTTT others(727): Show |
1 | a0001c0001t0001g0342 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.599-121_599-120ins others(734): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | ||||||
| chr9:91296197
|
C | CTTTTTTT others(727): Show |
4 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0044others(1): Show | 4 | HG02155.hp2 NA18948.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.599-121_599-120ins others(734): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | ||||||
| chr9:91296197
|
C | CTTTTTTT others(728): Show |
1 | a0001c0001t0001g0056 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.599-121_599-120ins others(735): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | ||||||
| chr9:91296197
|
C | CTTTTTTT others(727): Show |
1 | a0001c0001t0001g0054 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.599-121_599-120ins others(734): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | ||||||
| chr9:91296197
|
C | CTTTTTTT others(728): Show |
1 | a0001c0001t0001g0026 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.599-121_599-120ins others(735): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | ||||||
| chr9:91296197
|
C | CTTTTTTT others(729): Show |
1 | a0001c0001t0001g0340 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.599-121_599-120ins others(736): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | ||||||
| chr9:91296197
|
C | CTTTTTTT others(728): Show |
5 | a0001c0001t0001g0322a0001c0001t0001g0341a0001c0001t0001g0343others(2): Show | 5 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.599-121_599-120ins others(735): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | ||||||
| chr9:91296197
|
C | CTTTTTTT others(728): Show |
31 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(28): Show | 31 | HG00438.hp1 HG00597.hp1 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.599-121_599-120ins others(735): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | ||||||
| chr9:91296197
|
C | CTTTTTTT others(729): Show |
1 | a0001c0001t0001g0042 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.599-121_599-120ins others(736): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | ||||||
| chr9:91296197
|
C | CTTTTTTT others(730): Show |
1 | a0001c0001t0001g0033 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.599-121_599-120ins others(737): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | ||||||
| chr9:91296197
|
C | CTTTTTTT others(745): Show |
1 | a0001c0001t0001g0062 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.599-121_599-120ins others(752): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | ||||||
| chr9:91296197
|
C | CTTTTTTT others(748): Show |
2 | a0001c0001t0001g0059a0001c0001t0001g0063 | 2 | NA18955.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.599-121_599-120ins others(755): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | ||||||
| chr9:91296197
|
C | CTTTTTTT others(749): Show |
1 | a0001c0001t0001g0064 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.599-121_599-120ins others(756): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | ||||||
| chr9:91296197
|
C | CTTTTTTT others(750): Show |
1 | a0001c0001t0001g0061 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.599-121_599-120ins others(757): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | ||||||
| chr9:91296197
|
C | CTTTTTTT others(751): Show |
1 | a0001c0001t0001g0060 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.599-121_599-120ins others(758): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | ||||||
| chr9:91296197
|
C | CTTTTTTT others(752): Show |
1 | a0001c0001t0001g0346 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.599-121_599-120ins others(759): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | ||||||
| chr9:91296197
|
C | CTTTTTTT others(758): Show |
1 | a0001c0001t0001g0001 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.599-121_599-120ins others(765): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | ||||||
| chr9:91296200
|
A | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.599-123T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296200 | ||||||
| chr9:91296201
|
A | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.599-124T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296201 | ||||||
| chr9:91296204
|
A | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.599-127T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296204 | ||||||
| chr9:91296205
|
A | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.599-128T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296205 | ||||||
| chr9:91296374
|
T | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0196a0001c0001t0001g0197 | 4 | HG02895.hp1 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-297A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296374 | ||||||
| chr9:91296550
|
T | C | 1 | a0005c0005t0001g0012 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.599-473A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296550 | ||||||
| chr9:91296761
|
C | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.599-684G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296761 | ||||||
| chr9:91296832
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.599-755A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296832 | ||||||
| chr9:91296839
|
G | A | 4 | a0001c0001t0001g0332a0001c0001t0001g0333a0001c0001t0001g0334others(1): Show | 4 | NA18990.hp2 NA19005.hp1 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-762C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296839 | ||||||
| chr9:91296860
|
A | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0340 | 3 | HG00621.hp1 NA18612.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.599-783T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296860 | ||||||
| chr9:91296896
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0153 | 3 | HG01168.hp2 HG01169.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.599-819C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296896 | ||||||
| chr9:91297017
|
T | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.599-940A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91297017 | ||||||
| chr9:91297254
|
A | C | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.598+730T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91297254 | ||||||
| chr9:91297265
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.598+719C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91297265 | ||||||
| chr9:91297369
|
CACCT | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.598+611_598+614del others(4): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91297369 | ||||||
| chr9:91297536
|
G | A | 6 | a0001c0001t0001g0322a0001c0001t0001g0341a0001c0001t0001g0342others(3): Show | 6 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.598+448C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91297536 | ||||||
| chr9:91297554
|
AAGGGAGG others(5): Show |
A | 1 | a0001c0002t0004g0276 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.598+418_598+429del others(12): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91297554 | ||||||
| chr9:91297591
|
CTTTT | C | 54 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.598+389_598+392del others(4): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91297591 | ||||||
| chr9:91297596
|
T | A | 1 | a0001c0001t0001g0340 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.598+388A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91297596 | ||||||
| chr9:91297598
|
A | T | 1 | a0001c0001t0001g0340 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.598+386T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91297598 | ||||||
| chr9:91297619
|
G | T | 1 | a0001c0001t0001g0182 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.598+365C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91297619 | ||||||
| chr9:91297646
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.598+338C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91297646 | ||||||
| chr9:91297749
|
G | A | 45 | a0001c0001t0001g0005a0001c0001t0001g0170a0001c0001t0001g0171others(42): Show | 47 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.598+235C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91297749 | ||||||
| chr9:91297750
|
C | T | 2 | a0001c0001t0001g0058a0001c0001t0001g0252 | 2 | NA18942.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.598+234G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91297750 | ||||||
| chr9:91298244
|
C | CA | 346 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(343): Show | 357 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(354): Show |
intron_variant | MODIFIER | c.506-169dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91298244 | ||||||
| chr9:91298443
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.506-367A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91298443 | ||||||
| chr9:91298507
|
T | C | 1 | a0001c0001t0001g0332 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.506-431A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91298507 | ||||||
| chr9:91298681
|
C | T | 1 | a0001c0001t0001g0318 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.506-605G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91298681 | ||||||
| chr9:91298691
|
G | A | 1 | a0001c0001t0001g0332 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.506-615C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91298691 | ||||||
| chr9:91298696
|
G | C | 1 | a0001c0001t0001g0049 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.506-620C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91298696 | ||||||
| chr9:91298765
|
G | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.506-689C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91298765 | ||||||
| chr9:91298933
|
T | C | 2 | a0001c0001t0001g0292a0001c0001t0001g0293 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.506-857A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91298933 | ||||||
| chr9:91298945
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.506-869C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91298945 | ||||||
| chr9:91299161
|
G | C | 1 | a0001c0001t0001g0344 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.506-1085C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91299161 | ||||||
| chr9:91299351
|
A | G | 30 | a0001c0002t0001g0011a0001c0002t0001g0016a0001c0002t0001g0115others(27): Show | 31 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.506-1275T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91299351 | ||||||
| chr9:91299617
|
G | C | 15 | a0001c0001t0001g0005a0001c0001t0001g0170a0001c0001t0001g0171others(12): Show | 16 | HG02145.hp1 HG02451.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.506-1541C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91299617 | ||||||
| chr9:91299639
|
T | C | 27 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(24): Show | 28 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.506-1563A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91299639 | ||||||
| chr9:91299681
|
A | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(53): Show | 57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.506-1605T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91299681 | ||||||
| chr9:91299766
|
A | T | 15 | a0001c0001t0001g0007a0001c0001t0001g0200a0001c0001t0001g0201others(12): Show | 16 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.506-1690T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91299766 | ||||||
| chr9:91299780
|
C | T | 3 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107 | 3 | NA18978.hp1 NA19002.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.506-1704G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91299780 | ||||||
| chr9:91299781
|
G | A | 2 | a0001c0001t0001g0200a0001c0001t0001g0201 | 2 | HG00438.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.506-1705C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91299781 | ||||||
| chr9:91300039
|
A | T | 1 | a0001c0001t0001g0191 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.506-1963T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91300039 | ||||||
| chr9:91300110
|
AC | A | 30 | a0001c0002t0001g0011a0001c0002t0001g0016a0001c0002t0001g0115others(27): Show | 31 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.506-2035delG | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91300110 | ||||||
| chr9:91300179
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.506-2103G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91300179 | ||||||
| chr9:91300569
|
C | A | 1 | a0001c0002t0002g0259 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.506-2493G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91300569 | ||||||
| chr9:91300642
|
T | G | 41 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0065others(38): Show | 43 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.506-2566A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91300642 | ||||||
| chr9:91300696
|
C | T | 47 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0095others(44): Show | 47 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.506-2620G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91300696 | ||||||
| chr9:91300745
|
G | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.506-2669C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91300745 | ||||||
| chr9:91300822
|
T | A | 1 | a0001c0001t0001g0103 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.506-2746A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91300822 | ||||||
| chr9:91300838
|
A | G | 3 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0055 | 3 | HG00438.hp1 NA18940.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.506-2762T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91300838 | ||||||
| chr9:91300992
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.506-2916G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91300992 | ||||||
| chr9:91301369
|
A | T | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(125): Show | 131 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.506-3293T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91301369 | ||||||
| chr9:91301622
|
G | C | 1 | a0001c0001t0001g0063 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.506-3546C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91301622 | ||||||
| chr9:91301699
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.506-3623C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91301699 | ||||||
| chr9:91301784
|
C | T | 41 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(38): Show | 41 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.506-3708G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91301784 | ||||||
| chr9:91301973
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.506-3897C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91301973 | ||||||
| chr9:91301974
|
T | C | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.506-3898A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91301974 | ||||||
| chr9:91302058
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.506-3982A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91302058 | ||||||
| chr9:91302194
|
AGT | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(109): Show | 115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.506-4120_506-4119d others(4): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91302194 | ||||||
| chr9:91302195
|
G | C | 3 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0001g0101 | 3 | HG02280.hp2 HG02895.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.506-4119C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91302195 | ||||||
| chr9:91302344
|
C | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.506-4268G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91302344 | ||||||
| chr9:91302452
|
G | C | 1 | a0001c0001t0001g0251 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.506-4376C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91302452 | ||||||
| chr9:91302663
|
G | C | 1 | a0001c0001t0001g0191 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.506-4587C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91302663 | ||||||
| chr9:91302995
|
T | C | 3 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0331 | 3 | HG01168.hp1 HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.506-4919A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91302995 | ||||||
| chr9:91303352
|
G | A | 6 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0029others(3): Show | 6 | NA18960.hp2 NA18965.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.506-5276C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91303352 | ||||||
| chr9:91303369
|
C | T | 47 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0095others(44): Show | 47 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.506-5293G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91303369 | ||||||
| chr9:91303394
|
A | G | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(126): Show | 133 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.506-5318T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91303394 | ||||||
| chr9:91303424
|
G | A | 1 | a0001c0002t0001g0260 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.506-5348C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91303424 | ||||||
| chr9:91303751
|
T | C | 6 | a0001c0001t0001g0322a0001c0001t0001g0341a0001c0001t0001g0342others(3): Show | 6 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.506-5675A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91303751 | ||||||
| chr9:91303754
|
A | G | 1 | a0001c0001t0001g0238 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.506-5678T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91303754 | ||||||
| chr9:91303970
|
C | G | 1 | a0001c0001t0001g0326 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.506-5894G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91303970 | ||||||
| chr9:91303988
|
T | C | 1 | a0001c0001t0001g0173 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.506-5912A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91303988 | ||||||
| chr9:91304301
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.506-6225C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91304301 | ||||||
| chr9:91304473
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.506-6397G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91304473 | ||||||
| chr9:91304579
|
G | T | 2 | a0001c0001t0001g0033a0001c0001t0001g0039 | 2 | HG00544.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.506-6503C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91304579 | ||||||
| chr9:91304682
|
T | C | 40 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0065others(37): Show | 42 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.506-6606A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91304682 | ||||||
| chr9:91304915
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.506-6839C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91304915 | ||||||
| chr9:91305034
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.506-6958A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91305034 | ||||||
| chr9:91305152
|
A | G | 1 | a0001c0002t0001g0264 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.506-7076T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91305152 | ||||||
| chr9:91305212
|
TA | T | 12 | a0001c0001t0001g0017a0001c0001t0001g0280a0001c0001t0001g0281others(9): Show | 12 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.506-7137delT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91305212 | ||||||
| chr9:91305214
|
A | C | 1 | a0001c0001t0001g0170 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.506-7138T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91305214 | ||||||
| chr9:91305380
|
C | T | 1 | a0002c0003t0001g0015 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.506-7304G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91305380 | ||||||
| chr9:91305397
|
C | T | 4 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0001g0101others(1): Show | 4 | HG02280.hp2 HG02895.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.506-7321G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91305397 | ||||||
| chr9:91305687
|
C | G | 1 | a0001c0002t0001g0268 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.506-7611G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91305687 | ||||||
| chr9:91305718
|
C | T | 1 | a0001c0002t0001g0272 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.506-7642G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91305718 | ||||||
| chr9:91305759
|
T | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0214a0001c0001t0001g0215others(4): Show | 8 | HG01071.hp2 HG01106.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.506-7683A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91305759 | ||||||
| chr9:91306000
|
G | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.506-7924C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91306000 | ||||||
| chr9:91306244
|
C | T | 6 | a0001c0001t0001g0322a0001c0001t0001g0341a0001c0001t0001g0342others(3): Show | 6 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.506-8168G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91306244 | ||||||
| chr9:91306659
|
AT | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(109): Show | 115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.506-8584delA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91306659 | ||||||
| chr9:91306795
|
G | A | 1 | a0001c0001t0001g0023 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.506-8719C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91306795 | ||||||
| chr9:91307071
|
A | G | 1 | a0001c0001t0001g0123 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.506-8995T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91307071 | ||||||
| chr9:91307085
|
G | A | 3 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0166 | 3 | HG02257.hp2 HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.506-9009C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91307085 | ||||||
| chr9:91307166
|
G | A | 1 | a0001c0002t0004g0276 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.506-9090C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91307166 | ||||||
| chr9:91307192
|
T | C | 1 | a0001c0001t0001g0186 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.506-9116A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91307192 | ||||||
| chr9:91307347
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.506-9271C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91307347 | ||||||
| chr9:91307665
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.506-9589A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91307665 | ||||||
| chr9:91307898
|
G | C | 4 | a0001c0002t0001g0261a0001c0002t0001g0262a0001c0002t0001g0263others(1): Show | 4 | HG03098.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.506-9822C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91307898 | ||||||
| chr9:91308022
|
C | T | 46 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0091others(43): Show | 48 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.506-9946G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91308022 | ||||||
| chr9:91308348
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.506-10272C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91308348 | ||||||
| chr9:91308384
|
G | C | 3 | a0001c0001t0001g0018a0001c0001t0001g0046a0001c0001t0001g0057 | 3 | NA18969.hp1 NA18970.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.506-10308C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91308384 | ||||||
| chr9:91308462
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.506-10386G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91308462 | ||||||
| chr9:91308500
|
T | C | 57 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(54): Show | 59 | HG00408.hp2 HG00558.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.506-10424A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91308500 | ||||||
| chr9:91308733
|
C | T | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.506-10657G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91308733 | ||||||
| chr9:91308791
|
C | CT | 48 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0050others(45): Show | 49 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.506-10716dupA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91308791 | ||||||
| chr9:91309081
|
G | A | 15 | a0001c0001t0001g0005a0001c0001t0001g0170a0001c0001t0001g0171others(12): Show | 16 | HG02145.hp1 HG02451.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.506-11005C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91309081 | ||||||
| chr9:91309237
|
C | T | 1 | a0001c0001t0001g0326 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.506-11161G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91309237 | ||||||
| chr9:91309503
|
G | A | 15 | a0001c0001t0001g0005a0001c0001t0001g0170a0001c0001t0001g0171others(12): Show | 16 | HG02145.hp1 HG02451.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.506-11427C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91309503 | ||||||
| chr9:91309555
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.506-11479C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91309555 | ||||||
| chr9:91309662
|
G | C | 15 | a0001c0001t0001g0005a0001c0001t0001g0170a0001c0001t0001g0171others(12): Show | 16 | HG02145.hp1 HG02451.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.506-11586C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91309662 | ||||||
| chr9:91309687
|
G | A | 1 | a0001c0001t0001g0004 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.506-11611C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91309687 | ||||||
| chr9:91309803
|
G | A | 1 | a0001c0001t0001g0044 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.506-11727C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91309803 | ||||||
| chr9:91309831
|
T | C | 48 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0095others(45): Show | 48 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.506-11755A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91309831 | ||||||
| chr9:91309919
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.506-11843G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91309919 | ||||||
| chr9:91309935
|
C | CT | 48 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0095others(45): Show | 48 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.506-11860dupA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91309935 | ||||||
| chr9:91310115
|
G | A | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.506-12039C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91310115 | ||||||
| chr9:91310133
|
C | T | 6 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0076others(3): Show | 6 | NA18956.hp2 NA18959.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.506-12057G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91310133 | ||||||
| chr9:91310137
|
C | T | 1 | a0001c0001t0001g0240 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.506-12061G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91310137 | ||||||
| chr9:91310138
|
T | C | 1 | a0001c0001t0001g0087 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.506-12062A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91310138 | ||||||
| chr9:91310319
|
G | A | 2 | a0001c0001t0001g0234a0001c0001t0001g0237 | 2 | HG01934.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.506-12243C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91310319 | ||||||
| chr9:91310560
|
A | G | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.506-12484T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91310560 | ||||||
| chr9:91310729
|
A | T | 1 | a0001c0001t0001g0032 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.506-12653T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91310729 | ||||||
| chr9:91310905
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.506-12829G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91310905 | ||||||
| chr9:91310952
|
T | C | 1 | a0001c0002t0001g0273 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.506-12876A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91310952 | ||||||
| chr9:91310959
|
G | A | 3 | a0002c0003t0001g0013a0002c0003t0001g0014a0002c0003t0001g0015 | 3 | HG02451.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.506-12883C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91310959 | ||||||
| chr9:91311079
|
T | A | 1 | a0001c0001t0001g0223 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.506-13003A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91311079 | ||||||
| chr9:91311212
|
A | T | 1 | a0001c0001t0001g0060 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.506-13136T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91311212 | ||||||
| chr9:91311233
|
C | A | 1 | a0001c0001t0001g0082 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.506-13157G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91311233 | ||||||
| chr9:91311430
|
A | G | 1 | a0001c0001t0001g0173 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.506-13354T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91311430 | ||||||
| chr9:91311443
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.506-13367T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91311443 | ||||||
| chr9:91311752
|
C | T | 4 | a0001c0001t0001g0219a0001c0001t0001g0227a0001c0001t0001g0228others(1): Show | 4 | HG02129.hp2 HG02165.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.505+13566G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91311752 | ||||||
| chr9:91311940
|
G | C | 3 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279 | 3 | HG02257.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.505+13378C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91311940 | ||||||
| chr9:91312010
|
CT | C | 33 | a0001c0001t0001g0097a0001c0001t0001g0169a0001c0001t0001g0207others(30): Show | 34 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.505+13307delA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91312010 | ||||||
| chr9:91312087
|
T | C | 1 | a0001c0001t0001g0326 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.505+13231A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91312087 | ||||||
| chr9:91312129
|
A | T | 1 | a0001c0001t0001g0224 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.505+13189T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91312129 | ||||||
| chr9:91312178
|
A | G | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.505+13140T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91312178 | ||||||
| chr9:91312249
|
T | G | 345 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(342): Show | 356 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(353): Show |
intron_variant | MODIFIER | c.505+13069A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91312249 | ||||||
| chr9:91312408
|
A | G | 1 | a0001c0001t0001g0094 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.505+12910T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91312408 | ||||||
| chr9:91312469
|
T | C | 3 | a0001c0001t0001g0311a0001c0001t0001g0312a0001c0001t0001g0313 | 3 | HG00544.hp1 HG00673.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.505+12849A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91312469 | ||||||
| chr9:91312497
|
G | T | 1 | a0001c0002t0004g0276 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.505+12821C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91312497 | ||||||
| chr9:91312587
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.505+12731C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91312587 | ||||||
| chr9:91312599
|
G | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0060others(5): Show | 9 | HG03491.hp1 HG03492.hp1 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.505+12719C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91312599 | ||||||
| chr9:91312649
|
G | A | 1 | a0001c0001t0001g0343 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.505+12669C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91312649 | ||||||
| chr9:91312886
|
G | C | 12 | a0001c0001t0001g0017a0001c0001t0001g0280a0001c0001t0001g0281others(9): Show | 12 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.505+12432C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91312886 | ||||||
| chr9:91313029
|
G | GA | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.505+12288dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91313029 | ||||||
| chr9:91313069
|
CG | C | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(109): Show | 115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.505+12248delC | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91313069 | ||||||
| chr9:91313121
|
T | G | 3 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279 | 3 | HG02257.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.505+12197A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91313121 | ||||||
| chr9:91313296
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.505+12022G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91313296 | ||||||
| chr9:91313330
|
A | G | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.505+11988T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91313330 | ||||||
| chr9:91313444
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.505+11874C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91313444 | ||||||
| chr9:91313568
|
G | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.505+11750C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91313568 | ||||||
| chr9:91313711
|
C | CA | 137 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(134): Show | 141 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.505+11606dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91313711 | ||||||
| chr9:91313711
|
C | CAA | 6 | a0001c0001t0001g0107a0001c0001t0001g0163a0001c0001t0001g0189others(3): Show | 6 | HG00733.hp2 HG01175.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.505+11605_505+1160 others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91313711 | ||||||
| chr9:91313711
|
CA | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(50): Show | 54 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.505+11606delT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91313711 | ||||||
| chr9:91313822
|
TC | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(164): Show | 172 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(169): Show |
intron_variant | MODIFIER | c.505+11495delG | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91313822 | ||||||
| chr9:91313823
|
C | T | 49 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(46): Show | 49 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.505+11495G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91313823 | ||||||
| chr9:91313862
|
G | A | 27 | a0001c0002t0001g0011a0001c0002t0001g0016a0001c0002t0001g0115others(24): Show | 28 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.505+11456C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91313862 | ||||||
| chr9:91314002
|
C | T | 13 | a0001c0001t0001g0017a0001c0001t0001g0280a0001c0001t0001g0281others(10): Show | 13 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.505+11316G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314002 | ||||||
| chr9:91314087
|
G | A | 1 | a0001c0001t0001g0087 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.505+11231C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314087 | ||||||
| chr9:91314109
|
C | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.505+11209G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314109 | ||||||
| chr9:91314137
|
G | C | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.505+11181C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314137 | ||||||
| chr9:91314297
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.505+11021C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314297 | ||||||
| chr9:91314346
|
C | T | 235 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(232): Show | 242 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(239): Show |
intron_variant | MODIFIER | c.505+10972G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314346 | ||||||
| chr9:91314438
|
G | A | 48 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0058others(45): Show | 50 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.505+10880C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314438 | ||||||
| chr9:91314490
|
G | GA | 47 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0025others(44): Show | 49 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.505+10827dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314490 | ||||||
| chr9:91314490
|
GA | G | 15 | a0001c0001t0001g0005a0001c0001t0001g0170a0001c0001t0001g0171others(12): Show | 16 | HG02145.hp1 HG02451.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.505+10827delT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314490 | ||||||
| chr9:91314505
|
AAC | A | 11 | a0001c0001t0001g0277a0001c0001t0001g0279a0001c0001t0001g0280others(8): Show | 11 | HG00597.hp2 HG01109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.505+10811_505+1081 others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314505 | ||||||
| chr9:91314506
|
AC | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0281a0001c0001t0001g0282others(1): Show | 4 | HG00609.hp1 HG02602.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.505+10811delG | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314506 | ||||||
| chr9:91314529
|
G | A | 6 | a0001c0001t0001g0322a0001c0001t0001g0341a0001c0001t0001g0342others(3): Show | 6 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.505+10789C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314529 | ||||||
| chr9:91314545
|
C | A | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(122): Show | 128 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.505+10773G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314545 | ||||||
| chr9:91314583
|
T | TA | 11 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0001g0101others(8): Show | 11 | HG01243.hp1 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.505+10734dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314583 | ||||||
| chr9:91314698
|
C | T | 1 | a0001c0001t0001g0341 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.505+10620G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314698 | ||||||
| chr9:91314721
|
T | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.505+10597A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314721 | ||||||
| chr9:91314737
|
G | A | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.505+10581C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314737 | ||||||
| chr9:91314805
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.505+10513G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314805 | ||||||
| chr9:91314993
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.505+10325C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314993 | ||||||
| chr9:91315082
|
G | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.505+10236C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91315082 | ||||||
| chr9:91315230
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.505+10088G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91315230 | ||||||
| chr9:91315331
|
G | A | 5 | a0001c0001t0001g0119a0001c0001t0001g0139a0001c0001t0001g0140others(2): Show | 5 | HG01168.hp1 HG01884.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.505+9987C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91315331 | ||||||
| chr9:91315344
|
A | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0299a0001c0001t0001g0327others(1): Show | 5 | HG01952.hp2 HG01978.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.505+9974T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91315344 | ||||||
| chr9:91315347
|
C | T | 16 | a0001c0001t0001g0017a0001c0001t0001g0277a0001c0001t0001g0278others(13): Show | 16 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.505+9971G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91315347 | ||||||
| chr9:91315415
|
T | G | 2 | a0001c0001t0001g0292a0001c0001t0001g0293 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.505+9903A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91315415 | ||||||
| chr9:91315478
|
G | C | 6 | a0001c0001t0001g0322a0001c0001t0001g0341a0001c0001t0001g0342others(3): Show | 6 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.505+9840C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91315478 | ||||||
| chr9:91315519
|
C | T | 15 | a0001c0001t0001g0005a0001c0001t0001g0170a0001c0001t0001g0171others(12): Show | 16 | HG02145.hp1 HG02451.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.505+9799G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91315519 | ||||||
| chr9:91315652
|
T | C | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.505+9666A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91315652 | ||||||
| chr9:91315661
|
C | T | 4 | a0001c0002t0001g0261a0001c0002t0001g0262a0001c0002t0001g0263others(1): Show | 4 | HG03098.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.505+9657G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91315661 | ||||||
| chr9:91315796
|
C | T | 1 | a0001c0002t0004g0276 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.505+9522G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91315796 | ||||||
| chr9:91315797
|
G | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0055others(1): Show | 4 | HG00438.hp1 NA18940.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.505+9521C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91315797 | ||||||
| chr9:91315869
|
G | A | 4 | a0001c0001t0001g0202a0001c0001t0001g0208a0001c0001t0001g0210others(1): Show | 4 | HG02132.hp2 NA18977.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.505+9449C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91315869 | ||||||
| chr9:91316280
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.505+9038A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91316280 | ||||||
| chr9:91316411
|
G | A | 17 | a0001c0002t0001g0011a0001c0002t0001g0115a0001c0002t0001g0152others(14): Show | 18 | HG00639.hp2 HG01175.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.505+8907C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91316411 | ||||||
| chr9:91316484
|
C | A | 1 | a0001c0007t0001g0225 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.505+8834G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91316484 | ||||||
| chr9:91316961
|
G | C | 1 | a0001c0001t0001g0151 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.505+8357C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91316961 | ||||||
| chr9:91317177
|
G | A | 15 | a0001c0001t0001g0007a0001c0001t0001g0200a0001c0001t0001g0201others(12): Show | 16 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.505+8141C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91317177 | ||||||
| chr9:91317216
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.505+8102C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91317216 | ||||||
| chr9:91317329
|
C | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.505+7989G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91317329 | ||||||
| chr9:91317375
|
A | G | 1 | a0001c0001t0001g0024 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.505+7943T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91317375 | ||||||
| chr9:91317492
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.505+7826A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91317492 | ||||||
| chr9:91317885
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.505+7433A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91317885 | ||||||
| chr9:91317970
|
A | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.505+7348T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91317970 | ||||||
| chr9:91318187
|
T | TAAAAGTA others(301): Show |
6 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(3): Show | 6 | HG02132.hp1 NA18982.hp1 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.505+7130_505+7131i others(310): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91318187 | ||||||
| chr9:91318208
|
A | C | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.505+7110T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91318208 | ||||||
| chr9:91318319
|
G | A | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(110): Show | 116 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.505+6999C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91318319 | ||||||
| chr9:91318413
|
T | A | 1 | a0001c0001t0001g0108 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.505+6905A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91318413 | ||||||
| chr9:91318503
|
G | C | 3 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0331 | 3 | HG01168.hp1 HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.505+6815C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91318503 | ||||||
| chr9:91318542
|
A | C | 1 | a0001c0001t0001g0094 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.505+6776T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91318542 | ||||||
| chr9:91318679
|
T | G | 1 | a0001c0001t0001g0106 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.505+6639A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91318679 | ||||||
| chr9:91318696
|
T | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(53): Show | 57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.505+6622A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91318696 | ||||||
| chr9:91318701
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.505+6617G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91318701 | ||||||
| chr9:91318948
|
C | T | 1 | a0001c0001t0001g0202 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.505+6370G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91318948 | ||||||
| chr9:91318952
|
G | A | 1 | a0005c0005t0001g0012 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.505+6366C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91318952 | ||||||
| chr9:91319080
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.505+6238C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91319080 | ||||||
| chr9:91319150
|
A | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0196a0001c0001t0001g0197 | 4 | HG02895.hp1 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.505+6168T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91319150 | ||||||
| chr9:91319253
|
A | C | 2 | a0001c0001t0001g0297a0001c0001t0001g0323 | 2 | HG01081.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.505+6065T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91319253 | ||||||
| chr9:91319392
|
A | G | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(233): Show | 243 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(240): Show |
intron_variant | MODIFIER | c.505+5926T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91319392 | ||||||
| chr9:91319580
|
T | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(53): Show | 57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.505+5738A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91319580 | ||||||
| chr9:91319594
|
C | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0164 | 2 | HG01081.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.505+5724G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91319594 | ||||||
| chr9:91319631
|
G | A | 40 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0065others(37): Show | 42 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.505+5687C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91319631 | ||||||
| chr9:91319654
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.505+5664C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91319654 | ||||||
| chr9:91319656
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.505+5662C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91319656 | ||||||
| chr9:91319706
|
A | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | NA18968.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.505+5612T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91319706 | ||||||
| chr9:91319888
|
T | C | 1 | a0001c0001t0001g0052 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.505+5430A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91319888 | ||||||
| chr9:91320073
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.505+5245G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91320073 | ||||||
| chr9:91320289
|
C | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.505+5029G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91320289 | ||||||
| chr9:91320438
|
A | T | 42 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(39): Show | 42 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.505+4880T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91320438 | ||||||
| chr9:91320500
|
T | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.505+4818A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91320500 | ||||||
| chr9:91320557
|
T | C | 1 | a0001c0001t0001g0002 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.505+4761A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91320557 | ||||||
| chr9:91320619
|
C | T | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.505+4699G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91320619 | ||||||
| chr9:91321171
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.505+4147A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91321171 | ||||||
| chr9:91321508
|
A | T | 284 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(281): Show | 293 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(290): Show |
intron_variant | MODIFIER | c.505+3810T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91321508 | ||||||
| chr9:91321590
|
T | C | 40 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0065others(37): Show | 42 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.505+3728A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91321590 | ||||||
| chr9:91321828
|
G | C | 1 | a0001c0001t0001g0322 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.505+3490C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91321828 | ||||||
| chr9:91321966
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.505+3352G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91321966 | ||||||
| chr9:91322138
|
A | G | 3 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279 | 3 | HG02257.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.505+3180T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91322138 | ||||||
| chr9:91322483
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.505+2835G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91322483 | ||||||
| chr9:91322512
|
T | C | 14 | a0001c0001t0001g0017a0001c0001t0001g0238a0001c0001t0001g0280others(11): Show | 14 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.505+2806A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91322512 | ||||||
| chr9:91322649
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.505+2669A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91322649 | ||||||
| chr9:91322704
|
T | C | 1 | a0005c0005t0001g0012 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.505+2614A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91322704 | ||||||
| chr9:91322705
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0173 | 3 | HG02615.hp1 HG02809.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.505+2613G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91322705 | ||||||
| chr9:91322958
|
T | C | 4 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(1): Show | 4 | HG02257.hp1 HG02818.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.505+2360A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91322958 | ||||||
| chr9:91323116
|
C | T | 1 | a0001c0001t0001g0342 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.505+2202G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91323116 | ||||||
| chr9:91323546
|
C | T | 2 | a0001c0002t0001g0261a0001c0002t0001g0262 | 2 | HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.505+1772G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91323546 | ||||||
| chr9:91323621
|
C | CA | 7 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0049others(4): Show | 7 | HG02027.hp2 HG02602.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.505+1696dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91323621 | ||||||
| chr9:91323723
|
T | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.505+1595A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91323723 | ||||||
| chr9:91323747
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.505+1571T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91323747 | ||||||
| chr9:91323898
|
T | A | 42 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(39): Show | 42 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.505+1420A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91323898 | ||||||
| chr9:91324049
|
A | C | 1 | a0001c0001t0001g0281 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.505+1269T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324049 | ||||||
| chr9:91324178
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.505+1140T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324178 | ||||||
| chr9:91324282
|
C | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.505+1036G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324282 | ||||||
| chr9:91324390
|
C | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.505+928G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324390 | ||||||
| chr9:91324432
|
G | A | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.505+886C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324432 | ||||||
| chr9:91324432
|
G | C | 1 | a0001c0001t0001g0187 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.505+886C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324432 | ||||||
| chr9:91324520
|
T | TA | 53 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0020others(50): Show | 54 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.505+797dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324520 | ||||||
| chr9:91324547
|
T | TA | 30 | a0001c0002t0001g0011a0001c0002t0001g0016a0001c0002t0001g0115others(27): Show | 31 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.505+770dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324547 | ||||||
| chr9:91324547
|
TA | T | 16 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0046others(13): Show | 16 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.505+770delT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324547 | ||||||
| chr9:91324562
|
A | C | 25 | a0001c0002t0001g0011a0001c0002t0001g0016a0001c0002t0001g0115others(22): Show | 26 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.505+756T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324562 | ||||||
| chr9:91324563
|
A | C | 25 | a0001c0002t0001g0011a0001c0002t0001g0016a0001c0002t0001g0115others(22): Show | 26 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.505+755T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324563 | ||||||
| chr9:91324570
|
A | G | 1 | a0001c0001t0001g0094 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.505+748T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324570 | ||||||
| chr9:91324673
|
C | T | 3 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279 | 3 | HG02257.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.505+645G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324673 | ||||||
| chr9:91324719
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.505+599G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324719 | ||||||
| chr9:91324789
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.505+529G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324789 | ||||||
| chr9:91324869
|
A | T | 4 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0001g0101others(1): Show | 4 | HG02280.hp2 HG02895.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.505+449T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324869 | ||||||
| chr9:91324884
|
G | A | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | NA18954.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.505+434C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324884 | ||||||
| chr9:91325068
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.505+250C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91325068 | ||||||
| chr9:91325120
|
A | G | 48 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0095others(45): Show | 48 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.505+198T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91325120 | ||||||
| chr9:91325511
|
T | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(53): Show | 57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.419-107A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91325511 | ||||||
| chr9:91325672
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.419-268T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91325672 | ||||||
| chr9:91325706
|
T | C | 3 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085 | 3 | HG01255.hp1 HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.419-302A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91325706 | ||||||
| chr9:91325772
|
G | T | 40 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0065others(37): Show | 42 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.419-368C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91325772 | ||||||
| chr9:91325787
|
G | C | 1 | a0001c0001t0001g0299 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.419-383C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91325787 | ||||||
| chr9:91325799
|
A | C | 1 | a0001c0001t0001g0023 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.419-395T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91325799 | ||||||
| chr9:91325875
|
C | A | 1 | a0001c0001t0001g0030 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.419-471G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91325875 | ||||||
| chr9:91326354
|
T | C | 62 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(59): Show | 66 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.419-950A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91326354 | ||||||
| chr9:91326411
|
A | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0153 | 3 | HG01168.hp2 HG01169.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.419-1007T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91326411 | ||||||
| chr9:91326886
|
C | T | 1 | a0001c0001t0001g0219 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.419-1482G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91326886 | ||||||
| chr9:91326902
|
A | T | 1 | a0001c0001t0001g0164 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.419-1498T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91326902 | ||||||
| chr9:91327243
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.419-1839G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91327243 | ||||||
| chr9:91327338
|
T | C | 299 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(296): Show | 309 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.419-1934A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91327338 | ||||||
| chr9:91327447
|
G | A | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.419-2043C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91327447 | ||||||
| chr9:91327603
|
C | T | 1 | a0001c0001t0001g0326 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.419-2199G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91327603 | ||||||
| chr9:91327628
|
G | A | 15 | a0001c0001t0001g0068a0001c0001t0001g0070a0001c0001t0001g0073others(12): Show | 15 | HG00408.hp2 HG00673.hp1 NA18955.hp1 others(12): Show |
intron_variant | MODIFIER | c.419-2224C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91327628 | ||||||
| chr9:91327784
|
G | C | 1 | a0001c0001t0001g0305 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.419-2380C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91327784 | ||||||
| chr9:91327806
|
C | T | 2 | a0001c0002t0001g0115a0001c0002t0001g0152 | 2 | HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.419-2402G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91327806 | ||||||
| chr9:91327848
|
G | A | 23 | a0001c0002t0001g0011a0001c0002t0001g0016a0001c0002t0001g0258others(20): Show | 24 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.419-2444C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91327848 | ||||||
| chr9:91327923
|
T | C | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.419-2519A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91327923 | ||||||
| chr9:91327989
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.419-2585C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91327989 | ||||||
| chr9:91327989
|
G | T | 1 | a0001c0001t0001g0109 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.419-2585C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91327989 | ||||||
| chr9:91328070
|
C | T | 1 | a0001c0002t0001g0268 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.419-2666G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91328070 | ||||||
| chr9:91328116
|
A | G | 1 | a0001c0001t0001g0122 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.419-2712T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91328116 | ||||||
| chr9:91328204
|
C | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(231): Show | 240 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(237): Show |
intron_variant | MODIFIER | c.419-2800G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91328204 | ||||||
| chr9:91328301
|
C | T | 2 | a0001c0001t0001g0297a0001c0001t0001g0323 | 2 | HG01081.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.419-2897G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91328301 | ||||||
| chr9:91328560
|
C | T | 41 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0065others(38): Show | 43 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.419-3156G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91328560 | ||||||
| chr9:91328890
|
T | C | 3 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107 | 3 | NA18978.hp1 NA19002.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.419-3486A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91328890 | ||||||
| chr9:91328951
|
T | C | 1 | a0001c0001t0001g0163 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.419-3547A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91328951 | ||||||
| chr9:91329022
|
T | A | 16 | a0001c0001t0001g0010a0001c0001t0001g0296a0001c0001t0001g0306others(13): Show | 17 | HG00544.hp1 HG00673.hp2 HG02165.hp1 others(14): Show |
intron_variant | MODIFIER | c.419-3618A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91329022 | ||||||
| chr9:91329251
|
A | C | 3 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0072 | 3 | HG00558.hp2 NA19090.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.419-3847T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91329251 | ||||||
| chr9:91329304
|
G | GA | 29 | a0001c0001t0001g0188a0001c0002t0001g0011a0001c0002t0001g0016others(26): Show | 30 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.419-3901dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91329304 | ||||||
| chr9:91329304
|
GA | G | 7 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0060others(4): Show | 8 | HG03491.hp1 HG03492.hp1 HG03927.hp1 others(5): Show |
intron_variant | MODIFIER | c.419-3901delT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91329304 | ||||||
| chr9:91329311
|
A | AAAAAAC | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.419-3913_419-3908d others(8): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91329311 | ||||||
| chr9:91329575
|
A | G | 42 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(39): Show | 42 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.419-4171T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91329575 | ||||||
| chr9:91329649
|
A | C | 6 | a0001c0002t0001g0011a0001c0002t0001g0272a0001c0002t0001g0336others(3): Show | 7 | HG03017.hp1 NA18947.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.419-4245T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91329649 | ||||||
| chr9:91330130
|
G | A | 4 | a0001c0002t0001g0261a0001c0002t0001g0262a0001c0002t0001g0263others(1): Show | 4 | HG03098.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.419-4726C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91330130 | ||||||
| chr9:91330166
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.419-4762G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91330166 | ||||||
| chr9:91330189
|
G | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(53): Show | 57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.419-4785C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91330189 | ||||||
| chr9:91330203
|
G | A | 29 | a0001c0001t0001g0188a0001c0002t0001g0011a0001c0002t0001g0016others(26): Show | 30 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.419-4799C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91330203 | ||||||
| chr9:91330229
|
A | C | 1 | a0001c0001t0001g0282 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.419-4825T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91330229 | ||||||
| chr9:91330344
|
T | C | 6 | a0001c0001t0001g0322a0001c0001t0001g0341a0001c0001t0001g0342others(3): Show | 6 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.419-4940A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91330344 | ||||||
| chr9:91330351
|
G | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(53): Show | 57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.419-4947C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91330351 | ||||||
| chr9:91330371
|
T | C | 1 | a0001c0001t0001g0332 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.419-4967A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91330371 | ||||||
| chr9:91330755
|
C | T | 1 | a0001c0001t0001g0038 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.419-5351G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91330755 | ||||||
| chr9:91330910
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.419-5506A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91330910 | ||||||
| chr9:91330930
|
C | T | 3 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085 | 3 | HG01255.hp1 HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.419-5526G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91330930 | ||||||
| chr9:91331064
|
C | A | 3 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335 | 3 | NA18990.hp2 NA19005.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.419-5660G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91331064 | ||||||
| chr9:91331290
|
T | C | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.419-5886A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91331290 | ||||||
| chr9:91331450
|
A | C | 1 | a0001c0001t0001g0173 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.419-6046T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91331450 | ||||||
| chr9:91331597
|
C | G | 2 | a0001c0001t0001g0200a0001c0001t0001g0201 | 2 | HG00438.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.419-6193G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91331597 | ||||||
| chr9:91331609
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0031 | 2 | HG00438.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.419-6205G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91331609 | ||||||
| chr9:91331815
|
C | A | 1 | a0001c0001t0001g0064 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.419-6411G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91331815 | ||||||
| chr9:91331822
|
C | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(124): Show | 130 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.419-6418G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91331822 | ||||||
| chr9:91331885
|
T | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.419-6481A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91331885 | ||||||
| chr9:91331890
|
C | A | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.419-6486G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91331890 | ||||||
| chr9:91331940
|
G | A | 29 | a0001c0001t0001g0030a0001c0002t0001g0011a0001c0002t0001g0016others(26): Show | 30 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.419-6536C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91331940 | ||||||
| chr9:91332065
|
T | A | 1 | a0001c0001t0001g0317 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.419-6661A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91332065 | ||||||
| chr9:91332082
|
A | G | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.419-6678T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91332082 | ||||||
| chr9:91332240
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.419-6836C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91332240 | ||||||
| chr9:91332473
|
G | C | 1 | a0001c0001t0001g0064 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.419-7069C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91332473 | ||||||
| chr9:91332479
|
G | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.419-7075C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91332479 | ||||||
| chr9:91332647
|
T | C | 298 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(295): Show | 308 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(305): Show |
intron_variant | MODIFIER | c.419-7243A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91332647 | ||||||
| chr9:91332847
|
G | A | 1 | a0005c0005t0001g0012 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.419-7443C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91332847 | ||||||
| chr9:91332947
|
TC | T | 16 | a0001c0001t0001g0017a0001c0001t0001g0277a0001c0001t0001g0278others(13): Show | 16 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.419-7544delG | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91332947 | ||||||
| chr9:91332949
|
G | A | 10 | a0001c0001t0001g0008a0001c0001t0001g0240a0001c0001t0001g0241others(7): Show | 11 | HG00609.hp2 HG02155.hp1 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.419-7545C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91332949 | ||||||
| chr9:91332972
|
T | C | 10 | a0001c0001t0001g0017a0001c0001t0001g0281a0001c0001t0001g0282others(7): Show | 10 | HG00597.hp2 HG00609.hp1 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.419-7568A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91332972 | ||||||
| chr9:91333019
|
G | C | 1 | a0001c0002t0001g0267 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.419-7615C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91333019 | ||||||
| chr9:91333125
|
G | A | 3 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085 | 3 | HG01255.hp1 HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.419-7721C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91333125 | ||||||
| chr9:91333139
|
T | C | 1 | a0001c0002t0001g0272 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.419-7735A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91333139 | ||||||
| chr9:91333393
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.419-7989A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91333393 | ||||||
| chr9:91333790
|
T | C | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.419-8386A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91333790 | ||||||
| chr9:91333882
|
T | A | 1 | a0001c0001t0001g0246 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.419-8478A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91333882 | ||||||
| chr9:91333933
|
C | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.419-8529G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91333933 | ||||||
| chr9:91334035
|
C | T | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(108): Show | 114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.419-8631G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91334035 | ||||||
| chr9:91334193
|
A | G | 1 | a0001c0001t0001g0070 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.419-8789T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91334193 | ||||||
| chr9:91334302
|
G | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0066 | 3 | HG02280.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.419-8898C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91334302 | ||||||
| chr9:91334303
|
G | C | 2 | a0001c0001t0001g0002a0001c0001t0001g0066 | 3 | HG02280.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.419-8899C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91334303 | ||||||
| chr9:91334401
|
G | A | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.419-8997C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91334401 | ||||||
| chr9:91334420
|
C | G | 3 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335 | 3 | NA18990.hp2 NA19005.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.419-9016G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91334420 | ||||||
| chr9:91334470
|
C | CCTGCCCT others(72): Show |
112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(109): Show | 115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.419-9067_419-9066i others(81): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91334470 | ||||||
| chr9:91334494
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.419-9090A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91334494 | ||||||
| chr9:91334772
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.419-9368C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91334772 | ||||||
| chr9:91334824
|
T | C | 1 | a0001c0001t0001g0052 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.419-9420A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91334824 | ||||||
| chr9:91334838
|
G | A | 1 | a0001c0001t0001g0318 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.419-9434C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91334838 | ||||||
| chr9:91335051
|
C | T | 3 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279 | 3 | HG02257.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.419-9647G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91335051 | ||||||
| chr9:91335186
|
T | C | 1 | a0001c0002t0001g0268 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.419-9782A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91335186 | ||||||
| chr9:91335211
|
C | G | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.419-9807G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91335211 | ||||||
| chr9:91335221
|
A | C | 3 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0331 | 3 | HG01168.hp1 HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.419-9817T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91335221 | ||||||
| chr9:91335244
|
T | G | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.419-9840A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91335244 | ||||||
| chr9:91335348
|
T | TG | 299 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(296): Show | 309 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(306): Show |
intron_variant | MODIFIER | c.419-9945dupC | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91335348 | ||||||
| chr9:91335444
|
C | T | 41 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0065others(38): Show | 43 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.419-10040G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91335444 | ||||||
| chr9:91335462
|
A | G | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.419-10058T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91335462 | ||||||
| chr9:91335466
|
G | A | 1 | a0001c0002t0001g0265 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.419-10062C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91335466 | ||||||
| chr9:91335911
|
A | G | 1 | a0005c0005t0001g0012 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.419-10507T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91335911 | ||||||
| chr9:91336061
|
C | A | 1 | a0001c0001t0001g0192 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.419-10657G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91336061 | ||||||
| chr9:91336148
|
G | C | 4 | a0001c0002t0001g0261a0001c0002t0001g0262a0001c0002t0001g0263others(1): Show | 4 | HG03098.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.419-10744C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91336148 | ||||||
| chr9:91336224
|
CACAT | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.419-10824_419-1082 others(8): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91336224 | ||||||
| chr9:91336421
|
C | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.419-11017G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91336421 | ||||||
| chr9:91336490
|
C | T | 1 | a0001c0001t0001g0326 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.419-11086G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91336490 | ||||||
| chr9:91336817
|
T | A | 42 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(39): Show | 42 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.419-11413A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91336817 | ||||||
| chr9:91336972
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.419-11568A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91336972 | ||||||
| chr9:91337300
|
G | C | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.419-11896C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91337300 | ||||||
| chr9:91337361
|
T | C | 3 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0134 | 3 | HG01255.hp2 HG03491.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.419-11957A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91337361 | ||||||
| chr9:91337454
|
G | T | 1 | a0001c0001t0001g0181 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.419-12050C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91337454 | ||||||
| chr9:91337636
|
A | G | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.419-12232T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91337636 | ||||||
| chr9:91338378
|
T | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0214a0001c0001t0001g0215others(4): Show | 8 | HG01071.hp2 HG01106.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.419-12974A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91338378 | ||||||
| chr9:91338408
|
CAG | C | 12 | a0001c0001t0001g0017a0001c0001t0001g0280a0001c0001t0001g0281others(9): Show | 12 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.419-13006_419-1300 others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91338408 | ||||||
| chr9:91338570
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.419-13166T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91338570 | ||||||
| chr9:91338629
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.419-13225A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91338629 | ||||||
| chr9:91339065
|
C | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.419-13661G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91339065 | ||||||
| chr9:91339073
|
AAT | A | 5 | a0001c0002t0001g0016a0001c0002t0001g0266a0001c0002t0001g0267others(2): Show | 5 | HG01071.hp1 HG01106.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.419-13671_419-1367 others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91339073 | ||||||
| chr9:91339639
|
T | C | 42 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(39): Show | 42 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.419-14235A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91339639 | ||||||
| chr9:91339655
|
T | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.419-14251A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91339655 | ||||||
| chr9:91339872
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.419-14468C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91339872 | ||||||
| chr9:91339880
|
A | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.419-14476T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91339880 | ||||||
| chr9:91339910
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.419-14506G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91339910 | ||||||
| chr9:91340541
|
A | C | 1 | a0001c0001t0001g0033 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.419-15137T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91340541 | ||||||
| chr9:91340620
|
A | G | 41 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0065others(38): Show | 43 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.419-15216T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91340620 | ||||||
| chr9:91340627
|
A | C | 1 | a0001c0001t0001g0153 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.419-15223T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91340627 | ||||||
| chr9:91340799
|
A | C | 1 | a0001c0001t0001g0326 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.418+15084T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91340799 | ||||||
| chr9:91341008
|
T | C | 49 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0095others(46): Show | 49 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.418+14875A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91341008 | ||||||
| chr9:91341102
|
C | T | 1 | a0001c0001t0001g0326 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.418+14781G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91341102 | ||||||
| chr9:91341535
|
C | A | 1 | a0001c0001t0001g0042 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.418+14348G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91341535 | ||||||
| chr9:91341568
|
C | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.418+14315G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91341568 | ||||||
| chr9:91341757
|
G | C | 1 | a0001c0001t0001g0053 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.418+14126C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91341757 | ||||||
| chr9:91341978
|
C | G | 23 | a0001c0002t0001g0011a0001c0002t0001g0016a0001c0002t0001g0258others(20): Show | 24 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.418+13905G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91341978 | ||||||
| chr9:91341982
|
G | A | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.418+13901C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91341982 | ||||||
| chr9:91342058
|
A | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(53): Show | 57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.418+13825T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91342058 | ||||||
| chr9:91342245
|
T | C | 1 | a0001c0001t0001g0135 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.418+13638A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91342245 | ||||||
| chr9:91342591
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.418+13292A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91342591 | ||||||
| chr9:91342600
|
T | C | 29 | a0001c0001t0001g0226a0001c0002t0001g0011a0001c0002t0001g0016others(26): Show | 30 | HG00621.hp2 HG00639.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.418+13283A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91342600 | ||||||
| chr9:91342753
|
G | A | 3 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0040 | 3 | NA19002.hp1 NA19074.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.418+13130C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91342753 | ||||||
| chr9:91342822
|
C | T | 54 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.418+13061G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91342822 | ||||||
| chr9:91342981
|
G | A | 299 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(296): Show | 310 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(307): Show |
intron_variant | MODIFIER | c.418+12902C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91342981 | ||||||
| chr9:91343120
|
A | G | 1 | a0001c0001t0001g0173 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.418+12763T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91343120 | ||||||
| chr9:91343175
|
G | A | 188 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(185): Show | 196 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(193): Show |
intron_variant | MODIFIER | c.418+12708C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91343175 | ||||||
| chr9:91343446
|
A | G | 2 | a0001c0001t0001g0095a0001c0001t0001g0108 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.418+12437T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91343446 | ||||||
| chr9:91343447
|
C | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0108 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.418+12436G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91343447 | ||||||
| chr9:91343628
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.418+12255C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91343628 | ||||||
| chr9:91343670
|
T | C | 1 | a0001c0002t0001g0016 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.418+12213A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91343670 | ||||||
| chr9:91344274
|
T | C | 1 | a0001c0001t0001g0320 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.418+11609A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91344274 | ||||||
| chr9:91344375
|
C | CT | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172 | 3 | HG02451.hp1 HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.418+11507dupA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91344375 | ||||||
| chr9:91344460
|
T | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.418+11423A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91344460 | ||||||
| chr9:91344631
|
C | T | 3 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279 | 3 | HG02257.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.418+11252G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91344631 | ||||||
| chr9:91344661
|
A | T | 1 | a0001c0001t0001g0094 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.418+11222T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91344661 | ||||||
| chr9:91345009
|
GA | G | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(109): Show | 115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.418+10873delT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91345009 | ||||||
| chr9:91345065
|
G | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(107): Show | 113 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.418+10818C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91345065 | ||||||
| chr9:91345297
|
C | G | 7 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(4): Show | 7 | NA18950.hp1 NA18968.hp2 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.418+10586G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91345297 | ||||||
| chr9:91345306
|
T | C | 2 | a0001c0001t0001g0280a0001c0001t0001g0289 | 2 | HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.418+10577A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91345306 | ||||||
| chr9:91345314
|
A | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.418+10569T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91345314 | ||||||
| chr9:91345400
|
T | G | 1 | a0001c0001t0001g0091 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.418+10483A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91345400 | ||||||
| chr9:91345559
|
C | T | 1 | a0001c0001t0001g0068 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.418+10324G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91345559 | ||||||
| chr9:91345572
|
G | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.418+10311C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91345572 | ||||||
| chr9:91345630
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.418+10253C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91345630 | ||||||
| chr9:91345830
|
C | T | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.418+10053G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91345830 | ||||||
| chr9:91345832
|
C | CA | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(171): Show | 181 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.418+10050dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91345832 | ||||||
| chr9:91345832
|
C | CAA | 10 | a0001c0001t0001g0117a0001c0001t0001g0136a0001c0001t0001g0137others(7): Show | 10 | HG01361.hp2 HG02027.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.418+10049_418+1005 others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91345832 | ||||||
| chr9:91345865
|
C | G | 1 | a0001c0001t0001g0042 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.418+10018G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91345865 | ||||||
| chr9:91345921
|
T | C | 1 | a0001c0001t0001g0343 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.418+9962A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91345921 | ||||||
| chr9:91345931
|
G | A | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.418+9952C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91345931 | ||||||
| chr9:91346022
|
T | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.418+9861A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91346022 | ||||||
| chr9:91346024
|
C | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(107): Show | 113 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.418+9859G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91346024 | ||||||
| chr9:91346091
|
T | A | 1 | a0001c0001t0001g0211 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.418+9792A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91346091 | ||||||
| chr9:91346159
|
G | C | 1 | a0001c0001t0001g0033 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.418+9724C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91346159 | ||||||
| chr9:91346404
|
G | A | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147 | 3 | HG01243.hp1 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.418+9479C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91346404 | ||||||
| chr9:91346475
|
G | A | 82 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(79): Show | 84 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.418+9408C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91346475 | ||||||
| chr9:91346508
|
T | C | 29 | a0001c0001t0001g0148a0001c0002t0001g0011a0001c0002t0001g0016others(26): Show | 30 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.418+9375A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91346508 | ||||||
| chr9:91346860
|
T | TA | 16 | a0001c0001t0001g0032a0001c0001t0001g0247a0001c0001t0001g0277others(13): Show | 16 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.418+9022dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91346860 | ||||||
| chr9:91346860
|
T | TAAA | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.418+9020_418+9022d others(5): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91346860 | ||||||
| chr9:91346872
|
A | C | 4 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0001g0101others(1): Show | 4 | HG02280.hp2 HG02895.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.418+9011T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91346872 | ||||||
| chr9:91347099
|
C | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.418+8784G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347099 | ||||||
| chr9:91347124
|
T | A | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(167): Show | 178 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.418+8759A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347124 | ||||||
| chr9:91347212
|
T | G | 1 | a0001c0001t0001g0051 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.418+8671A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347212 | ||||||
| chr9:91347212
|
T | TTTTG | 44 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0052others(41): Show | 46 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.418+8667_418+8670d others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347212 | ||||||
| chr9:91347212
|
T | TTTTGTTT others(1): Show |
35 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0024others(32): Show | 35 | HG00438.hp1 HG00544.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.418+8663_418+8670d others(10): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347212 | ||||||
| chr9:91347212
|
T | TTTTGTTT others(5): Show |
32 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0023others(29): Show | 33 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.418+8659_418+8670d others(14): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347212 | ||||||
| chr9:91347212
|
T | TTTTGTTT others(9): Show |
1 | a0001c0001t0001g0022 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.418+8655_418+8670d others(18): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347212 | ||||||
| chr9:91347212
|
TTTTG | T | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(169): Show | 180 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.418+8667_418+8670d others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347212 | ||||||
| chr9:91347234
|
T | A | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.418+8649A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347234 | ||||||
| chr9:91347347
|
G | A | 5 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(2): Show | 5 | HG00735.hp2 HG01433.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.418+8536C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347347 | ||||||
| chr9:91347404
|
T | C | 2 | a0001c0001t0001g0033a0001c0001t0001g0039 | 2 | HG00544.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.418+8479A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347404 | ||||||
| chr9:91347445
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.418+8438C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347445 | ||||||
| chr9:91347537
|
C | G | 1 | a0001c0001t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.418+8346G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347537 | ||||||
| chr9:91347542
|
C | A | 1 | a0001c0002t0001g0273 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.418+8341G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347542 | ||||||
| chr9:91347542
|
C | G | 1 | a0001c0001t0001g0064 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.418+8341G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347542 | ||||||
| chr9:91347720
|
T | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.418+8163A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347720 | ||||||
| chr9:91347916
|
T | TA | 8 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0060others(5): Show | 9 | HG03491.hp1 HG03492.hp1 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.418+7966dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347916 | ||||||
| chr9:91347938
|
A | C | 2 | a0001c0002t0001g0115a0001c0002t0001g0152 | 2 | HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.418+7945T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347938 | ||||||
| chr9:91347963
|
T | TAAAAAAC others(335): Show |
1 | a0001c0001t0001g0047 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.418+7919_418+7920i others(344): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | ||||||
| chr9:91347963
|
T | TAAAAAAC others(309): Show |
1 | a0001c0001t0001g0020 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.418+7919_418+7920i others(318): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | ||||||
| chr9:91347963
|
T | TAAAAAAC others(310): Show |
1 | a0001c0001t0001g0021 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.418+7919_418+7920i others(319): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | ||||||
| chr9:91347963
|
T | TAAAAAAC others(312): Show |
1 | a0001c0001t0001g0022 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.418+7919_418+7920i others(321): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | ||||||
| chr9:91347963
|
T | TAAAAAAC others(315): Show |
1 | a0001c0001t0001g0023 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.418+7919_418+7920i others(324): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | ||||||
| chr9:91347963
|
T | TAAAAAAC others(317): Show |
2 | a0001c0001t0001g0024a0001c0001t0001g0025 | 2 | HG02074.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.418+7919_418+7920i others(326): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | ||||||
| chr9:91347963
|
T | TAAAAAAC others(319): Show |
1 | a0001c0001t0001g0026 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.418+7919_418+7920i others(328): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | ||||||
| chr9:91347963
|
T | TAAAAAAC others(320): Show |
7 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(4): Show | 7 | HG00438.hp1 NA18950.hp2 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.418+7919_418+7920i others(329): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | ||||||
| chr9:91347963
|
T | TAAAAAAC others(321): Show |
5 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(2): Show | 5 | HG00544.hp2 HG02602.hp1 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.418+7919_418+7920i others(330): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | ||||||
| chr9:91347963
|
T | TAAAAAAC others(323): Show |
6 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(3): Show | 6 | HG02132.hp1 NA18948.hp2 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.418+7919_418+7920i others(332): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | ||||||
| chr9:91347963
|
T | TAAAAAAC others(324): Show |
1 | a0001c0001t0001g0040 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.418+7919_418+7920i others(333): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | ||||||
| chr9:91347963
|
T | TAAAAAAC others(328): Show |
2 | a0001c0001t0001g0041a0001c0001t0001g0056 | 2 | HG02135.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.418+7919_418+7920i others(337): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | ||||||
| chr9:91347963
|
T | TAAAAAAC others(332): Show |
1 | a0001c0001t0001g0042 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.418+7919_418+7920i others(341): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | ||||||
| chr9:91347963
|
T | TAAAAAAC others(333): Show |
1 | a0001c0001t0001g0043 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.418+7919_418+7920i others(342): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | ||||||
| chr9:91347963
|
T | TAAAAAAC others(334): Show |
4 | a0001c0001t0001g0018a0001c0001t0001g0044a0001c0001t0001g0045others(1): Show | 4 | HG00621.hp1 NA18612.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.418+7919_418+7920i others(343): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | ||||||
| chr9:91347963
|
T | TAAAAAAC others(335): Show |
2 | a0001c0001t0001g0046a0001c0001t0001g0057 | 2 | NA18970.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.418+7919_418+7920i others(344): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | ||||||
| chr9:91347963
|
T | TAAAAAAC others(339): Show |
3 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050 | 3 | HG02015.hp1 HG02027.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.418+7919_418+7920i others(348): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | ||||||
| chr9:91347963
|
T | TAAAAAAC others(340): Show |
1 | a0001c0001t0001g0051 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.418+7919_418+7920i others(349): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | ||||||
| chr9:91347963
|
T | TAAAAAAC others(346): Show |
1 | a0001c0001t0001g0019 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.418+7919_418+7920i others(355): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | ||||||
| chr9:91348006
|
T | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(107): Show | 113 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.418+7877A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91348006 | ||||||
| chr9:91348008
|
A | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(107): Show | 113 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.418+7875T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91348008 | ||||||
| chr9:91348072
|
A | T | 1 | a0001c0001t0001g0120 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.418+7811T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91348072 | ||||||
| chr9:91348081
|
C | CA | 21 | a0001c0001t0001g0017a0001c0001t0001g0052a0001c0001t0001g0277others(18): Show | 21 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.418+7801dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91348081 | ||||||
| chr9:91348085
|
A | C | 2 | a0001c0001t0001g0002a0001c0001t0001g0066 | 3 | HG02280.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.418+7798T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91348085 | ||||||
| chr9:91348281
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.418+7602C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91348281 | ||||||
| chr9:91348325
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.418+7558C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91348325 | ||||||
| chr9:91348472
|
G | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.418+7411C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91348472 | ||||||
| chr9:91348522
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.418+7361G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91348522 | ||||||
| chr9:91348523
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.418+7360C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91348523 | ||||||
| chr9:91348672
|
G | C | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.418+7211C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91348672 | ||||||
| chr9:91348958
|
C | G | 1 | a0001c0001t0001g0182 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.418+6925G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91348958 | ||||||
| chr9:91349023
|
G | A | 46 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0091others(43): Show | 48 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.418+6860C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91349023 | ||||||
| chr9:91349206
|
T | C | 16 | a0001c0001t0001g0005a0001c0001t0001g0170a0001c0001t0001g0171others(13): Show | 17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.418+6677A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91349206 | ||||||
| chr9:91349369
|
G | C | 1 | a0001c0001t0001g0067 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.418+6514C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91349369 | ||||||
| chr9:91349508
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0197 | 3 | HG02895.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.418+6375C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91349508 | ||||||
| chr9:91349599
|
C | T | 2 | a0001c0001t0001g0327a0001c0001t0001g0328 | 2 | HG01978.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.418+6284G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91349599 | ||||||
| chr9:91349627
|
TTGTG | T | 5 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(2): Show | 5 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.418+6252_418+6255d others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91349627 | ||||||
| chr9:91349679
|
GAC | G | 170 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(167): Show | 175 | HG00544.hp1 HG00597.hp2 HG00609.hp1 others(172): Show |
intron_variant | MODIFIER | c.418+6202_418+6203d others(4): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91349679 | ||||||
| chr9:91349679
|
GACAC | G | 85 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(82): Show | 87 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.418+6200_418+6203d others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91349679 | ||||||
| chr9:91349683
|
C | G | 45 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0091others(42): Show | 47 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.418+6200G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91349683 | ||||||
| chr9:91349685
|
C | G | 1 | a0001c0001t0001g0219 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.418+6198G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91349685 | ||||||
| chr9:91349703
|
C | G | 1 | a0001c0001t0001g0094 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.418+6180G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91349703 | ||||||
| chr9:91349703
|
CAG | C | 61 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(58): Show | 64 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.418+6178_418+6179d others(4): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91349703 | ||||||
| chr9:91349726
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.418+6157C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91349726 | ||||||
| chr9:91350057
|
T | G | 1 | a0001c0001t0001g0251 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.418+5826A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91350057 | ||||||
| chr9:91350117
|
T | C | 30 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0002t0001g0011others(27): Show | 31 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.418+5766A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91350117 | ||||||
| chr9:91350314
|
C | A | 16 | a0001c0001t0001g0017a0001c0001t0001g0277a0001c0001t0001g0278others(13): Show | 16 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.418+5569G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91350314 | ||||||
| chr9:91350525
|
G | A | 16 | a0001c0001t0001g0017a0001c0001t0001g0277a0001c0001t0001g0278others(13): Show | 16 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.418+5358C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91350525 | ||||||
| chr9:91350758
|
C | CA | 36 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0175others(33): Show | 38 | HG00544.hp1 HG00673.hp2 HG01496.hp1 others(35): Show |
intron_variant | MODIFIER | c.418+5124dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91350758 | ||||||
| chr9:91350758
|
CA | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(106): Show | 112 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.418+5124delT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91350758 | ||||||
| chr9:91350827
|
T | C | 6 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.418+5056A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91350827 | ||||||
| chr9:91350852
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.418+5031T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91350852 | ||||||
| chr9:91350917
|
C | T | 27 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(24): Show | 28 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.418+4966G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91350917 | ||||||
| chr9:91350954
|
T | A | 1 | a0001c0001t0001g0287 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.418+4929A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91350954 | ||||||
| chr9:91351016
|
A | T | 1 | a0001c0001t0001g0251 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.418+4867T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91351016 | ||||||
| chr9:91351072
|
C | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.418+4811G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91351072 | ||||||
| chr9:91351182
|
G | C | 1 | a0001c0002t0004g0276 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.418+4701C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91351182 | ||||||
| chr9:91351372
|
C | G | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.418+4511G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91351372 | ||||||
| chr9:91351374
|
T | C | 1 | a0001c0001t0001g0326 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.418+4509A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91351374 | ||||||
| chr9:91351561
|
T | C | 1 | a0001c0001t0001g0094 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.418+4322A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91351561 | ||||||
| chr9:91351670
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.418+4213C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91351670 | ||||||
| chr9:91351736
|
T | C | 1 | a0001c0001t0001g0288 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.418+4147A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91351736 | ||||||
| chr9:91351882
|
C | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.418+4001G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91351882 | ||||||
| chr9:91351896
|
G | C | 1 | a0001c0001t0001g0197 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.418+3987C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91351896 | ||||||
| chr9:91352482
|
T | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.418+3401A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91352482 | ||||||
| chr9:91352619
|
C | G | 1 | a0001c0001t0001g0118 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.418+3264G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91352619 | ||||||
| chr9:91352632
|
T | C | 1 | a0001c0001t0001g0249 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.418+3251A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91352632 | ||||||
| chr9:91352948
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.418+2935C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91352948 | ||||||
| chr9:91353028
|
C | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | HG03491.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.418+2855G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91353028 | ||||||
| chr9:91353220
|
G | A | 27 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(24): Show | 28 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.418+2663C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91353220 | ||||||
| chr9:91353374
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.418+2509G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91353374 | ||||||
| chr9:91353377
|
G | A | 3 | a0001c0001t0001g0094a0001c0001t0001g0292a0001c0001t0001g0293 | 3 | HG01167.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.418+2506C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91353377 | ||||||
| chr9:91353409
|
T | A | 2 | a0001c0001t0001g0218a0001c0001t0001g0250 | 2 | HG01109.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.418+2474A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91353409 | ||||||
| chr9:91353820
|
C | CA | 33 | a0001c0001t0001g0006a0001c0001t0001g0182a0001c0001t0001g0183others(30): Show | 34 | HG00642.hp1 HG00733.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.418+2062dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91353820 | ||||||
| chr9:91353820
|
CA | C | 28 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(25): Show | 28 | HG01109.hp1 HG01167.hp2 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.418+2062delT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91353820 | ||||||
| chr9:91353820
|
CAAA | C | 42 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0056others(39): Show | 43 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.418+2060_418+2062d others(5): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91353820 | ||||||
| chr9:91353820
|
CAAAA | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0020others(44): Show | 48 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.418+2059_418+2062d others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91353820 | ||||||
| chr9:91353820
|
CAAAAA | C | 7 | a0001c0001t0001g0019a0001c0001t0001g0059a0001c0002t0001g0261others(4): Show | 7 | HG03098.hp1 HG03209.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.418+2058_418+2062d others(7): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91353820 | ||||||
| chr9:91353845
|
A | C | 2 | a0001c0001t0001g0002a0001c0001t0001g0066 | 3 | HG02280.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.418+2038T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91353845 | ||||||
| chr9:91353922
|
T | A | 1 | a0001c0001t0001g0057 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.418+1961A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91353922 | ||||||
| chr9:91353922
|
T | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.418+1961A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91353922 | ||||||
| chr9:91354029
|
G | A | 12 | a0001c0001t0001g0017a0001c0001t0001g0280a0001c0001t0001g0281others(9): Show | 12 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.418+1854C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91354029 | ||||||
| chr9:91354167
|
T | G | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.418+1716A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91354167 | ||||||
| chr9:91354168
|
C | CA | 40 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0065others(37): Show | 42 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.418+1714dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91354168 | ||||||
| chr9:91354204
|
A | C | 1 | a0001c0001t0001g0094 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.418+1679T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91354204 | ||||||
| chr9:91354522
|
C | G | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.418+1361G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91354522 | ||||||
| chr9:91354610
|
T | G | 27 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(24): Show | 28 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.418+1273A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91354610 | ||||||
| chr9:91354653
|
T | G | 1 | a0001c0001t0001g0335 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.418+1230A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91354653 | ||||||
| chr9:91354672
|
A | G | 6 | a0001c0002t0001g0258a0001c0002t0001g0260a0001c0002t0002g0255others(3): Show | 6 | HG02572.hp1 HG02896.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.418+1211T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91354672 | ||||||
| chr9:91354773
|
C | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0214a0001c0001t0001g0215others(2): Show | 6 | HG01071.hp2 HG01106.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.418+1110G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91354773 | ||||||
| chr9:91354873
|
T | C | 27 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(24): Show | 28 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.418+1010A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91354873 | ||||||
| chr9:91354887
|
TC | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(107): Show | 113 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.418+995delG | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91354887 | ||||||
| chr9:91354950
|
T | C | 1 | a0001c0002t0004g0276 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.418+933A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91354950 | ||||||
| chr9:91354956
|
C | T | 15 | a0001c0001t0001g0007a0001c0001t0001g0200a0001c0001t0001g0201others(12): Show | 16 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.418+927G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91354956 | ||||||
| chr9:91354993
|
A | C | 28 | a0001c0002t0001g0011a0001c0002t0001g0016a0001c0002t0001g0258others(25): Show | 29 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.418+890T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91354993 | ||||||
| chr9:91355230
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0196a0001c0001t0001g0197 | 4 | HG02895.hp1 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.418+653C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91355230 | ||||||
| chr9:91355248
|
T | C | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.418+635A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91355248 | ||||||
| chr9:91355824
|
T | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(123): Show | 129 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.418+59A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91355824 | ||||||
| chr9:91355976
|
C | T | 41 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0065others(38): Show | 43 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(40): Show |
splice_region_variant&intron_variant | LOW | c.331-6G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 2/9 | chr9 | 91355976 | ||||||
| chr9:91356005
|
G | GA | 42 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(39): Show | 42 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.331-36dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 2/9 | chr9 | 91356005 | ||||||
| chr9:91356215
|
C | CGTAG | 8 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0060others(5): Show | 9 | HG03491.hp1 HG03492.hp1 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.263-61_263-60insCT others(2): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91356215 | ||||||
| chr9:91356241
|
C | T | 28 | a0001c0002t0001g0011a0001c0002t0001g0016a0001c0002t0001g0258others(25): Show | 29 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.263-86G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91356241 | ||||||
| chr9:91356253
|
A | G | 1 | a0001c0001t0001g0295 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.263-98T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91356253 | ||||||
| chr9:91356639
|
A | G | 42 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0065others(39): Show | 44 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.263-484T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91356639 | ||||||
| chr9:91356643
|
A | G | 5 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(2): Show | 5 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.263-488T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91356643 | ||||||
| chr9:91356791
|
T | A | 1 | a0001c0001t0001g0058 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.263-636A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91356791 | ||||||
| chr9:91356792
|
G | C | 1 | a0001c0001t0001g0058 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.263-637C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91356792 | ||||||
| chr9:91357423
|
G | T | 28 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(25): Show | 29 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.263-1268C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91357423 | ||||||
| chr9:91357715
|
C | T | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(108): Show | 114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.263-1560G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91357715 | ||||||
| chr9:91357813
|
G | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.263-1658C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91357813 | ||||||
| chr9:91357815
|
G | A | 2 | a0001c0001t0001g0327a0001c0001t0001g0328 | 2 | HG01978.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.263-1660C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91357815 | ||||||
| chr9:91357816
|
G | C | 1 | a0001c0001t0001g0294 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.263-1661C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91357816 | ||||||
| chr9:91358069
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.263-1914A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91358069 | ||||||
| chr9:91358210
|
A | G | 1 | a0001c0001t0001g0294 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.263-2055T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91358210 | ||||||
| chr9:91358394
|
G | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0060others(5): Show | 9 | HG03491.hp1 HG03492.hp1 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.263-2239C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91358394 | ||||||
| chr9:91358467
|
T | C | 59 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(56): Show | 62 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.263-2312A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91358467 | ||||||
| chr9:91358939
|
T | A | 1 | a0001c0001t0001g0089 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.262+2689A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91358939 | ||||||
| chr9:91358999
|
T | A | 2 | a0001c0001t0001g0329a0001c0001t0001g0330 | 2 | NA18980.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.262+2629A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91358999 | ||||||
| chr9:91359048
|
G | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(108): Show | 114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.262+2580C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91359048 | ||||||
| chr9:91359085
|
A | T | 1 | a0001c0006t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.262+2543T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91359085 | ||||||
| chr9:91359288
|
C | T | 1 | a0001c0002t0001g0336 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.262+2340G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91359288 | ||||||
| chr9:91359306
|
T | C | 1 | a0001c0001t0001g0345 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.262+2322A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91359306 | ||||||
| chr9:91359493
|
G | C | 15 | a0001c0001t0001g0017a0001c0001t0001g0277a0001c0001t0001g0278others(12): Show | 15 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.262+2135C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91359493 | ||||||
| chr9:91359530
|
T | C | 2 | a0001c0006t0001g0291a0005c0005t0001g0012 | 2 | HG02976.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.262+2098A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91359530 | ||||||
| chr9:91359580
|
AAAAAGAA others(3): Show |
A | 3 | a0001c0001t0001g0065a0001c0001t0001g0292a0001c0001t0001g0293 | 3 | HG01167.hp1 HG01169.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.262+2038_262+2047d others(12): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91359580 | ||||||
| chr9:91359590
|
G | A | 39 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0294others(36): Show | 41 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.262+2038C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91359590 | ||||||
| chr9:91359603
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.262+2025C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91359603 | ||||||
| chr9:91359665
|
C | T | 1 | a0001c0001t0001g0003 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.262+1963G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91359665 | ||||||
| chr9:91359671
|
T | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.262+1957A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91359671 | ||||||
| chr9:91359826
|
C | A | 1 | a0001c0001t0001g0331 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.262+1802G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91359826 | ||||||
| chr9:91359895
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.262+1733T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91359895 | ||||||
| chr9:91360036
|
A | G | 1 | a0001c0001t0001g0018 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.262+1592T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91360036 | ||||||
| chr9:91360086
|
T | C | 4 | a0001c0001t0001g0332a0001c0001t0001g0333a0001c0001t0001g0334others(1): Show | 4 | NA18990.hp2 NA19005.hp1 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.262+1542A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91360086 | ||||||
| chr9:91360091
|
T | A | 5 | a0001c0002t0001g0011a0001c0002t0001g0336a0001c0002t0001g0337others(2): Show | 6 | NA18947.hp2 NA18965.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.262+1537A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91360091 | ||||||
| chr9:91360147
|
A | G | 26 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.262+1481T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91360147 | ||||||
| chr9:91360673
|
C | G | 1 | a0001c0001t0001g0065 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.262+955G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91360673 | ||||||
| chr9:91360793
|
A | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.262+835T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91360793 | ||||||
| chr9:91360805
|
T | C | 1 | a0001c0001t0001g0340 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.262+823A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91360805 | ||||||
| chr9:91361174
|
G | A | 5 | a0001c0001t0001g0341a0001c0001t0001g0342a0001c0001t0001g0343others(2): Show | 5 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.262+454C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91361174 | ||||||
| chr9:91361222
|
T | C | 1 | a0001c0001t0001g0017 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.262+406A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91361222 | ||||||
| chr9:91361223
|
C | A | 1 | a0001c0001t0001g0017 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.262+405G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91361223 | ||||||
| chr9:91361224
|
A | C | 1 | a0001c0001t0001g0017 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.262+404T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91361224 | ||||||
| chr9:91361417
|
G | A | 1 | a0001c0001t0001g0346 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.262+211C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91361417 | ||||||
| chr9:91361504
|
C | T | 1 | a0001c0002t0001g0016 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.262+124G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91361504 |