| geneid | 6801 |
|---|---|
| ensemblid | ENSG00000115808.13 |
| hgncid | 11424 |
| symbol | STRN |
| name | striatin |
| refseq_nuc | NM_003162.4 |
| refseq_prot | NP_003153.2 |
| ensembl_nuc | ENST00000263918.9 |
| ensembl_prot | ENSP00000263918.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 36837698 |
| end | 36966536 |
| strand | - |
| ver | v1.2 |
| region | chr2:36837698-36966536 |
| region5000 | chr2:36832698-36971536 |
| regionname0 | STRN_chr2_36837698_36966536 |
| regionname5000 | STRN_chr2_36832698_36971536 |
| 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 | 780 | 295 | 75 | 49 | 122 | 13 | 34 | 87 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0002 | 0/0 | 780 | 3 | 0 | 0 | 1 | 0 | 2 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0003 | 0/0 | 780 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0004 | 0/0 | 780 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0005 | 0/0 | 780 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0006 | 0/0 | 780 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| 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 | 2343 | 293 | 74 | 49 | 121 | 13 | 34 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| c0002 | 0/0 | 2343 | 3 | 0 | 0 | 1 | 0 | 2 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| c0003 | 0/0 | 2343 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| c0004 | 0/0 | 2343 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| c0005 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| c0006 | 0/0 | 2343 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| c0007 | 0/0 | 2343 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| c0008 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| 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 | 0/1 | 11809 | 30 | 2 | 5 | 16 | 1 | 5 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0002 | 0/0 | 11811 | 12 | 4 | 4 | 3 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0003 | 0/0 | 11805 | 5 | 0 | 1 | 3 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0004 | 0/0 | 11813 | 4 | 0 | 1 | 2 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0005 | 0/0 | 11811 | 4 | 0 | 0 | 4 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0006 | 1/0 | 11832 | 3 | 2 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0007 | 0/0 | 11815 | 3 | 3 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0008 | 0/0 | 11807 | 3 | 0 | 2 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0009 | 0/0 | 11809 | 3 | 0 | 0 | 0 | 2 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0010 | 0/0 | 11820 | 3 | 3 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0011 | 0/0 | 11798 | 3 | 0 | 0 | 3 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0012 | 0/0 | 11806 | 3 | 0 | 1 | 0 | 2 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0013 | 0/0 | 11799 | 3 | 0 | 1 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0014 | 0/0 | 11807 | 3 | 0 | 0 | 2 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0015 | 0/0 | 11807 | 3 | 0 | 0 | 2 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0016 | 0/0 | 11833 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0017 | 0/0 | 11786 | 2 | 2 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0018 | 0/0 | 11809 | 2 | 0 | 0 | 0 | 0 | 2 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0019 | 0/0 | 11817 | 2 | 2 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0020 | 0/0 | 11825 | 2 | 2 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0021 | 0/0 | 11805 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0022 | 0/0 | 11809 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0023 | 0/0 | 11809 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0024 | 0/0 | 11809 | 2 | 0 | 1 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0025 | 0/0 | 11809 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0026 | 0/0 | 11811 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0027 | 0/0 | 11815 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0028 | 0/0 | 11815 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0029 | 0/0 | 11805 | 2 | 1 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0030 | 0/0 | 11807 | 2 | 1 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0031 | 0/0 | 11799 | 2 | 0 | 1 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0032 | 0/0 | 11801 | 2 | 0 | 0 | 0 | 1 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0033 | 0/0 | 11809 | 2 | 2 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0034 | 0/0 | 11804 | 2 | 1 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0035 | 0/0 | 11808 | 2 | 0 | 0 | 0 | 0 | 2 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0036 | 0/0 | 11807 | 2 | 0 | 0 | 0 | 0 | 2 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0037 | 0/0 | 11811 | 2 | 0 | 0 | 1 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0038 | 0/0 | 11824 | 2 | 0 | 2 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0039 | 0/0 | 11830 | 2 | 2 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0040 | 0/0 | 11783 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0041 | 0/0 | 11797 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0042 | 0/0 | 11801 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0043 | 0/0 | 11803 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0044 | 0/0 | 11803 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0045 | 0/0 | 11812 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0046 | 0/0 | 11811 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0047 | 0/0 | 11810 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0048 | 0/0 | 11813 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0049 | 0/0 | 11808 | 2 | 1 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0050 | 0/0 | 11810 | 2 | 2 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0051 | 0/0 | 11786 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0052 | 0/0 | 11807 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0053 | 0/0 | 11806 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0054 | 0/0 | 11800 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0055 | 0/0 | 11788 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0056 | 0/0 | 11834 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0057 | 0/0 | 11834 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0058 | 0/0 | 11838 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0059 | 0/0 | 11840 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0060 | 0/0 | 11842 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0061 | 0/0 | 11842 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0062 | 0/0 | 11803 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0063 | 0/0 | 11810 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0064 | 0/0 | 11811 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0065 | 0/0 | 11829 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0066 | 0/0 | 11833 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0067 | 0/0 | 11831 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0068 | 0/0 | 11835 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0069 | 0/0 | 11833 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0070 | 0/0 | 11835 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0071 | 0/0 | 11837 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0072 | 0/0 | 11839 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0073 | 0/0 | 11841 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0074 | 0/0 | 11823 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0075 | 0/0 | 11823 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0076 | 0/0 | 11826 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0077 | 0/0 | 11821 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0078 | 0/0 | 11801 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0079 | 0/0 | 11828 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0080 | 0/0 | 11824 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0081 | 0/0 | 11824 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0082 | 0/0 | 11803 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0083 | 0/0 | 11830 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0084 | 0/0 | 11809 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0085 | 0/0 | 11807 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0086 | 0/0 | 11811 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0087 | 0/0 | 11807 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0088 | 0/0 | 11812 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0089 | 0/0 | 11810 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0090 | 0/0 | 11810 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0091 | 0/0 | 11807 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0092 | 0/0 | 11810 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0093 | 0/0 | 11810 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0094 | 0/0 | 11809 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0095 | 0/0 | 11809 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0096 | 0/0 | 11809 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0097 | 0/0 | 11808 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0098 | 0/0 | 11808 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0099 | 0/0 | 11809 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0100 | 0/0 | 11809 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0101 | 0/0 | 11811 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0102 | 0/0 | 11809 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0103 | 0/0 | 11785 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0104 | 0/0 | 11785 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0105 | 0/0 | 11783 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0106 | 0/0 | 11811 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0107 | 0/0 | 11811 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0108 | 0/0 | 11811 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0109 | 0/0 | 11811 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0110 | 0/0 | 11817 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0111 | 0/0 | 11821 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0112 | 0/0 | 11823 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0113 | 0/0 | 11803 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0114 | 0/0 | 11805 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0115 | 0/0 | 11818 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0116 | 0/0 | 11777 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0117 | 0/0 | 11799 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0118 | 0/0 | 11818 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0119 | 0/0 | 11801 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0120 | 0/0 | 11800 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0121 | 0/0 | 11800 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0122 | 0/0 | 11798 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0123 | 0/0 | 11799 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0124 | 0/0 | 11805 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0125 | 0/0 | 11802 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0126 | 0/0 | 11827 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0127 | 0/0 | 11805 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0128 | 0/0 | 11804 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0129 | 0/0 | 11803 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0130 | 0/0 | 11805 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0131 | 0/0 | 11808 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0132 | 0/0 | 11806 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0133 | 0/0 | 11807 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0134 | 0/0 | 11803 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0135 | 0/0 | 11805 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0136 | 0/0 | 11804 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0137 | 0/0 | 11805 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0138 | 0/0 | 11803 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0139 | 0/0 | 11811 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0140 | 0/0 | 11810 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0141 | 0/0 | 11813 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0142 | 0/0 | 11812 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0143 | 0/0 | 11814 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0144 | 0/0 | 11811 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0145 | 0/0 | 11821 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0146 | 0/0 | 11825 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0147 | 0/0 | 11827 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0148 | 0/0 | 11833 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0149 | 0/0 | 11817 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0150 | 0/0 | 11822 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0151 | 0/0 | 11824 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0152 | 0/0 | 11800 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0153 | 0/0 | 11824 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0154 | 0/0 | 11828 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0155 | 0/0 | 11830 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0156 | 0/0 | 11832 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0157 | 0/0 | 11799 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0158 | 0/0 | 11786 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0159 | 0/0 | 11785 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0160 | 0/0 | 11790 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0161 | 0/0 | 11789 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0162 | 0/0 | 11788 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0163 | 0/0 | 11801 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0164 | 0/0 | 11797 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0165 | 0/0 | 11800 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0166 | 0/0 | 11799 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0167 | 0/0 | 11801 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0168 | 0/0 | 11801 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0169 | 0/0 | 11799 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0170 | 0/0 | 11806 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0171 | 0/0 | 11805 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0172 | 0/0 | 11801 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0173 | 0/0 | 11793 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0174 | 0/0 | 11807 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0175 | 0/0 | 11806 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0176 | 0/0 | 11808 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0177 | 0/0 | 11808 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0178 | 0/0 | 11811 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0179 | 0/0 | 11810 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0180 | 0/0 | 11809 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0181 | 0/0 | 11807 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0182 | 0/0 | 11811 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0183 | 0/0 | 11810 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0184 | 0/0 | 11809 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0185 | 0/0 | 11814 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0186 | 0/0 | 11812 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0187 | 0/0 | 11811 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0188 | 0/0 | 11813 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0189 | 0/0 | 11812 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0190 | 0/0 | 11813 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0191 | 0/0 | 11820 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0192 | 0/0 | 11817 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0193 | 0/0 | 11799 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0194 | 0/0 | 11813 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0195 | 0/0 | 11804 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0196 | 0/0 | 11806 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| t0197 | 0/0 | 11812 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0154 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0173 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| 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 | 2343 | 293 | 74 | 49 | 121 | 13 | 34 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0003 | 0/0 | 2343 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0005 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0002c0002 | 0/0 | 2343 | 3 | 0 | 0 | 1 | 0 | 2 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0003c0006 | 0/0 | 2343 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0004c0004 | 0/0 | 2343 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0005c0007 | 0/0 | 2343 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0006c0008 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 14151 | 29 | 2 | 4 | 16 | 1 | 5 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0002 | 0/0 | 14153 | 12 | 4 | 4 | 3 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0003 | 0/0 | 14147 | 5 | 0 | 1 | 3 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0004 | 0/0 | 14155 | 4 | 0 | 1 | 2 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0005 | 0/0 | 14153 | 4 | 0 | 0 | 4 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0006 | 1/0 | 14174 | 3 | 2 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0007 | 0/0 | 14157 | 3 | 3 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0008 | 0/0 | 14149 | 3 | 0 | 2 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0009 | 0/0 | 14151 | 3 | 0 | 0 | 0 | 2 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0010 | 0/0 | 14162 | 3 | 3 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0011 | 0/0 | 14140 | 3 | 0 | 0 | 3 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0012 | 0/0 | 14148 | 3 | 0 | 1 | 0 | 2 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0013 | 0/0 | 14141 | 3 | 0 | 1 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0014 | 0/0 | 14149 | 3 | 0 | 0 | 2 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0015 | 0/0 | 14149 | 3 | 0 | 0 | 2 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0016 | 0/0 | 14175 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0017 | 0/0 | 14128 | 2 | 2 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0018 | 0/0 | 14151 | 2 | 0 | 0 | 0 | 0 | 2 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0019 | 0/0 | 14159 | 2 | 2 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0020 | 0/0 | 14167 | 2 | 2 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0021 | 0/0 | 14147 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0022 | 0/0 | 14151 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0023 | 0/0 | 14151 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0024 | 0/0 | 14151 | 2 | 0 | 1 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0025 | 0/0 | 14151 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0026 | 0/0 | 14153 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0027 | 0/0 | 14157 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0028 | 0/0 | 14157 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0029 | 0/0 | 14147 | 2 | 1 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0030 | 0/0 | 14149 | 2 | 1 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0031 | 0/0 | 14141 | 2 | 0 | 1 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0032 | 0/0 | 14143 | 2 | 0 | 0 | 0 | 1 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0033 | 0/0 | 14151 | 2 | 2 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0034 | 0/0 | 14146 | 2 | 1 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0035 | 0/0 | 14150 | 2 | 0 | 0 | 0 | 0 | 2 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0036 | 0/0 | 14149 | 2 | 0 | 0 | 0 | 0 | 2 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0037 | 0/0 | 14153 | 2 | 0 | 0 | 1 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0038 | 0/0 | 14166 | 2 | 0 | 2 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0039 | 0/0 | 14172 | 2 | 2 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0040 | 0/0 | 14125 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0041 | 0/0 | 14139 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0042 | 0/0 | 14143 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0043 | 0/0 | 14145 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0044 | 0/0 | 14145 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0045 | 0/0 | 14154 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0046 | 0/0 | 14153 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0047 | 0/0 | 14152 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0048 | 0/0 | 14155 | 2 | 0 | 0 | 2 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0049 | 0/0 | 14150 | 2 | 1 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0050 | 0/0 | 14152 | 2 | 2 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0051 | 0/0 | 14128 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0052 | 0/0 | 14149 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0053 | 0/0 | 14148 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0054 | 0/0 | 14142 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0055 | 0/0 | 14130 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0056 | 0/0 | 14176 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0057 | 0/0 | 14176 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0058 | 0/0 | 14180 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0059 | 0/0 | 14182 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0060 | 0/0 | 14184 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0061 | 0/0 | 14184 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0063 | 0/0 | 14152 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0064 | 0/0 | 14153 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0065 | 0/0 | 14171 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0067 | 0/0 | 14173 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0068 | 0/0 | 14177 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0069 | 0/0 | 14175 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0070 | 0/0 | 14177 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0072 | 0/0 | 14181 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0073 | 0/0 | 14183 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0074 | 0/0 | 14165 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0075 | 0/0 | 14165 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0076 | 0/0 | 14168 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0078 | 0/0 | 14143 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0079 | 0/0 | 14170 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0080 | 0/0 | 14166 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0081 | 0/0 | 14166 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0082 | 0/0 | 14145 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0083 | 0/0 | 14172 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0084 | 0/0 | 14151 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0085 | 0/0 | 14149 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0086 | 0/0 | 14153 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0087 | 0/0 | 14149 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0088 | 0/0 | 14154 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0089 | 0/0 | 14152 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0090 | 0/0 | 14152 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0091 | 0/0 | 14149 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0092 | 0/0 | 14152 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0093 | 0/0 | 14152 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0094 | 0/0 | 14151 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0095 | 0/0 | 14151 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0096 | 0/0 | 14151 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0097 | 0/0 | 14150 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0098 | 0/0 | 14150 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0099 | 0/0 | 14151 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0100 | 0/0 | 14151 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0101 | 0/0 | 14153 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0102 | 0/0 | 14151 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0103 | 0/0 | 14127 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0104 | 0/0 | 14127 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0105 | 0/0 | 14125 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0106 | 0/0 | 14153 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0107 | 0/0 | 14153 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0108 | 0/0 | 14153 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0109 | 0/0 | 14153 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0110 | 0/0 | 14159 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0111 | 0/0 | 14163 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0112 | 0/0 | 14165 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0113 | 0/0 | 14145 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0114 | 0/0 | 14147 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0115 | 0/0 | 14160 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0116 | 0/0 | 14119 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0117 | 0/0 | 14141 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0118 | 0/0 | 14160 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0119 | 0/0 | 14143 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0120 | 0/0 | 14142 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0121 | 0/0 | 14142 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0122 | 0/0 | 14140 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0124 | 0/0 | 14147 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0125 | 0/0 | 14144 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0126 | 0/0 | 14169 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0127 | 0/0 | 14147 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0129 | 0/0 | 14145 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0130 | 0/0 | 14147 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0131 | 0/0 | 14150 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0132 | 0/0 | 14148 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0133 | 0/0 | 14149 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0134 | 0/0 | 14145 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0135 | 0/0 | 14147 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0136 | 0/0 | 14146 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0137 | 0/0 | 14147 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0138 | 0/0 | 14145 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0139 | 0/0 | 14153 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0140 | 0/0 | 14152 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0141 | 0/0 | 14155 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0142 | 0/0 | 14154 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0143 | 0/0 | 14156 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0144 | 0/0 | 14153 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0145 | 0/0 | 14163 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0146 | 0/0 | 14167 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0147 | 0/0 | 14169 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0148 | 0/0 | 14175 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0149 | 0/0 | 14159 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0150 | 0/0 | 14164 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0151 | 0/0 | 14166 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0152 | 0/0 | 14142 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0154 | 0/0 | 14170 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0155 | 0/0 | 14172 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0156 | 0/0 | 14174 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0157 | 0/0 | 14141 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0158 | 0/0 | 14128 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0159 | 0/0 | 14127 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0160 | 0/0 | 14132 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0161 | 0/0 | 14131 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0162 | 0/0 | 14130 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0163 | 0/0 | 14143 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0164 | 0/0 | 14139 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0165 | 0/0 | 14142 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0166 | 0/0 | 14141 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0167 | 0/0 | 14143 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0168 | 0/0 | 14143 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0169 | 0/0 | 14141 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0170 | 0/0 | 14148 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0171 | 0/0 | 14147 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0172 | 0/0 | 14143 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0173 | 0/0 | 14135 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0174 | 0/0 | 14149 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0175 | 0/0 | 14148 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0176 | 0/0 | 14150 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0177 | 0/0 | 14150 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0178 | 0/0 | 14153 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0179 | 0/0 | 14152 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0180 | 0/0 | 14151 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0181 | 0/0 | 14149 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0182 | 0/0 | 14153 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0183 | 0/0 | 14152 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0184 | 0/0 | 14151 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0185 | 0/0 | 14156 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0186 | 0/0 | 14154 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0187 | 0/0 | 14153 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0189 | 0/0 | 14154 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0190 | 0/0 | 14155 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0191 | 0/0 | 14162 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0192 | 0/0 | 14159 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0193 | 0/0 | 14141 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0194 | 0/0 | 14155 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0195 | 0/0 | 14146 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0196 | 0/0 | 14148 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0001t0197 | 0/0 | 14154 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0003t0071 | 0/0 | 14179 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0001c0005t0153 | 0/0 | 14166 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0002c0002t0062 | 0/0 | 14145 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0002c0002t0066 | 0/0 | 14175 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0002c0002t0077 | 0/0 | 14163 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0003c0006t0128 | 0/0 | 14146 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0004c0004t0188 | 0/0 | 14155 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0005c0007t0001 | 0/0 | 14151 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| a0006c0008t0123 | 0/0 | 14141 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | copy fasta | chr2 | 36832698 | 36971536 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0001g0173 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0005g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0005g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0006g0154 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0006g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0007g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0007g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0007g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0008g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0008g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0008g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0009g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0009g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0009g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0010g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0010g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0010g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0011g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0011g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0011g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0012g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0012g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0012g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0013g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0013g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0013g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0014g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0014g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0014g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0015g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0015g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0015g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0016g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0016g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0017g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0017g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0018g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0018g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0019g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0019g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0020g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0020g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0021g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0021g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0022g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0022g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0023g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0023g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0024g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0024g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0025g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0025g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0026g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0026g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0027g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0027g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0028g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0028g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0029g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0029g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0030g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0030g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0031g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0031g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0032g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0032g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0033g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0033g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0034g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0034g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0035g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0035g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0036g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0036g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0037g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0037g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0038g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0038g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0039g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0039g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0040g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0040g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0041g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0041g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0042g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0042g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0043g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0043g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0044g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0044g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0045g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0045g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0046g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0046g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0047g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0047g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0048g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0048g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0049g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0049g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0050g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0050g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0051g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0052g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0053g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0054g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0055g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0056g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0057g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0058g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0059g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0060g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0061g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0063g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0064g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0065g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0067g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0068g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0069g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0070g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0072g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0073g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0074g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0075g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0076g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0078g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0079g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0080g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0081g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0082g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0083g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0084g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0085g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0086g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0087g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0088g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0089g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0090g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0091g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0092g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0093g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0094g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0095g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0096g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0097g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0098g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0099g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0100g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0101g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0102g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0103g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0104g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0105g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0106g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0107g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0108g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0109g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0110g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0111g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0112g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0113g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0114g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0115g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0116g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0117g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0118g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0119g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0120g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0121g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0122g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0124g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0125g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0126g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0127g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0129g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0130g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0131g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0132g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0133g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0134g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0135g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0136g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0137g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0138g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0139g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0140g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0141g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0142g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0143g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0144g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0145g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0146g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0147g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0148g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0149g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0150g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0151g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0152g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0154g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0155g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0156g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0157g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0158g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0159g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0160g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0161g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0162g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0163g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0164g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0165g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0166g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0167g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0168g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0169g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0170g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0171g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0172g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0173g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0174g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0175g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0176g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0177g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0178g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0179g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0180g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0181g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0182g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0183g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0184g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0185g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0186g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0187g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0189g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0190g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0191g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0192g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0193g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0194g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0195g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0196g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0001t0197g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0003t0071g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0001c0005t0153g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0002c0002t0062g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0002c0002t0066g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0002c0002t0077g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0003c0006t0128g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0004c0004t0188g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0005c0007t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| a0006c0008t0123g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0193 | g0055 | EUR | GBR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG00099 | hp2 | a0001 | c0001 | t0009 | g0189 | EUR | GBR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG00280 | hp1 | a0001 | c0001 | t0186 | g0035 | EUR | FIN | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0171 | EUR | FIN | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG00323 | hp1 | a0001 | c0001 | t0009 | g0147 | EUR | FIN | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG00323 | hp2 | a0001 | c0001 | t0138 | g0043 | EUR | FIN | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | CHS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG00423 | hp1 | a0001 | c0001 | t0047 | g0083 | EAS | CHS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG00423 | hp2 | a0001 | c0001 | t0027 | g0194 | EAS | CHS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG00438 | hp1 | a0001 | c0001 | t0027 | g0125 | EAS | CHS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG00438 | hp2 | a0001 | c0001 | t0072 | g0221 | EAS | CHS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0178 | EAS | CHS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG00544 | hp2 | a0001 | c0001 | t0191 | g0080 | EAS | CHS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG00558 | hp1 | a0001 | c0001 | t0112 | g0168 | EAS | CHS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG00558 | hp2 | a0001 | c0001 | t0021 | g0005 | EAS | CHS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG00597 | hp1 | a0001 | c0001 | t0165 | g0017 | EAS | CHS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG00597 | hp2 | a0001 | c0001 | t0070 | g0225 | EAS | CHS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG00621 | hp1 | a0001 | c0001 | t0005 | g0023 | EAS | CHS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG00621 | hp2 | a0001 | c0001 | t0051 | g0001 | EAS | CHS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG00639 | hp1 | a0001 | c0001 | t0109 | g0166 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG00639 | hp2 | a0001 | c0001 | t0116 | g0272 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG00642 | hp1 | a0001 | c0001 | t0183 | g0073 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG00642 | hp2 | a0001 | c0001 | t0012 | g0022 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG00673 | hp1 | a0001 | c0001 | t0170 | g0142 | EAS | CHS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG00673 | hp2 | a0001 | c0001 | t0119 | g0301 | EAS | CHS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG00735 | hp1 | a0001 | c0001 | t0008 | g0119 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG00735 | hp2 | a0001 | c0001 | t0132 | g0258 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG00738 | hp1 | a0001 | c0001 | t0094 | g0179 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG00738 | hp2 | a0001 | c0001 | t0083 | g0234 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG00741 | hp1 | a0001 | c0001 | t0126 | g0040 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG00741 | hp2 | a0001 | c0001 | t0159 | g0032 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01070 | hp1 | a0001 | c0001 | t0038 | g0212 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01070 | hp2 | a0001 | c0001 | t0180 | g0031 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01071 | hp2 | a0001 | c0001 | t0038 | g0213 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01106 | hp1 | a0001 | c0001 | t0034 | g0264 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01106 | hp2 | a0001 | c0001 | t0068 | g0262 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01168 | hp1 | a0001 | c0001 | t0105 | g0100 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01168 | hp2 | a0001 | c0001 | t0088 | g0182 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01175 | hp1 | a0001 | c0001 | t0124 | g0260 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01243 | hp1 | a0001 | c0001 | t0049 | g0299 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01243 | hp2 | a0001 | c0001 | t0030 | g0237 | AMR | PUR | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01255 | hp1 | a0001 | c0001 | t0106 | g0128 | AMR | CLM | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | CLM | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0181 | AMR | CLM | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01256 | hp2 | a0001 | c0001 | t0145 | g0276 | AMR | CLM | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01261 | hp1 | a0001 | c0001 | t0174 | g0014 | AMR | CLM | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01261 | hp2 | a0001 | c0001 | t0024 | g0153 | AMR | CLM | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01346 | hp1 | a0001 | c0001 | t0150 | g0208 | AMR | CLM | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01346 | hp2 | a0001 | c0001 | t0086 | g0102 | AMR | CLM | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01361 | hp1 | a0001 | c0001 | t0008 | g0047 | AMR | CLM | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01361 | hp2 | a0001 | c0001 | t0029 | g0155 | AMR | CLM | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | CLM | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01433 | hp2 | a0001 | c0001 | t0143 | g0278 | AMR | CLM | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01496 | hp1 | a0001 | c0001 | t0196 | g0298 | AMR | CLM | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01496 | hp2 | a0001 | c0001 | t0134 | g0041 | AMR | CLM | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01516 | hp1 | a0001 | c0001 | t0098 | g0150 | EUR | IBS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01516 | hp2 | a0001 | c0001 | t0012 | g0279 | EUR | IBS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | IBS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01517 | hp2 | a0001 | c0001 | t0012 | g0280 | EUR | IBS | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0246 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01884 | hp2 | a0001 | c0001 | t0067 | g0092 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0201 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01891 | hp2 | a0001 | c0001 | t0017 | g0242 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01934 | hp1 | a0001 | c0001 | t0013 | g0027 | AMR | PEL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01934 | hp2 | a0005 | c0007 | t0001 | g0167 | AMR | PEL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01952 | hp1 | a0001 | c0001 | t0031 | g0045 | AMR | PEL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01952 | hp2 | a0001 | c0001 | t0101 | g0172 | AMR | PEL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01993 | hp1 | a0001 | c0001 | t0162 | g0051 | AMR | PEL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PEL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | PEL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02004 | hp2 | a0001 | c0001 | t0122 | g0044 | AMR | PEL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02015 | hp1 | a0001 | c0001 | t0136 | g0175 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02015 | hp2 | a0001 | c0001 | t0044 | g0012 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02040 | hp1 | a0001 | c0001 | t0133 | g0265 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02040 | hp2 | a0001 | c0001 | t0016 | g0229 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02055 | hp1 | a0001 | c0001 | t0081 | g0233 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02055 | hp2 | a0001 | c0001 | t0108 | g0116 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02056 | hp1 | a0001 | c0001 | t0111 | g0204 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02056 | hp2 | a0001 | c0001 | t0013 | g0008 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02071 | hp1 | a0001 | c0001 | t0048 | g0195 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02071 | hp2 | a0001 | c0001 | t0011 | g0096 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02080 | hp2 | a0001 | c0001 | t0167 | g0007 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02083 | hp1 | a0001 | c0001 | t0173 | g0028 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02083 | hp2 | a0001 | c0003 | t0071 | g0223 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02129 | hp1 | a0001 | c0001 | t0127 | g0009 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02129 | hp2 | a0001 | c0001 | t0042 | g0263 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02135 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02135 | hp2 | a0004 | c0004 | t0188 | g0048 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02145 | hp2 | a0001 | c0001 | t0017 | g0240 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02155 | hp1 | a0001 | c0001 | t0028 | g0177 | EAS | CDX | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02155 | hp2 | a0001 | c0001 | t0040 | g0034 | EAS | CDX | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02258 | hp2 | a0001 | c0001 | t0195 | g0294 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02273 | hp1 | a0001 | c0001 | t0135 | g0036 | AMR | PEL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02280 | hp2 | a0001 | c0001 | t0141 | g0274 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PEL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02300 | hp2 | a0001 | c0001 | t0184 | g0302 | AMR | PEL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02451 | hp1 | a0001 | c0001 | t0059 | g0255 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02451 | hp2 | a0001 | c0001 | t0197 | g0300 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02523 | hp1 | a0001 | c0001 | t0092 | g0157 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02523 | hp2 | a0001 | c0001 | t0015 | g0039 | EAS | KHV | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02572 | hp1 | a0001 | c0001 | t0033 | g0283 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02572 | hp2 | a0001 | c0001 | t0050 | g0297 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02602 | hp1 | a0001 | c0001 | t0036 | g0095 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02602 | hp2 | a0001 | c0001 | t0166 | g0117 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02615 | hp1 | a0001 | c0001 | t0114 | g0288 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0198 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02630 | hp1 | a0001 | c0001 | t0058 | g0251 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02630 | hp2 | a0001 | c0001 | t0019 | g0090 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02647 | hp1 | a0001 | c0001 | t0056 | g0241 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02647 | hp2 | a0001 | c0001 | t0139 | g0270 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02683 | hp1 | a0001 | c0001 | t0037 | g0069 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02683 | hp2 | a0002 | c0002 | t0077 | g0226 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02698 | hp1 | a0001 | c0001 | t0176 | g0064 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0244 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02723 | hp2 | a0001 | c0001 | t0082 | g0232 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02818 | hp2 | a0001 | c0001 | t0061 | g0252 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02886 | hp1 | a0001 | c0005 | t0153 | g0216 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02886 | hp2 | a0001 | c0001 | t0064 | g0202 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02895 | hp1 | a0001 | c0001 | t0155 | g0207 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02895 | hp2 | a0001 | c0001 | t0131 | g0285 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02896 | hp1 | a0001 | c0001 | t0010 | g0291 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02896 | hp2 | a0001 | c0001 | t0130 | g0136 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02897 | hp1 | a0001 | c0001 | t0010 | g0290 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02897 | hp2 | a0001 | c0001 | t0033 | g0286 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02922 | hp1 | a0001 | c0001 | t0069 | g0093 | AFR | ESN | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02922 | hp2 | a0001 | c0001 | t0010 | g0292 | AFR | ESN | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02965 | hp1 | a0001 | c0001 | t0080 | g0235 | AFR | ESN | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02965 | hp2 | a0001 | c0001 | t0129 | g0273 | AFR | ESN | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02970 | hp1 | a0001 | c0001 | t0147 | g0250 | AFR | ESN | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02970 | hp2 | a0001 | c0001 | t0049 | g0296 | AFR | ESN | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02976 | hp1 | a0001 | c0001 | t0054 | g0275 | AFR | ESN | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02976 | hp2 | a0001 | c0001 | t0146 | g0249 | AFR | ESN | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03195 | hp1 | a0001 | c0001 | t0060 | g0254 | AFR | ESN | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03195 | hp2 | a0001 | c0001 | t0074 | g0217 | AFR | ESN | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03209 | hp1 | a0001 | c0001 | t0039 | g0215 | AFR | MSL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03209 | hp2 | a0001 | c0001 | t0019 | g0091 | AFR | MSL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03239 | hp1 | a0001 | c0001 | t0032 | g0071 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03239 | hp2 | a0001 | c0001 | t0097 | g0164 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03453 | hp1 | a0001 | c0001 | t0078 | g0253 | AFR | MSL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03453 | hp2 | a0001 | c0001 | t0030 | g0289 | AFR | MSL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03486 | hp1 | a0001 | c0001 | t0075 | g0218 | AFR | MSL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0197 | AFR | MSL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03490 | hp1 | a0001 | c0001 | t0113 | g0146 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03490 | hp2 | a0001 | c0001 | t0018 | g0228 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03491 | hp1 | a0001 | c0001 | t0031 | g0042 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03492 | hp1 | a0001 | c0001 | t0018 | g0222 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03540 | hp1 | a0001 | c0001 | t0034 | g0256 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03540 | hp2 | a0001 | c0001 | t0151 | g0205 | AFR | GWD | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03579 | hp1 | a0001 | c0001 | t0063 | g0203 | AFR | MSL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03579 | hp2 | a0001 | c0001 | t0039 | g0214 | AFR | MSL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03669 | hp1 | a0001 | c0001 | t0035 | g0268 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03669 | hp2 | a0001 | c0001 | t0065 | g0224 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03688 | hp1 | a0001 | c0001 | t0014 | g0094 | SAS | STU | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03688 | hp2 | a0001 | c0001 | t0093 | g0121 | SAS | STU | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03704 | hp1 | a0001 | c0001 | t0035 | g0282 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03831 | hp1 | a0001 | c0001 | t0073 | g0210 | SAS | BEB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0030 | SAS | BEB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03834 | hp1 | a0001 | c0001 | t0036 | g0070 | SAS | BEB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03834 | hp2 | a0001 | c0001 | t0009 | g0190 | SAS | BEB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03942 | hp1 | a0001 | c0001 | t0144 | g0046 | SAS | BEB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03942 | hp2 | a0001 | c0001 | t0024 | g0115 | SAS | BEB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG04184 | hp1 | a0001 | c0001 | t0157 | g0050 | SAS | BEB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG04184 | hp2 | a0001 | c0001 | t0096 | g0111 | SAS | BEB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG04199 | hp1 | a0001 | c0001 | t0015 | g0056 | SAS | STU | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG04199 | hp2 | a0001 | c0001 | t0104 | g0105 | SAS | STU | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG04204 | hp1 | a0001 | c0001 | t0154 | g0209 | SAS | STU | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG04204 | hp2 | a0001 | c0001 | t0125 | g0277 | SAS | STU | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | STU | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG04228 | hp2 | a0002 | c0002 | t0066 | g0220 | SAS | STU | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18522 | hp1 | a0001 | c0001 | t0156 | g0206 | AFR | YRI | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18522 | hp2 | a0001 | c0001 | t0076 | g0219 | AFR | YRI | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18906 | hp1 | a0001 | c0001 | t0084 | g0231 | AFR | YRI | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18906 | hp2 | a0001 | c0001 | t0120 | g0267 | AFR | YRI | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18940 | hp1 | a0001 | c0001 | t0043 | g0024 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18940 | hp2 | a0001 | c0001 | t0090 | g0127 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18941 | hp1 | a0001 | c0001 | t0025 | g0187 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18941 | hp2 | a0001 | c0001 | t0045 | g0085 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18943 | hp1 | a0001 | c0001 | t0140 | g0257 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18943 | hp2 | a0001 | c0001 | t0099 | g0110 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18945 | hp2 | a0001 | c0001 | t0185 | g0084 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18946 | hp1 | a0001 | c0001 | t0026 | g0120 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18946 | hp2 | a0001 | c0001 | t0041 | g0018 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18950 | hp1 | a0001 | c0001 | t0005 | g0065 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18950 | hp2 | a0001 | c0001 | t0037 | g0072 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18952 | hp1 | a0001 | c0001 | t0013 | g0010 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18952 | hp2 | a0001 | c0001 | t0117 | g0269 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18954 | hp2 | a0001 | c0001 | t0192 | g0199 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18959 | hp1 | a0001 | c0001 | t0100 | g0193 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18959 | hp2 | a0001 | c0001 | t0182 | g0053 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18961 | hp1 | a0001 | c0001 | t0015 | g0025 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18961 | hp2 | a0001 | c0001 | t0023 | g0140 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18962 | hp1 | a0001 | c0001 | t0160 | g0088 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18963 | hp1 | a0001 | c0001 | t0161 | g0052 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18963 | hp2 | a0001 | c0001 | t0107 | g0148 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18968 | hp1 | a0001 | c0001 | t0175 | g0081 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18968 | hp2 | a0001 | c0001 | t0087 | g0133 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18969 | hp2 | a0001 | c0001 | t0178 | g0060 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18970 | hp1 | a0001 | c0001 | t0044 | g0058 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18970 | hp2 | a0001 | c0001 | t0026 | g0170 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18972 | hp2 | a0001 | c0001 | t0011 | g0098 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18982 | hp1 | a0001 | c0001 | t0103 | g0169 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18982 | hp2 | a0001 | c0001 | t0005 | g0087 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18985 | hp1 | a0001 | c0001 | t0102 | g0109 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18985 | hp2 | a0001 | c0001 | t0043 | g0066 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18986 | hp1 | a0001 | c0001 | t0046 | g0062 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18986 | hp2 | a0002 | c0002 | t0062 | g0227 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18995 | hp1 | a0001 | c0001 | t0045 | g0082 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18998 | hp1 | a0001 | c0001 | t0158 | g0078 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19000 | hp1 | a0001 | c0001 | t0187 | g0049 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19000 | hp2 | a0001 | c0001 | t0089 | g0104 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19002 | hp1 | a0001 | c0001 | t0021 | g0002 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19002 | hp2 | a0001 | c0001 | t0040 | g0016 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19006 | hp1 | a0001 | c0001 | t0016 | g0230 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19006 | hp2 | a0001 | c0001 | t0168 | g0075 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19007 | hp1 | a0001 | c0001 | t0190 | g0063 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19007 | hp2 | a0001 | c0001 | t0028 | g0130 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19011 | hp2 | a0001 | c0001 | t0047 | g0079 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19012 | hp1 | a0001 | c0001 | t0177 | g0089 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19012 | hp2 | a0001 | c0001 | t0022 | g0108 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19043 | hp1 | a0001 | c0001 | t0020 | g0239 | AFR | LWK | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19043 | hp2 | a0001 | c0001 | t0057 | g0245 | AFR | LWK | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19054 | hp2 | a0001 | c0001 | t0171 | g0038 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19056 | hp2 | a0001 | c0001 | t0014 | g0015 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19060 | hp1 | a0001 | c0001 | t0023 | g0139 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19060 | hp2 | a0001 | c0001 | t0048 | g0196 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19063 | hp2 | a0001 | c0001 | t0164 | g0019 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19064 | hp1 | a0001 | c0001 | t0008 | g0103 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19064 | hp2 | a0001 | c0001 | t0172 | g0074 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19065 | hp1 | a0001 | c0001 | t0091 | g0122 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19065 | hp2 | a0001 | c0001 | t0042 | g0026 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19066 | hp1 | a0001 | c0001 | t0169 | g0011 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19070 | hp1 | a0001 | c0001 | t0163 | g0013 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19070 | hp2 | a0001 | c0001 | t0022 | g0135 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19080 | hp2 | a0001 | c0001 | t0014 | g0037 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19081 | hp1 | a0001 | c0001 | t0041 | g0029 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19086 | hp1 | a0001 | c0001 | t0011 | g0097 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19086 | hp2 | a0001 | c0001 | t0095 | g0112 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19088 | hp1 | a0001 | c0001 | t0179 | g0086 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19089 | hp1 | a0001 | c0001 | t0046 | g0059 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19090 | hp1 | a0001 | c0001 | t0025 | g0151 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19090 | hp2 | a0001 | c0001 | t0194 | g0021 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19091 | hp1 | a0001 | c0001 | t0181 | g0061 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19091 | hp2 | a0001 | c0001 | t0110 | g0191 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19240 | hp1 | a0001 | c0001 | t0085 | g0192 | AFR | YRI | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | YRI | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA20129 | hp1 | a0001 | c0001 | t0052 | g0261 | AFR | ASW | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA20129 | hp2 | a0001 | c0001 | t0029 | g0159 | AFR | ASW | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA20752 | hp1 | a0003 | c0006 | t0128 | g0271 | EUR | TSI | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA20752 | hp2 | a0001 | c0001 | t0189 | g0054 | EUR | TSI | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0162 | EUR | TSI | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA20805 | hp2 | a0001 | c0001 | t0032 | g0067 | EUR | TSI | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA20905 | hp1 | a0001 | c0001 | t0053 | g0068 | SAS | GIH | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA20905 | hp2 | a0001 | c0001 | t0142 | g0266 | SAS | GIH | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01123 | hp1 | a0001 | c0001 | t0121 | g0281 | AMR | CLM | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02109 | hp1 | a0001 | c0001 | t0055 | g0243 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02109 | hp2 | a0001 | c0001 | t0118 | g0293 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02559 | hp1 | a0001 | c0001 | t0079 | g0236 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG02559 | hp2 | a0001 | c0001 | t0152 | g0211 | AFR | ACB | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03471 | hp1 | a0001 | c0001 | t0115 | g0287 | AFR | MSL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG03471 | hp2 | a0001 | c0001 | t0149 | g0247 | AFR | MSL | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG06807 | hp1 | a0001 | c0001 | t0137 | g0259 | AFR | USA | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| HG06807 | hp2 | a0001 | c0001 | t0050 | g0295 | AFR | USA | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA20300 | hp1 | a0001 | c0001 | t0020 | g0238 | AFR | USA | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA20300 | hp2 | a0001 | c0001 | t0148 | g0248 | AFR | USA | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | LWK | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| NA21309 | hp2 | a0006 | c0008 | t0123 | g0284 | AFR | LWK | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0173 | REF | REF | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0006 | g0154 | REF | REF | STRN_chr2_36832698_36971536 | STRN | chr2 | 36832698 | 36971536 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:36855307
|
C | G | 1 | a0004 | 1 | HG02135.hp2 | missense_variant | MODERATE | c.1883G>C | p.Ser628Thr | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/18 | 1956/14174 | 1883/2343 | 628/780 | chr2 | 36855307 | ||
| chr2:36877898
|
G | A | 1 | a0003 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.1316C>T | p.Thr439Ile | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/18 | 1389/14174 | 1316/2343 | 439/780 | chr2 | 36877898 | ||
| chr2:36877976
|
G | C | 1 | a0005 | 1 | HG01934.hp2 | missense_variant | MODERATE | c.1238C>G | p.Ala413Gly | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/18 | 1311/14174 | 1238/2343 | 413/780 | chr2 | 36877976 | ||
| chr2:36883980
|
G | A | 1 | a0002 | 3 | HG02683.hp2 HG04228.hp2 NA18986.hp2 |
missense_variant | MODERATE | c.1138C>T | p.Pro380Ser | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/18 | 1211/14174 | 1138/2343 | 380/780 | chr2 | 36883980 | ||
| chr2:36902653
|
T | C | 1 | a0006 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.590A>G | p.Glu197Gly | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/18 | 663/14174 | 590/2343 | 197/780 | chr2 | 36902653 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:36849510
|
G | C | 1 | a0001c0005 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.2289C>G | p.Ser763Ser | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 2362/14174 | 2289/2343 | 763/780 | chr2 | 36849510 | ||
| chr2:36905574
|
A | G | 1 | a0001c0003 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.457T>C | p.Leu153Leu | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/18 | 530/14174 | 457/2343 | 153/780 | chr2 | 36905574 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:36837812
|
A | G | 3 | a0001c0001t0023a0001c0001t0027a0001c0001t0111 | 5 | HG00423.hp2 HG00438.hp1 HG02056.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*11644T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 11644 | chr2 | 36837812 | |||||
| chr2:36837861
|
C | T | 17 | a0001c0001t0016a0001c0001t0018a0001c0001t0019others(14): Show | 20 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*11595G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 11595 | chr2 | 36837861 | |||||
| chr2:36837995
|
T | G | 157 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(154): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
3_prime_UTR_variant | MODIFIER | c.*11461A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 11461 | chr2 | 36837995 | |||||
| chr2:36838011
|
G | A | 14 | a0001c0001t0016a0001c0001t0018a0001c0001t0019others(11): Show | 17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*11445C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 11445 | chr2 | 36838011 | |||||
| chr2:36838148
|
T | C | 4 | a0001c0001t0009a0001c0001t0024a0001c0001t0106others(1): Show | 7 | HG00099.hp2 HG00323.hp1 HG01255.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*11308A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 11308 | chr2 | 36838148 | |||||
| chr2:36838177
|
G | A | 17 | a0001c0001t0016a0001c0001t0018a0001c0001t0019others(14): Show | 20 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*11279C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 11279 | chr2 | 36838177 | |||||
| chr2:36838264
|
C | G | 1 | a0001c0001t0157 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11192G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 11192 | chr2 | 36838264 | |||||
| chr2:36838335
|
T | C | 1 | a0001c0001t0100 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11121A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 11121 | chr2 | 36838335 | |||||
| chr2:36838351
|
G | T | 1 | a0001c0001t0082 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11105C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 11105 | chr2 | 36838351 | |||||
| chr2:36838413
|
G | C | 1 | a0001c0001t0187 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11043C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 11043 | chr2 | 36838413 | |||||
| chr2:36838549
|
C | T | 153 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(150): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
3_prime_UTR_variant | MODIFIER | c.*10907G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 10907 | chr2 | 36838549 | |||||
| chr2:36838647
|
G | T | 185 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(182): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
3_prime_UTR_variant | MODIFIER | c.*10809C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 10809 | chr2 | 36838647 | |||||
| chr2:36838821
|
G | T | 1 | a0001c0001t0176 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10635C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 10635 | chr2 | 36838821 | |||||
| chr2:36838875
|
T | G | 106 | a0001c0001t0003a0001c0001t0005a0001c0001t0011others(103): Show | 142 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*10581A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 10581 | chr2 | 36838875 | |||||
| chr2:36838878
|
T | C | 1 | a0001c0001t0170 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10578A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 10578 | chr2 | 36838878 | |||||
| chr2:36838904
|
A | C | 1 | a0001c0001t0073 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10552T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 10552 | chr2 | 36838904 | |||||
| chr2:36838943
|
T | C | 2 | a0001c0001t0075a0001c0001t0076 | 2 | HG03486.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10513A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 10513 | chr2 | 36838943 | |||||
| chr2:36839020
|
C | T | 189 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(186): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
3_prime_UTR_variant | MODIFIER | c.*10436G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 10436 | chr2 | 36839020 | |||||
| chr2:36839043
|
A | G | 2 | a0001c0001t0174a0001c0001t0180 | 2 | HG01070.hp2 HG01261.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10413T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 10413 | chr2 | 36839043 | |||||
| chr2:36839103
|
G | A | 1 | a0001c0001t0108 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10353C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 10353 | chr2 | 36839103 | |||||
| chr2:36839354
|
A | C | 1 | a0001c0001t0125 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10102T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 10102 | chr2 | 36839354 | |||||
| chr2:36839365
|
T | C | 2 | a0001c0001t0078a0001c0001t0182 | 2 | HG03453.hp1 NA18959.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10091A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 10091 | chr2 | 36839365 | |||||
| chr2:36839388
|
G | A | 1 | a0001c0001t0024 | 2 | HG01261.hp2 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10068C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 10068 | chr2 | 36839388 | |||||
| chr2:36839781
|
C | T | 1 | a0001c0001t0095 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9675G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 9675 | chr2 | 36839781 | |||||
| chr2:36839782
|
G | A | 1 | a0001c0001t0096 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9674C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 9674 | chr2 | 36839782 | |||||
| chr2:36839795
|
T | C | 3 | a0001c0001t0074a0001c0001t0075a0001c0001t0076 | 3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9661A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 9661 | chr2 | 36839795 | |||||
| chr2:36839975
|
A | G | 1 | a0001c0001t0094 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9481T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 9481 | chr2 | 36839975 | |||||
| chr2:36839994
|
A | G | 103 | a0001c0001t0003a0001c0001t0005a0001c0001t0011others(100): Show | 139 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*9462T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 9462 | chr2 | 36839994 | |||||
| chr2:36840339
|
C | A | 1 | a0001c0001t0087 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9117G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 9117 | chr2 | 36840339 | |||||
| chr2:36840356
|
C | T | 161 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(158): Show | 256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*9100G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 9100 | chr2 | 36840356 | |||||
| chr2:36840456
|
T | C | 3 | a0001c0001t0007a0001c0001t0082a0001c0001t0084 | 5 | HG01891.hp1 HG02615.hp2 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*9000A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 9000 | chr2 | 36840456 | |||||
| chr2:36840538
|
A | ATT | 13 | a0001c0001t0016a0001c0001t0018a0001c0001t0019others(10): Show | 16 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*8916_*8917dupAA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 8917 | chr2 | 36840538 | |||||
| chr2:36840538
|
AT | A | 30 | a0001c0001t0010a0001c0001t0045a0001c0001t0047others(27): Show | 36 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*8917delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 8917 | chr2 | 36840538 | |||||
| chr2:36840538
|
ATT | A | 120 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(117): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*8916_*8917delAA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 8916 | chr2 | 36840538 | |||||
| chr2:36840538
|
ATTT | A | 8 | a0001c0001t0034a0001c0001t0051a0001c0001t0097others(5): Show | 9 | HG00621.hp2 HG01106.hp1 HG01496.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*8915_*8917delAAA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 8915 | chr2 | 36840538 | |||||
| chr2:36841129
|
C | A | 171 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(168): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
3_prime_UTR_variant | MODIFIER | c.*8327G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 8327 | chr2 | 36841129 | |||||
| chr2:36841129
|
C | T | 1 | a0001c0001t0068 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8327G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 8327 | chr2 | 36841129 | |||||
| chr2:36841164
|
C | CT | 28 | a0001c0001t0016a0001c0001t0018a0001c0001t0019others(25): Show | 34 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*8291dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 8291 | chr2 | 36841164 | |||||
| chr2:36841164
|
CT | C | 28 | a0001c0001t0011a0001c0001t0012a0001c0001t0035others(25): Show | 33 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*8291delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 8291 | chr2 | 36841164 | |||||
| chr2:36841279
|
T | A | 1 | a0001c0001t0007 | 3 | HG01891.hp1 HG02615.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8177A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 8177 | chr2 | 36841279 | |||||
| chr2:36841285
|
C | T | 97 | a0001c0001t0003a0001c0001t0005a0001c0001t0011others(94): Show | 133 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*8171G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 8171 | chr2 | 36841285 | |||||
| chr2:36841369
|
T | C | 1 | a0001c0001t0121 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8087A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 8087 | chr2 | 36841369 | |||||
| chr2:36841532
|
G | A | 2 | a0001c0001t0099a0001c0001t0118 | 2 | HG02109.hp2 NA18943.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7924C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 7924 | chr2 | 36841532 | |||||
| chr2:36841712
|
A | G | 189 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(186): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
3_prime_UTR_variant | MODIFIER | c.*7744T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 7744 | chr2 | 36841712 | |||||
| chr2:36841928
|
G | A | 1 | a0001c0001t0064 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7528C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 7528 | chr2 | 36841928 | |||||
| chr2:36842031
|
T | C | 1 | a0001c0001t0166 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7425A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 7425 | chr2 | 36842031 | |||||
| chr2:36842177
|
C | T | 148 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(145): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
3_prime_UTR_variant | MODIFIER | c.*7279G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 7279 | chr2 | 36842177 | |||||
| chr2:36842507
|
C | T | 164 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(161): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
3_prime_UTR_variant | MODIFIER | c.*6949G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 6949 | chr2 | 36842507 | |||||
| chr2:36842654
|
T | C | 1 | a0001c0001t0109 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6802A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 6802 | chr2 | 36842654 | |||||
| chr2:36842695
|
T | C | 2 | a0001c0001t0025a0001c0001t0051 | 3 | HG00621.hp2 NA18941.hp1 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6761A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 6761 | chr2 | 36842695 | |||||
| chr2:36842714
|
TTA | T | 10 | a0001c0001t0038a0001c0001t0039a0001c0001t0064others(7): Show | 12 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*6740_*6741delTA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 6740 | chr2 | 36842714 | |||||
| chr2:36842742
|
A | G | 153 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(150): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
3_prime_UTR_variant | MODIFIER | c.*6714T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 6714 | chr2 | 36842742 | |||||
| chr2:36842906
|
C | T | 2 | a0001c0001t0059a0001c0001t0060 | 2 | HG02451.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6550G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 6550 | chr2 | 36842906 | |||||
| chr2:36842920
|
T | C | 10 | a0001c0001t0038a0001c0001t0039a0001c0001t0064others(7): Show | 12 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*6536A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 6536 | chr2 | 36842920 | |||||
| chr2:36843169
|
G | A | 5 | a0001c0001t0049a0001c0001t0050a0001c0001t0195others(2): Show | 7 | HG01243.hp1 HG01496.hp1 HG02258.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6287C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 6287 | chr2 | 36843169 | |||||
| chr2:36843210
|
G | A | 1 | a0001c0001t0007 | 3 | HG01891.hp1 HG02615.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6246C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 6246 | chr2 | 36843210 | |||||
| chr2:36843693
|
A | G | 1 | a0001c0001t0167 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5763T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 5763 | chr2 | 36843693 | |||||
| chr2:36843813
|
C | T | 1 | a0001c0001t0149 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5643G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 5643 | chr2 | 36843813 | |||||
| chr2:36843944
|
T | C | 3 | a0001c0001t0034a0001c0001t0052a0001c0001t0137 | 4 | HG01106.hp1 HG03540.hp1 HG06807.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5512A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 5512 | chr2 | 36843944 | |||||
| chr2:36844321
|
T | G | 1 | a0001c0001t0057 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5135A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 5135 | chr2 | 36844321 | |||||
| chr2:36844355
|
G | C | 3 | a0001c0001t0146a0001c0001t0147a0001c0001t0148 | 3 | HG02970.hp1 HG02976.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5101C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 5101 | chr2 | 36844355 | |||||
| chr2:36844402
|
T | A | 1 | a0001c0001t0132 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5054A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 5054 | chr2 | 36844402 | |||||
| chr2:36844403
|
A | C | 1 | a0001c0001t0132 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5053T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 5053 | chr2 | 36844403 | |||||
| chr2:36844455
|
T | C | 1 | a0001c0001t0100 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5001A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 5001 | chr2 | 36844455 | |||||
| chr2:36844701
|
A | G | 4 | a0001c0001t0079a0001c0001t0080a0001c0001t0081others(1): Show | 4 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4755T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 4755 | chr2 | 36844701 | |||||
| chr2:36845123
|
C | G | 157 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(154): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
3_prime_UTR_variant | MODIFIER | c.*4333G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 4333 | chr2 | 36845123 | |||||
| chr2:36845357
|
AT | A | 7 | a0001c0001t0007a0001c0001t0010a0001c0001t0082others(4): Show | 11 | HG01891.hp1 HG02109.hp2 HG02615.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4098delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 4098 | chr2 | 36845357 | |||||
| chr2:36845545
|
A | C | 3 | a0001c0001t0007a0001c0001t0082a0001c0001t0084 | 5 | HG01891.hp1 HG02615.hp2 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3911T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3911 | chr2 | 36845545 | |||||
| chr2:36845674
|
C | G | 2 | a0001c0001t0022a0001c0001t0103 | 3 | NA18982.hp1 NA19012.hp2 NA19070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3782G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3782 | chr2 | 36845674 | |||||
| chr2:36845769
|
A | G | 1 | a0001c0001t0151 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3687T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3687 | chr2 | 36845769 | |||||
| chr2:36845883
|
AAACACAC others(26): Show |
A | 2 | a0001c0001t0122a0001c0001t0134 | 2 | HG01496.hp2 HG02004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3540_*3572delGCAT others(29): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3540 | chr2 | 36845883 | |||||
| chr2:36845884
|
AAC | A | 72 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(69): Show | 136 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*3570_*3571delGT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3570 | chr2 | 36845884 | |||||
| chr2:36845884
|
AACACACA others(24): Show |
A | 1 | a0001c0001t0164 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3541_*3571delCATG others(27): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3541 | chr2 | 36845884 | |||||
| chr2:36845884
|
AACACACA others(25): Show |
A | 51 | a0001c0001t0003a0001c0001t0005a0001c0001t0013others(48): Show | 71 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*3540_*3571delGCAT others(28): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3540 | chr2 | 36845884 | |||||
| chr2:36845884
|
AACACACA others(27): Show |
A | 9 | a0001c0001t0031a0001c0001t0032a0001c0001t0036others(6): Show | 12 | HG00323.hp2 HG01168.hp1 HG01952.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3538_*3571delGTGC others(30): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3538 | chr2 | 36845884 | |||||
| chr2:36845884
|
AACACACA others(35): Show |
A | 1 | a0001c0001t0173 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3530_*3571delGTGT others(38): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3530 | chr2 | 36845884 | |||||
| chr2:36845884
|
AACACACA others(37): Show |
A | 2 | a0001c0001t0017a0001c0001t0055 | 3 | HG01891.hp2 HG02109.hp1 HG02145.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3528_*3571delGTGT others(40): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3528 | chr2 | 36845884 | |||||
| chr2:36845885
|
ACACACAC others(23): Show |
A | 38 | a0001c0001t0011a0001c0001t0012a0001c0001t0014others(35): Show | 51 | HG00544.hp2 HG00639.hp2 HG00642.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*3541_*3570delCATG others(26): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3541 | chr2 | 36845885 | |||||
| chr2:36845887
|
ACACACAC others(21): Show |
A | 5 | a0001c0001t0113a0001c0001t0124a0001c0001t0139others(2): Show | 5 | HG01175.hp1 HG02647.hp2 HG03490.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3541_*3568delCATG others(24): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3541 | chr2 | 36845887 | |||||
| chr2:36845889
|
ACACACAC others(19): Show |
A | 1 | a0001c0001t0170 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3541_*3566delCATG others(22): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3541 | chr2 | 36845889 | |||||
| chr2:36845907
|
G | A | 2 | a0001c0001t0020a0001c0001t0088 | 3 | HG01168.hp2 NA19043.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3549C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3549 | chr2 | 36845907 | |||||
| chr2:36845910
|
T | C | 2 | a0001c0001t0020a0001c0001t0088 | 3 | HG01168.hp2 NA19043.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3546A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3546 | chr2 | 36845910 | |||||
| chr2:36845915
|
GCA | G | 9 | a0001c0001t0020a0001c0001t0058a0001c0001t0068others(6): Show | 10 | HG00738.hp2 HG01106.hp2 HG01168.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3539_*3540delTG | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3539 | chr2 | 36845915 | |||||
| chr2:36845915
|
GCACA | G | 11 | a0001c0001t0016a0001c0001t0018a0001c0001t0026others(8): Show | 14 | HG00438.hp2 HG00597.hp2 HG01952.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3537_*3540delTGTG | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3537 | chr2 | 36845915 | |||||
| chr2:36845915
|
GCACACA | G | 43 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(40): Show | 97 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*3535_*3540delTGTG others(2): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3535 | chr2 | 36845915 | |||||
| chr2:36845915
|
GCACACAC others(1): Show |
G | 7 | a0001c0001t0029a0001c0001t0039a0001c0001t0063others(4): Show | 9 | HG01361.hp2 HG02886.hp1 HG02886.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3533_*3540delTGTG others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3533 | chr2 | 36845915 | |||||
| chr2:36845915
|
GCACACAC others(3): Show |
G | 3 | a0001c0001t0021a0001c0001t0146a0001c0001t0147 | 4 | HG00558.hp2 HG02970.hp1 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3531_*3540delTGTG others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3531 | chr2 | 36845915 | |||||
| chr2:36845915
|
GCACACAC others(5): Show |
G | 5 | a0001c0001t0010a0001c0001t0076a0001c0001t0115others(2): Show | 7 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3529_*3540delTGTG others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3529 | chr2 | 36845915 | |||||
| chr2:36845915
|
GCACACAC others(7): Show |
G | 1 | a0001c0001t0007 | 3 | HG01891.hp1 HG02615.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3527_*3540delTGTG others(10): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3527 | chr2 | 36845915 | |||||
| chr2:36845915
|
GCACACAC others(9): Show |
G | 3 | a0001c0001t0074a0001c0001t0075a0001c0001t0149 | 3 | HG03195.hp2 HG03471.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3525_*3540delTGTG others(12): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3525 | chr2 | 36845915 | |||||
| chr2:36845920
|
C | T | 2 | a0001c0001t0020a0001c0001t0088 | 3 | HG01168.hp2 NA19043.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3536G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3536 | chr2 | 36845920 | |||||
| chr2:36845921
|
A | G | 2 | a0001c0001t0020a0001c0001t0088 | 3 | HG01168.hp2 NA19043.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3535T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3535 | chr2 | 36845921 | |||||
| chr2:36845986
|
A | AC | 5 | a0001c0001t0089a0001c0001t0090a0001c0001t0165others(2): Show | 5 | HG00597.hp1 HG02698.hp1 NA18940.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3469dupG | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3469 | chr2 | 36845986 | |||||
| chr2:36845987
|
C | A | 1 | a0001c0001t0083 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3469G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3469 | chr2 | 36845987 | |||||
| chr2:36845990
|
C | G | 1 | a0001c0001t0040 | 2 | HG02155.hp2 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3466G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3466 | chr2 | 36845990 | |||||
| chr2:36846029
|
A | AT | 145 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(142): Show | 235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
3_prime_UTR_variant | MODIFIER | c.*3426dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3426 | chr2 | 36846029 | |||||
| chr2:36846029
|
A | ATT | 8 | a0001c0001t0007a0001c0001t0010a0001c0001t0054others(5): Show | 12 | HG01891.hp1 HG02109.hp2 HG02615.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3425_*3426dupAA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3426 | chr2 | 36846029 | |||||
| chr2:36846029
|
AT | A | 12 | a0001c0001t0029a0001c0001t0038a0001c0001t0039others(9): Show | 15 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3426delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3426 | chr2 | 36846029 | |||||
| chr2:36846301
|
G | A | 3 | a0001c0001t0074a0001c0001t0075a0001c0001t0076 | 3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3155C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3155 | chr2 | 36846301 | |||||
| chr2:36846387
|
T | TTA | 19 | a0001c0001t0010a0001c0001t0031a0001c0001t0038others(16): Show | 24 | HG00673.hp1 HG00738.hp2 HG01070.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*3067_*3068dupTA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3068 | chr2 | 36846387 | |||||
| chr2:36846387
|
T | TTATA | 18 | a0001c0001t0016a0001c0001t0032a0001c0001t0044others(15): Show | 21 | HG00741.hp1 HG01106.hp2 HG01884.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3065_*3068dupTATA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3068 | chr2 | 36846387 | |||||
| chr2:36846387
|
T | TTATATA | 18 | a0001c0001t0003a0001c0001t0012a0001c0001t0014others(15): Show | 27 | HG00323.hp2 HG00408.hp2 HG00597.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*3063_*3068dupTATA others(2): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3068 | chr2 | 36846387 | |||||
| chr2:36846387
|
T | TTATATAT others(1): Show |
20 | a0001c0001t0015a0001c0001t0030a0001c0001t0035others(17): Show | 25 | HG01070.hp2 HG01243.hp1 HG01243.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*3061_*3068dupTATA others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3068 | chr2 | 36846387 | |||||
| chr2:36846387
|
T | TTATATAT others(3): Show |
15 | a0001c0001t0036a0001c0001t0039a0001c0001t0045others(12): Show | 21 | HG00423.hp1 HG00438.hp2 HG00642.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3059_*3068dupTATA others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3068 | chr2 | 36846387 | |||||
| chr2:36846387
|
T | TTATATAT others(5): Show |
10 | a0001c0001t0005a0001c0001t0037a0001c0001t0048others(7): Show | 15 | HG00280.hp1 HG00621.hp1 HG02071.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3057_*3068dupTATA others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3068 | chr2 | 36846387 | |||||
| chr2:36846387
|
T | TTATATAT others(7): Show |
5 | a0001c0001t0143a0001c0001t0144a0001c0001t0189others(2): Show | 5 | HG01433.hp2 HG02135.hp2 HG03942.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3055_*3068dupTATA others(10): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3068 | chr2 | 36846387 | |||||
| chr2:36846387
|
T | TTATATAT others(9): Show |
1 | a0001c0001t0190 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3053_*3068dupTATA others(12): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3068 | chr2 | 36846387 | |||||
| chr2:36846387
|
T | TTATATAT others(11): Show |
3 | a0001c0001t0148a0001c0001t0191a0001c0001t0192 | 3 | HG00544.hp2 NA18954.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3051_*3068dupTATA others(14): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3068 | chr2 | 36846387 | |||||
| chr2:36846387
|
T | TTATATAT others(13): Show |
1 | a0001c0001t0145 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3049_*3068dupTATA others(16): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3068 | chr2 | 36846387 | |||||
| chr2:36846387
|
T | TTTTATAT others(1): Show |
2 | a0001c0001t0033a0001c0001t0131 | 3 | HG02572.hp1 HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3068_*3069insTATA others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3068 | chr2 | 36846387 | |||||
| chr2:36846387
|
TTA | T | 10 | a0001c0001t0007a0001c0001t0011a0001c0001t0017others(7): Show | 16 | HG01891.hp1 HG01891.hp2 HG02056.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3067_*3068delTA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3067 | chr2 | 36846387 | |||||
| chr2:36846387
|
TTATATA | T | 2 | a0001c0001t0020a0002c0002t0077 | 3 | HG02683.hp2 NA19043.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3063_*3068delTATA others(2): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3063 | chr2 | 36846387 | |||||
| chr2:36846387
|
TTATATAT others(1): Show |
T | 3 | a0001c0001t0027a0001c0001t0028a0001c0001t0064 | 5 | HG00423.hp2 HG00438.hp1 HG02155.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3061_*3068delTATA others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3061 | chr2 | 36846387 | |||||
| chr2:36846387
|
TTATATAT others(3): Show |
T | 6 | a0001c0001t0004a0001c0001t0019a0001c0001t0063others(3): Show | 10 | HG00544.hp1 HG01256.hp1 HG01993.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3059_*3068delTATA others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3059 | chr2 | 36846387 | |||||
| chr2:36846387
|
TTATATAT others(5): Show |
T | 8 | a0001c0001t0002a0001c0001t0051a0001c0001t0086others(5): Show | 19 | HG00280.hp2 HG00621.hp2 HG00639.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3057_*3068delTATA others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3057 | chr2 | 36846387 | |||||
| chr2:36846387
|
TTATATAT others(7): Show |
T | 29 | a0001c0001t0001a0001c0001t0009a0001c0001t0021others(26): Show | 66 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*3055_*3068delTATA others(10): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3055 | chr2 | 36846387 | |||||
| chr2:36846387
|
TTATATAT others(9): Show |
T | 5 | a0001c0001t0008a0001c0001t0040a0001c0001t0087others(2): Show | 8 | HG00735.hp1 HG01168.hp2 HG01361.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3053_*3068delTATA others(12): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3053 | chr2 | 36846387 | |||||
| chr2:36846387
|
TTATATAT others(13): Show |
T | 1 | a0001c0001t0018 | 2 | HG03490.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3049_*3068delTATA others(16): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3049 | chr2 | 36846387 | |||||
| chr2:36846387
|
TTATATAT others(17): Show |
T | 2 | a0001c0001t0116a0002c0002t0062 | 2 | HG00639.hp2 NA18986.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3045_*3068delTATA others(20): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3045 | chr2 | 36846387 | |||||
| chr2:36846430
|
G | A | 1 | a0001c0001t0193 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3026C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3026 | chr2 | 36846430 | |||||
| chr2:36846430
|
G | T | 3 | a0001c0001t0010a0001c0001t0079a0001c0001t0115 | 5 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3026C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3026 | chr2 | 36846430 | |||||
| chr2:36846432
|
T | A | 1 | a0001c0001t0193 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3024A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 3024 | chr2 | 36846432 | |||||
| chr2:36846519
|
CATT | C | 3 | a0001c0001t0146a0001c0001t0147a0001c0001t0148 | 3 | HG02970.hp1 HG02976.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2934_*2936delAAT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 2934 | chr2 | 36846519 | |||||
| chr2:36846666
|
T | C | 188 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(185): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
3_prime_UTR_variant | MODIFIER | c.*2790A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 2790 | chr2 | 36846666 | |||||
| chr2:36846698
|
A | C | 1 | a0001c0001t0086 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2758T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 2758 | chr2 | 36846698 | |||||
| chr2:36846749
|
T | A | 1 | a0001c0001t0029 | 2 | HG01361.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2707A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 2707 | chr2 | 36846749 | |||||
| chr2:36846965
|
C | T | 2 | a0001c0001t0030a0001c0001t0114 | 3 | HG01243.hp2 HG02615.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2491G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 2491 | chr2 | 36846965 | |||||
| chr2:36846980
|
T | C | 3 | a0001c0001t0074a0001c0001t0075a0001c0001t0076 | 3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2476A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 2476 | chr2 | 36846980 | |||||
| chr2:36847114
|
C | T | 1 | a0001c0001t0085 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2342G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 2342 | chr2 | 36847114 | |||||
| chr2:36847185
|
T | C | 1 | a0001c0001t0020 | 2 | NA19043.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2271A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 2271 | chr2 | 36847185 | |||||
| chr2:36847808
|
G | A | 151 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(148): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*1648C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 1648 | chr2 | 36847808 | |||||
| chr2:36847825
|
A | G | 1 | a0001c0001t0016 | 2 | HG02040.hp2 NA19006.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1631T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 1631 | chr2 | 36847825 | |||||
| chr2:36847870
|
T | A | 106 | a0001c0001t0003a0001c0001t0005a0001c0001t0010others(103): Show | 144 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*1586A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 1586 | chr2 | 36847870 | |||||
| chr2:36847978
|
T | C | 1 | a0002c0002t0077 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1478A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 1478 | chr2 | 36847978 | |||||
| chr2:36848254
|
T | G | 160 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(157): Show | 255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
3_prime_UTR_variant | MODIFIER | c.*1202A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 1202 | chr2 | 36848254 | |||||
| chr2:36848735
|
G | C | 1 | a0001c0001t0149 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*721C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 721 | chr2 | 36848735 | |||||
| chr2:36848798
|
A | G | 1 | a0001c0001t0054 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*658T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 658 | chr2 | 36848798 | |||||
| chr2:36849208
|
C | T | 1 | a0001c0001t0053 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*248G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 248 | chr2 | 36849208 | |||||
| chr2:36849331
|
T | C | 9 | a0001c0001t0038a0001c0001t0039a0001c0001t0150others(6): Show | 11 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*125A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 125 | chr2 | 36849331 | |||||
| chr2:36849344
|
C | G | 1 | a0001c0001t0157 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*112G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 112 | chr2 | 36849344 | |||||
| chr2:36849353
|
G | C | 1 | a0001c0001t0194 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*103C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 103 | chr2 | 36849353 | |||||
| chr2:36849355
|
A | C | 53 | a0001c0001t0003a0001c0001t0005a0001c0001t0013others(50): Show | 75 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*101T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 101 | chr2 | 36849355 | |||||
| chr2:36849430
|
C | G | 1 | a0001c0001t0052 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*26G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 26 | chr2 | 36849430 | |||||
| chr2:36849451
|
T | C | 58 | a0001c0001t0003a0001c0001t0005a0001c0001t0013others(55): Show | 82 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*5A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 18/18 | 5 | chr2 | 36849451 | |||||
| chr2:36966519
|
G | T | 1 | a0001c0001t0051 | 1 | HG00621.hp2 | 5_prime_UTR_variant | MODIFIER | c.-56C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/18 | 56 | chr2 | 36966519 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:36849872
|
C | A | 288 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(285): Show | 288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.2087-72G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 16/17 | chr2 | 36849872 | ||||||
| chr2:36849894
|
C | G | 4 | a0001c0001t0032g0067a0001c0001t0032g0071a0001c0001t0105g0100others(1): Show | 4 | HG00323.hp2 HG01168.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.2087-94G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 16/17 | chr2 | 36849894 | ||||||
| chr2:36849979
|
T | C | 1 | a0001c0001t0190g0063 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2087-179A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 16/17 | chr2 | 36849979 | ||||||
| chr2:36850033
|
G | A | 244 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(241): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.2087-233C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 16/17 | chr2 | 36850033 | ||||||
| chr2:36850272
|
T | C | 1 | a0001c0001t0005g0023 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2087-472A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 16/17 | chr2 | 36850272 | ||||||
| chr2:36850316
|
A | C | 24 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(21): Show | 24 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.2087-516T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 16/17 | chr2 | 36850316 | ||||||
| chr2:36850690
|
A | C | 1 | a0001c0001t0134g0041 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2086+310T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 16/17 | chr2 | 36850690 | ||||||
| chr2:36850867
|
G | C | 1 | a0001c0003t0071g0223 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2086+133C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 16/17 | chr2 | 36850867 | ||||||
| chr2:36850952
|
A | AT | 119 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(116): Show | 119 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.2086+47dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 16/17 | chr2 | 36850952 | ||||||
| chr2:36850952
|
A | ATT | 139 | a0001c0001t0001g0186a0001c0001t0002g0145a0001c0001t0003g0020others(136): Show | 139 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.2086+46_2086+47dup others(2): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 16/17 | chr2 | 36850952 | ||||||
| chr2:36851189
|
A | G | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1979-82T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36851189 | ||||||
| chr2:36851206
|
C | T | 1 | a0001c0001t0081g0233 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1979-99G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36851206 | ||||||
| chr2:36851211
|
G | A | 13 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.1979-104C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36851211 | ||||||
| chr2:36851245
|
G | A | 13 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.1979-138C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36851245 | ||||||
| chr2:36851446
|
G | A | 3 | a0001c0001t0146g0249a0001c0001t0147g0250a0001c0001t0148g0248 | 3 | HG02970.hp1 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1979-339C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36851446 | ||||||
| chr2:36851483
|
AAAAAAAG others(5): Show |
A | 17 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1979-388_1979-377d others(14): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36851483 | ||||||
| chr2:36851562
|
C | T | 247 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1979-455G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36851562 | ||||||
| chr2:36851592
|
G | A | 2 | a0001c0001t0082g0232a0001c0001t0084g0231 | 2 | HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1979-485C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36851592 | ||||||
| chr2:36851617
|
T | C | 1 | a0001c0001t0196g0298 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1979-510A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36851617 | ||||||
| chr2:36851651
|
C | T | 1 | a0001c0001t0194g0021 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1979-544G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36851651 | ||||||
| chr2:36851696
|
A | G | 139 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(136): Show | 139 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.1979-589T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36851696 | ||||||
| chr2:36851929
|
C | T | 1 | a0001c0001t0106g0128 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1979-822G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36851929 | ||||||
| chr2:36852053
|
T | A | 17 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1979-946A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36852053 | ||||||
| chr2:36852055
|
T | C | 255 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(252): Show | 255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1979-948A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36852055 | ||||||
| chr2:36852275
|
A | G | 12 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(9): Show | 12 | HG00438.hp2 HG00597.hp2 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.1979-1168T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36852275 | ||||||
| chr2:36852363
|
C | A | 1 | a0001c0001t0010g0292 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1979-1256G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36852363 | ||||||
| chr2:36852440
|
T | C | 140 | a0001c0001t0001g0163a0001c0001t0001g0200a0001c0001t0003g0020others(137): Show | 140 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1979-1333A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36852440 | ||||||
| chr2:36852517
|
G | A | 245 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.1979-1410C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36852517 | ||||||
| chr2:36852698
|
C | T | 1 | a0001c0001t0157g0050 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1979-1591G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36852698 | ||||||
| chr2:36852773
|
T | A | 1 | a0001c0001t0151g0205 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1979-1666A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36852773 | ||||||
| chr2:36852933
|
G | T | 1 | a0001c0001t0151g0205 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1979-1826C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36852933 | ||||||
| chr2:36852963
|
C | A | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1979-1856G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36852963 | ||||||
| chr2:36853019
|
T | C | 1 | a0001c0001t0021g0002 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1979-1912A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36853019 | ||||||
| chr2:36853101
|
A | G | 254 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1979-1994T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36853101 | ||||||
| chr2:36853112
|
G | A | 2 | a0001c0001t0019g0090a0001c0001t0019g0091 | 2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1979-2005C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36853112 | ||||||
| chr2:36853156
|
C | CA | 234 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.1979-2050dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36853156 | ||||||
| chr2:36853156
|
C | CAA | 7 | a0001c0001t0004g0141a0001c0001t0004g0178a0001c0001t0027g0125others(4): Show | 7 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(4): Show |
intron_variant | MODIFIER | c.1979-2051_1979-205 others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36853156 | ||||||
| chr2:36853195
|
T | A | 3 | a0001c0001t0146g0249a0001c0001t0147g0250a0001c0001t0148g0248 | 3 | HG02970.hp1 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1978+2017A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36853195 | ||||||
| chr2:36853201
|
G | A | 290 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1978+2011C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36853201 | ||||||
| chr2:36853547
|
A | T | 1 | a0001c0001t0120g0267 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1978+1665T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36853547 | ||||||
| chr2:36853556
|
A | T | 3 | a0001c0001t0074g0217a0001c0001t0075g0218a0001c0001t0076g0219 | 3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1978+1656T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36853556 | ||||||
| chr2:36853568
|
C | T | 1 | a0001c0001t0025g0151 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1978+1644G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36853568 | ||||||
| chr2:36853609
|
C | T | 1 | a0001c0001t0003g0020 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1978+1603G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36853609 | ||||||
| chr2:36854069
|
T | TA | 140 | a0001c0001t0001g0163a0001c0001t0001g0200a0001c0001t0003g0020others(137): Show | 140 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1978+1142dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36854069 | ||||||
| chr2:36854380
|
A | G | 7 | a0001c0001t0049g0296a0001c0001t0049g0299a0001c0001t0050g0295others(4): Show | 7 | HG01243.hp1 HG01496.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1978+832T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36854380 | ||||||
| chr2:36854506
|
G | A | 15 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(12): Show | 15 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.1978+706C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36854506 | ||||||
| chr2:36854674
|
T | C | 1 | a0001c0001t0002g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1978+538A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36854674 | ||||||
| chr2:36854700
|
A | T | 3 | a0001c0001t0074g0217a0001c0001t0075g0218a0001c0001t0076g0219 | 3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1978+512T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36854700 | ||||||
| chr2:36854820
|
A | G | 1 | a0001c0001t0054g0275 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1978+392T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36854820 | ||||||
| chr2:36854891
|
G | A | 238 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(235): Show | 238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.1978+321C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36854891 | ||||||
| chr2:36854904
|
T | C | 1 | a0001c0001t0105g0100 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1978+308A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36854904 | ||||||
| chr2:36855099
|
TAA | T | 15 | a0001c0001t0031g0042a0001c0001t0031g0045a0001c0001t0032g0067others(12): Show | 15 | HG00323.hp2 HG00741.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.1978+111_1978+112d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36855099 | ||||||
| chr2:36855136
|
A | C | 1 | a0001c0001t0023g0140 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1978+76T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 15/17 | chr2 | 36855136 | ||||||
| chr2:36855552
|
C | T | 249 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(246): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.1838-200G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36855552 | ||||||
| chr2:36855764
|
T | C | 3 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201 | 3 | HG01891.hp1 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1838-412A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36855764 | ||||||
| chr2:36855772
|
A | T | 2 | a0001c0001t0063g0203a0001c0001t0064g0202 | 2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1838-420T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36855772 | ||||||
| chr2:36855787
|
C | T | 1 | a0001c0001t0085g0192 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1838-435G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36855787 | ||||||
| chr2:36855909
|
T | G | 3 | a0001c0001t0032g0067a0001c0001t0032g0071a0001c0001t0138g0043 | 3 | HG00323.hp2 HG03239.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1838-557A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36855909 | ||||||
| chr2:36855987
|
A | AC | 3 | a0001c0001t0004g0141a0001c0001t0004g0178a0001c0001t0028g0177 | 3 | HG00544.hp1 HG02155.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1838-636_1838-635i others(3): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36855987 | ||||||
| chr2:36855988
|
A | C | 245 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.1838-636T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36855988 | ||||||
| chr2:36855999
|
G | C | 284 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(281): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.1838-647C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36855999 | ||||||
| chr2:36856163
|
T | C | 1 | a0001c0001t0157g0050 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1838-811A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36856163 | ||||||
| chr2:36856247
|
T | C | 1 | a0001c0001t0187g0049 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1838-895A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36856247 | ||||||
| chr2:36856546
|
C | T | 1 | a0001c0001t0090g0127 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1838-1194G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36856546 | ||||||
| chr2:36856820
|
T | C | 5 | a0001c0001t0010g0290a0001c0001t0010g0291a0001c0001t0010g0292others(2): Show | 5 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1837+1036A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36856820 | ||||||
| chr2:36856999
|
G | A | 1 | a0001c0001t0058g0251 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1837+857C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36856999 | ||||||
| chr2:36857087
|
C | CT | 14 | a0001c0001t0009g0147a0001c0001t0009g0189a0001c0001t0009g0190others(11): Show | 14 | HG00099.hp2 HG00323.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.1837+768dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36857087 | ||||||
| chr2:36857087
|
C | CTT | 11 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.1837+767_1837+768d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36857087 | ||||||
| chr2:36857116
|
C | T | 1 | a0001c0001t0157g0050 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1837+740G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36857116 | ||||||
| chr2:36857134
|
C | T | 3 | a0001c0001t0146g0249a0001c0001t0147g0250a0001c0001t0148g0248 | 3 | HG02970.hp1 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1837+722G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36857134 | ||||||
| chr2:36857163
|
G | A | 3 | a0001c0001t0074g0217a0001c0001t0075g0218a0001c0001t0076g0219 | 3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1837+693C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36857163 | ||||||
| chr2:36857226
|
T | C | 251 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.1837+630A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36857226 | ||||||
| chr2:36857294
|
T | G | 4 | a0001c0001t0001g0003a0001c0001t0002g0004a0001c0001t0021g0002others(1): Show | 4 | HG00408.hp1 HG00558.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.1837+562A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36857294 | ||||||
| chr2:36857574
|
T | C | 268 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(265): Show | 268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1837+282A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36857574 | ||||||
| chr2:36857651
|
C | A | 7 | a0001c0001t0002g0101a0001c0001t0002g0126a0001c0001t0002g0145others(4): Show | 7 | HG00558.hp1 HG00639.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.1837+205G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36857651 | ||||||
| chr2:36857655
|
G | A | 1 | a0001c0001t0105g0100 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1837+201C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36857655 | ||||||
| chr2:36857663
|
AAAAACAA others(3): Show |
A | 1 | a0001c0001t0096g0111 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1837+183_1837+192d others(12): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36857663 | ||||||
| chr2:36857663
|
AAAAACAA others(8): Show |
A | 6 | a0001c0001t0010g0290a0001c0001t0010g0291a0001c0001t0010g0292others(3): Show | 6 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1837+178_1837+192d others(17): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36857663 | ||||||
| chr2:36857738
|
G | A | 3 | a0001c0001t0008g0103a0001c0001t0028g0130a0001c0001t0136g0175 | 3 | HG02015.hp1 NA19007.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1837+118C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 14/17 | chr2 | 36857738 | ||||||
| chr2:36858148
|
C | T | 1 | a0001c0001t0168g0075 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1670-125G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36858148 | ||||||
| chr2:36858217
|
A | T | 5 | a0001c0001t0010g0290a0001c0001t0010g0291a0001c0001t0010g0292others(2): Show | 5 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1670-194T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36858217 | ||||||
| chr2:36858331
|
G | A | 284 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(281): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.1670-308C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36858331 | ||||||
| chr2:36858622
|
C | T | 1 | a0001c0001t0007g0201 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1670-599G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36858622 | ||||||
| chr2:36858692
|
T | A | 1 | a0001c0001t0112g0168 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1670-669A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36858692 | ||||||
| chr2:36858797
|
C | G | 17 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1670-774G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36858797 | ||||||
| chr2:36858851
|
C | A | 1 | a0001c0001t0076g0219 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1670-828G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36858851 | ||||||
| chr2:36858918
|
G | A | 290 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1670-895C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36858918 | ||||||
| chr2:36858953
|
T | G | 1 | a0001c0001t0068g0262 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1670-930A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36858953 | ||||||
| chr2:36859054
|
G | C | 97 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(94): Show | 97 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.1670-1031C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36859054 | ||||||
| chr2:36859088
|
T | G | 1 | a0001c0001t0008g0103 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1670-1065A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36859088 | ||||||
| chr2:36859197
|
C | T | 11 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.1670-1174G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36859197 | ||||||
| chr2:36859261
|
T | C | 3 | a0001c0001t0035g0268a0001c0001t0132g0258a0001c0001t0145g0276 | 3 | HG00735.hp2 HG01256.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1670-1238A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36859261 | ||||||
| chr2:36859277
|
A | G | 290 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1670-1254T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36859277 | ||||||
| chr2:36859337
|
A | G | 289 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(286): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1670-1314T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36859337 | ||||||
| chr2:36859473
|
A | G | 1 | a0001c0001t0003g0113 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1670-1450T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36859473 | ||||||
| chr2:36859762
|
C | T | 1 | a0002c0002t0062g0227 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1669+1370G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36859762 | ||||||
| chr2:36859794
|
A | C | 4 | a0001c0001t0034g0256a0001c0001t0034g0264a0001c0001t0052g0261others(1): Show | 4 | HG01106.hp1 HG03540.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1669+1338T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36859794 | ||||||
| chr2:36859887
|
T | A | 250 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.1669+1245A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36859887 | ||||||
| chr2:36860100
|
T | C | 1 | a0001c0001t0075g0218 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1669+1032A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36860100 | ||||||
| chr2:36860302
|
C | A | 1 | a0001c0001t0100g0193 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1669+830G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36860302 | ||||||
| chr2:36860310
|
G | C | 2 | a0001c0001t0063g0203a0001c0001t0064g0202 | 2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1669+822C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36860310 | ||||||
| chr2:36860447
|
C | G | 1 | a0001c0001t0118g0293 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1669+685G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36860447 | ||||||
| chr2:36860520
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1669+612G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36860520 | ||||||
| chr2:36860625
|
T | C | 1 | a0001c0001t0076g0219 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1669+507A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36860625 | ||||||
| chr2:36860690
|
T | A | 3 | a0001c0001t0146g0249a0001c0001t0147g0250a0001c0001t0148g0248 | 3 | HG02970.hp1 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1669+442A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36860690 | ||||||
| chr2:36860797
|
A | G | 289 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(286): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1669+335T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36860797 | ||||||
| chr2:36860940
|
C | T | 283 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(280): Show | 283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.1669+192G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36860940 | ||||||
| chr2:36860949
|
T | C | 1 | a0001c0001t0054g0275 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1669+183A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36860949 | ||||||
| chr2:36860973
|
T | G | 4 | a0001c0001t0002g0123a0001c0001t0002g0129a0001c0001t0002g0158others(1): Show | 4 | HG02055.hp2 HG02145.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1669+159A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36860973 | ||||||
| chr2:36860974
|
A | G | 1 | a0001c0001t0105g0100 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1669+158T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 13/17 | chr2 | 36860974 | ||||||
| chr2:36861332
|
T | G | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1548-79A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36861332 | ||||||
| chr2:36861486
|
C | T | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1548-233G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36861486 | ||||||
| chr2:36861490
|
A | G | 1 | a0001c0001t0076g0219 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1548-237T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36861490 | ||||||
| chr2:36861640
|
A | G | 1 | a0001c0001t0048g0195 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1548-387T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36861640 | ||||||
| chr2:36861728
|
T | C | 283 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(280): Show | 283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.1548-475A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36861728 | ||||||
| chr2:36861731
|
GCA | G | 3 | a0001c0001t0051g0001a0001c0001t0061g0252a0001c0001t0078g0253 | 3 | HG00621.hp2 HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1548-480_1548-479d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36861731 | ||||||
| chr2:36861731
|
GCACA | G | 23 | a0001c0001t0010g0290a0001c0001t0010g0291a0001c0001t0010g0292others(20): Show | 23 | HG00099.hp1 HG01070.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.1548-482_1548-479d others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36861731 | ||||||
| chr2:36861731
|
GCACACA | G | 236 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(233): Show | 236 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.1548-484_1548-479d others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36861731 | ||||||
| chr2:36861731
|
GCACACAC others(1): Show |
G | 3 | a0001c0001t0001g0163a0001c0001t0014g0094a0001c0001t0157g0050 | 3 | HG02280.hp1 HG03688.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1548-486_1548-479d others(10): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36861731 | ||||||
| chr2:36861731
|
GCACACAC others(5): Show |
G | 17 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1548-490_1548-479d others(14): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36861731 | ||||||
| chr2:36861731
|
GCACACAC others(7): Show |
G | 1 | a0001c0001t0151g0205 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1548-492_1548-479d others(16): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36861731 | ||||||
| chr2:36861931
|
T | C | 2 | a0001c0001t0019g0090a0001c0001t0019g0091 | 2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1548-678A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36861931 | ||||||
| chr2:36861964
|
C | G | 17 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1548-711G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36861964 | ||||||
| chr2:36862017
|
A | G | 260 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(257): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.1548-764T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862017 | ||||||
| chr2:36862085
|
G | T | 2 | a0001c0001t0019g0090a0001c0001t0019g0091 | 2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1548-832C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862085 | ||||||
| chr2:36862147
|
T | C | 3 | a0001c0001t0074g0217a0001c0001t0075g0218a0001c0001t0076g0219 | 3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1548-894A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862147 | ||||||
| chr2:36862167
|
A | C | 290 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1548-914T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862167 | ||||||
| chr2:36862182
|
G | C | 260 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(257): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.1548-929C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862182 | ||||||
| chr2:36862239
|
A | G | 11 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.1548-986T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862239 | ||||||
| chr2:36862298
|
G | C | 20 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(17): Show | 20 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1548-1045C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862298 | ||||||
| chr2:36862542
|
GTCT | G | 3 | a0001c0001t0034g0264a0001c0001t0052g0261a0001c0001t0137g0259 | 3 | HG01106.hp1 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1548-1292_1548-129 others(7): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862542 | ||||||
| chr2:36862560
|
T | G | 2 | a0001c0001t0063g0203a0001c0001t0064g0202 | 2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1548-1307A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862560 | ||||||
| chr2:36862667
|
C | T | 1 | a0001c0001t0031g0042 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1548-1414G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862667 | ||||||
| chr2:36862740
|
C | CT | 12 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(9): Show | 12 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1548-1488dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862740 | ||||||
| chr2:36862740
|
CT | C | 22 | a0001c0001t0012g0279a0001c0001t0016g0229a0001c0001t0016g0230others(19): Show | 22 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.1548-1488delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862740 | ||||||
| chr2:36862797
|
C | T | 1 | a0001c0001t0088g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1548-1544G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862797 | ||||||
| chr2:36862815
|
A | T | 3 | a0001c0001t0074g0217a0001c0001t0075g0218a0001c0001t0076g0219 | 3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1548-1562T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862815 | ||||||
| chr2:36862828
|
G | A | 256 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(253): Show | 256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.1548-1575C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862828 | ||||||
| chr2:36862885
|
A | G | 280 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(277): Show | 280 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.1548-1632T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862885 | ||||||
| chr2:36862937
|
G | A | 1 | a0001c0001t0027g0125 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1548-1684C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36862937 | ||||||
| chr2:36863090
|
T | C | 106 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(103): Show | 106 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.1548-1837A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36863090 | ||||||
| chr2:36863134
|
G | T | 277 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1548-1881C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36863134 | ||||||
| chr2:36863306
|
T | C | 1 | a0001c0001t0054g0275 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1548-2053A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36863306 | ||||||
| chr2:36863426
|
T | C | 3 | a0001c0001t0074g0217a0001c0001t0075g0218a0001c0001t0076g0219 | 3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1548-2173A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36863426 | ||||||
| chr2:36863472
|
G | C | 7 | a0001c0001t0001g0132a0001c0001t0001g0149a0001c0001t0001g0165others(4): Show | 7 | HG01346.hp2 HG02698.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.1548-2219C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36863472 | ||||||
| chr2:36863556
|
A | C | 290 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1548-2303T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36863556 | ||||||
| chr2:36863565
|
T | C | 1 | a0001c0001t0100g0193 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1548-2312A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36863565 | ||||||
| chr2:36863651
|
C | T | 285 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(282): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.1548-2398G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36863651 | ||||||
| chr2:36863754
|
G | A | 103 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(100): Show | 103 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1548-2501C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36863754 | ||||||
| chr2:36863833
|
G | C | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1548-2580C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36863833 | ||||||
| chr2:36863969
|
G | C | 255 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(252): Show | 255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1548-2716C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36863969 | ||||||
| chr2:36864066
|
T | C | 1 | a0001c0001t0053g0068 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1548-2813A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36864066 | ||||||
| chr2:36864121
|
C | T | 1 | a0001c0001t0005g0023 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1548-2868G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36864121 | ||||||
| chr2:36864163
|
G | C | 7 | a0001c0001t0005g0023a0001c0001t0005g0065a0001c0001t0014g0015others(4): Show | 7 | HG00621.hp1 HG00642.hp1 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.1548-2910C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36864163 | ||||||
| chr2:36864248
|
C | A | 1 | a0001c0001t0005g0023 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1548-2995G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36864248 | ||||||
| chr2:36864291
|
T | C | 7 | a0001c0001t0039g0214a0001c0001t0039g0215a0001c0001t0151g0205others(4): Show | 7 | HG02559.hp2 HG02886.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1548-3038A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36864291 | ||||||
| chr2:36864317
|
G | A | 256 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(253): Show | 256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.1548-3064C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36864317 | ||||||
| chr2:36864336
|
C | A | 12 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(9): Show | 12 | HG00438.hp2 HG00597.hp2 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.1548-3083G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36864336 | ||||||
| chr2:36864383
|
G | A | 4 | a0001c0001t0020g0238a0001c0001t0020g0239a0001c0001t0063g0203others(1): Show | 4 | HG02886.hp2 HG03579.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1548-3130C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36864383 | ||||||
| chr2:36864563
|
T | C | 3 | a0001c0001t0146g0249a0001c0001t0147g0250a0001c0001t0148g0248 | 3 | HG02970.hp1 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1547+3251A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36864563 | ||||||
| chr2:36864598
|
A | T | 2 | a0001c0001t0117g0269a0001c0001t0140g0257 | 2 | NA18943.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.1547+3216T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36864598 | ||||||
| chr2:36864807
|
G | C | 1 | a0001c0003t0071g0223 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1547+3007C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36864807 | ||||||
| chr2:36864822
|
C | T | 4 | a0001c0001t0049g0296a0001c0001t0049g0299a0001c0001t0196g0298others(1): Show | 4 | HG01243.hp1 HG01496.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1547+2992G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36864822 | ||||||
| chr2:36865042
|
T | C | 1 | a0001c0001t0157g0050 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1547+2772A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36865042 | ||||||
| chr2:36865073
|
C | T | 2 | a0001c0001t0019g0090a0001c0001t0019g0091 | 2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1547+2741G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36865073 | ||||||
| chr2:36865472
|
T | C | 1 | a0001c0001t0152g0211 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1547+2342A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36865472 | ||||||
| chr2:36865603
|
C | A | 2 | a0001c0001t0034g0264a0001c0001t0137g0259 | 2 | HG01106.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1547+2211G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36865603 | ||||||
| chr2:36865608
|
T | C | 13 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.1547+2206A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36865608 | ||||||
| chr2:36865680
|
G | C | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1547+2134C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36865680 | ||||||
| chr2:36865717
|
G | A | 1 | a0001c0001t0148g0248 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1547+2097C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36865717 | ||||||
| chr2:36865767
|
G | A | 1 | a0001c0003t0071g0223 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1547+2047C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36865767 | ||||||
| chr2:36865802
|
C | T | 1 | a0001c0001t0075g0218 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1547+2012G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36865802 | ||||||
| chr2:36865813
|
A | C | 1 | a0001c0001t0040g0034 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1547+2001T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36865813 | ||||||
| chr2:36865859
|
G | C | 2 | a0001c0001t0063g0203a0001c0001t0064g0202 | 2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1547+1955C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36865859 | ||||||
| chr2:36865954
|
A | G | 1 | a0001c0001t0064g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1547+1860T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36865954 | ||||||
| chr2:36865973
|
T | G | 2 | a0001c0001t0019g0090a0001c0001t0019g0091 | 2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1547+1841A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36865973 | ||||||
| chr2:36866106
|
G | A | 1 | a0001c0001t0120g0267 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1547+1708C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36866106 | ||||||
| chr2:36866115
|
C | G | 2 | a0001c0001t0063g0203a0001c0001t0064g0202 | 2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1547+1699G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36866115 | ||||||
| chr2:36866252
|
G | C | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1547+1562C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36866252 | ||||||
| chr2:36866384
|
C | G | 3 | a0001c0001t0074g0217a0001c0001t0075g0218a0001c0001t0076g0219 | 3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1547+1430G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36866384 | ||||||
| chr2:36866407
|
T | C | 5 | a0001c0001t0010g0290a0001c0001t0010g0291a0001c0001t0010g0292others(2): Show | 5 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1547+1407A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36866407 | ||||||
| chr2:36866520
|
T | C | 1 | a0001c0001t0050g0295 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1547+1294A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36866520 | ||||||
| chr2:36866544
|
C | T | 283 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(280): Show | 283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.1547+1270G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36866544 | ||||||
| chr2:36866581
|
C | T | 244 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(241): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1547+1233G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36866581 | ||||||
| chr2:36866831
|
A | C | 4 | a0001c0001t0079g0236a0001c0001t0080g0235a0001c0001t0081g0233others(1): Show | 4 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1547+983T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36866831 | ||||||
| chr2:36866851
|
C | G | 1 | a0001c0001t0054g0275 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1547+963G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36866851 | ||||||
| chr2:36866859
|
T | G | 1 | a0001c0001t0169g0011 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1547+955A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36866859 | ||||||
| chr2:36866875
|
G | C | 1 | a0001c0001t0041g0029 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1547+939C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36866875 | ||||||
| chr2:36866984
|
C | A | 1 | a0001c0001t0149g0247 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1547+830G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36866984 | ||||||
| chr2:36866985
|
C | A | 1 | a0001c0001t0149g0247 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1547+829G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36866985 | ||||||
| chr2:36866986
|
A | C | 1 | a0001c0001t0149g0247 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1547+828T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36866986 | ||||||
| chr2:36867103
|
T | C | 1 | a0001c0001t0149g0247 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1547+711A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36867103 | ||||||
| chr2:36867193
|
T | C | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1547+621A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36867193 | ||||||
| chr2:36867240
|
G | A | 4 | a0001c0001t0002g0123a0001c0001t0002g0129a0001c0001t0002g0158others(1): Show | 4 | HG02055.hp2 HG02145.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1547+574C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36867240 | ||||||
| chr2:36867248
|
T | C | 17 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1547+566A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36867248 | ||||||
| chr2:36867359
|
C | A | 17 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1547+455G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36867359 | ||||||
| chr2:36867410
|
C | T | 2 | a0001c0001t0034g0264a0001c0001t0137g0259 | 2 | HG01106.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1547+404G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36867410 | ||||||
| chr2:36867470
|
T | C | 1 | a0001c0001t0105g0100 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1547+344A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36867470 | ||||||
| chr2:36867496
|
G | A | 1 | a0001c0001t0068g0262 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1547+318C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36867496 | ||||||
| chr2:36867556
|
A | C | 4 | a0001c0001t0002g0123a0001c0001t0002g0129a0001c0001t0002g0158others(1): Show | 4 | HG02055.hp2 HG02145.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1547+258T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36867556 | ||||||
| chr2:36867609
|
T | C | 1 | a0001c0001t0118g0293 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1547+205A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36867609 | ||||||
| chr2:36867661
|
C | T | 17 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1547+153G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36867661 | ||||||
| chr2:36867686
|
A | T | 1 | a0001c0001t0101g0172 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1547+128T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36867686 | ||||||
| chr2:36867754
|
T | A | 1 | a0001c0001t0002g0101 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1547+60A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36867754 | ||||||
| chr2:36867754
|
T | C | 3 | a0001c0001t0074g0217a0001c0001t0075g0218a0001c0001t0076g0219 | 3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1547+60A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36867754 | ||||||
| chr2:36867802
|
A | G | 274 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(271): Show | 274 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.1547+12T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 12/17 | chr2 | 36867802 | ||||||
| chr2:36867870
|
G | C | 1 | a0001c0001t0149g0247 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1500-9C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36867870 | ||||||
| chr2:36867983
|
G | A | 1 | a0001c0001t0078g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1500-122C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36867983 | ||||||
| chr2:36867996
|
G | C | 140 | a0001c0001t0001g0124a0001c0001t0001g0134a0001c0001t0001g0143others(137): Show | 140 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1500-135C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36867996 | ||||||
| chr2:36868025
|
G | T | 2 | a0001c0001t0063g0203a0001c0001t0064g0202 | 2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1500-164C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36868025 | ||||||
| chr2:36868054
|
A | G | 1 | a0001c0001t0174g0014 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1500-193T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36868054 | ||||||
| chr2:36868055
|
T | C | 5 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201others(2): Show | 5 | HG01891.hp1 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1500-194A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36868055 | ||||||
| chr2:36868063
|
T | C | 17 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1500-202A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36868063 | ||||||
| chr2:36868246
|
A | G | 1 | a0001c0001t0008g0047 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1500-385T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36868246 | ||||||
| chr2:36868254
|
G | GA | 108 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(105): Show | 108 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.1500-394dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36868254 | ||||||
| chr2:36868341
|
T | C | 3 | a0001c0001t0146g0249a0001c0001t0147g0250a0001c0001t0148g0248 | 3 | HG02970.hp1 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1500-480A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36868341 | ||||||
| chr2:36868375
|
C | T | 1 | a0001c0001t0157g0050 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1500-514G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36868375 | ||||||
| chr2:36868651
|
C | T | 251 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.1500-790G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36868651 | ||||||
| chr2:36868708
|
T | A | 1 | a0001c0001t0089g0104 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1499+846A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36868708 | ||||||
| chr2:36868752
|
T | C | 17 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1499+802A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36868752 | ||||||
| chr2:36868804
|
C | A | 248 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.1499+750G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36868804 | ||||||
| chr2:36868869
|
G | T | 2 | a0001c0001t0019g0090a0001c0001t0019g0091 | 2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1499+685C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36868869 | ||||||
| chr2:36868872
|
C | CT | 27 | a0001c0001t0001g0174a0001c0001t0016g0229a0001c0001t0016g0230others(24): Show | 27 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.1499+681dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36868872 | ||||||
| chr2:36868935
|
G | A | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1499+619C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36868935 | ||||||
| chr2:36869029
|
T | G | 3 | a0001c0001t0074g0217a0001c0001t0075g0218a0001c0001t0076g0219 | 3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1499+525A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36869029 | ||||||
| chr2:36869062
|
T | C | 1 | a0001c0001t0013g0010 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1499+492A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36869062 | ||||||
| chr2:36869069
|
G | A | 1 | a0001c0001t0132g0258 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1499+485C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36869069 | ||||||
| chr2:36869115
|
C | A | 17 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1499+439G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36869115 | ||||||
| chr2:36869258
|
T | C | 17 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1499+296A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36869258 | ||||||
| chr2:36869369
|
C | G | 1 | a0001c0001t0157g0050 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1499+185G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36869369 | ||||||
| chr2:36869483
|
T | C | 2 | a0001c0001t0001g0137a0001c0001t0002g0171 | 2 | HG00280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1499+71A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 11/17 | chr2 | 36869483 | ||||||
| chr2:36869775
|
T | C | 1 | a0001c0001t0068g0262 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1324-46A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36869775 | ||||||
| chr2:36869827
|
C | T | 244 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(241): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1324-98G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36869827 | ||||||
| chr2:36869866
|
T | C | 135 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(132): Show | 135 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.1324-137A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36869866 | ||||||
| chr2:36869880
|
C | T | 1 | a0001c0001t0105g0100 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1324-151G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36869880 | ||||||
| chr2:36869941
|
A | G | 3 | a0001c0001t0074g0217a0001c0001t0075g0218a0001c0001t0076g0219 | 3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1324-212T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36869941 | ||||||
| chr2:36870028
|
T | G | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1324-299A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36870028 | ||||||
| chr2:36870238
|
C | T | 5 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201others(2): Show | 5 | HG01891.hp1 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1324-509G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36870238 | ||||||
| chr2:36870239
|
A | G | 289 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(286): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1324-510T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36870239 | ||||||
| chr2:36870252
|
AAC | A | 262 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(259): Show | 262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.1324-525_1324-524d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36870252 | ||||||
| chr2:36870296
|
G | GA | 19 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(16): Show | 19 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.1324-568dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36870296 | ||||||
| chr2:36870296
|
GA | G | 242 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1324-568delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36870296 | ||||||
| chr2:36870458
|
C | T | 1 | a0001c0001t0098g0150 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1324-729G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36870458 | ||||||
| chr2:36870502
|
A | T | 4 | a0001c0001t0001g0003a0001c0001t0002g0004a0001c0001t0021g0002others(1): Show | 4 | HG00408.hp1 HG00558.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324-773T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36870502 | ||||||
| chr2:36870667
|
T | G | 1 | a0001c0001t0035g0282 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1324-938A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36870667 | ||||||
| chr2:36870720
|
T | C | 2 | a0001c0001t0046g0062a0001c0001t0159g0032 | 2 | HG00741.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1324-991A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36870720 | ||||||
| chr2:36870810
|
G | T | 3 | a0001c0001t0074g0217a0001c0001t0075g0218a0001c0001t0076g0219 | 3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1324-1081C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36870810 | ||||||
| chr2:36870845
|
G | A | 1 | a0001c0001t0149g0247 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1324-1116C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36870845 | ||||||
| chr2:36870902
|
A | T | 15 | a0001c0001t0020g0238a0001c0001t0020g0239a0001c0001t0038g0212others(12): Show | 15 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.1324-1173T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36870902 | ||||||
| chr2:36871176
|
A | G | 1 | a0001c0001t0003g0030 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1324-1447T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36871176 | ||||||
| chr2:36871200
|
T | G | 1 | a0001c0001t0015g0056 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1324-1471A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36871200 | ||||||
| chr2:36871277
|
C | T | 1 | a0001c0001t0095g0112 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1324-1548G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36871277 | ||||||
| chr2:36871475
|
C | G | 289 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(286): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1324-1746G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36871475 | ||||||
| chr2:36871947
|
G | A | 1 | a0001c0001t0068g0262 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1324-2218C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36871947 | ||||||
| chr2:36871986
|
G | A | 1 | a0002c0002t0062g0227 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1324-2257C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36871986 | ||||||
| chr2:36872196
|
T | C | 107 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(104): Show | 107 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.1324-2467A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36872196 | ||||||
| chr2:36872327
|
C | T | 17 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1324-2598G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36872327 | ||||||
| chr2:36872368
|
C | T | 21 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(18): Show | 21 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1324-2639G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36872368 | ||||||
| chr2:36872491
|
C | T | 1 | a0001c0001t0159g0032 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1324-2762G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36872491 | ||||||
| chr2:36872743
|
T | C | 3 | a0001c0001t0074g0217a0001c0001t0075g0218a0001c0001t0076g0219 | 3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1324-3014A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36872743 | ||||||
| chr2:36872792
|
T | C | 6 | a0001c0001t0003g0033a0001c0001t0157g0050a0001c0001t0174g0014others(3): Show | 6 | HG00099.hp1 HG01070.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.1324-3063A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36872792 | ||||||
| chr2:36872915
|
G | A | 1 | a0001c0001t0086g0102 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1324-3186C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36872915 | ||||||
| chr2:36873003
|
T | G | 4 | a0001c0001t0079g0236a0001c0001t0080g0235a0001c0001t0081g0233others(1): Show | 4 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324-3274A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36873003 | ||||||
| chr2:36873055
|
G | A | 16 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(13): Show | 16 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.1324-3326C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36873055 | ||||||
| chr2:36873062
|
GGGCTCAG others(3): Show |
G | 244 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(241): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1324-3343_1324-333 others(14): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36873062 | ||||||
| chr2:36873240
|
C | T | 3 | a0001c0001t0074g0217a0001c0001t0075g0218a0001c0001t0076g0219 | 3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1324-3511G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36873240 | ||||||
| chr2:36873273
|
T | C | 1 | a0001c0001t0149g0247 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1324-3544A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36873273 | ||||||
| chr2:36873491
|
C | G | 17 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1324-3762G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36873491 | ||||||
| chr2:36873521
|
T | C | 1 | a0001c0001t0182g0053 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1324-3792A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36873521 | ||||||
| chr2:36873623
|
T | C | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1324-3894A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36873623 | ||||||
| chr2:36873673
|
G | A | 3 | a0001c0001t0013g0027a0001c0001t0059g0255a0001c0001t0060g0254 | 3 | HG01934.hp1 HG02451.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1324-3944C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36873673 | ||||||
| chr2:36873809
|
G | GGCATGTG others(19): Show |
1 | a0001c0001t0013g0010 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1323+4056_1323+408 others(30): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36873809 | ||||||
| chr2:36873836
|
G | A | 2 | a0001c0001t0001g0132a0001c0001t0001g0149 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1323+4055C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36873836 | ||||||
| chr2:36873855
|
A | G | 1 | a0001c0001t0037g0072 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1323+4036T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36873855 | ||||||
| chr2:36873892
|
G | A | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1323+3999C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36873892 | ||||||
| chr2:36873923
|
C | T | 1 | a0001c0001t0070g0225 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1323+3968G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36873923 | ||||||
| chr2:36873941
|
CA | C | 278 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(275): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.1323+3949delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36873941 | ||||||
| chr2:36874024
|
G | C | 2 | a0001c0001t0048g0195a0001c0001t0048g0196 | 2 | HG02071.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1323+3867C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874024 | ||||||
| chr2:36874047
|
A | C | 243 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1323+3844T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874047 | ||||||
| chr2:36874075
|
G | A | 1 | a0001c0001t0157g0050 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1323+3816C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874075 | ||||||
| chr2:36874181
|
G | A | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1323+3710C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874181 | ||||||
| chr2:36874221
|
G | A | 1 | a0001c0001t0068g0262 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1323+3670C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874221 | ||||||
| chr2:36874263
|
C | CA | 8 | a0001c0001t0010g0290a0001c0001t0010g0291a0001c0001t0010g0292others(5): Show | 8 | HG00735.hp2 HG01256.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1323+3627dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874263 | ||||||
| chr2:36874274
|
A | C | 5 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201others(2): Show | 5 | HG01891.hp1 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1323+3617T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874274 | ||||||
| chr2:36874317
|
C | A | 5 | a0001c0001t0014g0037a0001c0001t0043g0066a0001c0001t0171g0038others(2): Show | 5 | NA18945.hp2 NA18968.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.1323+3574G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874317 | ||||||
| chr2:36874574
|
A | G | 2 | a0001c0001t0048g0195a0001c0001t0048g0196 | 2 | HG02071.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1323+3317T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874574 | ||||||
| chr2:36874717
|
T | TA | 16 | a0001c0001t0001g0143a0001c0001t0007g0197a0001c0001t0007g0198others(13): Show | 16 | HG01891.hp1 HG01891.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.1323+3173dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874717 | ||||||
| chr2:36874717
|
TA | T | 41 | a0001c0001t0001g0076a0001c0001t0001g0106a0001c0001t0001g0114others(38): Show | 41 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.1323+3173delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874717 | ||||||
| chr2:36874728
|
A | C | 26 | a0001c0001t0011g0096a0001c0001t0011g0097a0001c0001t0011g0098others(23): Show | 26 | HG00639.hp2 HG00673.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.1323+3163T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874728 | ||||||
| chr2:36874730
|
A | AAAC | 20 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(17): Show | 20 | HG00438.hp2 HG00738.hp2 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.1323+3160_1323+316 others(7): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874730 | ||||||
| chr2:36874730
|
A | C | 1 | a0001c0001t0068g0262 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1323+3161T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874730 | ||||||
| chr2:36874731
|
A | C | 13 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.1323+3160T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874731 | ||||||
| chr2:36874732
|
A | C | 2 | a0001c0001t0042g0263a0001c0001t0133g0265 | 2 | HG02040.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1323+3159T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874732 | ||||||
| chr2:36874767
|
G | A | 2 | a0001c0001t0023g0139a0001c0001t0023g0140 | 2 | NA18961.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1323+3124C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874767 | ||||||
| chr2:36874774
|
C | T | 11 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.1323+3117G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874774 | ||||||
| chr2:36874835
|
T | TG | 4 | a0001c0001t0079g0236a0001c0001t0080g0235a0001c0001t0081g0233others(1): Show | 4 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1323+3055_1323+305 others(5): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874835 | ||||||
| chr2:36874889
|
G | T | 1 | a0001c0001t0157g0050 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1323+3002C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874889 | ||||||
| chr2:36874986
|
G | A | 268 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(265): Show | 268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1323+2905C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36874986 | ||||||
| chr2:36875106
|
A | G | 135 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(132): Show | 135 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.1323+2785T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875106 | ||||||
| chr2:36875121
|
A | G | 15 | a0001c0001t0020g0238a0001c0001t0020g0239a0001c0001t0038g0212others(12): Show | 15 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.1323+2770T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875121 | ||||||
| chr2:36875224
|
C | A | 1 | a0001c0001t0176g0064 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1323+2667G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875224 | ||||||
| chr2:36875477
|
T | C | 107 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(104): Show | 107 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.1323+2414A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875477 | ||||||
| chr2:36875505
|
C | CA | 8 | a0001c0001t0007g0197a0001c0001t0016g0230a0001c0001t0018g0222others(5): Show | 8 | HG02109.hp1 HG02723.hp2 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1323+2385dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875505 | ||||||
| chr2:36875505
|
CA | C | 207 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1323+2385delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875505 | ||||||
| chr2:36875532
|
T | C | 20 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(17): Show | 20 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1323+2359A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875532 | ||||||
| chr2:36875572
|
C | T | 248 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.1323+2319G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875572 | ||||||
| chr2:36875573
|
CA | C | 289 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(286): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1323+2317delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875573 | ||||||
| chr2:36875659
|
A | AT | 290 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1323+2231dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875659 | ||||||
| chr2:36875711
|
C | T | 5 | a0001c0001t0010g0290a0001c0001t0010g0291a0001c0001t0010g0292others(2): Show | 5 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1323+2180G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875711 | ||||||
| chr2:36875726
|
G | A | 3 | a0001c0001t0003g0020a0001c0001t0003g0057a0004c0004t0188g0048 | 3 | HG00408.hp2 HG02135.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1323+2165C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875726 | ||||||
| chr2:36875729
|
T | C | 1 | a0003c0006t0128g0271 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1323+2162A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875729 | ||||||
| chr2:36875807
|
C | A | 1 | a0001c0001t0070g0225 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1323+2084G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875807 | ||||||
| chr2:36875813
|
T | A | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1323+2078A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875813 | ||||||
| chr2:36875920
|
G | A | 17 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1323+1971C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875920 | ||||||
| chr2:36875964
|
AT | A | 20 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(17): Show | 20 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1323+1926delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875964 | ||||||
| chr2:36875972
|
T | A | 7 | a0001c0001t0049g0296a0001c0001t0049g0299a0001c0001t0050g0295others(4): Show | 7 | HG01243.hp1 HG01496.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1323+1919A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875972 | ||||||
| chr2:36875996
|
G | A | 1 | a0001c0001t0093g0121 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1323+1895C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36875996 | ||||||
| chr2:36876063
|
G | C | 1 | a0003c0006t0128g0271 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1323+1828C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876063 | ||||||
| chr2:36876090
|
G | A | 1 | a0001c0001t0002g0126 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1323+1801C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876090 | ||||||
| chr2:36876144
|
C | G | 1 | a0003c0006t0128g0271 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1323+1747G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876144 | ||||||
| chr2:36876175
|
T | TGGGAGGA others(17): Show |
2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1323+1692_1323+171 others(28): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876175 | ||||||
| chr2:36876218
|
C | T | 10 | a0001c0001t0002g0101a0001c0001t0002g0126a0001c0001t0002g0145others(7): Show | 10 | HG00558.hp1 HG00639.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.1323+1673G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876218 | ||||||
| chr2:36876270
|
TA | T | 281 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(278): Show | 281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.1323+1620delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876270 | ||||||
| chr2:36876285
|
A | T | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1323+1606T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876285 | ||||||
| chr2:36876364
|
T | G | 4 | a0001c0001t0002g0123a0001c0001t0002g0129a0001c0001t0002g0158others(1): Show | 4 | HG02055.hp2 HG02145.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1323+1527A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876364 | ||||||
| chr2:36876433
|
T | C | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1323+1458A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876433 | ||||||
| chr2:36876547
|
G | A | 249 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(246): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.1323+1344C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876547 | ||||||
| chr2:36876652
|
G | C | 3 | a0001c0001t0074g0217a0001c0001t0075g0218a0001c0001t0076g0219 | 3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1323+1239C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876652 | ||||||
| chr2:36876751
|
AT | A | 248 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.1323+1139delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876751 | ||||||
| chr2:36876770
|
C | T | 2 | a0001c0001t0122g0044a0001c0001t0126g0040 | 2 | HG00741.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1323+1121G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876770 | ||||||
| chr2:36876876
|
T | C | 17 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1323+1015A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876876 | ||||||
| chr2:36876893
|
G | A | 5 | a0001c0001t0010g0290a0001c0001t0010g0291a0001c0001t0010g0292others(2): Show | 5 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1323+998C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876893 | ||||||
| chr2:36876937
|
A | G | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1323+954T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876937 | ||||||
| chr2:36876969
|
C | T | 1 | a0001c0001t0011g0096 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1323+922G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876969 | ||||||
| chr2:36876995
|
G | A | 2 | a0001c0001t0063g0203a0001c0001t0064g0202 | 2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1323+896C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36876995 | ||||||
| chr2:36877265
|
C | T | 289 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(286): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1323+626G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36877265 | ||||||
| chr2:36877354
|
C | T | 4 | a0001c0001t0079g0236a0001c0001t0080g0235a0001c0001t0081g0233others(1): Show | 4 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1323+537G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36877354 | ||||||
| chr2:36877372
|
C | A | 264 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.1323+519G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36877372 | ||||||
| chr2:36877579
|
A | C | 1 | a0001c0001t0054g0275 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1323+312T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36877579 | ||||||
| chr2:36877660
|
CT | C | 14 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201others(11): Show | 14 | HG01891.hp1 HG02109.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1323+230delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36877660 | ||||||
| chr2:36877666
|
G | C | 1 | a0001c0001t0008g0103 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1323+225C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36877666 | ||||||
| chr2:36877667
|
C | A | 5 | a0001c0001t0010g0290a0001c0001t0010g0291a0001c0001t0010g0292others(2): Show | 5 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1323+224G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36877667 | ||||||
| chr2:36877698
|
G | T | 1 | a0001c0001t0001g0173 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1323+193C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36877698 | ||||||
| chr2:36877787
|
C | T | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1323+104G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 10/17 | chr2 | 36877787 | ||||||
| chr2:36878035
|
G | A | 24 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(21): Show | 24 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(21): Show |
splice_region_variant&intron_variant | LOW | c.1187-8C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36878035 | ||||||
| chr2:36878119
|
G | A | 1 | a0001c0001t0008g0119 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1187-92C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36878119 | ||||||
| chr2:36878185
|
T | C | 4 | a0001c0001t0079g0236a0001c0001t0080g0235a0001c0001t0081g0233others(1): Show | 4 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1187-158A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36878185 | ||||||
| chr2:36878632
|
C | T | 8 | a0001c0001t0003g0020a0001c0001t0039g0214a0001c0001t0039g0215others(5): Show | 8 | HG02559.hp2 HG02886.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1187-605G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36878632 | ||||||
| chr2:36878858
|
T | C | 2 | a0001c0001t0049g0299a0001c0001t0196g0298 | 2 | HG01243.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1187-831A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36878858 | ||||||
| chr2:36878865
|
G | A | 1 | a0001c0001t0193g0055 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1187-838C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36878865 | ||||||
| chr2:36878973
|
G | C | 1 | a0001c0001t0028g0177 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1187-946C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36878973 | ||||||
| chr2:36879184
|
C | T | 4 | a0001c0001t0001g0003a0001c0001t0002g0004a0001c0001t0021g0002others(1): Show | 4 | HG00408.hp1 HG00558.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.1187-1157G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36879184 | ||||||
| chr2:36879268
|
C | T | 1 | a0004c0004t0188g0048 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1187-1241G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36879268 | ||||||
| chr2:36879285
|
A | G | 289 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(286): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1187-1258T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36879285 | ||||||
| chr2:36879315
|
C | A | 244 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(241): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1187-1288G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36879315 | ||||||
| chr2:36879417
|
C | CTG | 4 | a0001c0001t0079g0236a0001c0001t0080g0235a0001c0001t0081g0233others(1): Show | 4 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1187-1392_1187-139 others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36879417 | ||||||
| chr2:36879487
|
T | A | 1 | a0001c0001t0002g0171 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1187-1460A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36879487 | ||||||
| chr2:36879510
|
C | T | 2 | a0001c0001t0001g0132a0001c0001t0001g0149 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1187-1483G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36879510 | ||||||
| chr2:36879839
|
G | C | 7 | a0001c0001t0039g0214a0001c0001t0039g0215a0001c0001t0151g0205others(4): Show | 7 | HG02559.hp2 HG02886.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1187-1812C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36879839 | ||||||
| chr2:36879931
|
A | G | 2 | a0001c0001t0174g0014a0001c0001t0180g0031 | 2 | HG01070.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1187-1904T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36879931 | ||||||
| chr2:36879941
|
G | A | 1 | a0001c0001t0190g0063 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1187-1914C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36879941 | ||||||
| chr2:36880151
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1187-2124G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36880151 | ||||||
| chr2:36880205
|
C | T | 1 | a0001c0001t0186g0035 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1187-2178G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36880205 | ||||||
| chr2:36880831
|
T | C | 1 | a0001c0001t0044g0058 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1187-2804A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36880831 | ||||||
| chr2:36880856
|
T | C | 1 | a0001c0001t0016g0229 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1187-2829A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36880856 | ||||||
| chr2:36880957
|
T | C | 1 | a0001c0001t0079g0236 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1187-2930A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36880957 | ||||||
| chr2:36881068
|
A | AAAAAC | 20 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(17): Show | 20 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1186+2859_1186+286 others(9): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881068 | ||||||
| chr2:36881118
|
CT | C | 36 | a0001c0001t0001g0076a0001c0001t0001g0174a0001c0001t0002g0101others(33): Show | 36 | HG00423.hp2 HG00438.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1186+2813delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881118 | ||||||
| chr2:36881118
|
CTT | C | 194 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0099others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1186+2812_1186+281 others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881118 | ||||||
| chr2:36881118
|
CTTT | C | 29 | a0001c0001t0001g0132a0001c0001t0003g0030a0001c0001t0005g0087others(26): Show | 29 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.1186+2811_1186+281 others(7): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881118 | ||||||
| chr2:36881118
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1186+2804_1186+281 others(14): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881118 | ||||||
| chr2:36881265
|
C | A | 1 | a0001c0001t0187g0049 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1186+2667G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881265 | ||||||
| chr2:36881328
|
A | C | 1 | a0001c0001t0095g0112 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1186+2604T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881328 | ||||||
| chr2:36881331
|
T | C | 1 | a0001c0001t0002g0145 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1186+2601A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881331 | ||||||
| chr2:36881332
|
T | G | 1 | a0001c0001t0054g0275 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1186+2600A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881332 | ||||||
| chr2:36881347
|
T | C | 2 | a0001c0001t0001g0132a0001c0001t0001g0149 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1186+2585A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881347 | ||||||
| chr2:36881348
|
G | C | 1 | a0001c0001t0176g0064 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1186+2584C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881348 | ||||||
| chr2:36881399
|
A | G | 1 | a0001c0001t0068g0262 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1186+2533T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881399 | ||||||
| chr2:36881436
|
C | A | 1 | a0001c0001t0001g0174 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1186+2496G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881436 | ||||||
| chr2:36881494
|
T | C | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1186+2438A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881494 | ||||||
| chr2:36881530
|
A | G | 1 | a0001c0001t0058g0251 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1186+2402T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881530 | ||||||
| chr2:36881750
|
G | A | 3 | a0001c0001t0074g0217a0001c0001t0075g0218a0001c0001t0076g0219 | 3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1186+2182C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881750 | ||||||
| chr2:36881854
|
T | C | 1 | a0001c0001t0029g0155 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1186+2078A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881854 | ||||||
| chr2:36881937
|
T | C | 3 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201 | 3 | HG01891.hp1 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1186+1995A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36881937 | ||||||
| chr2:36882120
|
T | A | 2 | a0001c0001t0048g0195a0001c0001t0048g0196 | 2 | HG02071.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1186+1812A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36882120 | ||||||
| chr2:36882138
|
G | T | 284 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(281): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.1186+1794C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36882138 | ||||||
| chr2:36882199
|
GA | G | 4 | a0001c0001t0002g0123a0001c0001t0002g0129a0001c0001t0002g0158others(1): Show | 4 | HG02055.hp2 HG02145.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1186+1732delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36882199 | ||||||
| chr2:36882206
|
A | C | 1 | a0001c0001t0001g0174 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1186+1726T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36882206 | ||||||
| chr2:36882281
|
T | C | 17 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1186+1651A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36882281 | ||||||
| chr2:36882307
|
A | G | 5 | a0001c0001t0010g0290a0001c0001t0010g0291a0001c0001t0010g0292others(2): Show | 5 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1186+1625T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36882307 | ||||||
| chr2:36882385
|
G | A | 5 | a0001c0001t0010g0290a0001c0001t0010g0291a0001c0001t0010g0292others(2): Show | 5 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1186+1547C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36882385 | ||||||
| chr2:36882571
|
A | G | 3 | a0001c0001t0035g0268a0001c0001t0132g0258a0001c0001t0145g0276 | 3 | HG00735.hp2 HG01256.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1186+1361T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36882571 | ||||||
| chr2:36882601
|
T | C | 254 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1186+1331A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36882601 | ||||||
| chr2:36882696
|
G | C | 1 | a0001c0001t0149g0247 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1186+1236C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36882696 | ||||||
| chr2:36883300
|
CA | C | 20 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(17): Show | 20 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1186+631delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36883300 | ||||||
| chr2:36883323
|
G | A | 1 | a0001c0001t0129g0273 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1186+609C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36883323 | ||||||
| chr2:36883379
|
C | A | 1 | a0001c0001t0096g0111 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1186+553G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36883379 | ||||||
| chr2:36883541
|
G | C | 1 | a0001c0001t0117g0269 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1186+391C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36883541 | ||||||
| chr2:36883603
|
A | C | 2 | a0001c0001t0063g0203a0001c0001t0064g0202 | 2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1186+329T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36883603 | ||||||
| chr2:36883631
|
A | G | 1 | a0001c0001t0085g0192 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1186+301T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36883631 | ||||||
| chr2:36883778
|
C | T | 2 | a0001c0001t0168g0075a0001c0001t0172g0074 | 2 | NA19006.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1186+154G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36883778 | ||||||
| chr2:36883902
|
T | A | 99 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(96): Show | 99 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1186+30A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 9/17 | chr2 | 36883902 | ||||||
| chr2:36884111
|
A | G | 1 | a0001c0001t0142g0266 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1043-36T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36884111 | ||||||
| chr2:36884205
|
T | G | 1 | a0001c0001t0149g0247 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1043-130A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36884205 | ||||||
| chr2:36884266
|
T | C | 1 | a0001c0001t0149g0247 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1043-191A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36884266 | ||||||
| chr2:36884289
|
G | T | 1 | a0001c0001t0085g0192 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1043-214C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36884289 | ||||||
| chr2:36884314
|
A | G | 1 | a0001c0001t0149g0247 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1043-239T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36884314 | ||||||
| chr2:36884479
|
T | C | 1 | a0001c0001t0176g0064 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1043-404A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36884479 | ||||||
| chr2:36884741
|
T | C | 6 | a0001c0001t0010g0290a0001c0001t0010g0291a0001c0001t0010g0292others(3): Show | 6 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1043-666A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36884741 | ||||||
| chr2:36884823
|
T | C | 16 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201others(13): Show | 16 | HG01891.hp1 HG02109.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1043-748A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36884823 | ||||||
| chr2:36884837
|
T | A | 1 | a0002c0002t0062g0227 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1043-762A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36884837 | ||||||
| chr2:36884867
|
A | T | 2 | a0001c0001t0042g0263a0001c0001t0133g0265 | 2 | HG02040.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1043-792T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36884867 | ||||||
| chr2:36884920
|
T | C | 2 | a0001c0001t0011g0097a0001c0001t0011g0098 | 2 | NA18972.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1043-845A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36884920 | ||||||
| chr2:36885215
|
C | T | 244 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(241): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1043-1140G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36885215 | ||||||
| chr2:36885636
|
G | T | 2 | a0001c0001t0063g0203a0001c0001t0064g0202 | 2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1042+1080C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36885636 | ||||||
| chr2:36885640
|
G | A | 4 | a0001c0001t0004g0141a0001c0001t0004g0178a0001c0001t0028g0177others(1): Show | 4 | HG00544.hp1 HG02155.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.1042+1076C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36885640 | ||||||
| chr2:36885656
|
T | C | 2 | a0001c0001t0061g0252a0001c0001t0078g0253 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1042+1060A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36885656 | ||||||
| chr2:36885666
|
G | C | 2 | a0001c0001t0082g0232a0001c0001t0084g0231 | 2 | HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1042+1050C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36885666 | ||||||
| chr2:36885676
|
C | T | 1 | a0001c0001t0043g0024 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1042+1040G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36885676 | ||||||
| chr2:36885779
|
C | T | 1 | a0001c0001t0164g0019 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1042+937G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36885779 | ||||||
| chr2:36885817
|
T | G | 4 | a0001c0001t0011g0096a0001c0001t0011g0097a0001c0001t0011g0098others(1): Show | 4 | HG02071.hp2 HG02965.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.1042+899A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36885817 | ||||||
| chr2:36886013
|
T | C | 1 | a0001c0001t0096g0111 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1042+703A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36886013 | ||||||
| chr2:36886132
|
C | T | 4 | a0001c0001t0079g0236a0001c0001t0080g0235a0001c0001t0081g0233others(1): Show | 4 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1042+584G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36886132 | ||||||
| chr2:36886233
|
T | C | 1 | a0001c0001t0055g0243 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1042+483A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36886233 | ||||||
| chr2:36886271
|
T | C | 1 | a0001c0001t0004g0181 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1042+445A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36886271 | ||||||
| chr2:36886314
|
T | C | 1 | a0001c0001t0041g0018 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1042+402A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36886314 | ||||||
| chr2:36886478
|
GATTT | G | 6 | a0001c0001t0001g0077a0001c0001t0001g0183a0001c0001t0001g0184others(3): Show | 6 | NA18940.hp2 NA18955.hp1 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.1042+234_1042+237d others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 8/17 | chr2 | 36886478 | ||||||
| chr2:36887040
|
A | AAGAC | 5 | a0001c0001t0018g0222a0001c0001t0018g0228a0001c0001t0065g0224others(2): Show | 5 | HG02083.hp2 HG03490.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.932-218_932-215dup others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887040 | ||||||
| chr2:36887042
|
G | GAC | 3 | a0001c0001t0056g0241a0001c0001t0058g0251a0001c0001t0078g0253 | 3 | HG02630.hp1 HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.932-218_932-217dup others(2): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887042 | ||||||
| chr2:36887042
|
G | GACAGAC | 3 | a0001c0001t0016g0229a0001c0001t0073g0210a0002c0002t0077g0226 | 3 | HG02040.hp2 HG02683.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.932-217_932-216ins others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887042 | ||||||
| chr2:36887042
|
GACAC | G | 3 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201 | 3 | HG01891.hp1 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.932-220_932-217del others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887042 | ||||||
| chr2:36887042
|
GACACAC | G | 3 | a0001c0001t0067g0092a0001c0001t0069g0093a0001c0001t0082g0232 | 3 | HG01884.hp2 HG02723.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.932-222_932-217del others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887042 | ||||||
| chr2:36887042
|
GACACACA others(1): Show |
G | 3 | a0001c0001t0084g0231a0001c0001t0085g0192a0001c0001t0107g0148 | 3 | NA18906.hp1 NA18963.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.932-224_932-217del others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887042 | ||||||
| chr2:36887042
|
GACACACA others(3): Show |
G | 22 | a0001c0001t0001g0163a0001c0001t0001g0174a0001c0001t0002g0101others(19): Show | 22 | HG00423.hp2 HG00438.hp1 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.932-226_932-217del others(10): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887042 | ||||||
| chr2:36887042
|
GACACACA others(5): Show |
G | 220 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.932-228_932-217del others(12): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887042 | ||||||
| chr2:36887042
|
GACACACA others(7): Show |
G | 1 | a0003c0006t0128g0271 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.932-230_932-217del others(14): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887042 | ||||||
| chr2:36887044
|
C | CAG | 6 | a0001c0001t0019g0090a0001c0001t0019g0091a0001c0001t0068g0262others(3): Show | 6 | HG00438.hp2 HG01106.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.932-219_932-218ins others(2): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887044 | ||||||
| chr2:36887046
|
C | G | 6 | a0001c0001t0074g0217a0001c0001t0076g0219a0001c0001t0079g0236others(3): Show | 6 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.932-220G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887046 | ||||||
| chr2:36887052
|
C | G | 2 | a0001c0001t0067g0092a0001c0001t0069g0093 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.932-226G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887052 | ||||||
| chr2:36887084
|
C | CACAT | 4 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0064g0202others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-259_932-258ins others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887084 | ||||||
| chr2:36887084
|
C | T | 7 | a0001c0001t0020g0238a0001c0001t0020g0239a0001c0001t0039g0214others(4): Show | 7 | HG02886.hp1 HG02895.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.932-258G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887084 | ||||||
| chr2:36887086
|
C | T | 3 | a0001c0001t0146g0249a0001c0001t0147g0250a0001c0001t0148g0248 | 3 | HG02970.hp1 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.932-260G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887086 | ||||||
| chr2:36887266
|
A | AAAAT | 118 | a0001c0001t0001g0003a0001c0001t0001g0099a0001c0001t0001g0107others(115): Show | 118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.932-444_932-441dup others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887266 | ||||||
| chr2:36887266
|
A | AAAATAAA others(1): Show |
27 | a0001c0001t0001g0106a0001c0001t0001g0131a0001c0001t0001g0173others(24): Show | 27 | HG00280.hp1 HG01168.hp2 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.932-448_932-441dup others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887266 | ||||||
| chr2:36887266
|
A | AAAATAAA others(5): Show |
1 | a0001c0001t0026g0120 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.932-452_932-441dup others(12): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887266 | ||||||
| chr2:36887266
|
AAAAT | A | 25 | a0001c0001t0001g0156a0001c0001t0016g0229a0001c0001t0016g0230others(22): Show | 25 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.932-444_932-441del others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887266 | ||||||
| chr2:36887266
|
AAAATAAA others(1): Show |
A | 3 | a0001c0001t0040g0034a0001c0001t0174g0014a0001c0001t0180g0031 | 3 | HG01070.hp2 HG01261.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.932-448_932-441del others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887266 | ||||||
| chr2:36887266
|
AAAATAAA others(5): Show |
A | 4 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0150g0208others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-452_932-441del others(12): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887266 | ||||||
| chr2:36887316
|
C | T | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.932-490G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887316 | ||||||
| chr2:36887326
|
C | T | 2 | a0001c0001t0035g0268a0001c0001t0145g0276 | 2 | HG01256.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.932-500G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887326 | ||||||
| chr2:36887367
|
G | A | 244 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(241): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.932-541C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887367 | ||||||
| chr2:36887431
|
T | C | 15 | a0001c0001t0020g0238a0001c0001t0020g0239a0001c0001t0038g0212others(12): Show | 15 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.932-605A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887431 | ||||||
| chr2:36887487
|
C | CA | 3 | a0001c0001t0011g0096a0001c0001t0011g0097a0001c0001t0011g0098 | 3 | HG02071.hp2 NA18972.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.932-662dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887487 | ||||||
| chr2:36887671
|
G | C | 4 | a0001c0001t0034g0256a0001c0001t0034g0264a0001c0001t0052g0261others(1): Show | 4 | HG01106.hp1 HG03540.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-845C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887671 | ||||||
| chr2:36887703
|
T | A | 1 | a0001c0001t0024g0153 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.932-877A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887703 | ||||||
| chr2:36887832
|
A | G | 250 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.932-1006T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36887832 | ||||||
| chr2:36888093
|
C | A | 1 | a0001c0001t0078g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.932-1267G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36888093 | ||||||
| chr2:36888253
|
T | A | 289 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(286): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.932-1427A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36888253 | ||||||
| chr2:36888321
|
T | C | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.932-1495A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36888321 | ||||||
| chr2:36888639
|
A | ATG | 55 | a0001c0001t0003g0020a0001c0001t0003g0030a0001c0001t0003g0033others(52): Show | 55 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.932-1815_932-1814d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36888639 | ||||||
| chr2:36888639
|
A | ATGTG | 24 | a0001c0001t0005g0023a0001c0001t0005g0065a0001c0001t0012g0022others(21): Show | 24 | HG00323.hp2 HG00621.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.932-1817_932-1814d others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36888639 | ||||||
| chr2:36888639
|
A | ATGTGTG | 37 | a0001c0001t0008g0047a0001c0001t0011g0096a0001c0001t0011g0097others(34): Show | 37 | HG00597.hp1 HG00639.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.932-1819_932-1814d others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36888639 | ||||||
| chr2:36888639
|
A | ATGTGTGT others(1): Show |
16 | a0001c0001t0012g0279a0001c0001t0012g0280a0001c0001t0030g0237others(13): Show | 16 | HG01243.hp2 HG01433.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.932-1821_932-1814d others(10): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36888639 | ||||||
| chr2:36888639
|
A | ATGTGTGT others(3): Show |
9 | a0001c0001t0035g0268a0001c0001t0042g0263a0001c0001t0044g0012others(6): Show | 9 | HG00673.hp2 HG01256.hp2 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.932-1823_932-1814d others(12): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36888639 | ||||||
| chr2:36888639
|
A | ATGTGTGT others(5): Show |
1 | a0001c0001t0048g0195 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.932-1825_932-1814d others(14): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36888639 | ||||||
| chr2:36888639
|
A | ATGTGTGT others(7): Show |
1 | a0001c0001t0048g0196 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.932-1827_932-1814d others(16): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36888639 | ||||||
| chr2:36888639
|
A | G | 2 | a0001c0001t0189g0054a0001c0001t0193g0055 | 2 | HG00099.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.932-1813T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36888639 | ||||||
| chr2:36888639
|
ATG | A | 23 | a0001c0001t0001g0118a0001c0001t0001g0163a0001c0001t0016g0229others(20): Show | 23 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.932-1815_932-1814d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36888639 | ||||||
| chr2:36888639
|
ATGTG | A | 93 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(90): Show | 93 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.932-1817_932-1814d others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36888639 | ||||||
| chr2:36888639
|
ATGTGTG | A | 15 | a0001c0001t0001g0106a0001c0001t0001g0114a0001c0001t0001g0124others(12): Show | 15 | HG00621.hp2 HG01934.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.932-1819_932-1814d others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36888639 | ||||||
| chr2:36888639
|
ATGTGTGT others(3): Show |
A | 3 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201 | 3 | HG01891.hp1 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.932-1823_932-1814d others(12): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36888639 | ||||||
| chr2:36888949
|
G | A | 4 | a0001c0001t0002g0123a0001c0001t0002g0129a0001c0001t0002g0158others(1): Show | 4 | HG02055.hp2 HG02145.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-2123C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36888949 | ||||||
| chr2:36889270
|
G | A | 248 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.932-2444C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36889270 | ||||||
| chr2:36889419
|
A | T | 1 | a0001c0001t0001g0131 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.932-2593T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36889419 | ||||||
| chr2:36889460
|
G | T | 11 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.932-2634C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36889460 | ||||||
| chr2:36889468
|
A | AG | 248 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.932-2643_932-2642i others(3): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36889468 | ||||||
| chr2:36889554
|
G | C | 1 | a0001c0001t0032g0067 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.932-2728C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36889554 | ||||||
| chr2:36889619
|
G | T | 236 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(233): Show | 236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.932-2793C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36889619 | ||||||
| chr2:36889625
|
G | A | 1 | a0001c0001t0117g0269 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.932-2799C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36889625 | ||||||
| chr2:36889741
|
T | A | 1 | a0001c0001t0070g0225 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.932-2915A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36889741 | ||||||
| chr2:36889930
|
C | T | 128 | a0001c0001t0003g0020a0001c0001t0003g0030a0001c0001t0003g0033others(125): Show | 128 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.932-3104G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36889930 | ||||||
| chr2:36889939
|
A | G | 5 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201others(2): Show | 5 | HG01891.hp1 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.932-3113T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36889939 | ||||||
| chr2:36890136
|
G | A | 1 | a0001c0001t0149g0247 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.932-3310C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36890136 | ||||||
| chr2:36890299
|
A | T | 1 | a0003c0006t0128g0271 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.932-3473T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36890299 | ||||||
| chr2:36890353
|
G | A | 1 | a0001c0001t0120g0267 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.932-3527C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36890353 | ||||||
| chr2:36890359
|
G | C | 130 | a0001c0001t0003g0020a0001c0001t0003g0030a0001c0001t0003g0033others(127): Show | 130 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.932-3533C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36890359 | ||||||
| chr2:36890477
|
C | A | 1 | a0001c0001t0001g0131 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.931+3421G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36890477 | ||||||
| chr2:36890477
|
C | CT | 35 | a0001c0001t0001g0106a0001c0001t0001g0152a0001c0001t0001g0185others(32): Show | 35 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.931+3420dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36890477 | ||||||
| chr2:36890477
|
CT | C | 18 | a0001c0001t0009g0189a0001c0001t0010g0290a0001c0001t0010g0291others(15): Show | 18 | HG00099.hp2 HG02040.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.931+3420delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36890477 | ||||||
| chr2:36890478
|
T | C | 1 | a0001c0001t0001g0131 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.931+3420A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36890478 | ||||||
| chr2:36890710
|
C | T | 1 | a0001c0001t0015g0056 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.931+3188G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36890710 | ||||||
| chr2:36890782
|
C | T | 11 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.931+3116G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36890782 | ||||||
| chr2:36890987
|
G | T | 1 | a0001c0001t0090g0127 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.931+2911C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36890987 | ||||||
| chr2:36891145
|
T | G | 1 | a0001c0005t0153g0216 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.931+2753A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36891145 | ||||||
| chr2:36891383
|
G | A | 1 | a0001c0001t0074g0217 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.931+2515C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36891383 | ||||||
| chr2:36891385
|
G | A | 13 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.931+2513C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36891385 | ||||||
| chr2:36891516
|
C | G | 2 | a0001c0001t0032g0071a0001c0001t0138g0043 | 2 | HG00323.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.931+2382G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36891516 | ||||||
| chr2:36891522
|
C | CA | 104 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(101): Show | 104 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.931+2375dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36891522 | ||||||
| chr2:36891577
|
C | T | 7 | a0001c0001t0039g0214a0001c0001t0039g0215a0001c0001t0151g0205others(4): Show | 7 | HG02559.hp2 HG02886.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.931+2321G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36891577 | ||||||
| chr2:36891603
|
G | C | 7 | a0001c0001t0010g0290a0001c0001t0010g0291a0001c0001t0010g0292others(4): Show | 7 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.931+2295C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36891603 | ||||||
| chr2:36891626
|
A | T | 1 | a0001c0001t0110g0191 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.931+2272T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36891626 | ||||||
| chr2:36891798
|
C | G | 1 | a0001c0001t0063g0203 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.931+2100G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36891798 | ||||||
| chr2:36891918
|
T | C | 2 | a0001c0001t0082g0232a0001c0001t0084g0231 | 2 | HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.931+1980A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36891918 | ||||||
| chr2:36891935
|
C | A | 4 | a0001c0001t0001g0003a0001c0001t0002g0004a0001c0001t0021g0002others(1): Show | 4 | HG00408.hp1 HG00558.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+1963G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36891935 | ||||||
| chr2:36892027
|
T | G | 3 | a0001c0001t0074g0217a0001c0001t0075g0218a0001c0001t0076g0219 | 3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.931+1871A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36892027 | ||||||
| chr2:36892094
|
C | T | 290 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.931+1804G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36892094 | ||||||
| chr2:36892113
|
C | T | 249 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(246): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.931+1785G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36892113 | ||||||
| chr2:36892208
|
C | T | 35 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(32): Show | 35 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.931+1690G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36892208 | ||||||
| chr2:36892262
|
G | A | 1 | a0001c0001t0129g0273 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.931+1636C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36892262 | ||||||
| chr2:36892342
|
A | G | 4 | a0001c0001t0137g0259a0001c0001t0146g0249a0001c0001t0147g0250others(1): Show | 4 | HG02970.hp1 HG02976.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.931+1556T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36892342 | ||||||
| chr2:36892636
|
T | C | 1 | a0001c0001t0024g0153 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.931+1262A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36892636 | ||||||
| chr2:36892662
|
G | A | 1 | a0001c0001t0149g0247 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.931+1236C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36892662 | ||||||
| chr2:36892709
|
T | C | 1 | a0001c0001t0004g0181 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.931+1189A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36892709 | ||||||
| chr2:36892793
|
G | C | 1 | a0001c0001t0157g0050 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.931+1105C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36892793 | ||||||
| chr2:36893061
|
C | T | 1 | a0001c0001t0183g0073 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.931+837G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36893061 | ||||||
| chr2:36893294
|
C | CA | 5 | a0001c0001t0001g0131a0001c0001t0002g0145a0001c0001t0050g0295others(2): Show | 5 | HG02300.hp1 HG03195.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.931+603dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36893294 | ||||||
| chr2:36893303
|
C | A | 290 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.931+595G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36893303 | ||||||
| chr2:36893311
|
C | A | 254 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.931+587G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36893311 | ||||||
| chr2:36893312
|
G | A | 1 | a0001c0001t0073g0210 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.931+586C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36893312 | ||||||
| chr2:36893443
|
A | AT | 254 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.931+454dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36893443 | ||||||
| chr2:36893582
|
T | C | 6 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0057others(3): Show | 6 | HG00408.hp2 HG02135.hp2 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.931+316A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36893582 | ||||||
| chr2:36893593
|
A | G | 1 | a0001c0001t0025g0187 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.931+305T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36893593 | ||||||
| chr2:36893654
|
G | A | 35 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(32): Show | 35 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.931+244C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36893654 | ||||||
| chr2:36893750
|
A | G | 1 | a0001c0001t0149g0247 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.931+148T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 7/17 | chr2 | 36893750 | ||||||
| chr2:36894103
|
T | C | 1 | a0001c0001t0022g0108 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.796-70A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36894103 | ||||||
| chr2:36894512
|
A | G | 1 | a0001c0001t0092g0157 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.796-479T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36894512 | ||||||
| chr2:36894751
|
T | C | 17 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.796-718A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36894751 | ||||||
| chr2:36894809
|
A | C | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.796-776T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36894809 | ||||||
| chr2:36894942
|
G | C | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.796-909C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36894942 | ||||||
| chr2:36894993
|
C | T | 24 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(21): Show | 24 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.796-960G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36894993 | ||||||
| chr2:36895055
|
C | T | 17 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.796-1022G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36895055 | ||||||
| chr2:36895243
|
C | T | 1 | a0001c0001t0166g0117 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.796-1210G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36895243 | ||||||
| chr2:36895325
|
T | TA | 9 | a0001c0001t0003g0030a0001c0001t0079g0236a0001c0001t0080g0235others(6): Show | 9 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.796-1293dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36895325 | ||||||
| chr2:36895381
|
T | C | 1 | a0002c0002t0077g0226 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.796-1348A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36895381 | ||||||
| chr2:36895402
|
T | C | 1 | a0001c0001t0177g0089 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.796-1369A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36895402 | ||||||
| chr2:36895409
|
A | G | 102 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(99): Show | 102 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.796-1376T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36895409 | ||||||
| chr2:36895432
|
T | A | 2 | a0001c0001t0024g0115a0001c0001t0024g0153 | 2 | HG01261.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.796-1399A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36895432 | ||||||
| chr2:36895596
|
T | C | 1 | a0001c0001t0004g0162 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.796-1563A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36895596 | ||||||
| chr2:36895631
|
G | A | 73 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(70): Show | 73 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.796-1598C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36895631 | ||||||
| chr2:36895756
|
CA | C | 152 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(149): Show | 152 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.796-1724delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36895756 | ||||||
| chr2:36895756
|
CAA | C | 101 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(98): Show | 101 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.796-1725_796-1724d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36895756 | ||||||
| chr2:36895873
|
G | A | 2 | a0001c0001t0059g0255a0001c0001t0060g0254 | 2 | HG02451.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.796-1840C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36895873 | ||||||
| chr2:36895987
|
G | C | 1 | a0001c0001t0001g0184 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.796-1954C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36895987 | ||||||
| chr2:36895994
|
A | G | 25 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(22): Show | 25 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.796-1961T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36895994 | ||||||
| chr2:36896153
|
T | A | 76 | a0001c0001t0001g0184a0001c0001t0001g0200a0001c0001t0003g0020others(73): Show | 76 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.796-2120A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36896153 | ||||||
| chr2:36896156
|
A | G | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.796-2123T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36896156 | ||||||
| chr2:36896228
|
T | C | 1 | a0001c0001t0003g0033 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.796-2195A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36896228 | ||||||
| chr2:36896240
|
T | C | 104 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(101): Show | 104 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.796-2207A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36896240 | ||||||
| chr2:36896293
|
A | G | 1 | a0001c0001t0054g0275 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.796-2260T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36896293 | ||||||
| chr2:36896549
|
A | C | 1 | a0001c0001t0126g0040 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.796-2516T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36896549 | ||||||
| chr2:36896665
|
G | A | 1 | a0001c0001t0157g0050 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.796-2632C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36896665 | ||||||
| chr2:36896711
|
T | C | 17 | a0001c0001t0008g0047a0001c0001t0031g0042a0001c0001t0031g0045others(14): Show | 17 | HG00323.hp2 HG00642.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.796-2678A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36896711 | ||||||
| chr2:36896933
|
C | T | 12 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201others(9): Show | 12 | HG01891.hp1 HG02109.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.795+2590G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36896933 | ||||||
| chr2:36897006
|
A | G | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.795+2517T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897006 | ||||||
| chr2:36897060
|
G | A | 1 | a0001c0001t0173g0028 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.795+2463C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897060 | ||||||
| chr2:36897122
|
A | G | 254 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.795+2401T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897122 | ||||||
| chr2:36897310
|
C | A | 2 | a0001c0001t0082g0232a0001c0001t0084g0231 | 2 | HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.795+2213G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897310 | ||||||
| chr2:36897316
|
C | A | 15 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201others(12): Show | 15 | HG01891.hp1 HG02109.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.795+2207G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897316 | ||||||
| chr2:36897330
|
G | T | 254 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.795+2193C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897330 | ||||||
| chr2:36897400
|
G | A | 1 | a0001c0001t0054g0275 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.795+2123C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897400 | ||||||
| chr2:36897429
|
T | TAA | 102 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(99): Show | 102 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.795+2092_795+2093d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897429 | ||||||
| chr2:36897434
|
A | T | 14 | a0001c0001t0013g0008a0001c0001t0013g0010a0001c0001t0013g0027others(11): Show | 14 | HG00597.hp1 HG01934.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.795+2089T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897434 | ||||||
| chr2:36897435
|
AT | A | 4 | a0001c0001t0019g0090a0001c0001t0019g0091a0001c0001t0067g0092others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.795+2087delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897435 | ||||||
| chr2:36897436
|
T | A | 180 | a0001c0001t0003g0020a0001c0001t0003g0030a0001c0001t0003g0057others(177): Show | 180 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.795+2087A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897436 | ||||||
| chr2:36897438
|
T | A | 69 | a0001c0001t0008g0047a0001c0001t0011g0096a0001c0001t0011g0097others(66): Show | 69 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.795+2085A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897438 | ||||||
| chr2:36897443
|
A | AT | 9 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201others(6): Show | 9 | HG00738.hp2 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.795+2079dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897443 | ||||||
| chr2:36897443
|
A | T | 1 | a0001c0001t0085g0192 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.795+2080T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897443 | ||||||
| chr2:36897445
|
A | T | 228 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(225): Show | 228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.795+2078T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897445 | ||||||
| chr2:36897447
|
T | A | 3 | a0001c0001t0020g0238a0001c0001t0020g0239a0001c0001t0055g0243 | 3 | HG02109.hp1 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.795+2076A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897447 | ||||||
| chr2:36897462
|
G | A | 250 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.795+2061C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897462 | ||||||
| chr2:36897485
|
G | A | 6 | a0001c0001t0010g0290a0001c0001t0010g0291a0001c0001t0010g0292others(3): Show | 6 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.795+2038C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897485 | ||||||
| chr2:36897497
|
G | A | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.795+2026C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897497 | ||||||
| chr2:36897517
|
GCTCTGCC others(77): Show |
G | 1 | a0001c0001t0052g0261 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.795+1922_795+2005d others(86): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897517 | ||||||
| chr2:36897612
|
T | C | 102 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(99): Show | 102 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.795+1911A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897612 | ||||||
| chr2:36897683
|
C | T | 3 | a0001c0001t0146g0249a0001c0001t0147g0250a0001c0001t0148g0248 | 3 | HG02970.hp1 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.795+1840G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897683 | ||||||
| chr2:36897747
|
A | C | 1 | a0001c0001t0003g0020 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.795+1776T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897747 | ||||||
| chr2:36897960
|
G | C | 5 | a0001c0001t0030g0237a0001c0001t0033g0283a0001c0001t0033g0286others(2): Show | 5 | HG01243.hp2 HG02572.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.795+1563C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897960 | ||||||
| chr2:36897972
|
C | G | 6 | a0001c0001t0001g0077a0001c0001t0001g0183a0001c0001t0001g0184others(3): Show | 6 | NA18940.hp2 NA18955.hp1 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.795+1551G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897972 | ||||||
| chr2:36897985
|
G | A | 1 | a0001c0001t0118g0293 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.795+1538C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36897985 | ||||||
| chr2:36898092
|
T | C | 4 | a0001c0001t0012g0279a0001c0001t0012g0280a0001c0001t0035g0282others(1): Show | 4 | HG01433.hp2 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.795+1431A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36898092 | ||||||
| chr2:36898299
|
G | C | 246 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.795+1224C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36898299 | ||||||
| chr2:36898350
|
G | A | 16 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(13): Show | 16 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.795+1173C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36898350 | ||||||
| chr2:36898379
|
T | C | 4 | a0001c0001t0074g0217a0001c0001t0075g0218a0001c0001t0076g0219others(1): Show | 4 | HG03195.hp2 HG03453.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.795+1144A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36898379 | ||||||
| chr2:36898394
|
T | C | 1 | a0001c0001t0151g0205 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.795+1129A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36898394 | ||||||
| chr2:36898503
|
C | G | 290 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.795+1020G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36898503 | ||||||
| chr2:36898826
|
T | C | 1 | a0001c0001t0119g0301 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.795+697A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36898826 | ||||||
| chr2:36899016
|
C | G | 28 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(25): Show | 28 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.795+507G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36899016 | ||||||
| chr2:36899043
|
C | A | 290 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.795+480G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36899043 | ||||||
| chr2:36899417
|
G | T | 1 | a0001c0001t0178g0060 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.795+106C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36899417 | ||||||
| chr2:36899508
|
A | C | 7 | a0001c0001t0010g0290a0001c0001t0010g0291a0001c0001t0010g0292others(4): Show | 7 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.795+15T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 6/17 | chr2 | 36899508 | ||||||
| chr2:36899881
|
C | T | 2 | a0001c0001t0074g0217a0001c0001t0078g0253 | 2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.660-223G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36899881 | ||||||
| chr2:36900132
|
G | T | 249 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(246): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.660-474C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36900132 | ||||||
| chr2:36900250
|
G | A | 7 | a0001c0001t0001g0124a0001c0001t0001g0134a0001c0001t0001g0143others(4): Show | 7 | HG00621.hp2 HG02080.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.660-592C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36900250 | ||||||
| chr2:36900414
|
T | C | 4 | a0001c0001t0074g0217a0001c0001t0075g0218a0001c0001t0076g0219others(1): Show | 4 | HG03195.hp2 HG03453.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.660-756A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36900414 | ||||||
| chr2:36900801
|
C | G | 284 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(281): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.660-1143G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36900801 | ||||||
| chr2:36900848
|
G | A | 1 | a0001c0001t0003g0113 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.660-1190C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36900848 | ||||||
| chr2:36901003
|
G | GA | 18 | a0001c0001t0001g0137a0001c0001t0002g0171a0001c0001t0003g0030others(15): Show | 18 | HG00280.hp2 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.660-1346dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901003 | ||||||
| chr2:36901169
|
A | G | 1 | a0001c0001t0151g0205 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.659+1415T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901169 | ||||||
| chr2:36901272
|
G | C | 1 | a0001c0003t0071g0223 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.659+1312C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901272 | ||||||
| chr2:36901294
|
G | A | 1 | a0001c0001t0113g0146 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.659+1290C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901294 | ||||||
| chr2:36901449
|
G | A | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.659+1135C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901449 | ||||||
| chr2:36901551
|
CA | C | 258 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0099others(255): Show | 258 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.659+1032delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901551 | ||||||
| chr2:36901563
|
A | C | 3 | a0001c0001t0146g0249a0001c0001t0147g0250a0001c0001t0148g0248 | 3 | HG02970.hp1 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.659+1021T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901563 | ||||||
| chr2:36901567
|
AAAC | A | 13 | a0001c0001t0020g0238a0001c0001t0020g0239a0001c0001t0038g0212others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.659+1014_659+1016d others(5): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901567 | ||||||
| chr2:36901571
|
A | C | 13 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.659+1013T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901571 | ||||||
| chr2:36901663
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.659+921C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901663 | ||||||
| chr2:36901674
|
T | A | 21 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(18): Show | 21 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.659+910A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901674 | ||||||
| chr2:36901711
|
T | C | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.659+873A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901711 | ||||||
| chr2:36901783
|
G | C | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.659+801C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901783 | ||||||
| chr2:36901915
|
G | A | 1 | a0001c0001t0037g0069 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.659+669C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901915 | ||||||
| chr2:36901916
|
T | C | 3 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201 | 3 | HG01891.hp1 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.659+668A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901916 | ||||||
| chr2:36901941
|
T | A | 1 | a0001c0001t0145g0276 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.659+643A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901941 | ||||||
| chr2:36901978
|
A | T | 21 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(18): Show | 21 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.659+606T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36901978 | ||||||
| chr2:36902044
|
T | C | 3 | a0001c0001t0004g0141a0001c0001t0004g0178a0001c0001t0028g0177 | 3 | HG00544.hp1 HG02155.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.659+540A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36902044 | ||||||
| chr2:36902245
|
C | T | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.659+339G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36902245 | ||||||
| chr2:36902414
|
T | A | 1 | a0001c0001t0163g0013 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.659+170A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36902414 | ||||||
| chr2:36902475
|
A | ATAAT | 290 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.659+108_659+109ins others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 5/17 | chr2 | 36902475 | ||||||
| chr2:36902960
|
G | A | 1 | a0001c0001t0054g0275 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.492-209C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36902960 | ||||||
| chr2:36903010
|
G | C | 1 | a0001c0001t0055g0243 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.492-259C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36903010 | ||||||
| chr2:36903108
|
T | A | 2 | a0001c0001t0029g0155a0001c0001t0029g0159 | 2 | HG01361.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.492-357A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36903108 | ||||||
| chr2:36903180
|
C | T | 1 | a0001c0001t0061g0252 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.492-429G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36903180 | ||||||
| chr2:36903199
|
G | A | 2 | a0001c0001t0029g0155a0001c0001t0029g0159 | 2 | HG01361.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.492-448C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36903199 | ||||||
| chr2:36903227
|
T | C | 1 | a0002c0002t0066g0220 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.492-476A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36903227 | ||||||
| chr2:36903230
|
T | C | 3 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201 | 3 | HG01891.hp1 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.492-479A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36903230 | ||||||
| chr2:36903283
|
G | A | 1 | a0002c0002t0062g0227 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.492-532C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36903283 | ||||||
| chr2:36903515
|
A | C | 57 | a0001c0001t0008g0047a0001c0001t0011g0096a0001c0001t0011g0097others(54): Show | 57 | HG00323.hp2 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.492-764T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36903515 | ||||||
| chr2:36903515
|
A | T | 1 | a0001c0001t0037g0072 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.492-764T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36903515 | ||||||
| chr2:36903581
|
A | G | 25 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(22): Show | 25 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.492-830T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36903581 | ||||||
| chr2:36903619
|
G | A | 1 | a0003c0006t0128g0271 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.492-868C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36903619 | ||||||
| chr2:36903637
|
C | T | 3 | a0001c0001t0146g0249a0001c0001t0147g0250a0001c0001t0148g0248 | 3 | HG02970.hp1 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.492-886G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36903637 | ||||||
| chr2:36903738
|
G | C | 1 | a0001c0001t0037g0069 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.492-987C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36903738 | ||||||
| chr2:36903738
|
G | T | 6 | a0001c0001t0039g0214a0001c0001t0039g0215a0001c0001t0152g0211others(3): Show | 6 | HG02559.hp2 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.492-987C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36903738 | ||||||
| chr2:36903758
|
G | T | 1 | a0001c0001t0037g0072 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.492-1007C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36903758 | ||||||
| chr2:36903854
|
C | T | 13 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.492-1103G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36903854 | ||||||
| chr2:36904148
|
A | T | 250 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.491+1392T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904148 | ||||||
| chr2:36904288
|
G | A | 1 | a0001c0001t0065g0224 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.491+1252C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904288 | ||||||
| chr2:36904322
|
T | A | 6 | a0001c0001t0002g0123a0001c0001t0002g0129a0001c0001t0002g0158others(3): Show | 6 | HG01361.hp2 HG02055.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.491+1218A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904322 | ||||||
| chr2:36904328
|
C | T | 1 | a0001c0001t0054g0275 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.491+1212G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904328 | ||||||
| chr2:36904403
|
G | C | 254 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.491+1137C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904403 | ||||||
| chr2:36904548
|
C | T | 1 | a0001c0001t0003g0113 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.491+992G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904548 | ||||||
| chr2:36904549
|
G | A | 1 | a0001c0001t0061g0252 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.491+991C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904549 | ||||||
| chr2:36904554
|
T | C | 1 | a0001c0001t0151g0205 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.491+986A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904554 | ||||||
| chr2:36904557
|
T | C | 1 | a0001c0001t0063g0203 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.491+983A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904557 | ||||||
| chr2:36904669
|
T | C | 1 | a0001c0001t0105g0100 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.491+871A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904669 | ||||||
| chr2:36904686
|
G | C | 1 | a0001c0001t0091g0122 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.491+854C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904686 | ||||||
| chr2:36904720
|
C | T | 47 | a0001c0001t0008g0047a0001c0001t0011g0096a0001c0001t0011g0097others(44): Show | 47 | HG00639.hp2 HG00642.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.491+820G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904720 | ||||||
| chr2:36904734
|
A | G | 1 | a0001c0001t0001g0156 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.491+806T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904734 | ||||||
| chr2:36904747
|
G | C | 21 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(18): Show | 21 | HG00438.hp2 HG00597.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.491+793C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904747 | ||||||
| chr2:36904829
|
A | G | 1 | a0001c0001t0087g0133 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.491+711T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904829 | ||||||
| chr2:36904838
|
C | A | 3 | a0001c0001t0040g0016a0001c0001t0040g0034a0001c0001t0096g0111 | 3 | HG02155.hp2 HG04184.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.491+702G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904838 | ||||||
| chr2:36904838
|
C | CTGAA | 79 | a0001c0001t0003g0020a0001c0001t0003g0030a0001c0001t0003g0033others(76): Show | 79 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.491+698_491+701dup others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904838 | ||||||
| chr2:36904952
|
T | C | 1 | a0001c0001t0118g0293 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.491+588A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904952 | ||||||
| chr2:36904969
|
CT | C | 166 | a0001c0001t0002g0138a0001c0001t0003g0020a0001c0001t0003g0030others(163): Show | 166 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.491+570delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36904969 | ||||||
| chr2:36905031
|
G | A | 8 | a0001c0001t0009g0190a0001c0001t0010g0290a0001c0001t0010g0291others(5): Show | 8 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.491+509C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36905031 | ||||||
| chr2:36905032
|
C | T | 45 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0016g0229others(42): Show | 45 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.491+508G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36905032 | ||||||
| chr2:36905038
|
C | A | 1 | a0001c0001t0163g0013 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.491+502G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36905038 | ||||||
| chr2:36905096
|
A | G | 1 | a0001c0001t0001g0156 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.491+444T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36905096 | ||||||
| chr2:36905104
|
G | A | 1 | a0001c0001t0124g0260 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.491+436C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36905104 | ||||||
| chr2:36905117
|
G | A | 1 | a0001c0001t0151g0205 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.491+423C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36905117 | ||||||
| chr2:36905358
|
G | A | 2 | a0001c0001t0048g0195a0001c0001t0048g0196 | 2 | HG02071.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.491+182C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 4/17 | chr2 | 36905358 | ||||||
| chr2:36905663
|
T | G | 2 | a0001c0001t0063g0203a0001c0001t0064g0202 | 2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.413-45A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36905663 | ||||||
| chr2:36905984
|
C | T | 201 | a0001c0001t0003g0020a0001c0001t0003g0030a0001c0001t0003g0033others(198): Show | 201 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.413-366G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36905984 | ||||||
| chr2:36906137
|
T | C | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.413-519A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906137 | ||||||
| chr2:36906209
|
A | G | 2 | a0001c0001t0038g0212a0001c0001t0038g0213 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.413-591T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906209 | ||||||
| chr2:36906293
|
T | C | 1 | a0001c0001t0046g0062 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.413-675A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906293 | ||||||
| chr2:36906392
|
G | A | 1 | a0001c0001t0040g0016 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.413-774C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906392 | ||||||
| chr2:36906463
|
C | CAATGAAT others(1): Show |
32 | a0001c0001t0003g0033a0001c0001t0005g0006a0001c0001t0007g0197others(29): Show | 32 | HG00099.hp1 HG01243.hp1 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.413-853_413-846dup others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906463 | ||||||
| chr2:36906463
|
C | CAATGAAT others(5): Show |
102 | a0001c0001t0003g0020a0001c0001t0003g0057a0001c0001t0003g0113others(99): Show | 102 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.413-857_413-846dup others(12): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906463 | ||||||
| chr2:36906463
|
C | CAATGAAT others(9): Show |
8 | a0001c0001t0032g0067a0001c0001t0032g0071a0001c0001t0122g0044others(5): Show | 8 | HG00280.hp1 HG00735.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.413-861_413-846dup others(16): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906463 | ||||||
| chr2:36906463
|
C | CAATGAAT others(13): Show |
2 | a0001c0001t0014g0037a0001c0001t0138g0043 | 2 | HG00323.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.413-865_413-846dup others(20): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906463 | ||||||
| chr2:36906463
|
C | CAATGAAT others(17): Show |
2 | a0001c0001t0043g0066a0001c0001t0171g0038 | 2 | NA18985.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.413-869_413-846dup others(24): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906463 | ||||||
| chr2:36906493
|
G | A | 5 | a0001c0001t0003g0030a0001c0001t0005g0006a0001c0001t0044g0058others(2): Show | 5 | HG02135.hp1 HG02135.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.413-875C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906493 | ||||||
| chr2:36906514
|
T | A | 33 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0017g0240others(30): Show | 33 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.413-896A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906514 | ||||||
| chr2:36906538
|
C | A | 11 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0017g0240others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.413-920G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906538 | ||||||
| chr2:36906694
|
A | G | 56 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0007g0197others(53): Show | 56 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.413-1076T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906694 | ||||||
| chr2:36906696
|
C | T | 1 | a0001c0001t0003g0033 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.413-1078G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906696 | ||||||
| chr2:36906704
|
T | C | 4 | a0001c0001t0010g0290a0001c0001t0010g0291a0001c0001t0030g0289others(1): Show | 4 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.413-1086A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906704 | ||||||
| chr2:36906740
|
A | C | 1 | a0001c0001t0011g0096 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.413-1122T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906740 | ||||||
| chr2:36906868
|
C | G | 1 | a0001c0001t0157g0050 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.413-1250G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906868 | ||||||
| chr2:36906938
|
A | AAAC | 6 | a0001c0001t0003g0033a0001c0001t0157g0050a0001c0001t0174g0014others(3): Show | 6 | HG00099.hp1 HG01070.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.413-1321_413-1320i others(5): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906938 | ||||||
| chr2:36906938
|
A | AAC | 69 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(66): Show | 69 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.413-1321_413-1320i others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906938 | ||||||
| chr2:36906939
|
C | A | 75 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(72): Show | 75 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.413-1321G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906939 | ||||||
| chr2:36906939
|
C | CA | 73 | a0001c0001t0002g0123a0001c0001t0002g0129a0001c0001t0002g0158others(70): Show | 73 | HG00323.hp2 HG00639.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.413-1322dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906939 | ||||||
| chr2:36906949
|
C | A | 156 | a0001c0001t0001g0200a0001c0001t0002g0123a0001c0001t0002g0129others(153): Show | 156 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.413-1331G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906949 | ||||||
| chr2:36906968
|
T | C | 4 | a0001c0001t0079g0236a0001c0001t0080g0235a0001c0001t0081g0233others(1): Show | 4 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.413-1350A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36906968 | ||||||
| chr2:36907071
|
C | T | 7 | a0001c0001t0049g0296a0001c0001t0049g0299a0001c0001t0050g0295others(4): Show | 7 | HG01243.hp1 HG01496.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.413-1453G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36907071 | ||||||
| chr2:36907142
|
G | A | 31 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(28): Show | 31 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.413-1524C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36907142 | ||||||
| chr2:36907190
|
T | G | 1 | a0001c0001t0032g0071 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.413-1572A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36907190 | ||||||
| chr2:36907516
|
C | G | 1 | a0001c0001t0031g0045 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.413-1898G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36907516 | ||||||
| chr2:36907617
|
T | C | 2 | a0001c0001t0029g0155a0001c0001t0029g0159 | 2 | HG01361.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.413-1999A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36907617 | ||||||
| chr2:36907637
|
A | C | 3 | a0001c0001t0003g0033a0001c0001t0189g0054a0001c0001t0193g0055 | 3 | HG00099.hp1 HG01255.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.413-2019T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36907637 | ||||||
| chr2:36907718
|
G | A | 1 | a0001c0001t0029g0155 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.413-2100C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36907718 | ||||||
| chr2:36907869
|
G | A | 2 | a0001c0001t0117g0269a0001c0001t0140g0257 | 2 | NA18943.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.413-2251C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36907869 | ||||||
| chr2:36907960
|
C | T | 35 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(32): Show | 35 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.413-2342G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36907960 | ||||||
| chr2:36908074
|
C | T | 1 | a0001c0001t0085g0192 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.413-2456G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36908074 | ||||||
| chr2:36908301
|
G | C | 1 | a0001c0001t0048g0196 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.413-2683C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36908301 | ||||||
| chr2:36908314
|
A | C | 4 | a0001c0001t0014g0037a0001c0001t0043g0024a0001c0001t0043g0066others(1): Show | 4 | NA18940.hp1 NA18985.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.413-2696T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36908314 | ||||||
| chr2:36908357
|
C | G | 7 | a0001c0001t0010g0290a0001c0001t0010g0291a0001c0001t0010g0292others(4): Show | 7 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.413-2739G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36908357 | ||||||
| chr2:36908426
|
T | G | 5 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201others(2): Show | 5 | HG01891.hp1 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.413-2808A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36908426 | ||||||
| chr2:36908571
|
T | C | 1 | a0001c0001t0054g0275 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.413-2953A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36908571 | ||||||
| chr2:36908748
|
C | T | 1 | a0001c0001t0170g0142 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.413-3130G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36908748 | ||||||
| chr2:36908844
|
G | A | 1 | a0001c0001t0063g0203 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.413-3226C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36908844 | ||||||
| chr2:36908893
|
A | C | 158 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(155): Show | 158 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.413-3275T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36908893 | ||||||
| chr2:36908964
|
G | A | 1 | a0001c0001t0054g0275 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.413-3346C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36908964 | ||||||
| chr2:36908998
|
G | GA | 14 | a0001c0001t0021g0005a0001c0001t0038g0212a0001c0001t0038g0213others(11): Show | 14 | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.413-3381dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36908998 | ||||||
| chr2:36908998
|
G | GAA | 16 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0007g0197others(13): Show | 16 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.413-3382_413-3381d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36908998 | ||||||
| chr2:36908998
|
G | GAAA | 138 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(135): Show | 138 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.413-3383_413-3381d others(5): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36908998 | ||||||
| chr2:36908998
|
G | GAAAA | 12 | a0001c0001t0003g0033a0001c0001t0003g0113a0001c0001t0019g0090others(9): Show | 12 | HG00741.hp1 HG01255.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.413-3384_413-3381d others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36908998 | ||||||
| chr2:36909002
|
A | AAAC | 12 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(9): Show | 12 | HG00438.hp2 HG00597.hp2 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.413-3385_413-3384i others(5): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909002 | ||||||
| chr2:36909013
|
G | C | 2 | a0001c0001t0082g0232a0001c0001t0084g0231 | 2 | HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.413-3395C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909013 | ||||||
| chr2:36909031
|
G | A | 1 | a0001c0001t0054g0275 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.413-3413C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909031 | ||||||
| chr2:36909157
|
C | CA | 14 | a0001c0001t0024g0115a0001c0001t0038g0212a0001c0001t0038g0213others(11): Show | 14 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.413-3540dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909157 | ||||||
| chr2:36909157
|
CA | C | 61 | a0001c0001t0001g0077a0001c0001t0001g0183a0001c0001t0001g0184others(58): Show | 61 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.413-3540delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909157 | ||||||
| chr2:36909217
|
A | T | 1 | a0001c0001t0023g0140 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.413-3599T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909217 | ||||||
| chr2:36909255
|
T | C | 75 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(72): Show | 75 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.413-3637A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909255 | ||||||
| chr2:36909374
|
A | G | 12 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.413-3756T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909374 | ||||||
| chr2:36909492
|
C | T | 7 | a0001c0001t0039g0214a0001c0001t0039g0215a0001c0001t0151g0205others(4): Show | 7 | HG02559.hp2 HG02886.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.413-3874G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909492 | ||||||
| chr2:36909495
|
T | C | 189 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(186): Show | 189 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.413-3877A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909495 | ||||||
| chr2:36909617
|
T | C | 190 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(187): Show | 190 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.413-3999A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909617 | ||||||
| chr2:36909669
|
T | C | 2 | a0001c0001t0001g0186a0001c0001t0099g0110 | 2 | NA18943.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.413-4051A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909669 | ||||||
| chr2:36909746
|
A | G | 4 | a0001c0001t0079g0236a0001c0001t0080g0235a0001c0001t0081g0233others(1): Show | 4 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.413-4128T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909746 | ||||||
| chr2:36909764
|
T | C | 5 | a0001c0001t0039g0214a0001c0001t0039g0215a0001c0001t0155g0207others(2): Show | 5 | HG02886.hp1 HG02895.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.413-4146A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909764 | ||||||
| chr2:36909877
|
TAAAG | T | 3 | a0001c0001t0035g0268a0001c0001t0132g0258a0001c0001t0145g0276 | 3 | HG00735.hp2 HG01256.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.413-4263_413-4260d others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909877 | ||||||
| chr2:36909946
|
G | T | 1 | a0001c0001t0005g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.413-4328C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909946 | ||||||
| chr2:36909980
|
C | G | 58 | a0001c0001t0008g0047a0001c0001t0011g0096a0001c0001t0011g0097others(55): Show | 58 | HG00323.hp2 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.413-4362G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36909980 | ||||||
| chr2:36910110
|
C | T | 201 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(198): Show | 201 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.413-4492G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36910110 | ||||||
| chr2:36910122
|
G | A | 1 | a0001c0001t0068g0262 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.413-4504C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36910122 | ||||||
| chr2:36910127
|
C | T | 1 | a0001c0001t0004g0162 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.413-4509G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36910127 | ||||||
| chr2:36910152
|
G | T | 12 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.413-4534C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36910152 | ||||||
| chr2:36910161
|
G | A | 52 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0007g0197others(49): Show | 52 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.413-4543C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36910161 | ||||||
| chr2:36910173
|
C | CA | 53 | a0001c0001t0001g0107a0001c0001t0001g0149a0001c0001t0001g0165others(50): Show | 53 | HG00438.hp2 HG00597.hp2 HG01175.hp2 others(50): Show |
intron_variant | MODIFIER | c.413-4556dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36910173 | ||||||
| chr2:36910173
|
C | CAA | 7 | a0001c0001t0056g0241a0001c0001t0067g0092a0001c0001t0079g0236others(4): Show | 7 | HG00738.hp2 HG01884.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.413-4557_413-4556d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36910173 | ||||||
| chr2:36910173
|
CA | C | 10 | a0001c0001t0013g0010a0001c0001t0039g0214a0001c0001t0039g0215others(7): Show | 10 | HG02886.hp1 HG02895.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.413-4556delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36910173 | ||||||
| chr2:36910173
|
CAAAAAAA others(4): Show |
C | 58 | a0001c0001t0008g0047a0001c0001t0011g0096a0001c0001t0011g0097others(55): Show | 58 | HG00323.hp2 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.413-4566_413-4556d others(13): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36910173 | ||||||
| chr2:36910237
|
T | G | 1 | a0001c0001t0095g0112 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.413-4619A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36910237 | ||||||
| chr2:36910252
|
C | T | 48 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0007g0197others(45): Show | 48 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.413-4634G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36910252 | ||||||
| chr2:36910497
|
T | C | 16 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0007g0197others(13): Show | 16 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.413-4879A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36910497 | ||||||
| chr2:36910705
|
T | C | 1 | a0001c0001t0002g0123 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.413-5087A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36910705 | ||||||
| chr2:36910903
|
C | A | 181 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(178): Show | 181 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.412+5175G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36910903 | ||||||
| chr2:36910944
|
T | C | 1 | a0001c0001t0083g0234 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.412+5134A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36910944 | ||||||
| chr2:36911203
|
A | G | 3 | a0001c0001t0035g0268a0001c0001t0132g0258a0001c0001t0145g0276 | 3 | HG00735.hp2 HG01256.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.412+4875T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36911203 | ||||||
| chr2:36911207
|
G | C | 16 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(13): Show | 16 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.412+4871C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36911207 | ||||||
| chr2:36911243
|
C | T | 2 | a0001c0001t0118g0293a0001c0001t0191g0080 | 2 | HG00544.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.412+4835G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36911243 | ||||||
| chr2:36911322
|
C | G | 155 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(152): Show | 155 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.412+4756G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36911322 | ||||||
| chr2:36911421
|
G | A | 5 | a0001c0001t0023g0139a0001c0001t0023g0140a0001c0001t0027g0125others(2): Show | 5 | HG00423.hp2 HG00438.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.412+4657C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36911421 | ||||||
| chr2:36911511
|
T | C | 1 | a0001c0001t0064g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.412+4567A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36911511 | ||||||
| chr2:36911554
|
A | T | 1 | a0001c0001t0151g0205 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.412+4524T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36911554 | ||||||
| chr2:36911690
|
T | C | 3 | a0001c0001t0020g0238a0001c0001t0020g0239a0001c0001t0063g0203 | 3 | HG03579.hp1 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.412+4388A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36911690 | ||||||
| chr2:36912014
|
A | G | 17 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0007g0197others(14): Show | 17 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.412+4064T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36912014 | ||||||
| chr2:36912113
|
T | G | 1 | a0001c0001t0190g0063 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.412+3965A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36912113 | ||||||
| chr2:36912236
|
G | A | 1 | a0001c0001t0061g0252 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.412+3842C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36912236 | ||||||
| chr2:36912253
|
C | T | 2 | a0001c0001t0019g0090a0001c0001t0019g0091 | 2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.412+3825G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36912253 | ||||||
| chr2:36912260
|
G | A | 7 | a0001c0001t0005g0023a0001c0001t0005g0065a0001c0001t0012g0022others(4): Show | 7 | HG00621.hp1 HG00642.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.412+3818C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36912260 | ||||||
| chr2:36912273
|
T | C | 1 | a0001c0001t0170g0142 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.412+3805A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36912273 | ||||||
| chr2:36912345
|
C | G | 1 | a0001c0001t0075g0218 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.412+3733G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36912345 | ||||||
| chr2:36912384
|
T | C | 26 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(23): Show | 26 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.412+3694A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36912384 | ||||||
| chr2:36912392
|
T | A | 55 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0007g0197others(52): Show | 55 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.412+3686A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36912392 | ||||||
| chr2:36912403
|
T | A | 1 | a0001c0001t0040g0034 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.412+3675A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36912403 | ||||||
| chr2:36912580
|
T | C | 1 | a0001c0001t0065g0224 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.412+3498A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36912580 | ||||||
| chr2:36912701
|
G | T | 1 | a0001c0001t0156g0206 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.412+3377C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36912701 | ||||||
| chr2:36912704
|
T | C | 1 | a0001c0001t0003g0020 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.412+3374A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36912704 | ||||||
| chr2:36912996
|
A | G | 1 | a0001c0001t0125g0277 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.412+3082T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36912996 | ||||||
| chr2:36913072
|
G | A | 1 | a0001c0001t0029g0155 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.412+3006C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36913072 | ||||||
| chr2:36913228
|
T | C | 1 | a0001c0001t0106g0128 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.412+2850A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36913228 | ||||||
| chr2:36913449
|
T | C | 7 | a0001c0001t0010g0290a0001c0001t0010g0291a0001c0001t0010g0292others(4): Show | 7 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.412+2629A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36913449 | ||||||
| chr2:36913482
|
G | A | 1 | a0001c0001t0187g0049 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.412+2596C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36913482 | ||||||
| chr2:36913557
|
G | A | 47 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0016g0229others(44): Show | 47 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.412+2521C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36913557 | ||||||
| chr2:36913570
|
A | C | 187 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(184): Show | 187 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.412+2508T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36913570 | ||||||
| chr2:36913580
|
CA | C | 3 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201 | 3 | HG01891.hp1 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.412+2497delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36913580 | ||||||
| chr2:36913693
|
A | G | 1 | a0001c0001t0075g0218 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.412+2385T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36913693 | ||||||
| chr2:36913942
|
C | T | 156 | a0001c0001t0003g0020a0001c0001t0003g0030a0001c0001t0003g0033others(153): Show | 156 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.412+2136G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36913942 | ||||||
| chr2:36913943
|
G | A | 1 | a0001c0001t0149g0247 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.412+2135C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36913943 | ||||||
| chr2:36914017
|
C | A | 3 | a0001c0001t0074g0217a0001c0001t0075g0218a0001c0001t0076g0219 | 3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.412+2061G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36914017 | ||||||
| chr2:36914104
|
C | T | 1 | a0001c0001t0088g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.412+1974G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36914104 | ||||||
| chr2:36914156
|
A | G | 4 | a0001c0001t0033g0283a0001c0001t0033g0286a0001c0001t0131g0285others(1): Show | 4 | HG02572.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.412+1922T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36914156 | ||||||
| chr2:36914193
|
A | G | 185 | a0001c0001t0003g0020a0001c0001t0003g0030a0001c0001t0003g0033others(182): Show | 185 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.412+1885T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36914193 | ||||||
| chr2:36914269
|
T | C | 3 | a0001c0001t0020g0238a0001c0001t0020g0239a0001c0001t0063g0203 | 3 | HG03579.hp1 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.412+1809A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36914269 | ||||||
| chr2:36914352
|
C | T | 185 | a0001c0001t0003g0020a0001c0001t0003g0030a0001c0001t0003g0033others(182): Show | 185 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.412+1726G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36914352 | ||||||
| chr2:36914426
|
A | G | 4 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0150g0208others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+1652T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36914426 | ||||||
| chr2:36914904
|
A | G | 1 | a0001c0001t0054g0275 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.412+1174T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36914904 | ||||||
| chr2:36914966
|
G | C | 2 | a0001c0001t0019g0090a0001c0001t0019g0091 | 2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.412+1112C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36914966 | ||||||
| chr2:36914967
|
G | C | 3 | a0001c0001t0074g0217a0001c0001t0075g0218a0001c0001t0076g0219 | 3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.412+1111C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36914967 | ||||||
| chr2:36915135
|
T | C | 4 | a0001c0001t0146g0249a0001c0001t0147g0250a0001c0001t0148g0248others(1): Show | 4 | HG02970.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.412+943A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915135 | ||||||
| chr2:36915172
|
G | A | 12 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0017g0240others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.412+906C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915172 | ||||||
| chr2:36915228
|
CATAAAT | C | 3 | a0001c0001t0033g0283a0001c0001t0033g0286a0001c0001t0131g0285 | 3 | HG02572.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.412+844_412+849del others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915228 | ||||||
| chr2:36915232
|
A | AAT | 26 | a0001c0001t0001g0106a0001c0001t0001g0124a0001c0001t0001g0134others(23): Show | 26 | HG00621.hp2 HG01070.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.412+844_412+845dup others(2): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | ||||||
| chr2:36915232
|
A | AATAT | 15 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0001g0176others(12): Show | 15 | HG00438.hp1 HG00673.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.412+842_412+845dup others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | ||||||
| chr2:36915232
|
A | AATATAT | 18 | a0001c0001t0002g0126a0001c0001t0002g0145a0001c0001t0002g0171others(15): Show | 18 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(15): Show |
intron_variant | MODIFIER | c.412+840_412+845dup others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | ||||||
| chr2:36915232
|
A | AATATATA others(1): Show |
15 | a0001c0001t0001g0200a0001c0001t0002g0004a0001c0001t0003g0057others(12): Show | 15 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(12): Show |
intron_variant | MODIFIER | c.412+838_412+845dup others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | ||||||
| chr2:36915232
|
A | AATATATA others(3): Show |
18 | a0001c0001t0001g0077a0001c0001t0001g0184a0001c0001t0001g0186others(15): Show | 18 | HG00099.hp1 HG01993.hp1 HG02004.hp1 others(15): Show |
intron_variant | MODIFIER | c.412+836_412+845dup others(10): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | ||||||
| chr2:36915232
|
A | AATATATA others(5): Show |
15 | a0001c0001t0001g0183a0001c0001t0001g0185a0001c0001t0003g0033others(12): Show | 15 | HG00621.hp1 HG00642.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.412+834_412+845dup others(12): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | ||||||
| chr2:36915232
|
A | AATATATA others(7): Show |
13 | a0001c0001t0002g0123a0001c0001t0002g0160a0001c0001t0003g0020others(10): Show | 13 | HG01993.hp2 HG02055.hp2 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.412+832_412+845dup others(14): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | ||||||
| chr2:36915232
|
A | AATATATA others(9): Show |
3 | a0001c0001t0001g0003a0001c0001t0003g0113a0001c0001t0175g0081 | 3 | HG00408.hp1 NA18955.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.412+830_412+845dup others(16): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | ||||||
| chr2:36915232
|
A | AATATATA others(11): Show |
1 | a0001c0001t0050g0295 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.412+828_412+845dup others(18): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | ||||||
| chr2:36915232
|
A | AATATATA others(15): Show |
1 | a0001c0001t0043g0024 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.412+824_412+845dup others(22): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | ||||||
| chr2:36915232
|
A | AATATATA others(19): Show |
1 | a0001c0001t0047g0079 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.412+820_412+845dup others(26): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | ||||||
| chr2:36915232
|
AAT | A | 9 | a0001c0001t0004g0141a0001c0001t0004g0178a0001c0001t0049g0296others(6): Show | 9 | HG00544.hp1 HG01243.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.412+844_412+845del others(2): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | ||||||
| chr2:36915232
|
AATAT | A | 7 | a0001c0001t0020g0239a0001c0001t0037g0069a0001c0001t0097g0164others(4): Show | 7 | HG01256.hp2 HG02602.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.412+842_412+845del others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | ||||||
| chr2:36915232
|
AATATAT | A | 11 | a0001c0001t0010g0292a0001c0001t0020g0238a0001c0001t0034g0256others(8): Show | 11 | HG00639.hp2 HG01433.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.412+840_412+845del others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | ||||||
| chr2:36915232
|
AATATATA others(1): Show |
A | 34 | a0001c0001t0008g0047a0001c0001t0011g0096a0001c0001t0011g0097others(31): Show | 34 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.412+838_412+845del others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | ||||||
| chr2:36915232
|
AATATATA others(3): Show |
A | 1 | a0001c0001t0007g0197 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.412+836_412+845del others(10): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | ||||||
| chr2:36915232
|
AATATATA others(5): Show |
A | 5 | a0001c0001t0001g0180a0001c0001t0007g0198a0001c0001t0007g0201others(2): Show | 5 | HG01517.hp1 HG01891.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.412+834_412+845del others(12): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | ||||||
| chr2:36915232
|
AATATATA others(9): Show |
A | 14 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0017g0240others(11): Show | 14 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.412+830_412+845del others(16): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | ||||||
| chr2:36915232
|
AATATATA others(11): Show |
A | 33 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(30): Show | 33 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.412+828_412+845del others(18): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | ||||||
| chr2:36915232
|
AATATATA others(19): Show |
A | 18 | a0001c0001t0013g0008a0001c0001t0013g0010a0001c0001t0013g0027others(15): Show | 18 | HG00597.hp1 HG01934.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.412+820_412+845del others(26): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915232 | ||||||
| chr2:36915259
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0194g0021 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.412+818_412+819ins others(23): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915259 | ||||||
| chr2:36915274
|
A | T | 1 | a0004c0004t0188g0048 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.412+804T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915274 | ||||||
| chr2:36915334
|
G | A | 1 | a0001c0001t0001g0200 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.412+744C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915334 | ||||||
| chr2:36915399
|
T | A | 1 | a0001c0001t0001g0200 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.412+679A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915399 | ||||||
| chr2:36915460
|
T | C | 1 | a0001c0001t0031g0042 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.412+618A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915460 | ||||||
| chr2:36915526
|
A | C | 4 | a0001c0001t0079g0236a0001c0001t0080g0235a0001c0001t0081g0233others(1): Show | 4 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+552T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915526 | ||||||
| chr2:36915583
|
C | A | 1 | a0001c0001t0040g0016 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.412+495G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915583 | ||||||
| chr2:36915611
|
A | G | 40 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0007g0197others(37): Show | 40 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.412+467T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915611 | ||||||
| chr2:36915661
|
G | T | 2 | a0001c0001t0001g0107a0001c0001t0001g0174 | 2 | HG01071.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.412+417C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915661 | ||||||
| chr2:36915683
|
G | A | 1 | a0001c0001t0122g0044 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.412+395C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915683 | ||||||
| chr2:36915765
|
T | C | 2 | a0001c0001t0074g0217a0001c0001t0075g0218 | 2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.412+313A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915765 | ||||||
| chr2:36915786
|
C | G | 1 | a0001c0001t0159g0032 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.412+292G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915786 | ||||||
| chr2:36915946
|
A | G | 4 | a0001c0001t0014g0037a0001c0001t0043g0024a0001c0001t0043g0066others(1): Show | 4 | NA18940.hp1 NA18985.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.412+132T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915946 | ||||||
| chr2:36915997
|
A | G | 52 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0007g0197others(49): Show | 52 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.412+81T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36915997 | ||||||
| chr2:36916005
|
T | C | 1 | a0001c0001t0152g0211 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.412+73A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 3/17 | chr2 | 36916005 | ||||||
| chr2:36916230
|
T | C | 1 | a0001c0001t0041g0029 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.339-79A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36916230 | ||||||
| chr2:36916412
|
A | C | 1 | a0001c0001t0068g0262 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.339-261T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36916412 | ||||||
| chr2:36916496
|
TA | T | 6 | a0001c0001t0054g0275a0001c0001t0133g0265a0001c0001t0146g0249others(3): Show | 6 | HG02040.hp1 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.339-346delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36916496 | ||||||
| chr2:36916554
|
A | T | 1 | a0001c0001t0117g0269 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.339-403T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36916554 | ||||||
| chr2:36916772
|
T | C | 7 | a0001c0001t0039g0214a0001c0001t0039g0215a0001c0001t0151g0205others(4): Show | 7 | HG02559.hp2 HG02886.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.339-621A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36916772 | ||||||
| chr2:36916780
|
C | A | 1 | a0001c0001t0054g0275 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.339-629G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36916780 | ||||||
| chr2:36917044
|
T | TA | 6 | a0001c0001t0054g0275a0001c0001t0146g0249a0001c0001t0147g0250others(3): Show | 6 | HG02970.hp1 HG02976.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.339-894dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917044 | ||||||
| chr2:36917051
|
AT | A | 29 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0007g0197others(26): Show | 29 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.339-901delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917051 | ||||||
| chr2:36917052
|
T | A | 162 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(159): Show | 162 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.339-901A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917052 | ||||||
| chr2:36917053
|
A | T | 12 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(9): Show | 12 | HG00438.hp2 HG00597.hp2 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.339-902T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917053 | ||||||
| chr2:36917056
|
A | T | 1 | a0001c0001t0064g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.339-905T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917056 | ||||||
| chr2:36917069
|
T | TA | 12 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.339-919dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917069 | ||||||
| chr2:36917103
|
C | CAAT | 50 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0007g0197others(47): Show | 50 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.339-955_339-953dup others(3): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917103 | ||||||
| chr2:36917162
|
T | C | 1 | a0001c0001t0013g0027 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.339-1011A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917162 | ||||||
| chr2:36917173
|
T | C | 16 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(13): Show | 16 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.339-1022A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917173 | ||||||
| chr2:36917195
|
T | C | 12 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0017g0240others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.339-1044A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917195 | ||||||
| chr2:36917213
|
G | C | 1 | a0001c0001t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.339-1062C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917213 | ||||||
| chr2:36917213
|
G | GT | 16 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(13): Show | 16 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.339-1063dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917213 | ||||||
| chr2:36917249
|
C | A | 52 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0007g0197others(49): Show | 52 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.339-1098G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917249 | ||||||
| chr2:36917390
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.339-1239C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917390 | ||||||
| chr2:36917471
|
C | T | 11 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.339-1320G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917471 | ||||||
| chr2:36917529
|
CAAAAAAA others(9): Show |
C | 2 | a0001c0001t0022g0135a0001c0001t0126g0040 | 2 | HG00741.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.339-1394_339-1379d others(18): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917529 | ||||||
| chr2:36917532
|
A | T | 1 | a0001c0001t0068g0262 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.339-1381T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917532 | ||||||
| chr2:36917538
|
G | GA | 47 | a0001c0001t0004g0162a0001c0001t0006g0244a0001c0001t0006g0246others(44): Show | 47 | HG00438.hp2 HG00738.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.339-1388dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917538 | ||||||
| chr2:36917656
|
C | T | 12 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.339-1505G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917656 | ||||||
| chr2:36917830
|
GA | G | 12 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.339-1680delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917830 | ||||||
| chr2:36917903
|
T | C | 35 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0016g0229others(32): Show | 35 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.339-1752A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917903 | ||||||
| chr2:36917950
|
C | T | 12 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.339-1799G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917950 | ||||||
| chr2:36917964
|
T | C | 3 | a0001c0001t0014g0037a0001c0001t0043g0066a0001c0001t0171g0038 | 3 | NA18985.hp2 NA19054.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.339-1813A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36917964 | ||||||
| chr2:36918083
|
T | C | 12 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.339-1932A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36918083 | ||||||
| chr2:36918213
|
A | G | 1 | a0001c0001t0167g0007 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.339-2062T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36918213 | ||||||
| chr2:36918249
|
C | T | 31 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(28): Show | 31 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.339-2098G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36918249 | ||||||
| chr2:36918609
|
T | C | 5 | a0001c0001t0002g0144a0001c0001t0032g0067a0001c0001t0032g0071others(2): Show | 5 | HG00323.hp2 HG01168.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.339-2458A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36918609 | ||||||
| chr2:36918810
|
C | T | 4 | a0001c0001t0034g0256a0001c0001t0034g0264a0001c0001t0052g0261others(1): Show | 4 | HG01106.hp1 HG03540.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.339-2659G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36918810 | ||||||
| chr2:36918931
|
G | C | 1 | a0001c0001t0096g0111 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.339-2780C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36918931 | ||||||
| chr2:36918981
|
A | G | 1 | a0001c0001t0054g0275 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.339-2830T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36918981 | ||||||
| chr2:36919197
|
T | C | 1 | a0001c0001t0142g0266 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.339-3046A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36919197 | ||||||
| chr2:36919231
|
C | T | 1 | a0001c0001t0001g0185 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.339-3080G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36919231 | ||||||
| chr2:36919279
|
T | C | 5 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0002g0138others(2): Show | 5 | NA18943.hp2 NA18954.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.339-3128A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36919279 | ||||||
| chr2:36919549
|
G | A | 1 | a0001c0001t0096g0111 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.339-3398C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36919549 | ||||||
| chr2:36919562
|
A | C | 1 | a0001c0001t0125g0277 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.339-3411T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36919562 | ||||||
| chr2:36919621
|
A | G | 16 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(13): Show | 16 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.339-3470T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36919621 | ||||||
| chr2:36919634
|
C | T | 1 | a0001c0001t0064g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.339-3483G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36919634 | ||||||
| chr2:36919681
|
C | T | 31 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(28): Show | 31 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.339-3530G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36919681 | ||||||
| chr2:36919878
|
T | C | 1 | a0001c0001t0019g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.339-3727A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36919878 | ||||||
| chr2:36920065
|
T | C | 1 | a0001c0001t0100g0193 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.339-3914A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36920065 | ||||||
| chr2:36920085
|
GAATT | G | 171 | a0001c0001t0003g0020a0001c0001t0003g0030a0001c0001t0003g0033others(168): Show | 171 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.339-3938_339-3935d others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36920085 | ||||||
| chr2:36920179
|
G | A | 1 | a0001c0001t0001g0076 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.339-4028C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36920179 | ||||||
| chr2:36920426
|
G | A | 1 | a0001c0001t0016g0230 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.339-4275C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36920426 | ||||||
| chr2:36920437
|
G | A | 1 | a0001c0005t0153g0216 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.339-4286C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36920437 | ||||||
| chr2:36920492
|
G | C | 1 | a0001c0001t0085g0192 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.339-4341C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36920492 | ||||||
| chr2:36920638
|
C | CA | 9 | a0001c0001t0003g0033a0001c0001t0014g0094a0001c0001t0036g0095others(6): Show | 9 | HG00099.hp1 HG01255.hp2 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.338+4466dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36920638 | ||||||
| chr2:36920776
|
T | TA | 5 | a0001c0001t0039g0214a0001c0001t0039g0215a0001c0001t0155g0207others(2): Show | 5 | HG02886.hp1 HG02895.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.338+4328dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36920776 | ||||||
| chr2:36920829
|
C | T | 1 | a0001c0001t0054g0275 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.338+4276G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36920829 | ||||||
| chr2:36920832
|
T | G | 181 | a0001c0001t0003g0020a0001c0001t0003g0030a0001c0001t0003g0033others(178): Show | 181 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.338+4273A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36920832 | ||||||
| chr2:36920947
|
C | T | 4 | a0001c0001t0146g0249a0001c0001t0147g0250a0001c0001t0148g0248others(1): Show | 4 | HG02970.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.338+4158G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36920947 | ||||||
| chr2:36920973
|
A | G | 1 | a0001c0001t0182g0053 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.338+4132T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36920973 | ||||||
| chr2:36921087
|
T | A | 119 | a0001c0001t0002g0123a0001c0001t0002g0129a0001c0001t0002g0158others(116): Show | 119 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.338+4018A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36921087 | ||||||
| chr2:36921090
|
T | A | 3 | a0001c0001t0035g0268a0001c0001t0132g0258a0001c0001t0145g0276 | 3 | HG00735.hp2 HG01256.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.338+4015A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36921090 | ||||||
| chr2:36921122
|
T | C | 1 | a0001c0001t0037g0072 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.338+3983A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36921122 | ||||||
| chr2:36921398
|
CCTT | C | 12 | a0001c0001t0005g0087a0001c0001t0045g0082a0001c0001t0045g0085others(9): Show | 12 | HG00423.hp1 HG00544.hp2 NA18941.hp2 others(9): Show |
intron_variant | MODIFIER | c.338+3704_338+3706d others(5): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36921398 | ||||||
| chr2:36921503
|
G | A | 4 | a0001c0001t0146g0249a0001c0001t0147g0250a0001c0001t0148g0248others(1): Show | 4 | HG02970.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.338+3602C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36921503 | ||||||
| chr2:36921712
|
G | GTC | 186 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(183): Show | 186 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.338+3391_338+3392d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36921712 | ||||||
| chr2:36921760
|
C | T | 1 | a0001c0001t0003g0020 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.338+3345G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36921760 | ||||||
| chr2:36921865
|
A | T | 17 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0007g0197others(14): Show | 17 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.338+3240T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36921865 | ||||||
| chr2:36922073
|
G | C | 1 | a0001c0001t0073g0210 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.338+3032C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922073 | ||||||
| chr2:36922175
|
T | C | 1 | a0001c0001t0105g0100 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.338+2930A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922175 | ||||||
| chr2:36922355
|
T | C | 188 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(185): Show | 188 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.338+2750A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922355 | ||||||
| chr2:36922389
|
T | C | 1 | a0001c0001t0001g0114 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.338+2716A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922389 | ||||||
| chr2:36922458
|
G | A | 1 | a0001c0001t0064g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.338+2647C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922458 | ||||||
| chr2:36922482
|
G | A | 4 | a0001c0001t0079g0236a0001c0001t0080g0235a0001c0001t0081g0233others(1): Show | 4 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.338+2623C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922482 | ||||||
| chr2:36922518
|
C | CA | 11 | a0001c0001t0002g0145a0001c0001t0010g0292a0001c0001t0030g0289others(8): Show | 11 | HG00099.hp1 HG02109.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.338+2586dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922518 | ||||||
| chr2:36922518
|
CA | C | 97 | a0001c0001t0001g0183a0001c0001t0001g0188a0001c0001t0006g0244others(94): Show | 97 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.338+2586delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922518 | ||||||
| chr2:36922540
|
A | AT | 4 | a0001c0001t0038g0213a0001c0001t0121g0281a0001c0001t0150g0208others(1): Show | 4 | HG01071.hp2 HG01123.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.338+2564_338+2565i others(3): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922540 | ||||||
| chr2:36922540
|
A | T | 1 | a0001c0001t0038g0212 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.338+2565T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922540 | ||||||
| chr2:36922567
|
A | G | 17 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0007g0197others(14): Show | 17 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.338+2538T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922567 | ||||||
| chr2:36922621
|
C | T | 1 | a0001c0001t0058g0251 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.338+2484G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922621 | ||||||
| chr2:36922630
|
C | T | 5 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0121g0281others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.338+2475G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922630 | ||||||
| chr2:36922639
|
GTCA | G | 12 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0017g0240others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.338+2463_338+2465d others(5): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922639 | ||||||
| chr2:36922668
|
A | G | 1 | a0001c0001t0031g0042 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.338+2437T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922668 | ||||||
| chr2:36922816
|
T | TA | 12 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0017g0240others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.338+2288dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922816 | ||||||
| chr2:36922926
|
G | A | 2 | a0001c0001t0030g0237a0002c0002t0077g0226 | 2 | HG01243.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.338+2179C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922926 | ||||||
| chr2:36922998
|
T | A | 1 | a0001c0001t0063g0203 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.338+2107A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36922998 | ||||||
| chr2:36923013
|
G | A | 1 | a0001c0001t0049g0296 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.338+2092C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923013 | ||||||
| chr2:36923072
|
G | T | 32 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(29): Show | 32 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.338+2033C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923072 | ||||||
| chr2:36923140
|
G | GA | 18 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(15): Show | 18 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.338+1964dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923140 | ||||||
| chr2:36923162
|
A | C | 1 | a0001c0001t0187g0049 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.338+1943T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923162 | ||||||
| chr2:36923207
|
T | C | 13 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.338+1898A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923207 | ||||||
| chr2:36923280
|
C | T | 1 | a0001c0001t0031g0045 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.338+1825G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923280 | ||||||
| chr2:36923344
|
G | A | 12 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.338+1761C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923344 | ||||||
| chr2:36923388
|
T | C | 136 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(133): Show | 136 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.338+1717A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923388 | ||||||
| chr2:36923399
|
C | T | 1 | a0001c0001t0112g0168 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.338+1706G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923399 | ||||||
| chr2:36923445
|
C | CA | 38 | a0001c0001t0001g0184a0001c0001t0002g0145a0001c0001t0004g0141others(35): Show | 38 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.338+1659dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923445 | ||||||
| chr2:36923445
|
C | CAA | 10 | a0001c0001t0016g0230a0001c0001t0038g0213a0001c0001t0039g0214others(7): Show | 10 | HG01071.hp2 HG01123.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.338+1658_338+1659d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923445 | ||||||
| chr2:36923465
|
C | A | 12 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.338+1640G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923465 | ||||||
| chr2:36923499
|
G | A | 301 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(298): Show | 301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.338+1606C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923499 | ||||||
| chr2:36923507
|
T | TCTTTCCA others(24): Show |
1 | a0001c0001t0090g0127 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.338+1567_338+1597d others(33): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923507 | ||||||
| chr2:36923593
|
T | A | 1 | a0001c0001t0064g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.338+1512A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923593 | ||||||
| chr2:36923650
|
A | G | 135 | a0001c0001t0003g0020a0001c0001t0003g0030a0001c0001t0003g0033others(132): Show | 135 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.338+1455T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923650 | ||||||
| chr2:36923895
|
A | G | 7 | a0001c0001t0039g0214a0001c0001t0039g0215a0001c0001t0151g0205others(4): Show | 7 | HG02559.hp2 HG02886.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.338+1210T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36923895 | ||||||
| chr2:36924026
|
T | C | 1 | a0001c0001t0149g0247 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.338+1079A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36924026 | ||||||
| chr2:36924061
|
A | C | 5 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201others(2): Show | 5 | HG01891.hp1 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.338+1044T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36924061 | ||||||
| chr2:36924104
|
C | A | 2 | a0001c0001t0034g0264a0001c0001t0137g0259 | 2 | HG01106.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.338+1001G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36924104 | ||||||
| chr2:36924133
|
G | C | 12 | a0001c0001t0002g0101a0001c0001t0002g0126a0001c0001t0002g0145others(9): Show | 12 | HG00558.hp1 HG00639.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.338+972C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36924133 | ||||||
| chr2:36924355
|
C | CA | 33 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0007g0197others(30): Show | 33 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.338+749dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36924355 | ||||||
| chr2:36924355
|
C | CAA | 150 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(147): Show | 150 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.338+748_338+749dup others(2): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36924355 | ||||||
| chr2:36924535
|
G | T | 1 | a0001c0001t0064g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.338+570C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36924535 | ||||||
| chr2:36924545
|
T | C | 2 | a0001c0001t0001g0137a0001c0001t0002g0171 | 2 | HG00280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.338+560A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36924545 | ||||||
| chr2:36924652
|
A | G | 1 | a0001c0001t0027g0194 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.338+453T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36924652 | ||||||
| chr2:36924683
|
C | T | 1 | a0001c0001t0118g0293 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.338+422G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36924683 | ||||||
| chr2:36924796
|
C | A | 1 | a0001c0001t0157g0050 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.338+309G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36924796 | ||||||
| chr2:36924862
|
G | C | 4 | a0001c0001t0146g0249a0001c0001t0147g0250a0001c0001t0148g0248others(1): Show | 4 | HG02970.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.338+243C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36924862 | ||||||
| chr2:36924876
|
G | T | 12 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.338+229C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36924876 | ||||||
| chr2:36924946
|
C | T | 1 | a0001c0001t0177g0089 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.338+159G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36924946 | ||||||
| chr2:36924995
|
G | A | 75 | a0001c0001t0003g0020a0001c0001t0003g0030a0001c0001t0003g0033others(72): Show | 75 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.338+110C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36924995 | ||||||
| chr2:36925018
|
T | C | 1 | a0001c0001t0048g0195 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.338+87A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36925018 | ||||||
| chr2:36925028
|
C | T | 4 | a0001c0001t0001g0003a0001c0001t0002g0004a0001c0001t0021g0002others(1): Show | 4 | HG00408.hp1 HG00558.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.338+77G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 2/17 | chr2 | 36925028 | ||||||
| chr2:36925229
|
A | C | 52 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0007g0197others(49): Show | 52 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.235-21T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36925229 | ||||||
| chr2:36925282
|
T | C | 52 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0007g0197others(49): Show | 52 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.235-74A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36925282 | ||||||
| chr2:36925309
|
A | C | 2 | a0001c0001t0033g0286a0001c0001t0131g0285 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.235-101T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36925309 | ||||||
| chr2:36925434
|
A | G | 1 | a0003c0006t0128g0271 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.235-226T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36925434 | ||||||
| chr2:36925756
|
G | C | 132 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(129): Show | 132 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.235-548C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36925756 | ||||||
| chr2:36925824
|
A | C | 12 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0017g0240others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.235-616T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36925824 | ||||||
| chr2:36925977
|
T | G | 1 | a0001c0001t0090g0127 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.235-769A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36925977 | ||||||
| chr2:36926106
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.235-898G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36926106 | ||||||
| chr2:36926389
|
C | T | 13 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.235-1181G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36926389 | ||||||
| chr2:36926583
|
T | C | 1 | a0002c0002t0066g0220 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.235-1375A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36926583 | ||||||
| chr2:36926753
|
G | C | 4 | a0001c0001t0079g0236a0001c0001t0080g0235a0001c0001t0081g0233others(1): Show | 4 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-1545C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36926753 | ||||||
| chr2:36926772
|
A | G | 16 | a0001c0001t0002g0123a0001c0001t0002g0129a0001c0001t0002g0158others(13): Show | 16 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.235-1564T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36926772 | ||||||
| chr2:36926986
|
T | C | 1 | a0001c0001t0137g0259 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.235-1778A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36926986 | ||||||
| chr2:36927026
|
A | T | 5 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201others(2): Show | 5 | HG01891.hp1 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.235-1818T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927026 | ||||||
| chr2:36927041
|
T | G | 1 | a0001c0001t0067g0092 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.235-1833A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927041 | ||||||
| chr2:36927080
|
C | T | 2 | a0001c0001t0001g0176a0005c0007t0001g0167 | 2 | HG01934.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.235-1872G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927080 | ||||||
| chr2:36927282
|
T | A | 207 | a0001c0001t0001g0200a0001c0001t0002g0123a0001c0001t0002g0129others(204): Show | 207 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.235-2074A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927282 | ||||||
| chr2:36927315
|
CTGTGCAA | C | 16 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(13): Show | 16 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.235-2114_235-2108d others(9): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927315 | ||||||
| chr2:36927325
|
T | C | 35 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(32): Show | 35 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.235-2117A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927325 | ||||||
| chr2:36927381
|
T | C | 12 | a0001c0001t0001g0099a0001c0001t0001g0137a0001c0001t0001g0173others(9): Show | 12 | HG00280.hp2 HG00735.hp1 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.235-2173A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927381 | ||||||
| chr2:36927476
|
T | C | 1 | a0001c0001t0002g0004 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.235-2268A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927476 | ||||||
| chr2:36927524
|
A | AG | 51 | a0001c0001t0001g0003a0001c0001t0001g0107a0001c0001t0001g0124others(48): Show | 51 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.235-2317dupC | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927524 | ||||||
| chr2:36927524
|
A | AGG | 40 | a0001c0001t0001g0118a0001c0001t0002g0145a0001c0001t0002g0160others(37): Show | 40 | HG00597.hp1 HG00639.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.235-2318_235-2317d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927524 | ||||||
| chr2:36927524
|
A | AGGG | 28 | a0001c0001t0003g0113a0001c0001t0005g0023a0001c0001t0005g0065others(25): Show | 28 | HG00621.hp1 HG00642.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.235-2319_235-2317d others(5): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927524 | ||||||
| chr2:36927524
|
AG | A | 46 | a0001c0001t0001g0174a0001c0001t0001g0180a0001c0001t0002g0129others(43): Show | 46 | HG00323.hp2 HG00597.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.235-2317delC | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927524 | ||||||
| chr2:36927524
|
AGG | A | 17 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(14): Show | 17 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.235-2318_235-2317d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927524 | ||||||
| chr2:36927526
|
G | T | 1 | a0001c0001t0037g0072 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.235-2318C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927526 | ||||||
| chr2:36927528
|
G | T | 1 | a0001c0001t0091g0122 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.235-2320C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927528 | ||||||
| chr2:36927536
|
G | T | 9 | a0001c0001t0010g0290a0001c0001t0010g0291a0001c0001t0010g0292others(6): Show | 9 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.235-2328C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927536 | ||||||
| chr2:36927597
|
G | A | 5 | a0001c0001t0030g0237a0001c0001t0033g0283a0001c0001t0033g0286others(2): Show | 5 | HG01243.hp2 HG02572.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.235-2389C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927597 | ||||||
| chr2:36927723
|
A | G | 3 | a0001c0001t0003g0033a0001c0001t0189g0054a0001c0001t0193g0055 | 3 | HG00099.hp1 HG01255.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.235-2515T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927723 | ||||||
| chr2:36927838
|
T | C | 4 | a0001c0001t0012g0279a0001c0001t0012g0280a0001c0001t0035g0282others(1): Show | 4 | HG01433.hp2 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-2630A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927838 | ||||||
| chr2:36927870
|
T | C | 7 | a0001c0001t0010g0290a0001c0001t0010g0291a0001c0001t0010g0292others(4): Show | 7 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.235-2662A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927870 | ||||||
| chr2:36927875
|
T | C | 4 | a0001c0001t0034g0256a0001c0001t0034g0264a0001c0001t0052g0261others(1): Show | 4 | HG01106.hp1 HG03540.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-2667A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927875 | ||||||
| chr2:36927911
|
G | T | 1 | a0003c0006t0128g0271 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.235-2703C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927911 | ||||||
| chr2:36927920
|
G | A | 1 | a0001c0001t0076g0219 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.235-2712C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36927920 | ||||||
| chr2:36928097
|
T | A | 1 | a0001c0001t0003g0113 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.235-2889A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928097 | ||||||
| chr2:36928097
|
T | G | 1 | a0001c0001t0142g0266 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.235-2889A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928097 | ||||||
| chr2:36928106
|
G | C | 116 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(113): Show | 116 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.235-2898C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928106 | ||||||
| chr2:36928133
|
T | TA | 7 | a0001c0001t0007g0198a0001c0001t0011g0096a0001c0001t0011g0097others(4): Show | 7 | HG02056.hp1 HG02071.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.235-2926dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928133 | ||||||
| chr2:36928172
|
G | A | 32 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(29): Show | 32 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.235-2964C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928172 | ||||||
| chr2:36928227
|
A | C | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.235-3019T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928227 | ||||||
| chr2:36928228
|
G | C | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.235-3020C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928228 | ||||||
| chr2:36928274
|
T | C | 5 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0002g0138others(2): Show | 5 | NA18943.hp2 NA18954.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.235-3066A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928274 | ||||||
| chr2:36928310
|
A | C | 1 | a0001c0001t0035g0282 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.235-3102T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928310 | ||||||
| chr2:36928685
|
C | T | 3 | a0001c0001t0020g0238a0001c0001t0020g0239a0001c0001t0063g0203 | 3 | HG03579.hp1 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.235-3477G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928685 | ||||||
| chr2:36928745
|
C | T | 3 | a0001c0001t0074g0217a0001c0001t0075g0218a0001c0001t0076g0219 | 3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.235-3537G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928745 | ||||||
| chr2:36928805
|
C | T | 1 | a0001c0001t0003g0030 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.235-3597G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928805 | ||||||
| chr2:36928806
|
G | A | 12 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0017g0240others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.235-3598C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928806 | ||||||
| chr2:36928831
|
C | T | 1 | a0001c0001t0088g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.235-3623G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928831 | ||||||
| chr2:36928856
|
C | G | 32 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(29): Show | 32 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.235-3648G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928856 | ||||||
| chr2:36928931
|
G | C | 1 | a0001c0001t0096g0111 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.235-3723C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928931 | ||||||
| chr2:36928947
|
C | CA | 19 | a0001c0001t0003g0033a0001c0001t0003g0113a0001c0001t0022g0108others(16): Show | 19 | HG00673.hp2 HG00738.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.235-3740dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928947 | ||||||
| chr2:36928947
|
CA | C | 35 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(32): Show | 35 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.235-3740delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36928947 | ||||||
| chr2:36929048
|
C | T | 35 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(32): Show | 35 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.235-3840G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36929048 | ||||||
| chr2:36929074
|
A | G | 1 | a0001c0001t0096g0111 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.235-3866T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36929074 | ||||||
| chr2:36929095
|
T | A | 4 | a0001c0001t0146g0249a0001c0001t0147g0250a0001c0001t0148g0248others(1): Show | 4 | HG02970.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-3887A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36929095 | ||||||
| chr2:36929118
|
G | A | 3 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201 | 3 | HG01891.hp1 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.235-3910C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36929118 | ||||||
| chr2:36929183
|
T | C | 1 | a0001c0001t0193g0055 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.235-3975A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36929183 | ||||||
| chr2:36929415
|
G | A | 1 | a0001c0001t0051g0001 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.235-4207C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36929415 | ||||||
| chr2:36929477
|
A | T | 7 | a0001c0001t0049g0296a0001c0001t0049g0299a0001c0001t0050g0295others(4): Show | 7 | HG01243.hp1 HG01496.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.235-4269T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36929477 | ||||||
| chr2:36929483
|
G | C | 1 | a0001c0001t0031g0045 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.235-4275C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36929483 | ||||||
| chr2:36929506
|
T | G | 1 | a0002c0002t0077g0226 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.235-4298A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36929506 | ||||||
| chr2:36929738
|
C | A | 1 | a0001c0001t0036g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.235-4530G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36929738 | ||||||
| chr2:36929790
|
T | C | 22 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(19): Show | 22 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.235-4582A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36929790 | ||||||
| chr2:36929824
|
C | T | 2 | a0001c0001t0030g0289a0001c0001t0114g0288 | 2 | HG02615.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.235-4616G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36929824 | ||||||
| chr2:36930000
|
T | A | 4 | a0001c0001t0034g0256a0001c0001t0034g0264a0001c0001t0052g0261others(1): Show | 4 | HG01106.hp1 HG03540.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-4792A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36930000 | ||||||
| chr2:36930251
|
A | G | 1 | a0001c0001t0134g0041 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.235-5043T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36930251 | ||||||
| chr2:36930431
|
C | A | 1 | a0001c0001t0001g0180 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.235-5223G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36930431 | ||||||
| chr2:36930529
|
C | A | 21 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201others(18): Show | 21 | HG00323.hp2 HG00642.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.235-5321G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36930529 | ||||||
| chr2:36930787
|
C | T | 1 | a0003c0006t0128g0271 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.235-5579G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36930787 | ||||||
| chr2:36930979
|
G | C | 7 | a0001c0001t0010g0290a0001c0001t0010g0291a0001c0001t0010g0292others(4): Show | 7 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.235-5771C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36930979 | ||||||
| chr2:36930984
|
G | C | 1 | a0003c0006t0128g0271 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.235-5776C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36930984 | ||||||
| chr2:36931011
|
T | C | 1 | a0001c0001t0054g0275 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.235-5803A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36931011 | ||||||
| chr2:36931024
|
T | C | 115 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(112): Show | 115 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.235-5816A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36931024 | ||||||
| chr2:36931030
|
C | CA | 12 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0017g0240others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.235-5823dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36931030 | ||||||
| chr2:36931200
|
C | T | 4 | a0001c0001t0079g0236a0001c0001t0080g0235a0001c0001t0081g0233others(1): Show | 4 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-5992G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36931200 | ||||||
| chr2:36931241
|
G | T | 161 | a0001c0001t0003g0020a0001c0001t0003g0030a0001c0001t0003g0033others(158): Show | 161 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.235-6033C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36931241 | ||||||
| chr2:36931450
|
A | G | 1 | a0001c0001t0122g0044 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.235-6242T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36931450 | ||||||
| chr2:36931599
|
G | C | 1 | a0001c0001t0124g0260 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.235-6391C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36931599 | ||||||
| chr2:36931673
|
A | G | 1 | a0001c0001t0090g0127 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.235-6465T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36931673 | ||||||
| chr2:36931851
|
C | T | 4 | a0001c0001t0011g0096a0001c0001t0011g0097a0001c0001t0011g0098others(1): Show | 4 | HG02071.hp2 HG02965.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-6643G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36931851 | ||||||
| chr2:36931873
|
G | T | 1 | a0001c0001t0064g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.235-6665C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36931873 | ||||||
| chr2:36932097
|
T | A | 3 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201 | 3 | HG01891.hp1 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.235-6889A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36932097 | ||||||
| chr2:36932165
|
C | A | 12 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.235-6957G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36932165 | ||||||
| chr2:36932175
|
G | T | 2 | a0001c0001t0042g0263a0001c0001t0133g0265 | 2 | HG02040.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.235-6967C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36932175 | ||||||
| chr2:36932232
|
G | A | 1 | a0001c0001t0054g0275 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.235-7024C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36932232 | ||||||
| chr2:36932241
|
A | G | 35 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(32): Show | 35 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.235-7033T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36932241 | ||||||
| chr2:36932247
|
C | T | 1 | a0001c0001t0031g0042 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.235-7039G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36932247 | ||||||
| chr2:36932647
|
G | A | 1 | a0001c0001t0073g0210 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.235-7439C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36932647 | ||||||
| chr2:36932651
|
G | C | 16 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(13): Show | 16 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.235-7443C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36932651 | ||||||
| chr2:36932656
|
A | G | 201 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(198): Show | 201 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.235-7448T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36932656 | ||||||
| chr2:36932913
|
T | C | 4 | a0001c0001t0079g0236a0001c0001t0080g0235a0001c0001t0081g0233others(1): Show | 4 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-7705A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36932913 | ||||||
| chr2:36933045
|
AT | A | 12 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0017g0240others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.235-7838delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36933045 | ||||||
| chr2:36933054
|
T | A | 4 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0150g0208others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-7846A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36933054 | ||||||
| chr2:36933059
|
T | TAC | 96 | a0001c0001t0001g0099a0001c0001t0001g0173a0001c0001t0001g0200others(93): Show | 96 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.235-7853_235-7852d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36933059 | ||||||
| chr2:36933059
|
T | TACAC | 44 | a0001c0001t0003g0030a0001c0001t0005g0023a0001c0001t0005g0065others(41): Show | 44 | HG00323.hp2 HG00621.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.235-7855_235-7852d others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36933059 | ||||||
| chr2:36933059
|
TAC | T | 4 | a0001c0001t0068g0262a0001c0001t0146g0249a0001c0001t0147g0250others(1): Show | 4 | HG01106.hp2 HG02970.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-7853_235-7852d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36933059 | ||||||
| chr2:36933085
|
CAT | C | 15 | a0001c0001t0016g0230a0001c0001t0018g0222a0001c0001t0018g0228others(12): Show | 15 | HG00597.hp2 HG01884.hp2 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.235-7879_235-7878d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36933085 | ||||||
| chr2:36933087
|
T | C | 7 | a0001c0001t0016g0229a0001c0001t0020g0238a0001c0001t0020g0239others(4): Show | 7 | HG00438.hp2 HG02040.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.235-7879A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36933087 | ||||||
| chr2:36933185
|
T | A | 12 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.235-7977A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36933185 | ||||||
| chr2:36933191
|
T | C | 1 | a0001c0001t0001g0200 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.235-7983A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36933191 | ||||||
| chr2:36933378
|
C | A | 1 | a0002c0002t0066g0220 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.235-8170G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36933378 | ||||||
| chr2:36933630
|
G | T | 1 | a0001c0001t0003g0030 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.235-8422C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36933630 | ||||||
| chr2:36933657
|
T | A | 75 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(72): Show | 75 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.235-8449A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36933657 | ||||||
| chr2:36933883
|
G | A | 16 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(13): Show | 16 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.235-8675C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36933883 | ||||||
| chr2:36933927
|
C | G | 5 | a0001c0001t0030g0237a0001c0001t0033g0283a0001c0001t0033g0286others(2): Show | 5 | HG01243.hp2 HG02572.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.235-8719G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36933927 | ||||||
| chr2:36934025
|
C | T | 1 | a0001c0001t0064g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.235-8817G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36934025 | ||||||
| chr2:36934111
|
A | G | 6 | a0001c0001t0039g0214a0001c0001t0039g0215a0001c0001t0152g0211others(3): Show | 6 | HG02559.hp2 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.235-8903T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36934111 | ||||||
| chr2:36934343
|
T | C | 4 | a0001c0001t0146g0249a0001c0001t0147g0250a0001c0001t0148g0248others(1): Show | 4 | HG02970.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-9135A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36934343 | ||||||
| chr2:36934408
|
T | G | 6 | a0001c0001t0010g0290a0001c0001t0010g0291a0001c0001t0010g0292others(3): Show | 6 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.235-9200A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36934408 | ||||||
| chr2:36934480
|
A | C | 4 | a0001c0001t0002g0123a0001c0001t0002g0129a0001c0001t0002g0158others(1): Show | 4 | HG02055.hp2 HG02145.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-9272T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36934480 | ||||||
| chr2:36934480
|
A | G | 1 | a0001c0001t0098g0150 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.235-9272T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36934480 | ||||||
| chr2:36934567
|
G | A | 1 | a0001c0001t0120g0267 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.235-9359C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36934567 | ||||||
| chr2:36934570
|
T | C | 1 | a0001c0001t0112g0168 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.235-9362A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36934570 | ||||||
| chr2:36934661
|
T | G | 1 | a0001c0001t0064g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.235-9453A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36934661 | ||||||
| chr2:36934695
|
G | A | 1 | a0001c0001t0015g0025 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.235-9487C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36934695 | ||||||
| chr2:36934708
|
C | T | 1 | a0001c0001t0008g0047 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.235-9500G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36934708 | ||||||
| chr2:36934789
|
C | T | 1 | a0001c0001t0023g0140 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.235-9581G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36934789 | ||||||
| chr2:36934805
|
G | A | 5 | a0001c0001t0010g0290a0001c0001t0010g0291a0001c0001t0146g0249others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.235-9597C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36934805 | ||||||
| chr2:36935149
|
C | T | 1 | a0001c0001t0149g0247 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.235-9941G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36935149 | ||||||
| chr2:36935186
|
C | T | 1 | a0001c0001t0092g0157 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.235-9978G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36935186 | ||||||
| chr2:36935289
|
G | C | 1 | a0002c0002t0066g0220 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.235-10081C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36935289 | ||||||
| chr2:36935463
|
AT | A | 3 | a0001c0001t0020g0238a0001c0001t0020g0239a0001c0001t0063g0203 | 3 | HG03579.hp1 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.235-10256delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36935463 | ||||||
| chr2:36935558
|
A | C | 22 | a0001c0001t0001g0118a0001c0001t0007g0197a0001c0001t0007g0198others(19): Show | 22 | HG00323.hp2 HG00642.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.235-10350T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36935558 | ||||||
| chr2:36935752
|
C | G | 3 | a0001c0001t0074g0217a0001c0001t0075g0218a0001c0001t0076g0219 | 3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.235-10544G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36935752 | ||||||
| chr2:36935820
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.235-10612C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36935820 | ||||||
| chr2:36935832
|
T | C | 25 | a0001c0001t0011g0096a0001c0001t0011g0097a0001c0001t0011g0098others(22): Show | 25 | HG00639.hp2 HG00673.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.235-10624A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36935832 | ||||||
| chr2:36935948
|
T | G | 1 | a0001c0001t0054g0275 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.235-10740A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36935948 | ||||||
| chr2:36936233
|
C | T | 34 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(31): Show | 34 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.235-11025G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36936233 | ||||||
| chr2:36936244
|
T | C | 1 | a0001c0001t0054g0275 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.235-11036A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36936244 | ||||||
| chr2:36936272
|
G | A | 1 | a0001c0001t0190g0063 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.235-11064C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36936272 | ||||||
| chr2:36936405
|
A | T | 1 | a0001c0001t0030g0289 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.235-11197T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36936405 | ||||||
| chr2:36936446
|
G | A | 2 | a0001c0001t0001g0132a0001c0001t0001g0149 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.235-11238C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36936446 | ||||||
| chr2:36936524
|
T | C | 1 | a0001c0001t0125g0277 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.235-11316A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36936524 | ||||||
| chr2:36936553
|
G | T | 16 | a0001c0001t0008g0047a0001c0001t0031g0042a0001c0001t0031g0045others(13): Show | 16 | HG00323.hp2 HG00642.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.235-11345C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36936553 | ||||||
| chr2:36936634
|
A | G | 2 | a0001c0001t0174g0014a0001c0001t0180g0031 | 2 | HG01070.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.235-11426T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36936634 | ||||||
| chr2:36936724
|
G | A | 4 | a0001c0001t0034g0256a0001c0001t0034g0264a0001c0001t0052g0261others(1): Show | 4 | HG01106.hp1 HG03540.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-11516C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36936724 | ||||||
| chr2:36936901
|
T | G | 13 | a0001c0001t0001g0076a0001c0001t0001g0107a0001c0001t0001g0174others(10): Show | 13 | HG01071.hp1 HG01175.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.235-11693A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36936901 | ||||||
| chr2:36937040
|
G | A | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.235-11832C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36937040 | ||||||
| chr2:36937041
|
C | A | 7 | a0001c0001t0049g0296a0001c0001t0049g0299a0001c0001t0050g0295others(4): Show | 7 | HG01243.hp1 HG01496.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.235-11833G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36937041 | ||||||
| chr2:36937100
|
T | C | 13 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.235-11892A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36937100 | ||||||
| chr2:36937144
|
G | A | 1 | a0001c0001t0035g0282 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.235-11936C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36937144 | ||||||
| chr2:36937153
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.235-11945C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36937153 | ||||||
| chr2:36937342
|
CA | C | 242 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.235-12135delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36937342 | ||||||
| chr2:36937344
|
A | G | 1 | a0001c0001t0057g0245 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.235-12136T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36937344 | ||||||
| chr2:36937357
|
AAG | A | 30 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(27): Show | 30 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.235-12151_235-1215 others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36937357 | ||||||
| chr2:36937526
|
G | A | 2 | a0001c0001t0014g0094a0001c0001t0036g0095 | 2 | HG02602.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.235-12318C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36937526 | ||||||
| chr2:36937600
|
T | G | 16 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(13): Show | 16 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.235-12392A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36937600 | ||||||
| chr2:36937697
|
A | G | 4 | a0001c0001t0146g0249a0001c0001t0147g0250a0001c0001t0148g0248others(1): Show | 4 | HG02970.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-12489T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36937697 | ||||||
| chr2:36937714
|
T | G | 157 | a0001c0001t0001g0184a0001c0001t0001g0200a0001c0001t0002g0123others(154): Show | 157 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.235-12506A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36937714 | ||||||
| chr2:36937768
|
C | G | 151 | a0001c0001t0003g0020a0001c0001t0003g0030a0001c0001t0003g0033others(148): Show | 151 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.235-12560G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36937768 | ||||||
| chr2:36937825
|
C | T | 12 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.235-12617G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36937825 | ||||||
| chr2:36938276
|
A | C | 17 | a0001c0001t0008g0047a0001c0001t0031g0042a0001c0001t0031g0045others(14): Show | 17 | HG00323.hp2 HG00642.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.235-13068T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36938276 | ||||||
| chr2:36938370
|
G | T | 1 | a0001c0001t0064g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.235-13162C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36938370 | ||||||
| chr2:36938429
|
T | TA | 9 | a0001c0001t0029g0155a0001c0001t0029g0159a0001c0001t0038g0212others(6): Show | 9 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.235-13222dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36938429 | ||||||
| chr2:36938429
|
TA | T | 9 | a0001c0001t0001g0152a0001c0001t0032g0067a0001c0001t0052g0261others(6): Show | 9 | HG01516.hp1 HG02015.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.235-13222delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36938429 | ||||||
| chr2:36938440
|
A | G | 12 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0017g0240others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.235-13232T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36938440 | ||||||
| chr2:36938622
|
C | T | 34 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(31): Show | 34 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.235-13414G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36938622 | ||||||
| chr2:36938652
|
T | G | 1 | a0001c0001t0026g0120 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.235-13444A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36938652 | ||||||
| chr2:36938703
|
A | G | 4 | a0001c0001t0002g0123a0001c0001t0002g0129a0001c0001t0002g0158others(1): Show | 4 | HG02055.hp2 HG02145.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-13495T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36938703 | ||||||
| chr2:36938828
|
T | C | 2 | a0001c0001t0038g0212a0001c0001t0038g0213 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.235-13620A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36938828 | ||||||
| chr2:36938981
|
T | A | 12 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0017g0240others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.235-13773A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36938981 | ||||||
| chr2:36939152
|
C | T | 1 | a0001c0001t0017g0240 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.235-13944G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36939152 | ||||||
| chr2:36939178
|
G | A | 19 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(16): Show | 19 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.235-13970C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36939178 | ||||||
| chr2:36939218
|
G | A | 3 | a0001c0001t0009g0147a0001c0001t0018g0222a0001c0001t0018g0228 | 3 | HG00323.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.235-14010C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36939218 | ||||||
| chr2:36939223
|
G | A | 1 | a0001c0001t0140g0257 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.235-14015C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36939223 | ||||||
| chr2:36939262
|
G | A | 14 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(11): Show | 14 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.235-14054C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36939262 | ||||||
| chr2:36939270
|
G | A | 1 | a0001c0001t0061g0252 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.235-14062C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36939270 | ||||||
| chr2:36939289
|
G | A | 1 | a0001c0001t0013g0027 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.235-14081C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36939289 | ||||||
| chr2:36939332
|
C | A | 16 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(13): Show | 16 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.235-14124G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36939332 | ||||||
| chr2:36939377
|
C | T | 1 | a0001c0001t0076g0219 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.235-14169G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36939377 | ||||||
| chr2:36939445
|
T | C | 1 | a0001c0001t0035g0282 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.235-14237A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36939445 | ||||||
| chr2:36939543
|
T | C | 1 | a0001c0001t0002g0171 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.235-14335A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36939543 | ||||||
| chr2:36939560
|
T | A | 1 | a0001c0001t0089g0104 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.235-14352A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36939560 | ||||||
| chr2:36939774
|
G | C | 3 | a0001c0001t0036g0070a0001c0001t0144g0046a0001c0001t0183g0073 | 3 | HG00642.hp1 HG03834.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.235-14566C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36939774 | ||||||
| chr2:36939846
|
A | G | 33 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(30): Show | 33 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.235-14638T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36939846 | ||||||
| chr2:36940048
|
T | C | 116 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(113): Show | 116 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.235-14840A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36940048 | ||||||
| chr2:36940120
|
G | A | 1 | a0002c0002t0066g0220 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.235-14912C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36940120 | ||||||
| chr2:36940208
|
A | G | 7 | a0001c0001t0001g0124a0001c0001t0001g0134a0001c0001t0001g0143others(4): Show | 7 | HG00621.hp2 HG02080.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.235-15000T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36940208 | ||||||
| chr2:36940228
|
AAAGT | A | 6 | a0001c0001t0002g0123a0001c0001t0002g0129a0001c0001t0002g0158others(3): Show | 6 | HG01361.hp2 HG02055.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.235-15024_235-1502 others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36940228 | ||||||
| chr2:36940299
|
T | C | 16 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(13): Show | 16 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.235-15091A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36940299 | ||||||
| chr2:36940331
|
G | T | 1 | a0001c0001t0167g0007 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.235-15123C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36940331 | ||||||
| chr2:36940354
|
A | G | 33 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(30): Show | 33 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.235-15146T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36940354 | ||||||
| chr2:36940502
|
C | A | 4 | a0001c0001t0146g0249a0001c0001t0147g0250a0001c0001t0148g0248others(1): Show | 4 | HG02970.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-15294G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36940502 | ||||||
| chr2:36940603
|
G | A | 19 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(16): Show | 19 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.235-15395C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36940603 | ||||||
| chr2:36940805
|
G | C | 29 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(26): Show | 29 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.235-15597C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36940805 | ||||||
| chr2:36940823
|
C | G | 1 | a0001c0001t0065g0224 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.235-15615G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36940823 | ||||||
| chr2:36940836
|
C | CA | 58 | a0001c0001t0001g0106a0001c0001t0001g0149a0001c0001t0001g0163others(55): Show | 58 | HG00099.hp1 HG00621.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.235-15629dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36940836 | ||||||
| chr2:36940836
|
CA | C | 8 | a0001c0001t0010g0290a0001c0001t0015g0025a0001c0001t0026g0120others(5): Show | 8 | HG01243.hp2 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.235-15629delT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36940836 | ||||||
| chr2:36940836
|
CAAAAAAA others(4): Show |
C | 33 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(30): Show | 33 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.235-15639_235-1562 others(15): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36940836 | ||||||
| chr2:36941098
|
T | C | 2 | a0001c0001t0063g0203a0001c0001t0064g0202 | 2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.235-15890A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36941098 | ||||||
| chr2:36941120
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.235-15912G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36941120 | ||||||
| chr2:36941321
|
T | C | 1 | a0001c0001t0001g0076 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.235-16113A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36941321 | ||||||
| chr2:36941581
|
T | G | 1 | a0001c0001t0007g0197 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.235-16373A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36941581 | ||||||
| chr2:36941716
|
A | AT | 6 | a0001c0001t0036g0095a0001c0001t0043g0066a0001c0001t0051g0001others(3): Show | 6 | HG00621.hp2 HG02602.hp1 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.235-16509dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36941716 | ||||||
| chr2:36941716
|
A | ATTTTTTT others(5): Show |
2 | a0001c0001t0074g0217a0001c0001t0076g0219 | 2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.235-16520_235-1650 others(16): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36941716 | ||||||
| chr2:36941716
|
A | ATTTTTTT others(6): Show |
10 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(7): Show | 10 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.235-16521_235-1650 others(17): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36941716 | ||||||
| chr2:36941716
|
A | ATTTTTTT others(7): Show |
3 | a0001c0001t0063g0203a0001c0001t0154g0209a0001c0005t0153g0216 | 3 | HG02886.hp1 HG03579.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.235-16522_235-1650 others(18): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36941716 | ||||||
| chr2:36941716
|
A | ATTTTTTT others(8): Show |
1 | a0001c0001t0064g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.235-16523_235-1650 others(19): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36941716 | ||||||
| chr2:36941716
|
ATTTT | A | 16 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(13): Show | 16 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.235-16512_235-1650 others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36941716 | ||||||
| chr2:36941804
|
C | T | 1 | a0001c0001t0194g0021 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.235-16596G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36941804 | ||||||
| chr2:36941906
|
G | A | 184 | a0001c0001t0003g0020a0001c0001t0003g0030a0001c0001t0003g0033others(181): Show | 184 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.235-16698C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36941906 | ||||||
| chr2:36942003
|
T | C | 1 | a0001c0001t0069g0093 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.235-16795A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36942003 | ||||||
| chr2:36942325
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.235-17117A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36942325 | ||||||
| chr2:36942328
|
T | C | 13 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.235-17120A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36942328 | ||||||
| chr2:36942446
|
T | C | 1 | a0001c0001t0063g0203 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.235-17238A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36942446 | ||||||
| chr2:36942593
|
T | C | 1 | a0001c0001t0075g0218 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.235-17385A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36942593 | ||||||
| chr2:36942600
|
T | G | 1 | a0001c0001t0002g0126 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.235-17392A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36942600 | ||||||
| chr2:36942629
|
T | C | 5 | a0001c0001t0039g0214a0001c0001t0039g0215a0001c0001t0155g0207others(2): Show | 5 | HG02886.hp1 HG02895.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.235-17421A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36942629 | ||||||
| chr2:36942826
|
G | C | 2 | a0001c0001t0063g0203a0001c0001t0064g0202 | 2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.235-17618C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36942826 | ||||||
| chr2:36942898
|
G | GT | 118 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(115): Show | 118 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.235-17691dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36942898 | ||||||
| chr2:36942915
|
C | T | 2 | a0001c0001t0029g0155a0001c0001t0029g0159 | 2 | HG01361.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.235-17707G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36942915 | ||||||
| chr2:36943262
|
G | C | 1 | a0001c0001t0008g0047 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.235-18054C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36943262 | ||||||
| chr2:36943386
|
CTA | C | 17 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(14): Show | 17 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.235-18180_235-1817 others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36943386 | ||||||
| chr2:36943457
|
A | G | 1 | a0001c0001t0120g0267 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.235-18249T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36943457 | ||||||
| chr2:36943533
|
A | T | 4 | a0001c0001t0001g0003a0001c0001t0002g0004a0001c0001t0021g0002others(1): Show | 4 | HG00408.hp1 HG00558.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-18325T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36943533 | ||||||
| chr2:36943557
|
C | G | 1 | a0002c0002t0066g0220 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.235-18349G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36943557 | ||||||
| chr2:36943579
|
A | C | 17 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(14): Show | 17 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.235-18371T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36943579 | ||||||
| chr2:36943595
|
G | C | 6 | a0001c0001t0010g0290a0001c0001t0010g0291a0001c0001t0010g0292others(3): Show | 6 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.235-18387C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36943595 | ||||||
| chr2:36944038
|
T | G | 1 | a0001c0001t0088g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.235-18830A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36944038 | ||||||
| chr2:36944088
|
C | A | 2 | a0001c0001t0067g0092a0001c0001t0069g0093 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.235-18880G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36944088 | ||||||
| chr2:36944124
|
AAAAC | A | 4 | a0001c0001t0146g0249a0001c0001t0147g0250a0001c0001t0148g0248others(1): Show | 4 | HG02970.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-18920_235-1891 others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36944124 | ||||||
| chr2:36944154
|
A | G | 1 | a0001c0001t0087g0133 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.235-18946T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36944154 | ||||||
| chr2:36944165
|
C | A | 1 | a0001c0001t0001g0076 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.235-18957G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36944165 | ||||||
| chr2:36944244
|
G | A | 1 | a0001c0001t0058g0251 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.235-19036C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36944244 | ||||||
| chr2:36944254
|
C | T | 3 | a0001c0001t0080g0235a0001c0001t0081g0233a0001c0001t0083g0234 | 3 | HG00738.hp2 HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.235-19046G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36944254 | ||||||
| chr2:36944404
|
T | C | 55 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201others(52): Show | 55 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.235-19196A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36944404 | ||||||
| chr2:36944495
|
C | A | 31 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(28): Show | 31 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.235-19287G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36944495 | ||||||
| chr2:36945147
|
T | C | 5 | a0001c0001t0030g0237a0001c0001t0033g0283a0001c0001t0033g0286others(2): Show | 5 | HG01243.hp2 HG02572.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.235-19939A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36945147 | ||||||
| chr2:36945357
|
C | T | 7 | a0001c0001t0001g0132a0001c0001t0001g0149a0001c0001t0001g0165others(4): Show | 7 | HG01346.hp2 HG02698.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.235-20149G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36945357 | ||||||
| chr2:36945388
|
T | C | 149 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(146): Show | 149 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.235-20180A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36945388 | ||||||
| chr2:36945482
|
G | A | 116 | a0001c0001t0003g0020a0001c0001t0003g0030a0001c0001t0003g0033others(113): Show | 116 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.235-20274C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36945482 | ||||||
| chr2:36945549
|
C | T | 82 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(79): Show | 82 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.235-20341G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36945549 | ||||||
| chr2:36945602
|
T | G | 2 | a0001c0001t0016g0229a0001c0001t0016g0230 | 2 | HG02040.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.235-20394A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36945602 | ||||||
| chr2:36945764
|
T | C | 3 | a0001c0001t0011g0096a0001c0001t0011g0097a0001c0001t0011g0098 | 3 | HG02071.hp2 NA18972.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.234+20466A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36945764 | ||||||
| chr2:36945807
|
C | T | 1 | a0001c0001t0107g0148 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.234+20423G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36945807 | ||||||
| chr2:36945889
|
T | C | 139 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(136): Show | 139 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.234+20341A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36945889 | ||||||
| chr2:36946152
|
TAAATATT others(64): Show |
T | 5 | a0001c0001t0039g0214a0001c0001t0039g0215a0001c0001t0155g0207others(2): Show | 5 | HG02886.hp1 HG02895.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.234+20007_234+2007 others(75): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36946152 | ||||||
| chr2:36946578
|
C | T | 16 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(13): Show | 16 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.234+19652G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36946578 | ||||||
| chr2:36947160
|
T | C | 1 | a0001c0001t0001g0076 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.234+19070A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36947160 | ||||||
| chr2:36947410
|
T | C | 2 | a0001c0001t0045g0082a0001c0001t0113g0146 | 2 | HG03490.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.234+18820A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36947410 | ||||||
| chr2:36947540
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.234+18690G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36947540 | ||||||
| chr2:36947544
|
AACATATA others(8): Show |
A | 1 | a0001c0001t0139g0270 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.234+18671_234+1868 others(19): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36947544 | ||||||
| chr2:36947569
|
T | TTATA | 4 | a0001c0001t0146g0249a0001c0001t0147g0250a0001c0001t0148g0248others(1): Show | 4 | HG02970.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+18657_234+1866 others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36947569 | ||||||
| chr2:36947570
|
T | A | 18 | a0001c0001t0013g0008a0001c0001t0013g0010a0001c0001t0013g0027others(15): Show | 18 | HG00597.hp1 HG01934.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.234+18660A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36947570 | ||||||
| chr2:36947571
|
A | T | 31 | a0001c0001t0013g0008a0001c0001t0013g0010a0001c0001t0013g0027others(28): Show | 31 | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.234+18659T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36947571 | ||||||
| chr2:36947658
|
A | G | 1 | a0001c0001t0180g0031 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.234+18572T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36947658 | ||||||
| chr2:36947854
|
G | T | 1 | a0001c0001t0040g0016 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.234+18376C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36947854 | ||||||
| chr2:36948040
|
T | C | 1 | a0004c0004t0188g0048 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.234+18190A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948040 | ||||||
| chr2:36948081
|
C | CT | 59 | a0001c0001t0001g0076a0001c0001t0001g0106a0001c0001t0001g0107others(56): Show | 59 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.234+18148dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | ||||||
| chr2:36948081
|
C | CTT | 20 | a0001c0001t0001g0003a0001c0001t0001g0099a0001c0001t0001g0156others(17): Show | 20 | HG00408.hp1 HG01123.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.234+18147_234+1814 others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | ||||||
| chr2:36948081
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0058g0251 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.234+18138_234+1814 others(15): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | ||||||
| chr2:36948081
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0007g0201 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.234+18134_234+1814 others(19): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | ||||||
| chr2:36948081
|
C | CTTTTTTT others(11): Show |
1 | a0001c0001t0149g0247 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.234+18131_234+1814 others(22): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | ||||||
| chr2:36948081
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0084g0231 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.234+18130_234+1814 others(23): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | ||||||
| chr2:36948081
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0118g0293 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.234+18129_234+1814 others(24): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | ||||||
| chr2:36948081
|
C | CTTTTTTT others(15): Show |
1 | a0001c0001t0148g0248 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.234+18127_234+1814 others(26): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | ||||||
| chr2:36948081
|
C | CTTTTTTT others(22): Show |
1 | a0001c0001t0082g0232 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.234+18120_234+1814 others(33): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | ||||||
| chr2:36948081
|
C | CTTTTTTT others(27): Show |
1 | a0001c0001t0147g0250 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.234+18115_234+1814 others(38): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | ||||||
| chr2:36948081
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0113g0146 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.234+18136_234+1814 others(17): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | ||||||
| chr2:36948081
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0146g0249 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.234+18134_234+1814 others(19): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | ||||||
| chr2:36948081
|
CTTTTTTT others(10): Show |
C | 8 | a0001c0001t0003g0030a0001c0001t0005g0023a0001c0001t0011g0096others(5): Show | 8 | HG00621.hp1 HG02056.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.234+18132_234+1814 others(21): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | ||||||
| chr2:36948081
|
CTTTTTTT others(11): Show |
C | 124 | a0001c0001t0003g0020a0001c0001t0003g0033a0001c0001t0003g0057others(121): Show | 124 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.234+18131_234+1814 others(22): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | ||||||
| chr2:36948081
|
CTTTTTTT others(12): Show |
C | 20 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(17): Show | 20 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.234+18130_234+1814 others(23): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | ||||||
| chr2:36948081
|
CTTTTTTT others(14): Show |
C | 1 | a0001c0001t0126g0040 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.234+18128_234+1814 others(25): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | ||||||
| chr2:36948081
|
CTTTTTTT others(15): Show |
C | 15 | a0001c0001t0008g0047a0001c0001t0031g0042a0001c0001t0031g0045others(12): Show | 15 | HG00323.hp2 HG00642.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.234+18127_234+1814 others(26): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948081 | ||||||
| chr2:36948119
|
T | G | 1 | a0001c0001t0176g0064 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.234+18111A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948119 | ||||||
| chr2:36948167
|
T | G | 3 | a0001c0001t0074g0217a0001c0001t0075g0218a0001c0001t0076g0219 | 3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.234+18063A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948167 | ||||||
| chr2:36948280
|
T | G | 12 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0017g0240others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.234+17950A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948280 | ||||||
| chr2:36948301
|
T | C | 182 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(179): Show | 182 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.234+17929A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948301 | ||||||
| chr2:36948627
|
T | C | 4 | a0001c0001t0034g0256a0001c0001t0034g0264a0001c0001t0052g0261others(1): Show | 4 | HG01106.hp1 HG03540.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+17603A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948627 | ||||||
| chr2:36948648
|
T | C | 1 | a0001c0001t0132g0258 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.234+17582A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948648 | ||||||
| chr2:36948689
|
T | G | 1 | a0001c0001t0001g0076 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.234+17541A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948689 | ||||||
| chr2:36948820
|
G | C | 13 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.234+17410C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36948820 | ||||||
| chr2:36949067
|
T | A | 1 | a0001c0001t0157g0050 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.234+17163A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36949067 | ||||||
| chr2:36949070
|
G | A | 186 | a0001c0001t0003g0020a0001c0001t0003g0030a0001c0001t0003g0033others(183): Show | 186 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.234+17160C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36949070 | ||||||
| chr2:36949426
|
TAAAC | T | 21 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201others(18): Show | 21 | HG00323.hp2 HG00642.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.234+16800_234+1680 others(8): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36949426 | ||||||
| chr2:36949641
|
G | A | 21 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201others(18): Show | 21 | HG00323.hp2 HG00642.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.234+16589C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36949641 | ||||||
| chr2:36949780
|
T | G | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.234+16450A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36949780 | ||||||
| chr2:36950019
|
A | G | 1 | a0001c0001t0002g0160 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.234+16211T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36950019 | ||||||
| chr2:36950031
|
A | G | 1 | a0001c0001t0078g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.234+16199T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36950031 | ||||||
| chr2:36950096
|
G | A | 1 | a0001c0001t0177g0089 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.234+16134C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36950096 | ||||||
| chr2:36950115
|
A | G | 296 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(293): Show | 296 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.234+16115T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36950115 | ||||||
| chr2:36950212
|
T | G | 1 | a0001c0001t0016g0230 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.234+16018A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36950212 | ||||||
| chr2:36950213
|
G | GT | 59 | a0001c0001t0001g0156a0001c0001t0002g0004a0001c0001t0002g0123others(56): Show | 59 | HG00099.hp1 HG00597.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.234+16016dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36950213 | ||||||
| chr2:36950213
|
G | GTT | 54 | a0001c0001t0003g0020a0001c0001t0003g0033a0001c0001t0003g0057others(51): Show | 54 | HG00408.hp2 HG00597.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.234+16015_234+1601 others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36950213 | ||||||
| chr2:36950213
|
G | GTTT | 20 | a0001c0001t0003g0030a0001c0001t0005g0087a0001c0001t0012g0022others(17): Show | 20 | HG00423.hp1 HG00642.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.234+16014_234+1601 others(7): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36950213 | ||||||
| chr2:36950213
|
G | T | 5 | a0001c0001t0001g0200a0001c0001t0003g0113a0001c0001t0146g0249others(2): Show | 5 | HG02970.hp1 HG02976.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+16017C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36950213 | ||||||
| chr2:36950213
|
GT | G | 21 | a0001c0001t0001g0077a0001c0001t0001g0183a0001c0001t0001g0184others(18): Show | 21 | HG01070.hp1 HG01071.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.234+16016delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36950213 | ||||||
| chr2:36950292
|
C | T | 4 | a0001c0001t0033g0283a0001c0001t0033g0286a0001c0001t0131g0285others(1): Show | 4 | HG02572.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+15938G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36950292 | ||||||
| chr2:36950418
|
G | A | 5 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0002g0138others(2): Show | 5 | NA18943.hp2 NA18954.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+15812C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36950418 | ||||||
| chr2:36950589
|
T | C | 1 | a0001c0001t0036g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.234+15641A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36950589 | ||||||
| chr2:36951112
|
C | T | 152 | a0001c0001t0003g0020a0001c0001t0003g0030a0001c0001t0003g0033others(149): Show | 152 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.234+15118G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36951112 | ||||||
| chr2:36951168
|
A | C | 1 | a0001c0001t0031g0042 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.234+15062T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36951168 | ||||||
| chr2:36951276
|
G | C | 1 | a0001c0001t0001g0076 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.234+14954C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36951276 | ||||||
| chr2:36951480
|
G | C | 31 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(28): Show | 31 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.234+14750C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36951480 | ||||||
| chr2:36951596
|
T | C | 1 | a0001c0001t0106g0128 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.234+14634A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36951596 | ||||||
| chr2:36951728
|
T | C | 51 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201others(48): Show | 51 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.234+14502A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36951728 | ||||||
| chr2:36951906
|
G | C | 21 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(18): Show | 21 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.234+14324C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36951906 | ||||||
| chr2:36951958
|
C | T | 7 | a0001c0001t0049g0296a0001c0001t0049g0299a0001c0001t0050g0295others(4): Show | 7 | HG01243.hp1 HG01496.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.234+14272G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36951958 | ||||||
| chr2:36952063
|
A | G | 1 | a0001c0001t0194g0021 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.234+14167T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36952063 | ||||||
| chr2:36952290
|
G | A | 296 | a0001c0001t0001g0003a0001c0001t0001g0076a0001c0001t0001g0077others(293): Show | 296 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.234+13940C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36952290 | ||||||
| chr2:36952449
|
GAA | G | 51 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201others(48): Show | 51 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.234+13779_234+1378 others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36952449 | ||||||
| chr2:36952534
|
T | C | 1 | a0001c0001t0193g0055 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.234+13696A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36952534 | ||||||
| chr2:36953064
|
C | A | 49 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201others(46): Show | 49 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.234+13166G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36953064 | ||||||
| chr2:36953188
|
A | T | 1 | a0001c0001t0068g0262 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.234+13042T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36953188 | ||||||
| chr2:36953402
|
C | CT | 27 | a0001c0001t0001g0114a0001c0001t0002g0126a0001c0001t0003g0030others(24): Show | 27 | HG01255.hp1 HG01433.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.234+12827dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36953402 | ||||||
| chr2:36953518
|
T | C | 2 | a0001c0001t0014g0094a0001c0001t0036g0095 | 2 | HG02602.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.234+12712A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36953518 | ||||||
| chr2:36953545
|
G | A | 2 | a0001c0001t0048g0195a0001c0001t0048g0196 | 2 | HG02071.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.234+12685C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36953545 | ||||||
| chr2:36954126
|
G | T | 4 | a0001c0001t0079g0236a0001c0001t0080g0235a0001c0001t0081g0233others(1): Show | 4 | HG00738.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+12104C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36954126 | ||||||
| chr2:36954175
|
T | A | 1 | a0001c0001t0193g0055 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.234+12055A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36954175 | ||||||
| chr2:36954236
|
C | T | 1 | a0001c0001t0070g0225 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.234+11994G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36954236 | ||||||
| chr2:36954310
|
A | T | 1 | a0001c0001t0017g0240 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.234+11920T>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36954310 | ||||||
| chr2:36954340
|
G | C | 1 | a0001c0001t0085g0192 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.234+11890C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36954340 | ||||||
| chr2:36954466
|
T | G | 11 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.234+11764A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36954466 | ||||||
| chr2:36954515
|
C | A | 24 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201others(21): Show | 24 | HG00323.hp2 HG00642.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.234+11715G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36954515 | ||||||
| chr2:36954520
|
G | GA | 16 | a0001c0001t0001g0107a0001c0001t0002g0123a0001c0001t0002g0145others(13): Show | 16 | HG00621.hp1 HG00621.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.234+11709dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36954520 | ||||||
| chr2:36954521
|
A | G | 40 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0007g0197others(37): Show | 40 | HG00323.hp2 HG00642.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.234+11709T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36954521 | ||||||
| chr2:36954522
|
A | G | 2 | a0001c0001t0031g0042a0001c0001t0031g0045 | 2 | HG01952.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.234+11708T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36954522 | ||||||
| chr2:36954828
|
G | A | 1 | a0003c0006t0128g0271 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.234+11402C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36954828 | ||||||
| chr2:36955036
|
G | A | 3 | a0001c0001t0012g0279a0001c0001t0012g0280a0001c0001t0143g0278 | 3 | HG01433.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.234+11194C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36955036 | ||||||
| chr2:36955170
|
A | C | 2 | a0001c0001t0041g0029a0001c0001t0046g0059 | 2 | NA19081.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.234+11060T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36955170 | ||||||
| chr2:36955174
|
G | C | 1 | a0001c0001t0037g0072 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.234+11056C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36955174 | ||||||
| chr2:36955199
|
C | T | 16 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(13): Show | 16 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.234+11031G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36955199 | ||||||
| chr2:36955376
|
G | A | 11 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.234+10854C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36955376 | ||||||
| chr2:36955468
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.234+10762C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36955468 | ||||||
| chr2:36955621
|
G | A | 4 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0150g0208others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+10609C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36955621 | ||||||
| chr2:36955642
|
T | A | 1 | a0001c0001t0002g0145 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.234+10588A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36955642 | ||||||
| chr2:36955843
|
A | G | 7 | a0001c0001t0010g0290a0001c0001t0010g0291a0001c0001t0010g0292others(4): Show | 7 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.234+10387T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36955843 | ||||||
| chr2:36955896
|
T | C | 1 | a0001c0003t0071g0223 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.234+10334A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36955896 | ||||||
| chr2:36955905
|
T | C | 1 | a0001c0001t0187g0049 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.234+10325A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36955905 | ||||||
| chr2:36955910
|
A | G | 1 | a0001c0001t0022g0108 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.234+10320T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36955910 | ||||||
| chr2:36955921
|
G | C | 1 | a0001c0001t0195g0294 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.234+10309C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36955921 | ||||||
| chr2:36956098
|
T | G | 2 | a0001c0001t0010g0290a0001c0001t0010g0291 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.234+10132A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36956098 | ||||||
| chr2:36956146
|
A | G | 1 | a0001c0001t0004g0141 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.234+10084T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36956146 | ||||||
| chr2:36956160
|
G | T | 112 | a0001c0001t0003g0020a0001c0001t0003g0030a0001c0001t0003g0033others(109): Show | 112 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.234+10070C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36956160 | ||||||
| chr2:36956213
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.234+10017G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36956213 | ||||||
| chr2:36956344
|
C | A | 13 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.234+9886G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36956344 | ||||||
| chr2:36956468
|
C | A | 1 | a0001c0001t0086g0102 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.234+9762G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36956468 | ||||||
| chr2:36956649
|
T | C | 21 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201others(18): Show | 21 | HG00323.hp2 HG00642.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.234+9581A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36956649 | ||||||
| chr2:36956652
|
C | G | 4 | a0001c0001t0001g0003a0001c0001t0002g0004a0001c0001t0021g0002others(1): Show | 4 | HG00408.hp1 HG00558.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+9578G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36956652 | ||||||
| chr2:36956920
|
C | T | 1 | a0001c0001t0134g0041 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.234+9310G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36956920 | ||||||
| chr2:36956955
|
T | C | 1 | a0001c0001t0132g0258 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.234+9275A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36956955 | ||||||
| chr2:36956979
|
G | A | 1 | a0001c0001t0122g0044 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.234+9251C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36956979 | ||||||
| chr2:36957209
|
C | A | 2 | a0001c0001t0067g0092a0001c0001t0069g0093 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.234+9021G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957209 | ||||||
| chr2:36957273
|
A | G | 2 | a0001c0001t0042g0263a0001c0001t0133g0265 | 2 | HG02040.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.234+8957T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957273 | ||||||
| chr2:36957342
|
C | T | 196 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(193): Show | 196 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.234+8888G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957342 | ||||||
| chr2:36957446
|
G | T | 1 | a0001c0001t0151g0205 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.234+8784C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957446 | ||||||
| chr2:36957538
|
A | G | 1 | a0001c0001t0027g0125 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.234+8692T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957538 | ||||||
| chr2:36957611
|
C | T | 156 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(153): Show | 156 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.234+8619G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957611 | ||||||
| chr2:36957613
|
C | T | 7 | a0001c0001t0039g0214a0001c0001t0039g0215a0001c0001t0151g0205others(4): Show | 7 | HG02559.hp2 HG02886.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.234+8617G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957613 | ||||||
| chr2:36957654
|
TAAAAAAC | T | 4 | a0001c0001t0010g0290a0001c0001t0010g0291a0001c0001t0030g0289others(1): Show | 4 | HG02615.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+8569_234+8575d others(9): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957654 | ||||||
| chr2:36957672
|
C | CA | 24 | a0001c0001t0001g0124a0001c0001t0003g0020a0001c0001t0011g0098others(21): Show | 24 | HG00438.hp2 HG00597.hp2 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.234+8557dupT | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957672 | ||||||
| chr2:36957676
|
A | C | 1 | a0001c0001t0044g0058 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.234+8554T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957676 | ||||||
| chr2:36957742
|
G | GT | 4 | a0001c0001t0030g0237a0001c0001t0033g0286a0001c0001t0137g0259others(1): Show | 4 | HG01243.hp2 HG02897.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+8487dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957742 | ||||||
| chr2:36957742
|
G | GTT | 11 | a0001c0001t0012g0280a0001c0001t0033g0283a0001c0001t0034g0256others(8): Show | 11 | HG00639.hp2 HG01106.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.234+8487_234+8488i others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957742 | ||||||
| chr2:36957742
|
G | GTTT | 14 | a0001c0001t0011g0096a0001c0001t0011g0097a0001c0001t0011g0098others(11): Show | 14 | HG00673.hp2 HG00735.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.234+8487_234+8488i others(5): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957742 | ||||||
| chr2:36957742
|
G | GTTTT | 3 | a0001c0001t0042g0263a0001c0001t0125g0277a0001c0001t0133g0265 | 3 | HG02040.hp1 HG02129.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.234+8487_234+8488i others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957742 | ||||||
| chr2:36957744
|
C | CT | 32 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0114others(29): Show | 32 | HG00323.hp1 HG00423.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.234+8485dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957744 | ||||||
| chr2:36957744
|
C | CTTT | 37 | a0001c0001t0001g0200a0001c0001t0003g0030a0001c0001t0005g0065others(34): Show | 37 | HG00280.hp1 HG01993.hp1 HG02015.hp2 others(34): Show |
intron_variant | MODIFIER | c.234+8483_234+8485d others(5): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957744 | ||||||
| chr2:36957744
|
C | CTTTT | 31 | a0001c0001t0003g0033a0001c0001t0003g0057a0001c0001t0004g0141others(28): Show | 31 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.234+8482_234+8485d others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957744 | ||||||
| chr2:36957744
|
C | CTTTTT | 6 | a0001c0001t0003g0020a0001c0001t0036g0095a0001c0001t0048g0196others(3): Show | 6 | HG00099.hp1 HG02129.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.234+8481_234+8485d others(7): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957744 | ||||||
| chr2:36957744
|
C | T | 34 | a0001c0001t0011g0096a0001c0001t0011g0097a0001c0001t0011g0098others(31): Show | 34 | HG00639.hp2 HG00673.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.234+8486G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957744 | ||||||
| chr2:36957744
|
CT | C | 6 | a0001c0001t0001g0003a0001c0001t0009g0189a0001c0001t0009g0190others(3): Show | 6 | HG00099.hp2 HG00408.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.234+8485delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957744 | ||||||
| chr2:36957744
|
CTTTTTTT | C | 27 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(24): Show | 27 | HG00438.hp2 HG01070.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.234+8479_234+8485d others(9): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957744 | ||||||
| chr2:36957744
|
CTTTTTTT others(3): Show |
C | 6 | a0001c0001t0049g0296a0001c0001t0049g0299a0001c0001t0050g0295others(3): Show | 6 | HG01243.hp1 HG01496.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.234+8476_234+8485d others(12): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957744 | ||||||
| chr2:36957810
|
G | A | 1 | a0001c0001t0141g0274 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.234+8420C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957810 | ||||||
| chr2:36957876
|
G | A | 1 | a0001c0001t0023g0140 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.234+8354C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957876 | ||||||
| chr2:36957905
|
G | A | 1 | a0001c0001t0014g0015 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.234+8325C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957905 | ||||||
| chr2:36957914
|
C | A | 1 | a0001c0001t0177g0089 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.234+8316G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957914 | ||||||
| chr2:36957917
|
A | AT | 38 | a0001c0001t0001g0003a0001c0001t0001g0106a0001c0001t0001g0107others(35): Show | 38 | HG00408.hp1 HG00738.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.234+8312dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957917 | ||||||
| chr2:36957988
|
T | C | 156 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(153): Show | 156 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.234+8242A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36957988 | ||||||
| chr2:36958092
|
A | G | 13 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0039g0214others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.234+8138T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36958092 | ||||||
| chr2:36958147
|
G | A | 1 | a0001c0001t0110g0191 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.234+8083C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36958147 | ||||||
| chr2:36958461
|
C | T | 2 | a0001c0001t0012g0279a0001c0001t0012g0280 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.234+7769G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36958461 | ||||||
| chr2:36958550
|
T | G | 1 | a0001c0001t0170g0142 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.234+7680A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36958550 | ||||||
| chr2:36958579
|
T | A | 31 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(28): Show | 31 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.234+7651A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36958579 | ||||||
| chr2:36958649
|
G | A | 7 | a0001c0001t0010g0290a0001c0001t0010g0291a0001c0001t0010g0292others(4): Show | 7 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.234+7581C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36958649 | ||||||
| chr2:36958722
|
T | C | 21 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201others(18): Show | 21 | HG00323.hp2 HG00642.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.234+7508A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36958722 | ||||||
| chr2:36958895
|
G | T | 1 | a0001c0001t0089g0104 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.234+7335C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36958895 | ||||||
| chr2:36958940
|
C | G | 1 | a0001c0001t0051g0001 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.234+7290G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36958940 | ||||||
| chr2:36959016
|
T | A | 2 | a0001c0001t0048g0195a0001c0001t0048g0196 | 2 | HG02071.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.234+7214A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36959016 | ||||||
| chr2:36959029
|
T | C | 1 | a0001c0001t0065g0224 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.234+7201A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36959029 | ||||||
| chr2:36959092
|
G | C | 3 | a0001c0001t0074g0217a0001c0001t0075g0218a0001c0001t0076g0219 | 3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.234+7138C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36959092 | ||||||
| chr2:36959146
|
A | C | 2 | a0001c0001t0015g0025a0001c0001t0165g0017 | 2 | HG00597.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.234+7084T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36959146 | ||||||
| chr2:36959293
|
T | A | 3 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201 | 3 | HG01891.hp1 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.234+6937A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36959293 | ||||||
| chr2:36959437
|
G | A | 3 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201 | 3 | HG01891.hp1 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.234+6793C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36959437 | ||||||
| chr2:36959551
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.234+6679A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36959551 | ||||||
| chr2:36959635
|
AC | A | 4 | a0001c0001t0038g0212a0001c0001t0038g0213a0001c0001t0150g0208others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+6594delG | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36959635 | ||||||
| chr2:36959681
|
G | A | 3 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201 | 3 | HG01891.hp1 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.234+6549C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36959681 | ||||||
| chr2:36959845
|
T | C | 2 | a0001c0001t0074g0217a0001c0001t0075g0218 | 2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.234+6385A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36959845 | ||||||
| chr2:36959976
|
T | C | 1 | a0001c0001t0148g0248 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.234+6254A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36959976 | ||||||
| chr2:36960160
|
C | A | 1 | a0001c0001t0054g0275 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.234+6070G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36960160 | ||||||
| chr2:36960614
|
T | C | 1 | a0001c0001t0041g0029 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.234+5616A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36960614 | ||||||
| chr2:36960650
|
A | C | 29 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(26): Show | 29 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.234+5580T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36960650 | ||||||
| chr2:36960651
|
G | A | 16 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(13): Show | 16 | HG00438.hp2 HG00597.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.234+5579C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36960651 | ||||||
| chr2:36960997
|
A | C | 52 | a0001c0001t0011g0096a0001c0001t0011g0097a0001c0001t0011g0098others(49): Show | 52 | HG00597.hp1 HG00639.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.234+5233T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36960997 | ||||||
| chr2:36961039
|
G | C | 2 | a0001c0001t0063g0203a0001c0001t0064g0202 | 2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.234+5191C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36961039 | ||||||
| chr2:36961115
|
C | CT | 81 | a0001c0001t0001g0076a0001c0001t0001g0106a0001c0001t0001g0107others(78): Show | 81 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.234+5114dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36961115 | ||||||
| chr2:36961115
|
C | CTTTT | 11 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0007g0197others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.234+5111_234+5114d others(6): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36961115 | ||||||
| chr2:36961115
|
C | CTTTTT | 17 | a0001c0001t0017g0240a0001c0001t0031g0042a0001c0001t0032g0067others(14): Show | 17 | HG00323.hp2 HG00741.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.234+5110_234+5114d others(7): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36961115 | ||||||
| chr2:36961115
|
CT | C | 20 | a0001c0001t0010g0290a0001c0001t0010g0291a0001c0001t0010g0292others(17): Show | 20 | HG00597.hp2 HG01256.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.234+5114delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36961115 | ||||||
| chr2:36961115
|
CTT | C | 21 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(18): Show | 21 | HG00438.hp2 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.234+5113_234+5114d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36961115 | ||||||
| chr2:36961115
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0085g0192 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.234+5105_234+5114d others(12): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36961115 | ||||||
| chr2:36961285
|
AT | A | 27 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(24): Show | 27 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.234+4944delA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36961285 | ||||||
| chr2:36961290
|
T | A | 27 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(24): Show | 27 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.234+4940A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36961290 | ||||||
| chr2:36961472
|
C | T | 4 | a0001c0001t0146g0249a0001c0001t0147g0250a0001c0001t0148g0248others(1): Show | 4 | HG02970.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+4758G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36961472 | ||||||
| chr2:36961485
|
C | T | 4 | a0001c0001t0146g0249a0001c0001t0147g0250a0001c0001t0148g0248others(1): Show | 4 | HG02970.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+4745G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36961485 | ||||||
| chr2:36961718
|
G | C | 2 | a0001c0001t0063g0203a0001c0001t0064g0202 | 2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.234+4512C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36961718 | ||||||
| chr2:36961802
|
T | C | 1 | a0001c0001t0125g0277 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.234+4428A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36961802 | ||||||
| chr2:36961980
|
T | C | 66 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0007g0197others(63): Show | 66 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.234+4250A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36961980 | ||||||
| chr2:36962034
|
A | C | 2 | a0001c0001t0063g0203a0001c0001t0064g0202 | 2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.234+4196T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36962034 | ||||||
| chr2:36962047
|
A | C | 4 | a0001c0001t0146g0249a0001c0001t0147g0250a0001c0001t0148g0248others(1): Show | 4 | HG02970.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+4183T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36962047 | ||||||
| chr2:36962145
|
G | A | 1 | a0001c0001t0100g0193 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.234+4085C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36962145 | ||||||
| chr2:36962153
|
T | C | 193 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(190): Show | 193 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.234+4077A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36962153 | ||||||
| chr2:36962411
|
C | T | 2 | a0001c0001t0063g0203a0001c0001t0064g0202 | 2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.234+3819G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36962411 | ||||||
| chr2:36962481
|
A | C | 55 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201others(52): Show | 55 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.234+3749T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36962481 | ||||||
| chr2:36962531
|
C | CT | 50 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201others(47): Show | 50 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.234+3698dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36962531 | ||||||
| chr2:36962550
|
T | C | 1 | a0001c0001t0027g0194 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.234+3680A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36962550 | ||||||
| chr2:36962573
|
C | A | 2 | a0001c0001t0061g0252a0001c0001t0078g0253 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.234+3657G>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36962573 | ||||||
| chr2:36962627
|
A | G | 6 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0017g0240others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.234+3603T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36962627 | ||||||
| chr2:36962758
|
T | C | 21 | a0001c0001t0007g0197a0001c0001t0007g0198a0001c0001t0007g0201others(18): Show | 21 | HG00323.hp2 HG00642.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.234+3472A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36962758 | ||||||
| chr2:36962882
|
G | A | 29 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(26): Show | 29 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.234+3348C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36962882 | ||||||
| chr2:36962911
|
G | T | 1 | a0001c0001t0057g0245 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.234+3319C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36962911 | ||||||
| chr2:36963249
|
G | C | 31 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(28): Show | 31 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.234+2981C>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36963249 | ||||||
| chr2:36963273
|
C | G | 5 | a0001c0001t0030g0237a0001c0001t0033g0283a0001c0001t0033g0286others(2): Show | 5 | HG01243.hp2 HG02572.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+2957G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36963273 | ||||||
| chr2:36963286
|
T | C | 1 | a0004c0004t0188g0048 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.234+2944A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36963286 | ||||||
| chr2:36963390
|
G | A | 2 | a0001c0001t0059g0255a0001c0001t0060g0254 | 2 | HG02451.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.234+2840C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36963390 | ||||||
| chr2:36963430
|
A | G | 1 | a0001c0001t0034g0256 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.234+2800T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36963430 | ||||||
| chr2:36963431
|
T | C | 31 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(28): Show | 31 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.234+2799A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36963431 | ||||||
| chr2:36963552
|
A | G | 29 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(26): Show | 29 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.234+2678T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36963552 | ||||||
| chr2:36963583
|
C | T | 126 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(123): Show | 126 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.234+2647G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36963583 | ||||||
| chr2:36963618
|
T | G | 5 | a0001c0001t0012g0279a0001c0001t0012g0280a0001c0001t0035g0282others(2): Show | 5 | HG01123.hp1 HG01433.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+2612A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36963618 | ||||||
| chr2:36963783
|
C | G | 2 | a0001c0001t0020g0238a0001c0001t0020g0239 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.234+2447G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36963783 | ||||||
| chr2:36963836
|
A | G | 1 | a0001c0001t0008g0103 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.234+2394T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36963836 | ||||||
| chr2:36963845
|
T | TACTTGGG others(25): Show |
1 | a0001c0001t0187g0049 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.234+2353_234+2384d others(34): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36963845 | ||||||
| chr2:36963845
|
TACTTGGG others(25): Show |
T | 1 | a0001c0001t0086g0102 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.234+2353_234+2384d others(34): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36963845 | ||||||
| chr2:36964014
|
T | A | 1 | a0001c0001t0070g0225 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.234+2216A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36964014 | ||||||
| chr2:36964067
|
T | C | 5 | a0001c0001t0030g0237a0001c0001t0033g0283a0001c0001t0033g0286others(2): Show | 5 | HG01243.hp2 HG02572.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+2163A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36964067 | ||||||
| chr2:36964176
|
G | T | 1 | a0001c0001t0002g0101 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.234+2054C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36964176 | ||||||
| chr2:36964180
|
C | CG | 31 | a0001c0001t0001g0200a0001c0001t0003g0057a0001c0001t0005g0065others(28): Show | 31 | HG00099.hp1 HG00408.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.234+2049dupC | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36964180 | ||||||
| chr2:36964180
|
C | CGG | 55 | a0001c0001t0003g0020a0001c0001t0003g0030a0001c0001t0003g0033others(52): Show | 55 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.234+2048_234+2049d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36964180 | ||||||
| chr2:36964180
|
C | CGGG | 31 | a0001c0001t0006g0244a0001c0001t0013g0008a0001c0001t0013g0010others(28): Show | 31 | HG00438.hp2 HG00597.hp2 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.234+2047_234+2049d others(5): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36964180 | ||||||
| chr2:36964183
|
GGC | G | 43 | a0001c0001t0011g0096a0001c0001t0011g0097a0001c0001t0011g0098others(40): Show | 43 | HG00639.hp2 HG00673.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.234+2045_234+2046d others(4): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36964183 | ||||||
| chr2:36964185
|
C | G | 145 | a0001c0001t0001g0200a0001c0001t0003g0020a0001c0001t0003g0030others(142): Show | 145 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.234+2045G>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36964185 | ||||||
| chr2:36964186
|
G | A | 11 | a0001c0001t0005g0087a0001c0001t0045g0082a0001c0001t0045g0085others(8): Show | 11 | HG00423.hp1 HG00544.hp2 NA18941.hp2 others(8): Show |
intron_variant | MODIFIER | c.234+2044C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36964186 | ||||||
| chr2:36964193
|
A | C | 3 | a0001c0001t0074g0217a0001c0001t0075g0218a0001c0001t0076g0219 | 3 | HG03195.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.234+2037T>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36964193 | ||||||
| chr2:36964217
|
T | G | 1 | a0001c0001t0118g0293 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.234+2013A>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36964217 | ||||||
| chr2:36964243
|
T | C | 1 | a0001c0001t0177g0089 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.234+1987A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36964243 | ||||||
| chr2:36964272
|
G | GT | 16 | a0001c0001t0001g0099a0001c0001t0005g0006a0001c0001t0020g0238others(13): Show | 16 | HG01070.hp1 HG01071.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.234+1957dupA | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36964272 | ||||||
| chr2:36964568
|
T | C | 1 | a0001c0001t0119g0301 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.234+1662A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36964568 | ||||||
| chr2:36964694
|
T | C | 7 | a0001c0001t0049g0296a0001c0001t0049g0299a0001c0001t0050g0295others(4): Show | 7 | HG01243.hp1 HG01496.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.234+1536A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36964694 | ||||||
| chr2:36965083
|
A | G | 1 | a0001c0001t0030g0237 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.234+1147T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36965083 | ||||||
| chr2:36965107
|
CTCT | C | 30 | a0001c0001t0016g0229a0001c0001t0016g0230a0001c0001t0018g0222others(27): Show | 30 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.234+1120_234+1122d others(5): Show |
STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36965107 | ||||||
| chr2:36965262
|
T | C | 1 | a0001c0001t0119g0301 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.234+968A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36965262 | ||||||
| chr2:36965352
|
T | C | 195 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0200others(192): Show | 195 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.234+878A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36965352 | ||||||
| chr2:36965362
|
T | A | 2 | a0001c0001t0014g0094a0001c0001t0036g0095 | 2 | HG02602.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.234+868A>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36965362 | ||||||
| chr2:36965464
|
T | C | 74 | a0001c0001t0006g0244a0001c0001t0006g0246a0001c0001t0010g0290others(71): Show | 74 | HG00639.hp2 HG00673.hp2 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.234+766A>G | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36965464 | ||||||
| chr2:36965625
|
A | G | 3 | a0001c0001t0011g0096a0001c0001t0011g0097a0001c0001t0011g0098 | 3 | HG02071.hp2 NA18972.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.234+605T>C | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36965625 | ||||||
| chr2:36965723
|
C | T | 91 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0003g0020others(88): Show | 91 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.234+507G>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36965723 | ||||||
| chr2:36965824
|
G | A | 1 | a0001c0001t0184g0302 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.234+406C>T | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36965824 | ||||||
| chr2:36965932
|
G | T | 4 | a0001c0001t0001g0003a0001c0001t0002g0004a0001c0001t0021g0002others(1): Show | 4 | HG00408.hp1 HG00558.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.234+298C>A | STRN | ENSG00000115808.13 | transcript | ENST00000263918.9 | protein_coding | 1/17 | chr2 | 36965932 |