| geneid | 51130 |
|---|---|
| ensemblid | ENSG00000115239.24 |
| hgncid | 16013 |
| symbol | ASB3 |
| name | ankyrin repeat and SOCS box containing 3 |
| refseq_nuc | NM_016115.5 |
| refseq_prot | NP_057199.1 |
| ensembl_nuc | ENST00000263634.8 |
| ensembl_prot | ENSP00000263634.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 53669980 |
| end | 53786953 |
| strand | - |
| ver | v1.2 |
| region | chr2:53669980-53786953 |
| region5000 | chr2:53664980-53791953 |
| regionname0 | ASB3_chr2_53669980_53786953 |
| regionname5000 | ASB3_chr2_53664980_53791953 |
| 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 | 1/0 | 518 | 335 | 84 | 56 | 147 | 12 | 35 | 109 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0002 | 0/0 | 518 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0003 | 0/1 | 518 | 4 | 1 | 2 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0004 | 0/0 | 518 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0005 | 0/0 | 518 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0006 | 0/0 | 518 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0007 | 0/0 | 518 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0008 | 0/0 | 518 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| 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 | 1/0 | 1557 | 241 | 77 | 42 | 88 | 10 | 23 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| c0002 | 0/0 | 1557 | 49 | 1 | 0 | 39 | 2 | 7 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| c0003 | 0/0 | 1557 | 45 | 6 | 14 | 20 | 0 | 5 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| c0004 | 0/0 | 1557 | 5 | 5 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| c0005 | 0/1 | 1557 | 4 | 1 | 2 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| c0006 | 0/0 | 1557 | 2 | 0 | 0 | 2 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| c0007 | 0/0 | 1557 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| c0008 | 0/0 | 1557 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| c0009 | 0/0 | 1557 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| c0010 | 0/0 | 1557 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 670 | 151 | 43 | 27 | 55 | 7 | 18 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| t0002 | 0/0 | 670 | 74 | 10 | 5 | 50 | 2 | 7 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| t0003 | 0/0 | 669 | 42 | 10 | 9 | 19 | 2 | 2 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| t0004 | 0/0 | 671 | 27 | 13 | 5 | 7 | 0 | 2 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| t0005 | 0/1 | 663 | 14 | 1 | 7 | 0 | 2 | 3 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| t0006 | 0/0 | 671 | 9 | 1 | 1 | 6 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| t0007 | 0/0 | 669 | 8 | 1 | 1 | 5 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| t0008 | 0/0 | 668 | 8 | 5 | 1 | 2 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| t0009 | 0/0 | 669 | 5 | 0 | 1 | 4 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| t0010 | 0/0 | 670 | 4 | 4 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| t0011 | 0/0 | 670 | 3 | 0 | 1 | 0 | 1 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| t0012 | 0/0 | 670 | 2 | 0 | 0 | 2 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| t0013 | 0/0 | 671 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| t0014 | 0/0 | 670 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| t0015 | 0/0 | 670 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0008 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0055 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| 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 | 1/0 | 1557 | 241 | 77 | 42 | 88 | 10 | 23 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0001c0002 | 0/0 | 1557 | 49 | 1 | 0 | 39 | 2 | 7 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0001c0003 | 0/0 | 1557 | 45 | 6 | 14 | 20 | 0 | 5 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0002c0004 | 0/0 | 1557 | 5 | 5 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0003c0005 | 0/1 | 1557 | 4 | 1 | 2 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0004c0006 | 0/0 | 1557 | 2 | 0 | 0 | 2 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0005c0009 | 0/0 | 1557 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0006c0008 | 0/0 | 1557 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0007c0007 | 0/0 | 1557 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0008c0010 | 0/0 | 1557 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2226 | 144 | 43 | 24 | 53 | 5 | 18 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0001c0001t0002 | 0/0 | 2226 | 8 | 4 | 2 | 2 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0001c0001t0003 | 0/0 | 2225 | 41 | 10 | 9 | 18 | 2 | 2 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0001c0001t0004 | 0/0 | 2227 | 26 | 13 | 4 | 7 | 0 | 2 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0001c0001t0005 | 0/0 | 2219 | 2 | 0 | 0 | 0 | 2 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0001c0001t0006 | 0/0 | 2227 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0001c0001t0007 | 0/0 | 2225 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0001c0001t0008 | 0/0 | 2224 | 8 | 5 | 1 | 2 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0001c0001t0009 | 0/0 | 2225 | 5 | 0 | 1 | 4 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0001c0001t0011 | 0/0 | 2226 | 2 | 0 | 0 | 0 | 1 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0001c0001t0012 | 0/0 | 2226 | 2 | 0 | 0 | 2 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0001c0001t0015 | 0/0 | 2226 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0001c0002t0001 | 0/0 | 2226 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0001c0002t0002 | 0/0 | 2226 | 39 | 1 | 0 | 30 | 2 | 6 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0001c0002t0006 | 0/0 | 2227 | 5 | 0 | 0 | 5 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0001c0002t0007 | 0/0 | 2225 | 4 | 0 | 0 | 3 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0001c0003t0001 | 0/0 | 2226 | 3 | 0 | 3 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0001c0003t0002 | 0/0 | 2226 | 25 | 5 | 3 | 16 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0001c0003t0003 | 0/0 | 2225 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0001c0003t0004 | 0/0 | 2227 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0001c0003t0005 | 0/0 | 2219 | 7 | 0 | 5 | 0 | 0 | 2 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0001c0003t0006 | 0/0 | 2227 | 3 | 0 | 1 | 1 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0001c0003t0007 | 0/0 | 2225 | 3 | 1 | 0 | 2 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0001c0003t0011 | 0/0 | 2226 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0001c0003t0014 | 0/0 | 2226 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0002c0004t0010 | 0/0 | 2226 | 4 | 4 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0002c0004t0013 | 0/0 | 2227 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0003c0005t0005 | 0/1 | 2219 | 4 | 1 | 2 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0004c0006t0002 | 0/0 | 2226 | 2 | 0 | 0 | 2 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0005c0009t0001 | 0/0 | 2226 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0006c0008t0001 | 0/0 | 2226 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0007c0007t0005 | 0/0 | 2219 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| a0008c0010t0001 | 0/0 | 2226 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | copy fasta | chr2 | 53664980 | 53791953 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0055 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0004g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0005g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0007g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0008g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0008g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0008g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0008g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0008g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0008g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0008g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0008g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0009g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0009g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0009g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0009g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0009g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0011g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0011g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0012g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0012g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0001t0015g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0006g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0006g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0006g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0006g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0006g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0007g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0007g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0007g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0002t0007g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0004g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0005g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0005g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0005g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0005g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0005g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0005g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0005g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0006g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0006g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0006g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0007g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0007g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0007g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0011g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0001c0003t0014g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0002c0004t0010g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0002c0004t0010g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0002c0004t0010g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0002c0004t0010g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0002c0004t0013g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0003c0005t0005g0008 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0003c0005t0005g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0003c0005t0005g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0004c0006t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0004c0006t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0005c0009t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0006c0008t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0007c0007t0005g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| a0008c0010t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0008 | c0010 | t0001 | g0100 | EUR | GBR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0108 | EUR | GBR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | FIN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0245 | EUR | FIN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00323 | hp1 | a0001 | c0001 | t0011 | g0096 | EUR | FIN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0221 | EUR | FIN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0186 | EAS | CHS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | CHS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0220 | EAS | CHS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00438 | hp1 | a0001 | c0003 | t0002 | g0288 | EAS | CHS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0132 | EAS | CHS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00558 | hp2 | a0001 | c0003 | t0007 | g0284 | EAS | CHS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | CHS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00621 | hp2 | a0001 | c0003 | t0002 | g0310 | EAS | CHS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0266 | EAS | CHS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0248 | EAS | CHS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00733 | hp1 | a0001 | c0003 | t0005 | g0329 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01069 | hp1 | a0001 | c0003 | t0002 | g0302 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0336 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0168 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01071 | hp2 | a0001 | c0003 | t0002 | g0303 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0272 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0328 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01106 | hp2 | a0003 | c0005 | t0005 | g0008 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0189 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01167 | hp2 | a0001 | c0003 | t0001 | g0305 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01168 | hp1 | a0001 | c0003 | t0005 | g0312 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0306 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0182 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01175 | hp2 | a0001 | c0003 | t0002 | g0289 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01192 | hp1 | a0001 | c0003 | t0005 | g0342 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01255 | hp1 | a0001 | c0001 | t0008 | g0034 | AMR | CLM | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0256 | AMR | CLM | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01256 | hp2 | a0001 | c0003 | t0011 | g0330 | AMR | CLM | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0188 | AMR | CLM | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01257 | hp2 | a0001 | c0003 | t0005 | g0331 | AMR | CLM | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01261 | hp1 | a0001 | c0001 | t0007 | g0023 | AMR | CLM | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01261 | hp2 | a0003 | c0005 | t0005 | g0338 | AMR | CLM | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0159 | AMR | CLM | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0093 | AMR | CLM | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0203 | AMR | CLM | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0193 | EUR | IBS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0325 | EUR | IBS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01516 | hp1 | a0001 | c0001 | t0005 | g0003 | EUR | IBS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | IBS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0003 | EUR | IBS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0194 | EUR | IBS | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0114 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01928 | hp1 | a0001 | c0003 | t0004 | g0308 | AMR | PEL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0184 | AMR | PEL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01943 | hp2 | a0001 | c0003 | t0001 | g0307 | AMR | PEL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0049 | AMR | PEL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01952 | hp2 | a0001 | c0003 | t0006 | g0301 | AMR | PEL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0187 | AMR | PEL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0227 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0053 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02027 | hp2 | a0001 | c0002 | t0006 | g0244 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0236 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0255 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02056 | hp2 | a0001 | c0001 | t0012 | g0204 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0225 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02074 | hp2 | a0001 | c0003 | t0002 | g0291 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0223 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02083 | hp2 | a0001 | c0003 | t0002 | g0280 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0226 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0085 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0181 | AMR | PEL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02155 | hp1 | a0001 | c0003 | t0002 | g0286 | EAS | CDX | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0235 | EAS | CDX | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0127 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0044 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02293 | hp1 | a0001 | c0001 | t0009 | g0179 | AMR | PEL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02523 | hp1 | a0001 | c0003 | t0002 | g0322 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02602 | hp1 | a0001 | c0003 | t0005 | g0333 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0250 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0228 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0142 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0241 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0148 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0326 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0231 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02698 | hp2 | a0001 | c0001 | t0011 | g0095 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0169 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02735 | hp2 | a0007 | c0007 | t0005 | g0341 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0276 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02818 | hp2 | a0002 | c0004 | t0010 | g0137 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02896 | hp1 | a0001 | c0003 | t0002 | g0021 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02897 | hp1 | a0001 | c0003 | t0007 | g0022 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0118 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0339 | AFR | ESN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0143 | AFR | ESN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0029 | AFR | ESN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03041 | hp1 | a0001 | c0003 | t0002 | g0296 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0031 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03098 | hp1 | a0002 | c0004 | t0010 | g0139 | AFR | MSL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0119 | AFR | MSL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03130 | hp1 | a0002 | c0004 | t0010 | g0138 | AFR | ESN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | ESN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0275 | AFR | ESN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03139 | hp2 | a0002 | c0004 | t0010 | g0136 | AFR | ESN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0152 | AFR | ESN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | ESN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03209 | hp1 | a0002 | c0004 | t0013 | g0012 | AFR | MSL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0214 | AFR | MSL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0032 | AFR | MSL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0320 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | MSL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0273 | AFR | MSL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03486 | hp1 | a0001 | c0001 | t0008 | g0035 | AFR | MSL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0327 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0277 | AFR | ESN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | ESN | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03579 | hp1 | a0001 | c0001 | t0015 | g0013 | AFR | MSL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03579 | hp2 | a0001 | c0003 | t0002 | g0298 | AFR | MSL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0264 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03710 | hp2 | a0001 | c0003 | t0002 | g0299 | SAS | PJL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0267 | SAS | BEB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0205 | SAS | BEB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03834 | hp1 | a0001 | c0002 | t0007 | g0254 | SAS | BEB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0311 | SAS | BEB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03942 | hp1 | a0001 | c0003 | t0005 | g0332 | SAS | BEB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0324 | SAS | BEB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG04115 | hp1 | a0001 | c0003 | t0014 | g0304 | SAS | STU | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0123 | SAS | STU | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0247 | SAS | BEB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG04199 | hp1 | a0001 | c0003 | t0006 | g0294 | SAS | STU | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0265 | SAS | STU | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | STU | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | YRI | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0218 | AFR | YRI | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0261 | EAS | CHB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | YRI | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | YRI | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18939 | hp2 | a0001 | c0003 | t0002 | g0292 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18941 | hp1 | a0001 | c0001 | t0008 | g0209 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18941 | hp2 | a0001 | c0002 | t0002 | g0253 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18943 | hp2 | a0001 | c0003 | t0002 | g0281 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0224 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18945 | hp2 | a0006 | c0008 | t0001 | g0028 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18948 | hp2 | a0001 | c0003 | t0002 | g0290 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18950 | hp2 | a0001 | c0003 | t0006 | g0295 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0259 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18954 | hp1 | a0001 | c0002 | t0007 | g0239 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18959 | hp1 | a0001 | c0002 | t0007 | g0262 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0230 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18962 | hp2 | a0004 | c0006 | t0002 | g0234 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18964 | hp2 | a0001 | c0001 | t0008 | g0195 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0232 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18966 | hp1 | a0001 | c0003 | t0002 | g0293 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18967 | hp1 | a0001 | c0001 | t0004 | g0126 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18967 | hp2 | a0001 | c0003 | t0003 | g0309 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18968 | hp1 | a0001 | c0002 | t0002 | g0252 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18970 | hp1 | a0001 | c0003 | t0002 | g0283 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0240 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18972 | hp2 | a0001 | c0002 | t0006 | g0019 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0162 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18981 | hp1 | a0001 | c0003 | t0007 | g0285 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0257 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18982 | hp2 | a0001 | c0003 | t0002 | g0278 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0233 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18988 | hp2 | a0001 | c0003 | t0002 | g0282 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18989 | hp1 | a0004 | c0006 | t0002 | g0246 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0243 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19000 | hp2 | a0001 | c0001 | t0012 | g0208 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19001 | hp2 | a0001 | c0002 | t0006 | g0271 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19002 | hp2 | a0001 | c0003 | t0002 | g0300 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19006 | hp1 | a0001 | c0003 | t0002 | g0279 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0249 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | LWK | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19030 | hp2 | a0001 | c0001 | t0008 | g0033 | AFR | LWK | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | LWK | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19043 | hp2 | a0001 | c0003 | t0002 | g0297 | AFR | LWK | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19056 | hp2 | a0001 | c0002 | t0007 | g0242 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19057 | hp1 | a0001 | c0001 | t0009 | g0192 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0238 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19062 | hp2 | a0001 | c0002 | t0006 | g0219 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19063 | hp2 | a0001 | c0003 | t0002 | g0321 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19065 | hp2 | a0001 | c0001 | t0009 | g0200 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19066 | hp1 | a0001 | c0001 | t0009 | g0199 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19078 | hp2 | a0001 | c0002 | t0002 | g0260 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19079 | hp1 | a0001 | c0001 | t0009 | g0201 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0263 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19080 | hp2 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19083 | hp2 | a0001 | c0002 | t0006 | g0222 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0340 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19240 | hp1 | a0001 | c0003 | t0002 | g0287 | AFR | YRI | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | YRI | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ASW | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ASW | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0051 | EUR | TSI | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA20805 | hp2 | a0005 | c0009 | t0001 | g0160 | EUR | TSI | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01123 | hp1 | a0001 | c0003 | t0005 | g0335 | AMR | CLM | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0121 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0150 | AFR | ACB | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | MSL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0157 | AFR | MSL | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG06807 | hp1 | a0003 | c0005 | t0005 | g0337 | AFR | USA | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0146 | AFR | USA | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | USA | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | USA | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0005 | t0005 | g0008 | REF | REF | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0055 | REF | REF | ASB3_chr2_53664980_53791953 | ASB3 | chr2 | 53664980 | 53791953 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:53693919
|
C | A | 1 | a0006 | 1 | NA18945.hp2 | missense_variant | MODERATE | c.1334G>T | p.Arg445Leu | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/10 | 1480/2226 | 1334/1557 | 445/518 | chr2 | 53693919 | ||
| chr2:53693920
|
G | A | 1 | a0005 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.1333C>T | p.Arg445Cys | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/10 | 1479/2226 | 1333/1557 | 445/518 | chr2 | 53693920 | ||
| chr2:53694001
|
T | C | 1 | a0004 | 2 | NA18962.hp2 NA18989.hp1 |
missense_variant | MODERATE | c.1252A>G | p.Ser418Gly | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/10 | 1398/2226 | 1252/1557 | 418/518 | chr2 | 53694001 | ||
| chr2:53714544
|
A | G | 1 | a0007 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.820T>C | p.Cys274Arg | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/10 | 966/2226 | 820/1557 | 274/518 | chr2 | 53714544 | ||
| chr2:53728730
|
T | C | 1 | a0002 | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
missense_variant | MODERATE | c.586A>G | p.Ser196Gly | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/10 | 732/2226 | 586/1557 | 196/518 | chr2 | 53728730 | ||
| chr2:53728845
|
T | A | 1 | a0003 | 4 | HG01106.hp2 HG01261.hp2 HG06807.hp1 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.471A>T | p.Glu157Asp | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/10 | 617/2226 | 471/1557 | 157/518 | chr2 | 53728845 | ||
| chr2:53765485
|
G | C | 1 | a0008 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.88C>G | p.Leu30Val | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/10 | 234/2226 | 88/1557 | 30/518 | chr2 | 53765485 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:53728713
|
C | T | 3 | a0001c0003a0003c0005a0007c0007 | 50 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(47): Show |
splice_region_variant&synonymous_variant | LOW | c.603G>A | p.Ser201Ser | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/10 | 749/2226 | 603/1557 | 201/518 | chr2 | 53728713 | ||
| chr2:53765456
|
A | T | 2 | a0001c0002a0004c0006 | 51 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(48): Show |
synonymous_variant | LOW | c.117T>A | p.Ala39Ala | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/10 | 263/2226 | 117/1557 | 39/518 | chr2 | 53765456 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:53670114
|
A | G | 2 | a0001c0001t0011a0001c0003t0011 | 3 | HG00323.hp1 HG01256.hp2 HG02698.hp2 |
3_prime_UTR_variant | MODIFIER | c.*389T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 10/10 | 389 | chr2 | 53670114 | |||||
| chr2:53670130
|
G | A | 1 | a0001c0003t0014 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*373C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 10/10 | 373 | chr2 | 53670130 | |||||
| chr2:53670171
|
A | G | 1 | a0001c0001t0015 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*332T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 10/10 | 332 | chr2 | 53670171 | |||||
| chr2:53670292
|
A | AT | 6 | a0001c0001t0004a0001c0001t0006a0001c0002t0006others(3): Show | 37 | HG00438.hp2 HG01074.hp1 HG01346.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*210dupA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 10/10 | 210 | chr2 | 53670292 | |||||
| chr2:53670292
|
AT | A | 6 | a0001c0001t0003a0001c0001t0007a0001c0001t0009others(3): Show | 55 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*210delA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 10/10 | 210 | chr2 | 53670292 | |||||
| chr2:53670292
|
ATT | A | 1 | a0001c0001t0008 | 8 | HG01255.hp1 HG02976.hp1 HG03041.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*209_*210delAA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 10/10 | 209 | chr2 | 53670292 | |||||
| chr2:53670292
|
ATTTTTTT | A | 4 | a0001c0001t0005a0001c0003t0005a0003c0005t0005others(1): Show | 14 | HG00733.hp1 HG01106.hp2 HG01123.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*204_*210delAAAAAA others(1): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 10/10 | 204 | chr2 | 53670292 | |||||
| chr2:53670388
|
C | G | 15 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(12): Show | 106 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*115G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 10/10 | 115 | chr2 | 53670388 | |||||
| chr2:53670399
|
A | G | 2 | a0002c0004t0010a0002c0004t0013 | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*104T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 10/10 | 104 | chr2 | 53670399 | |||||
| chr2:53670431
|
G | A | 2 | a0001c0001t0009a0001c0001t0012 | 7 | HG02056.hp2 HG02293.hp1 NA19000.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*72C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 10/10 | 72 | chr2 | 53670431 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:53670895
|
T | C | 62 | a0001c0001t0001g0005a0001c0001t0001g0151a0001c0001t0001g0153others(59): Show | 65 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.1370-205A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53670895 | ||||||
| chr2:53670985
|
T | A | 3 | a0001c0001t0001g0015a0001c0001t0004g0014a0001c0001t0015g0013 | 3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1370-295A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53670985 | ||||||
| chr2:53670986
|
G | T | 3 | a0001c0001t0001g0015a0001c0001t0004g0014a0001c0001t0015g0013 | 3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1370-296C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53670986 | ||||||
| chr2:53671353
|
C | CGT | 105 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0038others(102): Show | 106 | HG00323.hp1 HG00423.hp1 HG00673.hp1 others(103): Show |
intron_variant | MODIFIER | c.1370-665_1370-664d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671353 | ||||||
| chr2:53671353
|
C | CGTGT | 73 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0030others(70): Show | 74 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.1370-667_1370-664d others(6): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671353 | ||||||
| chr2:53671353
|
C | CGTGTGT | 7 | a0001c0001t0001g0016a0001c0001t0001g0210a0001c0001t0002g0256others(4): Show | 7 | HG01255.hp2 HG02015.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1370-669_1370-664d others(8): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671353 | ||||||
| chr2:53671353
|
C | CGTGTGTG others(3): Show |
2 | a0001c0001t0004g0272a0001c0001t0004g0275 | 2 | HG01074.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1370-673_1370-664d others(12): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671353 | ||||||
| chr2:53671353
|
C | CGTGTGTG others(5): Show |
2 | a0001c0001t0001g0274a0001c0001t0004g0150 | 2 | HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1370-675_1370-664d others(14): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671353 | ||||||
| chr2:53671353
|
CGT | C | 58 | a0001c0001t0001g0046a0001c0001t0001g0054a0001c0001t0001g0064others(55): Show | 60 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.1370-665_1370-664d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671353 | ||||||
| chr2:53671353
|
CGTGT | C | 15 | a0001c0001t0001g0106a0001c0001t0001g0108a0001c0001t0001g0144others(12): Show | 16 | HG00099.hp2 HG00738.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.1370-667_1370-664d others(6): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671353 | ||||||
| chr2:53671353
|
CGTGTGT | C | 5 | a0001c0001t0003g0218a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1370-669_1370-664d others(8): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671353 | ||||||
| chr2:53671353
|
CGTGTGTG others(1): Show |
C | 3 | a0001c0001t0001g0211a0001c0001t0001g0216a0001c0001t0001g0217 | 3 | HG02572.hp2 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1370-671_1370-664d others(10): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671353 | ||||||
| chr2:53671353
|
CGTGTGTG others(7): Show |
C | 3 | a0001c0001t0001g0015a0001c0001t0004g0014a0001c0001t0015g0013 | 3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1370-677_1370-664d others(16): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671353 | ||||||
| chr2:53671514
|
C | G | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270 | 3 | HG02630.hp1 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1370-824G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671514 | ||||||
| chr2:53671531
|
G | A | 3 | a0001c0003t0002g0310a0001c0003t0002g0321a0001c0003t0002g0322 | 3 | HG00621.hp2 HG02523.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1370-841C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671531 | ||||||
| chr2:53671633
|
C | T | 1 | a0001c0001t0001g0328 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1370-943G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671633 | ||||||
| chr2:53671689
|
GCGGAGGT others(18): Show |
G | 3 | a0001c0001t0001g0015a0001c0001t0004g0014a0001c0001t0015g0013 | 3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1370-1024_1370-100 others(29): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671689 | ||||||
| chr2:53671691
|
G | A | 1 | a0001c0001t0003g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1370-1001C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671691 | ||||||
| chr2:53671695
|
GTTGCAGT others(175): Show |
G | 18 | a0001c0001t0001g0211a0001c0001t0001g0216a0001c0001t0001g0217others(15): Show | 18 | HG00408.hp2 HG01074.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1370-1187_1370-100 others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671695 | ||||||
| chr2:53671716
|
G | T | 3 | a0001c0001t0001g0015a0001c0001t0004g0014a0001c0001t0015g0013 | 3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1370-1026C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671716 | ||||||
| chr2:53671718
|
C | A | 3 | a0001c0001t0001g0015a0001c0001t0004g0014a0001c0001t0015g0013 | 3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1370-1028G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671718 | ||||||
| chr2:53671719
|
ACT | A | 3 | a0001c0001t0001g0015a0001c0001t0004g0014a0001c0001t0015g0013 | 3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1370-1031_1370-103 others(6): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671719 | ||||||
| chr2:53671759
|
C | CA | 10 | a0001c0001t0001g0015a0001c0001t0003g0218a0001c0001t0004g0014others(7): Show | 10 | HG02258.hp1 HG02818.hp2 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.1370-1070dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671759 | ||||||
| chr2:53671853
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1370-1163G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671853 | ||||||
| chr2:53671880
|
A | C | 18 | a0001c0001t0001g0211a0001c0001t0001g0216a0001c0001t0001g0217others(15): Show | 18 | HG00408.hp2 HG01074.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1370-1190T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671880 | ||||||
| chr2:53671884
|
C | T | 18 | a0001c0001t0001g0211a0001c0001t0001g0216a0001c0001t0001g0217others(15): Show | 18 | HG00408.hp2 HG01074.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1370-1194G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671884 | ||||||
| chr2:53671885
|
T | A | 18 | a0001c0001t0001g0211a0001c0001t0001g0216a0001c0001t0001g0217others(15): Show | 18 | HG00408.hp2 HG01074.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1370-1195A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671885 | ||||||
| chr2:53671886
|
T | A | 18 | a0001c0001t0001g0211a0001c0001t0001g0216a0001c0001t0001g0217others(15): Show | 18 | HG00408.hp2 HG01074.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1370-1196A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671886 | ||||||
| chr2:53671888
|
TATAAA | T | 18 | a0001c0001t0001g0211a0001c0001t0001g0216a0001c0001t0001g0217others(15): Show | 18 | HG00408.hp2 HG01074.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1370-1203_1370-119 others(9): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671888 | ||||||
| chr2:53671927
|
G | A | 10 | a0001c0001t0001g0016a0001c0001t0003g0043a0001c0001t0003g0044others(7): Show | 10 | HG01255.hp1 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1370-1237C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671927 | ||||||
| chr2:53671961
|
C | T | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1370-1271G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53671961 | ||||||
| chr2:53672301
|
C | T | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1370-1611G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53672301 | ||||||
| chr2:53672451
|
G | A | 1 | a0001c0003t0002g0299 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1370-1761C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53672451 | ||||||
| chr2:53672629
|
A | G | 51 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0001g0171others(48): Show | 53 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.1370-1939T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53672629 | ||||||
| chr2:53672631
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1370-1941A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53672631 | ||||||
| chr2:53672707
|
A | G | 10 | a0001c0001t0001g0005a0001c0001t0001g0158a0001c0001t0001g0161others(7): Show | 11 | HG00099.hp1 HG01099.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.1370-2017T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53672707 | ||||||
| chr2:53672741
|
G | C | 2 | a0001c0002t0002g0243a0001c0002t0006g0244 | 2 | HG02027.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1370-2051C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53672741 | ||||||
| chr2:53672781
|
G | A | 6 | a0001c0001t0001g0274a0001c0001t0004g0272a0001c0001t0004g0273others(3): Show | 6 | HG01074.hp1 HG02818.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1370-2091C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53672781 | ||||||
| chr2:53672960
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1370-2270A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53672960 | ||||||
| chr2:53673070
|
A | G | 1 | a0001c0001t0004g0324 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1370-2380T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53673070 | ||||||
| chr2:53673101
|
C | CA | 10 | a0001c0001t0001g0311a0001c0001t0001g0320a0001c0001t0001g0323others(7): Show | 10 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.1370-2412dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53673101 | ||||||
| chr2:53673259
|
G | A | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1370-2569C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53673259 | ||||||
| chr2:53673338
|
G | A | 1 | a0001c0002t0002g0241 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1370-2648C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53673338 | ||||||
| chr2:53673434
|
C | G | 19 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0002g0154others(16): Show | 19 | HG01243.hp2 HG01255.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1370-2744G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53673434 | ||||||
| chr2:53673535
|
G | C | 1 | a0002c0004t0013g0012 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1370-2845C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53673535 | ||||||
| chr2:53673634
|
T | C | 1 | a0001c0001t0001g0001 | 2 | HG03491.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1370-2944A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53673634 | ||||||
| chr2:53673664
|
G | C | 6 | a0001c0001t0003g0218a0002c0004t0010g0136a0002c0004t0010g0137others(3): Show | 6 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1370-2974C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53673664 | ||||||
| chr2:53673743
|
T | C | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1370-3053A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53673743 | ||||||
| chr2:53673815
|
T | C | 3 | a0001c0001t0002g0140a0001c0001t0002g0142a0001c0001t0006g0143 | 3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1370-3125A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53673815 | ||||||
| chr2:53673878
|
T | A | 1 | a0001c0001t0001g0120 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1370-3188A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53673878 | ||||||
| chr2:53674340
|
A | G | 52 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0001g0171others(49): Show | 54 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.1370-3650T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53674340 | ||||||
| chr2:53674642
|
G | C | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1370-3952C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53674642 | ||||||
| chr2:53674760
|
A | T | 218 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(215): Show | 223 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.1370-4070T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53674760 | ||||||
| chr2:53674829
|
C | G | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1370-4139G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53674829 | ||||||
| chr2:53674836
|
A | G | 212 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0016others(209): Show | 217 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.1370-4146T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53674836 | ||||||
| chr2:53674844
|
A | AAAATAAG others(8): Show |
1 | a0001c0001t0003g0172 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1370-4155_1370-415 others(19): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53674844 | ||||||
| chr2:53674847
|
A | ATAAGTAA others(3): Show |
1 | a0001c0001t0001g0176 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1370-4158_1370-415 others(14): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53674847 | ||||||
| chr2:53674848
|
A | T | 1 | a0001c0001t0001g0176 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1370-4158T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53674848 | ||||||
| chr2:53674849
|
G | A | 1 | a0001c0001t0003g0172 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1370-4159C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53674849 | ||||||
| chr2:53674850
|
C | A | 1 | a0001c0001t0001g0176 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1370-4160G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53674850 | ||||||
| chr2:53674850
|
C | T | 1 | a0001c0001t0003g0172 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1370-4160G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53674850 | ||||||
| chr2:53674874
|
C | T | 217 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(214): Show | 222 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.1370-4184G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53674874 | ||||||
| chr2:53674983
|
C | T | 1 | a0001c0001t0004g0014 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1370-4293G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53674983 | ||||||
| chr2:53675029
|
C | T | 213 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(210): Show | 218 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.1370-4339G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675029 | ||||||
| chr2:53675038
|
T | C | 1 | a0001c0001t0004g0123 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1370-4348A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675038 | ||||||
| chr2:53675090
|
C | T | 52 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0001g0171others(49): Show | 54 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.1370-4400G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675090 | ||||||
| chr2:53675226
|
T | A | 1 | a0001c0001t0001g0327 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1370-4536A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675226 | ||||||
| chr2:53675337
|
T | A | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4647A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675337 | ||||||
| chr2:53675342
|
A | T | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4652T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675342 | ||||||
| chr2:53675343
|
A | G | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4653T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675343 | ||||||
| chr2:53675345
|
A | T | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4655T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675345 | ||||||
| chr2:53675347
|
A | G | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4657T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675347 | ||||||
| chr2:53675348
|
A | G | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4658T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675348 | ||||||
| chr2:53675350
|
A | T | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4660T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675350 | ||||||
| chr2:53675352
|
G | A | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4662C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675352 | ||||||
| chr2:53675353
|
C | T | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4663G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675353 | ||||||
| chr2:53675356
|
A | G | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4666T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675356 | ||||||
| chr2:53675377
|
T | G | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4687A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675377 | ||||||
| chr2:53675384
|
A | T | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4694T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675384 | ||||||
| chr2:53675386
|
T | G | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4696A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675386 | ||||||
| chr2:53675387
|
T | G | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4697A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675387 | ||||||
| chr2:53675396
|
A | G | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4706T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675396 | ||||||
| chr2:53675399
|
G | T | 1 | a0001c0001t0001g0048 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1370-4709C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675399 | ||||||
| chr2:53675403
|
A | G | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4713T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675403 | ||||||
| chr2:53675416
|
A | T | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4726T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675416 | ||||||
| chr2:53675417
|
T | A | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4727A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675417 | ||||||
| chr2:53675421
|
A | T | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4731T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675421 | ||||||
| chr2:53675423
|
T | G | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4733A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675423 | ||||||
| chr2:53675425
|
T | G | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4735A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675425 | ||||||
| chr2:53675427
|
T | G | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4737A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675427 | ||||||
| chr2:53675432
|
A | C | 1 | a0001c0001t0001g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1370-4742T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675432 | ||||||
| chr2:53675434
|
G | A | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4744C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675434 | ||||||
| chr2:53675435
|
A | C | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4745T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675435 | ||||||
| chr2:53675437
|
C | T | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4747G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675437 | ||||||
| chr2:53675438
|
A | T | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4748T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675438 | ||||||
| chr2:53675439
|
A | T | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4749T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675439 | ||||||
| chr2:53675442
|
T | A | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4752A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675442 | ||||||
| chr2:53675447
|
G | C | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4757C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675447 | ||||||
| chr2:53675456
|
T | G | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4766A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675456 | ||||||
| chr2:53675457
|
T | G | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4767A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675457 | ||||||
| chr2:53675462
|
A | G | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4772T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675462 | ||||||
| chr2:53675466
|
A | G | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4776T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675466 | ||||||
| chr2:53675484
|
A | T | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4794T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675484 | ||||||
| chr2:53675485
|
A | T | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4795T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675485 | ||||||
| chr2:53675488
|
C | G | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4798G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675488 | ||||||
| chr2:53675489
|
A | C | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4799T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675489 | ||||||
| chr2:53675492
|
G | A | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4802C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675492 | ||||||
| chr2:53675493
|
A | T | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4803T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675493 | ||||||
| chr2:53675510
|
G | T | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4820C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675510 | ||||||
| chr2:53675512
|
T | G | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4822A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675512 | ||||||
| chr2:53675513
|
T | A | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4823A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675513 | ||||||
| chr2:53675516
|
T | C | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4826A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675516 | ||||||
| chr2:53675517
|
C | A | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4827G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675517 | ||||||
| chr2:53675519
|
G | C | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-4829C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675519 | ||||||
| chr2:53675707
|
T | A | 1 | a0001c0001t0004g0126 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1370-5017A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675707 | ||||||
| chr2:53675787
|
T | C | 6 | a0001c0002t0002g0238a0001c0002t0002g0257a0001c0002t0002g0259others(3): Show | 6 | NA18952.hp2 NA18954.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.1370-5097A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675787 | ||||||
| chr2:53675890
|
T | A | 1 | a0001c0001t0003g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1370-5200A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53675890 | ||||||
| chr2:53676024
|
A | G | 196 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0106others(193): Show | 200 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.1370-5334T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53676024 | ||||||
| chr2:53676051
|
T | A | 1 | a0001c0001t0007g0023 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1370-5361A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53676051 | ||||||
| chr2:53676161
|
A | C | 3 | a0001c0001t0001g0015a0001c0001t0004g0014a0001c0001t0015g0013 | 3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1370-5471T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53676161 | ||||||
| chr2:53676371
|
T | C | 9 | a0001c0003t0002g0288a0001c0003t0002g0289a0001c0003t0002g0290others(6): Show | 9 | HG00438.hp1 HG01069.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1370-5681A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53676371 | ||||||
| chr2:53676407
|
T | C | 4 | a0001c0001t0002g0140a0001c0001t0002g0142a0001c0001t0002g0154others(1): Show | 4 | HG01243.hp2 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1370-5717A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53676407 | ||||||
| chr2:53676608
|
C | T | 1 | a0001c0001t0003g0044 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1370-5918G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53676608 | ||||||
| chr2:53676672
|
T | C | 1 | a0001c0001t0001g0268 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1370-5982A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53676672 | ||||||
| chr2:53676730
|
T | A | 3 | a0002c0004t0010g0137a0002c0004t0010g0138a0002c0004t0010g0139 | 3 | HG02818.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1370-6040A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53676730 | ||||||
| chr2:53677218
|
T | C | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1370-6528A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53677218 | ||||||
| chr2:53677356
|
C | T | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1370-6666G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53677356 | ||||||
| chr2:53677388
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1370-6698G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53677388 | ||||||
| chr2:53677390
|
C | T | 1 | a0001c0003t0002g0287 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1370-6700G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53677390 | ||||||
| chr2:53677487
|
GT | G | 13 | a0001c0001t0001g0036a0001c0001t0005g0003a0001c0003t0005g0312others(10): Show | 15 | HG00733.hp1 HG01106.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.1370-6798delA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53677487 | ||||||
| chr2:53677495
|
T | A | 87 | a0001c0001t0002g0063a0001c0001t0002g0131a0001c0001t0002g0228others(84): Show | 87 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.1370-6805A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53677495 | ||||||
| chr2:53677496
|
A | T | 71 | a0001c0001t0001g0015a0001c0001t0001g0151a0001c0001t0001g0153others(68): Show | 73 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(70): Show |
intron_variant | MODIFIER | c.1370-6806T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53677496 | ||||||
| chr2:53677624
|
T | C | 11 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(8): Show | 11 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.1370-6934A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53677624 | ||||||
| chr2:53677671
|
A | C | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1370-6981T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53677671 | ||||||
| chr2:53677694
|
G | A | 1 | a0001c0002t0001g0258 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1370-7004C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53677694 | ||||||
| chr2:53677721
|
T | G | 52 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0001g0171others(49): Show | 54 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.1370-7031A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53677721 | ||||||
| chr2:53677830
|
T | C | 3 | a0001c0001t0001g0015a0001c0001t0004g0014a0001c0001t0015g0013 | 3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1370-7140A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53677830 | ||||||
| chr2:53677938
|
T | C | 1 | a0001c0001t0001g0109 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1370-7248A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53677938 | ||||||
| chr2:53677994
|
T | C | 1 | a0001c0001t0003g0187 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1370-7304A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53677994 | ||||||
| chr2:53678140
|
GGT | G | 335 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(332): Show | 343 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.1370-7452_1370-745 others(6): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53678140 | ||||||
| chr2:53678161
|
A | G | 142 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0106others(139): Show | 144 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.1370-7471T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53678161 | ||||||
| chr2:53678174
|
A | C | 59 | a0001c0001t0001g0099a0001c0001t0001g0151a0001c0001t0001g0153others(56): Show | 61 | HG00408.hp1 HG00621.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.1370-7484T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53678174 | ||||||
| chr2:53678188
|
G | C | 1 | a0001c0001t0003g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1370-7498C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53678188 | ||||||
| chr2:53678357
|
C | T | 3 | a0001c0001t0001g0117a0001c0001t0001g0191a0001c0001t0003g0118 | 3 | HG02886.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1370-7667G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53678357 | ||||||
| chr2:53678394
|
T | C | 3 | a0001c0001t0001g0048a0001c0001t0001g0081a0001c0001t0004g0082 | 3 | NA18943.hp1 NA18987.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1370-7704A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53678394 | ||||||
| chr2:53678706
|
G | C | 2 | a0001c0001t0001g0156a0001c0001t0004g0157 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1370-8016C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53678706 | ||||||
| chr2:53679219
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1370-8529A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679219 | ||||||
| chr2:53679239
|
C | T | 2 | a0001c0002t0002g0243a0001c0002t0006g0244 | 2 | HG02027.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1370-8549G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679239 | ||||||
| chr2:53679261
|
C | A | 4 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.1370-8571G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679261 | ||||||
| chr2:53679291
|
T | C | 1 | a0001c0003t0002g0281 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1370-8601A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679291 | ||||||
| chr2:53679321
|
T | A | 21 | a0001c0001t0001g0016a0001c0001t0001g0106a0001c0001t0001g0211others(18): Show | 21 | HG01074.hp1 HG01243.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.1370-8631A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679321 | ||||||
| chr2:53679373
|
A | G | 1 | a0001c0002t0002g0250 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1370-8683T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679373 | ||||||
| chr2:53679384
|
C | A | 14 | a0001c0001t0001g0015a0001c0001t0001g0211a0001c0001t0001g0216others(11): Show | 14 | HG01074.hp1 HG01243.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.1370-8694G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679384 | ||||||
| chr2:53679406
|
G | A | 10 | a0001c0001t0001g0016a0001c0001t0001g0106a0001c0001t0003g0043others(7): Show | 10 | HG01255.hp1 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1370-8716C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679406 | ||||||
| chr2:53679416
|
C | T | 3 | a0001c0001t0002g0140a0001c0001t0002g0142a0001c0001t0006g0143 | 3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1370-8726G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679416 | ||||||
| chr2:53679457
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1370-8767A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679457 | ||||||
| chr2:53679573
|
A | G | 1 | a0001c0001t0004g0114 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1370-8883T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679573 | ||||||
| chr2:53679593
|
G | A | 1 | a0001c0001t0003g0170 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1370-8903C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679593 | ||||||
| chr2:53679702
|
A | C | 1 | a0001c0001t0001g0057 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1370-9012T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679702 | ||||||
| chr2:53679741
|
A | G | 10 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(7): Show | 10 | HG00408.hp2 HG01081.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.1370-9051T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679741 | ||||||
| chr2:53679781
|
G | T | 4 | a0001c0001t0008g0035a0002c0004t0010g0137a0002c0004t0010g0138others(1): Show | 4 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1370-9091C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679781 | ||||||
| chr2:53679798
|
A | G | 193 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0106others(190): Show | 197 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1370-9108T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679798 | ||||||
| chr2:53679834
|
T | C | 10 | a0001c0001t0001g0211a0001c0001t0001g0216a0001c0001t0001g0217others(7): Show | 10 | HG01074.hp1 HG01261.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1370-9144A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679834 | ||||||
| chr2:53679940
|
G | A | 1 | a0001c0001t0002g0131 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1370-9250C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679940 | ||||||
| chr2:53679978
|
G | T | 1 | a0001c0001t0001g0327 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1370-9288C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53679978 | ||||||
| chr2:53680026
|
G | C | 3 | a0001c0001t0001g0015a0001c0001t0004g0014a0001c0001t0015g0013 | 3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1370-9336C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53680026 | ||||||
| chr2:53680131
|
A | T | 44 | a0001c0001t0001g0171a0001c0001t0001g0174a0001c0001t0001g0175others(41): Show | 46 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.1370-9441T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53680131 | ||||||
| chr2:53680238
|
C | A | 1 | a0001c0001t0009g0192 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1370-9548G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53680238 | ||||||
| chr2:53680424
|
T | A | 5 | a0001c0001t0001g0151a0001c0001t0003g0146a0001c0001t0003g0147others(2): Show | 5 | HG02630.hp2 HG02896.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1370-9734A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53680424 | ||||||
| chr2:53680460
|
T | C | 1 | a0001c0001t0001g0069 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1370-9770A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53680460 | ||||||
| chr2:53680495
|
G | C | 110 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(107): Show | 112 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1370-9805C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53680495 | ||||||
| chr2:53680637
|
T | C | 10 | a0001c0001t0001g0016a0001c0001t0001g0106a0001c0001t0003g0043others(7): Show | 10 | HG01255.hp1 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1370-9947A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53680637 | ||||||
| chr2:53680694
|
T | C | 3 | a0001c0001t0002g0140a0001c0001t0002g0142a0001c0001t0006g0143 | 3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1370-10004A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53680694 | ||||||
| chr2:53680737
|
A | T | 4 | a0001c0002t0002g0232a0001c0002t0002g0233a0001c0002t0002g0236others(1): Show | 4 | HG00673.hp1 HG02040.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1370-10047T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53680737 | ||||||
| chr2:53680738
|
T | C | 124 | a0001c0001t0001g0016a0001c0001t0001g0106a0001c0001t0001g0268others(121): Show | 126 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1370-10048A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53680738 | ||||||
| chr2:53680884
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0004g0014a0001c0001t0015g0013 | 3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1370-10194G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53680884 | ||||||
| chr2:53680921
|
G | C | 1 | a0001c0001t0001g0155 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1370-10231C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53680921 | ||||||
| chr2:53681254
|
T | C | 338 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(335): Show | 345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.1370-10564A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53681254 | ||||||
| chr2:53681289
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1370-10599G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53681289 | ||||||
| chr2:53681360
|
A | C | 3 | a0001c0001t0003g0043a0001c0001t0003g0044a0001c0001t0003g0127 | 3 | HG02257.hp2 HG02280.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1370-10670T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53681360 | ||||||
| chr2:53681505
|
C | G | 188 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0106others(185): Show | 192 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.1370-10815G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53681505 | ||||||
| chr2:53681736
|
G | C | 1 | a0001c0001t0001g0153 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1370-11046C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53681736 | ||||||
| chr2:53681886
|
G | A | 6 | a0001c0001t0001g0040a0001c0001t0001g0124a0001c0001t0001g0149others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.1370-11196C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53681886 | ||||||
| chr2:53681918
|
G | T | 9 | a0001c0001t0002g0063a0001c0002t0002g0220a0001c0002t0002g0223others(6): Show | 9 | HG00423.hp1 HG02015.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1370-11228C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53681918 | ||||||
| chr2:53681919
|
G | A | 9 | a0001c0001t0002g0063a0001c0002t0002g0220a0001c0002t0002g0223others(6): Show | 9 | HG00423.hp1 HG02015.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1370-11229C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53681919 | ||||||
| chr2:53681926
|
G | A | 1 | a0001c0001t0003g0169 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1370-11236C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53681926 | ||||||
| chr2:53681953
|
T | C | 1 | a0001c0001t0001g0120 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1370-11263A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53681953 | ||||||
| chr2:53682063
|
G | A | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1370-11373C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53682063 | ||||||
| chr2:53682157
|
C | T | 1 | a0001c0001t0003g0339 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1370-11467G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53682157 | ||||||
| chr2:53682159
|
C | CA | 52 | a0001c0001t0001g0086a0001c0001t0001g0128a0001c0001t0001g0151others(49): Show | 54 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1370-11470dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53682159 | ||||||
| chr2:53682218
|
G | C | 12 | a0001c0001t0005g0003a0001c0003t0005g0312a0001c0003t0005g0329others(9): Show | 14 | HG00733.hp1 HG01106.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.1370-11528C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53682218 | ||||||
| chr2:53682224
|
T | G | 9 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0315others(6): Show | 9 | HG01167.hp1 HG02615.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1370-11534A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53682224 | ||||||
| chr2:53682238
|
T | C | 1 | a0001c0001t0002g0256 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1370-11548A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53682238 | ||||||
| chr2:53682280
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1370-11590T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53682280 | ||||||
| chr2:53682307
|
A | G | 200 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0016others(197): Show | 205 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.1369+11577T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53682307 | ||||||
| chr2:53682540
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1369+11344C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53682540 | ||||||
| chr2:53682783
|
C | T | 4 | a0001c0001t0001g0176a0001c0001t0003g0172a0001c0001t0003g0180others(1): Show | 4 | HG00621.hp1 HG02080.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1369+11101G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53682783 | ||||||
| chr2:53682816
|
T | C | 76 | a0001c0001t0001g0016a0001c0001t0001g0106a0001c0001t0001g0151others(73): Show | 78 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.1369+11068A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53682816 | ||||||
| chr2:53682926
|
G | A | 11 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(8): Show | 11 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.1369+10958C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53682926 | ||||||
| chr2:53682947
|
C | A | 3 | a0001c0001t0002g0140a0001c0001t0002g0142a0001c0001t0006g0143 | 3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1369+10937G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53682947 | ||||||
| chr2:53683021
|
T | C | 118 | a0001c0001t0001g0037a0001c0001t0001g0057a0001c0001t0001g0058others(115): Show | 120 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1369+10863A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53683021 | ||||||
| chr2:53683110
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0004g0014a0001c0001t0015g0013 | 3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1369+10774C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53683110 | ||||||
| chr2:53683132
|
C | G | 10 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(7): Show | 10 | HG00408.hp2 HG01081.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.1369+10752G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53683132 | ||||||
| chr2:53683257
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0135 | 2 | NA18962.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1369+10627G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53683257 | ||||||
| chr2:53683261
|
C | T | 9 | a0001c0001t0001g0211a0001c0001t0001g0216a0001c0001t0001g0217others(6): Show | 9 | HG01074.hp1 HG02572.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1369+10623G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53683261 | ||||||
| chr2:53683335
|
A | G | 11 | a0001c0001t0001g0016a0001c0001t0001g0106a0001c0001t0003g0043others(8): Show | 11 | HG01255.hp1 HG02257.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1369+10549T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53683335 | ||||||
| chr2:53683336
|
TCTTTTAA others(3): Show |
T | 11 | a0001c0001t0001g0016a0001c0001t0001g0106a0001c0001t0003g0043others(8): Show | 11 | HG01255.hp1 HG02257.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1369+10538_1369+10 others(16): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53683336 | ||||||
| chr2:53683394
|
T | A | 1 | a0001c0001t0009g0192 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1369+10490A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53683394 | ||||||
| chr2:53683414
|
T | TG | 8 | a0001c0001t0001g0171a0001c0001t0001g0174a0001c0001t0001g0175others(5): Show | 8 | HG02080.hp2 HG02818.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.1369+10469dupC | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53683414 | ||||||
| chr2:53683415
|
G | GT | 16 | a0001c0001t0001g0129a0001c0001t0001g0311a0001c0001t0001g0319others(13): Show | 16 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.1369+10468dupA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53683415 | ||||||
| chr2:53683416
|
T | G | 48 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0001g0176others(45): Show | 50 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.1369+10468A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53683416 | ||||||
| chr2:53683659
|
T | G | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270 | 3 | HG02630.hp1 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1369+10225A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53683659 | ||||||
| chr2:53683971
|
T | C | 1 | a0001c0001t0001g0025 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1369+9913A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53683971 | ||||||
| chr2:53683997
|
C | T | 50 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0001g0171others(47): Show | 52 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.1369+9887G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53683997 | ||||||
| chr2:53684111
|
A | G | 1 | a0001c0003t0005g0342 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1369+9773T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53684111 | ||||||
| chr2:53684151
|
T | C | 1 | a0001c0001t0004g0272 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1369+9733A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53684151 | ||||||
| chr2:53684300
|
T | C | 2 | a0001c0001t0003g0167a0001c0001t0003g0340 | 2 | NA19080.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1369+9584A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53684300 | ||||||
| chr2:53684324
|
T | C | 1 | a0001c0001t0001g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1369+9560A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53684324 | ||||||
| chr2:53684447
|
G | T | 4 | a0001c0001t0003g0178a0001c0001t0003g0196a0001c0001t0003g0198others(1): Show | 4 | NA18955.hp1 NA18967.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1369+9437C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53684447 | ||||||
| chr2:53684452
|
C | T | 2 | a0001c0002t0002g0243a0001c0002t0006g0244 | 2 | HG02027.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1369+9432G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53684452 | ||||||
| chr2:53684482
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1369+9402T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53684482 | ||||||
| chr2:53684583
|
A | C | 1 | a0001c0001t0003g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1369+9301T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53684583 | ||||||
| chr2:53684612
|
T | C | 1 | a0001c0002t0002g0223 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1369+9272A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53684612 | ||||||
| chr2:53684676
|
G | C | 3 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0004g0157 | 3 | HG02109.hp2 HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1369+9208C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53684676 | ||||||
| chr2:53684832
|
A | T | 1 | a0001c0002t0002g0250 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1369+9052T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53684832 | ||||||
| chr2:53684845
|
A | G | 21 | a0001c0001t0001g0005a0001c0001t0001g0149a0001c0001t0001g0155others(18): Show | 22 | HG00099.hp1 HG01099.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.1369+9039T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53684845 | ||||||
| chr2:53684991
|
G | A | 10 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(7): Show | 10 | HG00408.hp2 HG01081.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.1369+8893C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53684991 | ||||||
| chr2:53685120
|
G | A | 5 | a0001c0001t0001g0149a0001c0001t0001g0166a0001c0001t0001g0210others(2): Show | 5 | HG01891.hp2 HG02559.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1369+8764C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53685120 | ||||||
| chr2:53685136
|
T | C | 5 | a0001c0001t0001g0171a0001c0001t0001g0174a0001c0001t0001g0175others(2): Show | 5 | HG02080.hp2 NA18968.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.1369+8748A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53685136 | ||||||
| chr2:53685202
|
A | C | 60 | a0001c0001t0001g0005a0001c0001t0001g0151a0001c0001t0001g0153others(57): Show | 63 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1369+8682T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53685202 | ||||||
| chr2:53685414
|
G | A | 1 | a0001c0003t0011g0330 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1369+8470C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53685414 | ||||||
| chr2:53685424
|
A | T | 1 | a0001c0001t0001g0311 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1369+8460T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53685424 | ||||||
| chr2:53685648
|
T | A | 1 | a0001c0002t0006g0244 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1369+8236A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53685648 | ||||||
| chr2:53685727
|
A | G | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1369+8157T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53685727 | ||||||
| chr2:53685975
|
A | T | 3 | a0001c0001t0001g0015a0001c0001t0004g0014a0001c0001t0015g0013 | 3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1369+7909T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53685975 | ||||||
| chr2:53686068
|
G | A | 1 | a0001c0003t0002g0281 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1369+7816C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53686068 | ||||||
| chr2:53686279
|
T | G | 3 | a0001c0001t0001g0038a0001c0001t0001g0088a0001c0001t0001g0090 | 3 | HG01074.hp2 HG01943.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1369+7605A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53686279 | ||||||
| chr2:53686472
|
C | A | 44 | a0001c0001t0005g0003a0001c0003t0002g0021a0001c0003t0002g0278others(41): Show | 46 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.1369+7412G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53686472 | ||||||
| chr2:53686593
|
A | G | 3 | a0001c0001t0001g0015a0001c0001t0004g0014a0001c0001t0015g0013 | 3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1369+7291T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53686593 | ||||||
| chr2:53686662
|
TA | T | 164 | a0001c0001t0001g0015a0001c0001t0001g0151a0001c0001t0001g0153others(161): Show | 168 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.1369+7221delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53686662 | ||||||
| chr2:53686728
|
C | T | 341 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(338): Show | 349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.1369+7156G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53686728 | ||||||
| chr2:53686759
|
C | G | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1369+7125G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53686759 | ||||||
| chr2:53686816
|
G | C | 2 | a0001c0001t0001g0319a0001c0001t0001g0323 | 2 | HG00408.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1369+7068C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53686816 | ||||||
| chr2:53686866
|
C | T | 1 | a0001c0001t0008g0029 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1369+7018G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53686866 | ||||||
| chr2:53687008
|
T | C | 6 | a0001c0001t0008g0029a0001c0001t0008g0031a0001c0001t0008g0032others(3): Show | 6 | HG01255.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1369+6876A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53687008 | ||||||
| chr2:53687024
|
G | T | 218 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(215): Show | 223 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.1369+6860C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53687024 | ||||||
| chr2:53687038
|
G | C | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1369+6846C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53687038 | ||||||
| chr2:53687105
|
C | A | 3 | a0001c0001t0001g0015a0001c0001t0004g0014a0001c0001t0015g0013 | 3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1369+6779G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53687105 | ||||||
| chr2:53687258
|
A | C | 3 | a0002c0004t0010g0137a0002c0004t0010g0138a0002c0004t0010g0139 | 3 | HG02818.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1369+6626T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53687258 | ||||||
| chr2:53687262
|
A | T | 51 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0001g0171others(48): Show | 53 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.1369+6622T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53687262 | ||||||
| chr2:53687462
|
G | C | 5 | a0001c0001t0001g0151a0001c0001t0003g0146a0001c0001t0003g0147others(2): Show | 5 | HG02630.hp2 HG02896.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1369+6422C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53687462 | ||||||
| chr2:53687521
|
G | A | 1 | a0001c0001t0003g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1369+6363C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53687521 | ||||||
| chr2:53687624
|
C | A | 1 | a0001c0001t0008g0031 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1369+6260G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53687624 | ||||||
| chr2:53687924
|
T | C | 55 | a0001c0001t0002g0063a0001c0001t0002g0131a0001c0001t0002g0228others(52): Show | 55 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.1369+5960A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53687924 | ||||||
| chr2:53687971
|
C | T | 1 | a0001c0002t0002g0243 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1369+5913G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53687971 | ||||||
| chr2:53687986
|
T | G | 1 | a0001c0001t0008g0029 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1369+5898A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53687986 | ||||||
| chr2:53688174
|
G | T | 17 | a0001c0001t0001g0005a0001c0001t0001g0149a0001c0001t0001g0155others(14): Show | 18 | HG00099.hp1 HG01099.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1369+5710C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53688174 | ||||||
| chr2:53688223
|
C | A | 2 | a0001c0001t0001g0207a0001c0001t0003g0206 | 2 | NA18987.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1369+5661G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53688223 | ||||||
| chr2:53688282
|
G | A | 1 | a0001c0001t0004g0272 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1369+5602C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53688282 | ||||||
| chr2:53688300
|
C | T | 99 | a0001c0001t0002g0063a0001c0001t0002g0131a0001c0001t0002g0228others(96): Show | 101 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1369+5584G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53688300 | ||||||
| chr2:53688318
|
G | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0149a0001c0001t0001g0155others(14): Show | 18 | HG00099.hp1 HG01099.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1369+5566C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53688318 | ||||||
| chr2:53688460
|
G | C | 1 | a0001c0001t0001g0048 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1369+5424C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53688460 | ||||||
| chr2:53688726
|
T | C | 106 | a0001c0001t0002g0063a0001c0001t0002g0131a0001c0001t0002g0140others(103): Show | 108 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.1369+5158A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53688726 | ||||||
| chr2:53688808
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1369+5076A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53688808 | ||||||
| chr2:53689033
|
A | T | 7 | a0001c0001t0001g0046a0001c0001t0001g0079a0001c0001t0001g0135others(4): Show | 7 | HG01243.hp1 HG01243.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1369+4851T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53689033 | ||||||
| chr2:53689082
|
T | G | 2 | a0001c0003t0002g0321a0001c0003t0002g0322 | 2 | HG02523.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1369+4802A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53689082 | ||||||
| chr2:53689526
|
C | G | 7 | a0001c0001t0001g0274a0001c0001t0004g0272a0001c0001t0004g0273others(4): Show | 7 | HG01074.hp1 HG01261.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1369+4358G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53689526 | ||||||
| chr2:53689534
|
T | C | 1 | a0001c0001t0003g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1369+4350A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53689534 | ||||||
| chr2:53689658
|
T | G | 1 | a0001c0001t0001g0107 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1369+4226A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53689658 | ||||||
| chr2:53689712
|
G | C | 117 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(114): Show | 119 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.1369+4172C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53689712 | ||||||
| chr2:53689811
|
G | C | 1 | a0001c0001t0001g0212 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1369+4073C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53689811 | ||||||
| chr2:53689839
|
TA | T | 3 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0004g0157 | 3 | HG02109.hp2 HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1369+4044delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53689839 | ||||||
| chr2:53689936
|
T | C | 15 | a0001c0001t0001g0151a0001c0001t0001g0211a0001c0001t0001g0216others(12): Show | 15 | HG01074.hp1 HG01261.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.1369+3948A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53689936 | ||||||
| chr2:53689989
|
T | C | 10 | a0001c0001t0001g0016a0001c0001t0003g0043a0001c0001t0003g0044others(7): Show | 10 | HG01255.hp1 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1369+3895A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53689989 | ||||||
| chr2:53690044
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1369+3840G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53690044 | ||||||
| chr2:53690057
|
G | A | 1 | a0001c0003t0002g0281 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1369+3827C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53690057 | ||||||
| chr2:53690105
|
A | G | 2 | a0002c0004t0010g0136a0002c0004t0013g0012 | 2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1369+3779T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53690105 | ||||||
| chr2:53690217
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1369+3667G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53690217 | ||||||
| chr2:53690251
|
A | T | 10 | a0001c0001t0001g0151a0001c0001t0003g0146a0001c0001t0003g0147others(7): Show | 10 | HG00323.hp1 HG01256.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1369+3633T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53690251 | ||||||
| chr2:53690255
|
T | A | 186 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(183): Show | 190 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1369+3629A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53690255 | ||||||
| chr2:53690259
|
T | A | 28 | a0001c0001t0001g0098a0001c0001t0001g0134a0001c0001t0001g0210others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.1369+3625A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53690259 | ||||||
| chr2:53690292
|
A | G | 2 | a0001c0001t0008g0034a0001c0001t0008g0035 | 2 | HG01255.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1369+3592T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53690292 | ||||||
| chr2:53690389
|
G | C | 1 | a0001c0001t0003g0167 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1369+3495C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53690389 | ||||||
| chr2:53690529
|
C | T | 99 | a0001c0001t0002g0063a0001c0001t0002g0131a0001c0001t0002g0228others(96): Show | 101 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1369+3355G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53690529 | ||||||
| chr2:53690560
|
G | A | 1 | a0001c0001t0003g0168 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1369+3324C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53690560 | ||||||
| chr2:53690623
|
G | GT | 63 | a0001c0001t0001g0005a0001c0001t0001g0151a0001c0001t0001g0153others(60): Show | 66 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.1369+3260dupA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53690623 | ||||||
| chr2:53690664
|
C | T | 99 | a0001c0001t0002g0063a0001c0001t0002g0131a0001c0001t0002g0228others(96): Show | 101 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1369+3220G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53690664 | ||||||
| chr2:53690684
|
T | G | 10 | a0001c0001t0001g0016a0001c0001t0003g0043a0001c0001t0003g0044others(7): Show | 10 | HG01255.hp1 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1369+3200A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53690684 | ||||||
| chr2:53690883
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1369+3001G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53690883 | ||||||
| chr2:53690969
|
A | T | 1 | a0001c0001t0001g0158 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1369+2915T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53690969 | ||||||
| chr2:53691108
|
C | G | 283 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(280): Show | 289 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(286): Show |
intron_variant | MODIFIER | c.1369+2776G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53691108 | ||||||
| chr2:53691110
|
A | C | 6 | a0001c0001t0001g0015a0001c0001t0002g0140a0001c0001t0002g0142others(3): Show | 6 | HG02258.hp1 HG02615.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1369+2774T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53691110 | ||||||
| chr2:53691262
|
G | C | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270 | 3 | HG02630.hp1 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1369+2622C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53691262 | ||||||
| chr2:53691304
|
G | A | 1 | a0001c0001t0005g0003 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1369+2580C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53691304 | ||||||
| chr2:53691353
|
A | G | 10 | a0001c0001t0001g0211a0001c0001t0001g0216a0001c0001t0001g0217others(7): Show | 10 | HG01074.hp1 HG01261.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1369+2531T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53691353 | ||||||
| chr2:53691466
|
G | A | 1 | a0001c0001t0004g0123 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1369+2418C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53691466 | ||||||
| chr2:53691751
|
C | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0141others(2): Show | 5 | HG00738.hp1 HG01884.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.1369+2133G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53691751 | ||||||
| chr2:53691805
|
C | T | 1 | a0001c0001t0003g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1369+2079G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53691805 | ||||||
| chr2:53692021
|
T | G | 1 | a0001c0001t0001g0072 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1369+1863A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53692021 | ||||||
| chr2:53692083
|
C | G | 3 | a0001c0003t0002g0286a0001c0003t0002g0292a0001c0003t0002g0293 | 3 | HG02155.hp1 NA18939.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1369+1801G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53692083 | ||||||
| chr2:53692210
|
G | A | 52 | a0001c0001t0002g0063a0001c0001t0002g0131a0001c0002t0002g0017others(49): Show | 52 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1369+1674C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53692210 | ||||||
| chr2:53692485
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1369+1399T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53692485 | ||||||
| chr2:53692526
|
C | G | 1 | a0001c0001t0002g0063 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1369+1358G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53692526 | ||||||
| chr2:53692630
|
C | T | 10 | a0001c0001t0001g0211a0001c0001t0001g0216a0001c0001t0001g0217others(7): Show | 10 | HG01074.hp1 HG01261.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1369+1254G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53692630 | ||||||
| chr2:53692631
|
T | C | 25 | a0001c0001t0001g0016a0001c0001t0001g0106a0001c0001t0001g0268others(22): Show | 25 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.1369+1253A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53692631 | ||||||
| chr2:53692646
|
G | C | 1 | a0001c0002t0002g0267 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1369+1238C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53692646 | ||||||
| chr2:53693214
|
G | C | 1 | a0001c0001t0004g0324 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1369+670C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53693214 | ||||||
| chr2:53693256
|
G | T | 1 | a0001c0003t0005g0312 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1369+628C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53693256 | ||||||
| chr2:53693457
|
G | A | 7 | a0001c0001t0001g0106a0001c0001t0008g0029a0001c0001t0008g0031others(4): Show | 7 | HG01255.hp1 HG02280.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1369+427C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53693457 | ||||||
| chr2:53693721
|
A | C | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0141others(2): Show | 5 | HG00738.hp1 HG01884.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.1369+163T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53693721 | ||||||
| chr2:53693793
|
C | T | 1 | a0001c0001t0001g0317 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1369+91G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53693793 | ||||||
| chr2:53693794
|
G | A | 173 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0106others(170): Show | 177 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.1369+90C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53693794 | ||||||
| chr2:53693833
|
A | G | 1 | a0001c0002t0002g0241 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1369+51T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 9/9 | chr2 | 53693833 | ||||||
| chr2:53694133
|
C | T | 99 | a0001c0001t0002g0063a0001c0001t0002g0131a0001c0001t0002g0228others(96): Show | 101 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1239-119G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53694133 | ||||||
| chr2:53694157
|
A | G | 7 | a0001c0001t0001g0274a0001c0001t0004g0272a0001c0001t0004g0273others(4): Show | 7 | HG01074.hp1 HG01261.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1239-143T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53694157 | ||||||
| chr2:53694184
|
C | G | 16 | a0001c0001t0001g0211a0001c0001t0001g0216a0001c0001t0001g0217others(13): Show | 16 | HG01074.hp1 HG01167.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.1239-170G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53694184 | ||||||
| chr2:53694617
|
G | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0202 | 2 | HG00733.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1239-603C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53694617 | ||||||
| chr2:53694646
|
A | G | 62 | a0001c0001t0001g0005a0001c0001t0001g0151a0001c0001t0001g0153others(59): Show | 65 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.1239-632T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53694646 | ||||||
| chr2:53694694
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1239-680A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53694694 | ||||||
| chr2:53694754
|
A | G | 62 | a0001c0001t0001g0005a0001c0001t0001g0151a0001c0001t0001g0153others(59): Show | 65 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.1239-740T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53694754 | ||||||
| chr2:53694800
|
T | C | 3 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0004g0157 | 3 | HG02109.hp2 HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1239-786A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53694800 | ||||||
| chr2:53694849
|
T | C | 4 | a0001c0001t0001g0149a0001c0001t0001g0166a0001c0001t0001g0210others(1): Show | 4 | HG01891.hp2 HG02559.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1239-835A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53694849 | ||||||
| chr2:53694884
|
C | T | 208 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0016others(205): Show | 213 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.1239-870G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53694884 | ||||||
| chr2:53694900
|
C | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0158a0001c0001t0001g0161others(7): Show | 11 | HG00099.hp1 HG01099.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.1239-886G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53694900 | ||||||
| chr2:53694987
|
G | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | HG03704.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1239-973C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53694987 | ||||||
| chr2:53695119
|
G | C | 219 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(216): Show | 224 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.1239-1105C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53695119 | ||||||
| chr2:53695134
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1239-1120C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53695134 | ||||||
| chr2:53695188
|
C | T | 6 | a0001c0001t0008g0029a0001c0001t0008g0031a0001c0001t0008g0032others(3): Show | 6 | HG01255.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1239-1174G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53695188 | ||||||
| chr2:53695319
|
C | T | 209 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(206): Show | 214 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.1239-1305G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53695319 | ||||||
| chr2:53695433
|
T | C | 10 | a0001c0001t0001g0211a0001c0001t0001g0216a0001c0001t0001g0217others(7): Show | 10 | HG01074.hp1 HG01261.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1239-1419A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53695433 | ||||||
| chr2:53695451
|
G | C | 1 | a0001c0002t0002g0230 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1239-1437C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53695451 | ||||||
| chr2:53695651
|
ATAATGCC others(2): Show |
A | 25 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0141others(22): Show | 25 | HG00738.hp1 HG01074.hp1 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.1239-1646_1239-163 others(13): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53695651 | ||||||
| chr2:53695688
|
A | T | 221 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(218): Show | 226 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.1239-1674T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53695688 | ||||||
| chr2:53695702
|
T | C | 1 | a0001c0003t0006g0294 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1239-1688A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53695702 | ||||||
| chr2:53695738
|
T | C | 1 | a0001c0002t0002g0231 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1239-1724A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53695738 | ||||||
| chr2:53695801
|
G | A | 1 | a0001c0001t0008g0195 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1239-1787C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53695801 | ||||||
| chr2:53695806
|
C | G | 211 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(208): Show | 216 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.1239-1792G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53695806 | ||||||
| chr2:53695911
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1239-1897A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53695911 | ||||||
| chr2:53695993
|
T | C | 4 | a0001c0001t0001g0149a0001c0001t0001g0166a0001c0001t0001g0210others(1): Show | 4 | HG01891.hp2 HG02559.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1239-1979A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53695993 | ||||||
| chr2:53696047
|
A | T | 1 | a0001c0002t0002g0238 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1239-2033T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53696047 | ||||||
| chr2:53696078
|
T | C | 61 | a0001c0001t0001g0005a0001c0001t0001g0151a0001c0001t0001g0153others(58): Show | 64 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.1239-2064A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53696078 | ||||||
| chr2:53696136
|
T | C | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0141others(2): Show | 5 | HG00738.hp1 HG01884.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.1239-2122A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53696136 | ||||||
| chr2:53696315
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1239-2301G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53696315 | ||||||
| chr2:53696340
|
C | T | 3 | a0001c0001t0002g0140a0001c0001t0002g0142a0001c0001t0006g0143 | 3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1239-2326G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53696340 | ||||||
| chr2:53696354
|
C | T | 4 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(1): Show | 4 | HG02630.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1239-2340G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53696354 | ||||||
| chr2:53696384
|
G | A | 7 | a0001c0001t0001g0015a0001c0001t0004g0014a0001c0001t0015g0013others(4): Show | 7 | HG02258.hp1 HG02818.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1239-2370C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53696384 | ||||||
| chr2:53696450
|
TA | T | 8 | a0001c0001t0001g0163a0001c0001t0001g0319a0001c0001t0004g0162others(5): Show | 8 | NA18973.hp2 NA18975.hp1 NA18975.hp2 others(5): Show |
intron_variant | MODIFIER | c.1239-2437delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53696450 | ||||||
| chr2:53696546
|
G | C | 1 | a0001c0001t0003g0183 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1239-2532C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53696546 | ||||||
| chr2:53696639
|
T | C | 4 | a0001c0001t0002g0140a0001c0001t0002g0142a0001c0001t0002g0154others(1): Show | 4 | HG01243.hp2 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1239-2625A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53696639 | ||||||
| chr2:53696647
|
T | C | 1 | a0001c0003t0002g0278 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1239-2633A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53696647 | ||||||
| chr2:53696763
|
C | T | 1 | a0001c0003t0006g0294 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1239-2749G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53696763 | ||||||
| chr2:53696784
|
T | C | 3 | a0001c0001t0001g0120a0001c0001t0004g0027a0006c0008t0001g0028 | 3 | NA18945.hp2 NA18955.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1239-2770A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53696784 | ||||||
| chr2:53696816
|
T | G | 1 | a0001c0001t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1239-2802A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53696816 | ||||||
| chr2:53696817
|
G | A | 7 | a0001c0001t0001g0037a0001c0001t0001g0058a0001c0001t0001g0074others(4): Show | 7 | NA18959.hp2 NA18978.hp1 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.1239-2803C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53696817 | ||||||
| chr2:53696879
|
G | A | 2 | a0001c0001t0001g0149a0001c0001t0004g0150 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1239-2865C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53696879 | ||||||
| chr2:53697167
|
C | T | 206 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(203): Show | 210 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.1238+3104G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53697167 | ||||||
| chr2:53697286
|
T | C | 90 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(87): Show | 93 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.1238+2985A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53697286 | ||||||
| chr2:53697458
|
GC | G | 55 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0003g0218others(52): Show | 56 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.1238+2812delG | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53697458 | ||||||
| chr2:53697560
|
A | C | 12 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(9): Show | 12 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.1238+2711T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53697560 | ||||||
| chr2:53697591
|
C | G | 50 | a0001c0001t0003g0339a0001c0003t0001g0305a0001c0003t0001g0306others(47): Show | 51 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.1238+2680G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53697591 | ||||||
| chr2:53697864
|
C | G | 1 | a0001c0001t0001g0025 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1238+2407G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53697864 | ||||||
| chr2:53697879
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1238+2392G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53697879 | ||||||
| chr2:53697950
|
GTCTCAAT others(7): Show |
G | 1 | a0001c0002t0002g0223 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1238+2307_1238+232 others(18): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53697950 | ||||||
| chr2:53698198
|
C | T | 4 | a0001c0001t0001g0149a0001c0001t0001g0166a0001c0001t0001g0210others(1): Show | 4 | HG01891.hp2 HG02559.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1238+2073G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53698198 | ||||||
| chr2:53698261
|
T | G | 36 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(33): Show | 37 | HG00099.hp1 HG00408.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.1238+2010A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53698261 | ||||||
| chr2:53698359
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1238+1912G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53698359 | ||||||
| chr2:53698514
|
C | T | 1 | a0001c0001t0003g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1238+1757G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53698514 | ||||||
| chr2:53698557
|
C | A | 3 | a0001c0001t0003g0043a0001c0001t0003g0044a0001c0001t0003g0127 | 3 | HG02257.hp2 HG02280.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1238+1714G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53698557 | ||||||
| chr2:53698623
|
C | A | 1 | a0001c0001t0001g0166 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1238+1648G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53698623 | ||||||
| chr2:53699030
|
T | A | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1238+1241A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53699030 | ||||||
| chr2:53699145
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1238+1126G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53699145 | ||||||
| chr2:53699166
|
T | C | 222 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(219): Show | 226 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.1238+1105A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53699166 | ||||||
| chr2:53699416
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1238+855G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53699416 | ||||||
| chr2:53699426
|
T | C | 1 | a0001c0001t0003g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1238+845A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53699426 | ||||||
| chr2:53699441
|
G | A | 5 | a0001c0003t0002g0288a0001c0003t0002g0290a0001c0003t0002g0291others(2): Show | 5 | HG00438.hp1 HG02074.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.1238+830C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53699441 | ||||||
| chr2:53699495
|
A | C | 19 | a0001c0001t0001g0005a0001c0001t0001g0149a0001c0001t0001g0155others(16): Show | 20 | HG00099.hp1 HG01099.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.1238+776T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53699495 | ||||||
| chr2:53699650
|
C | CAA | 77 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0001g0174others(74): Show | 79 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.1238+619_1238+620d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53699650 | ||||||
| chr2:53699739
|
GC | G | 61 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0001g0174others(58): Show | 63 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(60): Show |
intron_variant | MODIFIER | c.1238+531delG | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53699739 | ||||||
| chr2:53699769
|
T | G | 1 | a0001c0001t0001g0108 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1238+502A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53699769 | ||||||
| chr2:53700175
|
A | C | 1 | a0001c0002t0002g0248 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1238+96T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53700175 | ||||||
| chr2:53700176
|
T | TAC | 65 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0001g0174others(62): Show | 67 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.1238+93_1238+94dup others(2): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53700176 | ||||||
| chr2:53700233
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1238+38A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 8/9 | chr2 | 53700233 | ||||||
| chr2:53700551
|
A | C | 1 | a0001c0001t0008g0035 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.981-23T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53700551 | ||||||
| chr2:53700629
|
T | C | 2 | a0001c0003t0002g0279a0001c0003t0002g0300 | 2 | NA19002.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.981-101A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53700629 | ||||||
| chr2:53700711
|
C | T | 1 | a0001c0002t0006g0222 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.981-183G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53700711 | ||||||
| chr2:53700786
|
T | TA | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.981-259dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53700786 | ||||||
| chr2:53700795
|
T | A | 1 | a0001c0001t0001g0166 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.981-267A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53700795 | ||||||
| chr2:53701003
|
T | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0141others(2): Show | 5 | HG00738.hp1 HG01884.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.981-475A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53701003 | ||||||
| chr2:53701005
|
T | C | 1 | a0001c0003t0002g0299 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.981-477A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53701005 | ||||||
| chr2:53701129
|
A | G | 24 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(21): Show | 25 | HG00099.hp1 HG00738.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.981-601T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53701129 | ||||||
| chr2:53701182
|
C | T | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.981-654G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53701182 | ||||||
| chr2:53701220
|
C | T | 8 | a0001c0001t0001g0149a0001c0001t0001g0155a0001c0001t0001g0156others(5): Show | 8 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.981-692G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53701220 | ||||||
| chr2:53701245
|
C | T | 3 | a0001c0001t0002g0140a0001c0001t0002g0142a0001c0001t0006g0143 | 3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.981-717G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53701245 | ||||||
| chr2:53701288
|
T | A | 1 | a0001c0001t0004g0011 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.981-760A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53701288 | ||||||
| chr2:53701299
|
T | C | 55 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0001g0174others(52): Show | 57 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.981-771A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53701299 | ||||||
| chr2:53701328
|
C | G | 63 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0141others(60): Show | 64 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.981-800G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53701328 | ||||||
| chr2:53701367
|
T | C | 1 | a0001c0001t0004g0026 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.981-839A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53701367 | ||||||
| chr2:53701442
|
T | C | 9 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0315others(6): Show | 9 | HG01167.hp1 HG02615.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.981-914A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53701442 | ||||||
| chr2:53701501
|
G | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0149a0001c0001t0001g0155others(15): Show | 19 | HG00099.hp1 HG01099.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.981-973C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53701501 | ||||||
| chr2:53701587
|
T | A | 1 | a0001c0001t0001g0317 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.981-1059A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53701587 | ||||||
| chr2:53701898
|
C | A | 1 | a0001c0001t0001g0092 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.981-1370G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53701898 | ||||||
| chr2:53701975
|
C | T | 1 | a0001c0001t0003g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.981-1447G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53701975 | ||||||
| chr2:53702054
|
C | T | 3 | a0001c0001t0001g0141a0001c0001t0001g0144a0001c0001t0001g0145 | 3 | HG00738.hp1 HG01884.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.981-1526G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53702054 | ||||||
| chr2:53702079
|
A | C | 3 | a0001c0001t0002g0140a0001c0001t0002g0142a0001c0001t0006g0143 | 3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.981-1551T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53702079 | ||||||
| chr2:53702275
|
G | A | 6 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0003g0146others(3): Show | 6 | HG02630.hp2 HG02896.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.981-1747C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53702275 | ||||||
| chr2:53702279
|
C | T | 49 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(46): Show | 50 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.981-1751G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53702279 | ||||||
| chr2:53702409
|
C | G | 14 | a0001c0001t0001g0037a0001c0001t0001g0057a0001c0001t0001g0058others(11): Show | 14 | HG02132.hp1 NA18944.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.981-1881G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53702409 | ||||||
| chr2:53702436
|
ATGGATAA others(4): Show |
A | 1 | a0001c0003t0002g0298 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.981-1919_981-1909d others(13): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53702436 | ||||||
| chr2:53702492
|
A | C | 13 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(10): Show | 13 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.981-1964T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53702492 | ||||||
| chr2:53702542
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.981-2014G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53702542 | ||||||
| chr2:53702549
|
T | C | 3 | a0001c0001t0002g0140a0001c0001t0002g0142a0001c0001t0006g0143 | 3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.981-2021A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53702549 | ||||||
| chr2:53702718
|
C | T | 106 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(103): Show | 109 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.981-2190G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53702718 | ||||||
| chr2:53702769
|
A | T | 1 | a0001c0001t0003g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.981-2241T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53702769 | ||||||
| chr2:53703457
|
A | G | 2 | a0001c0001t0001g0046a0001c0001t0001g0135 | 2 | NA18962.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.981-2929T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53703457 | ||||||
| chr2:53703460
|
A | T | 3 | a0001c0001t0002g0140a0001c0001t0002g0142a0001c0001t0006g0143 | 3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.981-2932T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53703460 | ||||||
| chr2:53703484
|
G | A | 49 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(46): Show | 50 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.981-2956C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53703484 | ||||||
| chr2:53703543
|
G | A | 1 | a0001c0003t0002g0289 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.981-3015C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53703543 | ||||||
| chr2:53703546
|
C | G | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.981-3018G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53703546 | ||||||
| chr2:53703682
|
T | C | 56 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(53): Show | 56 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.981-3154A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53703682 | ||||||
| chr2:53703712
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.981-3184G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53703712 | ||||||
| chr2:53703717
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.981-3189C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53703717 | ||||||
| chr2:53703927
|
C | T | 55 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0001g0174others(52): Show | 57 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.981-3399G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53703927 | ||||||
| chr2:53704053
|
G | A | 111 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0268others(108): Show | 112 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.981-3525C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704053 | ||||||
| chr2:53704082
|
G | C | 3 | a0001c0001t0003g0178a0001c0001t0003g0196a0001c0001t0003g0198 | 3 | NA18955.hp1 NA18986.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.981-3554C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704082 | ||||||
| chr2:53704088
|
G | C | 1 | a0001c0001t0001g0115 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.981-3560C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704088 | ||||||
| chr2:53704142
|
C | G | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0141others(2): Show | 5 | HG00738.hp1 HG01884.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.981-3614G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704142 | ||||||
| chr2:53704339
|
C | G | 1 | a0001c0001t0001g0317 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.981-3811G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704339 | ||||||
| chr2:53704359
|
C | CA | 53 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0036others(50): Show | 54 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.981-3832dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704359 | ||||||
| chr2:53704359
|
CA | C | 116 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0268others(113): Show | 117 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.981-3832delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704359 | ||||||
| chr2:53704359
|
CAA | C | 26 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0141others(23): Show | 26 | HG00738.hp1 HG01169.hp1 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.981-3833_981-3832d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704359 | ||||||
| chr2:53704359
|
CAAA | C | 53 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0001g0174others(50): Show | 55 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.981-3834_981-3832d others(5): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704359 | ||||||
| chr2:53704393
|
T | C | 1 | a0001c0001t0001g0334 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.981-3865A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704393 | ||||||
| chr2:53704425
|
A | G | 4 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0004g0014others(1): Show | 4 | HG02258.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.981-3897T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704425 | ||||||
| chr2:53704488
|
G | C | 3 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0004g0157 | 3 | HG02109.hp2 HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.981-3960C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704488 | ||||||
| chr2:53704791
|
A | T | 1 | a0001c0003t0002g0310 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.981-4263T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704791 | ||||||
| chr2:53704869
|
C | T | 115 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0268others(112): Show | 116 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.981-4341G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704869 | ||||||
| chr2:53704871
|
C | T | 2 | a0001c0001t0001g0202a0001c0001t0003g0203 | 2 | HG01358.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.981-4343G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704871 | ||||||
| chr2:53704969
|
A | G | 1 | a0002c0004t0013g0012 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.981-4441T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704969 | ||||||
| chr2:53704997
|
G | C | 50 | a0001c0001t0003g0339a0001c0003t0001g0305a0001c0003t0001g0306others(47): Show | 51 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.981-4469C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53704997 | ||||||
| chr2:53705295
|
G | A | 3 | a0001c0001t0001g0040a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG00280.hp1 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.981-4767C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53705295 | ||||||
| chr2:53705310
|
C | T | 2 | a0001c0002t0002g0243a0001c0002t0006g0244 | 2 | HG02027.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.981-4782G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53705310 | ||||||
| chr2:53705361
|
C | A | 56 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(53): Show | 56 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.981-4833G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53705361 | ||||||
| chr2:53705532
|
T | G | 224 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(221): Show | 228 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.981-5004A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53705532 | ||||||
| chr2:53705705
|
T | A | 3 | a0001c0001t0001g0120a0001c0001t0004g0027a0006c0008t0001g0028 | 3 | NA18945.hp2 NA18955.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.981-5177A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53705705 | ||||||
| chr2:53705934
|
T | A | 15 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(12): Show | 15 | HG00408.hp2 HG01081.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.981-5406A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53705934 | ||||||
| chr2:53705943
|
C | G | 15 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(12): Show | 15 | HG00408.hp2 HG01081.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.981-5415G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53705943 | ||||||
| chr2:53705947
|
T | C | 15 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(12): Show | 15 | HG00408.hp2 HG01081.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.981-5419A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53705947 | ||||||
| chr2:53705949
|
C | T | 15 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(12): Show | 15 | HG00408.hp2 HG01081.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.981-5421G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53705949 | ||||||
| chr2:53705951
|
G | T | 15 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(12): Show | 15 | HG00408.hp2 HG01081.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.981-5423C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53705951 | ||||||
| chr2:53705979
|
T | C | 1 | a0001c0001t0003g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.981-5451A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53705979 | ||||||
| chr2:53706015
|
T | A | 5 | a0001c0001t0001g0149a0001c0001t0001g0166a0001c0001t0001g0210others(2): Show | 5 | HG01891.hp2 HG02559.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.981-5487A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53706015 | ||||||
| chr2:53706163
|
A | G | 15 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(12): Show | 15 | HG00408.hp2 HG01081.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.981-5635T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53706163 | ||||||
| chr2:53706208
|
G | C | 1 | a0001c0001t0003g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.981-5680C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53706208 | ||||||
| chr2:53706301
|
A | G | 1 | a0001c0001t0001g0311 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.981-5773T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53706301 | ||||||
| chr2:53706653
|
G | T | 5 | a0001c0001t0001g0149a0001c0001t0001g0166a0001c0001t0001g0210others(2): Show | 5 | HG01891.hp2 HG02559.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.981-6125C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53706653 | ||||||
| chr2:53706686
|
C | A | 69 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(66): Show | 72 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.981-6158G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53706686 | ||||||
| chr2:53706769
|
T | A | 1 | a0001c0001t0002g0229 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.981-6241A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53706769 | ||||||
| chr2:53706887
|
A | C | 16 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(13): Show | 16 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.981-6359T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53706887 | ||||||
| chr2:53706944
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.981-6416G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53706944 | ||||||
| chr2:53706957
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.981-6429C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53706957 | ||||||
| chr2:53707014
|
C | G | 92 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(89): Show | 95 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.981-6486G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53707014 | ||||||
| chr2:53707023
|
T | A | 4 | a0001c0001t0002g0140a0001c0001t0002g0142a0001c0001t0002g0154others(1): Show | 4 | HG01243.hp2 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.981-6495A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53707023 | ||||||
| chr2:53707191
|
C | G | 3 | a0001c0001t0002g0140a0001c0001t0002g0142a0001c0001t0006g0143 | 3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.981-6663G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53707191 | ||||||
| chr2:53707201
|
A | C | 1 | a0001c0001t0002g0131 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.981-6673T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53707201 | ||||||
| chr2:53707405
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.981-6877C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53707405 | ||||||
| chr2:53707646
|
C | CA | 77 | a0001c0001t0001g0005a0001c0001t0001g0107a0001c0001t0001g0149others(74): Show | 78 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.980+6737dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53707646 | ||||||
| chr2:53707698
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0097 | 2 | HG03490.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.980+6686G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53707698 | ||||||
| chr2:53707767
|
G | C | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.980+6617C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53707767 | ||||||
| chr2:53707961
|
C | CA | 12 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0001g0091others(9): Show | 12 | HG00323.hp1 HG00738.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.980+6422dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53707961 | ||||||
| chr2:53707961
|
CA | C | 181 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0141others(178): Show | 184 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.980+6422delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53707961 | ||||||
| chr2:53707974
|
A | G | 7 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0003g0146others(4): Show | 7 | HG02630.hp2 HG02896.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.980+6410T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53707974 | ||||||
| chr2:53708126
|
G | A | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.980+6258C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53708126 | ||||||
| chr2:53708131
|
C | A | 4 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0004g0014others(1): Show | 4 | HG02258.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.980+6253G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53708131 | ||||||
| chr2:53708222
|
G | GT | 7 | a0001c0001t0009g0179a0001c0001t0009g0192a0001c0001t0009g0199others(4): Show | 7 | HG02056.hp2 HG02293.hp1 NA19000.hp2 others(4): Show |
intron_variant | MODIFIER | c.980+6161dupA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53708222 | ||||||
| chr2:53708243
|
C | T | 4 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.980+6141G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53708243 | ||||||
| chr2:53708363
|
T | C | 3 | a0001c0001t0002g0140a0001c0001t0002g0142a0001c0001t0006g0143 | 3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.980+6021A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53708363 | ||||||
| chr2:53708381
|
T | C | 1 | a0001c0001t0004g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.980+6003A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53708381 | ||||||
| chr2:53708388
|
A | G | 16 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(13): Show | 16 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.980+5996T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53708388 | ||||||
| chr2:53708596
|
G | A | 1 | a0001c0001t0003g0184 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.980+5788C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53708596 | ||||||
| chr2:53708618
|
A | G | 6 | a0001c0001t0008g0029a0001c0001t0008g0031a0001c0001t0008g0032others(3): Show | 6 | HG01255.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.980+5766T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53708618 | ||||||
| chr2:53708665
|
A | C | 6 | a0001c0001t0008g0029a0001c0001t0008g0031a0001c0001t0008g0032others(3): Show | 6 | HG01255.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.980+5719T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53708665 | ||||||
| chr2:53708990
|
T | C | 1 | a0001c0002t0002g0247 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.980+5394A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53708990 | ||||||
| chr2:53708992
|
T | C | 6 | a0001c0001t0001g0274a0001c0001t0004g0272a0001c0001t0004g0273others(3): Show | 6 | HG01074.hp1 HG02818.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.980+5392A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53708992 | ||||||
| chr2:53709099
|
T | C | 6 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0315others(3): Show | 6 | HG01167.hp1 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.980+5285A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53709099 | ||||||
| chr2:53709116
|
G | A | 77 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(74): Show | 80 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.980+5268C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53709116 | ||||||
| chr2:53709123
|
T | C | 219 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(216): Show | 223 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.980+5261A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53709123 | ||||||
| chr2:53709320
|
G | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0158a0001c0001t0001g0161others(7): Show | 11 | HG00099.hp1 HG01099.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.980+5064C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53709320 | ||||||
| chr2:53709359
|
G | A | 57 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0066others(54): Show | 58 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.980+5025C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53709359 | ||||||
| chr2:53709416
|
A | T | 77 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(74): Show | 80 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.980+4968T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53709416 | ||||||
| chr2:53709440
|
T | G | 16 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(13): Show | 16 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.980+4944A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53709440 | ||||||
| chr2:53709671
|
A | G | 16 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(13): Show | 16 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.980+4713T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53709671 | ||||||
| chr2:53709729
|
G | C | 1 | a0002c0004t0010g0136 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.980+4655C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53709729 | ||||||
| chr2:53709734
|
C | G | 57 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(54): Show | 57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.980+4650G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53709734 | ||||||
| chr2:53709813
|
G | A | 57 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(54): Show | 57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.980+4571C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53709813 | ||||||
| chr2:53709823
|
T | A | 2 | a0001c0001t0003g0181a0001c0001t0003g0182 | 2 | HG01175.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.980+4561A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53709823 | ||||||
| chr2:53709828
|
G | A | 1 | a0001c0002t0002g0263 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.980+4556C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53709828 | ||||||
| chr2:53709907
|
G | C | 1 | a0004c0006t0002g0234 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.980+4477C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53709907 | ||||||
| chr2:53710040
|
C | T | 203 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(200): Show | 206 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.980+4344G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53710040 | ||||||
| chr2:53710100
|
A | C | 1 | a0001c0001t0003g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.980+4284T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53710100 | ||||||
| chr2:53710279
|
A | G | 4 | a0001c0001t0001g0149a0001c0001t0001g0166a0001c0001t0001g0210others(1): Show | 4 | HG01891.hp2 HG02559.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.980+4105T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53710279 | ||||||
| chr2:53710330
|
T | C | 1 | a0001c0001t0004g0082 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.980+4054A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53710330 | ||||||
| chr2:53710333
|
T | C | 3 | a0001c0001t0002g0140a0001c0001t0002g0142a0001c0001t0006g0143 | 3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.980+4051A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53710333 | ||||||
| chr2:53710365
|
A | T | 213 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(210): Show | 217 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.980+4019T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53710365 | ||||||
| chr2:53710378
|
T | A | 13 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(10): Show | 13 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.980+4006A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53710378 | ||||||
| chr2:53710467
|
G | C | 1 | a0001c0003t0007g0285 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.980+3917C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53710467 | ||||||
| chr2:53710601
|
T | G | 1 | a0002c0004t0010g0136 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.980+3783A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53710601 | ||||||
| chr2:53710803
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.980+3581T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53710803 | ||||||
| chr2:53710816
|
T | C | 3 | a0001c0001t0002g0140a0001c0001t0002g0142a0001c0001t0006g0143 | 3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.980+3568A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53710816 | ||||||
| chr2:53710864
|
C | T | 1 | a0001c0002t0002g0251 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.980+3520G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53710864 | ||||||
| chr2:53710897
|
C | A | 1 | a0001c0001t0003g0184 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.980+3487G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53710897 | ||||||
| chr2:53710901
|
G | C | 218 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(215): Show | 222 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.980+3483C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53710901 | ||||||
| chr2:53710970
|
CA | C | 202 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(199): Show | 205 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.980+3413delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53710970 | ||||||
| chr2:53711027
|
G | C | 4 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0004g0014others(1): Show | 4 | HG02258.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.980+3357C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53711027 | ||||||
| chr2:53711082
|
G | A | 1 | a0001c0002t0002g0263 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.980+3302C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53711082 | ||||||
| chr2:53711286
|
T | C | 4 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0004g0014others(1): Show | 4 | HG02258.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.980+3098A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53711286 | ||||||
| chr2:53711355
|
T | C | 1 | a0001c0001t0003g0188 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.980+3029A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53711355 | ||||||
| chr2:53711557
|
T | C | 1 | a0002c0004t0013g0012 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.980+2827A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53711557 | ||||||
| chr2:53711635
|
A | G | 2 | a0001c0003t0007g0284a0001c0003t0007g0285 | 2 | HG00558.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.980+2749T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53711635 | ||||||
| chr2:53711639
|
T | G | 3 | a0001c0001t0003g0043a0001c0001t0003g0044a0001c0001t0003g0127 | 3 | HG02257.hp2 HG02280.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.980+2745A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53711639 | ||||||
| chr2:53711761
|
G | A | 1 | a0001c0001t0003g0152 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.980+2623C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53711761 | ||||||
| chr2:53711908
|
C | T | 53 | a0001c0001t0001g0066a0001c0001t0001g0083a0001c0001t0001g0112others(50): Show | 54 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.980+2476G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53711908 | ||||||
| chr2:53711949
|
T | C | 10 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(7): Show | 10 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.980+2435A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53711949 | ||||||
| chr2:53712001
|
C | T | 4 | a0001c0001t0001g0048a0001c0001t0001g0078a0001c0001t0001g0081others(1): Show | 4 | HG02129.hp1 NA18943.hp1 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.980+2383G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712001 | ||||||
| chr2:53712057
|
T | G | 3 | a0001c0001t0001g0015a0001c0001t0004g0014a0001c0001t0015g0013 | 3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.980+2327A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712057 | ||||||
| chr2:53712147
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.980+2237A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712147 | ||||||
| chr2:53712216
|
C | CA | 11 | a0001c0001t0001g0130a0001c0001t0001g0151a0001c0001t0001g0211others(8): Show | 11 | HG02572.hp2 HG02818.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.980+2167dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712216 | ||||||
| chr2:53712216
|
CA | C | 30 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(27): Show | 31 | HG00099.hp1 HG00738.hp1 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.980+2167delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712216 | ||||||
| chr2:53712242
|
G | T | 3 | a0001c0003t0002g0286a0001c0003t0002g0292a0001c0003t0002g0293 | 3 | HG02155.hp1 NA18939.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.980+2142C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712242 | ||||||
| chr2:53712290
|
T | C | 52 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0001g0174others(49): Show | 54 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.980+2094A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712290 | ||||||
| chr2:53712411
|
C | T | 227 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(224): Show | 231 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.980+1973G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712411 | ||||||
| chr2:53712539
|
G | A | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.980+1845C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712539 | ||||||
| chr2:53712602
|
CA | C | 4 | a0001c0002t0002g0220a0001c0002t0002g0225a0001c0002t0002g0226others(1): Show | 4 | HG00423.hp1 HG02074.hp1 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.980+1781delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712602 | ||||||
| chr2:53712635
|
T | C | 1 | a0001c0001t0003g0339 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.980+1749A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712635 | ||||||
| chr2:53712745
|
A | AAC | 21 | a0001c0001t0001g0046a0001c0001t0001g0050a0001c0001t0001g0054others(18): Show | 21 | HG00438.hp2 HG01074.hp1 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.980+1637_980+1638d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712745 | ||||||
| chr2:53712745
|
AAC | A | 114 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0066others(111): Show | 115 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.980+1637_980+1638d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712745 | ||||||
| chr2:53712767
|
C | T | 1 | a0001c0001t0004g0275 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.980+1617G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712767 | ||||||
| chr2:53712769
|
G | GGC | 10 | a0001c0001t0001g0113a0001c0001t0001g0311a0001c0001t0002g0228others(7): Show | 10 | HG01255.hp1 HG02280.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.980+1613_980+1614d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712769 | ||||||
| chr2:53712772
|
G | A | 2 | a0001c0003t0002g0302a0001c0003t0002g0303 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.980+1612C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712772 | ||||||
| chr2:53712774
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.980+1610C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712774 | ||||||
| chr2:53712778
|
G | A | 3 | a0001c0001t0001g0141a0001c0001t0001g0144a0001c0001t0001g0145 | 3 | HG00738.hp1 HG01884.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.980+1606C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712778 | ||||||
| chr2:53712780
|
G | A | 55 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0001g0174others(52): Show | 57 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.980+1604C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712780 | ||||||
| chr2:53712822
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.980+1562C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712822 | ||||||
| chr2:53712825
|
C | T | 4 | a0001c0001t0001g0149a0001c0001t0001g0166a0001c0001t0001g0210others(1): Show | 4 | HG01891.hp2 HG02559.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.980+1559G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712825 | ||||||
| chr2:53712946
|
G | A | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.980+1438C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53712946 | ||||||
| chr2:53713109
|
G | A | 55 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0001g0174others(52): Show | 57 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.980+1275C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53713109 | ||||||
| chr2:53713333
|
T | A | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.980+1051A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53713333 | ||||||
| chr2:53713383
|
T | C | 4 | a0001c0001t0001g0149a0001c0001t0001g0166a0001c0001t0001g0210others(1): Show | 4 | HG01891.hp2 HG02559.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.980+1001A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53713383 | ||||||
| chr2:53713586
|
G | T | 215 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(212): Show | 219 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.980+798C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53713586 | ||||||
| chr2:53713651
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.980+733C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53713651 | ||||||
| chr2:53713925
|
T | A | 12 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(9): Show | 12 | HG00408.hp2 HG01081.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.980+459A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53713925 | ||||||
| chr2:53713988
|
A | T | 123 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0066others(120): Show | 124 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.980+396T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53713988 | ||||||
| chr2:53714052
|
T | G | 1 | a0001c0001t0001g0079 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.980+332A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53714052 | ||||||
| chr2:53714086
|
T | C | 1 | a0001c0003t0014g0304 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.980+298A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53714086 | ||||||
| chr2:53714103
|
C | T | 1 | a0001c0001t0001g0068 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.980+281G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53714103 | ||||||
| chr2:53714131
|
T | A | 3 | a0001c0001t0001g0211a0001c0001t0001g0216a0001c0001t0001g0217 | 3 | HG02572.hp2 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.980+253A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53714131 | ||||||
| chr2:53714143
|
A | G | 1 | a0001c0001t0001g0318 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.980+241T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53714143 | ||||||
| chr2:53714186
|
G | C | 4 | a0001c0001t0001g0149a0001c0001t0001g0166a0001c0001t0001g0210others(1): Show | 4 | HG01891.hp2 HG02559.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.980+198C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53714186 | ||||||
| chr2:53714218
|
G | A | 1 | a0001c0001t0008g0035 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.980+166C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53714218 | ||||||
| chr2:53714276
|
T | A | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.980+108A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53714276 | ||||||
| chr2:53714305
|
C | T | 6 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0003g0146others(3): Show | 6 | HG02630.hp2 HG02896.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.980+79G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53714305 | ||||||
| chr2:53714375
|
T | C | 7 | a0001c0001t0009g0179a0001c0001t0009g0192a0001c0001t0009g0199others(4): Show | 7 | HG02056.hp2 HG02293.hp1 NA19000.hp2 others(4): Show |
intron_variant | MODIFIER | c.980+9A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 7/9 | chr2 | 53714375 | ||||||
| chr2:53714607
|
T | C | 1 | a0001c0001t0003g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.783-26A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53714607 | ||||||
| chr2:53714622
|
T | C | 6 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0003g0146others(3): Show | 6 | HG02630.hp2 HG02896.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.783-41A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53714622 | ||||||
| chr2:53714806
|
T | C | 12 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(9): Show | 12 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.783-225A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53714806 | ||||||
| chr2:53715001
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.783-420G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53715001 | ||||||
| chr2:53715204
|
A | G | 13 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(10): Show | 13 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.783-623T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53715204 | ||||||
| chr2:53715216
|
C | A | 3 | a0001c0001t0002g0140a0001c0001t0002g0142a0001c0001t0006g0143 | 3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.783-635G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53715216 | ||||||
| chr2:53715230
|
A | G | 57 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(54): Show | 57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.783-649T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53715230 | ||||||
| chr2:53715242
|
A | G | 3 | a0001c0001t0001g0158a0001c0001t0001g0163a0001c0001t0004g0162 | 3 | NA18951.hp1 NA18973.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.783-661T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53715242 | ||||||
| chr2:53715312
|
G | T | 8 | a0001c0001t0001g0024a0001c0001t0001g0133a0001c0001t0001g0212others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.783-731C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53715312 | ||||||
| chr2:53715346
|
C | A | 8 | a0001c0001t0001g0024a0001c0001t0001g0133a0001c0001t0001g0212others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.783-765G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53715346 | ||||||
| chr2:53715441
|
C | A | 2 | a0001c0001t0001g0024a0001c0001t0004g0121 | 2 | HG02486.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.783-860G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53715441 | ||||||
| chr2:53715452
|
G | C | 14 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(11): Show | 14 | HG00438.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.783-871C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53715452 | ||||||
| chr2:53715564
|
A | G | 3 | a0002c0004t0010g0137a0002c0004t0010g0138a0002c0004t0010g0139 | 3 | HG02818.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.783-983T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53715564 | ||||||
| chr2:53715662
|
C | G | 12 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(9): Show | 12 | HG00408.hp2 HG01081.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.782+904G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53715662 | ||||||
| chr2:53715672
|
T | C | 13 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(10): Show | 13 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.782+894A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53715672 | ||||||
| chr2:53715788
|
C | T | 3 | a0001c0001t0002g0140a0001c0001t0002g0142a0001c0001t0006g0143 | 3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.782+778G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53715788 | ||||||
| chr2:53715843
|
T | C | 13 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(10): Show | 13 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.782+723A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53715843 | ||||||
| chr2:53715947
|
T | TATTGACT others(48): Show |
1 | a0001c0001t0005g0003 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.782+564_782+618dup others(55): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53715947 | ||||||
| chr2:53716002
|
C | T | 145 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(142): Show | 149 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.782+564G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53716002 | ||||||
| chr2:53716024
|
G | C | 57 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(54): Show | 57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.782+542C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53716024 | ||||||
| chr2:53716202
|
G | A | 1 | a0001c0001t0003g0205 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.782+364C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53716202 | ||||||
| chr2:53716249
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.782+317C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53716249 | ||||||
| chr2:53716251
|
C | A | 1 | a0001c0002t0002g0231 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.782+315G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53716251 | ||||||
| chr2:53716404
|
G | C | 1 | a0001c0002t0002g0247 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.782+162C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53716404 | ||||||
| chr2:53716559
|
C | T | 57 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(54): Show | 57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
splice_region_variant&intron_variant | LOW | c.782+7G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 6/9 | chr2 | 53716559 | ||||||
| chr2:53716813
|
G | C | 3 | a0001c0003t0005g0329a0001c0003t0005g0332a0001c0003t0005g0333 | 3 | HG00733.hp1 HG02602.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.605-70C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53716813 | ||||||
| chr2:53716833
|
C | G | 3 | a0001c0001t0002g0140a0001c0001t0002g0142a0001c0001t0006g0143 | 3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.605-90G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53716833 | ||||||
| chr2:53716995
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.605-252A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53716995 | ||||||
| chr2:53717105
|
A | C | 40 | a0001c0001t0001g0066a0001c0001t0001g0083a0001c0001t0001g0112others(37): Show | 41 | HG00558.hp2 HG00621.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.605-362T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53717105 | ||||||
| chr2:53717205
|
T | A | 52 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0001g0174others(49): Show | 54 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.605-462A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53717205 | ||||||
| chr2:53717226
|
G | A | 101 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0066others(98): Show | 102 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.605-483C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53717226 | ||||||
| chr2:53717229
|
A | C | 8 | a0001c0001t0001g0024a0001c0001t0001g0133a0001c0001t0001g0212others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.605-486T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53717229 | ||||||
| chr2:53717229
|
A | G | 98 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0036others(95): Show | 100 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.605-486T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53717229 | ||||||
| chr2:53717290
|
C | A | 97 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0025others(94): Show | 99 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.605-547G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53717290 | ||||||
| chr2:53717323
|
T | G | 1 | a0001c0002t0007g0242 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.605-580A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53717323 | ||||||
| chr2:53717355
|
G | A | 1 | a0001c0003t0005g0333 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.605-612C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53717355 | ||||||
| chr2:53717606
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.605-863G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53717606 | ||||||
| chr2:53717659
|
A | T | 1 | a0001c0001t0003g0127 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.605-916T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53717659 | ||||||
| chr2:53717676
|
G | A | 107 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0066others(104): Show | 108 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.605-933C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53717676 | ||||||
| chr2:53718175
|
G | A | 101 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0066others(98): Show | 102 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.605-1432C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53718175 | ||||||
| chr2:53718203
|
G | A | 91 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0025others(88): Show | 93 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.605-1460C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53718203 | ||||||
| chr2:53718279
|
G | A | 92 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0025others(89): Show | 94 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.605-1536C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53718279 | ||||||
| chr2:53718284
|
A | T | 92 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0025others(89): Show | 94 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.605-1541T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53718284 | ||||||
| chr2:53718286
|
G | C | 3 | a0001c0001t0001g0015a0001c0001t0004g0014a0001c0001t0015g0013 | 3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.605-1543C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53718286 | ||||||
| chr2:53718286
|
G | T | 92 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0025others(89): Show | 94 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.605-1543C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53718286 | ||||||
| chr2:53718287
|
T | TA | 92 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0025others(89): Show | 94 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.605-1545_605-1544i others(3): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53718287 | ||||||
| chr2:53718297
|
T | C | 100 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0025others(97): Show | 102 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.605-1554A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53718297 | ||||||
| chr2:53718348
|
T | C | 2 | a0001c0001t0001g0024a0001c0001t0004g0121 | 2 | HG02486.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.605-1605A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53718348 | ||||||
| chr2:53718451
|
A | G | 1 | a0001c0002t0002g0263 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.605-1708T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53718451 | ||||||
| chr2:53718574
|
A | G | 1 | a0001c0001t0001g0270 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.605-1831T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53718574 | ||||||
| chr2:53718661
|
T | C | 1 | a0001c0001t0001g0120 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.605-1918A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53718661 | ||||||
| chr2:53718742
|
G | A | 1 | a0001c0001t0004g0011 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.605-1999C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53718742 | ||||||
| chr2:53718773
|
A | G | 57 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(54): Show | 57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.605-2030T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53718773 | ||||||
| chr2:53718984
|
G | A | 1 | a0001c0001t0001g0175 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.605-2241C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53718984 | ||||||
| chr2:53719151
|
T | C | 2 | a0001c0001t0001g0037a0001c0001t0001g0058 | 2 | NA18981.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.605-2408A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53719151 | ||||||
| chr2:53719175
|
G | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0124 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.605-2432C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53719175 | ||||||
| chr2:53719280
|
G | T | 1 | a0001c0001t0001g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.605-2537C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53719280 | ||||||
| chr2:53719294
|
G | A | 5 | a0001c0001t0001g0039a0001c0001t0001g0062a0001c0001t0001g0069others(2): Show | 6 | HG00558.hp1 HG01516.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.605-2551C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53719294 | ||||||
| chr2:53719502
|
A | T | 16 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(13): Show | 16 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.605-2759T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53719502 | ||||||
| chr2:53719648
|
C | G | 9 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0315others(6): Show | 9 | HG01167.hp1 HG02615.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.605-2905G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53719648 | ||||||
| chr2:53719685
|
A | T | 1 | a0002c0004t0010g0136 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.605-2942T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53719685 | ||||||
| chr2:53719706
|
G | T | 1 | a0002c0004t0013g0012 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.605-2963C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53719706 | ||||||
| chr2:53719963
|
C | A | 61 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0268others(58): Show | 61 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.605-3220G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53719963 | ||||||
| chr2:53720046
|
G | A | 3 | a0001c0001t0002g0140a0001c0001t0002g0142a0001c0001t0006g0143 | 3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.605-3303C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53720046 | ||||||
| chr2:53720138
|
C | CA | 8 | a0001c0001t0001g0094a0001c0001t0001g0149a0001c0001t0001g0166others(5): Show | 8 | HG01891.hp2 HG02080.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.605-3396dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53720138 | ||||||
| chr2:53720138
|
CA | C | 170 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(167): Show | 172 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.605-3396delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53720138 | ||||||
| chr2:53720138
|
CAA | C | 57 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(54): Show | 57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.605-3397_605-3396d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53720138 | ||||||
| chr2:53720278
|
C | T | 216 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(213): Show | 219 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(216): Show |
intron_variant | MODIFIER | c.605-3535G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53720278 | ||||||
| chr2:53720397
|
T | A | 6 | a0001c0001t0008g0029a0001c0001t0008g0031a0001c0001t0008g0032others(3): Show | 6 | HG01255.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.605-3654A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53720397 | ||||||
| chr2:53720580
|
G | C | 57 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0066others(54): Show | 58 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.605-3837C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53720580 | ||||||
| chr2:53720707
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.605-3964C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53720707 | ||||||
| chr2:53720820
|
C | A | 1 | a0008c0010t0001g0100 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.605-4077G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53720820 | ||||||
| chr2:53720899
|
T | C | 2 | a0001c0001t0003g0167a0001c0001t0003g0340 | 2 | NA19080.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.605-4156A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53720899 | ||||||
| chr2:53720963
|
A | G | 3 | a0002c0004t0010g0137a0002c0004t0010g0138a0002c0004t0010g0139 | 3 | HG02818.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.605-4220T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53720963 | ||||||
| chr2:53720989
|
C | T | 2 | a0001c0001t0001g0117a0001c0001t0003g0118 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.605-4246G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53720989 | ||||||
| chr2:53720991
|
C | T | 1 | a0001c0001t0003g0043 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.605-4248G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53720991 | ||||||
| chr2:53721123
|
T | TATAA | 115 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0025others(112): Show | 118 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.605-4384_605-4381d others(6): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721123 | ||||||
| chr2:53721123
|
T | TATAAATA others(1): Show |
11 | a0001c0001t0001g0056a0001c0001t0001g0062a0001c0001t0001g0074others(8): Show | 12 | HG00558.hp1 HG01257.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.605-4388_605-4381d others(10): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721123 | ||||||
| chr2:53721123
|
TATAA | T | 14 | a0001c0001t0001g0116a0001c0001t0001g0166a0001c0001t0001g0210others(11): Show | 14 | HG00408.hp2 HG01069.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.605-4384_605-4381d others(6): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721123 | ||||||
| chr2:53721123
|
TATAAATA others(1): Show |
T | 8 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0120others(5): Show | 8 | HG01081.hp1 HG01243.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.605-4388_605-4381d others(10): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721123 | ||||||
| chr2:53721123
|
TATAAATA others(5): Show |
T | 3 | a0001c0001t0001g0040a0001c0001t0001g0124a0001c0003t0002g0296 | 3 | HG01070.hp2 HG01071.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.605-4392_605-4381d others(14): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721123 | ||||||
| chr2:53721285
|
T | C | 57 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(54): Show | 57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.605-4542A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721285 | ||||||
| chr2:53721344
|
C | G | 1 | a0001c0003t0002g0292 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.605-4601G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721344 | ||||||
| chr2:53721352
|
C | T | 4 | a0001c0001t0001g0042a0001c0001t0001g0051a0001c0001t0001g0084others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.605-4609G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721352 | ||||||
| chr2:53721398
|
C | CA | 15 | a0001c0001t0001g0010a0001c0001t0001g0325a0001c0001t0003g0172others(12): Show | 15 | HG01515.hp2 HG02145.hp1 HG02602.hp1 others(12): Show |
intron_variant | MODIFIER | c.605-4656dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721398 | ||||||
| chr2:53721398
|
C | CAA | 16 | a0001c0001t0001g0313a0001c0001t0001g0315a0001c0001t0001g0317others(13): Show | 16 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.605-4657_605-4656d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721398 | ||||||
| chr2:53721398
|
CA | C | 141 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0025others(138): Show | 143 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.605-4656delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721398 | ||||||
| chr2:53721430
|
A | ACATAGTG others(1): Show |
20 | a0001c0002t0002g0017a0001c0002t0002g0018a0001c0002t0002g0020others(17): Show | 20 | HG00673.hp1 HG00673.hp2 HG02040.hp1 others(17): Show |
intron_variant | MODIFIER | c.605-4695_605-4688d others(10): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721430 | ||||||
| chr2:53721512
|
G | A | 53 | a0001c0001t0001g0066a0001c0001t0001g0083a0001c0001t0001g0112others(50): Show | 54 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.605-4769C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721512 | ||||||
| chr2:53721799
|
C | A | 13 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(10): Show | 13 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.605-5056G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721799 | ||||||
| chr2:53721854
|
T | C | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0141others(2): Show | 5 | HG00738.hp1 HG01884.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.605-5111A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721854 | ||||||
| chr2:53721854
|
T | G | 2 | a0001c0001t0001g0133a0001c0001t0004g0114 | 2 | HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.605-5111A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721854 | ||||||
| chr2:53721936
|
C | T | 286 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(283): Show | 291 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.605-5193G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721936 | ||||||
| chr2:53721965
|
G | A | 1 | a0001c0001t0004g0026 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.605-5222C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721965 | ||||||
| chr2:53721987
|
T | C | 14 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0315others(11): Show | 14 | HG01167.hp1 HG02615.hp2 HG02818.hp2 others(11): Show |
intron_variant | MODIFIER | c.605-5244A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53721987 | ||||||
| chr2:53722086
|
G | C | 1 | a0008c0010t0001g0100 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.605-5343C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53722086 | ||||||
| chr2:53722100
|
A | G | 13 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(10): Show | 13 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.605-5357T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53722100 | ||||||
| chr2:53722156
|
T | C | 9 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0315others(6): Show | 9 | HG01167.hp1 HG02615.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.605-5413A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53722156 | ||||||
| chr2:53722173
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.605-5430A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53722173 | ||||||
| chr2:53722179
|
A | T | 8 | a0001c0001t0003g0218a0001c0001t0008g0029a0001c0001t0008g0031others(5): Show | 8 | HG01255.hp1 HG02976.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.605-5436T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53722179 | ||||||
| chr2:53722193
|
T | G | 1 | a0001c0001t0001g0025 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.605-5450A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53722193 | ||||||
| chr2:53722348
|
C | G | 1 | a0001c0001t0003g0185 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.605-5605G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53722348 | ||||||
| chr2:53722404
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.605-5661C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53722404 | ||||||
| chr2:53722413
|
T | C | 9 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0315others(6): Show | 9 | HG01167.hp1 HG02615.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.605-5670A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53722413 | ||||||
| chr2:53722496
|
T | C | 18 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0141others(15): Show | 18 | HG00408.hp2 HG00738.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.605-5753A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53722496 | ||||||
| chr2:53722538
|
T | C | 1 | a0001c0001t0002g0229 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.605-5795A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53722538 | ||||||
| chr2:53722679
|
T | C | 3 | a0001c0001t0011g0096a0001c0003t0002g0291a0001c0003t0003g0309 | 3 | HG00323.hp1 HG02074.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.605-5936A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53722679 | ||||||
| chr2:53722808
|
C | T | 53 | a0001c0001t0001g0066a0001c0001t0001g0083a0001c0001t0001g0112others(50): Show | 54 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.604+5904G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53722808 | ||||||
| chr2:53722985
|
A | C | 1 | a0001c0003t0002g0299 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.604+5727T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53722985 | ||||||
| chr2:53723165
|
C | T | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0141others(2): Show | 5 | HG00738.hp1 HG01884.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.604+5547G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53723165 | ||||||
| chr2:53723189
|
T | C | 1 | a0001c0001t0003g0197 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.604+5523A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53723189 | ||||||
| chr2:53723234
|
A | C | 57 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(54): Show | 57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.604+5478T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53723234 | ||||||
| chr2:53723248
|
A | T | 22 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0153others(19): Show | 22 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.604+5464T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53723248 | ||||||
| chr2:53723394
|
C | T | 1 | a0001c0001t0004g0026 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.604+5318G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53723394 | ||||||
| chr2:53723397
|
T | C | 3 | a0002c0004t0010g0137a0002c0004t0010g0138a0002c0004t0010g0139 | 3 | HG02818.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.604+5315A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53723397 | ||||||
| chr2:53723544
|
A | C | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.604+5168T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53723544 | ||||||
| chr2:53723569
|
A | G | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.604+5143T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53723569 | ||||||
| chr2:53723615
|
C | T | 2 | a0001c0001t0001g0024a0001c0001t0004g0121 | 2 | HG02486.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.604+5097G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53723615 | ||||||
| chr2:53723647
|
T | A | 3 | a0001c0003t0002g0296a0001c0003t0002g0297a0001c0003t0002g0298 | 3 | HG03041.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.604+5065A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53723647 | ||||||
| chr2:53723737
|
C | A | 3 | a0001c0001t0001g0166a0001c0001t0001g0210a0001c0003t0002g0281 | 3 | HG01891.hp2 NA18943.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.604+4975G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53723737 | ||||||
| chr2:53723875
|
A | G | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.604+4837T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53723875 | ||||||
| chr2:53724171
|
G | A | 2 | a0001c0003t0001g0305a0001c0003t0001g0306 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.604+4541C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53724171 | ||||||
| chr2:53724199
|
T | C | 51 | a0001c0001t0003g0218a0001c0001t0003g0339a0001c0003t0001g0305others(48): Show | 52 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.604+4513A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53724199 | ||||||
| chr2:53724252
|
A | G | 12 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(9): Show | 12 | HG00408.hp2 HG01081.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.604+4460T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53724252 | ||||||
| chr2:53724317
|
G | T | 1 | a0001c0001t0001g0116 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.604+4395C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53724317 | ||||||
| chr2:53724395
|
A | G | 1 | a0001c0001t0003g0169 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.604+4317T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53724395 | ||||||
| chr2:53724418
|
G | A | 1 | a0001c0001t0004g0114 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.604+4294C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53724418 | ||||||
| chr2:53724460
|
A | C | 4 | a0002c0004t0010g0137a0002c0004t0010g0138a0002c0004t0010g0139others(1): Show | 4 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.604+4252T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53724460 | ||||||
| chr2:53724565
|
C | T | 3 | a0001c0001t0001g0062a0001c0001t0001g0069a0001c0001t0002g0131 | 3 | HG00558.hp1 NA18747.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.604+4147G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53724565 | ||||||
| chr2:53724736
|
A | G | 1 | a0001c0001t0003g0186 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.604+3976T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53724736 | ||||||
| chr2:53724897
|
A | G | 1 | a0001c0001t0003g0205 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.604+3815T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53724897 | ||||||
| chr2:53724902
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0004g0014 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.604+3810G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53724902 | ||||||
| chr2:53724981
|
A | G | 55 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0001g0174others(52): Show | 57 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.604+3731T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53724981 | ||||||
| chr2:53725041
|
A | G | 83 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(80): Show | 86 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.604+3671T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53725041 | ||||||
| chr2:53725256
|
T | G | 3 | a0001c0001t0003g0043a0001c0001t0003g0044a0001c0001t0003g0127 | 3 | HG02257.hp2 HG02280.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.604+3456A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53725256 | ||||||
| chr2:53725377
|
C | T | 1 | a0001c0001t0003g0185 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.604+3335G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53725377 | ||||||
| chr2:53725428
|
G | A | 46 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0001g0174others(43): Show | 48 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.604+3284C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53725428 | ||||||
| chr2:53725453
|
TA | T | 8 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0153others(5): Show | 8 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.604+3258delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53725453 | ||||||
| chr2:53725496
|
C | T | 1 | a0001c0002t0002g0261 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.604+3216G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53725496 | ||||||
| chr2:53725662
|
G | A | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.604+3050C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53725662 | ||||||
| chr2:53725683
|
C | A | 1 | a0001c0001t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.604+3029G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53725683 | ||||||
| chr2:53725796
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.604+2916A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53725796 | ||||||
| chr2:53725871
|
T | A | 1 | a0001c0001t0001g0153 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.604+2841A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53725871 | ||||||
| chr2:53726026
|
G | T | 1 | a0001c0001t0008g0029 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.604+2686C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726026 | ||||||
| chr2:53726231
|
G | A | 2 | a0001c0001t0001g0117a0001c0001t0003g0118 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.604+2481C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726231 | ||||||
| chr2:53726251
|
A | C | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.604+2461T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726251 | ||||||
| chr2:53726257
|
A | AT | 85 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0057others(82): Show | 85 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.604+2454dupA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726257 | ||||||
| chr2:53726257
|
A | ATT | 11 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0003g0146others(8): Show | 11 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.604+2453_604+2454d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726257 | ||||||
| chr2:53726257
|
AT | A | 9 | a0001c0001t0001g0039a0001c0001t0001g0065a0001c0001t0001g0101others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.604+2454delA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726257 | ||||||
| chr2:53726314
|
G | A | 2 | a0001c0001t0001g0098a0001c0001t0001g0134 | 2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.604+2398C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726314 | ||||||
| chr2:53726322
|
G | A | 2 | a0001c0003t0002g0279a0001c0003t0002g0300 | 2 | NA19002.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.604+2390C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726322 | ||||||
| chr2:53726519
|
C | G | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.604+2193G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726519 | ||||||
| chr2:53726597
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.604+2115A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726597 | ||||||
| chr2:53726631
|
T | C | 1 | a0001c0003t0003g0309 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.604+2081A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726631 | ||||||
| chr2:53726687
|
T | C | 3 | a0001c0001t0001g0039a0001c0001t0001g0097a0001c0001t0005g0003 | 4 | HG01516.hp1 HG01517.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.604+2025A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726687 | ||||||
| chr2:53726692
|
A | T | 4 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0004g0014others(1): Show | 4 | HG02258.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.604+2020T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726692 | ||||||
| chr2:53726720
|
G | A | 1 | a0001c0002t0002g0247 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.604+1992C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726720 | ||||||
| chr2:53726759
|
C | A | 3 | a0001c0001t0001g0211a0001c0001t0001g0216a0001c0001t0001g0217 | 3 | HG02572.hp2 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.604+1953G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726759 | ||||||
| chr2:53726809
|
G | T | 3 | a0001c0001t0001g0015a0001c0001t0004g0014a0001c0001t0015g0013 | 3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.604+1903C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726809 | ||||||
| chr2:53726830
|
C | G | 216 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(213): Show | 220 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.604+1882G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726830 | ||||||
| chr2:53726903
|
G | A | 1 | a0001c0001t0001g0153 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.604+1809C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726903 | ||||||
| chr2:53726986
|
A | G | 30 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(27): Show | 31 | HG00099.hp1 HG00408.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.604+1726T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53726986 | ||||||
| chr2:53727113
|
T | C | 3 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0004g0157 | 3 | HG02109.hp2 HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.604+1599A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53727113 | ||||||
| chr2:53727125
|
A | C | 1 | a0001c0001t0008g0032 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.604+1587T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53727125 | ||||||
| chr2:53727131
|
C | T | 2 | a0001c0003t0002g0289a0001c0003t0006g0301 | 2 | HG01175.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.604+1581G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53727131 | ||||||
| chr2:53727215
|
G | C | 7 | a0001c0002t0002g0017a0001c0002t0002g0018a0001c0002t0002g0020others(4): Show | 7 | HG00673.hp2 HG02056.hp1 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.604+1497C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53727215 | ||||||
| chr2:53727466
|
TA | T | 57 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0256others(54): Show | 57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.604+1245delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53727466 | ||||||
| chr2:53727528
|
T | C | 1 | a0001c0001t0008g0032 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.604+1184A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53727528 | ||||||
| chr2:53727544
|
C | G | 177 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0141others(174): Show | 180 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.604+1168G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53727544 | ||||||
| chr2:53727563
|
G | C | 3 | a0001c0001t0001g0015a0001c0001t0004g0014a0001c0001t0015g0013 | 3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.604+1149C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53727563 | ||||||
| chr2:53727676
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.604+1036A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53727676 | ||||||
| chr2:53727705
|
A | G | 1 | a0001c0001t0001g0153 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.604+1007T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53727705 | ||||||
| chr2:53727752
|
G | C | 2 | a0001c0002t0002g0221a0001c0002t0002g0245 | 2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.604+960C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53727752 | ||||||
| chr2:53727757
|
C | G | 1 | a0001c0001t0008g0034 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.604+955G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53727757 | ||||||
| chr2:53727806
|
A | T | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.604+906T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53727806 | ||||||
| chr2:53728051
|
T | A | 57 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(54): Show | 57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.604+661A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53728051 | ||||||
| chr2:53728052
|
A | T | 1 | a0001c0001t0003g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.604+660T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53728052 | ||||||
| chr2:53728157
|
G | T | 1 | a0001c0001t0001g0158 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.604+555C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53728157 | ||||||
| chr2:53728206
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.604+506A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53728206 | ||||||
| chr2:53728334
|
C | T | 37 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(34): Show | 37 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.604+378G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53728334 | ||||||
| chr2:53728341
|
G | A | 204 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 208 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.604+371C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53728341 | ||||||
| chr2:53728352
|
A | C | 196 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(193): Show | 200 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.604+360T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53728352 | ||||||
| chr2:53728376
|
A | C | 117 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0268others(114): Show | 118 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.604+336T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53728376 | ||||||
| chr2:53728460
|
G | T | 5 | a0001c0001t0001g0005a0001c0001t0001g0161a0001c0001t0001g0165others(2): Show | 6 | HG01099.hp1 HG01106.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.604+252C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53728460 | ||||||
| chr2:53728524
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.604+188G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53728524 | ||||||
| chr2:53728604
|
C | T | 57 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(54): Show | 57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.604+108G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53728604 | ||||||
| chr2:53728684
|
C | A | 1 | a0001c0001t0001g0125 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.604+28G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 5/9 | chr2 | 53728684 | ||||||
| chr2:53729156
|
A | G | 1 | a0001c0001t0015g0013 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.468+302T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 4/9 | chr2 | 53729156 | ||||||
| chr2:53729234
|
T | C | 7 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0003g0146others(4): Show | 7 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.468+224A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 4/9 | chr2 | 53729234 | ||||||
| chr2:53729239
|
T | C | 2 | a0001c0001t0003g0180a0001c0001t0003g0183 | 2 | HG00621.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.468+219A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 4/9 | chr2 | 53729239 | ||||||
| chr2:53729701
|
A | G | 12 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(9): Show | 12 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.356-131T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53729701 | ||||||
| chr2:53729710
|
T | A | 1 | a0001c0001t0001g0076 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.356-140A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53729710 | ||||||
| chr2:53729721
|
C | A | 1 | a0001c0002t0002g0250 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.356-151G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53729721 | ||||||
| chr2:53729746
|
T | G | 55 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0003g0218others(52): Show | 56 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.356-176A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53729746 | ||||||
| chr2:53729779
|
T | TAAAAGAC others(318): Show |
1 | a0001c0001t0001g0038 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.356-210_356-209ins others(325): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53729779 | ||||||
| chr2:53729843
|
C | A | 78 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(75): Show | 81 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.356-273G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53729843 | ||||||
| chr2:53729902
|
C | T | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.356-332G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53729902 | ||||||
| chr2:53729947
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0061others(1): Show | 5 | NA18983.hp1 NA19004.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.356-377G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53729947 | ||||||
| chr2:53729961
|
G | C | 77 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(74): Show | 80 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.356-391C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53729961 | ||||||
| chr2:53729983
|
T | A | 2 | a0001c0001t0001g0065a0001c0001t0001g0080 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.356-413A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53729983 | ||||||
| chr2:53730039
|
T | C | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.356-469A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53730039 | ||||||
| chr2:53730135
|
T | C | 1 | a0001c0001t0008g0029 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.356-565A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53730135 | ||||||
| chr2:53730203
|
T | C | 56 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(53): Show | 56 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.356-633A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53730203 | ||||||
| chr2:53730224
|
A | G | 1 | a0001c0001t0001g0327 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.356-654T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53730224 | ||||||
| chr2:53730238
|
T | C | 8 | a0001c0001t0001g0024a0001c0001t0001g0133a0001c0001t0001g0212others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.356-668A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53730238 | ||||||
| chr2:53730329
|
C | T | 2 | a0001c0003t0007g0284a0001c0003t0007g0285 | 2 | HG00558.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.356-759G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53730329 | ||||||
| chr2:53730553
|
G | A | 1 | a0001c0001t0003g0339 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.356-983C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53730553 | ||||||
| chr2:53730645
|
A | C | 1 | a0001c0002t0002g0257 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.356-1075T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53730645 | ||||||
| chr2:53730665
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.356-1095C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53730665 | ||||||
| chr2:53730682
|
T | C | 3 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176 | 3 | HG02080.hp1 NA18968.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.356-1112A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53730682 | ||||||
| chr2:53730837
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0004g0014a0001c0001t0015g0013 | 3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.356-1267C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53730837 | ||||||
| chr2:53730935
|
A | C | 56 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(53): Show | 56 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.356-1365T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53730935 | ||||||
| chr2:53730999
|
C | T | 193 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(190): Show | 197 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.356-1429G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53730999 | ||||||
| chr2:53731079
|
C | T | 4 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(1): Show | 4 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.356-1509G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731079 | ||||||
| chr2:53731121
|
A | G | 78 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(75): Show | 81 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.356-1551T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731121 | ||||||
| chr2:53731172
|
C | T | 1 | a0001c0001t0003g0127 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.356-1602G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731172 | ||||||
| chr2:53731183
|
C | T | 3 | a0001c0003t0005g0312a0001c0003t0011g0330a0007c0007t0005g0341 | 3 | HG01168.hp1 HG01256.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.356-1613G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731183 | ||||||
| chr2:53731271
|
A | G | 60 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(57): Show | 61 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.356-1701T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731271 | ||||||
| chr2:53731272
|
C | T | 37 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(34): Show | 37 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.356-1702G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731272 | ||||||
| chr2:53731345
|
T | A | 78 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(75): Show | 81 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.356-1775A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731345 | ||||||
| chr2:53731408
|
A | AAAAAC | 78 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(75): Show | 81 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.356-1843_356-1839d others(7): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731408 | ||||||
| chr2:53731497
|
G | A | 1 | a0001c0001t0001g0153 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.356-1927C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731497 | ||||||
| chr2:53731542
|
T | C | 1 | a0001c0001t0003g0043 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.356-1972A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731542 | ||||||
| chr2:53731692
|
G | A | 3 | a0001c0001t0002g0140a0001c0001t0002g0142a0001c0001t0006g0143 | 3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.356-2122C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731692 | ||||||
| chr2:53731713
|
C | T | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.356-2143G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731713 | ||||||
| chr2:53731724
|
C | T | 195 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(192): Show | 199 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.356-2154G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731724 | ||||||
| chr2:53731753
|
A | C | 1 | a0001c0003t0002g0289 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.356-2183T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731753 | ||||||
| chr2:53731782
|
C | A | 116 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0268others(113): Show | 117 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.356-2212G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731782 | ||||||
| chr2:53731801
|
C | T | 1 | a0001c0003t0002g0296 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.356-2231G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731801 | ||||||
| chr2:53731816
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.356-2246G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731816 | ||||||
| chr2:53731845
|
G | A | 1 | a0001c0002t0002g0226 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.356-2275C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731845 | ||||||
| chr2:53731905
|
G | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.356-2335C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53731905 | ||||||
| chr2:53732027
|
G | A | 3 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0004g0157 | 3 | HG02109.hp2 HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.356-2457C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53732027 | ||||||
| chr2:53732061
|
C | T | 37 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(34): Show | 37 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.356-2491G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53732061 | ||||||
| chr2:53732084
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.356-2514C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53732084 | ||||||
| chr2:53732207
|
C | T | 9 | a0001c0001t0001g0165a0001c0002t0002g0220a0001c0002t0002g0223others(6): Show | 9 | HG00423.hp1 HG02015.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.356-2637G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53732207 | ||||||
| chr2:53732432
|
C | T | 90 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(87): Show | 93 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.356-2862G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53732432 | ||||||
| chr2:53732500
|
T | C | 56 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(53): Show | 56 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.356-2930A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53732500 | ||||||
| chr2:53732525
|
T | C | 1 | a0001c0001t0001g0173 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.356-2955A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53732525 | ||||||
| chr2:53732759
|
C | T | 1 | a0001c0001t0003g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.356-3189G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53732759 | ||||||
| chr2:53732827
|
G | C | 56 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(53): Show | 56 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.356-3257C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53732827 | ||||||
| chr2:53732956
|
G | C | 12 | a0001c0001t0001g0141a0001c0001t0001g0144a0001c0001t0001g0145others(9): Show | 12 | HG00738.hp1 HG01167.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.356-3386C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53732956 | ||||||
| chr2:53733092
|
C | T | 1 | a0008c0010t0001g0100 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.356-3522G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53733092 | ||||||
| chr2:53733297
|
G | C | 1 | a0001c0001t0012g0204 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.356-3727C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53733297 | ||||||
| chr2:53733445
|
CT | C | 148 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(145): Show | 152 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.356-3876delA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53733445 | ||||||
| chr2:53733491
|
G | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0124 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.356-3921C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53733491 | ||||||
| chr2:53733615
|
T | C | 2 | a0001c0002t0002g0264a0001c0002t0002g0265 | 2 | HG03669.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.356-4045A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53733615 | ||||||
| chr2:53733716
|
C | T | 11 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(8): Show | 11 | HG00408.hp2 HG01081.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.356-4146G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53733716 | ||||||
| chr2:53733810
|
G | A | 54 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0001g0174others(51): Show | 56 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.356-4240C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53733810 | ||||||
| chr2:53733835
|
A | G | 220 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(217): Show | 224 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.356-4265T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53733835 | ||||||
| chr2:53733915
|
C | G | 4 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0004g0014others(1): Show | 4 | HG02258.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.356-4345G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53733915 | ||||||
| chr2:53733990
|
G | C | 1 | a0001c0001t0001g0326 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.356-4420C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53733990 | ||||||
| chr2:53734071
|
G | A | 2 | a0001c0003t0002g0292a0001c0003t0002g0293 | 2 | NA18939.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.356-4501C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53734071 | ||||||
| chr2:53734118
|
C | G | 56 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(53): Show | 56 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.356-4548G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53734118 | ||||||
| chr2:53734275
|
C | G | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.356-4705G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53734275 | ||||||
| chr2:53734438
|
T | C | 84 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(81): Show | 87 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.356-4868A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53734438 | ||||||
| chr2:53734613
|
T | C | 2 | a0001c0001t0001g0313a0001c0001t0001g0314 | 2 | HG01167.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.356-5043A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53734613 | ||||||
| chr2:53734717
|
C | T | 1 | a0001c0001t0001g0315 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.356-5147G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53734717 | ||||||
| chr2:53734723
|
G | A | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.356-5153C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53734723 | ||||||
| chr2:53734874
|
G | C | 1 | a0001c0002t0006g0271 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.356-5304C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53734874 | ||||||
| chr2:53734891
|
A | AT | 6 | a0001c0001t0001g0141a0001c0001t0001g0144a0001c0001t0001g0145others(3): Show | 6 | HG00738.hp1 HG01884.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.356-5322dupA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53734891 | ||||||
| chr2:53734918
|
G | GT | 62 | a0001c0001t0001g0074a0001c0001t0001g0086a0001c0001t0001g0097others(59): Show | 62 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.356-5349dupA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53734918 | ||||||
| chr2:53734918
|
GT | G | 129 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(126): Show | 132 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.356-5349delA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53734918 | ||||||
| chr2:53735016
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.356-5446A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53735016 | ||||||
| chr2:53735172
|
G | A | 56 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0003g0218others(53): Show | 57 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.356-5602C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53735172 | ||||||
| chr2:53735212
|
G | A | 52 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0001g0174others(49): Show | 54 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.356-5642C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53735212 | ||||||
| chr2:53735215
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.356-5645G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53735215 | ||||||
| chr2:53735345
|
T | G | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.356-5775A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53735345 | ||||||
| chr2:53735485
|
T | TA | 169 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(166): Show | 171 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.356-5916dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53735485 | ||||||
| chr2:53735485
|
T | TAA | 7 | a0001c0001t0003g0218a0001c0002t0002g0260a0001c0002t0002g0267others(4): Show | 7 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.356-5917_356-5916d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53735485 | ||||||
| chr2:53735519
|
CATAGAT | C | 5 | a0001c0002t0002g0230a0001c0002t0002g0251a0001c0002t0002g0252others(2): Show | 5 | NA18941.hp2 NA18961.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.356-5955_356-5950d others(8): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53735519 | ||||||
| chr2:53735591
|
C | T | 55 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0001g0174others(52): Show | 57 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.356-6021G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53735591 | ||||||
| chr2:53735642
|
A | C | 3 | a0002c0004t0010g0137a0002c0004t0010g0138a0002c0004t0010g0139 | 3 | HG02818.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.356-6072T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53735642 | ||||||
| chr2:53735699
|
A | C | 221 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(218): Show | 225 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.356-6129T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53735699 | ||||||
| chr2:53735792
|
T | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0004g0014others(2): Show | 5 | HG02258.hp1 HG02970.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.356-6222A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53735792 | ||||||
| chr2:53735911
|
A | G | 1 | a0001c0001t0001g0025 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.356-6341T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53735911 | ||||||
| chr2:53735998
|
T | TA | 71 | a0001c0001t0001g0111a0001c0001t0001g0149a0001c0001t0001g0151others(68): Show | 71 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.356-6429dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53735998 | ||||||
| chr2:53735998
|
TA | T | 15 | a0001c0001t0001g0038a0001c0001t0001g0060a0001c0001t0001g0065others(12): Show | 15 | HG00733.hp1 HG01069.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.356-6429delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53735998 | ||||||
| chr2:53736105
|
A | C | 56 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0003g0218others(53): Show | 57 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.356-6535T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53736105 | ||||||
| chr2:53736179
|
T | C | 3 | a0002c0004t0010g0137a0002c0004t0010g0138a0002c0004t0010g0139 | 3 | HG02818.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.356-6609A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53736179 | ||||||
| chr2:53736450
|
G | A | 1 | a0001c0001t0001g0153 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.356-6880C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53736450 | ||||||
| chr2:53736479
|
G | A | 203 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(200): Show | 207 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.356-6909C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53736479 | ||||||
| chr2:53736561
|
T | G | 1 | a0001c0001t0001g0109 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.356-6991A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53736561 | ||||||
| chr2:53736567
|
C | T | 1 | a0001c0003t0002g0299 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.356-6997G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53736567 | ||||||
| chr2:53736700
|
G | GA | 52 | a0001c0001t0001g0130a0001c0001t0002g0228a0001c0001t0002g0229others(49): Show | 52 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.356-7131dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53736700 | ||||||
| chr2:53736700
|
GA | G | 82 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(79): Show | 85 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.356-7131delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53736700 | ||||||
| chr2:53736700
|
GAA | G | 55 | a0001c0001t0003g0339a0001c0001t0008g0209a0001c0003t0001g0305others(52): Show | 56 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.356-7132_356-7131d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53736700 | ||||||
| chr2:53736874
|
C | G | 2 | a0001c0001t0001g0149a0001c0001t0004g0150 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.356-7304G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53736874 | ||||||
| chr2:53737028
|
T | C | 77 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(74): Show | 80 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.356-7458A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53737028 | ||||||
| chr2:53737031
|
A | G | 1 | a0001c0001t0003g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.356-7461T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53737031 | ||||||
| chr2:53737150
|
T | C | 224 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(221): Show | 228 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.356-7580A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53737150 | ||||||
| chr2:53737222
|
C | T | 1 | a0001c0001t0003g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.356-7652G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53737222 | ||||||
| chr2:53737369
|
A | G | 62 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(59): Show | 63 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.356-7799T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53737369 | ||||||
| chr2:53737429
|
A | C | 1 | a0001c0001t0001g0047 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.356-7859T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53737429 | ||||||
| chr2:53737502
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.356-7932C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53737502 | ||||||
| chr2:53737509
|
A | G | 5 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0003g0172others(2): Show | 5 | HG00621.hp1 HG02080.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.356-7939T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53737509 | ||||||
| chr2:53737582
|
C | T | 1 | a0001c0001t0003g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.356-8012G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53737582 | ||||||
| chr2:53737601
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.356-8031G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53737601 | ||||||
| chr2:53737724
|
G | GA | 20 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0111others(17): Show | 20 | HG00423.hp2 HG01109.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.356-8155dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53737724 | ||||||
| chr2:53737724
|
GA | G | 19 | a0001c0001t0001g0065a0001c0001t0001g0077a0001c0001t0001g0102others(16): Show | 19 | HG00408.hp2 HG01081.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.356-8155delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53737724 | ||||||
| chr2:53737787
|
G | A | 3 | a0001c0001t0003g0007a0001c0001t0003g0170a0001c0001t0003g0190 | 4 | NA18944.hp2 NA18950.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.356-8217C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53737787 | ||||||
| chr2:53738026
|
T | C | 7 | a0001c0002t0002g0017a0001c0002t0002g0018a0001c0002t0002g0020others(4): Show | 7 | HG00673.hp2 HG02056.hp1 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.356-8456A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53738026 | ||||||
| chr2:53738124
|
G | T | 2 | a0003c0005t0005g0008a0003c0005t0005g0337 | 3 | HG01106.hp2 HG06807.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.356-8554C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53738124 | ||||||
| chr2:53738131
|
A | C | 1 | a0001c0001t0004g0114 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.356-8561T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53738131 | ||||||
| chr2:53738205
|
T | C | 7 | a0001c0001t0001g0217a0001c0001t0001g0274a0001c0001t0004g0272others(4): Show | 7 | HG01074.hp1 HG02572.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.356-8635A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53738205 | ||||||
| chr2:53738252
|
G | A | 213 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(210): Show | 217 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.356-8682C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53738252 | ||||||
| chr2:53738274
|
T | G | 2 | a0001c0001t0002g0154a0002c0004t0013g0012 | 2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.356-8704A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53738274 | ||||||
| chr2:53738387
|
C | A | 77 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(74): Show | 80 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.356-8817G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53738387 | ||||||
| chr2:53738430
|
T | A | 1 | a0001c0001t0003g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.356-8860A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53738430 | ||||||
| chr2:53738470
|
G | C | 77 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(74): Show | 80 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.356-8900C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53738470 | ||||||
| chr2:53738532
|
A | G | 1 | a0001c0003t0002g0288 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.356-8962T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53738532 | ||||||
| chr2:53738551
|
T | C | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.356-8981A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53738551 | ||||||
| chr2:53738640
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.356-9070A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53738640 | ||||||
| chr2:53738684
|
G | A | 50 | a0001c0001t0003g0339a0001c0003t0001g0305a0001c0003t0001g0306others(47): Show | 51 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.356-9114C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53738684 | ||||||
| chr2:53738720
|
G | C | 1 | a0001c0002t0002g0247 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.356-9150C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53738720 | ||||||
| chr2:53738913
|
T | C | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.356-9343A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53738913 | ||||||
| chr2:53739002
|
C | A | 1 | a0001c0001t0001g0064 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.356-9432G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53739002 | ||||||
| chr2:53739084
|
T | C | 1 | a0001c0003t0002g0296 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.356-9514A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53739084 | ||||||
| chr2:53739111
|
G | C | 78 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(75): Show | 81 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.356-9541C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53739111 | ||||||
| chr2:53739126
|
G | A | 1 | a0001c0001t0006g0143 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.356-9556C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53739126 | ||||||
| chr2:53739364
|
G | C | 1 | a0001c0001t0001g0129 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.356-9794C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53739364 | ||||||
| chr2:53739712
|
G | T | 1 | a0001c0001t0001g0042 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.356-10142C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53739712 | ||||||
| chr2:53739955
|
T | C | 3 | a0001c0001t0001g0211a0001c0001t0001g0216a0001c0001t0001g0217 | 3 | HG02572.hp2 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.356-10385A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53739955 | ||||||
| chr2:53740034
|
A | G | 3 | a0001c0001t0001g0211a0001c0001t0001g0216a0001c0001t0001g0217 | 3 | HG02572.hp2 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.356-10464T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53740034 | ||||||
| chr2:53740109
|
A | G | 84 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(81): Show | 87 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.356-10539T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53740109 | ||||||
| chr2:53740132
|
C | A | 3 | a0001c0001t0001g0050a0001c0001t0001g0059a0001c0001t0004g0126 | 3 | NA18965.hp1 NA18967.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.356-10562G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53740132 | ||||||
| chr2:53740194
|
G | C | 1 | a0002c0004t0010g0136 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.355+10589C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53740194 | ||||||
| chr2:53740200
|
C | T | 2 | a0001c0001t0003g0167a0001c0001t0003g0340 | 2 | NA19080.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.355+10583G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53740200 | ||||||
| chr2:53740224
|
C | T | 1 | a0001c0002t0002g0233 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.355+10559G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53740224 | ||||||
| chr2:53740349
|
G | C | 3 | a0001c0001t0002g0140a0001c0001t0002g0142a0001c0001t0006g0143 | 3 | HG02615.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.355+10434C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53740349 | ||||||
| chr2:53740443
|
T | G | 3 | a0001c0001t0003g0043a0001c0001t0003g0044a0001c0001t0003g0127 | 3 | HG02257.hp2 HG02280.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.355+10340A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53740443 | ||||||
| chr2:53740559
|
T | A | 46 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0153others(43): Show | 46 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.355+10224A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53740559 | ||||||
| chr2:53740646
|
T | C | 1 | a0001c0001t0003g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.355+10137A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53740646 | ||||||
| chr2:53740693
|
T | C | 14 | a0001c0001t0003g0218a0001c0001t0003g0339a0001c0003t0005g0312others(11): Show | 15 | HG00733.hp1 HG01106.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.355+10090A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53740693 | ||||||
| chr2:53740870
|
A | G | 57 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(54): Show | 57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.355+9913T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53740870 | ||||||
| chr2:53740900
|
G | A | 341 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(338): Show | 349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.355+9883C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53740900 | ||||||
| chr2:53740968
|
C | G | 4 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0004g0014others(1): Show | 4 | HG02258.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.355+9815G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53740968 | ||||||
| chr2:53740979
|
A | G | 1 | a0001c0001t0001g0120 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.355+9804T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53740979 | ||||||
| chr2:53741021
|
T | C | 2 | a0001c0001t0001g0078a0001c0001t0001g0153 | 2 | HG02129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.355+9762A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53741021 | ||||||
| chr2:53741097
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.355+9686G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53741097 | ||||||
| chr2:53741637
|
C | T | 204 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 208 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.355+9146G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53741637 | ||||||
| chr2:53741828
|
A | G | 11 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0050others(8): Show | 11 | HG00438.hp2 HG02027.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.355+8955T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53741828 | ||||||
| chr2:53742107
|
T | C | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.355+8676A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53742107 | ||||||
| chr2:53742432
|
C | T | 45 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0153others(42): Show | 45 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.355+8351G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53742432 | ||||||
| chr2:53742461
|
T | A | 1 | a0001c0001t0001g0141 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.355+8322A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53742461 | ||||||
| chr2:53742734
|
TA | T | 204 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 208 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.355+8048delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53742734 | ||||||
| chr2:53742789
|
A | C | 78 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(75): Show | 81 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.355+7994T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53742789 | ||||||
| chr2:53742880
|
A | C | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.355+7903T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53742880 | ||||||
| chr2:53743102
|
C | A | 14 | a0001c0001t0003g0218a0001c0001t0003g0339a0001c0003t0005g0312others(11): Show | 15 | HG00733.hp1 HG01106.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.355+7681G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53743102 | ||||||
| chr2:53743127
|
G | T | 54 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0256others(51): Show | 54 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.355+7656C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53743127 | ||||||
| chr2:53743164
|
C | CT | 13 | a0001c0001t0001g0040a0001c0001t0001g0058a0001c0001t0001g0066others(10): Show | 13 | HG00423.hp2 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.355+7618dupA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53743164 | ||||||
| chr2:53743164
|
CT | C | 160 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(157): Show | 165 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.355+7618delA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53743164 | ||||||
| chr2:53743209
|
T | G | 2 | a0001c0001t0001g0015a0001c0001t0004g0014 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.355+7574A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53743209 | ||||||
| chr2:53743800
|
C | T | 78 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(75): Show | 81 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.355+6983G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53743800 | ||||||
| chr2:53743874
|
C | T | 57 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(54): Show | 57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.355+6909G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53743874 | ||||||
| chr2:53743882
|
A | C | 78 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(75): Show | 81 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.355+6901T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53743882 | ||||||
| chr2:53743949
|
A | C | 4 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0108others(1): Show | 5 | HG00099.hp2 HG01081.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.355+6834T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53743949 | ||||||
| chr2:53743957
|
C | T | 45 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0153others(42): Show | 45 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.355+6826G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53743957 | ||||||
| chr2:53744042
|
C | CA | 56 | a0001c0001t0001g0058a0001c0001t0001g0122a0001c0001t0001g0149others(53): Show | 56 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.355+6740dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744042 | ||||||
| chr2:53744099
|
G | A | 1 | a0002c0004t0010g0136 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.355+6684C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744099 | ||||||
| chr2:53744114
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.355+6669G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744114 | ||||||
| chr2:53744129
|
C | G | 1 | a0001c0001t0004g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.355+6654G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744129 | ||||||
| chr2:53744195
|
T | C | 57 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(54): Show | 57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.355+6588A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744195 | ||||||
| chr2:53744220
|
C | CA | 6 | a0001c0001t0001g0111a0001c0001t0001g0174a0001c0001t0001g0175others(3): Show | 6 | HG02080.hp1 NA18968.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.355+6562dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744220 | ||||||
| chr2:53744245
|
G | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0004g0014others(2): Show | 5 | HG02258.hp1 HG02970.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.355+6538C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744245 | ||||||
| chr2:53744265
|
T | G | 6 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0315others(3): Show | 6 | HG01167.hp1 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.355+6518A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744265 | ||||||
| chr2:53744363
|
AG | A | 45 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0153others(42): Show | 45 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.355+6419delC | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744363 | ||||||
| chr2:53744372
|
G | A | 45 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0153others(42): Show | 45 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.355+6411C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744372 | ||||||
| chr2:53744379
|
T | C | 45 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0153others(42): Show | 45 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.355+6404A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744379 | ||||||
| chr2:53744384
|
C | CAAAA | 32 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(29): Show | 32 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.355+6395_355+6398d others(6): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744384 | ||||||
| chr2:53744384
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0003g0152 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.355+6398_355+6399i others(15): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744384 | ||||||
| chr2:53744384
|
C | CAAAAAAA others(7): Show |
4 | a0001c0001t0003g0146a0001c0001t0003g0147a0001c0001t0003g0148others(1): Show | 4 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.355+6398_355+6399i others(16): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744384 | ||||||
| chr2:53744384
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0151 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.355+6398_355+6399i others(17): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744384 | ||||||
| chr2:53744384
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0153 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.355+6398_355+6399i others(18): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744384 | ||||||
| chr2:53744392
|
T | A | 44 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0153others(41): Show | 44 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.355+6391A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744392 | ||||||
| chr2:53744396
|
T | A | 45 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0153others(42): Show | 45 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.355+6387A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744396 | ||||||
| chr2:53744400
|
A | T | 2 | a0001c0001t0001g0048a0001c0001t0001g0068 | 2 | NA18952.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.355+6383T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744400 | ||||||
| chr2:53744406
|
A | T | 18 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0003g0218others(15): Show | 19 | HG00733.hp1 HG01106.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.355+6377T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744406 | ||||||
| chr2:53744503
|
T | C | 13 | a0001c0001t0003g0339a0001c0003t0005g0312a0001c0003t0005g0329others(10): Show | 14 | HG00733.hp1 HG01106.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.355+6280A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744503 | ||||||
| chr2:53744534
|
T | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0004g0014others(2): Show | 5 | HG02258.hp1 HG02970.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.355+6249A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744534 | ||||||
| chr2:53744681
|
G | A | 1 | a0001c0001t0004g0272 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.355+6102C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53744681 | ||||||
| chr2:53745008
|
C | T | 1 | a0001c0001t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.355+5775G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53745008 | ||||||
| chr2:53745163
|
T | G | 5 | a0001c0001t0001g0040a0001c0001t0001g0113a0001c0001t0001g0124others(2): Show | 5 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.355+5620A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53745163 | ||||||
| chr2:53745331
|
T | A | 4 | a0001c0001t0009g0200a0001c0001t0009g0201a0001c0001t0012g0204others(1): Show | 4 | HG02056.hp2 NA19000.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.355+5452A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53745331 | ||||||
| chr2:53745473
|
G | C | 45 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0153others(42): Show | 45 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.355+5310C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53745473 | ||||||
| chr2:53745556
|
G | A | 159 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(156): Show | 163 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.355+5227C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53745556 | ||||||
| chr2:53745769
|
CA | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0004g0014others(2): Show | 5 | HG02258.hp1 HG02970.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.355+5013delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53745769 | ||||||
| chr2:53746155
|
G | A | 1 | a0001c0002t0007g0254 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.355+4628C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53746155 | ||||||
| chr2:53746165
|
G | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0004g0014others(2): Show | 5 | HG02258.hp1 HG02970.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.355+4618C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53746165 | ||||||
| chr2:53746249
|
T | C | 1 | a0001c0001t0001g0133 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.355+4534A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53746249 | ||||||
| chr2:53746424
|
A | G | 2 | a0001c0001t0003g0181a0001c0001t0003g0182 | 2 | HG01175.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.355+4359T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53746424 | ||||||
| chr2:53746457
|
C | T | 3 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0003g0172 | 3 | HG02080.hp2 NA18747.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.355+4326G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53746457 | ||||||
| chr2:53746485
|
C | CTTT | 84 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(81): Show | 87 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.355+4295_355+4297d others(5): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53746485 | ||||||
| chr2:53746609
|
G | T | 4 | a0001c0001t0001g0042a0001c0001t0001g0051a0001c0001t0001g0084others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.355+4174C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53746609 | ||||||
| chr2:53746652
|
G | A | 3 | a0002c0004t0010g0137a0002c0004t0010g0138a0002c0004t0010g0139 | 3 | HG02818.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.355+4131C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53746652 | ||||||
| chr2:53746669
|
G | A | 1 | a0001c0001t0001g0318 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.355+4114C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53746669 | ||||||
| chr2:53746687
|
C | G | 1 | a0001c0001t0004g0123 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.355+4096G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53746687 | ||||||
| chr2:53746728
|
C | G | 3 | a0001c0003t0005g0342a0003c0005t0005g0008a0003c0005t0005g0337 | 4 | HG01106.hp2 HG01192.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.355+4055G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53746728 | ||||||
| chr2:53746758
|
A | G | 85 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(82): Show | 88 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.355+4025T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53746758 | ||||||
| chr2:53746837
|
T | C | 12 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(9): Show | 12 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.355+3946A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53746837 | ||||||
| chr2:53746904
|
A | G | 17 | a0001c0003t0002g0278a0001c0003t0002g0279a0001c0003t0002g0280others(14): Show | 17 | HG00558.hp2 HG00621.hp2 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.355+3879T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53746904 | ||||||
| chr2:53747071
|
T | C | 1 | a0001c0001t0003g0203 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.355+3712A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53747071 | ||||||
| chr2:53747086
|
T | G | 142 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(139): Show | 145 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.355+3697A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53747086 | ||||||
| chr2:53747212
|
A | G | 5 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0004g0014others(2): Show | 5 | HG02258.hp1 HG02970.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.355+3571T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53747212 | ||||||
| chr2:53747420
|
C | A | 1 | a0001c0002t0002g0249 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.355+3363G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53747420 | ||||||
| chr2:53747557
|
G | A | 13 | a0001c0001t0003g0339a0001c0003t0005g0312a0001c0003t0005g0329others(10): Show | 14 | HG00733.hp1 HG01106.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.355+3226C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53747557 | ||||||
| chr2:53747958
|
T | C | 2 | a0001c0001t0003g0167a0001c0001t0003g0340 | 2 | NA19080.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.355+2825A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53747958 | ||||||
| chr2:53747999
|
A | G | 5 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0004g0014others(2): Show | 5 | HG02258.hp1 HG02970.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.355+2784T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53747999 | ||||||
| chr2:53748010
|
C | A | 1 | a0001c0001t0004g0114 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.355+2773G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53748010 | ||||||
| chr2:53748093
|
CAT | C | 6 | a0001c0001t0001g0041a0001c0001t0001g0103a0001c0001t0001g0104others(3): Show | 6 | HG01109.hp1 HG01884.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.355+2688_355+2689d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53748093 | ||||||
| chr2:53748299
|
T | C | 46 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0153others(43): Show | 46 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.355+2484A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53748299 | ||||||
| chr2:53748404
|
C | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.355+2379G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53748404 | ||||||
| chr2:53748428
|
T | A | 4 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(1): Show | 4 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.355+2355A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53748428 | ||||||
| chr2:53748510
|
G | A | 1 | a0001c0001t0001g0336 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.355+2273C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53748510 | ||||||
| chr2:53748689
|
G | C | 1 | a0001c0001t0004g0272 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.355+2094C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53748689 | ||||||
| chr2:53748744
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.355+2039A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53748744 | ||||||
| chr2:53748805
|
C | T | 1 | a0001c0002t0002g0231 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.355+1978G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53748805 | ||||||
| chr2:53748806
|
C | T | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.355+1977G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53748806 | ||||||
| chr2:53748919
|
C | A | 1 | a0002c0004t0013g0012 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.355+1864G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53748919 | ||||||
| chr2:53749176
|
G | C | 45 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0153others(42): Show | 45 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.355+1607C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53749176 | ||||||
| chr2:53749253
|
A | C | 13 | a0001c0001t0003g0339a0001c0003t0005g0312a0001c0003t0005g0329others(10): Show | 14 | HG00733.hp1 HG01106.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.355+1530T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53749253 | ||||||
| chr2:53749554
|
C | G | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.355+1229G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53749554 | ||||||
| chr2:53749590
|
T | C | 58 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(55): Show | 58 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.355+1193A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53749590 | ||||||
| chr2:53749846
|
A | G | 45 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0153others(42): Show | 45 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.355+937T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53749846 | ||||||
| chr2:53750737
|
T | A | 1 | a0001c0001t0001g0098 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.355+46A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 3/9 | chr2 | 53750737 | ||||||
| chr2:53750968
|
T | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.197-27A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53750968 | ||||||
| chr2:53751321
|
A | T | 1 | a0001c0001t0008g0035 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.197-380T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53751321 | ||||||
| chr2:53751342
|
C | T | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.197-401G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53751342 | ||||||
| chr2:53751569
|
T | A | 55 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0001g0174others(52): Show | 57 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.197-628A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53751569 | ||||||
| chr2:53751596
|
C | A | 1 | a0001c0002t0002g0250 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.197-655G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53751596 | ||||||
| chr2:53751632
|
G | C | 5 | a0001c0001t0001g0274a0001c0001t0004g0273a0001c0001t0004g0275others(2): Show | 5 | HG02818.hp1 HG03139.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-691C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53751632 | ||||||
| chr2:53751676
|
A | G | 25 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(22): Show | 26 | HG00408.hp2 HG00733.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.197-735T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53751676 | ||||||
| chr2:53751979
|
G | A | 5 | a0001c0001t0008g0031a0001c0001t0008g0032a0001c0001t0008g0033others(2): Show | 5 | HG01255.hp1 HG03041.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.197-1038C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53751979 | ||||||
| chr2:53751991
|
G | A | 4 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0004g0014others(1): Show | 4 | HG02258.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-1050C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53751991 | ||||||
| chr2:53752592
|
G | A | 7 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0003g0146others(4): Show | 7 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.197-1651C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53752592 | ||||||
| chr2:53752635
|
C | G | 2 | a0001c0003t0002g0297a0001c0003t0002g0298 | 2 | HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.197-1694G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53752635 | ||||||
| chr2:53752716
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.197-1775T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53752716 | ||||||
| chr2:53752727
|
G | A | 7 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0003g0146others(4): Show | 7 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.197-1786C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53752727 | ||||||
| chr2:53752747
|
T | C | 57 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(54): Show | 57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.197-1806A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53752747 | ||||||
| chr2:53753038
|
C | A | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.197-2097G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53753038 | ||||||
| chr2:53753044
|
T | TA | 4 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0004g0014others(1): Show | 4 | HG02258.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-2104_197-2103i others(3): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53753044 | ||||||
| chr2:53753045
|
T | A | 18 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0003g0218others(15): Show | 19 | HG00733.hp1 HG01106.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.197-2104A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53753045 | ||||||
| chr2:53753152
|
C | T | 1 | a0001c0001t0003g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.197-2211G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53753152 | ||||||
| chr2:53753248
|
A | G | 1 | a0001c0002t0002g0251 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.197-2307T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53753248 | ||||||
| chr2:53753451
|
G | C | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.197-2510C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53753451 | ||||||
| chr2:53753648
|
T | G | 2 | a0001c0001t0001g0207a0001c0001t0003g0206 | 2 | NA18987.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.197-2707A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53753648 | ||||||
| chr2:53753652
|
G | GT | 84 | a0001c0001t0001g0066a0001c0001t0001g0083a0001c0001t0001g0112others(81): Show | 86 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.197-2712dupA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53753652 | ||||||
| chr2:53753652
|
G | GTT | 15 | a0001c0001t0003g0340a0001c0003t0001g0305a0001c0003t0001g0306others(12): Show | 15 | HG00438.hp1 HG01069.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.197-2713_197-2712d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53753652 | ||||||
| chr2:53753668
|
A | G | 23 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0133others(20): Show | 24 | HG00099.hp1 HG01099.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.197-2727T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53753668 | ||||||
| chr2:53753698
|
G | A | 5 | a0001c0001t0008g0031a0001c0001t0008g0032a0001c0001t0008g0033others(2): Show | 5 | HG01255.hp1 HG03041.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.197-2757C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53753698 | ||||||
| chr2:53753740
|
G | A | 4 | a0001c0002t0002g0230a0001c0002t0002g0251a0001c0002t0002g0252others(1): Show | 4 | NA18941.hp2 NA18961.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-2799C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53753740 | ||||||
| chr2:53753761
|
C | A | 1 | a0001c0001t0003g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.197-2820G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53753761 | ||||||
| chr2:53753810
|
A | AT | 40 | a0001c0001t0001g0005a0001c0001t0001g0078a0001c0001t0001g0081others(37): Show | 41 | HG00099.hp1 HG00621.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.197-2870dupA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53753810 | ||||||
| chr2:53753921
|
G | A | 1 | a0001c0001t0003g0203 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.197-2980C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53753921 | ||||||
| chr2:53753982
|
C | A | 57 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(54): Show | 57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.197-3041G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53753982 | ||||||
| chr2:53754005
|
A | T | 57 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(54): Show | 57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.197-3064T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53754005 | ||||||
| chr2:53754108
|
CA | C | 4 | a0001c0001t0003g0178a0001c0001t0003g0196a0001c0001t0003g0197others(1): Show | 4 | NA18955.hp1 NA18986.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-3168delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53754108 | ||||||
| chr2:53754328
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.197-3387C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53754328 | ||||||
| chr2:53754405
|
G | A | 45 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0153others(42): Show | 45 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.197-3464C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53754405 | ||||||
| chr2:53754518
|
T | G | 12 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(9): Show | 12 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.197-3577A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53754518 | ||||||
| chr2:53754594
|
G | A | 1 | a0001c0001t0004g0011 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.197-3653C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53754594 | ||||||
| chr2:53754632
|
T | C | 6 | a0001c0001t0008g0029a0001c0001t0008g0031a0001c0001t0008g0032others(3): Show | 6 | HG01255.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.197-3691A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53754632 | ||||||
| chr2:53754701
|
C | G | 1 | a0001c0001t0001g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.197-3760G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53754701 | ||||||
| chr2:53754979
|
T | C | 2 | a0001c0001t0001g0211a0001c0001t0001g0216 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.197-4038A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53754979 | ||||||
| chr2:53755201
|
T | G | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.197-4260A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53755201 | ||||||
| chr2:53755246
|
G | A | 1 | a0001c0001t0004g0026 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.197-4305C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53755246 | ||||||
| chr2:53755265
|
G | C | 1 | a0001c0002t0002g0224 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.197-4324C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53755265 | ||||||
| chr2:53755603
|
T | A | 46 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0153others(43): Show | 46 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.197-4662A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53755603 | ||||||
| chr2:53755616
|
G | A | 1 | a0001c0001t0004g0277 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.197-4675C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53755616 | ||||||
| chr2:53755643
|
A | G | 47 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0153others(44): Show | 47 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.197-4702T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53755643 | ||||||
| chr2:53755715
|
A | G | 2 | a0003c0005t0005g0008a0003c0005t0005g0337 | 3 | HG01106.hp2 HG06807.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.197-4774T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53755715 | ||||||
| chr2:53755791
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.197-4850G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53755791 | ||||||
| chr2:53755821
|
G | A | 61 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(58): Show | 61 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.197-4880C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53755821 | ||||||
| chr2:53755917
|
C | G | 4 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(1): Show | 4 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-4976G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53755917 | ||||||
| chr2:53755970
|
T | C | 52 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0001g0174others(49): Show | 54 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.197-5029A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53755970 | ||||||
| chr2:53755970
|
T | G | 5 | a0001c0001t0001g0057a0001c0001t0001g0073a0001c0001t0001g0077others(2): Show | 5 | NA18963.hp2 NA18964.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-5029A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53755970 | ||||||
| chr2:53755977
|
AC | A | 25 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(22): Show | 26 | HG00099.hp1 HG01099.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.197-5037delG | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53755977 | ||||||
| chr2:53755980
|
C | G | 3 | a0001c0001t0001g0015a0001c0001t0004g0014a0001c0001t0015g0013 | 3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.197-5039G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53755980 | ||||||
| chr2:53755986
|
C | A | 1 | a0001c0003t0002g0299 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.197-5045G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53755986 | ||||||
| chr2:53755987
|
C | G | 1 | a0001c0001t0001g0113 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.197-5046G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53755987 | ||||||
| chr2:53756098
|
GGAGGCTG others(4): Show |
G | 2 | a0001c0001t0001g0099a0001c0001t0001g0336 | 2 | HG00733.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.197-5168_197-5158d others(13): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53756098 | ||||||
| chr2:53756176
|
T | A | 1 | a0001c0001t0003g0167 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.197-5235A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53756176 | ||||||
| chr2:53756310
|
T | C | 4 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0215others(1): Show | 4 | HG02451.hp1 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-5369A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53756310 | ||||||
| chr2:53756362
|
T | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.197-5421A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53756362 | ||||||
| chr2:53756396
|
G | C | 23 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0133others(20): Show | 24 | HG00099.hp1 HG01099.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.197-5455C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53756396 | ||||||
| chr2:53756397
|
C | A | 23 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0133others(20): Show | 24 | HG00099.hp1 HG01099.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.197-5456G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53756397 | ||||||
| chr2:53756398
|
A | T | 23 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0133others(20): Show | 24 | HG00099.hp1 HG01099.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.197-5457T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53756398 | ||||||
| chr2:53756547
|
T | C | 229 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(226): Show | 233 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.197-5606A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53756547 | ||||||
| chr2:53756601
|
C | G | 1 | a0001c0001t0008g0031 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.197-5660G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53756601 | ||||||
| chr2:53756709
|
A | G | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.197-5768T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53756709 | ||||||
| chr2:53756722
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.197-5781G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53756722 | ||||||
| chr2:53756787
|
A | T | 12 | a0001c0001t0001g0141a0001c0001t0001g0144a0001c0001t0001g0145others(9): Show | 12 | HG00738.hp1 HG01167.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.197-5846T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53756787 | ||||||
| chr2:53756882
|
T | C | 57 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(54): Show | 57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.197-5941A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53756882 | ||||||
| chr2:53756932
|
A | C | 39 | a0001c0001t0001g0153a0001c0001t0003g0340a0001c0003t0001g0305others(36): Show | 39 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.197-5991T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53756932 | ||||||
| chr2:53757117
|
A | G | 53 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0001g0174others(50): Show | 55 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.197-6176T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757117 | ||||||
| chr2:53757128
|
G | A | 2 | a0001c0003t0002g0021a0001c0003t0007g0022 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.197-6187C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757128 | ||||||
| chr2:53757198
|
G | A | 2 | a0001c0001t0001g0320a0001c0001t0001g0327 | 2 | HG03239.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.197-6257C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757198 | ||||||
| chr2:53757213
|
A | G | 92 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(89): Show | 95 | HG00099.hp1 HG00408.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.197-6272T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757213 | ||||||
| chr2:53757233
|
G | C | 1 | a0001c0001t0004g0272 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.197-6292C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757233 | ||||||
| chr2:53757289
|
G | A | 2 | a0001c0001t0001g0202a0001c0001t0003g0203 | 2 | HG01358.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.197-6348C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757289 | ||||||
| chr2:53757291
|
C | A | 7 | a0001c0001t0001g0037a0001c0001t0001g0058a0001c0001t0001g0074others(4): Show | 7 | NA18959.hp2 NA18978.hp1 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.197-6350G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757291 | ||||||
| chr2:53757316
|
G | A | 6 | a0001c0001t0008g0029a0001c0001t0008g0031a0001c0001t0008g0032others(3): Show | 6 | HG01255.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.197-6375C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757316 | ||||||
| chr2:53757361
|
C | A | 1 | a0001c0001t0001g0311 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.197-6420G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757361 | ||||||
| chr2:53757362
|
G | A | 2 | a0001c0002t0002g0225a0001c0002t0002g0226 | 2 | HG02074.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.197-6421C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757362 | ||||||
| chr2:53757366
|
G | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0080 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.197-6425C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757366 | ||||||
| chr2:53757390
|
G | A | 1 | a0001c0001t0002g0131 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.197-6449C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757390 | ||||||
| chr2:53757579
|
T | C | 1 | a0001c0001t0001g0323 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.197-6638A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757579 | ||||||
| chr2:53757686
|
A | G | 189 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(186): Show | 192 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.197-6745T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757686 | ||||||
| chr2:53757820
|
T | C | 223 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(220): Show | 227 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.197-6879A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757820 | ||||||
| chr2:53757846
|
T | C | 59 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(56): Show | 59 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.197-6905A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757846 | ||||||
| chr2:53757886
|
A | C | 1 | a0001c0002t0002g0263 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.197-6945T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53757886 | ||||||
| chr2:53758033
|
G | A | 1 | a0001c0002t0007g0254 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.197-7092C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53758033 | ||||||
| chr2:53758193
|
G | A | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.196+7184C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53758193 | ||||||
| chr2:53758275
|
A | C | 1 | a0008c0010t0001g0100 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.196+7102T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53758275 | ||||||
| chr2:53758329
|
C | T | 56 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0036others(53): Show | 57 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.196+7048G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53758329 | ||||||
| chr2:53758362
|
G | A | 1 | a0001c0002t0006g0271 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.196+7015C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53758362 | ||||||
| chr2:53758615
|
G | A | 7 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0003g0146others(4): Show | 7 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.196+6762C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53758615 | ||||||
| chr2:53758705
|
A | T | 53 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0256others(50): Show | 53 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.196+6672T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53758705 | ||||||
| chr2:53758729
|
G | A | 53 | a0001c0001t0002g0228a0001c0001t0002g0229a0001c0001t0002g0256others(50): Show | 53 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.196+6648C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53758729 | ||||||
| chr2:53758755
|
C | T | 1 | a0001c0001t0004g0011 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.196+6622G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53758755 | ||||||
| chr2:53758844
|
A | T | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.196+6533T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53758844 | ||||||
| chr2:53759232
|
G | A | 6 | a0001c0001t0001g0141a0001c0001t0001g0144a0001c0001t0001g0145others(3): Show | 6 | HG00738.hp1 HG01884.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.196+6145C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53759232 | ||||||
| chr2:53759379
|
A | G | 1 | a0001c0001t0008g0195 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.196+5998T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53759379 | ||||||
| chr2:53759456
|
A | G | 57 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(54): Show | 57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.196+5921T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53759456 | ||||||
| chr2:53759509
|
C | T | 1 | a0001c0001t0004g0132 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.196+5868G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53759509 | ||||||
| chr2:53759561
|
G | T | 23 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(20): Show | 24 | HG00408.hp2 HG00733.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.196+5816C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53759561 | ||||||
| chr2:53759593
|
C | T | 84 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(81): Show | 87 | HG00408.hp1 HG00621.hp1 HG00738.hp1 others(84): Show |
intron_variant | MODIFIER | c.196+5784G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53759593 | ||||||
| chr2:53759630
|
G | C | 2 | a0001c0003t0002g0282a0001c0003t0002g0283 | 2 | NA18970.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.196+5747C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53759630 | ||||||
| chr2:53759725
|
G | A | 1 | a0001c0001t0004g0011 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.196+5652C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53759725 | ||||||
| chr2:53759747
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.196+5630G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53759747 | ||||||
| chr2:53759748
|
G | A | 57 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(54): Show | 57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.196+5629C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53759748 | ||||||
| chr2:53759795
|
A | T | 2 | a0001c0003t0002g0282a0001c0003t0002g0283 | 2 | NA18970.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.196+5582T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53759795 | ||||||
| chr2:53759802
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.196+5575C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53759802 | ||||||
| chr2:53759813
|
G | A | 1 | a0001c0001t0001g0326 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.196+5564C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53759813 | ||||||
| chr2:53759881
|
C | T | 38 | a0001c0001t0001g0153a0001c0003t0001g0305a0001c0003t0001g0306others(35): Show | 38 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.196+5496G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53759881 | ||||||
| chr2:53759906
|
G | C | 13 | a0001c0001t0003g0339a0001c0003t0005g0312a0001c0003t0005g0329others(10): Show | 14 | HG00733.hp1 HG01106.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.196+5471C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53759906 | ||||||
| chr2:53760287
|
G | A | 2 | a0001c0001t0001g0166a0001c0001t0001g0210 | 2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.196+5090C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53760287 | ||||||
| chr2:53760414
|
C | T | 1 | a0001c0001t0001g0313 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.196+4963G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53760414 | ||||||
| chr2:53760422
|
A | G | 146 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(143): Show | 149 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.196+4955T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53760422 | ||||||
| chr2:53760470
|
GC | G | 4 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(1): Show | 4 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+4906delG | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53760470 | ||||||
| chr2:53760644
|
TA | T | 84 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(81): Show | 87 | HG00408.hp1 HG00621.hp1 HG00738.hp1 others(84): Show |
intron_variant | MODIFIER | c.196+4732delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53760644 | ||||||
| chr2:53760708
|
T | A | 1 | a0001c0001t0001g0328 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.196+4669A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53760708 | ||||||
| chr2:53760752
|
G | T | 1 | a0001c0003t0002g0287 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.196+4625C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53760752 | ||||||
| chr2:53760753
|
A | G | 222 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(219): Show | 226 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.196+4624T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53760753 | ||||||
| chr2:53760754
|
T | C | 222 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(219): Show | 226 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.196+4623A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53760754 | ||||||
| chr2:53760793
|
G | A | 57 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(54): Show | 57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.196+4584C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53760793 | ||||||
| chr2:53760885
|
A | G | 221 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(218): Show | 225 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.196+4492T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53760885 | ||||||
| chr2:53760957
|
T | C | 1 | a0001c0001t0003g0167 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.196+4420A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53760957 | ||||||
| chr2:53761003
|
C | T | 1 | a0001c0001t0003g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.196+4374G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53761003 | ||||||
| chr2:53761093
|
G | A | 19 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0057others(16): Show | 19 | HG00423.hp2 HG02132.hp1 NA18612.hp1 others(16): Show |
intron_variant | MODIFIER | c.196+4284C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53761093 | ||||||
| chr2:53761098
|
G | T | 3 | a0001c0001t0001g0213a0001c0001t0001g0215a0001c0001t0004g0214 | 3 | HG03209.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.196+4279C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53761098 | ||||||
| chr2:53761383
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.196+3994C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53761383 | ||||||
| chr2:53761425
|
G | GA | 8 | a0001c0001t0001g0141a0001c0001t0001g0144a0001c0001t0001g0145others(5): Show | 8 | HG00738.hp1 HG01884.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.196+3951dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53761425 | ||||||
| chr2:53761698
|
G | T | 3 | a0001c0001t0003g0193a0001c0001t0003g0194a0001c0001t0003g0205 | 3 | HG01515.hp1 HG01517.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.196+3679C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53761698 | ||||||
| chr2:53761826
|
C | G | 1 | a0001c0003t0002g0296 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.196+3551G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53761826 | ||||||
| chr2:53761942
|
G | T | 1 | a0001c0003t0002g0296 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.196+3435C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53761942 | ||||||
| chr2:53762030
|
G | T | 7 | a0001c0002t0002g0220a0001c0002t0002g0223a0001c0002t0002g0224others(4): Show | 7 | HG00423.hp1 HG02074.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.196+3347C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53762030 | ||||||
| chr2:53762035
|
T | C | 1 | a0001c0001t0001g0153 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.196+3342A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53762035 | ||||||
| chr2:53762107
|
G | T | 112 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(109): Show | 116 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.196+3270C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53762107 | ||||||
| chr2:53762153
|
T | C | 3 | a0001c0001t0001g0004a0001c0001t0001g0108a0001c0001t0001g0122 | 4 | HG00099.hp2 HG01081.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+3224A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53762153 | ||||||
| chr2:53762171
|
C | CTG | 85 | a0001c0001t0001g0050a0001c0001t0001g0269a0001c0001t0001g0311others(82): Show | 86 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.196+3204_196+3205d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53762171 | ||||||
| chr2:53762171
|
C | CTGTG | 4 | a0001c0001t0002g0154a0001c0001t0003g0340a0001c0001t0004g0324others(1): Show | 4 | HG01243.hp2 HG03942.hp2 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+3202_196+3205d others(6): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53762171 | ||||||
| chr2:53762171
|
CTG | C | 49 | a0001c0001t0001g0145a0001c0001t0001g0171a0001c0001t0001g0173others(46): Show | 51 | HG00408.hp1 HG00621.hp1 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.196+3204_196+3205d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53762171 | ||||||
| chr2:53762171
|
CTGTGTG | C | 5 | a0001c0001t0001g0274a0001c0001t0004g0273a0001c0001t0004g0275others(2): Show | 5 | HG02818.hp1 HG03139.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+3200_196+3205d others(8): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53762171 | ||||||
| chr2:53762334
|
G | A | 5 | a0001c0003t0005g0312a0001c0003t0005g0331a0001c0003t0005g0335others(2): Show | 5 | HG01123.hp1 HG01168.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+3043C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53762334 | ||||||
| chr2:53762440
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.196+2937C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53762440 | ||||||
| chr2:53762608
|
T | C | 11 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(8): Show | 11 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.196+2769A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53762608 | ||||||
| chr2:53762847
|
A | C | 12 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(9): Show | 12 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.196+2530T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53762847 | ||||||
| chr2:53763296
|
T | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0004g0014others(2): Show | 5 | HG02258.hp1 HG02970.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.196+2081A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53763296 | ||||||
| chr2:53763395
|
C | T | 164 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(161): Show | 167 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.196+1982G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53763395 | ||||||
| chr2:53763564
|
G | A | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270 | 3 | HG02630.hp1 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.196+1813C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53763564 | ||||||
| chr2:53763581
|
A | C | 3 | a0001c0001t0001g0166a0001c0001t0001g0210a0001c0001t0003g0339 | 3 | HG01891.hp2 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.196+1796T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53763581 | ||||||
| chr2:53763582
|
A | G | 1 | a0001c0001t0009g0192 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.196+1795T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53763582 | ||||||
| chr2:53763781
|
G | T | 1 | a0001c0001t0001g0113 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.196+1596C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53763781 | ||||||
| chr2:53763785
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.196+1592A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53763785 | ||||||
| chr2:53763840
|
C | G | 5 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0004g0014others(2): Show | 5 | HG02258.hp1 HG02970.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.196+1537G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53763840 | ||||||
| chr2:53763941
|
G | C | 2 | a0001c0003t0002g0282a0001c0003t0002g0283 | 2 | NA18970.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.196+1436C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53763941 | ||||||
| chr2:53763961
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.196+1416G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53763961 | ||||||
| chr2:53764085
|
A | T | 57 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(54): Show | 57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.196+1292T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53764085 | ||||||
| chr2:53764156
|
T | C | 58 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(55): Show | 58 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.196+1221A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53764156 | ||||||
| chr2:53764440
|
A | C | 2 | a0001c0003t0007g0284a0001c0003t0007g0285 | 2 | HG00558.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.196+937T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53764440 | ||||||
| chr2:53764542
|
C | G | 4 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(1): Show | 4 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+835G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53764542 | ||||||
| chr2:53764570
|
A | C | 193 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(190): Show | 197 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.196+807T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53764570 | ||||||
| chr2:53764604
|
A | T | 193 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(190): Show | 197 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.196+773T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53764604 | ||||||
| chr2:53764671
|
T | C | 1 | a0007c0007t0005g0341 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.196+706A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53764671 | ||||||
| chr2:53764733
|
C | T | 1 | a0001c0003t0002g0310 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.196+644G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53764733 | ||||||
| chr2:53764758
|
G | C | 6 | a0001c0001t0001g0141a0001c0001t0001g0144a0001c0001t0001g0145others(3): Show | 6 | HG00738.hp1 HG01884.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.196+619C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53764758 | ||||||
| chr2:53764962
|
A | C | 1 | a0002c0004t0010g0136 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.196+415T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53764962 | ||||||
| chr2:53765032
|
G | A | 1 | a0001c0001t0004g0114 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.196+345C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53765032 | ||||||
| chr2:53765041
|
C | A | 2 | a0001c0003t0007g0284a0001c0003t0007g0285 | 2 | HG00558.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.196+336G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53765041 | ||||||
| chr2:53765174
|
G | A | 2 | a0001c0001t0001g0207a0001c0001t0003g0206 | 2 | NA18987.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.196+203C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 2/9 | chr2 | 53765174 | ||||||
| chr2:53765645
|
G | C | 3 | a0001c0001t0001g0141a0001c0001t0001g0144a0001c0001t0001g0145 | 3 | HG00738.hp1 HG01884.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-13-60C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53765645 | ||||||
| chr2:53765722
|
T | G | 47 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0153others(44): Show | 47 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.-13-137A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53765722 | ||||||
| chr2:53765726
|
A | G | 1 | a0001c0001t0003g0339 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-13-141T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53765726 | ||||||
| chr2:53765900
|
TTCTTTGG others(22): Show |
T | 24 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(21): Show | 25 | HG00408.hp2 HG00733.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.-13-344_-13-316del others(29): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53765900 | ||||||
| chr2:53765936
|
G | A | 2 | a0001c0003t0002g0297a0001c0003t0002g0298 | 2 | HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-13-351C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53765936 | ||||||
| chr2:53766109
|
T | C | 1 | a0001c0003t0006g0294 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-13-524A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53766109 | ||||||
| chr2:53766245
|
A | G | 57 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(54): Show | 57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.-13-660T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53766245 | ||||||
| chr2:53766326
|
G | C | 2 | a0001c0001t0001g0024a0001c0001t0004g0121 | 2 | HG02486.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-13-741C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53766326 | ||||||
| chr2:53766329
|
T | C | 6 | a0001c0001t0001g0024a0001c0001t0001g0212a0001c0001t0001g0213others(3): Show | 6 | HG02451.hp1 HG02486.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-744A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53766329 | ||||||
| chr2:53766350
|
G | A | 137 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0149others(134): Show | 138 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.-13-765C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53766350 | ||||||
| chr2:53766366
|
G | A | 57 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(54): Show | 57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.-13-781C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53766366 | ||||||
| chr2:53766377
|
T | C | 2 | a0001c0001t0001g0054a0001c0001t0004g0053 | 2 | HG02027.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.-13-792A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53766377 | ||||||
| chr2:53766456
|
A | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0108a0001c0001t0001g0122 | 4 | HG00099.hp2 HG01081.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13-871T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53766456 | ||||||
| chr2:53766465
|
G | C | 1 | a0001c0001t0008g0035 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-13-880C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53766465 | ||||||
| chr2:53766482
|
T | A | 2 | a0001c0001t0001g0133a0001c0001t0004g0114 | 2 | HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-13-897A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53766482 | ||||||
| chr2:53766535
|
T | C | 4 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0004g0014others(1): Show | 4 | HG02258.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13-950A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53766535 | ||||||
| chr2:53766788
|
C | T | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-1203G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53766788 | ||||||
| chr2:53766923
|
T | G | 6 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0315others(3): Show | 6 | HG01167.hp1 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-13-1338A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53766923 | ||||||
| chr2:53767023
|
C | A | 51 | a0001c0002t0001g0258a0001c0002t0002g0017a0001c0002t0002g0018others(48): Show | 51 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.-13-1438G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53767023 | ||||||
| chr2:53767161
|
G | A | 1 | a0002c0004t0013g0012 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-13-1576C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53767161 | ||||||
| chr2:53767356
|
A | G | 57 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(54): Show | 57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.-13-1771T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53767356 | ||||||
| chr2:53767400
|
T | C | 1 | a0001c0001t0003g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-13-1815A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53767400 | ||||||
| chr2:53767441
|
C | G | 1 | a0001c0001t0001g0153 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-13-1856G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53767441 | ||||||
| chr2:53767465
|
C | T | 2 | a0001c0003t0002g0302a0001c0003t0002g0303 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-13-1880G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53767465 | ||||||
| chr2:53767615
|
A | C | 1 | a0002c0004t0013g0012 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-13-2030T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53767615 | ||||||
| chr2:53767683
|
C | T | 45 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0153others(42): Show | 45 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.-13-2098G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53767683 | ||||||
| chr2:53767730
|
T | C | 9 | a0001c0001t0001g0005a0001c0001t0001g0158a0001c0001t0001g0161others(6): Show | 10 | HG01099.hp1 HG01106.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.-13-2145A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53767730 | ||||||
| chr2:53767746
|
C | T | 1 | a0001c0001t0005g0003 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-13-2161G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53767746 | ||||||
| chr2:53767786
|
C | A | 2 | a0001c0001t0001g0101a0001c0001t0001g0102 | 2 | NA18612.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.-13-2201G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53767786 | ||||||
| chr2:53767792
|
G | A | 38 | a0001c0001t0001g0153a0001c0003t0001g0305a0001c0003t0001g0306others(35): Show | 38 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.-13-2207C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53767792 | ||||||
| chr2:53768243
|
C | T | 139 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(136): Show | 142 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-13-2658G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53768243 | ||||||
| chr2:53768359
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-13-2774C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53768359 | ||||||
| chr2:53768543
|
C | T | 204 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(201): Show | 208 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.-13-2958G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53768543 | ||||||
| chr2:53768596
|
T | G | 79 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(76): Show | 82 | HG00408.hp1 HG00621.hp1 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.-13-3011A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53768596 | ||||||
| chr2:53768607
|
T | C | 1 | a0001c0001t0001g0001 | 2 | HG03491.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-13-3022A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53768607 | ||||||
| chr2:53768684
|
A | G | 1 | a0002c0004t0010g0136 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-13-3099T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53768684 | ||||||
| chr2:53768753
|
A | C | 12 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(9): Show | 12 | HG00408.hp2 HG01069.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-13-3168T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53768753 | ||||||
| chr2:53768753
|
A | G | 141 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(138): Show | 144 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.-13-3168T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53768753 | ||||||
| chr2:53768780
|
T | C | 1 | a0001c0003t0014g0304 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-13-3195A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53768780 | ||||||
| chr2:53768818
|
A | G | 1 | a0001c0001t0002g0131 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-13-3233T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53768818 | ||||||
| chr2:53768939
|
A | C | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-13-3354T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53768939 | ||||||
| chr2:53768940
|
C | A | 82 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(79): Show | 85 | HG00408.hp1 HG00621.hp1 HG00738.hp1 others(82): Show |
intron_variant | MODIFIER | c.-13-3355G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53768940 | ||||||
| chr2:53768947
|
A | T | 1 | a0001c0003t0014g0304 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-13-3362T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53768947 | ||||||
| chr2:53769103
|
G | A | 4 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(1): Show | 4 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13-3518C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53769103 | ||||||
| chr2:53769167
|
G | C | 1 | a0001c0001t0012g0204 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-13-3582C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53769167 | ||||||
| chr2:53769351
|
C | T | 1 | a0001c0001t0003g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-13-3766G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53769351 | ||||||
| chr2:53769418
|
T | C | 24 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(21): Show | 24 | HG01358.hp1 HG01515.hp1 HG01517.hp2 others(21): Show |
intron_variant | MODIFIER | c.-13-3833A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53769418 | ||||||
| chr2:53769419
|
A | T | 1 | a0001c0002t0002g0227 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-13-3834T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53769419 | ||||||
| chr2:53769429
|
A | G | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-13-3844T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53769429 | ||||||
| chr2:53769446
|
G | C | 229 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(226): Show | 233 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.-13-3861C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53769446 | ||||||
| chr2:53769730
|
C | A | 1 | a0001c0003t0006g0295 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-13-4145G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53769730 | ||||||
| chr2:53769783
|
G | A | 7 | a0001c0001t0001g0041a0001c0001t0001g0103a0001c0001t0001g0104others(4): Show | 7 | HG01109.hp1 HG01884.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-4198C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53769783 | ||||||
| chr2:53769799
|
G | A | 3 | a0001c0003t0002g0296a0001c0003t0002g0297a0001c0003t0002g0298 | 3 | HG03041.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-13-4214C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53769799 | ||||||
| chr2:53769915
|
T | C | 7 | a0001c0001t0001g0045a0001c0001t0008g0029a0001c0001t0008g0031others(4): Show | 7 | HG01255.hp1 HG02257.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-4330A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53769915 | ||||||
| chr2:53769937
|
C | T | 1 | a0001c0001t0009g0179 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-13-4352G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53769937 | ||||||
| chr2:53770021
|
C | A | 45 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0001g0174others(42): Show | 47 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.-13-4436G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770021 | ||||||
| chr2:53770183
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0108a0001c0001t0001g0122 | 4 | HG00099.hp2 HG01081.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13-4598C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770183 | ||||||
| chr2:53770204
|
C | CA | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-4620dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770204 | ||||||
| chr2:53770209
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-13-4624A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770209 | ||||||
| chr2:53770328
|
G | C | 2 | a0001c0002t0001g0258a0001c0002t0002g0257 | 2 | NA18975.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.-13-4743C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770328 | ||||||
| chr2:53770411
|
T | C | 1 | a0001c0001t0001g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-13-4826A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770411 | ||||||
| chr2:53770487
|
C | T | 22 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(19): Show | 23 | HG01099.hp1 HG01106.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.-13-4902G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770487 | ||||||
| chr2:53770498
|
T | TA | 7 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(4): Show | 7 | HG01952.hp1 HG03927.hp2 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-4914dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770498 | ||||||
| chr2:53770498
|
TA | T | 101 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0036others(98): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.-13-4914delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770498 | ||||||
| chr2:53770498
|
TAA | T | 38 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(35): Show | 39 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.-13-4915_-13-4914d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770498 | ||||||
| chr2:53770498
|
TAAA | T | 56 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0149others(53): Show | 57 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.-13-4916_-13-4914d others(5): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770498 | ||||||
| chr2:53770498
|
TAAAA | T | 58 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(55): Show | 58 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.-13-4917_-13-4914d others(6): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770498 | ||||||
| chr2:53770539
|
T | A | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-13-4954A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770539 | ||||||
| chr2:53770612
|
G | A | 341 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(338): Show | 349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.-13-5027C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770612 | ||||||
| chr2:53770650
|
A | G | 2 | a0001c0001t0001g0054a0001c0001t0004g0053 | 2 | HG02027.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.-13-5065T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770650 | ||||||
| chr2:53770852
|
A | G | 3 | a0001c0001t0003g0146a0001c0001t0003g0147a0001c0001t0003g0148 | 3 | HG02630.hp2 HG02896.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-13-5267T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770852 | ||||||
| chr2:53770873
|
T | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0004g0014others(2): Show | 5 | HG02258.hp1 HG02970.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-5288A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53770873 | ||||||
| chr2:53771118
|
C | A | 1 | a0001c0003t0004g0308 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-13-5533G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53771118 | ||||||
| chr2:53771185
|
A | G | 8 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0153others(5): Show | 8 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13-5600T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53771185 | ||||||
| chr2:53771218
|
C | T | 4 | a0001c0001t0001g0040a0001c0001t0001g0124a0001c0001t0001g0125others(1): Show | 4 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13-5633G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53771218 | ||||||
| chr2:53771219
|
C | T | 55 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0001g0174others(52): Show | 57 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.-13-5634G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53771219 | ||||||
| chr2:53771301
|
G | T | 2 | a0001c0001t0001g0015a0001c0001t0004g0014 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-13-5716C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53771301 | ||||||
| chr2:53771317
|
C | A | 56 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(53): Show | 56 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.-13-5732G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53771317 | ||||||
| chr2:53771374
|
G | C | 2 | a0001c0003t0005g0332a0001c0003t0005g0333 | 2 | HG02602.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-13-5789C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53771374 | ||||||
| chr2:53771421
|
G | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0004g0014others(2): Show | 5 | HG02258.hp1 HG02970.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-5836C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53771421 | ||||||
| chr2:53771443
|
T | A | 1 | a0001c0001t0005g0003 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-13-5858A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53771443 | ||||||
| chr2:53771520
|
T | A | 1 | a0001c0001t0003g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-13-5935A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53771520 | ||||||
| chr2:53771571
|
A | C | 1 | a0001c0001t0001g0153 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-13-5986T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53771571 | ||||||
| chr2:53771703
|
T | C | 1 | a0001c0003t0005g0342 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-13-6118A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53771703 | ||||||
| chr2:53771711
|
G | T | 7 | a0001c0002t0002g0220a0001c0002t0002g0223a0001c0002t0002g0224others(4): Show | 7 | HG00423.hp1 HG02074.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-6126C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53771711 | ||||||
| chr2:53771789
|
T | C | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-6204A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53771789 | ||||||
| chr2:53771883
|
T | A | 1 | a0001c0001t0003g0339 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-13-6298A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53771883 | ||||||
| chr2:53772040
|
A | C | 5 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(2): Show | 5 | HG02080.hp1 NA18968.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-6455T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772040 | ||||||
| chr2:53772108
|
A | G | 2 | a0001c0002t0002g0264a0001c0002t0002g0265 | 2 | HG03669.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-13-6523T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772108 | ||||||
| chr2:53772121
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0004g0014 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-13-6536C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772121 | ||||||
| chr2:53772186
|
G | GT | 83 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(80): Show | 86 | HG00408.hp1 HG00621.hp1 HG00738.hp1 others(83): Show |
intron_variant | MODIFIER | c.-13-6602dupA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772186 | ||||||
| chr2:53772186
|
G | T | 1 | a0001c0001t0001g0052 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-13-6601C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772186 | ||||||
| chr2:53772205
|
A | C | 1 | a0001c0001t0001g0323 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-13-6620T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772205 | ||||||
| chr2:53772237
|
C | G | 1 | a0001c0001t0001g0051 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-13-6652G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772237 | ||||||
| chr2:53772335
|
T | C | 9 | a0001c0001t0001g0005a0001c0001t0001g0158a0001c0001t0001g0161others(6): Show | 10 | HG01099.hp1 HG01106.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.-13-6750A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772335 | ||||||
| chr2:53772366
|
A | G | 1 | a0001c0001t0001g0050 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-13-6781T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772366 | ||||||
| chr2:53772416
|
C | T | 1 | a0001c0001t0001g0048 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-13-6831G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772416 | ||||||
| chr2:53772425
|
T | C | 3 | a0001c0001t0001g0030a0001c0001t0003g0167a0001c0001t0003g0340 | 3 | HG03669.hp2 NA19080.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-13-6840A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772425 | ||||||
| chr2:53772501
|
T | G | 1 | a0001c0001t0004g0276 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-13-6916A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772501 | ||||||
| chr2:53772529
|
C | T | 1 | a0002c0004t0010g0136 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-13-6944G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772529 | ||||||
| chr2:53772637
|
T | G | 58 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(55): Show | 58 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.-13-7052A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772637 | ||||||
| chr2:53772702
|
GTGTTTT | G | 55 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0001g0174others(52): Show | 57 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.-13-7123_-13-7118d others(8): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772702 | ||||||
| chr2:53772825
|
T | A | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-13-7240A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772825 | ||||||
| chr2:53772883
|
T | C | 1 | a0001c0002t0002g0267 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-13-7298A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53772883 | ||||||
| chr2:53773085
|
A | T | 1 | a0001c0001t0004g0114 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-13-7500T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773085 | ||||||
| chr2:53773125
|
G | A | 2 | a0001c0001t0001g0133a0001c0001t0004g0114 | 2 | HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-13-7540C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773125 | ||||||
| chr2:53773130
|
G | A | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-13-7545C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773130 | ||||||
| chr2:53773293
|
T | A | 3 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0130 | 3 | HG02015.hp2 HG03710.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.-13-7708A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773293 | ||||||
| chr2:53773321
|
C | CAAGATAT others(25): Show |
2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-13-7737_-13-7736i others(34): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773321 | ||||||
| chr2:53773322
|
C | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-13-7737G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773322 | ||||||
| chr2:53773323
|
T | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-13-7738A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773323 | ||||||
| chr2:53773324
|
A | G | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-7739T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773324 | ||||||
| chr2:53773326
|
G | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-13-7741C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773326 | ||||||
| chr2:53773401
|
C | CT | 8 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0153others(5): Show | 8 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13-7817dupA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773401 | ||||||
| chr2:53773418
|
CTG | C | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-7835_-13-7834d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773418 | ||||||
| chr2:53773500
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-13-7915C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773500 | ||||||
| chr2:53773503
|
T | C | 2 | a0001c0003t0005g0332a0001c0003t0005g0333 | 2 | HG02602.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-13-7918A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773503 | ||||||
| chr2:53773681
|
G | A | 1 | a0001c0001t0003g0339 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-13-8096C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773681 | ||||||
| chr2:53773719
|
G | A | 2 | a0001c0003t0002g0302a0001c0003t0002g0303 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-13-8134C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773719 | ||||||
| chr2:53773801
|
G | A | 7 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0003g0146others(4): Show | 7 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13-8216C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773801 | ||||||
| chr2:53773905
|
C | G | 1 | a0001c0001t0004g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-13-8320G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53773905 | ||||||
| chr2:53774008
|
C | G | 3 | a0002c0004t0010g0137a0002c0004t0010g0138a0002c0004t0010g0139 | 3 | HG02818.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-13-8423G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53774008 | ||||||
| chr2:53774033
|
C | CA | 8 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0153others(5): Show | 8 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13-8449dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53774033 | ||||||
| chr2:53774093
|
A | G | 1 | a0001c0001t0001g0048 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-13-8508T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53774093 | ||||||
| chr2:53774499
|
G | A | 3 | a0001c0001t0001g0213a0001c0001t0001g0215a0001c0001t0004g0214 | 3 | HG03209.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-13-8914C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53774499 | ||||||
| chr2:53774659
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-13-9074G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53774659 | ||||||
| chr2:53774710
|
A | G | 1 | a0001c0001t0001g0046 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-13-9125T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53774710 | ||||||
| chr2:53774927
|
C | A | 49 | a0001c0001t0003g0339a0001c0003t0001g0305a0001c0003t0001g0306others(46): Show | 50 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.-13-9342G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53774927 | ||||||
| chr2:53775131
|
G | A | 6 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0315others(3): Show | 6 | HG01167.hp1 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-13-9546C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53775131 | ||||||
| chr2:53775339
|
T | TTG | 59 | a0001c0001t0001g0117a0001c0001t0001g0269a0001c0001t0001g0270others(56): Show | 59 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.-13-9756_-13-9755d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53775339 | ||||||
| chr2:53775366
|
T | A | 70 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0171others(67): Show | 71 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.-13-9781A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53775366 | ||||||
| chr2:53775368
|
T | C | 8 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0153others(5): Show | 8 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13-9783A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53775368 | ||||||
| chr2:53775385
|
T | C | 1 | a0001c0001t0001g0120 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-13-9800A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53775385 | ||||||
| chr2:53775404
|
G | A | 78 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(75): Show | 81 | HG00408.hp1 HG00621.hp1 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.-13-9819C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53775404 | ||||||
| chr2:53775422
|
C | G | 4 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(1): Show | 4 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13-9837G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53775422 | ||||||
| chr2:53775611
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0122 | 3 | HG01081.hp2 HG01099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.-13-10026C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53775611 | ||||||
| chr2:53775723
|
G | A | 8 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0153others(5): Show | 8 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13-10138C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53775723 | ||||||
| chr2:53775876
|
C | G | 70 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0042others(67): Show | 71 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.-13-10291G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53775876 | ||||||
| chr2:53776034
|
A | G | 2 | a0001c0003t0002g0321a0001c0003t0002g0322 | 2 | HG02523.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.-13-10449T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53776034 | ||||||
| chr2:53776269
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-14+10552G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53776269 | ||||||
| chr2:53776640
|
A | G | 224 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(221): Show | 228 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.-14+10181T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53776640 | ||||||
| chr2:53776751
|
C | T | 5 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0003g0218others(2): Show | 5 | HG02258.hp1 HG02970.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14+10070G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53776751 | ||||||
| chr2:53776764
|
A | C | 1 | a0001c0001t0001g0001 | 2 | HG03491.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-14+10057T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53776764 | ||||||
| chr2:53776823
|
A | C | 1 | a0001c0001t0001g0041 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-14+9998T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53776823 | ||||||
| chr2:53776853
|
G | C | 4 | a0001c0001t0001g0040a0001c0001t0001g0124a0001c0001t0001g0125others(1): Show | 4 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+9968C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53776853 | ||||||
| chr2:53777095
|
C | G | 4 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(1): Show | 4 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+9726G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53777095 | ||||||
| chr2:53777351
|
T | G | 6 | a0001c0001t0001g0141a0001c0001t0001g0144a0001c0001t0001g0145others(3): Show | 6 | HG00738.hp1 HG01884.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14+9470A>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53777351 | ||||||
| chr2:53777421
|
G | A | 1 | a0001c0001t0003g0152 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-14+9400C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53777421 | ||||||
| chr2:53777589
|
C | CT | 57 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(54): Show | 57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.-14+9231dupA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53777589 | ||||||
| chr2:53777660
|
C | T | 1 | a0001c0001t0003g0340 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-14+9161G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53777660 | ||||||
| chr2:53777698
|
G | A | 1 | a0001c0001t0001g0311 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-14+9123C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53777698 | ||||||
| chr2:53777726
|
A | G | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+9095T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53777726 | ||||||
| chr2:53777983
|
C | T | 56 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(53): Show | 56 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.-14+8838G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53777983 | ||||||
| chr2:53778010
|
G | A | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-14+8811C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53778010 | ||||||
| chr2:53778149
|
C | CA | 9 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0334others(6): Show | 9 | HG01358.hp2 HG01952.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-14+8671dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53778149 | ||||||
| chr2:53778149
|
CA | C | 85 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0036others(82): Show | 87 | HG00323.hp2 HG00408.hp1 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.-14+8671delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53778149 | ||||||
| chr2:53778149
|
CAA | C | 22 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0016others(19): Show | 23 | HG01070.hp1 HG01099.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.-14+8670_-14+8671d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53778149 | ||||||
| chr2:53778281
|
A | G | 6 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0315others(3): Show | 6 | HG01167.hp1 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14+8540T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53778281 | ||||||
| chr2:53778423
|
T | C | 1 | a0001c0001t0004g0011 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-14+8398A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53778423 | ||||||
| chr2:53778792
|
G | T | 1 | a0001c0001t0004g0272 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-14+8029C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53778792 | ||||||
| chr2:53778810
|
C | T | 76 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(73): Show | 79 | HG00408.hp1 HG00621.hp1 HG00738.hp1 others(76): Show |
intron_variant | MODIFIER | c.-14+8011G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53778810 | ||||||
| chr2:53778926
|
T | C | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-14+7895A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53778926 | ||||||
| chr2:53778962
|
C | T | 211 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(208): Show | 215 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.-14+7859G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53778962 | ||||||
| chr2:53778975
|
C | T | 1 | a0001c0001t0001g0319 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-14+7846G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53778975 | ||||||
| chr2:53778986
|
A | C | 3 | a0001c0001t0001g0211a0001c0001t0001g0216a0001c0001t0001g0217 | 3 | HG02572.hp2 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-14+7835T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53778986 | ||||||
| chr2:53779002
|
A | G | 1 | a0001c0001t0003g0167 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-14+7819T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53779002 | ||||||
| chr2:53779018
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-14+7803G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53779018 | ||||||
| chr2:53779421
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-14+7400C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53779421 | ||||||
| chr2:53779621
|
G | A | 76 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(73): Show | 79 | HG00408.hp1 HG00621.hp1 HG00738.hp1 others(76): Show |
intron_variant | MODIFIER | c.-14+7200C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53779621 | ||||||
| chr2:53779886
|
T | C | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+6935A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53779886 | ||||||
| chr2:53779999
|
G | A | 4 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(1): Show | 4 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+6822C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53779999 | ||||||
| chr2:53780034
|
A | C | 61 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(58): Show | 62 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-14+6787T>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53780034 | ||||||
| chr2:53780197
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-14+6624T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53780197 | ||||||
| chr2:53780349
|
T | C | 2 | a0001c0002t0002g0264a0001c0002t0002g0265 | 2 | HG03669.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-14+6472A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53780349 | ||||||
| chr2:53780514
|
C | T | 56 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(53): Show | 56 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.-14+6307G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53780514 | ||||||
| chr2:53780515
|
G | A | 2 | a0001c0001t0001g0207a0001c0001t0003g0206 | 2 | NA18987.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.-14+6306C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53780515 | ||||||
| chr2:53780554
|
G | A | 3 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0004g0157 | 3 | HG02109.hp2 HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-14+6267C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53780554 | ||||||
| chr2:53781131
|
G | A | 1 | a0001c0001t0008g0029 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-14+5690C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53781131 | ||||||
| chr2:53781271
|
G | A | 9 | a0001c0001t0001g0005a0001c0001t0001g0158a0001c0001t0001g0161others(6): Show | 10 | HG01099.hp1 HG01106.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14+5550C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53781271 | ||||||
| chr2:53781273
|
G | A | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270 | 3 | HG02630.hp1 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-14+5548C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53781273 | ||||||
| chr2:53781373
|
T | C | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+5448A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53781373 | ||||||
| chr2:53781412
|
C | CA | 7 | a0001c0001t0001g0166a0001c0001t0002g0131a0001c0001t0004g0132others(4): Show | 7 | HG00438.hp2 HG01069.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14+5408dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53781412 | ||||||
| chr2:53781412
|
CA | C | 57 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(54): Show | 57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.-14+5408delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53781412 | ||||||
| chr2:53781466
|
G | T | 7 | a0001c0003t0002g0278a0001c0003t0002g0280a0001c0003t0002g0281others(4): Show | 7 | HG00558.hp2 HG02083.hp2 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14+5355C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53781466 | ||||||
| chr2:53781490
|
TC | T | 8 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0153others(5): Show | 8 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-14+5330delG | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53781490 | ||||||
| chr2:53781498
|
T | C | 1 | a0001c0001t0004g0011 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-14+5323A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53781498 | ||||||
| chr2:53781635
|
A | T | 65 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0311others(62): Show | 66 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.-14+5186T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53781635 | ||||||
| chr2:53781665
|
T | C | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+5156A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53781665 | ||||||
| chr2:53781670
|
T | C | 46 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0001g0174others(43): Show | 48 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.-14+5151A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53781670 | ||||||
| chr2:53781781
|
C | T | 1 | a0001c0001t0008g0029 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-14+5040G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53781781 | ||||||
| chr2:53782124
|
C | T | 2 | a0001c0001t0004g0027a0006c0008t0001g0028 | 2 | NA18945.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.-14+4697G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53782124 | ||||||
| chr2:53782153
|
G | C | 1 | a0001c0002t0002g0266 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-14+4668C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53782153 | ||||||
| chr2:53782182
|
C | T | 59 | a0001c0001t0001g0311a0001c0001t0001g0319a0001c0001t0001g0320others(56): Show | 60 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.-14+4639G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53782182 | ||||||
| chr2:53782370
|
T | C | 6 | a0001c0001t0001g0274a0001c0001t0004g0272a0001c0001t0004g0273others(3): Show | 6 | HG01074.hp1 HG02818.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14+4451A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53782370 | ||||||
| chr2:53782425
|
G | C | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-14+4396C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53782425 | ||||||
| chr2:53782543
|
C | G | 16 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(13): Show | 17 | HG01099.hp1 HG01106.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.-14+4278G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53782543 | ||||||
| chr2:53782707
|
C | T | 212 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(209): Show | 216 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.-14+4114G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53782707 | ||||||
| chr2:53783075
|
G | T | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+3746C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53783075 | ||||||
| chr2:53783077
|
A | AT | 6 | a0001c0001t0004g0026a0002c0004t0010g0136a0002c0004t0010g0137others(3): Show | 6 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14+3743dupA | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53783077 | ||||||
| chr2:53783077
|
A | T | 1 | a0001c0003t0002g0279 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-14+3744T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53783077 | ||||||
| chr2:53783174
|
T | C | 1 | a0001c0001t0001g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-14+3647A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53783174 | ||||||
| chr2:53783223
|
C | G | 1 | a0001c0001t0001g0025 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-14+3598G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53783223 | ||||||
| chr2:53783273
|
C | A | 1 | a0001c0001t0001g0153 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14+3548G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53783273 | ||||||
| chr2:53783371
|
CTGTATTT others(17): Show |
C | 1 | a0001c0001t0002g0154 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-14+3426_-14+3449d others(26): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53783371 | ||||||
| chr2:53783427
|
T | C | 4 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+3394A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53783427 | ||||||
| chr2:53783739
|
C | A | 3 | a0003c0005t0005g0008a0003c0005t0005g0337a0003c0005t0005g0338 | 4 | HG01106.hp2 HG01261.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+3082G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53783739 | ||||||
| chr2:53783764
|
C | T | 1 | a0002c0004t0010g0136 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-14+3057G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53783764 | ||||||
| chr2:53783856
|
C | A | 1 | a0001c0001t0004g0277 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-14+2965G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53783856 | ||||||
| chr2:53784138
|
T | C | 2 | a0001c0001t0001g0216a0001c0001t0001g0217 | 2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-14+2683A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53784138 | ||||||
| chr2:53784148
|
G | A | 4 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(1): Show | 4 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+2673C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53784148 | ||||||
| chr2:53784150
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-14+2671C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53784150 | ||||||
| chr2:53784182
|
T | C | 1 | a0001c0001t0008g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-14+2639A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53784182 | ||||||
| chr2:53784242
|
C | T | 126 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0268others(123): Show | 127 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.-14+2579G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53784242 | ||||||
| chr2:53784432
|
C | A | 1 | a0001c0001t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-14+2389G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53784432 | ||||||
| chr2:53784546
|
C | G | 5 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+2275G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53784546 | ||||||
| chr2:53784614
|
C | T | 7 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0003g0146others(4): Show | 7 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14+2207G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53784614 | ||||||
| chr2:53785323
|
T | C | 1 | a0007c0007t0005g0341 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-14+1498A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53785323 | ||||||
| chr2:53785433
|
T | TA | 125 | a0001c0001t0001g0134a0001c0001t0001g0149a0001c0001t0001g0151others(122): Show | 126 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.-14+1387dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53785433 | ||||||
| chr2:53785433
|
T | TAA | 6 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(3): Show | 6 | HG01192.hp1 HG02630.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14+1386_-14+1387d others(4): Show |
ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53785433 | ||||||
| chr2:53785433
|
TA | T | 65 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(62): Show | 68 | HG00408.hp1 HG00621.hp1 HG01070.hp1 others(65): Show |
intron_variant | MODIFIER | c.-14+1387delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53785433 | ||||||
| chr2:53785529
|
C | G | 1 | a0001c0001t0001g0311 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-14+1292G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53785529 | ||||||
| chr2:53785576
|
C | A | 4 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(1): Show | 4 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+1245G>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53785576 | ||||||
| chr2:53785673
|
C | T | 1 | a0001c0003t0002g0310 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-14+1148G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53785673 | ||||||
| chr2:53785688
|
CA | C | 8 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0153others(5): Show | 8 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-14+1132delT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53785688 | ||||||
| chr2:53785693
|
A | T | 8 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0153others(5): Show | 8 | HG02559.hp2 HG02630.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-14+1128T>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53785693 | ||||||
| chr2:53785743
|
G | C | 3 | a0002c0004t0010g0137a0002c0004t0010g0138a0002c0004t0010g0139 | 3 | HG02818.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-14+1078C>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53785743 | ||||||
| chr2:53785761
|
G | T | 6 | a0001c0001t0001g0141a0001c0001t0001g0144a0001c0001t0001g0145others(3): Show | 6 | HG00738.hp1 HG01884.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14+1060C>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53785761 | ||||||
| chr2:53785773
|
C | T | 34 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0307others(31): Show | 34 | HG00438.hp1 HG00558.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.-14+1048G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53785773 | ||||||
| chr2:53785781
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-14+1040C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53785781 | ||||||
| chr2:53785973
|
T | TA | 54 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(51): Show | 54 | HG00280.hp2 HG00323.hp2 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.-14+847dupT | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53785973 | ||||||
| chr2:53785983
|
T | A | 1 | a0001c0002t0006g0271 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-14+838A>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53785983 | ||||||
| chr2:53786098
|
G | A | 6 | a0001c0001t0001g0274a0001c0001t0004g0272a0001c0001t0004g0273others(3): Show | 6 | HG01074.hp1 HG02818.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14+723C>T | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53786098 | ||||||
| chr2:53786118
|
C | T | 4 | a0002c0004t0010g0136a0002c0004t0010g0137a0002c0004t0010g0138others(1): Show | 4 | HG02818.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+703G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53786118 | ||||||
| chr2:53786390
|
C | T | 151 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(148): Show | 154 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.-14+431G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53786390 | ||||||
| chr2:53786407
|
T | C | 222 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(219): Show | 226 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.-14+414A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53786407 | ||||||
| chr2:53786446
|
C | T | 4 | a0001c0002t0002g0017a0001c0002t0002g0018a0001c0002t0002g0020others(1): Show | 4 | NA18971.hp2 NA18972.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14+375G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53786446 | ||||||
| chr2:53786516
|
T | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-14+305A>G | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53786516 | ||||||
| chr2:53786560
|
C | G | 5 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0004g0014others(2): Show | 5 | HG02258.hp1 HG02970.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14+261G>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53786560 | ||||||
| chr2:53786701
|
C | T | 1 | a0001c0001t0004g0011 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-14+120G>A | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53786701 | ||||||
| chr2:53786792
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-14+29T>C | ASB3 | ENSG00000115239.24 | transcript | ENST00000263634.8 | protein_coding | 1/9 | chr2 | 53786792 |