Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 27130 |
|---|---|
| ensemblid | ENSG00000119509.13 |
| hgncid | 17870 |
| symbol | INVS |
| name | inversin |
| refseq_nuc | NM_014425.5 |
| refseq_prot | NP_055240.2 |
| ensembl_nuc | ENST00000262457.7 |
| ensembl_prot | ENSP00000262457.2 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 100099243 |
| end | 100302175 |
| strand | + |
| ver | v1.2 |
| region | chr9:100099243-100302175 |
| region5000 | chr9:100094243-100307175 |
| regionname0 | INVS_chr9_100099243_100302175 |
| regionname5000 | INVS_chr9_100094243_100307175 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1065 | 169 | 63 | 40 | 41 | 9 | 14 | 22 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0002 | 0/0 | 1065 | 7 | 2 | 4 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0003 | 0/0 | 1065 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0004 | 0/0 | 1065 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0005 | 0/0 | 1065 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0006 | 0/0 | 1065 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0007 | 0/0 | 283 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 3198 | 94 | 39 | 21 | 21 | 4 | 8 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| c0002 | 1/0 | 3198 | 72 | 21 | 19 | 20 | 5 | 6 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| c0003 | 0/0 | 3198 | 7 | 2 | 4 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| c0004 | 0/0 | 3198 | 2 | 2 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| c0005 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| c0006 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| c0007 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| c0008 | 0/0 | 3198 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| c0009 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| c0010 | 0/0 | 3198 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| c0011 | 0/0 | 4195 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1692 | 48 | 32 | 11 | 2 | 1 | 2 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| t0002 | 0/0 | 1694 | 25 | 0 | 8 | 14 | 1 | 2 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| t0003 | 1/1 | 1700 | 19 | 0 | 12 | 1 | 2 | 2 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| t0004 | 0/0 | 1698 | 19 | 1 | 1 | 14 | 1 | 2 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| t0005 | 0/0 | 1706 | 7 | 7 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| t0006 | 0/0 | 1704 | 6 | 1 | 4 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| t0007 | 0/0 | 1696 | 6 | 6 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| t0008 | 0/0 | 1694 | 6 | 3 | 0 | 3 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| t0009 | 0/0 | 1696 | 5 | 0 | 2 | 2 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| t0010 | 0/0 | 1698 | 4 | 0 | 0 | 2 | 1 | 1 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| t0011 | 0/0 | 1684 | 4 | 4 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| t0012 | 0/0 | 1682 | 4 | 4 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| t0013 | 0/0 | 1710 | 4 | 0 | 1 | 0 | 1 | 2 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| t0014 | 0/0 | 1698 | 3 | 0 | 0 | 3 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| t0015 | 0/0 | 1716 | 3 | 0 | 2 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| t0016 | 0/0 | 1712 | 2 | 1 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| t0017 | 0/0 | 1708 | 2 | 0 | 2 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| t0018 | 0/0 | 1694 | 2 | 0 | 0 | 0 | 2 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| t0019 | 0/0 | 1704 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| t0020 | 0/0 | 1716 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| t0021 | 0/0 | 1710 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| t0022 | 0/0 | 1708 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| t0023 | 0/0 | 1708 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| t0024 | 0/0 | 1698 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| t0025 | 0/0 | 1696 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| t0026 | 0/0 | 1690 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| t0027 | 0/0 | 1722 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| t0028 | 0/0 | 1720 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| t0029 | 0/0 | 1714 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| t0030 | 0/0 | 1692 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| t0031 | 0/0 | 1698 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0047 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0090 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3198 | 94 | 39 | 21 | 21 | 4 | 8 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0002 | 1/0 | 3198 | 72 | 21 | 19 | 20 | 5 | 6 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0004 | 0/0 | 3198 | 2 | 2 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0009 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0002c0003 | 0/0 | 3198 | 7 | 2 | 4 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0003c0005 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0003c0008 | 0/0 | 3198 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0004c0010 | 0/0 | 3198 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0005c0006 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0006c0007 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0007c0011 | 0/0 | 4195 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4889 | 14 | 11 | 3 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0001t0003 | 0/1 | 4897 | 16 | 0 | 10 | 1 | 2 | 2 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0001t0004 | 0/0 | 4895 | 19 | 1 | 1 | 14 | 1 | 2 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0001t0005 | 0/0 | 4903 | 7 | 7 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0001t0007 | 0/0 | 4893 | 5 | 5 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0001t0008 | 0/0 | 4891 | 2 | 2 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0001t0010 | 0/0 | 4895 | 3 | 0 | 0 | 2 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0001t0011 | 0/0 | 4881 | 3 | 3 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0001t0012 | 0/0 | 4879 | 4 | 4 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0001t0013 | 0/0 | 4907 | 4 | 0 | 1 | 0 | 1 | 2 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0001t0014 | 0/0 | 4895 | 3 | 0 | 0 | 3 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0001t0015 | 0/0 | 4913 | 3 | 0 | 2 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0001t0016 | 0/0 | 4909 | 2 | 1 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0001t0017 | 0/0 | 4905 | 2 | 0 | 2 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0001t0019 | 0/0 | 4901 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0001t0024 | 0/0 | 4895 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0001t0026 | 0/0 | 4887 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0001t0027 | 0/0 | 4919 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0001t0028 | 0/0 | 4917 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0001t0029 | 0/0 | 4911 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0001t0031 | 0/0 | 4895 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0002t0001 | 0/0 | 4889 | 32 | 19 | 8 | 2 | 1 | 2 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0002t0002 | 0/0 | 4891 | 24 | 0 | 8 | 13 | 1 | 2 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0002t0003 | 1/0 | 4897 | 2 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0002t0008 | 0/0 | 4891 | 4 | 1 | 0 | 3 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0002t0009 | 0/0 | 4893 | 5 | 0 | 2 | 2 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0002t0010 | 0/0 | 4895 | 1 | 0 | 0 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0002t0018 | 0/0 | 4891 | 2 | 0 | 0 | 0 | 2 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0002t0025 | 0/0 | 4893 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0002t0030 | 0/0 | 4889 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0004t0001 | 0/0 | 4889 | 2 | 2 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0001c0009t0007 | 0/0 | 4893 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0002c0003t0006 | 0/0 | 4901 | 6 | 1 | 4 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0002c0003t0023 | 0/0 | 4905 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0003c0005t0022 | 0/0 | 4905 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0003c0008t0021 | 0/0 | 4907 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0004c0010t0003 | 0/0 | 4897 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0005c0006t0020 | 0/0 | 4913 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0006c0007t0011 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| a0007c0011t0002 | 0/0 | 5888 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | copy fasta | chr9 | 100094243 | 100307175 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0003g0090 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0005g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0007g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0007g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0007g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0007g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0007g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0008g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0008g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0010g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0010g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0010g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0011g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0011g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0011g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0012g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0012g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0012g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0012g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0013g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0013g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0013g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0013g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0014g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0014g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0014g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0015g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0015g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0015g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0016g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0016g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0017g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0017g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0019g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0024g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0026g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0027g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0028g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0029g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0031g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0003g0047 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0008g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0008g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0008g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0008g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0009g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0009g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0009g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0009g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0009g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0010g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0018g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0018g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0025g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0030g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0004t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0004t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0009t0007g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0002c0003t0006g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0002c0003t0006g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0002c0003t0006g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0002c0003t0006g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0002c0003t0006g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0002c0003t0006g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0002c0003t0023g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0003c0005t0022g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0003c0008t0021g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0004c0010t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0005c0006t0020g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0006c0007t0011g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0007c0011t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0048 | EUR | GBR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0041 | EUR | GBR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0128 | EUR | FIN | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0055 | EUR | FIN | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00323 | hp1 | a0001 | c0001 | t0013 | g0016 | EUR | FIN | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00323 | hp2 | a0001 | c0002 | t0010 | g0170 | EUR | FIN | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00423 | hp1 | a0001 | c0002 | t0008 | g0168 | EAS | CHS | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00423 | hp2 | a0001 | c0001 | t0031 | g0077 | EAS | CHS | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00544 | hp1 | a0001 | c0002 | t0008 | g0166 | EAS | CHS | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0075 | EAS | CHS | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0064 | EAS | CHS | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00609 | hp2 | a0001 | c0002 | t0009 | g0122 | EAS | CHS | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00621 | hp1 | a0001 | c0001 | t0014 | g0081 | EAS | CHS | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0137 | EAS | CHS | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0141 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00642 | hp2 | a0001 | c0001 | t0017 | g0017 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0154 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00733 | hp2 | a0003 | c0008 | t0021 | g0001 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00735 | hp1 | a0002 | c0003 | t0006 | g0084 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00735 | hp2 | a0001 | c0002 | t0009 | g0150 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00738 | hp1 | a0002 | c0003 | t0006 | g0096 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00738 | hp2 | a0001 | c0001 | t0017 | g0018 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0114 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00741 | hp2 | a0001 | c0001 | t0015 | g0020 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0116 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0178 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0140 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0179 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0073 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0152 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01081 | hp2 | a0001 | c0001 | t0024 | g0182 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01106 | hp1 | a0001 | c0001 | t0013 | g0079 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0042 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0171 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0176 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0155 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01168 | hp1 | a0001 | c0001 | t0015 | g0019 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0159 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01169 | hp1 | a0001 | c0002 | t0002 | g0160 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0177 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01175 | hp1 | a0002 | c0003 | t0006 | g0097 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0163 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01192 | hp1 | a0001 | c0002 | t0009 | g0169 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0094 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0092 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0173 | AMR | CLM | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0095 | AMR | CLM | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0151 | AMR | CLM | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01433 | hp2 | a0001 | c0002 | t0003 | g0115 | AMR | CLM | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0130 | AMR | CLM | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01496 | hp2 | a0004 | c0010 | t0003 | g0044 | AMR | CLM | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01516 | hp1 | a0001 | c0002 | t0018 | g0149 | EUR | IBS | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0043 | EUR | IBS | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0161 | AMR | PEL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0046 | AMR | PEL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0175 | AMR | PEL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01975 | hp2 | a0002 | c0003 | t0006 | g0085 | AMR | PEL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0034 | AFR | ACB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02055 | hp2 | a0002 | c0003 | t0023 | g0089 | AFR | ACB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0069 | EAS | KHV | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02056 | hp2 | a0007 | c0011 | t0002 | g0104 | EAS | KHV | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0119 | EAS | KHV | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0062 | EAS | KHV | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | KHV | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0156 | EAS | KHV | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0068 | EAS | KHV | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0139 | EAS | KHV | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | ACB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02145 | hp2 | a0001 | c0001 | t0027 | g0030 | AFR | ACB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0065 | EAS | CDX | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0138 | EAS | CDX | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02280 | hp1 | a0001 | c0001 | t0012 | g0134 | AFR | ACB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02280 | hp2 | a0001 | c0001 | t0016 | g0011 | AFR | ACB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02451 | hp1 | a0001 | c0001 | t0019 | g0066 | AFR | ACB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | ACB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02523 | hp1 | a0001 | c0001 | t0010 | g0126 | EAS | KHV | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0056 | EAS | KHV | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02602 | hp1 | a0001 | c0001 | t0015 | g0074 | SAS | PJL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0153 | SAS | PJL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0107 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02647 | hp1 | a0001 | c0001 | t0007 | g0063 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02647 | hp2 | a0001 | c0001 | t0008 | g0032 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02717 | hp1 | a0001 | c0001 | t0026 | g0029 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02809 | hp1 | a0001 | c0009 | t0007 | g0052 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0102 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0051 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | ESN | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0142 | AFR | ESN | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0023 | AFR | ESN | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02970 | hp2 | a0001 | c0001 | t0012 | g0136 | AFR | ESN | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0133 | AFR | ESN | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | ESN | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0058 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03098 | hp1 | a0003 | c0005 | t0022 | g0002 | AFR | MSL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03098 | hp2 | a0001 | c0001 | t0011 | g0061 | AFR | MSL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0106 | AFR | ESN | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0057 | AFR | ESN | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03139 | hp2 | a0001 | c0001 | t0012 | g0135 | AFR | ESN | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03209 | hp1 | a0001 | c0001 | t0029 | g0008 | AFR | MSL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03209 | hp2 | a0006 | c0007 | t0011 | g0181 | AFR | MSL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | MSL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03225 | hp2 | a0001 | c0004 | t0001 | g0109 | AFR | MSL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0050 | SAS | PJL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0129 | SAS | PJL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0098 | AFR | MSL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03453 | hp2 | a0001 | c0001 | t0011 | g0101 | AFR | MSL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03490 | hp1 | a0001 | c0002 | t0030 | g0113 | SAS | PJL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0093 | SAS | PJL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0164 | AFR | ESN | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0013 | AFR | ESN | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03540 | hp1 | a0001 | c0004 | t0001 | g0110 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03669 | hp1 | a0001 | c0001 | t0010 | g0127 | SAS | PJL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03669 | hp2 | a0001 | c0001 | t0013 | g0078 | SAS | PJL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03831 | hp1 | a0001 | c0001 | t0013 | g0082 | SAS | BEB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03831 | hp2 | a0001 | c0002 | t0009 | g0147 | SAS | BEB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0049 | SAS | BEB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0158 | SAS | BEB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA18522 | hp1 | a0001 | c0001 | t0011 | g0100 | AFR | YRI | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA18522 | hp2 | a0001 | c0002 | t0008 | g0105 | AFR | YRI | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0060 | AFR | YRI | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0028 | AFR | YRI | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0120 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0070 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA18970 | hp1 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA18983 | hp1 | a0001 | c0001 | t0010 | g0157 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA18983 | hp2 | a0001 | c0002 | t0008 | g0174 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA18999 | hp1 | a0001 | c0001 | t0004 | g0054 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0121 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0125 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0118 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19012 | hp2 | a0001 | c0001 | t0004 | g0071 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0112 | AFR | LWK | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19030 | hp2 | a0005 | c0006 | t0020 | g0099 | AFR | LWK | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | LWK | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19043 | hp2 | a0001 | c0002 | t0025 | g0165 | AFR | LWK | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19058 | hp1 | a0001 | c0002 | t0009 | g0132 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0067 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19082 | hp1 | a0001 | c0001 | t0014 | g0080 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19082 | hp2 | a0001 | c0002 | t0002 | g0124 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0123 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19084 | hp2 | a0001 | c0001 | t0014 | g0076 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0103 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0072 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0031 | AFR | YRI | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0053 | AFR | YRI | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0172 | AFR | ASW | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ASW | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA20805 | hp1 | a0002 | c0003 | t0006 | g0086 | EUR | TSI | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA20805 | hp2 | a0001 | c0002 | t0018 | g0146 | EUR | TSI | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0087 | SAS | GIH | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0111 | SAS | GIH | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01123 | hp1 | a0001 | c0001 | t0016 | g0027 | AMR | CLM | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0088 | AMR | CLM | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0022 | AFR | ACB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02109 | hp2 | a0001 | c0001 | t0028 | g0059 | AFR | ACB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0131 | AFR | ACB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0180 | AFR | ACB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03471 | hp1 | a0001 | c0001 | t0012 | g0162 | AFR | MSL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | LWK | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA21309 | hp2 | a0002 | c0003 | t0006 | g0091 | AFR | LWK | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0090 | REF | REF | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0003 | g0047 | REF | REF | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:100126394
|
C | G | 1 | a0007 | 1 | HG02056.hp2 | missense_variant | MODERATE | c.118C>G | p.Leu40Val | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/17 | 316/4897 | 118/3198 | 40/1065 | chr9 | 100126394 | ||
| chr9:100240112
|
C | CCAACAAA others(990): Show |
1 | a0007 | 1 | HG02056.hp2 | frameshift_variant&stop_gained | HIGH | c.668_669insCAACAAAG others(989): Show |
p.Pro224fs | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 6/17 | 867/4897 | 669/3198 | 223/1065 | chr9 | 100240112 | ||
| chr9:100240114
|
C | A | 1 | a0007 | 1 | HG02056.hp2 | missense_variant | MODERATE | c.670C>A | p.Pro224Thr | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 6/17 | 868/4897 | 670/3198 | 224/1065 | chr9 | 100240114 | ||
| chr9:100240169
|
C | T | 1 | a0004 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.725C>T | p.Ser242Leu | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 6/17 | 923/4897 | 725/3198 | 242/1065 | chr9 | 100240169 | ||
| chr9:100284480
|
G | A | 1 | a0005 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.1945G>A | p.Val649Met | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/17 | 2143/4897 | 1945/3198 | 649/1065 | chr9 | 100284480 | ||
| chr9:100292373
|
A | G | 1 | a0003 | 2 | HG00733.hp2 HG03098.hp1 |
missense_variant | MODERATE | c.2116A>G | p.Arg706Gly | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/17 | 2314/4897 | 2116/3198 | 706/1065 | chr9 | 100292373 | ||
| chr9:100292659
|
G | A | 1 | a0002 | 7 | HG00735.hp1 HG00738.hp1 HG01175.hp1 others(4): Show |
missense_variant | MODERATE | c.2402G>A | p.Gly801Glu | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/17 | 2600/4897 | 2402/3198 | 801/1065 | chr9 | 100292659 | ||
| chr9:100292743
|
G | A | 1 | a0006 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.2486G>A | p.Arg829His | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/17 | 2684/4897 | 2486/3198 | 829/1065 | chr9 | 100292743 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:100104623
|
C | T | 1 | a0001c0004 | 2 | HG03225.hp2 HG03540.hp1 |
synonymous_variant | LOW | c.102C>T | p.Ile34Ile | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/17 | 300/4897 | 102/3198 | 34/1065 | chr9 | 100104623 | ||
| chr9:100229827
|
G | C | 1 | a0003c0005 | 1 | HG03098.hp1 | splice_region_variant&synonymous_variant | LOW | c.615G>C | p.Leu205Leu | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/17 | 813/4897 | 615/3198 | 205/1065 | chr9 | 100229827 | ||
| chr9:100240113
|
T | A | 1 | a0007c0011 | 1 | HG02056.hp2 | synonymous_variant | LOW | c.669T>A | p.Thr223Thr | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 6/17 | 867/4897 | 669/3198 | 223/1065 | chr9 | 100240113 | ||
| chr9:100284536
|
C | T | 1 | a0001c0009 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.2001C>T | p.Gly667Gly | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/17 | 2199/4897 | 2001/3198 | 667/1065 | chr9 | 100284536 | ||
| chr9:100292669
|
T | C | 8 | a0001c0001a0001c0009a0002c0003others(5): Show | 107 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(104): Show |
synonymous_variant | LOW | c.2412T>C | p.Ser804Ser | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/17 | 2610/4897 | 2412/3198 | 804/1065 | chr9 | 100292669 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:100099249
|
A | T | 1 | a0001c0001t0031 | 1 | HG00423.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-192A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/17 | chr9 | 100099249 | ||||||
| chr9:100099286
|
C | T | 1 | a0001c0002t0018 | 2 | HG01516.hp1 NA20805.hp2 |
5_prime_UTR_variant | MODIFIER | c.-155C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/17 | 5236 | chr9 | 100099286 | |||||
| chr9:100099312
|
C | A | 1 | a0001c0001t0019 | 1 | HG02451.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-129C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/17 | chr9 | 100099312 | ||||||
| chr9:100099331
|
T | G | 6 | a0001c0001t0010a0001c0002t0002a0001c0002t0009others(3): Show | 36 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(33): Show |
5_prime_UTR_variant | MODIFIER | c.-110T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/17 | 5191 | chr9 | 100099331 | |||||
| chr9:100099390
|
G | T | 1 | a0001c0002t0030 | 1 | HG03490.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-51G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/17 | chr9 | 100099390 | ||||||
| chr9:100301002
|
G | A | 2 | a0001c0001t0014a0001c0001t0031 | 4 | HG00423.hp2 HG00621.hp1 NA19082.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*328G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 328 | chr9 | 100301002 | |||||
| chr9:100301138
|
A | ATC | 1 | a0001c0001t0005 | 7 | HG02451.hp2 HG02717.hp2 HG02922.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*465_*466dupTC | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 467 | INFO_REALIGN_3_PRIME | chr9 | 100301138 | ||||
| chr9:100301139
|
T | TCACA | 2 | a0001c0001t0019a0002c0003t0006 | 7 | HG00735.hp1 HG00738.hp1 HG01175.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*502_*505dupCACA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 506 | INFO_REALIGN_3_PRIME | chr9 | 100301139 | ||||
| chr9:100301139
|
T | TCACACAC others(1): Show |
2 | a0002c0003t0023a0003c0005t0022 | 2 | HG02055.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*498_*505dupCACACA others(2): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 506 | INFO_REALIGN_3_PRIME | chr9 | 100301139 | ||||
| chr9:100301139
|
T | TCACACAC others(3): Show |
1 | a0003c0008t0021 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*496_*505dupCACACA others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 506 | INFO_REALIGN_3_PRIME | chr9 | 100301139 | ||||
| chr9:100301139
|
T | TCACACAC others(9): Show |
1 | a0005c0006t0020 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*490_*505dupCACACA others(10): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 506 | INFO_REALIGN_3_PRIME | chr9 | 100301139 | ||||
| chr9:100301139
|
T | TCTCA | 1 | a0001c0001t0017 | 2 | HG00642.hp2 HG00738.hp2 |
3_prime_UTR_variant | MODIFIER | c.*466_*467insTCAC | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 467 | INFO_REALIGN_3_PRIME | chr9 | 100301139 | ||||
| chr9:100301139
|
T | TCTCACA | 1 | a0001c0001t0013 | 4 | HG00323.hp1 HG01106.hp1 HG03669.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*466_*467insTCACAC | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 467 | INFO_REALIGN_3_PRIME | chr9 | 100301139 | ||||
| chr9:100301139
|
T | TCTCACAC others(1): Show |
1 | a0001c0001t0016 | 2 | HG01123.hp1 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*466_*467insTCACAC others(2): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 467 | INFO_REALIGN_3_PRIME | chr9 | 100301139 | ||||
| chr9:100301139
|
T | TCTCACAC others(3): Show |
1 | a0001c0001t0029 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*466_*467insTCACAC others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 467 | INFO_REALIGN_3_PRIME | chr9 | 100301139 | ||||
| chr9:100301139
|
T | TCTCACAC others(5): Show |
1 | a0001c0001t0015 | 3 | HG00741.hp2 HG01168.hp1 HG02602.hp1 |
3_prime_UTR_variant | MODIFIER | c.*466_*467insTCACAC others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 467 | INFO_REALIGN_3_PRIME | chr9 | 100301139 | ||||
| chr9:100301139
|
T | TCTCACAC others(9): Show |
1 | a0001c0001t0028 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*466_*467insTCACAC others(10): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 467 | INFO_REALIGN_3_PRIME | chr9 | 100301139 | ||||
| chr9:100301139
|
T | TCTCACAC others(11): Show |
1 | a0001c0001t0027 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*466_*467insTCACAC others(12): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 467 | INFO_REALIGN_3_PRIME | chr9 | 100301139 | ||||
| chr9:100301139
|
TCA | T | 6 | a0001c0001t0004a0001c0001t0010a0001c0001t0014others(3): Show | 28 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*504_*505delCA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 504 | INFO_REALIGN_3_PRIME | chr9 | 100301139 | ||||
| chr9:100301139
|
TCACA | T | 2 | a0001c0001t0007a0001c0009t0007 | 6 | HG02647.hp1 HG02809.hp1 HG02897.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*502_*505delCACA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 502 | INFO_REALIGN_3_PRIME | chr9 | 100301139 | ||||
| chr9:100301139
|
TCACACAC others(9): Show |
T | 2 | a0001c0001t0011a0006c0007t0011 | 4 | HG03098.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*490_*505delCACACA others(10): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 490 | INFO_REALIGN_3_PRIME | chr9 | 100301139 | ||||
| chr9:100301139
|
TCACACAC others(11): Show |
T | 1 | a0001c0001t0012 | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*488_*505delCACACA others(12): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 488 | INFO_REALIGN_3_PRIME | chr9 | 100301139 | ||||
| chr9:100301170
|
CACACACA others(3): Show |
C | 1 | a0001c0001t0026 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*498_*507delCACACA others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 498 | INFO_REALIGN_3_PRIME | chr9 | 100301170 | ||||
| chr9:100301172
|
CACACACA others(1): Show |
C | 4 | a0001c0001t0001a0001c0002t0001a0001c0002t0030others(1): Show | 49 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*500_*507delCACACA others(2): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 500 | INFO_REALIGN_3_PRIME | chr9 | 100301172 | ||||
| chr9:100301174
|
CACACAT | C | 5 | a0001c0001t0008a0001c0002t0002a0001c0002t0008others(2): Show | 33 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*502_*507delCACATA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 502 | INFO_REALIGN_3_PRIME | chr9 | 100301174 | ||||
| chr9:100301176
|
CACAT | C | 2 | a0001c0002t0009a0001c0002t0025 | 6 | HG00609.hp2 HG00735.hp2 HG01192.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*504_*507delCATA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 504 | INFO_REALIGN_3_PRIME | chr9 | 100301176 | ||||
| chr9:100301180
|
T | C | 8 | a0001c0001t0005a0001c0001t0013a0001c0001t0015others(5): Show | 21 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*506T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 506 | chr9 | 100301180 | |||||
| chr9:100301363
|
G | A | 12 | a0001c0001t0001a0001c0001t0008a0001c0001t0026others(9): Show | 89 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*689G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 689 | chr9 | 100301363 | |||||
| chr9:100301438
|
T | C | 2 | a0003c0005t0022a0003c0008t0021 | 2 | HG00733.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*764T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 764 | chr9 | 100301438 | |||||
| chr9:100301544
|
G | T | 12 | a0001c0001t0001a0001c0001t0008a0001c0001t0026others(9): Show | 89 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*870G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 870 | chr9 | 100301544 | |||||
| chr9:100301709
|
T | G | 1 | a0001c0001t0024 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1035T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 1035 | chr9 | 100301709 | |||||
| chr9:100301752
|
G | GAGAT | 8 | a0001c0001t0005a0001c0001t0013a0001c0001t0015others(5): Show | 21 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1082_*1085dupTAGA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 1086 | INFO_REALIGN_3_PRIME | chr9 | 100301752 | ||||
| chr9:100301778
|
T | C | 3 | a0001c0001t0011a0001c0001t0012a0006c0007t0011 | 8 | HG02280.hp1 HG02970.hp2 HG03098.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1104T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 1104 | chr9 | 100301778 | |||||
| chr9:100301871
|
A | G | 23 | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(20): Show | 113 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*1197A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 1197 | chr9 | 100301871 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:100099732
|
T | C | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-25+316T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100099732 | ||||||
| chr9:100099948
|
C | T | 2 | a0001c0001t0024g0182a0006c0007t0011g0181 | 2 | HG01081.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-25+532C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100099948 | ||||||
| chr9:100100001
|
C | T | 1 | a0001c0002t0001g0180 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-25+585C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100001 | ||||||
| chr9:100100073
|
T | C | 1 | a0001c0002t0001g0003 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-25+657T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100073 | ||||||
| chr9:100100239
|
A | G | 4 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0003g0178others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25+823A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100239 | ||||||
| chr9:100100257
|
T | C | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.-25+841T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100257 | ||||||
| chr9:100100361
|
T | G | 1 | a0001c0002t0002g0041 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-25+945T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100361 | ||||||
| chr9:100100569
|
T | C | 2 | a0001c0001t0024g0182a0006c0007t0011g0181 | 2 | HG01081.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-25+1153T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100569 | ||||||
| chr9:100100575
|
T | TATATAAT others(17): Show |
1 | a0001c0001t0003g0042 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-25+1183_-25+1206d others(26): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100575 | |||||
| chr9:100100599
|
C | T | 120 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0026others(117): Show | 120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.-25+1183C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100599 | ||||||
| chr9:100100617
|
T | A | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-25+1201T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100617 | ||||||
| chr9:100100628
|
AAT | A | 9 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+1221_-25+1222d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100628 | |||||
| chr9:100100634
|
T | C | 9 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(6): Show | 9 | HG02280.hp2 HG02451.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-25+1218T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100634 | ||||||
| chr9:100100637
|
ATT | A | 2 | a0001c0001t0011g0100a0001c0001t0011g0101 | 2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-25+1222_-25+1223d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100637 | ||||||
| chr9:100100638
|
T | A | 2 | a0001c0001t0024g0182a0006c0007t0011g0181 | 2 | HG01081.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-25+1222T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100638 | ||||||
| chr9:100100638
|
TTA | T | 2 | a0001c0002t0001g0098a0001c0002t0008g0174 | 2 | HG03453.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-25+1228_-25+1229d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100638 | |||||
| chr9:100100638
|
TTATATAT others(47): Show |
T | 1 | a0001c0002t0002g0175 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-25+1228_-25+1281d others(56): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100638 | |||||
| chr9:100100639
|
T | A | 11 | a0001c0001t0003g0043a0001c0001t0005g0005a0001c0001t0005g0006others(8): Show | 11 | HG01516.hp2 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-25+1223T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100639 | ||||||
| chr9:100100640
|
A | ATATGTAT others(133): Show |
1 | a0006c0007t0011g0181 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-25+1227_-25+1228i others(142): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100640 | |||||
| chr9:100100640
|
A | ATATGTAT others(157): Show |
1 | a0001c0001t0024g0182 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-25+1227_-25+1228i others(166): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100640 | |||||
| chr9:100100641
|
T | C | 1 | a0001c0002t0001g0014 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-25+1225T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100641 | ||||||
| chr9:100100649
|
T | C | 39 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(36): Show | 39 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.-25+1233T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100649 | ||||||
| chr9:100100649
|
T | TATATATA others(68): Show |
9 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(6): Show | 9 | HG02280.hp2 HG02451.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-25+1238_-25+1239i others(77): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100649 | |||||
| chr9:100100654
|
AAT | A | 20 | a0001c0001t0003g0042a0001c0001t0003g0087a0001c0001t0003g0088others(17): Show | 20 | HG00735.hp1 HG00738.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.-25+1247_-25+1248d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100654 | |||||
| chr9:100100663
|
ATT | A | 2 | a0001c0001t0011g0100a0001c0001t0011g0101 | 2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-25+1248_-25+1249d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100663 | ||||||
| chr9:100100664
|
TTA | T | 40 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(37): Show | 40 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.-25+1254_-25+1255d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100664 | |||||
| chr9:100100665
|
T | A | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-25+1249T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100665 | ||||||
| chr9:100100671
|
TGTAC | T | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-25+1256_-25+1259d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100671 | ||||||
| chr9:100100672
|
G | A | 1 | a0001c0002t0030g0113 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-25+1256G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100672 | ||||||
| chr9:100100673
|
T | C | 1 | a0001c0002t0030g0113 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-25+1257T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100673 | ||||||
| chr9:100100675
|
C | CATATAAT others(113): Show |
3 | a0002c0003t0006g0084a0002c0003t0006g0085a0002c0003t0006g0086 | 3 | HG00735.hp1 HG01975.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-25+1271_-25+1272i others(122): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100675 | |||||
| chr9:100100675
|
C | CATATAAT others(117): Show |
2 | a0001c0001t0003g0042a0001c0001t0003g0087 | 2 | HG01106.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-25+1279_-25+1280i others(126): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100675 | |||||
| chr9:100100675
|
C | T | 86 | a0001c0001t0001g0108a0001c0001t0001g0144a0001c0001t0001g0145others(83): Show | 86 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.-25+1259C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100675 | ||||||
| chr9:100100688
|
TATTA | T | 9 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(6): Show | 9 | HG02280.hp2 HG02451.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-25+1273_-25+1276d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100688 | ||||||
| chr9:100100690
|
TTA | T | 69 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(66): Show | 69 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.-25+1280_-25+1281d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100690 | |||||
| chr9:100100692
|
A | ATATGTAC others(141): Show |
1 | a0001c0001t0003g0048 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-25+1279_-25+1280i others(150): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100692 | |||||
| chr9:100100692
|
A | ATATGTAC others(141): Show |
12 | a0001c0001t0003g0088a0001c0001t0003g0090a0001c0001t0003g0092others(9): Show | 12 | HG01069.hp2 HG01071.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.-25+1279_-25+1280i others(150): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100692 | |||||
| chr9:100100692
|
A | ATATGTAC others(37): Show |
1 | a0001c0001t0001g0033 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-25+1279_-25+1280i others(46): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100692 | |||||
| chr9:100100692
|
A | ATATGTAT others(109): Show |
1 | a0001c0001t0011g0100 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-25+1279_-25+1280i others(118): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100692 | |||||
| chr9:100100692
|
A | ATATGTAT others(109): Show |
1 | a0001c0001t0011g0101 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-25+1279_-25+1280i others(118): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100692 | |||||
| chr9:100100696
|
A | G | 4 | a0001c0001t0003g0083a0001c0002t0001g0172a0003c0005t0022g0002others(1): Show | 4 | HG00733.hp2 HG02083.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25+1280A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100696 | ||||||
| chr9:100100698
|
G | A | 80 | a0001c0001t0001g0108a0001c0001t0001g0144a0001c0001t0001g0145others(77): Show | 80 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.-25+1282G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100698 | ||||||
| chr9:100100699
|
T | C | 78 | a0001c0001t0001g0108a0001c0001t0001g0144a0001c0001t0001g0145others(75): Show | 78 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.-25+1283T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100699 | ||||||
| chr9:100100701
|
C | T | 91 | a0001c0001t0001g0108a0001c0001t0001g0144a0001c0001t0001g0145others(88): Show | 91 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.-25+1285C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100701 | ||||||
| chr9:100100707
|
A | ATATATGT others(29): Show |
1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-25+1296_-25+1297i others(38): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100707 | |||||
| chr9:100100716
|
T | A | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-25+1300T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100716 | ||||||
| chr9:100100722
|
G | A | 32 | a0001c0001t0003g0042a0001c0001t0003g0048a0001c0001t0003g0087others(29): Show | 32 | HG00140.hp1 HG00280.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.-25+1306G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100722 | ||||||
| chr9:100100723
|
TAC | T | 28 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(25): Show | 28 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.-25+1309_-25+1310d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100723 | |||||
| chr9:100100725
|
C | CAT | 123 | a0001c0001t0001g0108a0001c0001t0001g0144a0001c0001t0001g0145others(120): Show | 123 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.-25+1313_-25+1314d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100725 | |||||
| chr9:100100725
|
C | CATATATA others(21): Show |
3 | a0002c0003t0006g0084a0002c0003t0006g0085a0002c0003t0006g0086 | 3 | HG00735.hp1 HG01975.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-25+1314_-25+1315i others(30): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100725 | |||||
| chr9:100100725
|
C | CATATATA others(147): Show |
2 | a0002c0003t0006g0096a0002c0003t0006g0097 | 2 | HG00738.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.-25+1314_-25+1315i others(156): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100725 | |||||
| chr9:100100725
|
C | T | 17 | a0001c0001t0001g0033a0001c0001t0003g0178a0001c0001t0003g0179others(14): Show | 17 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.-25+1309C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100725 | ||||||
| chr9:100100730
|
AAT | A | 10 | a0001c0001t0001g0033a0001c0001t0005g0005a0001c0001t0005g0006others(7): Show | 10 | HG01109.hp1 HG02280.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-25+1323_-25+1324d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100730 | |||||
| chr9:100100731
|
A | T | 28 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(25): Show | 28 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.-25+1315A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100731 | ||||||
| chr9:100100740
|
T | A | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-25+1324T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100740 | ||||||
| chr9:100100749
|
C | T | 92 | a0001c0001t0001g0033a0001c0001t0001g0108a0001c0001t0001g0144others(89): Show | 92 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.-25+1333C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100749 | ||||||
| chr9:100100754
|
A | AATATATA others(118): Show |
1 | a0001c0001t0016g0027 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-25+1347_-25+1348i others(127): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100754 | |||||
| chr9:100100754
|
A | ATAATATA others(52): Show |
1 | a0001c0001t0003g0043 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-25+1338_-25+1339i others(61): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100754 | ||||||
| chr9:100100763
|
A | ATTATATG others(78): Show |
1 | a0001c0001t0001g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-25+1347_-25+1348i others(87): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100763 | ||||||
| chr9:100100763
|
A | ATTATATG others(87): Show |
2 | a0001c0001t0001g0035a0001c0001t0008g0034 | 2 | HG02055.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-25+1347_-25+1348i others(96): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100763 | ||||||
| chr9:100100763
|
A | ATTATATG others(85): Show |
9 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(6): Show | 9 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.-25+1347_-25+1348i others(94): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100763 | ||||||
| chr9:100100763
|
A | T | 14 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(11): Show | 14 | HG01081.hp2 HG01975.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-25+1347A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100763 | ||||||
| chr9:100100764
|
A | T | 93 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(90): Show | 93 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.-25+1348A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100764 | ||||||
| chr9:100100765
|
T | C | 1 | a0001c0002t0030g0113 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-25+1349T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100765 | ||||||
| chr9:100100773
|
T | C | 16 | a0001c0001t0001g0015a0001c0001t0004g0064a0001c0001t0004g0065others(13): Show | 16 | HG00609.hp1 HG00609.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-25+1357T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100773 | ||||||
| chr9:100100778
|
A | AAT | 4 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0002t0030g0113others(1): Show | 4 | HG02523.hp1 HG03490.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25+1369_-25+1370d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100778 | |||||
| chr9:100100778
|
AATATATA others(2): Show |
A | 2 | a0001c0001t0001g0015a0001c0002t0009g0169 | 2 | HG01192.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-25+1371_-25+1379d others(11): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100778 | |||||
| chr9:100100779
|
A | ATATATAT others(8): Show |
69 | a0001c0001t0001g0108a0001c0001t0001g0144a0001c0001t0001g0145others(66): Show | 69 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.-25+1370_-25+1371i others(17): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100779 | |||||
| chr9:100100779
|
A | ATATATAT others(32): Show |
1 | a0001c0002t0010g0170 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-25+1370_-25+1371i others(41): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100779 | |||||
| chr9:100100783
|
ATATTATA others(12): Show |
A | 1 | a0001c0002t0002g0175 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-25+1368_-25+1386d others(21): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100783 | ||||||
| chr9:100100784
|
T | TA | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-25+1369dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100784 | |||||
| chr9:100100786
|
T | TATTATAT others(5): Show |
1 | a0001c0002t0001g0171 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-25+1370_-25+1371i others(14): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100786 | ||||||
| chr9:100100786
|
T | TTATATGT others(111): Show |
1 | a0001c0001t0008g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-25+1375_-25+1376i others(120): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100786 | |||||
| chr9:100100786
|
TTATATAT others(4): Show |
T | 8 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0026others(5): Show | 8 | HG02109.hp1 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-25+1376_-25+1386d others(13): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100786 | |||||
| chr9:100100787
|
T | A | 70 | a0001c0001t0001g0108a0001c0001t0001g0144a0001c0001t0001g0145others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.-25+1371T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100787 | ||||||
| chr9:100100787
|
T | TATATGTA others(255): Show |
3 | a0001c0001t0007g0028a0001c0001t0026g0029a0001c0001t0027g0030 | 3 | HG02145.hp2 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-25+1375_-25+1376i others(264): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100787 | |||||
| chr9:100100787
|
T | TATATGTA others(329): Show |
2 | a0001c0002t0001g0003a0001c0002t0001g0031 | 2 | HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-25+1375_-25+1376i others(338): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100787 | |||||
| chr9:100100788
|
A | G | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-25+1372A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100788 | ||||||
| chr9:100100791
|
T | TGTAC | 5 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0002t0030g0113others(2): Show | 5 | HG00733.hp2 HG02523.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25+1375_-25+1376i others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100791 | ||||||
| chr9:100100796
|
A | G | 4 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(1): Show | 4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25+1380A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100796 | ||||||
| chr9:100100796
|
A | T | 6 | a0001c0001t0007g0028a0001c0001t0008g0032a0001c0001t0026g0029others(3): Show | 6 | HG02145.hp2 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+1380A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100796 | ||||||
| chr9:100100797
|
A | T | 73 | a0001c0001t0001g0015a0001c0001t0001g0108a0001c0001t0001g0144others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.-25+1381A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100797 | ||||||
| chr9:100100802
|
T | TA | 5 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0002t0030g0113others(2): Show | 5 | HG00733.hp2 HG02523.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25+1386_-25+1387i others(3): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100802 | ||||||
| chr9:100100803
|
G | A | 21 | a0001c0001t0003g0042a0001c0001t0003g0048a0001c0001t0003g0087others(18): Show | 21 | HG00140.hp1 HG00735.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.-25+1387G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100803 | ||||||
| chr9:100100803
|
G | T | 5 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0002t0030g0113others(2): Show | 5 | HG00733.hp2 HG02523.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25+1387G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100803 | ||||||
| chr9:100100804
|
T | C | 15 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(12): Show | 15 | HG01109.hp1 HG01123.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.-25+1388T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100804 | ||||||
| chr9:100100806
|
T | C | 71 | a0001c0001t0001g0108a0001c0001t0001g0144a0001c0001t0001g0145others(68): Show | 71 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.-25+1390T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100806 | ||||||
| chr9:100100810
|
T | A | 19 | a0001c0001t0003g0042a0001c0001t0003g0087a0001c0001t0003g0088others(16): Show | 19 | HG00735.hp1 HG00738.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.-25+1394T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100810 | ||||||
| chr9:100100810
|
TA | T | 5 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0002t0030g0113others(2): Show | 5 | HG00733.hp2 HG02523.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25+1396delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100810 | |||||
| chr9:100100811
|
A | AAT | 29 | a0001c0001t0003g0048a0001c0001t0004g0054a0001c0001t0004g0055others(26): Show | 29 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.-25+1403_-25+1404d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100811 | |||||
| chr9:100100811
|
A | AATATATA others(21): Show |
2 | a0001c0001t0004g0049a0001c0001t0004g0050 | 2 | HG03239.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-25+1404_-25+1405i others(30): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100811 | |||||
| chr9:100100811
|
A | T | 19 | a0001c0001t0003g0042a0001c0001t0003g0087a0001c0001t0003g0088others(16): Show | 19 | HG00735.hp1 HG00738.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.-25+1395A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100811 | ||||||
| chr9:100100812
|
A | ATATATAT others(4): Show |
1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-25+1404_-25+1405i others(13): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100812 | |||||
| chr9:100100812
|
A | G | 5 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0002t0030g0113others(2): Show | 5 | HG00733.hp2 HG02523.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25+1396A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100812 | ||||||
| chr9:100100820
|
A | ATG | 4 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(1): Show | 4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25+1404_-25+1405i others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100820 | ||||||
| chr9:100100820
|
A | ATT | 6 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0037others(3): Show | 6 | HG01109.hp1 HG01123.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+1404_-25+1405i others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100820 | ||||||
| chr9:100100820
|
A | T | 80 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0039others(77): Show | 80 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.-25+1404A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100820 | ||||||
| chr9:100100821
|
A | T | 9 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0026others(6): Show | 9 | HG01192.hp1 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+1405A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100821 | ||||||
| chr9:100100825
|
AT | A | 9 | a0001c0002t0001g0114a0001c0002t0001g0116a0001c0002t0001g0128others(6): Show | 9 | HG00280.hp1 HG00741.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+1410delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100825 | ||||||
| chr9:100100825
|
ATGT | A | 5 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0002t0030g0113others(2): Show | 5 | HG00733.hp2 HG02523.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25+1410_-25+1412d others(5): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100825 | ||||||
| chr9:100100828
|
T | C | 14 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(11): Show | 14 | HG01109.hp1 HG01123.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-25+1412T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100828 | ||||||
| chr9:100100830
|
T | C | 1 | a0001c0002t0009g0169 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-25+1414T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100830 | ||||||
| chr9:100100835
|
AAT | A | 8 | a0001c0001t0007g0028a0001c0001t0024g0182a0001c0001t0026g0029others(5): Show | 8 | HG01081.hp2 HG01192.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-25+1429_-25+1430d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100835 | |||||
| chr9:100100836
|
A | T | 5 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0002t0030g0113others(2): Show | 5 | HG00733.hp2 HG02523.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25+1420A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100836 | ||||||
| chr9:100100837
|
T | A | 5 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0002t0030g0113others(2): Show | 5 | HG00733.hp2 HG02523.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25+1421T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100837 | ||||||
| chr9:100100837
|
T | TATAAATA others(6): Show |
2 | a0001c0002t0002g0118a0001c0002t0002g0119 | 2 | HG02080.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-25+1424_-25+1425i others(15): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100837 | |||||
| chr9:100100837
|
T | TATAATAT others(5): Show |
69 | a0001c0001t0001g0108a0001c0001t0001g0144a0001c0001t0001g0145others(66): Show | 69 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.-25+1424_-25+1425i others(14): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100837 | |||||
| chr9:100100837
|
T | TATATATT others(63): Show |
2 | a0001c0001t0011g0100a0001c0001t0011g0101 | 2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-25+1427_-25+1428i others(72): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100837 | |||||
| chr9:100100843
|
T | G | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-25+1427T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100843 | ||||||
| chr9:100100843
|
TATAA | T | 9 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(6): Show | 9 | HG02109.hp1 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+1428_-25+1431d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100843 | ||||||
| chr9:100100844
|
A | G | 1 | a0001c0002t0002g0041 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-25+1428A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100844 | ||||||
| chr9:100100846
|
A | T | 23 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(20): Show | 23 | HG01109.hp1 HG01123.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-25+1430A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100846 | ||||||
| chr9:100100853
|
G | A | 1 | a0001c0002t0009g0132 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-25+1437G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100853 | ||||||
| chr9:100100854
|
T | C | 23 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(20): Show | 23 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.-25+1438T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100854 | ||||||
| chr9:100100861
|
AAT | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(14): Show | 17 | HG01346.hp2 HG02109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-25+1454_-25+1455d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100861 | |||||
| chr9:100100862
|
A | ATATATAA others(6): Show |
75 | a0001c0001t0001g0108a0001c0001t0001g0144a0001c0001t0001g0145others(72): Show | 75 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.-25+1452_-25+1453i others(15): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100862 | |||||
| chr9:100100863
|
T | TATAAATT others(346): Show |
1 | a0001c0001t0005g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-25+1450_-25+1451i others(355): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100863 | |||||
| chr9:100100863
|
T | TATAAATT others(348): Show |
1 | a0001c0001t0005g0006 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-25+1450_-25+1451i others(357): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100863 | |||||
| chr9:100100863
|
T | TATAAATT others(324): Show |
3 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0016g0011 | 3 | HG02280.hp2 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-25+1450_-25+1451i others(333): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100863 | |||||
| chr9:100100863
|
T | TATAAATT others(348): Show |
4 | a0001c0001t0005g0007a0001c0001t0005g0009a0001c0001t0005g0010others(1): Show | 4 | HG02717.hp2 HG02922.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25+1450_-25+1451i others(357): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100863 | |||||
| chr9:100100863
|
T | TATAATAT others(5): Show |
1 | a0001c0002t0009g0169 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-25+1450_-25+1451i others(14): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100863 | |||||
| chr9:100100863
|
T | TATATAGA others(167): Show |
1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-25+1452_-25+1453i others(176): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100863 | |||||
| chr9:100100863
|
T | TATATATA others(115): Show |
2 | a0001c0001t0001g0033a0001c0001t0001g0037 | 2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-25+1479_-25+1480i others(124): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100863 | |||||
| chr9:100100863
|
T | TATATATT others(63): Show |
1 | a0006c0007t0011g0181 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-25+1453_-25+1454i others(72): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100863 | |||||
| chr9:100100863
|
T | TATATATT others(87): Show |
1 | a0001c0001t0024g0182 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-25+1453_-25+1454i others(96): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100863 | |||||
| chr9:100100872
|
T | A | 1 | a0001c0002t0009g0169 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-25+1456T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100872 | ||||||
| chr9:100100880
|
T | C | 7 | a0001c0001t0008g0032a0001c0001t0013g0016a0001c0001t0015g0019others(4): Show | 7 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.-25+1464T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100880 | ||||||
| chr9:100100887
|
A | AAT | 14 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0038others(11): Show | 14 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-25+1478_-25+1479d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100887 | |||||
| chr9:100100897
|
ATATATG | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(6): Show | 9 | HG02109.hp1 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+1487_-25+1492d others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100897 | |||||
| chr9:100100904
|
T | C | 7 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0038others(4): Show | 7 | HG01123.hp1 HG02055.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-25+1488T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100904 | ||||||
| chr9:100100904
|
T | TATATATA | 9 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(6): Show | 9 | HG02280.hp2 HG02451.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-25+1489_-25+1495d others(9): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100904 | |||||
| chr9:100100905
|
A | ATATATAT | 2 | a0001c0001t0001g0033a0001c0001t0001g0037 | 2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-25+1495_-25+1501d others(9): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100905 | |||||
| chr9:100100907
|
A | G | 4 | a0001c0002t0001g0167a0001c0002t0008g0166a0001c0002t0008g0168others(1): Show | 4 | HG00423.hp1 HG00544.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25+1491A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100907 | ||||||
| chr9:100100912
|
T | A | 34 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(31): Show | 34 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.-25+1496T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100912 | ||||||
| chr9:100100917
|
T | TA | 2 | a0001c0001t0008g0032a0001c0001t0016g0027 | 2 | HG01123.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-25+1501_-25+1502i others(3): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100917 | ||||||
| chr9:100100918
|
G | A | 16 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0038others(13): Show | 16 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.-25+1502G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100918 | ||||||
| chr9:100100918
|
G | T | 2 | a0001c0001t0008g0032a0001c0001t0016g0027 | 2 | HG01123.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-25+1502G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100918 | ||||||
| chr9:100100918
|
GTA | G | 9 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(6): Show | 9 | HG02109.hp1 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+1511_-25+1512d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100918 | |||||
| chr9:100100919
|
TA | T | 5 | a0001c0001t0007g0028a0001c0001t0026g0029a0001c0001t0027g0030others(2): Show | 5 | HG02145.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25+1504delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100919 | ||||||
| chr9:100100920
|
A | ATTATATA others(136): Show |
1 | a0001c0001t0001g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-25+1505_-25+1506i others(145): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100920 | |||||
| chr9:100100921
|
TA | T | 10 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0039others(7): Show | 10 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.-25+1506delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100921 | ||||||
| chr9:100100922
|
A | ATATAATA others(5): Show |
2 | a0001c0001t0001g0033a0001c0001t0001g0037 | 2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-25+1510_-25+1511i others(14): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100922 | |||||
| chr9:100100926
|
A | G | 2 | a0001c0001t0008g0032a0001c0001t0016g0027 | 2 | HG01123.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-25+1510A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100926 | ||||||
| chr9:100100927
|
T | A | 10 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(7): Show | 10 | HG02280.hp2 HG02451.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-25+1511T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100927 | ||||||
| chr9:100100927
|
T | TG | 5 | a0001c0001t0007g0028a0001c0001t0026g0029a0001c0001t0027g0030others(2): Show | 5 | HG02145.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25+1511_-25+1512i others(3): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100927 | ||||||
| chr9:100100928
|
A | ATATATAA others(38): Show |
2 | a0001c0001t0008g0032a0001c0001t0016g0027 | 2 | HG01123.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-25+1512_-25+1513i others(47): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100928 | ||||||
| chr9:100100928
|
A | ATGCATAT others(138): Show |
5 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0039others(2): Show | 5 | HG02055.hp1 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-25+1512_-25+1513i others(147): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100928 | ||||||
| chr9:100100928
|
A | ATGCATAT others(90): Show |
5 | a0001c0001t0013g0016a0001c0001t0015g0019a0001c0001t0015g0020others(2): Show | 5 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(2): Show |
intron_variant | MODIFIER | c.-25+1512_-25+1513i others(99): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100928 | ||||||
| chr9:100100928
|
A | ATGT | 2 | a0001c0001t0001g0033a0001c0001t0001g0037 | 2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-25+1512_-25+1513i others(5): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100928 | ||||||
| chr9:100100928
|
A | T | 15 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(12): Show | 15 | HG02145.hp2 HG02280.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.-25+1512A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100928 | ||||||
| chr9:100100929
|
A | ATATATTA others(6): Show |
9 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(6): Show | 9 | HG02280.hp2 HG02451.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-25+1518_-25+1519i others(15): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100929 | |||||
| chr9:100100929
|
A | ATATATTA others(80): Show |
1 | a0001c0001t0005g0010 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-25+1518_-25+1519i others(89): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100929 | |||||
| chr9:100100929
|
A | G | 1 | a0001c0001t0001g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-25+1513A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100929 | ||||||
| chr9:100100938
|
A | T | 15 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(12): Show | 15 | HG01081.hp2 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-25+1522A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100938 | ||||||
| chr9:100100946
|
A | G | 9 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(6): Show | 9 | HG02109.hp1 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+1530A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100946 | ||||||
| chr9:100100946
|
AC | A | 6 | a0001c0001t0004g0064a0001c0001t0004g0065a0001c0001t0004g0067others(3): Show | 6 | HG00609.hp1 HG02056.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+1531delC | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100946 | ||||||
| chr9:100100947
|
CA | C | 2 | a0001c0001t0004g0062a0001c0002t0025g0165 | 2 | HG02080.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-25+1532delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100947 | ||||||
| chr9:100100955
|
T | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(6): Show | 9 | HG02109.hp1 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+1539T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100955 | ||||||
| chr9:100100957
|
A | ATATATAT others(28): Show |
1 | a0001c0001t0004g0049 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-25+1558_-25+1592d others(37): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100957 | |||||
| chr9:100100964
|
TAA | T | 69 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0004g0121others(66): Show | 69 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.-25+1549_-25+1550d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100964 | ||||||
| chr9:100100965
|
A | T | 16 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(13): Show | 16 | HG02109.hp1 HG02145.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.-25+1549A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100965 | ||||||
| chr9:100100967
|
T | TATATGC | 9 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(6): Show | 9 | HG02109.hp1 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+1555_-25+1556i others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100967 | |||||
| chr9:100100968
|
ATATAT | A | 3 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0008g0105 | 3 | HG02622.hp1 HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-25+1558_-25+1562d others(7): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100968 | |||||
| chr9:100100970
|
ATAT | A | 4 | a0001c0001t0001g0108a0001c0002t0001g0102a0001c0002t0001g0133others(1): Show | 4 | HG02886.hp1 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25+1558_-25+1560d others(5): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100970 | |||||
| chr9:100100972
|
A | G | 2 | a0001c0001t0011g0100a0001c0001t0011g0101 | 2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-25+1556A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100972 | ||||||
| chr9:100100974
|
T | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(6): Show | 9 | HG02109.hp1 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+1558T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100974 | ||||||
| chr9:100100978
|
T | C | 11 | a0001c0001t0004g0121a0001c0002t0002g0103a0001c0002t0002g0117others(8): Show | 11 | HG00609.hp2 HG02056.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.-25+1562T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100978 | ||||||
| chr9:100100984
|
A | T | 9 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(6): Show | 9 | HG02109.hp1 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+1568A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100984 | ||||||
| chr9:100101000
|
A | ATAATGCA others(3): Show |
1 | a0001c0001t0001g0026 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-25+1584_-25+1585i others(12): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100101000 | ||||||
| chr9:100101000
|
A | ATAATGCA others(5): Show |
8 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(5): Show | 8 | HG02109.hp1 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-25+1584_-25+1585i others(14): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100101000 | ||||||
| chr9:100101010
|
T | TTATATAT others(92): Show |
1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-25+1599_-25+1600i others(101): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100101010 | |||||
| chr9:100101073
|
TACAC | T | 3 | a0001c0001t0007g0028a0001c0001t0026g0029a0001c0001t0027g0030 | 3 | HG02145.hp2 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-25+1667_-25+1670d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100101073 | |||||
| chr9:100101098
|
C | T | 4 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(1): Show | 4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25+1682C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100101098 | ||||||
| chr9:100101133
|
A | G | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-25+1717A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100101133 | ||||||
| chr9:100101475
|
C | T | 9 | a0001c0001t0004g0058a0001c0001t0007g0051a0001c0001t0007g0053others(6): Show | 9 | HG02109.hp2 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+2059C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100101475 | ||||||
| chr9:100101539
|
C | A | 76 | a0001c0001t0001g0108a0001c0001t0001g0144a0001c0001t0001g0145others(73): Show | 76 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.-25+2123C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100101539 | ||||||
| chr9:100101546
|
T | A | 5 | a0001c0002t0001g0014a0001c0002t0001g0021a0001c0002t0001g0022others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-25+2130T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100101546 | ||||||
| chr9:100101885
|
T | C | 2 | a0001c0002t0002g0103a0001c0002t0002g0117 | 2 | NA18964.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-25+2469T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100101885 | ||||||
| chr9:100101908
|
G | A | 4 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(1): Show | 4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25+2492G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100101908 | ||||||
| chr9:100102053
|
G | A | 4 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(1): Show | 4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24-2445G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100102053 | ||||||
| chr9:100102131
|
G | GT | 156 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-24-2366dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100102131 | |||||
| chr9:100102287
|
C | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.-24-2211C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100102287 | ||||||
| chr9:100102576
|
A | G | 1 | a0001c0001t0013g0082 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-24-1922A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100102576 | ||||||
| chr9:100102772
|
G | A | 3 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136 | 3 | HG02280.hp1 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-24-1726G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100102772 | ||||||
| chr9:100103429
|
C | G | 1 | a0001c0001t0001g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-24-1069C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100103429 | ||||||
| chr9:100104687
|
G | T | 1 | a0001c0001t0019g0066 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.106+60G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100104687 | ||||||
| chr9:100104839
|
T | A | 1 | a0001c0001t0007g0057 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.106+212T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100104839 | ||||||
| chr9:100105545
|
G | T | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106+918G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100105545 | ||||||
| chr9:100105850
|
C | CT | 48 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0037others(45): Show | 48 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.106+1248dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100105850 | |||||
| chr9:100105850
|
C | CTT | 39 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0010g0157others(36): Show | 39 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.106+1247_106+1248d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100105850 | |||||
| chr9:100105850
|
CT | C | 5 | a0001c0001t0003g0087a0001c0001t0004g0067a0001c0001t0004g0070others(2): Show | 5 | HG00323.hp1 NA18522.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.106+1248delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100105850 | |||||
| chr9:100106193
|
C | T | 72 | a0001c0001t0001g0108a0001c0001t0001g0144a0001c0001t0001g0145others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.106+1566C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100106193 | ||||||
| chr9:100106357
|
C | G | 9 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(6): Show | 9 | HG02280.hp2 HG02451.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.106+1730C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100106357 | ||||||
| chr9:100106389
|
C | T | 1 | a0001c0001t0008g0034 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.106+1762C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100106389 | ||||||
| chr9:100106402
|
C | A | 36 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0010g0157others(33): Show | 36 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.106+1775C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100106402 | ||||||
| chr9:100106487
|
A | G | 35 | a0001c0001t0003g0042a0001c0001t0003g0048a0001c0001t0003g0087others(32): Show | 35 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.106+1860A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100106487 | ||||||
| chr9:100106809
|
A | G | 1 | a0001c0002t0001g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.106+2182A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100106809 | ||||||
| chr9:100106945
|
T | C | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106+2318T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100106945 | ||||||
| chr9:100106949
|
AAAG | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.106+2328_106+2330d others(5): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100106949 | |||||
| chr9:100107047
|
C | G | 4 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(1): Show | 4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+2420C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100107047 | ||||||
| chr9:100107246
|
T | C | 1 | a0001c0002t0001g0111 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.106+2619T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100107246 | ||||||
| chr9:100107564
|
G | A | 77 | a0001c0001t0001g0108a0001c0001t0001g0144a0001c0001t0001g0145others(74): Show | 77 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.106+2937G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100107564 | ||||||
| chr9:100108023
|
C | A | 2 | a0001c0001t0004g0071a0001c0001t0004g0072 | 2 | NA19012.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.106+3396C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100108023 | ||||||
| chr9:100108378
|
C | A | 1 | a0001c0001t0001g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.106+3751C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100108378 | ||||||
| chr9:100108434
|
T | C | 1 | a0001c0001t0013g0079 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.106+3807T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100108434 | ||||||
| chr9:100108556
|
T | C | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.106+3929T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100108556 | ||||||
| chr9:100108619
|
C | T | 1 | a0001c0002t0009g0132 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.106+3992C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100108619 | ||||||
| chr9:100109246
|
C | T | 1 | a0001c0001t0003g0048 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.106+4619C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100109246 | ||||||
| chr9:100109304
|
A | G | 79 | a0001c0001t0001g0108a0001c0001t0001g0144a0001c0001t0001g0145others(76): Show | 79 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.106+4677A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100109304 | ||||||
| chr9:100109553
|
C | T | 78 | a0001c0001t0001g0108a0001c0001t0001g0144a0001c0001t0001g0145others(75): Show | 78 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.106+4926C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100109553 | ||||||
| chr9:100109856
|
G | A | 1 | a0001c0002t0008g0174 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.106+5229G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100109856 | ||||||
| chr9:100109913
|
C | T | 1 | a0001c0002t0001g0180 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.106+5286C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100109913 | ||||||
| chr9:100109959
|
G | A | 77 | a0001c0001t0001g0108a0001c0001t0001g0144a0001c0001t0001g0145others(74): Show | 77 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.106+5332G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100109959 | ||||||
| chr9:100110168
|
C | A | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106+5541C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100110168 | ||||||
| chr9:100110175
|
A | G | 1 | a0001c0001t0001g0004 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.106+5548A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100110175 | ||||||
| chr9:100110441
|
T | C | 9 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.106+5814T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100110441 | ||||||
| chr9:100110483
|
G | A | 2 | a0001c0001t0003g0043a0001c0001t0003g0073 | 2 | HG01074.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.106+5856G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100110483 | ||||||
| chr9:100110775
|
T | A | 120 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(117): Show | 120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.106+6148T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100110775 | ||||||
| chr9:100111027
|
T | G | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.106+6400T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100111027 | ||||||
| chr9:100111178
|
A | G | 2 | a0001c0001t0001g0108a0001c0002t0001g0112 | 2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.106+6551A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100111178 | ||||||
| chr9:100111302
|
G | T | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106+6675G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100111302 | ||||||
| chr9:100111487
|
T | C | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106+6860T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100111487 | ||||||
| chr9:100111741
|
G | A | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106+7114G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100111741 | ||||||
| chr9:100111742
|
C | T | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106+7115C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100111742 | ||||||
| chr9:100111808
|
G | C | 1 | a0001c0002t0001g0102 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.106+7181G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100111808 | ||||||
| chr9:100111960
|
T | C | 1 | a0006c0007t0011g0181 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.106+7333T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100111960 | ||||||
| chr9:100111977
|
A | ACTTT | 11 | a0001c0001t0004g0058a0001c0001t0007g0051a0001c0001t0007g0053others(8): Show | 11 | HG02109.hp2 HG02647.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.106+7371_106+7374d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100111977 | |||||
| chr9:100112028
|
C | T | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106+7401C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100112028 | ||||||
| chr9:100112171
|
T | C | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106+7544T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100112171 | ||||||
| chr9:100112444
|
T | A | 1 | a0001c0002t0018g0146 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.106+7817T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100112444 | ||||||
| chr9:100112665
|
T | TA | 7 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(4): Show | 7 | HG00621.hp2 HG01081.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.106+8052dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100112665 | |||||
| chr9:100112945
|
T | C | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106+8318T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100112945 | ||||||
| chr9:100112961
|
C | A | 1 | a0001c0001t0007g0028 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.106+8334C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100112961 | ||||||
| chr9:100113261
|
GTTA | G | 77 | a0001c0001t0001g0108a0001c0001t0001g0144a0001c0001t0001g0145others(74): Show | 77 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.106+8639_106+8641d others(5): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100113261 | |||||
| chr9:100113461
|
A | G | 1 | a0001c0001t0003g0094 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.106+8834A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100113461 | ||||||
| chr9:100113542
|
A | G | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106+8915A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100113542 | ||||||
| chr9:100113558
|
TTTTG | T | 17 | a0001c0001t0001g0145a0001c0001t0003g0092a0001c0001t0003g0093others(14): Show | 17 | HG00140.hp2 HG00733.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.106+8963_106+8966d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100113558 | |||||
| chr9:100113826
|
T | C | 1 | a0001c0002t0001g0128 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.106+9199T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100113826 | ||||||
| chr9:100113899
|
T | C | 120 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(117): Show | 120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.106+9272T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100113899 | ||||||
| chr9:100114026
|
A | C | 25 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0001t0010g0157others(22): Show | 25 | HG00609.hp2 HG00621.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.106+9399A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100114026 | ||||||
| chr9:100114114
|
A | G | 1 | a0001c0001t0013g0079 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.106+9487A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100114114 | ||||||
| chr9:100114143
|
G | A | 1 | a0001c0002t0002g0148 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.106+9516G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100114143 | ||||||
| chr9:100114204
|
A | T | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106+9577A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100114204 | ||||||
| chr9:100114391
|
CT | C | 64 | a0001c0001t0001g0025a0001c0001t0001g0108a0001c0001t0003g0042others(61): Show | 64 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.106+9792delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100114391 | |||||
| chr9:100114391
|
CTT | C | 98 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0026others(95): Show | 98 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.106+9791_106+9792d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100114391 | |||||
| chr9:100114391
|
CTTT | C | 7 | a0001c0001t0001g0033a0001c0001t0024g0182a0001c0002t0002g0152others(4): Show | 7 | HG01074.hp2 HG01081.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.106+9790_106+9792d others(5): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100114391 | |||||
| chr9:100114537
|
G | T | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106+9910G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100114537 | ||||||
| chr9:100114686
|
G | A | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106+10059G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100114686 | ||||||
| chr9:100114839
|
G | C | 120 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(117): Show | 120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.106+10212G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100114839 | ||||||
| chr9:100114955
|
G | A | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106+10328G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100114955 | ||||||
| chr9:100115267
|
G | A | 1 | a0001c0002t0001g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.106+10640G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100115267 | ||||||
| chr9:100115300
|
TTA | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.106+10685_106+1068 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100115300 | |||||
| chr9:100115351
|
A | G | 77 | a0001c0001t0001g0108a0001c0001t0001g0144a0001c0001t0001g0145others(74): Show | 77 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.106+10724A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100115351 | ||||||
| chr9:100115353
|
G | A | 2 | a0001c0001t0003g0092a0001c0001t0003g0093 | 2 | HG01243.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.106+10726G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100115353 | ||||||
| chr9:100115453
|
C | T | 1 | a0001c0002t0008g0174 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.106+10826C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100115453 | ||||||
| chr9:100115605
|
C | G | 4 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(1): Show | 4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-10778C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100115605 | ||||||
| chr9:100115789
|
A | G | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.107-10594A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100115789 | ||||||
| chr9:100115792
|
A | T | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.107-10591A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100115792 | ||||||
| chr9:100115806
|
C | T | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.107-10577C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100115806 | ||||||
| chr9:100115858
|
C | G | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.107-10525C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100115858 | ||||||
| chr9:100115869
|
A | T | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.107-10514A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100115869 | ||||||
| chr9:100116001
|
G | A | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.107-10382G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100116001 | ||||||
| chr9:100116094
|
CTTTCTTT others(2): Show |
C | 2 | a0001c0001t0004g0056a0001c0001t0004g0062 | 2 | HG02080.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.107-10276_107-1026 others(13): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100116094 | |||||
| chr9:100116107
|
CT | C | 117 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(114): Show | 117 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.107-10262delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100116107 | |||||
| chr9:100116190
|
G | A | 9 | a0001c0001t0004g0058a0001c0001t0007g0051a0001c0001t0007g0053others(6): Show | 9 | HG02109.hp2 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.107-10193G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100116190 | ||||||
| chr9:100116239
|
G | C | 1 | a0001c0001t0004g0049 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.107-10144G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100116239 | ||||||
| chr9:100116327
|
T | G | 3 | a0001c0002t0001g0140a0001c0002t0001g0180a0001c0002t0025g0165 | 3 | HG01071.hp1 HG02559.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-10056T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100116327 | ||||||
| chr9:100116368
|
C | A | 1 | a0001c0002t0001g0133 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.107-10015C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100116368 | ||||||
| chr9:100116460
|
G | C | 75 | a0001c0001t0001g0108a0001c0001t0001g0144a0001c0001t0001g0145others(72): Show | 75 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.107-9923G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100116460 | ||||||
| chr9:100116477
|
C | G | 1 | a0001c0002t0001g0131 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.107-9906C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100116477 | ||||||
| chr9:100116540
|
T | G | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(30): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.107-9843T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100116540 | ||||||
| chr9:100117054
|
A | G | 120 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(117): Show | 120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.107-9329A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100117054 | ||||||
| chr9:100117097
|
G | A | 119 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(116): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.107-9286G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100117097 | ||||||
| chr9:100117232
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.107-9151G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100117232 | ||||||
| chr9:100117334
|
G | C | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.107-9049G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100117334 | ||||||
| chr9:100117477
|
C | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.107-8906C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100117477 | ||||||
| chr9:100117522
|
A | G | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.107-8861A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100117522 | ||||||
| chr9:100117564
|
C | T | 42 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(39): Show | 42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.107-8819C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100117564 | ||||||
| chr9:100117609
|
G | GC | 45 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(42): Show | 45 | HG00140.hp2 HG00544.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.107-8766dupC | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100117609 | |||||
| chr9:100118302
|
G | A | 3 | a0001c0002t0001g0102a0001c0002t0001g0107a0001c0002t0008g0105 | 3 | HG02622.hp1 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.107-8081G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100118302 | ||||||
| chr9:100118661
|
G | T | 1 | a0007c0011t0002g0104 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.107-7722G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100118661 | ||||||
| chr9:100119173
|
T | A | 77 | a0001c0001t0001g0108a0001c0001t0001g0144a0001c0001t0001g0145others(74): Show | 77 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.107-7210T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100119173 | ||||||
| chr9:100119189
|
C | G | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.107-7194C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100119189 | ||||||
| chr9:100119435
|
T | C | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.107-6948T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100119435 | ||||||
| chr9:100119495
|
C | G | 76 | a0001c0001t0001g0108a0001c0001t0001g0144a0001c0001t0001g0145others(73): Show | 76 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.107-6888C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100119495 | ||||||
| chr9:100120260
|
A | T | 1 | a0001c0001t0016g0027 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.107-6123A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100120260 | ||||||
| chr9:100120263
|
C | A | 1 | a0001c0001t0016g0027 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.107-6120C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100120263 | ||||||
| chr9:100120458
|
C | G | 2 | a0001c0001t0011g0100a0001c0001t0011g0101 | 2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.107-5925C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100120458 | ||||||
| chr9:100121051
|
A | G | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.107-5332A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100121051 | ||||||
| chr9:100121709
|
T | TC | 5 | a0001c0001t0007g0028a0001c0001t0026g0029a0001c0001t0027g0030others(2): Show | 5 | HG02145.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-4673dupC | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100121709 | |||||
| chr9:100121894
|
C | T | 120 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(117): Show | 120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.107-4489C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100121894 | ||||||
| chr9:100122133
|
T | C | 1 | a0001c0001t0001g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.107-4250T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100122133 | ||||||
| chr9:100122168
|
T | C | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.107-4215T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100122168 | ||||||
| chr9:100122576
|
C | CT | 72 | a0001c0001t0001g0108a0001c0001t0001g0144a0001c0001t0001g0145others(69): Show | 72 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.107-3782dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100122576 | |||||
| chr9:100122576
|
C | CTT | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.107-3783_107-3782d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100122576 | |||||
| chr9:100122576
|
C | CTTT | 10 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0008g0032others(7): Show | 10 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.107-3784_107-3782d others(5): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100122576 | |||||
| chr9:100122657
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.107-3726T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100122657 | ||||||
| chr9:100122864
|
G | A | 153 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(150): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.107-3519G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100122864 | ||||||
| chr9:100122880
|
A | G | 117 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(114): Show | 117 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.107-3503A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100122880 | ||||||
| chr9:100123149
|
T | C | 1 | a0001c0002t0001g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.107-3234T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100123149 | ||||||
| chr9:100123449
|
T | C | 1 | a0001c0001t0003g0088 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.107-2934T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100123449 | ||||||
| chr9:100123629
|
G | A | 76 | a0001c0001t0001g0108a0001c0001t0001g0144a0001c0001t0001g0145others(73): Show | 76 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.107-2754G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100123629 | ||||||
| chr9:100123997
|
C | G | 35 | a0001c0001t0003g0042a0001c0001t0003g0048a0001c0001t0003g0087others(32): Show | 35 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.107-2386C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100123997 | ||||||
| chr9:100124177
|
A | AGT | 37 | a0001c0001t0001g0040a0001c0001t0003g0087a0001c0001t0003g0178others(34): Show | 37 | HG00280.hp2 HG00735.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.107-2169_107-2168d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100124177 | |||||
| chr9:100124177
|
A | AGTGT | 21 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0026others(18): Show | 21 | HG00140.hp1 HG00323.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.107-2171_107-2168d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100124177 | |||||
| chr9:100124177
|
A | AGTGTGT | 5 | a0001c0001t0001g0015a0001c0001t0003g0095a0001c0001t0004g0049others(2): Show | 5 | HG01346.hp2 HG02809.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.107-2173_107-2168d others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100124177 | |||||
| chr9:100124177
|
A | AGTGTGTG others(1): Show |
3 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0002t0001g0024 | 3 | HG01243.hp1 HG02630.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.107-2175_107-2168d others(10): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100124177 | |||||
| chr9:100124177
|
AGT | A | 50 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0004g0068others(47): Show | 50 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.107-2169_107-2168d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100124177 | |||||
| chr9:100124177
|
AGTGT | A | 34 | a0001c0001t0001g0035a0001c0001t0003g0043a0001c0001t0003g0073others(31): Show | 34 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.107-2171_107-2168d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100124177 | |||||
| chr9:100124177
|
AGTGTGTG others(3): Show |
A | 2 | a0001c0004t0001g0109a0001c0004t0001g0110 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.107-2177_107-2168d others(12): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100124177 | |||||
| chr9:100124312
|
C | G | 2 | a0001c0002t0018g0146a0001c0002t0018g0149 | 2 | HG01516.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.107-2071C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100124312 | ||||||
| chr9:100124526
|
C | A | 1 | a0001c0002t0001g0129 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.107-1857C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100124526 | ||||||
| chr9:100124546
|
T | TA | 20 | a0001c0001t0003g0042a0001c0001t0003g0087a0001c0001t0003g0088others(17): Show | 20 | HG00735.hp1 HG00738.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.107-1821dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100124546 | |||||
| chr9:100124546
|
T | TAA | 41 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(38): Show | 41 | HG00323.hp1 HG00738.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.107-1822_107-1821d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100124546 | |||||
| chr9:100124654
|
T | A | 42 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(39): Show | 42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.107-1729T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100124654 | ||||||
| chr9:100124666
|
G | A | 117 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(114): Show | 117 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.107-1717G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100124666 | ||||||
| chr9:100125018
|
G | A | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.107-1365G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100125018 | ||||||
| chr9:100125147
|
G | T | 2 | a0001c0002t0002g0159a0001c0002t0002g0160 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.107-1236G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100125147 | ||||||
| chr9:100125309
|
T | C | 1 | a0001c0002t0001g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.107-1074T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100125309 | ||||||
| chr9:100125321
|
G | A | 1 | a0001c0002t0009g0122 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.107-1062G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100125321 | ||||||
| chr9:100125681
|
AT | A | 104 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0026others(101): Show | 104 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.107-681delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100125681 | |||||
| chr9:100125742
|
A | G | 1 | a0001c0002t0002g0158 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.107-641A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100125742 | ||||||
| chr9:100126039
|
T | C | 73 | a0001c0001t0001g0108a0001c0001t0004g0121a0001c0001t0010g0126others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.107-344T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100126039 | ||||||
| chr9:100126156
|
C | G | 1 | a0001c0002t0001g0143 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.107-227C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100126156 | ||||||
| chr9:100126595
|
C | T | 1 | a0001c0001t0013g0016 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+46C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100126595 | ||||||
| chr9:100127087
|
T | C | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+538T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100127087 | ||||||
| chr9:100127577
|
G | A | 1 | a0001c0002t0002g0175 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.273+1028G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100127577 | ||||||
| chr9:100127696
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.273+1147T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100127696 | ||||||
| chr9:100127775
|
G | A | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+1226G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100127775 | ||||||
| chr9:100127797
|
T | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.273+1248T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100127797 | ||||||
| chr9:100128432
|
C | A | 1 | a0001c0001t0001g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.273+1883C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100128432 | ||||||
| chr9:100128729
|
G | T | 1 | a0001c0002t0010g0170 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.273+2180G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100128729 | ||||||
| chr9:100128854
|
A | G | 4 | a0001c0001t0001g0108a0001c0002t0001g0112a0001c0004t0001g0109others(1): Show | 4 | HG02886.hp1 HG03225.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+2305A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100128854 | ||||||
| chr9:100129124
|
A | C | 1 | a0001c0001t0001g0026 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.273+2575A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100129124 | ||||||
| chr9:100129239
|
T | C | 1 | a0001c0002t0001g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.273+2690T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100129239 | ||||||
| chr9:100129551
|
A | G | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+3002A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100129551 | ||||||
| chr9:100129659
|
A | G | 1 | a0001c0001t0004g0067 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.273+3110A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100129659 | ||||||
| chr9:100130278
|
G | A | 1 | a0001c0001t0004g0055 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.273+3729G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100130278 | ||||||
| chr9:100130320
|
A | G | 1 | a0001c0001t0019g0066 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.273+3771A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100130320 | ||||||
| chr9:100130460
|
C | T | 118 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(115): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.273+3911C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100130460 | ||||||
| chr9:100130574
|
C | G | 3 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182 | 3 | HG01081.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.273+4025C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100130574 | ||||||
| chr9:100130593
|
A | G | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+4044A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100130593 | ||||||
| chr9:100130595
|
T | A | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+4046T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100130595 | ||||||
| chr9:100130647
|
C | G | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+4098C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100130647 | ||||||
| chr9:100130709
|
T | C | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+4160T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100130709 | ||||||
| chr9:100131433
|
A | C | 9 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.273+4884A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100131433 | ||||||
| chr9:100131473
|
C | G | 42 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(39): Show | 42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.273+4924C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100131473 | ||||||
| chr9:100131674
|
G | A | 1 | a0001c0001t0024g0182 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.273+5125G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100131674 | ||||||
| chr9:100131763
|
A | G | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+5214A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100131763 | ||||||
| chr9:100131964
|
T | C | 1 | a0001c0001t0010g0126 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.273+5415T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100131964 | ||||||
| chr9:100131973
|
C | T | 70 | a0001c0001t0001g0108a0001c0001t0010g0126a0001c0001t0010g0127others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.273+5424C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100131973 | ||||||
| chr9:100132117
|
G | A | 1 | a0001c0002t0025g0165 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.273+5568G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100132117 | ||||||
| chr9:100132226
|
CATGA | C | 96 | a0001c0001t0001g0108a0001c0001t0003g0088a0001c0001t0003g0090others(93): Show | 96 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.273+5712_273+5715d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100132226 | |||||
| chr9:100132226
|
CATGAATG others(1): Show |
C | 57 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(54): Show | 57 | HG00140.hp1 HG00323.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.273+5708_273+5715d others(10): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100132226 | |||||
| chr9:100132226
|
CATGAATG others(5): Show |
C | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+5704_273+5715d others(14): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100132226 | |||||
| chr9:100132403
|
G | T | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+5854G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100132403 | ||||||
| chr9:100132436
|
T | C | 118 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(115): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.273+5887T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100132436 | ||||||
| chr9:100132777
|
A | AT | 42 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(39): Show | 42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.273+6240dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100132777 | |||||
| chr9:100132777
|
AT | A | 72 | a0001c0001t0001g0108a0001c0001t0010g0126a0001c0001t0010g0127others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.273+6240delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100132777 | |||||
| chr9:100132964
|
G | A | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+6415G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100132964 | ||||||
| chr9:100132975
|
C | T | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+6426C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100132975 | ||||||
| chr9:100133008
|
G | A | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+6459G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100133008 | ||||||
| chr9:100133065
|
A | G | 1 | a0001c0002t0002g0175 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.273+6516A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100133065 | ||||||
| chr9:100133338
|
A | ATG | 13 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(10): Show | 13 | HG00140.hp1 HG01071.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.273+6813_273+6814d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133338 | |||||
| chr9:100133338
|
A | ATGTG | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+6811_273+6814d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133338 | |||||
| chr9:100133338
|
ATG | A | 6 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0011g0100others(3): Show | 6 | HG01081.hp1 HG01081.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.273+6813_273+6814d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133338 | |||||
| chr9:100133423
|
T | C | 1 | a0001c0001t0010g0157 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.273+6874T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100133423 | ||||||
| chr9:100133477
|
T | TGAAACTT others(307): Show |
1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+6938_273+6939i others(316): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133477 | |||||
| chr9:100133764
|
T | TAC | 17 | a0001c0001t0003g0048a0001c0001t0003g0083a0001c0001t0003g0088others(14): Show | 17 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.273+7255_273+7256d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133764 | |||||
| chr9:100133764
|
T | TACAC | 2 | a0001c0001t0007g0057a0005c0006t0020g0099 | 2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.273+7253_273+7256d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133764 | |||||
| chr9:100133764
|
T | TACACAC | 6 | a0001c0001t0001g0144a0001c0001t0012g0134a0001c0001t0012g0135others(3): Show | 6 | HG01081.hp1 HG02280.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.273+7251_273+7256d others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133764 | |||||
| chr9:100133764
|
T | TACACACA others(1): Show |
5 | a0001c0001t0001g0145a0001c0002t0001g0142a0001c0002t0001g0161others(2): Show | 5 | HG01243.hp2 HG01952.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.273+7249_273+7256d others(10): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133764 | |||||
| chr9:100133764
|
T | TACACACA others(3): Show |
3 | a0001c0002t0002g0158a0001c0002t0018g0146a0001c0004t0001g0110 | 3 | HG03540.hp1 HG03927.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.273+7247_273+7256d others(12): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133764 | |||||
| chr9:100133764
|
T | TACACACA others(5): Show |
10 | a0001c0002t0001g0111a0001c0002t0001g0141a0001c0002t0001g0143others(7): Show | 10 | HG00323.hp2 HG00609.hp2 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.273+7245_273+7256d others(14): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133764 | |||||
| chr9:100133764
|
T | TACACACA others(7): Show |
14 | a0001c0002t0001g0106a0001c0002t0001g0116a0001c0002t0001g0130others(11): Show | 14 | HG00735.hp2 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.273+7243_273+7256d others(16): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133764 | |||||
| chr9:100133764
|
T | TACACACA others(9): Show |
12 | a0001c0001t0010g0127a0001c0002t0001g0102a0001c0002t0001g0107others(9): Show | 12 | HG00140.hp2 HG00621.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.273+7241_273+7256d others(18): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133764 | |||||
| chr9:100133764
|
T | TACACACA others(11): Show |
12 | a0001c0001t0010g0126a0001c0002t0001g0114a0001c0002t0001g0128others(9): Show | 12 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.273+7239_273+7256d others(20): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133764 | |||||
| chr9:100133764
|
T | TACACACA others(13): Show |
10 | a0001c0001t0001g0108a0001c0001t0010g0157a0001c0002t0001g0112others(7): Show | 10 | HG00733.hp2 HG01109.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.273+7237_273+7256d others(22): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133764 | |||||
| chr9:100133764
|
T | TACACACA others(15): Show |
3 | a0001c0002t0001g0129a0001c0002t0001g0172a0001c0002t0001g0180 | 3 | HG02559.hp2 HG03239.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.273+7235_273+7256d others(24): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133764 | |||||
| chr9:100133764
|
T | TACACACA others(17): Show |
2 | a0001c0002t0001g0167a0001c0002t0002g0175 | 2 | HG01975.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.273+7233_273+7256d others(26): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133764 | |||||
| chr9:100133764
|
TAC | T | 5 | a0001c0001t0003g0042a0001c0001t0003g0087a0001c0001t0011g0100others(2): Show | 5 | HG01106.hp2 HG02055.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.273+7255_273+7256d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133764 | |||||
| chr9:100133764
|
TACACACA others(3): Show |
T | 35 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(32): Show | 35 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.273+7247_273+7256d others(12): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133764 | |||||
| chr9:100133796
|
CACACACA others(3): Show |
C | 3 | a0001c0001t0007g0028a0001c0001t0026g0029a0001c0001t0027g0030 | 3 | HG02145.hp2 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.273+7255_273+7264d others(12): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133796 | |||||
| chr9:100133806
|
T | C | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+7257T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100133806 | ||||||
| chr9:100133956
|
A | G | 118 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(115): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.273+7407A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100133956 | ||||||
| chr9:100134015
|
T | C | 2 | a0001c0001t0024g0182a0006c0007t0011g0181 | 2 | HG01081.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.273+7466T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100134015 | ||||||
| chr9:100134126
|
G | A | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+7577G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100134126 | ||||||
| chr9:100134182
|
C | T | 2 | a0001c0002t0001g0003a0001c0002t0001g0031 | 2 | HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.273+7633C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100134182 | ||||||
| chr9:100134339
|
G | A | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+7790G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100134339 | ||||||
| chr9:100134639
|
T | TA | 19 | a0001c0001t0003g0042a0001c0001t0003g0048a0001c0001t0003g0087others(16): Show | 19 | HG00140.hp1 HG00735.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.273+8091dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100134639 | |||||
| chr9:100134862
|
G | A | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+8313G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100134862 | ||||||
| chr9:100134922
|
T | C | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+8373T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100134922 | ||||||
| chr9:100135072
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.273+8523C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100135072 | ||||||
| chr9:100135146
|
T | C | 1 | a0001c0002t0001g0142 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.273+8597T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100135146 | ||||||
| chr9:100135730
|
C | T | 2 | a0001c0002t0002g0123a0001c0002t0002g0124 | 2 | NA19082.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.273+9181C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100135730 | ||||||
| chr9:100135797
|
T | C | 1 | a0001c0001t0003g0048 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.273+9248T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100135797 | ||||||
| chr9:100135965
|
T | C | 1 | a0001c0002t0025g0165 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.273+9416T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100135965 | ||||||
| chr9:100136443
|
C | G | 42 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(39): Show | 42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.273+9894C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100136443 | ||||||
| chr9:100136462
|
C | T | 4 | a0001c0002t0001g0102a0001c0002t0001g0106a0001c0002t0001g0107others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+9913C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100136462 | ||||||
| chr9:100136505
|
A | G | 3 | a0001c0001t0007g0028a0001c0001t0026g0029a0001c0001t0027g0030 | 3 | HG02145.hp2 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.273+9956A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100136505 | ||||||
| chr9:100136600
|
G | A | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+10051G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100136600 | ||||||
| chr9:100136717
|
A | G | 1 | a0001c0002t0002g0156 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.273+10168A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100136717 | ||||||
| chr9:100136725
|
C | T | 1 | a0001c0002t0001g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.273+10176C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100136725 | ||||||
| chr9:100136789
|
C | G | 42 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(39): Show | 42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.273+10240C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100136789 | ||||||
| chr9:100136933
|
G | A | 9 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.273+10384G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100136933 | ||||||
| chr9:100137234
|
T | G | 1 | a0001c0002t0009g0147 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.273+10685T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100137234 | ||||||
| chr9:100137357
|
A | G | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+10808A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100137357 | ||||||
| chr9:100137560
|
C | CACTAGAT | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+11011_273+1101 others(11): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100137560 | ||||||
| chr9:100138212
|
C | G | 42 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(39): Show | 42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.273+11663C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100138212 | ||||||
| chr9:100138283
|
A | G | 118 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(115): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.273+11734A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100138283 | ||||||
| chr9:100138384
|
T | C | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+11835T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100138384 | ||||||
| chr9:100138401
|
C | T | 11 | a0001c0002t0002g0103a0001c0002t0002g0117a0001c0002t0002g0118others(8): Show | 11 | HG00609.hp2 HG01192.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.273+11852C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100138401 | ||||||
| chr9:100138561
|
G | A | 1 | a0001c0002t0002g0124 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.273+12012G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100138561 | ||||||
| chr9:100138631
|
AAG | A | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(30): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.273+12085_273+1208 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100138631 | |||||
| chr9:100138700
|
C | CT | 11 | a0001c0001t0005g0013a0001c0001t0012g0134a0001c0001t0012g0135others(8): Show | 11 | HG00733.hp2 HG02083.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.273+12169dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100138700 | |||||
| chr9:100138700
|
C | CTT | 64 | a0001c0001t0001g0108a0001c0001t0010g0126a0001c0001t0010g0127others(61): Show | 64 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.273+12168_273+1216 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100138700 | |||||
| chr9:100138809
|
C | T | 2 | a0001c0001t0003g0083a0001c0001t0004g0070 | 2 | HG02083.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.273+12260C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100138809 | ||||||
| chr9:100138895
|
T | TG | 42 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(39): Show | 42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.273+12349dupG | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100138895 | |||||
| chr9:100138996
|
G | A | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+12447G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100138996 | ||||||
| chr9:100139002
|
G | A | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+12453G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100139002 | ||||||
| chr9:100139333
|
C | A | 1 | a0001c0002t0001g0024 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.273+12784C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100139333 | ||||||
| chr9:100139423
|
C | T | 7 | a0001c0001t0003g0088a0001c0001t0003g0090a0001c0001t0003g0094others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.273+12874C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100139423 | ||||||
| chr9:100139458
|
A | G | 1 | a0001c0002t0002g0137 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.273+12909A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100139458 | ||||||
| chr9:100139720
|
G | A | 1 | a0001c0001t0004g0068 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.273+13171G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100139720 | ||||||
| chr9:100139942
|
C | T | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+13393C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100139942 | ||||||
| chr9:100140198
|
A | G | 1 | a0001c0001t0003g0042 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.273+13649A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100140198 | ||||||
| chr9:100140260
|
C | T | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+13711C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100140260 | ||||||
| chr9:100140382
|
C | T | 4 | a0001c0002t0002g0152a0001c0002t0002g0154a0001c0002t0002g0155others(1): Show | 4 | HG00733.hp1 HG01074.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+13833C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100140382 | ||||||
| chr9:100140517
|
G | A | 1 | a0001c0002t0001g0140 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.273+13968G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100140517 | ||||||
| chr9:100140650
|
A | G | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+14101A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100140650 | ||||||
| chr9:100140673
|
C | T | 2 | a0001c0001t0004g0056a0001c0001t0004g0062 | 2 | HG02080.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.273+14124C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100140673 | ||||||
| chr9:100140814
|
G | A | 4 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(1): Show | 4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+14265G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100140814 | ||||||
| chr9:100141029
|
T | A | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+14480T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100141029 | ||||||
| chr9:100141547
|
C | T | 2 | a0001c0001t0011g0100a0001c0001t0011g0101 | 2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.273+14998C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100141547 | ||||||
| chr9:100141884
|
G | A | 1 | a0001c0002t0001g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.273+15335G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100141884 | ||||||
| chr9:100142582
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.273+16033C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100142582 | ||||||
| chr9:100142709
|
T | C | 70 | a0001c0001t0001g0108a0001c0001t0004g0121a0001c0001t0010g0126others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.273+16160T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100142709 | ||||||
| chr9:100142956
|
A | C | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+16407A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100142956 | ||||||
| chr9:100143045
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.273+16496G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100143045 | ||||||
| chr9:100143127
|
G | A | 1 | a0001c0001t0003g0095 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.273+16578G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100143127 | ||||||
| chr9:100143166
|
C | G | 118 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(115): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.273+16617C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100143166 | ||||||
| chr9:100143291
|
C | T | 1 | a0001c0001t0010g0157 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.273+16742C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100143291 | ||||||
| chr9:100143334
|
A | G | 5 | a0001c0001t0007g0028a0001c0001t0026g0029a0001c0001t0027g0030others(2): Show | 5 | HG02145.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.273+16785A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100143334 | ||||||
| chr9:100143612
|
G | T | 42 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(39): Show | 42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.273+17063G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100143612 | ||||||
| chr9:100143757
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.273+17208G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100143757 | ||||||
| chr9:100143827
|
T | C | 1 | a0001c0002t0009g0147 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.273+17278T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100143827 | ||||||
| chr9:100143853
|
C | T | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+17304C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100143853 | ||||||
| chr9:100143911
|
C | T | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+17362C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100143911 | ||||||
| chr9:100143971
|
G | A | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+17422G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100143971 | ||||||
| chr9:100144167
|
T | C | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+17618T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100144167 | ||||||
| chr9:100144226
|
G | T | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+17677G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100144226 | ||||||
| chr9:100144310
|
G | A | 1 | a0001c0002t0002g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.273+17761G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100144310 | ||||||
| chr9:100144345
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.273+17796C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100144345 | ||||||
| chr9:100144824
|
C | T | 2 | a0001c0001t0011g0100a0001c0001t0011g0101 | 2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.273+18275C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100144824 | ||||||
| chr9:100144922
|
G | T | 4 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(1): Show | 4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+18373G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100144922 | ||||||
| chr9:100144927
|
A | G | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+18378A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100144927 | ||||||
| chr9:100145366
|
C | T | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+18817C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100145366 | ||||||
| chr9:100145367
|
G | A | 34 | a0001c0001t0003g0042a0001c0001t0003g0048a0001c0001t0003g0087others(31): Show | 34 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.273+18818G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100145367 | ||||||
| chr9:100145385
|
G | A | 2 | a0001c0001t0007g0028a0001c0001t0026g0029 | 2 | HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.273+18836G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100145385 | ||||||
| chr9:100145429
|
G | A | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+18880G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100145429 | ||||||
| chr9:100145690
|
G | A | 1 | a0001c0001t0003g0087 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.273+19141G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100145690 | ||||||
| chr9:100145794
|
G | T | 69 | a0001c0001t0001g0108a0001c0001t0010g0126a0001c0001t0010g0127others(66): Show | 69 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.273+19245G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100145794 | ||||||
| chr9:100145823
|
C | T | 1 | a0001c0001t0004g0049 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.273+19274C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100145823 | ||||||
| chr9:100146017
|
G | A | 4 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(1): Show | 4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+19468G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100146017 | ||||||
| chr9:100146086
|
T | TC | 11 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0002t0001g0114others(8): Show | 11 | HG00280.hp1 HG00741.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.273+19543dupC | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100146086 | |||||
| chr9:100146086
|
TC | T | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+19543delC | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100146086 | |||||
| chr9:100146121
|
C | G | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+19572C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100146121 | ||||||
| chr9:100146232
|
G | C | 6 | a0001c0001t0004g0049a0001c0001t0004g0050a0001c0001t0004g0054others(3): Show | 6 | HG00280.hp2 HG02080.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.273+19683G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100146232 | ||||||
| chr9:100146298
|
T | TGGCG | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+19752_273+1975 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100146298 | |||||
| chr9:100146439
|
G | A | 71 | a0001c0001t0001g0108a0001c0001t0010g0126a0001c0001t0010g0127others(68): Show | 71 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.273+19890G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100146439 | ||||||
| chr9:100146750
|
T | C | 9 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(6): Show | 9 | HG02109.hp1 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.273+20201T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100146750 | ||||||
| chr9:100146790
|
A | T | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+20241A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100146790 | ||||||
| chr9:100146921
|
G | A | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+20372G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100146921 | ||||||
| chr9:100146956
|
CT | C | 29 | a0001c0001t0001g0108a0001c0002t0001g0111a0001c0002t0001g0112others(26): Show | 29 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.273+20409delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100146956 | |||||
| chr9:100147069
|
T | G | 2 | a0001c0001t0024g0182a0006c0007t0011g0181 | 2 | HG01081.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.273+20520T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100147069 | ||||||
| chr9:100147479
|
T | C | 1 | a0001c0001t0010g0127 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.273+20930T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100147479 | ||||||
| chr9:100147491
|
G | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.273+20942G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100147491 | ||||||
| chr9:100147662
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.273+21113G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100147662 | ||||||
| chr9:100147949
|
C | T | 1 | a0001c0002t0002g0151 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.273+21400C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100147949 | ||||||
| chr9:100148020
|
C | CA | 16 | a0001c0001t0001g0108a0001c0001t0004g0049a0001c0001t0004g0071others(13): Show | 16 | HG00735.hp1 HG01175.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.273+21492dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100148020 | |||||
| chr9:100148020
|
CAAAAAA | C | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+21487_273+2149 others(10): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100148020 | |||||
| chr9:100148382
|
G | A | 1 | a0001c0001t0003g0043 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.273+21833G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100148382 | ||||||
| chr9:100148611
|
G | A | 2 | a0001c0002t0002g0151a0001c0002t0009g0150 | 2 | HG00735.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.273+22062G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100148611 | ||||||
| chr9:100148820
|
A | G | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+22271A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100148820 | ||||||
| chr9:100148941
|
T | C | 4 | a0001c0002t0001g0102a0001c0002t0001g0106a0001c0002t0001g0107others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+22392T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100148941 | ||||||
| chr9:100149043
|
C | T | 120 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(117): Show | 120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.273+22494C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100149043 | ||||||
| chr9:100149049
|
CA | C | 70 | a0001c0001t0001g0108a0001c0001t0010g0126a0001c0001t0010g0127others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.273+22514delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100149049 | |||||
| chr9:100149306
|
GC | G | 4 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(1): Show | 4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+22760delC | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100149306 | |||||
| chr9:100149385
|
G | T | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+22836G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100149385 | ||||||
| chr9:100149402
|
C | G | 4 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(1): Show | 4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+22853C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100149402 | ||||||
| chr9:100149424
|
T | C | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+22875T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100149424 | ||||||
| chr9:100150194
|
C | G | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+23645C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100150194 | ||||||
| chr9:100150248
|
T | C | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+23699T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100150248 | ||||||
| chr9:100150438
|
G | A | 80 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(77): Show | 80 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.273+23889G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100150438 | ||||||
| chr9:100150476
|
G | T | 1 | a0001c0001t0015g0020 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.273+23927G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100150476 | ||||||
| chr9:100150775
|
G | A | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+24226G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100150775 | ||||||
| chr9:100150978
|
A | G | 4 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(1): Show | 4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+24429A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100150978 | ||||||
| chr9:100151117
|
C | G | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+24568C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100151117 | ||||||
| chr9:100151132
|
A | T | 1 | a0001c0002t0002g0173 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.273+24583A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100151132 | ||||||
| chr9:100151154
|
T | A | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+24605T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100151154 | ||||||
| chr9:100151532
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0008g0034 | 2 | HG02055.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.273+24983C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100151532 | ||||||
| chr9:100151644
|
A | G | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+25095A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100151644 | ||||||
| chr9:100151664
|
T | C | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+25115T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100151664 | ||||||
| chr9:100151869
|
A | T | 1 | a0001c0001t0003g0048 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.273+25320A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100151869 | ||||||
| chr9:100151987
|
G | A | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+25438G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100151987 | ||||||
| chr9:100152035
|
A | C | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+25486A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100152035 | ||||||
| chr9:100152079
|
T | C | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+25530T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100152079 | ||||||
| chr9:100152132
|
T | C | 1 | a0001c0002t0001g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.273+25583T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100152132 | ||||||
| chr9:100152168
|
C | T | 1 | a0001c0001t0004g0075 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.273+25619C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100152168 | ||||||
| chr9:100152214
|
T | G | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+25665T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100152214 | ||||||
| chr9:100152226
|
C | CTTTT | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+25679_273+2568 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100152226 | |||||
| chr9:100152387
|
A | T | 4 | a0001c0001t0014g0076a0001c0001t0014g0080a0001c0001t0014g0081others(1): Show | 4 | HG00423.hp2 HG00621.hp1 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+25838A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100152387 | ||||||
| chr9:100152409
|
A | C | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+25860A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100152409 | ||||||
| chr9:100152739
|
T | A | 2 | a0001c0001t0003g0176a0001c0001t0003g0177 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.273+26190T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100152739 | ||||||
| chr9:100152774
|
C | T | 2 | a0001c0001t0015g0019a0001c0001t0015g0020 | 2 | HG00741.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.273+26225C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100152774 | ||||||
| chr9:100152885
|
T | C | 2 | a0001c0001t0024g0182a0006c0007t0011g0181 | 2 | HG01081.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.273+26336T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100152885 | ||||||
| chr9:100153005
|
T | TTG | 6 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(3): Show | 6 | HG01081.hp2 HG03209.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.273+26482_273+2648 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100153005 | |||||
| chr9:100153005
|
T | TTGTG | 8 | a0001c0002t0001g0003a0001c0002t0001g0014a0001c0002t0001g0021others(5): Show | 8 | HG02109.hp1 HG02145.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.273+26480_273+2648 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100153005 | |||||
| chr9:100153005
|
T | TTGTGTG | 20 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(17): Show | 20 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.273+26478_273+2648 others(10): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100153005 | |||||
| chr9:100153005
|
T | TTGTGTGT others(1): Show |
7 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(4): Show | 7 | HG01109.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.273+26476_273+2648 others(12): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100153005 | |||||
| chr9:100153005
|
T | TTGTGTGT others(3): Show |
2 | a0001c0001t0008g0032a0001c0001t0008g0034 | 2 | HG02055.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.273+26474_273+2648 others(14): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100153005 | |||||
| chr9:100153005
|
TTG | T | 37 | a0001c0001t0003g0042a0001c0001t0003g0048a0001c0001t0003g0087others(34): Show | 37 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.273+26482_273+2648 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100153005 | |||||
| chr9:100153013
|
G | GTGTA | 3 | a0001c0001t0007g0028a0001c0001t0026g0029a0001c0001t0027g0030 | 3 | HG02145.hp2 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.273+26467_273+2646 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100153013 | |||||
| chr9:100153044
|
C | G | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+26495C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100153044 | ||||||
| chr9:100153141
|
G | A | 4 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(1): Show | 4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+26592G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100153141 | ||||||
| chr9:100153263
|
TA | T | 76 | a0001c0001t0001g0108a0001c0001t0001g0144a0001c0001t0010g0126others(73): Show | 76 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.273+26727delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100153263 | |||||
| chr9:100153718
|
G | A | 1 | a0001c0001t0013g0016 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+27169G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100153718 | ||||||
| chr9:100153897
|
G | C | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.273+27348G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100153897 | ||||||
| chr9:100154088
|
C | T | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+27539C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100154088 | ||||||
| chr9:100154256
|
TTGGGCTT others(33): Show |
T | 1 | a0002c0003t0006g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.273+27712_273+2775 others(44): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154256 | |||||
| chr9:100154331
|
A | AT | 42 | a0001c0001t0001g0108a0001c0001t0003g0088a0001c0001t0004g0049others(39): Show | 42 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.273+27810dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154331 | |||||
| chr9:100154331
|
A | ATT | 9 | a0001c0002t0001g0112a0001c0002t0001g0114a0001c0002t0001g0131others(6): Show | 9 | HG00423.hp1 HG00741.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.273+27809_273+2781 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154331 | |||||
| chr9:100154331
|
A | ATTT | 6 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(3): Show | 6 | HG01109.hp1 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.273+27808_273+2781 others(7): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154331 | |||||
| chr9:100154331
|
A | ATTTT | 6 | a0001c0001t0001g0040a0001c0001t0008g0032a0001c0001t0008g0034others(3): Show | 6 | HG01081.hp2 HG02055.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.273+27807_273+2781 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154331 | |||||
| chr9:100154331
|
A | ATTTTTTT others(4): Show |
3 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0026 | 3 | HG02486.hp1 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.273+27800_273+2781 others(15): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154331 | |||||
| chr9:100154331
|
A | ATTTTTTT others(6): Show |
1 | a0001c0002t0001g0024 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.273+27798_273+2781 others(17): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154331 | |||||
| chr9:100154331
|
A | ATTTTTTT others(7): Show |
2 | a0001c0002t0001g0022a0001c0002t0001g0023 | 2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.273+27797_273+2781 others(18): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154331 | |||||
| chr9:100154331
|
A | ATTTTTTT others(8): Show |
5 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(2): Show | 5 | HG02451.hp2 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.273+27796_273+2781 others(19): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154331 | |||||
| chr9:100154331
|
A | ATTTTTTT others(9): Show |
4 | a0001c0001t0001g0004a0001c0001t0005g0009a0001c0001t0015g0019others(1): Show | 4 | HG01168.hp1 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+27795_273+2781 others(20): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154331 | |||||
| chr9:100154331
|
A | ATTTTTTT others(10): Show |
7 | a0001c0001t0005g0013a0001c0001t0013g0016a0001c0001t0015g0020others(4): Show | 7 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.273+27794_273+2781 others(21): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154331 | |||||
| chr9:100154331
|
A | ATTTTTTT others(11): Show |
1 | a0001c0001t0005g0010 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.273+27793_273+2781 others(22): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154331 | |||||
| chr9:100154331
|
A | ATTTTTTT others(13): Show |
1 | a0001c0002t0001g0014 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.273+27791_273+2781 others(24): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154331 | |||||
| chr9:100154331
|
A | ATTTTTTT others(15): Show |
2 | a0001c0001t0007g0028a0001c0001t0026g0029 | 2 | HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.273+27789_273+2781 others(26): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154331 | |||||
| chr9:100154331
|
A | ATTTTTTT others(17): Show |
1 | a0001c0001t0027g0030 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.273+27787_273+2781 others(28): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154331 | |||||
| chr9:100154331
|
ATTTTTTT others(3): Show |
A | 5 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.273+27801_273+2781 others(14): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154331 | |||||
| chr9:100154978
|
C | CA | 4 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(1): Show | 4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+28431dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154978 | |||||
| chr9:100155135
|
C | T | 4 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0013g0082others(1): Show | 4 | HG01106.hp1 HG02602.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+28586C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100155135 | ||||||
| chr9:100155162
|
G | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.273+28613G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100155162 | ||||||
| chr9:100155254
|
A | C | 179 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(176): Show | 179 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.273+28705A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100155254 | ||||||
| chr9:100155368
|
G | A | 5 | a0001c0002t0002g0041a0001c0002t0002g0138a0001c0002t0002g0139others(2): Show | 5 | HG00140.hp2 HG00323.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.273+28819G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100155368 | ||||||
| chr9:100155404
|
T | A | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+28855T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100155404 | ||||||
| chr9:100155813
|
G | A | 1 | a0001c0002t0018g0149 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.273+29264G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100155813 | ||||||
| chr9:100156024
|
T | C | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+29475T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100156024 | ||||||
| chr9:100156257
|
C | CT | 12 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0012g0162others(9): Show | 12 | HG00323.hp1 HG00733.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.273+29729dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100156257 | |||||
| chr9:100156257
|
C | CTT | 34 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(31): Show | 34 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.273+29728_273+2972 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100156257 | |||||
| chr9:100156499
|
A | G | 119 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(116): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.273+29950A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100156499 | ||||||
| chr9:100156574
|
T | C | 9 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.273+30025T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100156574 | ||||||
| chr9:100156723
|
T | C | 2 | a0001c0001t0007g0063a0001c0002t0001g0060 | 2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.273+30174T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100156723 | ||||||
| chr9:100156823
|
TA | T | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+30280delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100156823 | |||||
| chr9:100156931
|
C | CAT | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+30394_273+3039 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100156931 | |||||
| chr9:100156941
|
T | TAC | 4 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(1): Show | 4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+30393_273+3039 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100156941 | |||||
| chr9:100156943
|
T | C | 6 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(3): Show | 6 | HG00733.hp2 HG01081.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.273+30394T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100156943 | ||||||
| chr9:100156943
|
T | TAC | 71 | a0001c0001t0001g0108a0001c0001t0004g0121a0001c0001t0010g0126others(68): Show | 71 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.273+30406_273+3040 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100156943 | |||||
| chr9:100156943
|
T | TACAC | 37 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(34): Show | 37 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.273+30404_273+3040 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100156943 | |||||
| chr9:100156971
|
TATTC | T | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+30429_273+3043 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100156971 | |||||
| chr9:100157156
|
A | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.273+30607A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100157156 | ||||||
| chr9:100157251
|
A | G | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+30702A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100157251 | ||||||
| chr9:100157267
|
C | CTTTTTTT others(3): Show |
34 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(31): Show | 34 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.273+30724_273+3073 others(14): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100157267 | |||||
| chr9:100157267
|
C | CTTTTTTT others(4): Show |
6 | a0001c0001t0001g0033a0001c0001t0008g0034a0001c0001t0026g0029others(3): Show | 6 | HG01109.hp1 HG02055.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.273+30723_273+3073 others(15): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100157267 | |||||
| chr9:100157267
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0007g0028a0001c0001t0027g0030 | 2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.273+30722_273+3073 others(16): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100157267 | |||||
| chr9:100157273
|
T | C | 38 | a0001c0001t0004g0121a0001c0001t0010g0126a0001c0001t0010g0127others(35): Show | 38 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.273+30724T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100157273 | ||||||
| chr9:100157380
|
T | G | 2 | a0001c0002t0008g0166a0001c0002t0008g0168 | 2 | HG00423.hp1 HG00544.hp1 |
intron_variant | MODIFIER | c.273+30831T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100157380 | ||||||
| chr9:100157410
|
G | A | 6 | a0001c0001t0004g0049a0001c0001t0004g0050a0001c0001t0004g0054others(3): Show | 6 | HG00280.hp2 HG02080.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.273+30861G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100157410 | ||||||
| chr9:100157509
|
G | A | 1 | a0002c0003t0023g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.273+30960G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100157509 | ||||||
| chr9:100157561
|
G | A | 5 | a0001c0001t0007g0028a0001c0001t0026g0029a0001c0001t0027g0030others(2): Show | 5 | HG02145.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.273+31012G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100157561 | ||||||
| chr9:100157779
|
T | C | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+31230T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100157779 | ||||||
| chr9:100158072
|
T | G | 2 | a0001c0001t0015g0019a0001c0001t0015g0020 | 2 | HG00741.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.273+31523T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100158072 | ||||||
| chr9:100158091
|
T | C | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(30): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.273+31542T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100158091 | ||||||
| chr9:100158226
|
T | C | 1 | a0001c0002t0002g0154 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.273+31677T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100158226 | ||||||
| chr9:100158314
|
G | GA | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+31772dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100158314 | |||||
| chr9:100158524
|
A | G | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+31975A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100158524 | ||||||
| chr9:100158754
|
C | T | 118 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(115): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.273+32205C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100158754 | ||||||
| chr9:100158758
|
G | A | 1 | a0002c0003t0006g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.273+32209G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100158758 | ||||||
| chr9:100158874
|
A | G | 1 | a0007c0011t0002g0104 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.273+32325A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100158874 | ||||||
| chr9:100158964
|
A | G | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+32415A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100158964 | ||||||
| chr9:100159005
|
G | T | 1 | a0001c0002t0002g0139 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.273+32456G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100159005 | ||||||
| chr9:100159108
|
C | A | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+32559C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100159108 | ||||||
| chr9:100160025
|
T | C | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+33476T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100160025 | ||||||
| chr9:100160069
|
T | C | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+33520T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100160069 | ||||||
| chr9:100160182
|
C | A | 4 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(1): Show | 4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+33633C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100160182 | ||||||
| chr9:100160505
|
G | T | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+33956G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100160505 | ||||||
| chr9:100160574
|
G | A | 4 | a0001c0002t0002g0152a0001c0002t0002g0154a0001c0002t0002g0155others(1): Show | 4 | HG00733.hp1 HG01074.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+34025G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100160574 | ||||||
| chr9:100160689
|
TC | T | 42 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(39): Show | 42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.273+34144delC | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100160689 | |||||
| chr9:100160702
|
G | A | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+34153G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100160702 | ||||||
| chr9:100160836
|
C | T | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+34287C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100160836 | ||||||
| chr9:100160880
|
G | A | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+34331G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100160880 | ||||||
| chr9:100160939
|
A | C | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.273+34390A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100160939 | ||||||
| chr9:100160940
|
G | C | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.273+34391G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100160940 | ||||||
| chr9:100160943
|
A | G | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.273+34394A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100160943 | ||||||
| chr9:100160944
|
GACTC | G | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.273+34396_273+3439 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100160944 | ||||||
| chr9:100160954
|
C | CA | 6 | a0001c0001t0004g0049a0001c0001t0004g0068a0001c0001t0011g0061others(3): Show | 6 | HG01175.hp1 HG02055.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.273+34427dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100160954 | |||||
| chr9:100160954
|
CA | C | 68 | a0001c0001t0001g0108a0001c0001t0001g0144a0001c0001t0003g0095others(65): Show | 68 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.273+34427delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100160954 | |||||
| chr9:100160954
|
CAAA | C | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.273+34425_273+3442 others(7): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100160954 | |||||
| chr9:100161069
|
G | C | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+34520G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100161069 | ||||||
| chr9:100161141
|
C | T | 34 | a0001c0001t0003g0042a0001c0001t0003g0048a0001c0001t0003g0087others(31): Show | 34 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.273+34592C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100161141 | ||||||
| chr9:100161204
|
T | C | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.273+34655T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100161204 | ||||||
| chr9:100161326
|
T | C | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+34777T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100161326 | ||||||
| chr9:100161364
|
C | CA | 31 | a0001c0001t0001g0108a0001c0001t0003g0042a0001c0001t0003g0073others(28): Show | 31 | HG00423.hp1 HG00423.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.273+34843dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100161364 | |||||
| chr9:100161364
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0024g0182 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.273+34823_273+3482 others(17): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100161364 | |||||
| chr9:100161364
|
C | CAAAAAAA others(7): Show |
1 | a0006c0007t0011g0181 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.273+34823_273+3482 others(18): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100161364 | |||||
| chr9:100161364
|
CA | C | 12 | a0001c0001t0001g0144a0001c0001t0003g0176a0001c0001t0004g0058others(9): Show | 12 | HG01081.hp1 HG01167.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.273+34843delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100161364 | |||||
| chr9:100161366
|
A | AAACAAAA others(7): Show |
1 | a0001c0001t0026g0029 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.273+34819_273+3482 others(18): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100161366 | |||||
| chr9:100161373
|
A | C | 2 | a0001c0001t0011g0100a0001c0001t0011g0101 | 2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.273+34824A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100161373 | ||||||
| chr9:100161376
|
A | AAAACAAA others(8): Show |
1 | a0001c0002t0001g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.273+34830_273+3483 others(19): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100161376 | |||||
| chr9:100161377
|
A | AAACAAAA others(7): Show |
36 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(33): Show | 36 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.273+34830_273+3483 others(18): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100161377 | |||||
| chr9:100161377
|
A | AAACAAAA others(6): Show |
1 | a0001c0001t0001g0026 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.273+34830_273+3483 others(17): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100161377 | |||||
| chr9:100161377
|
A | C | 1 | a0001c0001t0026g0029 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.273+34828A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100161377 | ||||||
| chr9:100161380
|
A | C | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+34831A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100161380 | ||||||
| chr9:100161388
|
A | AACAAAAA others(6): Show |
2 | a0001c0001t0011g0100a0001c0001t0011g0101 | 2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.273+34840_273+3484 others(17): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100161388 | |||||
| chr9:100161388
|
A | C | 40 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(37): Show | 40 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.273+34839A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100161388 | ||||||
| chr9:100161436
|
T | G | 5 | a0001c0001t0004g0064a0001c0001t0004g0065a0001c0001t0004g0067others(2): Show | 5 | HG00609.hp1 HG02056.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.273+34887T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100161436 | ||||||
| chr9:100161481
|
G | A | 118 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(115): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.273+34932G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100161481 | ||||||
| chr9:100161613
|
A | AGATG | 2 | a0001c0004t0001g0110a0005c0006t0020g0099 | 2 | HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.273+35094_273+3509 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100161613 | |||||
| chr9:100161696
|
T | C | 1 | a0001c0002t0002g0148 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.273+35147T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100161696 | ||||||
| chr9:100162081
|
G | A | 2 | a0001c0001t0003g0043a0001c0001t0003g0073 | 2 | HG01074.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.273+35532G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100162081 | ||||||
| chr9:100162150
|
G | T | 1 | a0001c0001t0007g0053 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.273+35601G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100162150 | ||||||
| chr9:100162418
|
C | T | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(30): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.273+35869C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100162418 | ||||||
| chr9:100162583
|
A | C | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.273+36034A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100162583 | ||||||
| chr9:100162783
|
T | C | 1 | a0001c0001t0017g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.273+36234T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100162783 | ||||||
| chr9:100162826
|
C | CA | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.273+36290dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100162826 | |||||
| chr9:100162984
|
G | A | 1 | a0002c0003t0006g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.273+36435G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100162984 | ||||||
| chr9:100163003
|
A | G | 4 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(1): Show | 4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+36454A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100163003 | ||||||
| chr9:100163140
|
G | T | 1 | a0001c0001t0001g0015 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.273+36591G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100163140 | ||||||
| chr9:100163186
|
A | AT | 75 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0108others(72): Show | 75 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.273+36656dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100163186 | |||||
| chr9:100163186
|
A | ATT | 31 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(28): Show | 31 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.273+36655_273+3665 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100163186 | |||||
| chr9:100163186
|
A | ATTT | 6 | a0001c0001t0005g0005a0001c0001t0011g0100a0001c0001t0011g0101others(3): Show | 6 | HG01081.hp2 HG02451.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.273+36654_273+3665 others(7): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100163186 | |||||
| chr9:100163322
|
C | T | 40 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(37): Show | 40 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.273+36773C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100163322 | ||||||
| chr9:100163354
|
A | C | 2 | a0001c0002t0002g0151a0001c0002t0009g0150 | 2 | HG00735.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.273+36805A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100163354 | ||||||
| chr9:100163524
|
T | A | 9 | a0001c0001t0003g0092a0001c0001t0003g0093a0002c0003t0006g0084others(6): Show | 9 | HG00735.hp1 HG00738.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.273+36975T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100163524 | ||||||
| chr9:100163554
|
G | A | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+37005G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100163554 | ||||||
| chr9:100163822
|
G | T | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+37273G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100163822 | ||||||
| chr9:100163929
|
G | GCA | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(30): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.273+37383_273+3738 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100163929 | |||||
| chr9:100164135
|
G | A | 1 | a0001c0002t0009g0132 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.273+37586G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100164135 | ||||||
| chr9:100164337
|
A | G | 76 | a0001c0001t0001g0108a0001c0001t0010g0126a0001c0001t0010g0127others(73): Show | 76 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.273+37788A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100164337 | ||||||
| chr9:100164407
|
GT | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.273+37868delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100164407 | |||||
| chr9:100164495
|
T | C | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+37946T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100164495 | ||||||
| chr9:100164569
|
T | C | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.273+38020T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100164569 | ||||||
| chr9:100164615
|
T | C | 4 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(1): Show | 4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+38066T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100164615 | ||||||
| chr9:100164896
|
C | CT | 22 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(19): Show | 22 | HG00609.hp2 HG00741.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.273+38364dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100164896 | |||||
| chr9:100165229
|
A | C | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+38680A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100165229 | ||||||
| chr9:100165254
|
T | A | 118 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(115): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.273+38705T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100165254 | ||||||
| chr9:100165508
|
A | G | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+38959A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100165508 | ||||||
| chr9:100165724
|
G | A | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+39175G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100165724 | ||||||
| chr9:100166096
|
C | G | 5 | a0001c0001t0007g0028a0001c0001t0026g0029a0001c0001t0027g0030others(2): Show | 5 | HG02145.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.273+39547C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100166096 | ||||||
| chr9:100166164
|
A | G | 119 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(116): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.273+39615A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100166164 | ||||||
| chr9:100166330
|
A | G | 1 | a0001c0002t0001g0142 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.273+39781A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100166330 | ||||||
| chr9:100166772
|
A | T | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+40223A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100166772 | ||||||
| chr9:100166965
|
C | T | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+40416C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100166965 | ||||||
| chr9:100167047
|
A | G | 2 | a0001c0001t0003g0092a0001c0001t0003g0093 | 2 | HG01243.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.273+40498A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100167047 | ||||||
| chr9:100167050
|
G | A | 9 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.273+40501G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100167050 | ||||||
| chr9:100167141
|
G | T | 1 | a0001c0002t0001g0131 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.273+40592G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100167141 | ||||||
| chr9:100167173
|
G | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.273+40624G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100167173 | ||||||
| chr9:100167583
|
C | T | 5 | a0001c0001t0007g0028a0001c0001t0026g0029a0001c0001t0027g0030others(2): Show | 5 | HG02145.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.273+41034C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100167583 | ||||||
| chr9:100167655
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.273+41106C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100167655 | ||||||
| chr9:100167660
|
T | C | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.273+41111T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100167660 | ||||||
| chr9:100167823
|
C | T | 3 | a0001c0001t0016g0027a0001c0001t0017g0017a0001c0001t0017g0018 | 3 | HG00642.hp2 HG00738.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.273+41274C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100167823 | ||||||
| chr9:100167975
|
C | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.273+41426C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100167975 | ||||||
| chr9:100168180
|
G | A | 1 | a0001c0002t0009g0122 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.273+41631G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100168180 | ||||||
| chr9:100168493
|
G | A | 4 | a0001c0002t0001g0102a0001c0002t0001g0106a0001c0002t0001g0107others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+41944G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100168493 | ||||||
| chr9:100168828
|
C | T | 2 | a0001c0001t0014g0076a0001c0001t0014g0081 | 2 | HG00621.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.273+42279C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100168828 | ||||||
| chr9:100168904
|
G | A | 1 | a0001c0002t0002g0137 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.273+42355G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100168904 | ||||||
| chr9:100169033
|
C | A | 1 | a0001c0002t0001g0003 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.273+42484C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100169033 | ||||||
| chr9:100169145
|
T | C | 1 | a0001c0001t0016g0011 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.273+42596T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100169145 | ||||||
| chr9:100169213
|
T | C | 1 | a0001c0001t0013g0082 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.273+42664T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100169213 | ||||||
| chr9:100169297
|
A | G | 1 | a0001c0001t0007g0051 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.273+42748A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100169297 | ||||||
| chr9:100169341
|
T | C | 72 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(69): Show | 72 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.273+42792T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100169341 | ||||||
| chr9:100169913
|
T | G | 1 | a0001c0002t0002g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.273+43364T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100169913 | ||||||
| chr9:100169978
|
A | T | 29 | a0001c0001t0001g0108a0001c0001t0010g0157a0001c0002t0001g0111others(26): Show | 29 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.273+43429A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100169978 | ||||||
| chr9:100170108
|
C | T | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+43559C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100170108 | ||||||
| chr9:100170276
|
G | C | 1 | a0001c0002t0030g0113 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.273+43727G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100170276 | ||||||
| chr9:100170323
|
A | G | 1 | a0001c0002t0009g0169 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.273+43774A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100170323 | ||||||
| chr9:100170393
|
CAAA | C | 116 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(113): Show | 116 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.273+43860_273+4386 others(7): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100170393 | |||||
| chr9:100170564
|
C | CA | 5 | a0001c0001t0001g0004a0001c0001t0001g0108a0001c0002t0001g0112others(2): Show | 5 | HG02886.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.273+44025dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100170564 | |||||
| chr9:100170580
|
TA | T | 5 | a0001c0002t0001g0014a0001c0002t0001g0021a0001c0002t0001g0022others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.273+44037delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100170580 | |||||
| chr9:100170950
|
T | C | 1 | a0001c0002t0001g0133 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.273+44401T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100170950 | ||||||
| chr9:100170999
|
T | G | 1 | a0001c0001t0005g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.273+44450T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100170999 | ||||||
| chr9:100171059
|
G | A | 5 | a0001c0001t0007g0028a0001c0001t0026g0029a0001c0001t0027g0030others(2): Show | 5 | HG02145.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.273+44510G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100171059 | ||||||
| chr9:100171244
|
T | C | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+44695T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100171244 | ||||||
| chr9:100171354
|
T | A | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+44805T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100171354 | ||||||
| chr9:100171365
|
C | CA | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.273+44817dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100171365 | |||||
| chr9:100171385
|
T | G | 2 | a0001c0001t0024g0182a0006c0007t0011g0181 | 2 | HG01081.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.273+44836T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100171385 | ||||||
| chr9:100171654
|
A | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.273+45105A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100171654 | ||||||
| chr9:100171829
|
T | A | 118 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(115): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.273+45280T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100171829 | ||||||
| chr9:100171902
|
C | T | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.273+45353C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100171902 | ||||||
| chr9:100172008
|
T | G | 121 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(118): Show | 121 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.273+45459T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100172008 | ||||||
| chr9:100172498
|
A | G | 37 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(34): Show | 37 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.273+45949A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100172498 | ||||||
| chr9:100172838
|
G | C | 120 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(117): Show | 120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.273+46289G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100172838 | ||||||
| chr9:100173170
|
G | C | 1 | a0001c0002t0001g0024 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.273+46621G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100173170 | ||||||
| chr9:100173301
|
C | T | 2 | a0001c0001t0004g0056a0001c0001t0004g0062 | 2 | HG02080.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.273+46752C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100173301 | ||||||
| chr9:100173460
|
G | A | 1 | a0001c0002t0002g0154 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.273+46911G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100173460 | ||||||
| chr9:100173544
|
A | G | 2 | a0001c0002t0002g0153a0001c0002t0002g0158 | 2 | HG02602.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.273+46995A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100173544 | ||||||
| chr9:100173557
|
G | A | 4 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(1): Show | 4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+47008G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100173557 | ||||||
| chr9:100173687
|
T | C | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+47138T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100173687 | ||||||
| chr9:100173867
|
G | A | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+47318G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100173867 | ||||||
| chr9:100173888
|
T | C | 1 | a0001c0001t0016g0027 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.273+47339T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100173888 | ||||||
| chr9:100174100
|
A | C | 4 | a0001c0001t0010g0157a0001c0002t0001g0167a0001c0002t0008g0166others(1): Show | 4 | HG00423.hp1 HG00544.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+47551A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100174100 | ||||||
| chr9:100174223
|
C | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.273+47674C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100174223 | ||||||
| chr9:100174593
|
C | T | 1 | a0001c0001t0003g0087 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.273+48044C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100174593 | ||||||
| chr9:100174895
|
G | C | 4 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0013g0082others(1): Show | 4 | HG01106.hp1 HG02602.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+48346G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100174895 | ||||||
| chr9:100175251
|
T | C | 42 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(39): Show | 42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.273+48702T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100175251 | ||||||
| chr9:100175287
|
C | G | 1 | a0001c0002t0002g0151 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.273+48738C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100175287 | ||||||
| chr9:100175575
|
C | G | 2 | a0001c0001t0024g0182a0006c0007t0011g0181 | 2 | HG01081.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.273+49026C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100175575 | ||||||
| chr9:100175699
|
C | T | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+49150C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100175699 | ||||||
| chr9:100175925
|
T | G | 4 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(1): Show | 4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+49376T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100175925 | ||||||
| chr9:100175969
|
A | G | 4 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0013g0082others(1): Show | 4 | HG01106.hp1 HG02602.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+49420A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100175969 | ||||||
| chr9:100176392
|
G | C | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.274-49670G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100176392 | ||||||
| chr9:100176455
|
T | C | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.274-49607T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100176455 | ||||||
| chr9:100176569
|
C | T | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.274-49493C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100176569 | ||||||
| chr9:100176705
|
T | C | 1 | a0001c0002t0008g0174 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.274-49357T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100176705 | ||||||
| chr9:100176911
|
G | A | 37 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(34): Show | 37 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.274-49151G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100176911 | ||||||
| chr9:100177038
|
C | T | 2 | a0001c0001t0011g0100a0001c0001t0011g0101 | 2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.274-49024C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100177038 | ||||||
| chr9:100177088
|
C | T | 1 | a0001c0002t0001g0131 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.274-48974C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100177088 | ||||||
| chr9:100177150
|
G | A | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-48912G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100177150 | ||||||
| chr9:100177575
|
G | C | 1 | a0001c0002t0002g0123 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.274-48487G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100177575 | ||||||
| chr9:100177767
|
C | T | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.274-48295C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100177767 | ||||||
| chr9:100178109
|
A | C | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(30): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.274-47953A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100178109 | ||||||
| chr9:100178275
|
T | A | 4 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(1): Show | 4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-47787T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100178275 | ||||||
| chr9:100178293
|
A | C | 77 | a0001c0001t0001g0108a0001c0001t0004g0121a0001c0001t0010g0126others(74): Show | 77 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.274-47769A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100178293 | ||||||
| chr9:100178315
|
G | A | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.274-47747G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100178315 | ||||||
| chr9:100178458
|
C | G | 1 | a0001c0002t0002g0041 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.274-47604C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100178458 | ||||||
| chr9:100178495
|
G | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-47567G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100178495 | ||||||
| chr9:100178702
|
A | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-47360A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100178702 | ||||||
| chr9:100178707
|
A | G | 4 | a0001c0002t0002g0152a0001c0002t0002g0154a0001c0002t0002g0155others(1): Show | 4 | HG00733.hp1 HG01074.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-47355A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100178707 | ||||||
| chr9:100178937
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.274-47125C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100178937 | ||||||
| chr9:100178994
|
G | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-47068G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100178994 | ||||||
| chr9:100179023
|
A | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-47039A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100179023 | ||||||
| chr9:100179128
|
C | A | 2 | a0001c0001t0024g0182a0006c0007t0011g0181 | 2 | HG01081.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.274-46934C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100179128 | ||||||
| chr9:100179176
|
G | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.274-46886G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100179176 | ||||||
| chr9:100179202
|
C | T | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.274-46860C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100179202 | ||||||
| chr9:100179230
|
C | T | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-46832C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100179230 | ||||||
| chr9:100179260
|
A | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-46802A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100179260 | ||||||
| chr9:100179309
|
G | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-46753G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100179309 | ||||||
| chr9:100179437
|
A | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-46625A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100179437 | ||||||
| chr9:100179515
|
T | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-46547T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100179515 | ||||||
| chr9:100179656
|
A | C | 1 | a0001c0002t0001g0129 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.274-46406A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100179656 | ||||||
| chr9:100179687
|
A | C | 1 | a0001c0002t0001g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.274-46375A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100179687 | ||||||
| chr9:100179792
|
C | A | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.274-46270C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100179792 | ||||||
| chr9:100179881
|
A | G | 4 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(1): Show | 4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-46181A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100179881 | ||||||
| chr9:100180203
|
G | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.274-45859G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100180203 | ||||||
| chr9:100180344
|
GT | G | 104 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(101): Show | 104 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.274-45709delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100180344 | |||||
| chr9:100180605
|
A | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-45457A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100180605 | ||||||
| chr9:100180916
|
A | T | 2 | a0001c0001t0003g0176a0001c0001t0003g0177 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.274-45146A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100180916 | ||||||
| chr9:100181057
|
G | T | 3 | a0001c0001t0016g0027a0001c0001t0017g0017a0001c0001t0017g0018 | 3 | HG00642.hp2 HG00738.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.274-45005G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100181057 | ||||||
| chr9:100181375
|
A | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-44687A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100181375 | ||||||
| chr9:100181508
|
A | C | 63 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(60): Show | 63 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.274-44554A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100181508 | ||||||
| chr9:100181560
|
G | A | 1 | a0001c0002t0030g0113 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.274-44502G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100181560 | ||||||
| chr9:100181776
|
G | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-44286G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100181776 | ||||||
| chr9:100181866
|
C | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-44196C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100181866 | ||||||
| chr9:100181953
|
A | G | 2 | a0001c0001t0004g0046a0004c0010t0003g0044 | 2 | HG01496.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.274-44109A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100181953 | ||||||
| chr9:100182114
|
T | C | 1 | a0001c0002t0001g0003 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.274-43948T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100182114 | ||||||
| chr9:100182137
|
C | T | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-43925C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100182137 | ||||||
| chr9:100182233
|
A | T | 1 | a0001c0002t0009g0169 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.274-43829A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100182233 | ||||||
| chr9:100182357
|
A | G | 2 | a0001c0002t0002g0151a0001c0002t0009g0150 | 2 | HG00735.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.274-43705A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100182357 | ||||||
| chr9:100182494
|
C | T | 60 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0048others(57): Show | 60 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.274-43568C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100182494 | ||||||
| chr9:100182574
|
C | T | 40 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(37): Show | 40 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.274-43488C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100182574 | ||||||
| chr9:100182645
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.274-43417G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100182645 | ||||||
| chr9:100182753
|
A | G | 5 | a0001c0002t0001g0141a0001c0002t0001g0142a0001c0002t0001g0161others(2): Show | 5 | HG00642.hp1 HG01175.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-43309A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100182753 | ||||||
| chr9:100182811
|
G | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-43251G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100182811 | ||||||
| chr9:100183017
|
C | G | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.274-43045C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100183017 | ||||||
| chr9:100183248
|
A | G | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.274-42814A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100183248 | ||||||
| chr9:100183720
|
G | A | 2 | a0001c0001t0024g0182a0006c0007t0011g0181 | 2 | HG01081.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.274-42342G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100183720 | ||||||
| chr9:100183794
|
G | GA | 21 | a0001c0001t0003g0042a0001c0001t0003g0088a0001c0001t0004g0058others(18): Show | 21 | HG00735.hp2 HG01106.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.274-42246dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100183794 | |||||
| chr9:100183794
|
GA | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-42246delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100183794 | |||||
| chr9:100183795
|
A | G | 2 | a0001c0001t0003g0176a0001c0001t0003g0177 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.274-42267A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100183795 | ||||||
| chr9:100183852
|
C | G | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-42210C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100183852 | ||||||
| chr9:100183940
|
G | A | 4 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(1): Show | 4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-42122G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100183940 | ||||||
| chr9:100183955
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.274-42107A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100183955 | ||||||
| chr9:100184314
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.274-41748A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100184314 | ||||||
| chr9:100184437
|
C | T | 9 | a0001c0001t0004g0058a0001c0001t0007g0051a0001c0001t0007g0053others(6): Show | 9 | HG02109.hp2 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.274-41625C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100184437 | ||||||
| chr9:100184460
|
T | G | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.274-41602T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100184460 | ||||||
| chr9:100184463
|
G | A | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-41599G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100184463 | ||||||
| chr9:100184520
|
T | C | 1 | a0001c0002t0001g0003 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.274-41542T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100184520 | ||||||
| chr9:100184793
|
A | G | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-41269A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100184793 | ||||||
| chr9:100184842
|
A | G | 1 | a0001c0002t0002g0041 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.274-41220A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100184842 | ||||||
| chr9:100184891
|
C | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-41171C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100184891 | ||||||
| chr9:100185022
|
G | A | 2 | a0001c0001t0003g0042a0001c0001t0003g0087 | 2 | HG01106.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.274-41040G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100185022 | ||||||
| chr9:100185220
|
GATT | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-40832_274-4083 others(7): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185220 | |||||
| chr9:100185474
|
T | G | 1 | a0001c0001t0013g0016 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.274-40588T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100185474 | ||||||
| chr9:100185489
|
A | G | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.274-40573A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100185489 | ||||||
| chr9:100185516
|
A | AAT | 3 | a0001c0002t0002g0124a0001c0002t0002g0137a0001c0002t0008g0174 | 3 | HG00621.hp2 NA18983.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.274-40505_274-4050 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | |||||
| chr9:100185516
|
A | AATAT | 8 | a0001c0001t0010g0126a0001c0001t0010g0127a0001c0002t0001g0106others(5): Show | 8 | HG00733.hp1 HG00733.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.274-40507_274-4050 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | |||||
| chr9:100185516
|
A | AATATAT | 8 | a0001c0002t0001g0112a0001c0002t0001g0116a0001c0002t0001g0133others(5): Show | 8 | HG01069.hp1 HG01975.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.274-40509_274-4050 others(10): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | |||||
| chr9:100185516
|
A | AATATATA others(1): Show |
8 | a0001c0002t0001g0107a0001c0002t0001g0131a0001c0002t0001g0141others(5): Show | 8 | HG00323.hp2 HG00642.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.274-40511_274-4050 others(12): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | |||||
| chr9:100185516
|
A | AATATATA others(3): Show |
10 | a0001c0002t0001g0102a0001c0002t0001g0114a0001c0002t0002g0123others(7): Show | 10 | HG00423.hp1 HG00544.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.274-40513_274-4050 others(14): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | |||||
| chr9:100185516
|
A | AATATATA others(5): Show |
4 | a0001c0002t0001g0171a0001c0002t0002g0041a0001c0002t0002g0155others(1): Show | 4 | HG00140.hp2 HG01109.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-40515_274-4050 others(16): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | |||||
| chr9:100185516
|
A | AATATATA others(7): Show |
1 | a0001c0002t0002g0152 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.274-40517_274-4050 others(18): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | |||||
| chr9:100185516
|
A | AATATATA others(11): Show |
2 | a0001c0002t0002g0120a0001c0002t0002g0158 | 2 | HG03927.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.274-40521_274-4050 others(22): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | |||||
| chr9:100185516
|
AAT | A | 10 | a0001c0001t0001g0108a0001c0002t0001g0128a0001c0002t0001g0129others(7): Show | 10 | HG00280.hp1 HG01168.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.274-40505_274-4050 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | |||||
| chr9:100185516
|
AATAT | A | 3 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0002t0009g0122 | 3 | HG00609.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.274-40507_274-4050 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | |||||
| chr9:100185516
|
AATATATA others(1): Show |
A | 4 | a0001c0001t0016g0011a0001c0001t0024g0182a0001c0002t0001g0022others(1): Show | 4 | HG01081.hp2 HG02109.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-40511_274-4050 others(12): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | |||||
| chr9:100185516
|
AATATATA others(3): Show |
A | 3 | a0001c0001t0005g0013a0001c0001t0029g0008a0001c0002t0001g0023 | 3 | HG02970.hp1 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.274-40513_274-4050 others(14): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | |||||
| chr9:100185516
|
AATATATA others(5): Show |
A | 9 | a0001c0001t0004g0067a0001c0001t0005g0005a0001c0001t0005g0006others(6): Show | 9 | HG02451.hp2 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-40515_274-4050 others(16): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | |||||
| chr9:100185516
|
AATATATA others(7): Show |
A | 19 | a0001c0001t0001g0025a0001c0001t0001g0144a0001c0001t0001g0145others(16): Show | 19 | HG00609.hp1 HG01081.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.274-40517_274-4050 others(18): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | |||||
| chr9:100185516
|
AATATATA others(9): Show |
A | 58 | a0001c0001t0001g0015a0001c0001t0003g0042a0001c0001t0003g0048others(55): Show | 58 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.274-40519_274-4050 others(20): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | |||||
| chr9:100185516
|
AATATATA others(11): Show |
A | 15 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0033others(12): Show | 15 | HG01074.hp1 HG01109.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.274-40521_274-4050 others(22): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | |||||
| chr9:100185516
|
AATATATA others(17): Show |
A | 1 | a0001c0002t0001g0111 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.274-40527_274-4050 others(28): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | |||||
| chr9:100185516
|
AATATATA others(19): Show |
A | 5 | a0001c0001t0010g0157a0001c0002t0001g0140a0001c0002t0001g0143others(2): Show | 5 | HG01071.hp1 HG02559.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-40529_274-4050 others(30): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | |||||
| chr9:100185516
|
AATATATA others(25): Show |
A | 1 | a0001c0002t0002g0138 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.274-40535_274-4050 others(36): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | |||||
| chr9:100185560
|
C | T | 1 | a0001c0001t0004g0056 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.274-40502C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100185560 | ||||||
| chr9:100185695
|
G | A | 1 | a0001c0001t0019g0066 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.274-40367G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100185695 | ||||||
| chr9:100185735
|
A | G | 61 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0048others(58): Show | 61 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.274-40327A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100185735 | ||||||
| chr9:100185774
|
G | T | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.274-40288G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100185774 | ||||||
| chr9:100186186
|
G | A | 63 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(60): Show | 63 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.274-39876G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100186186 | ||||||
| chr9:100186198
|
G | A | 1 | a0001c0002t0001g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.274-39864G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100186198 | ||||||
| chr9:100186384
|
A | C | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-39678A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100186384 | ||||||
| chr9:100186403
|
A | G | 181 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(178): Show | 181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.274-39659A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100186403 | ||||||
| chr9:100186938
|
A | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-39124A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100186938 | ||||||
| chr9:100187004
|
G | A | 62 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(59): Show | 62 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.274-39058G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100187004 | ||||||
| chr9:100187005
|
T | G | 1 | a0001c0001t0004g0069 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.274-39057T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100187005 | ||||||
| chr9:100187078
|
G | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-38984G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100187078 | ||||||
| chr9:100187163
|
T | C | 1 | a0001c0002t0010g0170 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.274-38899T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100187163 | ||||||
| chr9:100187515
|
T | C | 1 | a0001c0002t0002g0173 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.274-38547T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100187515 | ||||||
| chr9:100187525
|
C | CT | 64 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0048others(61): Show | 64 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.274-38518dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100187525 | |||||
| chr9:100187525
|
C | CTTTTTTT others(3): Show |
6 | a0001c0001t0001g0038a0001c0001t0005g0006a0001c0001t0005g0007others(3): Show | 6 | HG01168.hp1 HG02622.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.274-38527_274-3851 others(14): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100187525 | |||||
| chr9:100187525
|
C | CTTTTTTT others(4): Show |
19 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0026others(16): Show | 19 | HG00323.hp1 HG00738.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.274-38528_274-3851 others(15): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100187525 | |||||
| chr9:100187525
|
C | CTTTTTTT others(5): Show |
11 | a0001c0001t0001g0033a0001c0001t0001g0039a0001c0001t0005g0013others(8): Show | 11 | HG00642.hp2 HG01081.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.274-38529_274-3851 others(16): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100187525 | |||||
| chr9:100187525
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0016g0011 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.274-38531_274-3851 others(18): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100187525 | |||||
| chr9:100187712
|
G | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-38350G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100187712 | ||||||
| chr9:100187755
|
A | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-38307A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100187755 | ||||||
| chr9:100188033
|
C | T | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.274-38029C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100188033 | ||||||
| chr9:100188178
|
G | A | 1 | a0001c0002t0009g0132 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.274-37884G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100188178 | ||||||
| chr9:100188255
|
G | A | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-37807G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100188255 | ||||||
| chr9:100188268
|
A | C | 1 | a0001c0001t0016g0027 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.274-37794A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100188268 | ||||||
| chr9:100188307
|
G | A | 1 | a0001c0001t0004g0056 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.274-37755G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100188307 | ||||||
| chr9:100188444
|
T | G | 105 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(102): Show | 105 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.274-37618T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100188444 | ||||||
| chr9:100188635
|
CT | C | 39 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(36): Show | 39 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.274-37411delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100188635 | |||||
| chr9:100188941
|
G | A | 63 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(60): Show | 63 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.274-37121G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100188941 | ||||||
| chr9:100189106
|
C | CT | 28 | a0001c0001t0001g0145a0001c0001t0003g0043a0001c0001t0003g0073others(25): Show | 28 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.274-36935dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100189106 | |||||
| chr9:100189106
|
C | CTTTTTTT | 29 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(26): Show | 29 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.274-36941_274-3693 others(11): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100189106 | |||||
| chr9:100189106
|
CT | C | 11 | a0001c0001t0003g0048a0001c0001t0012g0134a0001c0001t0012g0135others(8): Show | 11 | HG00140.hp1 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.274-36935delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100189106 | |||||
| chr9:100189106
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0002t0008g0166a0001c0002t0008g0168 | 2 | HG00423.hp1 HG00544.hp1 |
intron_variant | MODIFIER | c.274-36944_274-3693 others(14): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100189106 | |||||
| chr9:100189346
|
T | C | 4 | a0001c0001t0001g0108a0001c0002t0001g0112a0001c0004t0001g0109others(1): Show | 4 | HG02886.hp1 HG03225.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-36716T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100189346 | ||||||
| chr9:100189420
|
C | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-36642C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100189420 | ||||||
| chr9:100189422
|
T | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-36640T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100189422 | ||||||
| chr9:100189440
|
T | C | 1 | a0001c0002t0002g0148 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.274-36622T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100189440 | ||||||
| chr9:100189493
|
G | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-36569G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100189493 | ||||||
| chr9:100189777
|
C | T | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-36285C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100189777 | ||||||
| chr9:100190456
|
G | T | 1 | a0001c0001t0001g0144 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.274-35606G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100190456 | ||||||
| chr9:100190484
|
C | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-35578C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100190484 | ||||||
| chr9:100190606
|
T | C | 61 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0048others(58): Show | 61 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.274-35456T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100190606 | ||||||
| chr9:100190649
|
T | C | 1 | a0001c0002t0008g0174 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.274-35413T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100190649 | ||||||
| chr9:100190674
|
G | A | 1 | a0001c0002t0002g0120 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.274-35388G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100190674 | ||||||
| chr9:100191044
|
A | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-35018A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100191044 | ||||||
| chr9:100191110
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.274-34952C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100191110 | ||||||
| chr9:100191113
|
G | A | 3 | a0001c0002t0001g0167a0001c0002t0008g0166a0001c0002t0008g0168 | 3 | HG00423.hp1 HG00544.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.274-34949G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100191113 | ||||||
| chr9:100191719
|
A | G | 3 | a0001c0001t0003g0083a0001c0001t0004g0070a0001c0001t0004g0075 | 3 | HG00544.hp2 HG02083.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.274-34343A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100191719 | ||||||
| chr9:100192248
|
A | AGT | 28 | a0001c0001t0003g0042a0001c0001t0003g0087a0001c0001t0003g0092others(25): Show | 28 | HG00280.hp1 HG00642.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.274-33779_274-3377 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100192248 | |||||
| chr9:100192248
|
A | AGTGT | 33 | a0001c0001t0003g0043a0001c0001t0003g0048a0001c0001t0003g0073others(30): Show | 33 | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.274-33781_274-3377 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100192248 | |||||
| chr9:100192248
|
A | AGTGTGT | 15 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0040others(12): Show | 15 | HG00280.hp2 HG00423.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.274-33783_274-3377 others(10): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100192248 | |||||
| chr9:100192248
|
A | AGTGTGTG others(1): Show |
21 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0026others(18): Show | 21 | HG00741.hp2 HG01109.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.274-33785_274-3377 others(12): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100192248 | |||||
| chr9:100192248
|
A | AGTGTGTG others(3): Show |
9 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0039others(6): Show | 9 | HG00323.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-33787_274-3377 others(14): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100192248 | |||||
| chr9:100192248
|
AGT | A | 3 | a0001c0002t0001g0021a0001c0002t0008g0105a0004c0010t0003g0044 | 3 | HG01496.hp2 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.274-33779_274-3377 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100192248 | |||||
| chr9:100192248
|
AGTGT | A | 5 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0002t0001g0102others(2): Show | 5 | HG01081.hp1 HG01243.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-33781_274-3377 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100192248 | |||||
| chr9:100192407
|
G | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-33655G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100192407 | ||||||
| chr9:100192814
|
A | C | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-33248A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100192814 | ||||||
| chr9:100192830
|
T | A | 1 | a0001c0001t0001g0004 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.274-33232T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100192830 | ||||||
| chr9:100192956
|
A | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-33106A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100192956 | ||||||
| chr9:100192978
|
C | CTT | 35 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(32): Show | 35 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.274-33069_274-3306 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100192978 | |||||
| chr9:100193081
|
A | T | 1 | a0001c0001t0010g0157 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.274-32981A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100193081 | ||||||
| chr9:100193305
|
A | T | 4 | a0001c0001t0001g0108a0001c0002t0001g0112a0001c0004t0001g0109others(1): Show | 4 | HG02886.hp1 HG03225.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-32757A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100193305 | ||||||
| chr9:100193307
|
A | G | 4 | a0001c0001t0014g0076a0001c0001t0014g0080a0001c0001t0014g0081others(1): Show | 4 | HG00423.hp2 HG00621.hp1 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-32755A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100193307 | ||||||
| chr9:100193776
|
A | G | 62 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(59): Show | 62 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.274-32286A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100193776 | ||||||
| chr9:100193931
|
A | C | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-32131A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100193931 | ||||||
| chr9:100194109
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.274-31953G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100194109 | ||||||
| chr9:100194116
|
T | A | 1 | a0001c0002t0001g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.274-31946T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100194116 | ||||||
| chr9:100194453
|
T | C | 2 | a0001c0002t0002g0123a0001c0002t0002g0124 | 2 | NA19082.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.274-31609T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100194453 | ||||||
| chr9:100194475
|
ATCGTCTT others(10): Show |
A | 2 | a0001c0002t0008g0166a0001c0002t0008g0168 | 2 | HG00423.hp1 HG00544.hp1 |
intron_variant | MODIFIER | c.274-31585_274-3156 others(21): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100194475 | |||||
| chr9:100194503
|
GT | G | 68 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(65): Show | 68 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.274-31549delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100194503 | |||||
| chr9:100194505
|
T | G | 7 | a0001c0001t0004g0049a0001c0001t0004g0050a0001c0001t0004g0054others(4): Show | 7 | HG00280.hp2 HG02080.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.274-31557T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100194505 | ||||||
| chr9:100194616
|
G | C | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.274-31446G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100194616 | ||||||
| chr9:100194964
|
C | G | 1 | a0001c0001t0016g0011 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.274-31098C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100194964 | ||||||
| chr9:100194987
|
C | T | 2 | a0001c0002t0001g0133a0001c0002t0001g0172 | 2 | HG02976.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.274-31075C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100194987 | ||||||
| chr9:100195251
|
C | T | 1 | a0001c0002t0002g0154 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.274-30811C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100195251 | ||||||
| chr9:100195423
|
A | C | 107 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(104): Show | 107 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.274-30639A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100195423 | ||||||
| chr9:100195493
|
A | AT | 106 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(103): Show | 106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.274-30558dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100195493 | |||||
| chr9:100195542
|
C | T | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.274-30520C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100195542 | ||||||
| chr9:100195557
|
G | A | 11 | a0001c0002t0002g0103a0001c0002t0002g0117a0001c0002t0002g0118others(8): Show | 11 | HG00609.hp2 HG01192.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.274-30505G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100195557 | ||||||
| chr9:100195601
|
G | C | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-30461G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100195601 | ||||||
| chr9:100195708
|
G | A | 61 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0048others(58): Show | 61 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.274-30354G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100195708 | ||||||
| chr9:100195725
|
T | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.274-30337T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100195725 | ||||||
| chr9:100195824
|
A | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-30238A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100195824 | ||||||
| chr9:100195886
|
A | T | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.274-30176A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100195886 | ||||||
| chr9:100195957
|
G | T | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.274-30105G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100195957 | ||||||
| chr9:100195962
|
G | A | 9 | a0001c0001t0004g0058a0001c0001t0007g0051a0001c0001t0007g0053others(6): Show | 9 | HG02109.hp2 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.274-30100G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100195962 | ||||||
| chr9:100195970
|
A | G | 4 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(1): Show | 4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-30092A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100195970 | ||||||
| chr9:100196317
|
G | A | 158 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(155): Show | 158 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.274-29745G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100196317 | ||||||
| chr9:100196454
|
G | A | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(30): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.274-29608G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100196454 | ||||||
| chr9:100196888
|
GT | G | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-29167delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100196888 | |||||
| chr9:100197093
|
G | A | 1 | a0001c0002t0001g0102 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.274-28969G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100197093 | ||||||
| chr9:100197587
|
C | G | 61 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0048others(58): Show | 61 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.274-28475C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100197587 | ||||||
| chr9:100197636
|
A | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-28426A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100197636 | ||||||
| chr9:100197715
|
G | T | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.274-28347G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100197715 | ||||||
| chr9:100197791
|
G | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-28271G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100197791 | ||||||
| chr9:100197817
|
G | C | 2 | a0001c0002t0018g0146a0001c0002t0018g0149 | 2 | HG01516.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.274-28245G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100197817 | ||||||
| chr9:100197969
|
C | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-28093C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100197969 | ||||||
| chr9:100198244
|
T | C | 1 | a0001c0001t0001g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.274-27818T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100198244 | ||||||
| chr9:100198264
|
A | AT | 5 | a0001c0001t0001g0026a0001c0002t0001g0161a0001c0002t0001g0172others(2): Show | 5 | HG01952.hp1 HG03471.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-27747dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | |||||
| chr9:100198264
|
A | ATTTTTTT others(7): Show |
1 | a0001c0002t0001g0171 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.274-27760_274-2774 others(18): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | |||||
| chr9:100198264
|
AT | A | 7 | a0001c0001t0011g0100a0001c0002t0001g0114a0001c0002t0001g0128others(4): Show | 7 | HG00280.hp1 HG00741.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.274-27747delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | |||||
| chr9:100198264
|
ATTTT | A | 7 | a0001c0001t0001g0036a0001c0002t0002g0103a0001c0002t0002g0152others(4): Show | 7 | HG00323.hp2 HG01074.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.274-27750_274-2774 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | |||||
| chr9:100198264
|
ATTTTT | A | 15 | a0001c0001t0007g0028a0001c0001t0010g0127a0001c0001t0027g0030others(12): Show | 15 | HG00733.hp1 HG01167.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.274-27751_274-2774 others(9): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | |||||
| chr9:100198264
|
ATTTTTT | A | 15 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0039others(12): Show | 15 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.274-27752_274-2774 others(10): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | |||||
| chr9:100198264
|
ATTTTTTT | A | 11 | a0001c0001t0001g0025a0001c0001t0001g0033a0001c0001t0001g0035others(8): Show | 11 | HG00735.hp2 HG01109.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.274-27753_274-2774 others(11): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | |||||
| chr9:100198264
|
ATTTTTTT others(1): Show |
A | 7 | a0001c0001t0001g0037a0001c0001t0015g0019a0001c0001t0017g0018others(4): Show | 7 | HG00738.hp2 HG01168.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.274-27754_274-2774 others(12): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | |||||
| chr9:100198264
|
ATTTTTTT others(6): Show |
A | 1 | a0001c0002t0001g0167 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.274-27759_274-2774 others(17): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | |||||
| chr9:100198264
|
ATTTTTTT others(8): Show |
A | 7 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(4): Show | 7 | HG00140.hp2 HG00733.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.274-27761_274-2774 others(19): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | |||||
| chr9:100198264
|
ATTTTTTT others(11): Show |
A | 1 | a0001c0002t0002g0137 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.274-27764_274-2774 others(22): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | |||||
| chr9:100198264
|
ATTTTTTT others(13): Show |
A | 2 | a0001c0001t0024g0182a0001c0002t0001g0107 | 2 | HG01081.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.274-27766_274-2774 others(24): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | |||||
| chr9:100198264
|
ATTTTTTT others(14): Show |
A | 5 | a0001c0001t0001g0145a0001c0002t0001g0102a0001c0002t0001g0106others(2): Show | 5 | HG01243.hp2 HG02886.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-27767_274-2774 others(25): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | |||||
| chr9:100198264
|
ATTTTTTT others(15): Show |
A | 2 | a0001c0001t0001g0144a0001c0002t0002g0119 | 2 | HG01081.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.274-27768_274-2774 others(26): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | |||||
| chr9:100198264
|
ATTTTTTT others(17): Show |
A | 11 | a0001c0001t0003g0042a0001c0001t0003g0087a0001c0001t0003g0092others(8): Show | 11 | HG01106.hp1 HG01106.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.274-27770_274-2774 others(28): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | |||||
| chr9:100198264
|
ATTTTTTT others(18): Show |
A | 51 | a0001c0001t0003g0043a0001c0001t0003g0048a0001c0001t0003g0073others(48): Show | 51 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.274-27771_274-2774 others(29): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | |||||
| chr9:100198264
|
ATTTTTTT others(19): Show |
A | 1 | a0001c0001t0013g0016 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.274-27772_274-2774 others(30): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | |||||
| chr9:100198264
|
ATTTTTTT others(20): Show |
A | 8 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(5): Show | 8 | HG00741.hp2 HG02451.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.274-27773_274-2774 others(31): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | |||||
| chr9:100198264
|
ATTTTTTT others(21): Show |
A | 1 | a0001c0002t0002g0158 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.274-27774_274-2774 others(32): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | |||||
| chr9:100198591
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.274-27471C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100198591 | ||||||
| chr9:100198713
|
C | G | 1 | a0001c0002t0002g0137 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.274-27349C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100198713 | ||||||
| chr9:100198718
|
G | A | 2 | a0001c0001t0011g0100a0001c0001t0011g0101 | 2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.274-27344G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100198718 | ||||||
| chr9:100198724
|
C | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-27338C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100198724 | ||||||
| chr9:100198803
|
G | C | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.274-27259G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100198803 | ||||||
| chr9:100198833
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.274-27229C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100198833 | ||||||
| chr9:100199389
|
G | T | 1 | a0001c0001t0007g0028 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.274-26673G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100199389 | ||||||
| chr9:100199434
|
T | C | 1 | a0001c0002t0002g0119 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.274-26628T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100199434 | ||||||
| chr9:100199656
|
C | T | 1 | a0001c0002t0002g0175 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.274-26406C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100199656 | ||||||
| chr9:100199657
|
G | A | 1 | a0001c0002t0001g0143 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.274-26405G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100199657 | ||||||
| chr9:100199662
|
C | T | 1 | a0001c0002t0001g0130 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.274-26400C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100199662 | ||||||
| chr9:100199678
|
A | G | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.274-26384A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100199678 | ||||||
| chr9:100199830
|
T | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-26232T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100199830 | ||||||
| chr9:100199830
|
T | G | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.274-26232T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100199830 | ||||||
| chr9:100199859
|
C | T | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.274-26203C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100199859 | ||||||
| chr9:100200136
|
A | G | 1 | a0001c0001t0003g0043 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.274-25926A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100200136 | ||||||
| chr9:100200299
|
G | T | 1 | a0001c0002t0002g0119 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.274-25763G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100200299 | ||||||
| chr9:100200347
|
G | A | 2 | a0001c0001t0001g0035a0001c0001t0008g0034 | 2 | HG02055.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.274-25715G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100200347 | ||||||
| chr9:100200545
|
A | C | 1 | a0002c0003t0006g0084 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.274-25517A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100200545 | ||||||
| chr9:100200585
|
G | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-25477G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100200585 | ||||||
| chr9:100201196
|
C | T | 1 | a0001c0001t0004g0075 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.274-24866C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100201196 | ||||||
| chr9:100201379
|
T | C | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-24683T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100201379 | ||||||
| chr9:100201547
|
T | G | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-24515T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100201547 | ||||||
| chr9:100201865
|
C | T | 1 | a0001c0001t0003g0073 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.274-24197C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100201865 | ||||||
| chr9:100201958
|
G | A | 2 | a0001c0002t0001g0133a0001c0002t0001g0172 | 2 | HG02976.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.274-24104G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100201958 | ||||||
| chr9:100202086
|
A | G | 2 | a0001c0001t0015g0019a0001c0001t0015g0020 | 2 | HG00741.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.274-23976A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100202086 | ||||||
| chr9:100202092
|
G | GT | 100 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(97): Show | 100 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.274-23957dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100202092 | |||||
| chr9:100202624
|
C | T | 1 | a0001c0001t0003g0088 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.274-23438C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100202624 | ||||||
| chr9:100203100
|
G | A | 34 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(31): Show | 34 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.274-22962G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100203100 | ||||||
| chr9:100203341
|
C | T | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.274-22721C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100203341 | ||||||
| chr9:100203501
|
C | CT | 68 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(65): Show | 68 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.274-22542dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100203501 | |||||
| chr9:100203501
|
C | CTTT | 28 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(25): Show | 28 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.274-22544_274-2254 others(7): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100203501 | |||||
| chr9:100203501
|
C | CTTTT | 6 | a0001c0001t0007g0028a0001c0001t0026g0029a0001c0001t0027g0030others(3): Show | 6 | HG02145.hp2 HG02717.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.274-22545_274-2254 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100203501 | |||||
| chr9:100203521
|
G | T | 27 | a0001c0001t0003g0043a0001c0001t0003g0073a0001c0001t0003g0083others(24): Show | 27 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.274-22541G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100203521 | ||||||
| chr9:100203662
|
G | A | 34 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(31): Show | 34 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.274-22400G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100203662 | ||||||
| chr9:100203774
|
C | T | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-22288C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100203774 | ||||||
| chr9:100203785
|
C | G | 1 | a0001c0001t0011g0100 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.274-22277C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100203785 | ||||||
| chr9:100203819
|
A | G | 2 | a0001c0001t0003g0042a0001c0001t0003g0087 | 2 | HG01106.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.274-22243A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100203819 | ||||||
| chr9:100203841
|
C | T | 2 | a0001c0001t0003g0092a0001c0001t0003g0093 | 2 | HG01243.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.274-22221C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100203841 | ||||||
| chr9:100203988
|
A | G | 63 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(60): Show | 63 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.274-22074A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100203988 | ||||||
| chr9:100204029
|
A | G | 4 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(1): Show | 4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-22033A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100204029 | ||||||
| chr9:100204083
|
A | G | 1 | a0001c0001t0013g0078 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.274-21979A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100204083 | ||||||
| chr9:100204104
|
A | T | 3 | a0001c0001t0007g0028a0001c0001t0026g0029a0001c0001t0027g0030 | 3 | HG02145.hp2 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.274-21958A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100204104 | ||||||
| chr9:100204681
|
G | C | 1 | a0001c0001t0007g0063 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.274-21381G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100204681 | ||||||
| chr9:100204744
|
A | C | 4 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(1): Show | 4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-21318A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100204744 | ||||||
| chr9:100204786
|
A | G | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-21276A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100204786 | ||||||
| chr9:100204938
|
G | A | 2 | a0001c0001t0004g0046a0004c0010t0003g0044 | 2 | HG01496.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.274-21124G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100204938 | ||||||
| chr9:100205093
|
CTG | C | 2 | a0001c0001t0005g0012a0001c0001t0005g0013 | 2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.274-20966_274-2096 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100205093 | |||||
| chr9:100205159
|
T | C | 2 | a0001c0001t0007g0028a0001c0001t0026g0029 | 2 | HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.274-20903T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100205159 | ||||||
| chr9:100205310
|
A | T | 1 | a0001c0002t0001g0003 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.274-20752A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100205310 | ||||||
| chr9:100205491
|
CAGTT | C | 5 | a0001c0001t0001g0108a0001c0002t0001g0102a0001c0002t0001g0106others(2): Show | 5 | HG02622.hp1 HG02886.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-20569_274-2056 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100205491 | |||||
| chr9:100205611
|
G | T | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.274-20451G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100205611 | ||||||
| chr9:100205721
|
C | T | 42 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(39): Show | 42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.274-20341C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100205721 | ||||||
| chr9:100206031
|
A | G | 6 | a0001c0001t0013g0016a0001c0001t0015g0019a0001c0001t0015g0020others(3): Show | 6 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.274-20031A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100206031 | ||||||
| chr9:100206112
|
C | T | 1 | a0001c0001t0003g0042 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.274-19950C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100206112 | ||||||
| chr9:100206240
|
G | A | 1 | a0001c0002t0002g0152 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.274-19822G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100206240 | ||||||
| chr9:100206341
|
T | C | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(30): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.274-19721T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100206341 | ||||||
| chr9:100206430
|
C | T | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-19632C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100206430 | ||||||
| chr9:100206468
|
C | T | 1 | a0001c0002t0009g0132 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.274-19594C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100206468 | ||||||
| chr9:100206524
|
T | A | 9 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0012g0134others(6): Show | 9 | HG01081.hp2 HG02280.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-19538T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100206524 | ||||||
| chr9:100206565
|
G | T | 5 | a0001c0001t0004g0064a0001c0001t0004g0065a0001c0001t0004g0067others(2): Show | 5 | HG00609.hp1 HG02056.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-19497G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100206565 | ||||||
| chr9:100207177
|
A | AC | 42 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(39): Show | 42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.274-18883dupC | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100207177 | |||||
| chr9:100207180
|
G | A | 1 | a0001c0001t0014g0076 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.274-18882G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100207180 | ||||||
| chr9:100207180
|
G | C | 42 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(39): Show | 42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.274-18882G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100207180 | ||||||
| chr9:100207280
|
A | AT | 4 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0013g0082others(1): Show | 4 | HG01106.hp1 HG02602.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-18776dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100207280 | |||||
| chr9:100207577
|
C | T | 42 | a0001c0001t0004g0121a0001c0001t0010g0126a0001c0001t0010g0127others(39): Show | 42 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.274-18485C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100207577 | ||||||
| chr9:100207650
|
A | C | 1 | a0001c0001t0001g0039 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.274-18412A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100207650 | ||||||
| chr9:100207650
|
A | T | 41 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(38): Show | 41 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.274-18412A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100207650 | ||||||
| chr9:100207971
|
GATTAC | G | 6 | a0001c0001t0013g0016a0001c0001t0015g0019a0001c0001t0015g0020others(3): Show | 6 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.274-18089_274-1808 others(9): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100207971 | |||||
| chr9:100207976
|
C | G | 36 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(33): Show | 36 | HG01081.hp2 HG01109.hp1 HG02055.hp1 others(33): Show |
intron_variant | MODIFIER | c.274-18086C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100207976 | ||||||
| chr9:100208031
|
T | TG | 4 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(1): Show | 4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-18030dupG | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100208031 | |||||
| chr9:100208080
|
A | G | 1 | a0001c0001t0017g0018 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.274-17982A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100208080 | ||||||
| chr9:100208169
|
A | G | 42 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(39): Show | 42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.274-17893A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100208169 | ||||||
| chr9:100208484
|
G | T | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-17578G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100208484 | ||||||
| chr9:100208830
|
T | C | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(30): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.274-17232T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100208830 | ||||||
| chr9:100209508
|
T | C | 5 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-16554T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100209508 | ||||||
| chr9:100209769
|
C | CA | 7 | a0001c0001t0010g0157a0001c0002t0001g0161a0001c0002t0001g0163others(4): Show | 7 | HG00423.hp1 HG01109.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.274-16267dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100209769 | |||||
| chr9:100209769
|
CA | C | 90 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0043others(87): Show | 90 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.274-16267delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100209769 | |||||
| chr9:100209769
|
CAAAAA | C | 29 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(26): Show | 29 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.274-16271_274-1626 others(9): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100209769 | |||||
| chr9:100209769
|
CAAAAAA | C | 12 | a0001c0001t0007g0028a0001c0001t0008g0032a0001c0001t0011g0100others(9): Show | 12 | HG00323.hp1 HG01081.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.274-16272_274-1626 others(10): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100209769 | |||||
| chr9:100209808
|
G | A | 42 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(39): Show | 42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.274-16254G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100209808 | ||||||
| chr9:100209908
|
G | A | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-16154G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100209908 | ||||||
| chr9:100210035
|
A | G | 1 | a0001c0001t0003g0048 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.274-16027A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100210035 | ||||||
| chr9:100210054
|
C | G | 61 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(58): Show | 61 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.274-16008C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100210054 | ||||||
| chr9:100210061
|
T | G | 4 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(1): Show | 4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-16001T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100210061 | ||||||
| chr9:100210355
|
G | A | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-15707G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100210355 | ||||||
| chr9:100210426
|
A | G | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.274-15636A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100210426 | ||||||
| chr9:100210719
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.274-15343C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100210719 | ||||||
| chr9:100210779
|
A | G | 1 | a0001c0001t0004g0069 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.274-15283A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100210779 | ||||||
| chr9:100210834
|
C | G | 1 | a0001c0001t0001g0039 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.274-15228C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100210834 | ||||||
| chr9:100211096
|
C | T | 2 | a0001c0004t0001g0109a0001c0004t0001g0110 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.274-14966C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100211096 | ||||||
| chr9:100211437
|
C | A | 103 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(100): Show | 103 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.274-14625C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100211437 | ||||||
| chr9:100211638
|
T | C | 1 | a0001c0001t0008g0034 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.274-14424T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100211638 | ||||||
| chr9:100211716
|
A | G | 2 | a0001c0001t0003g0083a0001c0001t0004g0070 | 2 | HG02083.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.274-14346A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100211716 | ||||||
| chr9:100212455
|
CTCT | C | 5 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-13603_274-1360 others(7): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100212455 | |||||
| chr9:100212465
|
G | C | 42 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(39): Show | 42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.274-13597G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100212465 | ||||||
| chr9:100212745
|
C | T | 5 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-13317C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100212745 | ||||||
| chr9:100213037
|
T | C | 5 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-13025T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100213037 | ||||||
| chr9:100213116
|
G | A | 2 | a0001c0002t0002g0151a0001c0002t0009g0150 | 2 | HG00735.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.274-12946G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100213116 | ||||||
| chr9:100213200
|
T | TG | 62 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(59): Show | 62 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.274-12855dupG | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100213200 | |||||
| chr9:100213378
|
T | C | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(30): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.274-12684T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100213378 | ||||||
| chr9:100213637
|
C | G | 42 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(39): Show | 42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.274-12425C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100213637 | ||||||
| chr9:100213692
|
C | T | 9 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0012g0134others(6): Show | 9 | HG01081.hp2 HG02280.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-12370C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100213692 | ||||||
| chr9:100213720
|
C | T | 9 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0012g0134others(6): Show | 9 | HG01081.hp2 HG02280.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-12342C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100213720 | ||||||
| chr9:100213814
|
A | C | 9 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0012g0134others(6): Show | 9 | HG01081.hp2 HG02280.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-12248A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100213814 | ||||||
| chr9:100213886
|
A | G | 9 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0012g0134others(6): Show | 9 | HG01081.hp2 HG02280.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-12176A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100213886 | ||||||
| chr9:100214089
|
G | T | 42 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(39): Show | 42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.274-11973G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100214089 | ||||||
| chr9:100214135
|
A | T | 59 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0048others(56): Show | 59 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.274-11927A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100214135 | ||||||
| chr9:100214259
|
T | C | 42 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(39): Show | 42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.274-11803T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100214259 | ||||||
| chr9:100214271
|
A | C | 9 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.274-11791A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100214271 | ||||||
| chr9:100214362
|
G | A | 101 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(98): Show | 101 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.274-11700G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100214362 | ||||||
| chr9:100214541
|
T | C | 1 | a0001c0002t0025g0165 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.274-11521T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100214541 | ||||||
| chr9:100214568
|
A | C | 9 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0012g0134others(6): Show | 9 | HG01081.hp2 HG02280.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-11494A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100214568 | ||||||
| chr9:100214846
|
C | G | 9 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0012g0134others(6): Show | 9 | HG01081.hp2 HG02280.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-11216C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100214846 | ||||||
| chr9:100215013
|
C | T | 28 | a0001c0001t0004g0121a0001c0001t0010g0126a0001c0001t0010g0127others(25): Show | 28 | HG00609.hp2 HG00621.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.274-11049C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100215013 | ||||||
| chr9:100215179
|
T | C | 1 | a0001c0001t0008g0034 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.274-10883T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100215179 | ||||||
| chr9:100215645
|
A | G | 1 | a0001c0002t0002g0158 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.274-10417A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100215645 | ||||||
| chr9:100215791
|
G | A | 5 | a0001c0001t0007g0028a0001c0001t0026g0029a0001c0001t0027g0030others(2): Show | 5 | HG02145.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-10271G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100215791 | ||||||
| chr9:100216115
|
A | G | 1 | a0001c0001t0004g0075 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.274-9947A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100216115 | ||||||
| chr9:100216329
|
AC | A | 4 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(1): Show | 4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-9731delC | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100216329 | |||||
| chr9:100216358
|
G | C | 1 | a0001c0002t0002g0158 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.274-9704G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100216358 | ||||||
| chr9:100216374
|
C | T | 9 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(6): Show | 9 | HG02280.hp2 HG02451.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-9688C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100216374 | ||||||
| chr9:100216452
|
G | A | 4 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(1): Show | 4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-9610G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100216452 | ||||||
| chr9:100216752
|
C | T | 62 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(59): Show | 62 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.274-9310C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100216752 | ||||||
| chr9:100216766
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.274-9296C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100216766 | ||||||
| chr9:100216962
|
A | G | 104 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(101): Show | 104 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.274-9100A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100216962 | ||||||
| chr9:100217016
|
T | C | 62 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(59): Show | 62 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.274-9046T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100217016 | ||||||
| chr9:100217064
|
G | A | 1 | a0001c0001t0007g0063 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.274-8998G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100217064 | ||||||
| chr9:100217230
|
A | G | 3 | a0001c0001t0004g0071a0001c0001t0004g0072a0001c0001t0004g0121 | 3 | NA19005.hp1 NA19012.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.274-8832A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100217230 | ||||||
| chr9:100217274
|
A | G | 9 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.274-8788A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100217274 | ||||||
| chr9:100217447
|
C | T | 42 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(39): Show | 42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.274-8615C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100217447 | ||||||
| chr9:100217632
|
C | T | 5 | a0001c0001t0004g0064a0001c0001t0004g0065a0001c0001t0004g0067others(2): Show | 5 | HG00609.hp1 HG02056.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-8430C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100217632 | ||||||
| chr9:100217836
|
C | T | 1 | a0001c0002t0002g0125 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.274-8226C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100217836 | ||||||
| chr9:100217918
|
G | A | 1 | a0001c0002t0001g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.274-8144G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100217918 | ||||||
| chr9:100218077
|
A | G | 2 | a0001c0001t0004g0071a0001c0001t0004g0072 | 2 | NA19012.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.274-7985A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100218077 | ||||||
| chr9:100218387
|
C | T | 103 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(100): Show | 103 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.274-7675C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100218387 | ||||||
| chr9:100218391
|
G | A | 9 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0012g0134others(6): Show | 9 | HG01081.hp2 HG02280.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-7671G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100218391 | ||||||
| chr9:100218550
|
C | G | 2 | a0001c0001t0011g0100a0001c0001t0011g0101 | 2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.274-7512C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100218550 | ||||||
| chr9:100218985
|
A | G | 42 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(39): Show | 42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.274-7077A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100218985 | ||||||
| chr9:100219266
|
G | A | 42 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(39): Show | 42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.274-6796G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100219266 | ||||||
| chr9:100219274
|
A | G | 42 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(39): Show | 42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.274-6788A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100219274 | ||||||
| chr9:100219290
|
T | C | 60 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0048others(57): Show | 60 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.274-6772T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100219290 | ||||||
| chr9:100219881
|
G | GATATATA others(23): Show |
1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.274-6163_274-6162i others(32): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100219881 | |||||
| chr9:100219881
|
GATATATA others(1): Show |
G | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(30): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.274-6170_274-6163d others(10): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100219881 | |||||
| chr9:100220136
|
T | A | 64 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(61): Show | 64 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.274-5926T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100220136 | ||||||
| chr9:100220137
|
T | A | 105 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(102): Show | 105 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.274-5925T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100220137 | ||||||
| chr9:100220421
|
T | G | 1 | a0001c0001t0004g0050 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.274-5641T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100220421 | ||||||
| chr9:100220598
|
T | G | 1 | a0001c0001t0001g0015 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.274-5464T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100220598 | ||||||
| chr9:100220783
|
G | T | 1 | a0001c0002t0001g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.274-5279G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100220783 | ||||||
| chr9:100220803
|
C | T | 1 | a0001c0001t0011g0100 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.274-5259C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100220803 | ||||||
| chr9:100220814
|
T | A | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.274-5248T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100220814 | ||||||
| chr9:100220974
|
C | CA | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-5074dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100220974 | |||||
| chr9:100220974
|
C | CAA | 58 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0048others(55): Show | 58 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.274-5075_274-5074d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100220974 | |||||
| chr9:100220974
|
C | CAAA | 7 | a0001c0001t0004g0056a0001c0001t0012g0134a0001c0001t0012g0135others(4): Show | 7 | HG01175.hp1 HG02280.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.274-5076_274-5074d others(5): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100220974 | |||||
| chr9:100221047
|
A | G | 5 | a0001c0001t0007g0028a0001c0001t0026g0029a0001c0001t0027g0030others(2): Show | 5 | HG02145.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-5015A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100221047 | ||||||
| chr9:100221052
|
A | G | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(30): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.274-5010A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100221052 | ||||||
| chr9:100221305
|
A | AT | 67 | a0001c0001t0001g0015a0001c0001t0003g0042a0001c0001t0003g0043others(64): Show | 67 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.274-4741dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100221305 | |||||
| chr9:100221305
|
A | ATT | 30 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0026others(27): Show | 30 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.274-4742_274-4741d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100221305 | |||||
| chr9:100221399
|
C | G | 1 | a0001c0002t0008g0174 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.274-4663C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100221399 | ||||||
| chr9:100221588
|
C | CCTTATCA others(9): Show |
38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-4472_274-4471i others(18): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100221588 | |||||
| chr9:100221621
|
G | T | 1 | a0001c0001t0001g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.274-4441G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100221621 | ||||||
| chr9:100221762
|
G | A | 5 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-4300G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100221762 | ||||||
| chr9:100221934
|
GA | G | 5 | a0001c0001t0004g0050a0001c0001t0004g0054a0001c0001t0004g0055others(2): Show | 5 | HG00280.hp2 HG02080.hp2 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-4121delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100221934 | |||||
| chr9:100221937
|
A | C | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(30): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.274-4125A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100221937 | ||||||
| chr9:100221981
|
A | C | 1 | a0001c0001t0004g0049 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.274-4081A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100221981 | ||||||
| chr9:100222302
|
A | G | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(30): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.274-3760A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100222302 | ||||||
| chr9:100222475
|
T | C | 5 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-3587T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100222475 | ||||||
| chr9:100222605
|
G | A | 5 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-3457G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100222605 | ||||||
| chr9:100222685
|
G | A | 104 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(101): Show | 104 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.274-3377G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100222685 | ||||||
| chr9:100222730
|
C | T | 5 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-3332C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100222730 | ||||||
| chr9:100222819
|
CT | C | 19 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(16): Show | 19 | HG01109.hp1 HG02055.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.274-3226delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100222819 | |||||
| chr9:100223020
|
G | C | 5 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-3042G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100223020 | ||||||
| chr9:100223078
|
CATTT | C | 2 | a0001c0001t0001g0033a0001c0001t0001g0037 | 2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.274-2967_274-2964d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100223078 | |||||
| chr9:100223088
|
T | G | 1 | a0001c0002t0008g0174 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.274-2974T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100223088 | ||||||
| chr9:100223490
|
C | CACCT | 7 | a0001c0001t0003g0088a0001c0001t0003g0090a0001c0001t0003g0094others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.274-2570_274-2567d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100223490 | |||||
| chr9:100223608
|
A | G | 1 | a0001c0001t0004g0121 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.274-2454A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100223608 | ||||||
| chr9:100223639
|
G | A | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(30): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.274-2423G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100223639 | ||||||
| chr9:100223957
|
T | C | 1 | a0001c0002t0009g0122 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.274-2105T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100223957 | ||||||
| chr9:100223975
|
A | T | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.274-2087A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100223975 | ||||||
| chr9:100224071
|
A | G | 1 | a0001c0002t0001g0129 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.274-1991A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100224071 | ||||||
| chr9:100224078
|
A | C | 5 | a0001c0001t0007g0028a0001c0001t0026g0029a0001c0001t0027g0030others(2): Show | 5 | HG02145.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-1984A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100224078 | ||||||
| chr9:100224610
|
T | C | 2 | a0001c0002t0002g0159a0001c0002t0002g0160 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.274-1452T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100224610 | ||||||
| chr9:100224984
|
A | C | 19 | a0001c0001t0003g0042a0001c0001t0003g0048a0001c0001t0003g0087others(16): Show | 19 | HG00140.hp1 HG00735.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.274-1078A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100224984 | ||||||
| chr9:100225054
|
G | T | 1 | a0001c0002t0018g0149 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.274-1008G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100225054 | ||||||
| chr9:100225062
|
G | GT | 13 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0005g0005others(10): Show | 13 | HG01081.hp1 HG01243.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.274-987dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100225062 | |||||
| chr9:100225062
|
GT | G | 5 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-987delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100225062 | |||||
| chr9:100225158
|
C | T | 3 | a0001c0001t0011g0100a0001c0001t0011g0101a0006c0007t0011g0181 | 3 | HG03209.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.274-904C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100225158 | ||||||
| chr9:100225178
|
C | G | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.274-884C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100225178 | ||||||
| chr9:100225182
|
C | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-880C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100225182 | ||||||
| chr9:100225203
|
G | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-859G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100225203 | ||||||
| chr9:100225218
|
C | A | 1 | a0001c0001t0004g0055 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.274-844C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100225218 | ||||||
| chr9:100225253
|
C | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-809C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100225253 | ||||||
| chr9:100225339
|
CG | C | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(30): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.274-722delG | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100225339 | ||||||
| chr9:100225341
|
C | A | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(30): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.274-721C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100225341 | ||||||
| chr9:100225459
|
G | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-603G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100225459 | ||||||
| chr9:100225500
|
G | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-562G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100225500 | ||||||
| chr9:100225731
|
T | C | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-331T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100225731 | ||||||
| chr9:100225746
|
A | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-316A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100225746 | ||||||
| chr9:100225750
|
CA | C | 5 | a0001c0001t0001g0108a0001c0002t0001g0102a0001c0002t0001g0112others(2): Show | 5 | HG02886.hp1 HG02886.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-304delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100225750 | |||||
| chr9:100225754
|
A | AG | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-308_274-307ins others(1): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100225754 | ||||||
| chr9:100225908
|
T | TATCTC | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-153_274-152ins others(5): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100225908 | |||||
| chr9:100225952
|
G | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-110G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100225952 | ||||||
| chr9:100226046
|
CTT | C | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-15_274-14delTT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100226046 | ||||||
| chr9:100226600
|
T | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.447+365T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100226600 | ||||||
| chr9:100226612
|
A | C | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.447+377A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100226612 | ||||||
| chr9:100226706
|
G | A | 61 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(58): Show | 61 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.447+471G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100226706 | ||||||
| chr9:100226810
|
C | CA | 56 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0048others(53): Show | 56 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.447+600dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr9 | 100226810 | |||||
| chr9:100226810
|
C | CAA | 8 | a0001c0001t0004g0054a0001c0001t0004g0067a0001c0001t0004g0075others(5): Show | 8 | HG00544.hp2 HG01175.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.447+599_447+600dup others(2): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr9 | 100226810 | |||||
| chr9:100226810
|
CAAAA | C | 30 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(27): Show | 30 | HG00323.hp1 HG00738.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.447+597_447+600del others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr9 | 100226810 | |||||
| chr9:100226935
|
C | T | 2 | a0001c0001t0011g0100a0001c0001t0011g0101 | 2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.447+700C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100226935 | ||||||
| chr9:100226963
|
C | T | 5 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.447+728C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100226963 | ||||||
| chr9:100227264
|
G | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.447+1029G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100227264 | ||||||
| chr9:100227360
|
G | T | 1 | a0001c0001t0008g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.447+1125G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100227360 | ||||||
| chr9:100227514
|
ACAG | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.447+1283_447+1285d others(5): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr9 | 100227514 | |||||
| chr9:100227610
|
G | A | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(30): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.447+1375G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100227610 | ||||||
| chr9:100227700
|
T | TAA | 35 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(32): Show | 35 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.447+1478_447+1479d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr9 | 100227700 | |||||
| chr9:100227991
|
C | CT | 6 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0002t0001g0003others(3): Show | 6 | HG00735.hp2 HG01081.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.448-1652dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr9 | 100227991 | |||||
| chr9:100227991
|
C | CTT | 95 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(92): Show | 95 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.448-1653_448-1652d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr9 | 100227991 | |||||
| chr9:100227991
|
CT | C | 6 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0024g0182others(3): Show | 6 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.448-1652delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr9 | 100227991 | |||||
| chr9:100228032
|
C | A | 1 | a0001c0001t0001g0026 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.448-1628C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100228032 | ||||||
| chr9:100228159
|
T | C | 1 | a0001c0001t0001g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.448-1501T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100228159 | ||||||
| chr9:100228175
|
G | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.448-1485G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100228175 | ||||||
| chr9:100228300
|
T | C | 2 | a0001c0001t0011g0100a0001c0001t0011g0101 | 2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.448-1360T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100228300 | ||||||
| chr9:100228413
|
T | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.448-1247T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100228413 | ||||||
| chr9:100228513
|
G | A | 41 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(38): Show | 41 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.448-1147G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100228513 | ||||||
| chr9:100228530
|
C | G | 5 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.448-1130C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100228530 | ||||||
| chr9:100228530
|
C | T | 1 | a0001c0002t0001g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.448-1130C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100228530 | ||||||
| chr9:100228913
|
A | T | 1 | a0001c0002t0001g0140 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.448-747A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100228913 | ||||||
| chr9:100229032
|
G | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.448-628G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100229032 | ||||||
| chr9:100229132
|
T | G | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.448-528T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100229132 | ||||||
| chr9:100229301
|
A | G | 1 | a0001c0001t0011g0101 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.448-359A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100229301 | ||||||
| chr9:100229402
|
G | A | 3 | a0001c0001t0011g0100a0001c0001t0011g0101a0006c0007t0011g0181 | 3 | HG03209.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.448-258G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100229402 | ||||||
| chr9:100229557
|
C | T | 1 | a0001c0002t0002g0117 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.448-103C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100229557 | ||||||
| chr9:100230048
|
C | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.615+221C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100230048 | ||||||
| chr9:100230054
|
C | T | 102 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(99): Show | 102 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.615+227C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100230054 | ||||||
| chr9:100230119
|
A | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.615+292A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100230119 | ||||||
| chr9:100230267
|
CCT | C | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.615+443_615+444del others(2): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr9 | 100230267 | |||||
| chr9:100230276
|
G | A | 5 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.615+449G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100230276 | ||||||
| chr9:100230362
|
A | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.615+535A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100230362 | ||||||
| chr9:100230405
|
A | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.615+578A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100230405 | ||||||
| chr9:100230440
|
T | C | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.615+613T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100230440 | ||||||
| chr9:100230444
|
G | A | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(30): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+617G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100230444 | ||||||
| chr9:100230469
|
TG | T | 6 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(3): Show | 6 | HG02451.hp2 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+643delG | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100230469 | ||||||
| chr9:100230532
|
A | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.615+705A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100230532 | ||||||
| chr9:100230674
|
G | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.615+847G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100230674 | ||||||
| chr9:100230688
|
T | C | 4 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0003g0178others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.615+861T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100230688 | ||||||
| chr9:100230893
|
G | A | 62 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(59): Show | 62 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.615+1066G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100230893 | ||||||
| chr9:100231018
|
T | C | 3 | a0001c0001t0004g0071a0001c0001t0004g0072a0001c0001t0004g0121 | 3 | NA19005.hp1 NA19012.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.615+1191T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100231018 | ||||||
| chr9:100231213
|
TTAAAG | T | 5 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.615+1389_615+1393d others(7): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr9 | 100231213 | |||||
| chr9:100231293
|
AT | A | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.615+1474delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr9 | 100231293 | |||||
| chr9:100231337
|
C | T | 1 | a0001c0002t0001g0143 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.615+1510C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100231337 | ||||||
| chr9:100231359
|
AT | A | 5 | a0001c0002t0001g0141a0001c0002t0001g0142a0001c0002t0001g0161others(2): Show | 5 | HG00642.hp1 HG01175.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.615+1540delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr9 | 100231359 | |||||
| chr9:100231379
|
G | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.615+1552G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100231379 | ||||||
| chr9:100231457
|
A | G | 62 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(59): Show | 62 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.615+1630A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100231457 | ||||||
| chr9:100231582
|
C | T | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(30): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+1755C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100231582 | ||||||
| chr9:100231664
|
C | G | 2 | a0001c0002t0001g0141a0001c0002t0001g0163 | 2 | HG00642.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.615+1837C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100231664 | ||||||
| chr9:100231900
|
C | G | 5 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.615+2073C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100231900 | ||||||
| chr9:100231927
|
G | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.615+2100G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100231927 | ||||||
| chr9:100232192
|
T | C | 1 | a0001c0001t0004g0070 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.615+2365T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100232192 | ||||||
| chr9:100232199
|
GT | G | 7 | a0001c0001t0003g0088a0001c0001t0003g0090a0001c0001t0003g0094others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.615+2382delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr9 | 100232199 | |||||
| chr9:100232567
|
C | T | 3 | a0001c0001t0011g0100a0001c0001t0011g0101a0006c0007t0011g0181 | 3 | HG03209.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.615+2740C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100232567 | ||||||
| chr9:100232989
|
G | A | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(30): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+3162G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100232989 | ||||||
| chr9:100233131
|
G | A | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(30): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+3304G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100233131 | ||||||
| chr9:100233781
|
A | G | 4 | a0001c0002t0002g0152a0001c0002t0002g0154a0001c0002t0002g0155others(1): Show | 4 | HG00733.hp1 HG01074.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.615+3954A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100233781 | ||||||
| chr9:100234074
|
T | C | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.615+4247T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100234074 | ||||||
| chr9:100234588
|
G | T | 1 | a0001c0001t0001g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.615+4761G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100234588 | ||||||
| chr9:100234689
|
T | G | 1 | a0001c0001t0024g0182 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.615+4862T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100234689 | ||||||
| chr9:100235215
|
C | G | 1 | a0001c0001t0005g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.616-4845C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100235215 | ||||||
| chr9:100235272
|
G | C | 3 | a0001c0002t0001g0142a0001c0002t0001g0161a0001c0002t0001g0164 | 3 | HG01952.hp1 HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.616-4788G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100235272 | ||||||
| chr9:100235278
|
T | C | 1 | a0001c0001t0028g0059 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.616-4782T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100235278 | ||||||
| chr9:100235535
|
C | T | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(30): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.616-4525C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100235535 | ||||||
| chr9:100236149
|
G | A | 1 | a0007c0011t0002g0104 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.616-3911G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100236149 | ||||||
| chr9:100236299
|
T | G | 105 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(102): Show | 105 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.616-3761T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100236299 | ||||||
| chr9:100236403
|
A | G | 9 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(6): Show | 9 | HG02280.hp2 HG02451.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.616-3657A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100236403 | ||||||
| chr9:100236489
|
G | A | 2 | a0001c0001t0005g0005a0001c0001t0005g0010 | 2 | HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.616-3571G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100236489 | ||||||
| chr9:100236564
|
G | A | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.616-3496G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100236564 | ||||||
| chr9:100236669
|
G | A | 47 | a0001c0001t0001g0108a0001c0001t0010g0126a0001c0001t0010g0127others(44): Show | 47 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.616-3391G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100236669 | ||||||
| chr9:100236690
|
T | A | 1 | a0001c0002t0002g0139 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.616-3370T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100236690 | ||||||
| chr9:100236746
|
G | T | 1 | a0001c0001t0017g0017 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.616-3314G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100236746 | ||||||
| chr9:100236750
|
A | C | 111 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(108): Show | 111 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.616-3310A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100236750 | ||||||
| chr9:100237105
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.616-2955C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100237105 | ||||||
| chr9:100237267
|
A | C | 3 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0023 | 3 | HG02109.hp1 HG02897.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.616-2793A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100237267 | ||||||
| chr9:100237823
|
T | C | 60 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0048others(57): Show | 60 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.616-2237T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100237823 | ||||||
| chr9:100238026
|
A | G | 1 | a0001c0001t0013g0016 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.616-2034A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100238026 | ||||||
| chr9:100238035
|
C | T | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.616-2025C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100238035 | ||||||
| chr9:100238068
|
G | A | 2 | a0001c0001t0004g0046a0004c0010t0003g0044 | 2 | HG01496.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.616-1992G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100238068 | ||||||
| chr9:100238323
|
G | A | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(30): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.616-1737G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100238323 | ||||||
| chr9:100238377
|
G | A | 4 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0003g0178others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.616-1683G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100238377 | ||||||
| chr9:100238832
|
A | G | 2 | a0001c0001t0001g0035a0001c0001t0008g0034 | 2 | HG02055.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.616-1228A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100238832 | ||||||
| chr9:100238946
|
C | A | 2 | a0001c0001t0015g0019a0001c0001t0015g0020 | 2 | HG00741.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.616-1114C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100238946 | ||||||
| chr9:100239183
|
G | T | 1 | a0001c0001t0007g0028 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.616-877G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100239183 | ||||||
| chr9:100239605
|
T | G | 60 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0048others(57): Show | 60 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.616-455T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100239605 | ||||||
| chr9:100239736
|
C | T | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.616-324C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100239736 | ||||||
| chr9:100239770
|
A | G | 7 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(4): Show | 7 | HG00733.hp2 HG02280.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.616-290A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100239770 | ||||||
| chr9:100239787
|
C | T | 59 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0048others(56): Show | 59 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.616-273C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100239787 | ||||||
| chr9:100240041
|
T | C | 6 | a0001c0002t0001g0014a0001c0002t0001g0021a0001c0002t0001g0022others(3): Show | 6 | HG02109.hp1 HG02145.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-19T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100240041 | ||||||
| chr9:100240264
|
G | A | 1 | a0001c0002t0002g0139 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.796+24G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 6/16 | chr9 | 100240264 | ||||||
| chr9:100240474
|
A | G | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.796+234A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 6/16 | chr9 | 100240474 | ||||||
| chr9:100240756
|
A | T | 1 | a0001c0002t0001g0023 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.796+516A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 6/16 | chr9 | 100240756 | ||||||
| chr9:100240794
|
T | C | 3 | a0001c0001t0011g0100a0001c0001t0011g0101a0006c0007t0011g0181 | 3 | HG03209.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.796+554T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 6/16 | chr9 | 100240794 | ||||||
| chr9:100240834
|
G | A | 1 | a0001c0001t0004g0062 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.796+594G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 6/16 | chr9 | 100240834 | ||||||
| chr9:100240944
|
G | A | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(30): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.796+704G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 6/16 | chr9 | 100240944 | ||||||
| chr9:100241151
|
T | G | 7 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(4): Show | 7 | HG00733.hp2 HG02280.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.796+911T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 6/16 | chr9 | 100241151 | ||||||
| chr9:100241350
|
C | A | 105 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(102): Show | 105 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.796+1110C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 6/16 | chr9 | 100241350 | ||||||
| chr9:100241682
|
G | A | 1 | a0001c0002t0001g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.797-888G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 6/16 | chr9 | 100241682 | ||||||
| chr9:100241996
|
A | G | 62 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(59): Show | 62 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.797-574A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 6/16 | chr9 | 100241996 | ||||||
| chr9:100242264
|
T | C | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(30): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.797-306T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 6/16 | chr9 | 100242264 | ||||||
| chr9:100242285
|
G | A | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.797-285G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 6/16 | chr9 | 100242285 | ||||||
| chr9:100243437
|
A | G | 1 | a0001c0002t0002g0139 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.906+758A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100243437 | ||||||
| chr9:100243487
|
G | A | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.906+808G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100243487 | ||||||
| chr9:100243533
|
T | C | 105 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(102): Show | 105 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.906+854T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100243533 | ||||||
| chr9:100243604
|
G | A | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.906+925G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100243604 | ||||||
| chr9:100243677
|
G | T | 2 | a0001c0004t0001g0109a0001c0004t0001g0110 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.906+998G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100243677 | ||||||
| chr9:100243741
|
A | G | 5 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.906+1062A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100243741 | ||||||
| chr9:100243747
|
C | T | 3 | a0001c0001t0007g0028a0001c0001t0026g0029a0001c0001t0027g0030 | 3 | HG02145.hp2 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.906+1068C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100243747 | ||||||
| chr9:100243768
|
G | A | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(30): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.906+1089G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100243768 | ||||||
| chr9:100243840
|
G | A | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(30): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.906+1161G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100243840 | ||||||
| chr9:100243874
|
A | G | 103 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(100): Show | 103 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.906+1195A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100243874 | ||||||
| chr9:100244049
|
G | A | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.906+1370G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100244049 | ||||||
| chr9:100244304
|
C | T | 1 | a0001c0002t0001g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.906+1625C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100244304 | ||||||
| chr9:100244364
|
A | G | 1 | a0001c0002t0001g0130 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.906+1685A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100244364 | ||||||
| chr9:100244824
|
A | C | 1 | a0001c0002t0001g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.907-1792A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100244824 | ||||||
| chr9:100244859
|
C | A | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(30): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.907-1757C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100244859 | ||||||
| chr9:100245132
|
C | T | 59 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0048others(56): Show | 59 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.907-1484C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100245132 | ||||||
| chr9:100245208
|
A | T | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(30): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.907-1408A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100245208 | ||||||
| chr9:100245558
|
G | T | 1 | a0001c0001t0010g0126 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.907-1058G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100245558 | ||||||
| chr9:100245955
|
T | A | 41 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(38): Show | 41 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.907-661T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100245955 | ||||||
| chr9:100246106
|
T | C | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.907-510T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100246106 | ||||||
| chr9:100246156
|
AAAAAAAG others(6): Show |
A | 1 | a0001c0002t0001g0116 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.907-448_907-436del others(13): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr9 | 100246156 | |||||
| chr9:100246163
|
G | A | 37 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(34): Show | 37 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.907-453G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100246163 | ||||||
| chr9:100246182
|
A | G | 2 | a0001c0001t0011g0100a0001c0001t0011g0101 | 2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.907-434A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100246182 | ||||||
| chr9:100246209
|
A | T | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(30): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.907-407A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100246209 | ||||||
| chr9:100246378
|
G | A | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.907-238G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100246378 | ||||||
| chr9:100246578
|
T | C | 1 | a0001c0002t0010g0170 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.907-38T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100246578 | ||||||
| chr9:100247029
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1078+242C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100247029 | ||||||
| chr9:100247133
|
G | T | 104 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(101): Show | 104 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.1078+346G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100247133 | ||||||
| chr9:100247672
|
TAAA | T | 104 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(101): Show | 104 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.1078+890_1078+892d others(5): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr9 | 100247672 | |||||
| chr9:100247832
|
G | A | 33 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(30): Show | 33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.1078+1045G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100247832 | ||||||
| chr9:100247910
|
G | A | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1078+1123G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100247910 | ||||||
| chr9:100247965
|
C | T | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1078+1178C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100247965 | ||||||
| chr9:100248007
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1078+1220G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100248007 | ||||||
| chr9:100248390
|
A | G | 1 | a0004c0010t0003g0044 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1078+1603A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100248390 | ||||||
| chr9:100248635
|
C | T | 1 | a0001c0002t0001g0021 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1078+1848C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100248635 | ||||||
| chr9:100248665
|
A | C | 33 | a0001c0001t0003g0042a0001c0001t0003g0048a0001c0001t0003g0087others(30): Show | 33 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.1078+1878A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100248665 | ||||||
| chr9:100248993
|
GCTT | G | 102 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(99): Show | 102 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1078+2211_1078+221 others(7): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr9 | 100248993 | |||||
| chr9:100249031
|
G | A | 59 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0048others(56): Show | 59 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.1078+2244G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100249031 | ||||||
| chr9:100249305
|
C | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(35): Show | 38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.1078+2518C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100249305 | ||||||
| chr9:100249401
|
A | T | 1 | a0001c0002t0030g0113 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1078+2614A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100249401 | ||||||
| chr9:100249408
|
T | A | 1 | a0001c0002t0001g0140 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1078+2621T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100249408 | ||||||
| chr9:100249421
|
T | G | 9 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(6): Show | 9 | HG02280.hp2 HG02451.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1078+2634T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100249421 | ||||||
| chr9:100249538
|
G | A | 181 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(178): Show | 181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.1079-2745G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100249538 | ||||||
| chr9:100249589
|
G | C | 1 | a0001c0002t0009g0169 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1079-2694G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100249589 | ||||||
| chr9:100249826
|
C | T | 1 | a0001c0002t0002g0154 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1079-2457C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100249826 | ||||||
| chr9:100249853
|
C | G | 1 | a0001c0001t0016g0011 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1079-2430C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100249853 | ||||||
| chr9:100249963
|
G | T | 3 | a0001c0001t0007g0028a0001c0001t0026g0029a0001c0001t0027g0030 | 3 | HG02145.hp2 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1079-2320G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100249963 | ||||||
| chr9:100250546
|
G | GTGTT | 105 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(102): Show | 105 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.1079-1735_1079-173 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr9 | 100250546 | |||||
| chr9:100250848
|
T | C | 1 | a0006c0007t0011g0181 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1079-1435T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100250848 | ||||||
| chr9:100250849
|
C | T | 1 | a0006c0007t0011g0181 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1079-1434C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100250849 | ||||||
| chr9:100251564
|
T | G | 1 | a0001c0001t0004g0058 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1079-719T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100251564 | ||||||
| chr9:100251704
|
G | A | 24 | a0001c0001t0003g0043a0001c0001t0003g0073a0001c0001t0003g0083others(21): Show | 24 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.1079-579G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100251704 | ||||||
| chr9:100251832
|
T | C | 1 | a0001c0002t0001g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1079-451T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100251832 | ||||||
| chr9:100251915
|
T | C | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1079-368T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100251915 | ||||||
| chr9:100252075
|
T | G | 1 | a0001c0002t0002g0124 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1079-208T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100252075 | ||||||
| chr9:100252257
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1079-26A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100252257 | ||||||
| chr9:100252736
|
C | T | 102 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(99): Show | 102 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1235-171C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 9/16 | chr9 | 100252736 | ||||||
| chr9:100252902
|
T | C | 56 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0048others(53): Show | 56 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(53): Show |
splice_region_variant&intron_variant | LOW | c.1235-5T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 9/16 | chr9 | 100252902 | ||||||
| chr9:100253415
|
CT | C | 99 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(96): Show | 99 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1464+290delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 100253415 | |||||
| chr9:100253426
|
T | A | 1 | a0001c0002t0002g0119 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1464+290T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100253426 | ||||||
| chr9:100253588
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1464+452C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100253588 | ||||||
| chr9:100253618
|
A | G | 1 | a0001c0002t0001g0024 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1464+482A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100253618 | ||||||
| chr9:100253680
|
T | G | 9 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1464+544T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100253680 | ||||||
| chr9:100253865
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1464+729G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100253865 | ||||||
| chr9:100253986
|
G | A | 57 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0048others(54): Show | 57 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.1464+850G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100253986 | ||||||
| chr9:100254045
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1464+909G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100254045 | ||||||
| chr9:100254117
|
A | G | 62 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(59): Show | 62 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.1464+981A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100254117 | ||||||
| chr9:100254234
|
A | G | 3 | a0001c0001t0011g0100a0001c0001t0011g0101a0006c0007t0011g0181 | 3 | HG03209.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1464+1098A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100254234 | ||||||
| chr9:100254376
|
C | T | 1 | a0001c0002t0002g0139 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1464+1240C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100254376 | ||||||
| chr9:100254556
|
C | T | 103 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(100): Show | 103 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1464+1420C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100254556 | ||||||
| chr9:100254657
|
T | C | 35 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(32): Show | 35 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1464+1521T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100254657 | ||||||
| chr9:100254658
|
G | A | 35 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(32): Show | 35 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1464+1522G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100254658 | ||||||
| chr9:100254824
|
A | G | 104 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(101): Show | 104 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.1464+1688A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100254824 | ||||||
| chr9:100255256
|
A | C | 4 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0013g0082others(1): Show | 4 | HG01106.hp1 HG02602.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1464+2120A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100255256 | ||||||
| chr9:100255390
|
A | G | 1 | a0003c0008t0021g0001 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1464+2254A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100255390 | ||||||
| chr9:100255407
|
C | G | 35 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(32): Show | 35 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1464+2271C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100255407 | ||||||
| chr9:100255487
|
G | C | 1 | a0001c0002t0009g0147 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1464+2351G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100255487 | ||||||
| chr9:100255536
|
C | T | 103 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(100): Show | 103 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1464+2400C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100255536 | ||||||
| chr9:100255633
|
G | C | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1464+2497G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100255633 | ||||||
| chr9:100255899
|
G | A | 6 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(3): Show | 6 | HG02451.hp2 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1464+2763G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100255899 | ||||||
| chr9:100256095
|
T | G | 9 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1464+2959T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100256095 | ||||||
| chr9:100256113
|
G | C | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1464+2977G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100256113 | ||||||
| chr9:100256171
|
A | C | 2 | a0001c0004t0001g0109a0001c0004t0001g0110 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1464+3035A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100256171 | ||||||
| chr9:100256201
|
T | C | 1 | a0001c0001t0004g0070 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1464+3065T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100256201 | ||||||
| chr9:100256363
|
C | A | 2 | a0001c0001t0001g0036a0005c0006t0020g0099 | 2 | HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1464+3227C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100256363 | ||||||
| chr9:100256559
|
A | G | 35 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(32): Show | 35 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1464+3423A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100256559 | ||||||
| chr9:100257641
|
G | C | 1 | a0001c0002t0001g0130 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1464+4505G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100257641 | ||||||
| chr9:100257783
|
A | C | 3 | a0001c0001t0011g0100a0001c0001t0011g0101a0006c0007t0011g0181 | 3 | HG03209.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1464+4647A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100257783 | ||||||
| chr9:100257817
|
C | T | 1 | a0001c0002t0008g0174 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1464+4681C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100257817 | ||||||
| chr9:100258342
|
G | A | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1464+5206G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100258342 | ||||||
| chr9:100258355
|
C | T | 56 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0048others(53): Show | 56 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.1464+5219C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100258355 | ||||||
| chr9:100258413
|
G | A | 3 | a0001c0001t0011g0061a0001c0001t0027g0030a0001c0001t0028g0059 | 3 | HG02109.hp2 HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1464+5277G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100258413 | ||||||
| chr9:100258477
|
G | A | 1 | a0001c0002t0001g0024 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1464+5341G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100258477 | ||||||
| chr9:100258715
|
G | A | 5 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1464+5579G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100258715 | ||||||
| chr9:100258860
|
G | C | 61 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(58): Show | 61 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.1464+5724G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100258860 | ||||||
| chr9:100259053
|
G | A | 1 | a0001c0002t0002g0156 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1465-5769G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100259053 | ||||||
| chr9:100259088
|
C | T | 7 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0012g0134others(4): Show | 7 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1465-5734C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100259088 | ||||||
| chr9:100259121
|
C | T | 1 | a0001c0002t0008g0174 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1465-5701C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100259121 | ||||||
| chr9:100259252
|
C | T | 103 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(100): Show | 103 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1465-5570C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100259252 | ||||||
| chr9:100259312
|
C | G | 1 | a0001c0002t0002g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1465-5510C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100259312 | ||||||
| chr9:100259365
|
A | G | 103 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(100): Show | 103 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1465-5457A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100259365 | ||||||
| chr9:100259557
|
C | CT | 96 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0026others(93): Show | 96 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.1465-5248dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 100259557 | |||||
| chr9:100259557
|
C | CTT | 6 | a0001c0001t0004g0075a0001c0001t0012g0134a0001c0001t0012g0135others(3): Show | 6 | HG00544.hp2 HG02280.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1465-5249_1465-524 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 100259557 | |||||
| chr9:100259581
|
A | T | 5 | a0001c0001t0004g0064a0001c0001t0004g0065a0001c0001t0004g0067others(2): Show | 5 | HG00609.hp1 HG02056.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.1465-5241A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100259581 | ||||||
| chr9:100259802
|
G | A | 1 | a0001c0002t0001g0133 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1465-5020G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100259802 | ||||||
| chr9:100259903
|
G | A | 4 | a0001c0001t0014g0076a0001c0001t0014g0080a0001c0001t0014g0081others(1): Show | 4 | HG00423.hp2 HG00621.hp1 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.1465-4919G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100259903 | ||||||
| chr9:100260113
|
G | A | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1465-4709G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100260113 | ||||||
| chr9:100260171
|
A | G | 3 | a0001c0001t0011g0100a0001c0001t0011g0101a0006c0007t0011g0181 | 3 | HG03209.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1465-4651A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100260171 | ||||||
| chr9:100260186
|
C | CT | 19 | a0001c0001t0003g0042a0001c0001t0003g0048a0001c0001t0003g0087others(16): Show | 19 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.1465-4616dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 100260186 | |||||
| chr9:100260186
|
C | CTT | 16 | a0001c0001t0003g0088a0001c0001t0003g0090a0001c0001t0003g0092others(13): Show | 16 | HG00735.hp1 HG00738.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.1465-4617_1465-461 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 100260186 | |||||
| chr9:100260186
|
CT | C | 6 | a0001c0001t0004g0058a0001c0001t0012g0134a0001c0001t0012g0135others(3): Show | 6 | HG02280.hp1 HG02970.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1465-4616delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 100260186 | |||||
| chr9:100260193
|
T | C | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1465-4629T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100260193 | ||||||
| chr9:100260198
|
T | C | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1465-4624T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100260198 | ||||||
| chr9:100260312
|
C | T | 1 | a0001c0002t0001g0171 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1465-4510C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100260312 | ||||||
| chr9:100260357
|
T | C | 1 | a0001c0002t0001g0111 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1465-4465T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100260357 | ||||||
| chr9:100260709
|
A | G | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1465-4113A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100260709 | ||||||
| chr9:100261069
|
A | G | 1 | a0006c0007t0011g0181 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1465-3753A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100261069 | ||||||
| chr9:100261095
|
A | G | 1 | a0001c0002t0008g0166 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1465-3727A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100261095 | ||||||
| chr9:100261117
|
T | G | 3 | a0001c0002t0001g0114a0001c0002t0001g0116a0001c0002t0003g0115 | 3 | HG00741.hp1 HG01069.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1465-3705T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100261117 | ||||||
| chr9:100261299
|
T | C | 3 | a0001c0001t0011g0061a0001c0001t0027g0030a0001c0001t0028g0059 | 3 | HG02109.hp2 HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1465-3523T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100261299 | ||||||
| chr9:100261896
|
T | A | 1 | a0006c0007t0011g0181 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1465-2926T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100261896 | ||||||
| chr9:100261950
|
GT | G | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1465-2870delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 100261950 | |||||
| chr9:100261997
|
T | G | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1465-2825T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100261997 | ||||||
| chr9:100262038
|
A | AT | 41 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(38): Show | 41 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.1465-2774dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 100262038 | |||||
| chr9:100262088
|
T | C | 103 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(100): Show | 103 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1465-2734T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100262088 | ||||||
| chr9:100262197
|
A | G | 5 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1465-2625A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100262197 | ||||||
| chr9:100262238
|
CA | C | 103 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(100): Show | 103 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1465-2573delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 100262238 | |||||
| chr9:100262638
|
TA | T | 30 | a0001c0001t0001g0025a0001c0001t0001g0108a0001c0001t0011g0061others(27): Show | 30 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.1465-2161delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 100262638 | |||||
| chr9:100262638
|
TAA | T | 37 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0026others(34): Show | 37 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.1465-2162_1465-216 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 100262638 | |||||
| chr9:100262638
|
TAAA | T | 53 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0048others(50): Show | 53 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.1465-2163_1465-216 others(7): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 100262638 | |||||
| chr9:100262742
|
CTTGT | C | 56 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0048others(53): Show | 56 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.1465-2065_1465-206 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 100262742 | |||||
| chr9:100262942
|
T | C | 1 | a0001c0002t0001g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1465-1880T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100262942 | ||||||
| chr9:100262960
|
G | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1465-1862G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100262960 | ||||||
| chr9:100263167
|
T | TAGAAGTG others(320): Show |
4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1465-1639_1465-163 others(331): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 100263167 | |||||
| chr9:100263297
|
T | C | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1465-1525T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100263297 | ||||||
| chr9:100263511
|
T | C | 5 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1465-1311T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100263511 | ||||||
| chr9:100263552
|
C | T | 61 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(58): Show | 61 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.1465-1270C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100263552 | ||||||
| chr9:100263656
|
T | A | 1 | a0001c0001t0031g0077 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1465-1166T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100263656 | ||||||
| chr9:100264275
|
T | G | 1 | a0001c0002t0030g0113 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1465-547T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100264275 | ||||||
| chr9:100264496
|
T | C | 5 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1465-326T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100264496 | ||||||
| chr9:100264618
|
C | CA | 40 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(37): Show | 40 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.1465-188dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 100264618 | |||||
| chr9:100264618
|
CA | C | 61 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0048others(58): Show | 61 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.1465-188delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 100264618 | |||||
| chr9:100264731
|
G | A | 2 | a0001c0001t0011g0100a0001c0001t0011g0101 | 2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1465-91G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100264731 | ||||||
| chr9:100264944
|
C | CT | 7 | a0001c0001t0011g0100a0001c0001t0011g0101a0001c0001t0012g0134others(4): Show | 7 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1571+32dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | 100264944 | |||||
| chr9:100265165
|
G | A | 7 | a0002c0003t0006g0084a0002c0003t0006g0085a0002c0003t0006g0086others(4): Show | 7 | HG00735.hp1 HG00738.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1571+237G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100265165 | ||||||
| chr9:100265225
|
G | A | 1 | a0001c0002t0002g0158 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1571+297G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100265225 | ||||||
| chr9:100265408
|
A | C | 35 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(32): Show | 35 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1571+480A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100265408 | ||||||
| chr9:100265573
|
C | G | 62 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(59): Show | 62 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.1571+645C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100265573 | ||||||
| chr9:100265710
|
G | A | 1 | a0001c0002t0001g0102 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1571+782G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100265710 | ||||||
| chr9:100265923
|
A | T | 42 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(39): Show | 42 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.1571+995A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100265923 | ||||||
| chr9:100266040
|
A | G | 1 | a0001c0001t0001g0004 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1571+1112A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100266040 | ||||||
| chr9:100266281
|
C | T | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1571+1353C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100266281 | ||||||
| chr9:100266770
|
G | C | 1 | a0001c0001t0003g0087 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1571+1842G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100266770 | ||||||
| chr9:100266957
|
C | G | 5 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1571+2029C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100266957 | ||||||
| chr9:100267019
|
T | TA | 75 | a0001c0001t0001g0108a0001c0001t0001g0145a0001c0001t0007g0028others(72): Show | 75 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.1571+2115dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | 100267019 | |||||
| chr9:100267019
|
T | TAA | 58 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0048others(55): Show | 58 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1571+2114_1571+211 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | 100267019 | |||||
| chr9:100267019
|
TA | T | 39 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(36): Show | 39 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.1571+2115delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | 100267019 | |||||
| chr9:100267121
|
C | T | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1571+2193C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100267121 | ||||||
| chr9:100267421
|
A | G | 59 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(56): Show | 59 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.1571+2493A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100267421 | ||||||
| chr9:100267557
|
A | G | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1571+2629A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100267557 | ||||||
| chr9:100267806
|
G | T | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1571+2878G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100267806 | ||||||
| chr9:100267885
|
G | A | 1 | a0001c0002t0001g0180 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1571+2957G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100267885 | ||||||
| chr9:100268037
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1571+3109C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100268037 | ||||||
| chr9:100269173
|
T | C | 2 | a0001c0004t0001g0109a0001c0004t0001g0110 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1572-3691T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100269173 | ||||||
| chr9:100269371
|
AT | A | 35 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(32): Show | 35 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1572-3485delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | 100269371 | |||||
| chr9:100269790
|
G | A | 1 | a0001c0002t0008g0174 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1572-3074G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100269790 | ||||||
| chr9:100269805
|
T | C | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1572-3059T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100269805 | ||||||
| chr9:100270042
|
AT | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1572-2821delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100270042 | ||||||
| chr9:100270048
|
T | G | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1572-2816T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100270048 | ||||||
| chr9:100270050
|
A | G | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1572-2814A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100270050 | ||||||
| chr9:100270121
|
A | AT | 60 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(57): Show | 60 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.1572-2733dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | 100270121 | |||||
| chr9:100270609
|
G | A | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1572-2255G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100270609 | ||||||
| chr9:100270748
|
C | CA | 26 | a0001c0001t0004g0049a0001c0001t0004g0062a0001c0001t0004g0068others(23): Show | 26 | HG00609.hp2 HG00621.hp1 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.1572-2092dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | 100270748 | |||||
| chr9:100270748
|
C | CAA | 25 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0026others(22): Show | 25 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.1572-2093_1572-209 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | 100270748 | |||||
| chr9:100270748
|
C | CAAA | 11 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0036others(8): Show | 11 | HG00741.hp2 HG01106.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1572-2094_1572-209 others(7): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | 100270748 | |||||
| chr9:100270853
|
A | G | 104 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(101): Show | 104 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.1572-2011A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100270853 | ||||||
| chr9:100271070
|
A | G | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1572-1794A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100271070 | ||||||
| chr9:100271136
|
G | C | 62 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(59): Show | 62 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.1572-1728G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100271136 | ||||||
| chr9:100271557
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1572-1307T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100271557 | ||||||
| chr9:100271648
|
C | T | 1 | a0002c0003t0023g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1572-1216C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100271648 | ||||||
| chr9:100271800
|
C | A | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1572-1064C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100271800 | ||||||
| chr9:100271907
|
C | T | 1 | a0001c0001t0007g0053 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1572-957C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100271907 | ||||||
| chr9:100271908
|
A | G | 104 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(101): Show | 104 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.1572-956A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100271908 | ||||||
| chr9:100272044
|
TTTTTAGT others(75): Show |
T | 1 | a0001c0001t0003g0090 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1572-819_1572-738d others(84): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100272044 | ||||||
| chr9:100272059
|
G | T | 1 | a0001c0001t0001g0144 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1572-805G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100272059 | ||||||
| chr9:100272090
|
A | G | 1 | a0001c0002t0001g0111 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1572-774A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100272090 | ||||||
| chr9:100272160
|
G | T | 1 | a0001c0001t0028g0059 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1572-704G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100272160 | ||||||
| chr9:100272429
|
A | G | 1 | a0001c0002t0002g0158 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1572-435A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100272429 | ||||||
| chr9:100272546
|
G | A | 56 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0048others(53): Show | 56 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.1572-318G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100272546 | ||||||
| chr9:100273180
|
T | G | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1784+104T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100273180 | ||||||
| chr9:100273219
|
T | G | 1 | a0001c0002t0002g0041 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1784+143T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100273219 | ||||||
| chr9:100273473
|
G | C | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1784+397G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100273473 | ||||||
| chr9:100273527
|
C | CT | 42 | a0001c0001t0001g0108a0001c0001t0004g0121a0001c0002t0001g0003others(39): Show | 42 | HG00323.hp2 HG00609.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.1784+478dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr9 | 100273527 | |||||
| chr9:100273527
|
C | CTT | 5 | a0001c0002t0001g0014a0001c0002t0002g0041a0001c0002t0009g0147others(2): Show | 5 | HG00140.hp2 HG01192.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.1784+477_1784+478d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr9 | 100273527 | |||||
| chr9:100273527
|
CT | C | 12 | a0001c0001t0005g0013a0001c0001t0008g0034a0001c0001t0011g0061others(9): Show | 12 | HG02055.hp1 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1784+478delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr9 | 100273527 | |||||
| chr9:100273527
|
CTT | C | 26 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(23): Show | 26 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.1784+477_1784+478d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr9 | 100273527 | |||||
| chr9:100273527
|
CTTTTTTT others(8): Show |
C | 61 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(58): Show | 61 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.1784+464_1784+478d others(17): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr9 | 100273527 | |||||
| chr9:100273682
|
C | T | 1 | a0001c0002t0008g0166 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1784+606C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100273682 | ||||||
| chr9:100273694
|
C | T | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1784+618C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100273694 | ||||||
| chr9:100273728
|
G | C | 1 | a0001c0001t0004g0058 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1784+652G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100273728 | ||||||
| chr9:100273787
|
C | T | 58 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(55): Show | 58 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1784+711C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100273787 | ||||||
| chr9:100273975
|
C | T | 11 | a0001c0001t0004g0121a0001c0002t0002g0103a0001c0002t0002g0117others(8): Show | 11 | HG00609.hp2 HG02056.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1784+899C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100273975 | ||||||
| chr9:100274122
|
C | T | 1 | a0001c0001t0004g0056 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1784+1046C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100274122 | ||||||
| chr9:100274345
|
C | CA | 35 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(32): Show | 35 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1784+1270dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr9 | 100274345 | |||||
| chr9:100274515
|
C | CT | 7 | a0001c0002t0001g0114a0001c0002t0001g0116a0001c0002t0001g0128others(4): Show | 7 | HG00280.hp1 HG00741.hp1 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.1784+1448dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr9 | 100274515 | |||||
| chr9:100274566
|
A | G | 103 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(100): Show | 103 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1784+1490A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100274566 | ||||||
| chr9:100274597
|
C | T | 61 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(58): Show | 61 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.1784+1521C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100274597 | ||||||
| chr9:100275007
|
C | T | 3 | a0001c0002t0001g0142a0001c0002t0001g0161a0001c0002t0001g0164 | 3 | HG01952.hp1 HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1784+1931C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100275007 | ||||||
| chr9:100275666
|
T | G | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1784+2590T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100275666 | ||||||
| chr9:100275763
|
G | A | 1 | a0001c0002t0001g0107 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1784+2687G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100275763 | ||||||
| chr9:100275840
|
A | G | 1 | a0001c0001t0007g0028 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1784+2764A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100275840 | ||||||
| chr9:100275911
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1784+2835C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100275911 | ||||||
| chr9:100276371
|
C | G | 103 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(100): Show | 103 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1784+3295C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100276371 | ||||||
| chr9:100276374
|
G | T | 1 | a0001c0001t0001g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1784+3298G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100276374 | ||||||
| chr9:100276438
|
T | C | 56 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0048others(53): Show | 56 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.1784+3362T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100276438 | ||||||
| chr9:100276489
|
C | T | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1784+3413C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100276489 | ||||||
| chr9:100276554
|
G | A | 1 | a0001c0001t0004g0056 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1784+3478G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100276554 | ||||||
| chr9:100276915
|
T | C | 103 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(100): Show | 103 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1784+3839T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100276915 | ||||||
| chr9:100277015
|
G | A | 3 | a0001c0001t0011g0061a0001c0001t0027g0030a0001c0001t0028g0059 | 3 | HG02109.hp2 HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1784+3939G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100277015 | ||||||
| chr9:100277821
|
C | T | 1 | a0001c0001t0027g0030 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1784+4745C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100277821 | ||||||
| chr9:100278231
|
C | CA | 7 | a0001c0001t0005g0007a0001c0001t0005g0009a0001c0002t0002g0138others(4): Show | 7 | HG01167.hp2 HG01975.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1784+5179dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr9 | 100278231 | |||||
| chr9:100278231
|
C | CAA | 95 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(92): Show | 95 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.1784+5178_1784+517 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr9 | 100278231 | |||||
| chr9:100278231
|
C | CAAA | 12 | a0001c0001t0001g0040a0001c0001t0001g0108a0001c0001t0005g0013others(9): Show | 12 | HG00735.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1784+5177_1784+517 others(7): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr9 | 100278231 | |||||
| chr9:100278231
|
C | CAAAAAAA others(4): Show |
4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1784+5169_1784+517 others(15): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr9 | 100278231 | |||||
| chr9:100278381
|
G | A | 64 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(61): Show | 64 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1784+5305G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100278381 | ||||||
| chr9:100278646
|
T | C | 5 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1784+5570T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100278646 | ||||||
| chr9:100278667
|
T | C | 1 | a0001c0001t0011g0101 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1784+5591T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100278667 | ||||||
| chr9:100278729
|
T | C | 1 | a0001c0001t0003g0095 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1785-5591T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100278729 | ||||||
| chr9:100278837
|
A | C | 63 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(60): Show | 63 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.1785-5483A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100278837 | ||||||
| chr9:100278867
|
C | G | 64 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(61): Show | 64 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1785-5453C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100278867 | ||||||
| chr9:100279062
|
G | A | 40 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(37): Show | 40 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.1785-5258G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100279062 | ||||||
| chr9:100279156
|
G | A | 3 | a0001c0002t0001g0142a0001c0002t0001g0161a0001c0002t0001g0164 | 3 | HG01952.hp1 HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1785-5164G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100279156 | ||||||
| chr9:100279524
|
A | G | 1 | a0001c0001t0004g0054 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1785-4796A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100279524 | ||||||
| chr9:100279987
|
C | G | 1 | a0001c0001t0008g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1785-4333C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100279987 | ||||||
| chr9:100280129
|
T | G | 3 | a0001c0001t0011g0100a0001c0001t0011g0101a0006c0007t0011g0181 | 3 | HG03209.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1785-4191T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100280129 | ||||||
| chr9:100280808
|
C | G | 40 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(37): Show | 40 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.1785-3512C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100280808 | ||||||
| chr9:100280999
|
T | C | 58 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(55): Show | 58 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1785-3321T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100280999 | ||||||
| chr9:100281037
|
T | C | 58 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(55): Show | 58 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1785-3283T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100281037 | ||||||
| chr9:100281061
|
T | G | 1 | a0001c0001t0024g0182 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1785-3259T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100281061 | ||||||
| chr9:100281689
|
T | C | 19 | a0001c0001t0003g0042a0001c0001t0003g0087a0001c0001t0003g0088others(16): Show | 19 | HG00735.hp1 HG00738.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.1785-2631T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100281689 | ||||||
| chr9:100281733
|
A | C | 62 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(59): Show | 62 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.1785-2587A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100281733 | ||||||
| chr9:100281740
|
T | C | 1 | a0001c0001t0003g0088 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1785-2580T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100281740 | ||||||
| chr9:100282017
|
G | T | 35 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(32): Show | 35 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1785-2303G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100282017 | ||||||
| chr9:100282075
|
A | G | 1 | a0001c0001t0024g0182 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1785-2245A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100282075 | ||||||
| chr9:100282103
|
C | G | 3 | a0001c0001t0011g0061a0001c0001t0027g0030a0001c0001t0028g0059 | 3 | HG02109.hp2 HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1785-2217C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100282103 | ||||||
| chr9:100282170
|
C | A | 32 | a0001c0001t0003g0042a0001c0001t0003g0048a0001c0001t0003g0087others(29): Show | 32 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.1785-2150C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100282170 | ||||||
| chr9:100282546
|
T | C | 4 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0013g0082others(1): Show | 4 | HG01106.hp1 HG02602.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1785-1774T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100282546 | ||||||
| chr9:100282813
|
G | GTA | 35 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(32): Show | 35 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1785-1504_1785-150 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr9 | 100282813 | |||||
| chr9:100282927
|
T | C | 1 | a0001c0001t0004g0058 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1785-1393T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100282927 | ||||||
| chr9:100283196
|
C | T | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1785-1124C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100283196 | ||||||
| chr9:100283324
|
A | G | 6 | a0001c0001t0011g0061a0001c0001t0011g0100a0001c0001t0011g0101others(3): Show | 6 | HG00733.hp2 HG03098.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1785-996A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100283324 | ||||||
| chr9:100283582
|
C | T | 3 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0023 | 3 | HG02109.hp1 HG02897.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1785-738C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100283582 | ||||||
| chr9:100283799
|
C | T | 106 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(103): Show | 106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.1785-521C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100283799 | ||||||
| chr9:100283870
|
T | C | 1 | a0001c0001t0012g0135 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1785-450T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100283870 | ||||||
| chr9:100284026
|
G | A | 5 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1785-294G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100284026 | ||||||
| chr9:100284634
|
G | A | 37 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(34): Show | 37 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.2068+31G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100284634 | ||||||
| chr9:100284889
|
T | C | 107 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(104): Show | 107 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.2068+286T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100284889 | ||||||
| chr9:100284928
|
G | T | 1 | a0001c0001t0019g0066 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2068+325G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100284928 | ||||||
| chr9:100285097
|
A | G | 4 | a0001c0001t0011g0061a0001c0001t0011g0100a0001c0001t0011g0101others(1): Show | 4 | HG03098.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2068+494A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100285097 | ||||||
| chr9:100285358
|
C | G | 57 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0048others(54): Show | 57 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.2068+755C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100285358 | ||||||
| chr9:100285467
|
C | A | 6 | a0001c0001t0011g0061a0001c0001t0011g0100a0001c0001t0011g0101others(3): Show | 6 | HG00733.hp2 HG03098.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2068+864C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100285467 | ||||||
| chr9:100285634
|
G | A | 2 | a0001c0001t0013g0078a0001c0001t0015g0074 | 2 | HG02602.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.2068+1031G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100285634 | ||||||
| chr9:100285673
|
C | T | 1 | a0001c0001t0004g0054 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2068+1070C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100285673 | ||||||
| chr9:100285918
|
T | C | 1 | a0001c0002t0001g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2068+1315T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100285918 | ||||||
| chr9:100286057
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2068+1454G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100286057 | ||||||
| chr9:100286067
|
A | G | 59 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(56): Show | 59 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.2068+1464A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100286067 | ||||||
| chr9:100286071
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2068+1468G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100286071 | ||||||
| chr9:100286118
|
T | C | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2068+1515T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100286118 | ||||||
| chr9:100286169
|
T | C | 1 | a0001c0001t0024g0182 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2068+1566T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100286169 | ||||||
| chr9:100286395
|
A | C | 25 | a0001c0001t0003g0043a0001c0001t0003g0073a0001c0001t0003g0083others(22): Show | 25 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.2068+1792A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100286395 | ||||||
| chr9:100286730
|
T | C | 1 | a0001c0002t0001g0143 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2068+2127T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100286730 | ||||||
| chr9:100286962
|
T | C | 59 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(56): Show | 59 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.2068+2359T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100286962 | ||||||
| chr9:100286975
|
C | G | 1 | a0001c0002t0010g0170 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2068+2372C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100286975 | ||||||
| chr9:100287174
|
A | G | 1 | a0001c0002t0002g0152 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2068+2571A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100287174 | ||||||
| chr9:100287204
|
G | A | 1 | a0001c0001t0003g0042 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2068+2601G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100287204 | ||||||
| chr9:100287276
|
G | A | 1 | a0001c0002t0001g0107 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2068+2673G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100287276 | ||||||
| chr9:100287351
|
C | T | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2068+2748C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100287351 | ||||||
| chr9:100287582
|
T | C | 4 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(1): Show | 4 | HG02486.hp1 HG02809.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2068+2979T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100287582 | ||||||
| chr9:100287827
|
G | A | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2068+3224G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100287827 | ||||||
| chr9:100287846
|
T | C | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2068+3243T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100287846 | ||||||
| chr9:100287939
|
G | T | 2 | a0001c0001t0027g0030a0001c0001t0028g0059 | 2 | HG02109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2068+3336G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100287939 | ||||||
| chr9:100288065
|
C | T | 4 | a0001c0002t0002g0152a0001c0002t0002g0154a0001c0002t0002g0155others(1): Show | 4 | HG00733.hp1 HG01074.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.2068+3462C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100288065 | ||||||
| chr9:100288125
|
C | T | 64 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(61): Show | 64 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.2068+3522C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100288125 | ||||||
| chr9:100288255
|
C | A | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2068+3652C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100288255 | ||||||
| chr9:100288669
|
G | A | 1 | a0001c0002t0002g0137 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2069-3657G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100288669 | ||||||
| chr9:100288855
|
G | A | 56 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0048others(53): Show | 56 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.2069-3471G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100288855 | ||||||
| chr9:100288896
|
G | A | 1 | a0001c0002t0010g0170 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2069-3430G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100288896 | ||||||
| chr9:100288923
|
C | T | 43 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(40): Show | 43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.2069-3403C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100288923 | ||||||
| chr9:100288968
|
TG | T | 37 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(34): Show | 37 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.2069-3356delG | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr9 | 100288968 | |||||
| chr9:100288973
|
G | A | 5 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.2069-3353G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100288973 | ||||||
| chr9:100289046
|
A | G | 1 | a0001c0001t0017g0018 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2069-3280A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100289046 | ||||||
| chr9:100289995
|
G | A | 2 | a0001c0001t0001g0035a0001c0001t0008g0034 | 2 | HG02055.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2069-2331G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100289995 | ||||||
| chr9:100290086
|
G | GT | 65 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(62): Show | 65 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.2069-2230dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr9 | 100290086 | |||||
| chr9:100290317
|
A | C | 1 | a0001c0001t0003g0048 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2069-2009A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100290317 | ||||||
| chr9:100290389
|
G | A | 35 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(32): Show | 35 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.2069-1937G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100290389 | ||||||
| chr9:100290516
|
A | C | 107 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(104): Show | 107 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.2069-1810A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100290516 | ||||||
| chr9:100290632
|
G | A | 2 | a0001c0002t0002g0103a0001c0002t0002g0117 | 2 | NA18964.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2069-1694G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100290632 | ||||||
| chr9:100290903
|
A | G | 5 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.2069-1423A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100290903 | ||||||
| chr9:100290913
|
A | T | 1 | a0001c0001t0004g0056 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2069-1413A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100290913 | ||||||
| chr9:100291071
|
AT | A | 40 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(37): Show | 40 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.2069-1243delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr9 | 100291071 | |||||
| chr9:100291224
|
C | T | 1 | a0001c0002t0003g0115 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2069-1102C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100291224 | ||||||
| chr9:100291256
|
A | G | 155 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(152): Show | 155 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.2069-1070A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100291256 | ||||||
| chr9:100291317
|
C | A | 1 | a0001c0002t0009g0132 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2069-1009C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100291317 | ||||||
| chr9:100291461
|
TGA | T | 4 | a0001c0001t0011g0061a0001c0001t0011g0100a0001c0001t0011g0101others(1): Show | 4 | HG03098.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2069-860_2069-859d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr9 | 100291461 | |||||
| chr9:100291562
|
C | T | 1 | a0004c0010t0003g0044 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2069-764C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100291562 | ||||||
| chr9:100291579
|
T | G | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2069-747T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100291579 | ||||||
| chr9:100291795
|
C | CT | 2 | a0001c0001t0027g0030a0001c0001t0028g0059 | 2 | HG02109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2069-530dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr9 | 100291795 | |||||
| chr9:100291908
|
A | C | 107 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(104): Show | 107 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.2069-418A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100291908 | ||||||
| chr9:100292048
|
C | A | 1 | a0001c0002t0001g0171 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2069-278C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100292048 | ||||||
| chr9:100292286
|
C | A | 1 | a0001c0001t0005g0006 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2069-40C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100292286 | ||||||
| chr9:100293554
|
T | C | 1 | a0001c0001t0008g0034 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2786+511T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100293554 | ||||||
| chr9:100293656
|
G | A | 65 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(62): Show | 65 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.2786+613G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100293656 | ||||||
| chr9:100293715
|
G | T | 62 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(59): Show | 62 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.2786+672G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100293715 | ||||||
| chr9:100293885
|
G | A | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2786+842G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100293885 | ||||||
| chr9:100293985
|
C | T | 106 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(103): Show | 106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.2786+942C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100293985 | ||||||
| chr9:100294011
|
TACA | T | 5 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.2786+973_2786+975d others(5): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr9 | 100294011 | |||||
| chr9:100294337
|
T | C | 1 | a0001c0002t0009g0122 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2786+1294T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100294337 | ||||||
| chr9:100294707
|
G | A | 1 | a0001c0009t0007g0052 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2786+1664G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100294707 | ||||||
| chr9:100294808
|
T | A | 1 | a0001c0002t0001g0143 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2786+1765T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100294808 | ||||||
| chr9:100294879
|
C | T | 2 | a0001c0002t0001g0098a0001c0002t0001g0172 | 2 | HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2786+1836C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100294879 | ||||||
| chr9:100295235
|
A | T | 59 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(56): Show | 59 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.2787-1682A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100295235 | ||||||
| chr9:100295268
|
T | C | 1 | a0001c0002t0008g0166 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2787-1649T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100295268 | ||||||
| chr9:100295439
|
A | G | 25 | a0001c0001t0003g0043a0001c0001t0003g0073a0001c0001t0003g0083others(22): Show | 25 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.2787-1478A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100295439 | ||||||
| chr9:100295649
|
C | A | 2 | a0003c0005t0022g0002a0003c0008t0021g0001 | 2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2787-1268C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100295649 | ||||||
| chr9:100295811
|
C | G | 57 | a0001c0001t0003g0042a0001c0001t0003g0043a0001c0001t0003g0048others(54): Show | 57 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.2787-1106C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100295811 | ||||||
| chr9:100295943
|
C | T | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2787-974C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100295943 | ||||||
| chr9:100296204
|
A | G | 2 | a0001c0002t0001g0098a0001c0002t0001g0172 | 2 | HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2787-713A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100296204 | ||||||
| chr9:100296389
|
C | T | 4 | a0001c0001t0012g0134a0001c0001t0012g0135a0001c0001t0012g0136others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2787-528C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100296389 | ||||||
| chr9:100296417
|
G | T | 90 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0003g0042others(87): Show | 90 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.2787-500G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100296417 | ||||||
| chr9:100296487
|
G | A | 4 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0013g0082others(1): Show | 4 | HG01106.hp1 HG02602.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.2787-430G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100296487 | ||||||
| chr9:100296506
|
C | T | 8 | a0001c0001t0011g0061a0001c0001t0011g0100a0001c0001t0011g0101others(5): Show | 8 | HG02280.hp1 HG02970.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.2787-411C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100296506 | ||||||
| chr9:100296649
|
C | T | 19 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0009others(16): Show | 19 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.2787-268C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100296649 | ||||||
| chr9:100296894
|
C | G | 21 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(18): Show | 21 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.2787-23C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100296894 | ||||||
| chr9:100297194
|
A | G | 115 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(112): Show | 115 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.3016+48A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 15/16 | chr9 | 100297194 | ||||||
| chr9:100297553
|
G | A | 4 | a0001c0002t0002g0152a0001c0002t0002g0154a0001c0002t0002g0155others(1): Show | 4 | HG00733.hp1 HG01074.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.3017-383G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 15/16 | chr9 | 100297553 | ||||||
| chr9:100297931
|
T | G | 1 | a0001c0001t0013g0082 | 1 | HG03831.hp1 | splice_region_variant&intron_variant | LOW | c.3017-5T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 15/16 | chr9 | 100297931 | ||||||
| chr9:100298104
|
T | G | 124 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(121): Show | 124 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.3091+94T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | chr9 | 100298104 | ||||||
| chr9:100298350
|
A | G | 2 | a0001c0002t0001g0102a0001c0002t0001g0133 | 2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.3091+340A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | chr9 | 100298350 | ||||||
| chr9:100298389
|
A | G | 1 | a0001c0001t0003g0073 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3091+379A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | chr9 | 100298389 | ||||||
| chr9:100298437
|
G | A | 24 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(21): Show | 24 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.3091+427G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | chr9 | 100298437 | ||||||
| chr9:100298597
|
G | T | 1 | a0001c0002t0008g0174 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3091+587G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | chr9 | 100298597 | ||||||
| chr9:100298636
|
C | T | 21 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(18): Show | 21 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.3091+626C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | chr9 | 100298636 | ||||||
| chr9:100298874
|
AAAAC | A | 25 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(22): Show | 25 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.3091+876_3091+879d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100298874 | |||||
| chr9:100299084
|
A | G | 92 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(89): Show | 92 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.3091+1074A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | chr9 | 100299084 | ||||||
| chr9:100299207
|
T | C | 1 | a0001c0001t0013g0082 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3091+1197T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | chr9 | 100299207 | ||||||
| chr9:100299501
|
CCAGCCTT others(80): Show |
C | 2 | a0001c0002t0002g0119a0001c0002t0009g0150 | 2 | HG00735.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.3092-1012_3092-926 others(90): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299501 | |||||
| chr9:100299554
|
C | CAACACAC others(93): Show |
2 | a0001c0001t0005g0005a0001c0001t0005g0010 | 2 | HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3092-978_3092-977i others(102): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299554 | |||||
| chr9:100299554
|
C | CAACACAC others(91): Show |
1 | a0001c0001t0005g0006 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3092-978_3092-977i others(100): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299554 | |||||
| chr9:100299554
|
C | CAACACAC others(75): Show |
1 | a0001c0001t0028g0059 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3092-980_3092-979i others(84): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299554 | |||||
| chr9:100299555
|
A | AAC | 13 | a0001c0001t0004g0045a0001c0001t0004g0058a0001c0001t0004g0065others(10): Show | 13 | HG01496.hp2 HG02056.hp1 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.3092-979_3092-978d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299555 | |||||
| chr9:100299555
|
A | AACACACA others(9): Show |
1 | a0003c0005t0022g0002 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3092-993_3092-978d others(18): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299555 | |||||
| chr9:100299555
|
A | AACACACA others(11): Show |
1 | a0003c0008t0021g0001 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3092-995_3092-978d others(20): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299555 | |||||
| chr9:100299555
|
A | AACACACA others(13): Show |
1 | a0001c0001t0001g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3092-997_3092-978d others(22): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299555 | |||||
| chr9:100299555
|
A | AACACACA others(19): Show |
1 | a0001c0001t0001g0144 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3092-1003_3092-978 others(29): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299555 | |||||
| chr9:100299555
|
AAC | A | 8 | a0001c0001t0004g0067a0001c0001t0011g0061a0001c0001t0011g0100others(5): Show | 8 | HG02145.hp2 HG02280.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.3092-979_3092-978d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299555 | |||||
| chr9:100299555
|
AACAC | A | 11 | a0001c0001t0003g0048a0001c0001t0003g0092a0001c0001t0003g0093others(8): Show | 11 | HG00140.hp1 HG00735.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.3092-981_3092-978d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299555 | |||||
| chr9:100299555
|
AACACACA others(15): Show |
A | 86 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0026others(83): Show | 86 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.3092-999_3092-978d others(24): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299555 | |||||
| chr9:100299557
|
C | CACACACA others(93): Show |
2 | a0001c0001t0005g0012a0001c0001t0005g0013 | 2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3092-978_3092-977i others(102): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299557 | |||||
| chr9:100299557
|
C | CACACACA others(85): Show |
1 | a0001c0001t0005g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3092-978_3092-977i others(94): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299557 | |||||
| chr9:100299557
|
C | CACACACA others(83): Show |
2 | a0001c0001t0005g0007a0001c0001t0016g0011 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3092-978_3092-977i others(92): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299557 | |||||
| chr9:100299557
|
C | CACACACA others(79): Show |
7 | a0001c0001t0013g0078a0001c0001t0013g0079a0001c0001t0013g0082others(4): Show | 7 | HG00741.hp2 HG01106.hp1 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.3092-978_3092-977i others(88): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299557 | |||||
| chr9:100299557
|
C | CACACACA others(73): Show |
1 | a0001c0001t0029g0008 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3092-980_3092-979i others(82): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299557 | |||||
| chr9:100299568
|
A | AGCCTTGC others(37): Show |
1 | a0001c0001t0001g0015 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3092-1000_3092-999 others(47): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | chr9 | 100299568 | ||||||
| chr9:100299569
|
C | G | 1 | a0001c0001t0001g0015 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3092-999C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | chr9 | 100299569 | ||||||
| chr9:100299604
|
CCCA | C | 6 | a0001c0001t0004g0064a0001c0001t0004g0065a0001c0001t0004g0067others(3): Show | 6 | HG00609.hp1 HG02056.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.3092-960_3092-958d others(5): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299604 | |||||
| chr9:100299635
|
G | GAC | 11 | a0001c0001t0004g0050a0001c0001t0004g0054a0001c0001t0004g0055others(8): Show | 11 | HG00280.hp2 HG00741.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.3092-888_3092-887d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299635 | |||||
| chr9:100299635
|
G | GACAAACA others(77): Show |
1 | a0001c0001t0013g0016 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3092-930_3092-929i others(86): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299635 | |||||
| chr9:100299635
|
G | GACAC | 2 | a0001c0001t0010g0126a0001c0001t0010g0127 | 2 | HG02523.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.3092-890_3092-887d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299635 | |||||
| chr9:100299635
|
GAC | G | 21 | a0001c0001t0003g0043a0001c0001t0003g0073a0001c0001t0003g0095others(18): Show | 21 | HG00609.hp1 HG01074.hp1 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.3092-888_3092-887d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299635 | |||||
| chr9:100299635
|
GACAC | G | 8 | a0001c0001t0003g0178a0001c0001t0003g0179a0001c0001t0004g0121others(5): Show | 8 | HG00642.hp2 HG00738.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.3092-890_3092-887d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299635 | |||||
| chr9:100299635
|
GACACAC | G | 20 | a0001c0001t0003g0042a0001c0001t0003g0048a0001c0001t0003g0087others(17): Show | 20 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.3092-892_3092-887d others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299635 | |||||
| chr9:100299635
|
GACACACA others(1): Show |
G | 7 | a0001c0001t0004g0049a0001c0001t0011g0061a0001c0001t0011g0100others(4): Show | 7 | HG00733.hp2 HG02280.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.3092-894_3092-887d others(10): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299635 | |||||
| chr9:100299635
|
GACACACA others(7): Show |
G | 1 | a0006c0007t0011g0181 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3092-900_3092-887d others(16): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299635 | |||||
| chr9:100299635
|
GACACACA others(15): Show |
G | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.3092-908_3092-887d others(24): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299635 | |||||
| chr9:100299635
|
GACACACA others(19): Show |
G | 90 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(87): Show | 90 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.3092-912_3092-887d others(28): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299635 | |||||
| chr9:100299987
|
A | T | 1 | a0005c0006t0020g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3092-581A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | chr9 | 100299987 | ||||||
| chr9:100300094
|
C | T | 87 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0025others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.3092-474C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | chr9 | 100300094 | ||||||
| chr9:100300430
|
T | C | 1 | a0001c0001t0019g0066 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3092-138T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | chr9 | 100300430 |