Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9719 |
|---|---|
| ensemblid | ENSG00000197859.11 |
| hgncid | 14631 |
| symbol | ADAMTSL2 |
| name | ADAMTS like 2 |
| refseq_nuc | NM_014694.4 |
| refseq_prot | NP_055509.2 |
| ensembl_nuc | ENST00000651351.2 |
| ensembl_prot | ENSP00000498961.2 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 133534704 |
| end | 133575519 |
| strand | + |
| ver | v1.2 |
| region | chr9:133534704-133575519 |
| region5000 | chr9:133529704-133580519 |
| regionname0 | ADAMTSL2_chr9_133534704_133575519 |
| regionname5000 | ADAMTSL2_chr9_133529704_133580519 |
| 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 | 951 | 105 | 38 | 20 | 20 | 10 | 15 | 5 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0002 | 0/0 | 951 | 40 | 8 | 4 | 21 | 3 | 4 | 5 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0003 | 0/0 | 951 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0004 | 0/0 | 951 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0005 | 0/0 | 951 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0006 | 0/0 | 951 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0007 | 0/0 | 951 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| 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 | 0/0 | 2856 | 29 | 19 | 5 | 0 | 2 | 3 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0002 | 0/0 | 2856 | 23 | 4 | 2 | 13 | 3 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0003 | 1/1 | 2856 | 18 | 0 | 3 | 10 | 0 | 3 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0004 | 0/0 | 2856 | 12 | 1 | 2 | 8 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0005 | 0/0 | 2856 | 10 | 0 | 2 | 3 | 3 | 2 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0006 | 0/0 | 2856 | 10 | 7 | 3 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0007 | 0/0 | 2856 | 7 | 0 | 3 | 0 | 2 | 2 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0008 | 0/0 | 2856 | 4 | 0 | 0 | 1 | 0 | 3 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0009 | 0/0 | 2856 | 3 | 3 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0010 | 0/0 | 2856 | 3 | 0 | 0 | 1 | 1 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0011 | 0/0 | 2856 | 3 | 0 | 2 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0012 | 0/0 | 2856 | 2 | 0 | 0 | 2 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0013 | 0/0 | 2856 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0014 | 0/0 | 2856 | 2 | 0 | 1 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0015 | 0/0 | 2856 | 2 | 0 | 0 | 2 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0016 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0017 | 0/0 | 2856 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0018 | 0/0 | 2856 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0019 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0020 | 0/0 | 2856 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0021 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0022 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0023 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0024 | 0/0 | 2856 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0025 | 0/0 | 2856 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0026 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0027 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0028 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0029 | 0/0 | 2856 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0030 | 0/0 | 2856 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0031 | 0/0 | 2856 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0032 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0033 | 0/0 | 2856 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0034 | 0/0 | 2856 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0035 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0036 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| c0037 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| 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 | 1020 | 52 | 27 | 12 | 3 | 5 | 5 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| t0002 | 0/1 | 1019 | 40 | 1 | 4 | 21 | 3 | 10 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| t0003 | 1/0 | 1020 | 38 | 5 | 7 | 16 | 4 | 5 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| t0004 | 0/0 | 1020 | 6 | 6 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| t0005 | 0/0 | 1019 | 4 | 3 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| t0006 | 0/0 | 1020 | 2 | 1 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| t0007 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| t0008 | 0/0 | 1019 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| t0009 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| t0010 | 0/0 | 1020 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| t0011 | 0/0 | 1019 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| t0012 | 0/0 | 1019 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| t0013 | 0/0 | 1020 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| t0014 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| t0015 | 0/0 | 1020 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| t0016 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| 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 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0026 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0076 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| 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 | 0/0 | 2856 | 29 | 19 | 5 | 0 | 2 | 3 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0003 | 1/1 | 2856 | 18 | 0 | 3 | 10 | 0 | 3 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0005 | 0/0 | 2856 | 10 | 0 | 2 | 3 | 3 | 2 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0006 | 0/0 | 2856 | 10 | 7 | 3 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0007 | 0/0 | 2856 | 7 | 0 | 3 | 0 | 2 | 2 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0008 | 0/0 | 2856 | 4 | 0 | 0 | 1 | 0 | 3 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0010 | 0/0 | 2856 | 3 | 0 | 0 | 1 | 1 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0011 | 0/0 | 2856 | 3 | 0 | 2 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0012 | 0/0 | 2856 | 2 | 0 | 0 | 2 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0013 | 0/0 | 2856 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0015 | 0/0 | 2856 | 2 | 0 | 0 | 2 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0016 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0019 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0020 | 0/0 | 2856 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0021 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0022 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0023 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0024 | 0/0 | 2856 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0025 | 0/0 | 2856 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0026 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0027 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0028 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0031 | 0/0 | 2856 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0032 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0033 | 0/0 | 2856 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0035 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0002c0002 | 0/0 | 2856 | 23 | 4 | 2 | 13 | 3 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0002c0004 | 0/0 | 2856 | 12 | 1 | 2 | 8 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0002c0009 | 0/0 | 2856 | 3 | 3 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0002c0018 | 0/0 | 2856 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0002c0029 | 0/0 | 2856 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0003c0036 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0003c0037 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0004c0014 | 0/0 | 2856 | 2 | 0 | 1 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0005c0034 | 0/0 | 2856 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0006c0017 | 0/0 | 2856 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0007c0030 | 0/0 | 2856 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3875 | 18 | 9 | 5 | 0 | 2 | 2 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0001t0002 | 0/0 | 3874 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0001t0003 | 0/0 | 3875 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0001t0004 | 0/0 | 3875 | 6 | 6 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0001t0007 | 0/0 | 3875 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0001t0009 | 0/0 | 3875 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0001t0014 | 0/0 | 3875 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0003t0001 | 0/0 | 3875 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0003t0002 | 0/1 | 3874 | 13 | 0 | 2 | 8 | 0 | 2 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0003t0003 | 1/0 | 3875 | 4 | 0 | 1 | 1 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0005t0001 | 0/0 | 3875 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0005t0002 | 0/0 | 3874 | 7 | 0 | 1 | 3 | 2 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0005t0003 | 0/0 | 3875 | 2 | 0 | 1 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0006t0001 | 0/0 | 3875 | 6 | 4 | 2 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0006t0005 | 0/0 | 3874 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0006t0006 | 0/0 | 3875 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0006t0008 | 0/0 | 3874 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0007t0001 | 0/0 | 3875 | 7 | 0 | 3 | 0 | 2 | 2 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0008t0002 | 0/0 | 3874 | 4 | 0 | 0 | 1 | 0 | 3 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0010t0001 | 0/0 | 3875 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0010t0002 | 0/0 | 3874 | 2 | 0 | 0 | 0 | 1 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0011t0001 | 0/0 | 3875 | 3 | 0 | 2 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0012t0002 | 0/0 | 3874 | 2 | 0 | 0 | 2 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0013t0001 | 0/0 | 3875 | 2 | 2 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0015t0002 | 0/0 | 3874 | 2 | 0 | 0 | 2 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0016t0001 | 0/0 | 3875 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0019t0006 | 0/0 | 3875 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0020t0012 | 0/0 | 3874 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0021t0016 | 0/0 | 3875 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0022t0001 | 0/0 | 3875 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0023t0001 | 0/0 | 3875 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0024t0005 | 0/0 | 3874 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0025t0002 | 0/0 | 3874 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0026t0001 | 0/0 | 3875 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0027t0001 | 0/0 | 3875 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0028t0001 | 0/0 | 3875 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0031t0011 | 0/0 | 3874 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0032t0005 | 0/0 | 3874 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0033t0015 | 0/0 | 3875 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0001c0035t0003 | 0/0 | 3875 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0002c0002t0002 | 0/0 | 3874 | 4 | 1 | 0 | 3 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0002c0002t0003 | 0/0 | 3875 | 18 | 3 | 2 | 9 | 3 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0002c0002t0010 | 0/0 | 3875 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0002c0004t0001 | 0/0 | 3875 | 2 | 1 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0002c0004t0002 | 0/0 | 3874 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0002c0004t0003 | 0/0 | 3875 | 9 | 0 | 2 | 6 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0002c0009t0001 | 0/0 | 3875 | 3 | 3 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0002c0018t0003 | 0/0 | 3875 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0002c0029t0003 | 0/0 | 3875 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0003c0036t0001 | 0/0 | 3875 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0003c0037t0001 | 0/0 | 3875 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0004c0014t0002 | 0/0 | 3874 | 2 | 0 | 1 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0005c0034t0003 | 0/0 | 3875 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0006c0017t0002 | 0/0 | 3874 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| a0007c0030t0013 | 0/0 | 3875 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | copy fasta | chr9 | 133529704 | 133580519 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0001t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0001t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0001t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0001t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0001t0007g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0001t0009g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0001t0014g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0003t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0003t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0003t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0003t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0003t0002g0076 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0003t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0003t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0003t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0003t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0003t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0003t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0003t0003g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0003t0003g0026 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0003t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0003t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0005t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0005t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0005t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0005t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0005t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0005t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0005t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0005t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0005t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0005t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0006t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0006t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0006t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0006t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0006t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0006t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0006t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0006t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0006t0006g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0006t0008g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0007t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0007t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0007t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0007t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0007t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0007t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0007t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0008t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0008t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0008t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0008t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0010t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0010t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0010t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0011t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0011t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0011t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0012t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0012t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0013t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0013t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0015t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0015t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0016t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0019t0006g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0020t0012g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0021t0016g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0022t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0023t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0024t0005g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0025t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0026t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0027t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0028t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0031t0011g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0032t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0033t0015g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0001c0035t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0002t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0002t0003g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0002t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0002t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0002t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0002t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0002t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0002t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0002t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0002t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0002t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0002t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0002t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0002t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0002t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0002t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0002t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0002t0010g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0004t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0004t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0004t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0004t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0004t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0004t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0004t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0004t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0004t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0004t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0004t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0004t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0009t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0009t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0009t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0018t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0002c0029t0003g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0003c0036t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0003c0037t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0004c0014t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0004c0014t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0005c0034t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0006c0017t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| a0007c0030t0013g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0005 | t0003 | g0014 | EUR | GBR | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG00099 | hp2 | a0002 | c0002 | t0003 | g0030 | EUR | GBR | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG00140 | hp1 | a0007 | c0030 | t0013 | g0083 | EUR | GBR | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG00140 | hp2 | a0001 | c0005 | t0002 | g0145 | EUR | GBR | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG00280 | hp1 | a0002 | c0002 | t0003 | g0102 | EUR | FIN | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | FIN | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | FIN | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG00323 | hp2 | a0001 | c0007 | t0001 | g0147 | EUR | FIN | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0046 | EAS | CHS | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG00438 | hp2 | a0001 | c0015 | t0002 | g0148 | EAS | CHS | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG00544 | hp1 | a0001 | c0012 | t0002 | g0048 | EAS | CHS | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG00544 | hp2 | a0002 | c0004 | t0003 | g0068 | EAS | CHS | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG00597 | hp1 | a0001 | c0003 | t0002 | g0061 | EAS | CHS | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG00597 | hp2 | a0002 | c0004 | t0002 | g0058 | EAS | CHS | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG00609 | hp1 | a0006 | c0017 | t0002 | g0031 | EAS | CHS | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG00609 | hp2 | a0001 | c0005 | t0002 | g0143 | EAS | CHS | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG00621 | hp1 | a0001 | c0005 | t0002 | g0064 | EAS | CHS | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG00621 | hp2 | a0002 | c0004 | t0003 | g0063 | EAS | CHS | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG00738 | hp1 | a0001 | c0011 | t0001 | g0062 | AMR | PUR | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG01070 | hp1 | a0001 | c0006 | t0001 | g0103 | AMR | PUR | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG01070 | hp2 | a0001 | c0005 | t0002 | g0050 | AMR | PUR | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG01071 | hp1 | a0002 | c0002 | t0003 | g0019 | AMR | PUR | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG01071 | hp2 | a0001 | c0006 | t0001 | g0104 | AMR | PUR | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG01192 | hp1 | a0001 | c0003 | t0002 | g0054 | AMR | PUR | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG01255 | hp1 | a0001 | c0007 | t0001 | g0042 | AMR | CLM | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG01255 | hp2 | a0001 | c0006 | t0006 | g0109 | AMR | CLM | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG01257 | hp1 | a0001 | c0003 | t0002 | g0097 | AMR | CLM | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG01257 | hp2 | a0004 | c0014 | t0002 | g0098 | AMR | CLM | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG01261 | hp1 | a0001 | c0007 | t0001 | g0073 | AMR | CLM | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG01261 | hp2 | a0001 | c0031 | t0011 | g0004 | AMR | CLM | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG01433 | hp1 | a0002 | c0002 | t0003 | g0101 | AMR | CLM | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG01433 | hp2 | a0001 | c0020 | t0012 | g0005 | AMR | CLM | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG01496 | hp1 | a0001 | c0003 | t0003 | g0055 | AMR | CLM | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG01496 | hp2 | a0001 | c0011 | t0001 | g0007 | AMR | CLM | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG01515 | hp1 | a0001 | c0010 | t0002 | g0075 | EUR | IBS | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG01515 | hp2 | a0002 | c0002 | t0003 | g0095 | EUR | IBS | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG01884 | hp1 | a0002 | c0002 | t0003 | g0151 | AFR | ACB | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG01943 | hp1 | a0001 | c0007 | t0001 | g0131 | AMR | PEL | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG01975 | hp1 | a0005 | c0034 | t0003 | g0037 | AMR | PEL | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02015 | hp1 | a0001 | c0003 | t0002 | g0092 | EAS | KHV | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02015 | hp2 | a0002 | c0002 | t0003 | g0036 | EAS | KHV | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02040 | hp1 | a0002 | c0004 | t0003 | g0067 | EAS | KHV | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02040 | hp2 | a0001 | c0010 | t0001 | g0084 | EAS | KHV | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02056 | hp1 | a0002 | c0002 | t0010 | g0039 | EAS | KHV | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02056 | hp2 | a0002 | c0002 | t0002 | g0028 | EAS | KHV | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02080 | hp1 | a0001 | c0033 | t0015 | g0135 | EAS | KHV | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0027 | EAS | KHV | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02083 | hp1 | a0001 | c0003 | t0002 | g0069 | EAS | KHV | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02083 | hp2 | a0001 | c0003 | t0002 | g0133 | EAS | KHV | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02129 | hp1 | a0001 | c0003 | t0002 | g0057 | EAS | KHV | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02129 | hp2 | a0001 | c0008 | t0002 | g0090 | EAS | KHV | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02132 | hp1 | a0002 | c0002 | t0003 | g0066 | EAS | KHV | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02132 | hp2 | a0001 | c0003 | t0002 | g0141 | EAS | KHV | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02155 | hp1 | a0002 | c0002 | t0003 | g0071 | EAS | CDX | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02155 | hp2 | a0002 | c0002 | t0003 | g0096 | EAS | CDX | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02165 | hp1 | a0002 | c0004 | t0003 | g0044 | EAS | CDX | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02165 | hp2 | a0002 | c0002 | t0003 | g0021 | EAS | CDX | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02258 | hp1 | a0001 | c0006 | t0001 | g0080 | AFR | ACB | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02273 | hp2 | a0002 | c0004 | t0003 | g0038 | AMR | PEL | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02280 | hp1 | a0001 | c0035 | t0003 | g0020 | AFR | ACB | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02280 | hp2 | a0001 | c0027 | t0001 | g0010 | AFR | ACB | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02300 | hp1 | a0001 | c0005 | t0003 | g0070 | AMR | PEL | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02300 | hp2 | a0002 | c0004 | t0003 | g0047 | AMR | PEL | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02451 | hp1 | a0002 | c0009 | t0001 | g0124 | AFR | ACB | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0002 | AFR | GWD | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02602 | hp1 | a0001 | c0005 | t0001 | g0127 | SAS | PJL | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02602 | hp2 | a0001 | c0003 | t0002 | g0049 | SAS | PJL | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02615 | hp1 | a0002 | c0002 | t0003 | g0053 | AFR | GWD | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02615 | hp2 | a0001 | c0006 | t0005 | g0125 | AFR | GWD | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | GWD | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02622 | hp2 | a0001 | c0006 | t0001 | g0081 | AFR | GWD | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02647 | hp1 | a0001 | c0001 | t0007 | g0112 | AFR | GWD | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02647 | hp2 | a0003 | c0036 | t0001 | g0113 | AFR | GWD | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02723 | hp1 | a0001 | c0016 | t0001 | g0087 | AFR | GWD | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02723 | hp2 | a0003 | c0037 | t0001 | g0114 | AFR | GWD | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02809 | hp1 | a0001 | c0001 | t0009 | g0001 | AFR | GWD | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02809 | hp2 | a0001 | c0013 | t0001 | g0108 | AFR | GWD | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | GWD | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02896 | hp2 | a0001 | c0021 | t0016 | g0129 | AFR | GWD | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02922 | hp1 | a0001 | c0019 | t0006 | g0117 | AFR | ESN | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02922 | hp2 | a0001 | c0028 | t0001 | g0116 | AFR | ESN | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02965 | hp1 | a0002 | c0009 | t0001 | g0016 | AFR | ESN | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02965 | hp2 | a0001 | c0013 | t0001 | g0015 | AFR | ESN | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02970 | hp2 | a0001 | c0001 | t0014 | g0118 | AFR | ESN | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0035 | AFR | ESN | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG03041 | hp1 | a0001 | c0006 | t0008 | g0074 | AFR | GWD | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG03041 | hp2 | a0001 | c0022 | t0001 | g0059 | AFR | GWD | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG03130 | hp1 | a0001 | c0006 | t0001 | g0128 | AFR | ESN | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | ESN | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG03225 | hp1 | a0002 | c0002 | t0003 | g0152 | AFR | MSL | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG03239 | hp2 | a0001 | c0005 | t0002 | g0085 | SAS | PJL | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0150 | AFR | MSL | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG03453 | hp2 | a0001 | c0023 | t0001 | g0119 | AFR | MSL | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG03492 | hp1 | a0001 | c0007 | t0001 | g0142 | SAS | PJL | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG03654 | hp1 | a0001 | c0010 | t0002 | g0088 | SAS | PJL | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG03654 | hp2 | a0001 | c0008 | t0002 | g0045 | SAS | PJL | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG03710 | hp1 | a0001 | c0003 | t0002 | g0107 | SAS | PJL | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG03710 | hp2 | a0001 | c0007 | t0001 | g0032 | SAS | PJL | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG03834 | hp1 | a0002 | c0002 | t0003 | g0022 | SAS | BEB | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG03942 | hp1 | a0001 | c0025 | t0002 | g0089 | SAS | BEB | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG03942 | hp2 | a0001 | c0008 | t0002 | g0105 | SAS | BEB | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG04199 | hp1 | a0002 | c0004 | t0003 | g0093 | SAS | STU | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG04199 | hp2 | a0002 | c0029 | t0003 | g0011 | SAS | STU | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG04228 | hp1 | a0001 | c0008 | t0002 | g0024 | SAS | STU | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG04228 | hp2 | a0004 | c0014 | t0002 | g0034 | SAS | STU | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| NA18612 | hp1 | a0001 | c0015 | t0002 | g0072 | EAS | CHB | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| NA18612 | hp2 | a0002 | c0002 | t0003 | g0099 | EAS | CHB | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| NA18747 | hp1 | a0002 | c0002 | t0003 | g0134 | EAS | CHB | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| NA18747 | hp2 | a0001 | c0003 | t0002 | g0086 | EAS | CHB | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| NA18945 | hp1 | a0001 | c0003 | t0003 | g0091 | EAS | JPT | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| NA18945 | hp2 | a0002 | c0004 | t0001 | g0051 | EAS | JPT | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| NA18951 | hp1 | a0001 | c0012 | t0002 | g0139 | EAS | JPT | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| NA18951 | hp2 | a0002 | c0002 | t0003 | g0065 | EAS | JPT | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| NA18964 | hp1 | a0002 | c0004 | t0003 | g0082 | EAS | JPT | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| NA18964 | hp2 | a0001 | c0003 | t0001 | g0140 | EAS | JPT | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| NA18973 | hp1 | a0001 | c0003 | t0002 | g0033 | EAS | JPT | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| NA18973 | hp2 | a0002 | c0002 | t0003 | g0121 | EAS | JPT | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| NA18983 | hp1 | a0001 | c0005 | t0002 | g0144 | EAS | JPT | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| NA18983 | hp2 | a0002 | c0004 | t0003 | g0094 | EAS | JPT | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| NA19043 | hp1 | a0001 | c0006 | t0005 | g0137 | AFR | LWK | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| NA19043 | hp2 | a0002 | c0004 | t0001 | g0106 | AFR | LWK | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| NA20752 | hp1 | a0001 | c0007 | t0001 | g0060 | EUR | TSI | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| NA20752 | hp2 | a0001 | c0005 | t0002 | g0136 | EUR | TSI | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| NA20805 | hp1 | a0001 | c0011 | t0001 | g0029 | EUR | TSI | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| NA20805 | hp2 | a0001 | c0024 | t0005 | g0126 | EUR | TSI | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| NA20905 | hp1 | a0002 | c0018 | t0003 | g0110 | SAS | GIH | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| NA20905 | hp2 | a0001 | c0003 | t0003 | g0003 | SAS | GIH | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0079 | AFR | ACB | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02109 | hp2 | a0001 | c0006 | t0001 | g0111 | AFR | ACB | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02559 | hp1 | a0001 | c0032 | t0005 | g0100 | AFR | ACB | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG02559 | hp2 | a0001 | c0026 | t0001 | g0123 | AFR | ACB | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG06807 | hp1 | a0002 | c0009 | t0001 | g0149 | AFR | USA | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | USA | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0002 | g0076 | REF | REF | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0003 | g0026 | REF | REF | ADAMTSL2_chr9_133529704_133580519 | ADAMTSL2 | chr9 | 133529704 | 133580519 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:133536800
|
A | G | 1 | a0003 | 2 | HG02647.hp2 HG02723.hp2 |
missense_variant&splice_region_variant | MODERATE | c.88A>G | p.Thr30Ala | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 2/19 | 452/3875 | 88/2856 | 30/951 | chr9 | 133536800 | ||
| chr9:133538387
|
C | T | 1 | a0005 | 1 | HG01975.hp1 | missense_variant | MODERATE | c.272C>T | p.Thr91Met | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/19 | 636/3875 | 272/2856 | 91/951 | chr9 | 133538387 | ||
| chr9:133554507
|
G | A | 3 | a0002a0005a0006 | 42 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(39): Show |
missense_variant | MODERATE | c.1090G>A | p.Val364Ile | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 10/19 | 1454/3875 | 1090/2856 | 364/951 | chr9 | 133554507 | ||
| chr9:133554639
|
G | A | 1 | a0007 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.1222G>A | p.Glu408Lys | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 10/19 | 1586/3875 | 1222/2856 | 408/951 | chr9 | 133554639 | ||
| chr9:133568440
|
G | A | 1 | a0004 | 2 | HG01257.hp2 HG04228.hp2 |
missense_variant | MODERATE | c.2042G>A | p.Arg681Gln | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 14/19 | 2406/3875 | 2042/2856 | 681/951 | chr9 | 133568440 | ||
| chr9:133568482
|
C | A | 1 | a0006 | 1 | HG00609.hp1 | missense_variant | MODERATE | c.2084C>A | p.Ser695Tyr | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 14/19 | 2448/3875 | 2084/2856 | 695/951 | chr9 | 133568482 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:133537419
|
A | G | 1 | a0001c0035 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.105A>G | p.Thr35Thr | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 3/19 | 469/3875 | 105/2856 | 35/951 | chr9 | 133537419 | ||
| chr9:133538394
|
G | A | 1 | a0001c0016 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.279G>A | p.Thr93Thr | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/19 | 643/3875 | 279/2856 | 93/951 | chr9 | 133538394 | ||
| chr9:133547048
|
C | T | 26 | a0001c0001a0001c0005a0001c0006others(23): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
synonymous_variant | LOW | c.774C>T | p.Asp258Asp | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/19 | 1138/3875 | 774/2856 | 258/951 | chr9 | 133547048 | ||
| chr9:133547111
|
C | T | 1 | a0001c0033 | 1 | HG02080.hp1 | synonymous_variant | LOW | c.837C>T | p.Ile279Ile | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/19 | 1201/3875 | 837/2856 | 279/951 | chr9 | 133547111 | ||
| chr9:133547114
|
A | T | 26 | a0001c0001a0001c0005a0001c0006others(23): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
synonymous_variant | LOW | c.840A>T | p.Ala280Ala | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/19 | 1204/3875 | 840/2856 | 280/951 | chr9 | 133547114 | ||
| chr9:133547133
|
A | C | 26 | a0001c0001a0001c0005a0001c0006others(23): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
synonymous_variant | LOW | c.859A>C | p.Arg287Arg | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/19 | 1223/3875 | 859/2856 | 287/951 | chr9 | 133547133 | ||
| chr9:133547174
|
C | T | 7 | a0001c0010a0001c0011a0001c0015others(4): Show | 12 | HG00140.hp1 HG00438.hp2 HG00738.hp1 others(9): Show |
synonymous_variant | LOW | c.900C>T | p.Ile300Ile | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/19 | 1264/3875 | 900/2856 | 300/951 | chr9 | 133547174 | ||
| chr9:133554647
|
C | T | 4 | a0001c0026a0001c0027a0001c0028others(1): Show | 4 | HG02280.hp2 HG02559.hp2 HG02723.hp2 others(1): Show |
synonymous_variant | LOW | c.1230C>T | p.Ala410Ala | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 10/19 | 1594/3875 | 1230/2856 | 410/951 | chr9 | 133554647 | ||
| chr9:133554662
|
C | T | 1 | a0001c0025 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.1245C>T | p.Cys415Cys | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 10/19 | 1609/3875 | 1245/2856 | 415/951 | chr9 | 133554662 | ||
| chr9:133555838
|
C | T | 1 | a0001c0019 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.1557C>T | p.Ser519Ser | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/19 | 1921/3875 | 1557/2856 | 519/951 | chr9 | 133555838 | ||
| chr9:133555922
|
C | T | 8 | a0001c0006a0001c0007a0001c0024others(5): Show | 23 | HG00323.hp2 HG01070.hp1 HG01071.hp2 others(20): Show |
synonymous_variant | LOW | c.1641C>T | p.His547His | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/19 | 2005/3875 | 1641/2856 | 547/951 | chr9 | 133555922 | ||
| chr9:133568420
|
C | T | 7 | a0001c0007a0001c0022a0001c0023others(4): Show | 13 | HG00323.hp2 HG01255.hp1 HG01261.hp1 others(10): Show |
synonymous_variant | LOW | c.2022C>T | p.Pro674Pro | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 14/19 | 2386/3875 | 2022/2856 | 674/951 | chr9 | 133568420 | ||
| chr9:133568447
|
C | T | 1 | a0002c0009 | 3 | HG02451.hp1 HG02965.hp1 HG06807.hp1 |
synonymous_variant | LOW | c.2049C>T | p.Pro683Pro | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 14/19 | 2413/3875 | 2049/2856 | 683/951 | chr9 | 133568447 | ||
| chr9:133568656
|
G | A | 5 | a0001c0008a0001c0012a0001c0015others(2): Show | 11 | HG00438.hp2 HG00544.hp1 HG01257.hp2 others(8): Show |
synonymous_variant | LOW | c.2142G>A | p.Ser714Ser | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 15/19 | 2506/3875 | 2142/2856 | 714/951 | chr9 | 133568656 | ||
| chr9:133569422
|
C | T | 1 | a0001c0021 | 1 | HG02896.hp2 | synonymous_variant | LOW | c.2259C>T | p.Cys753Cys | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 16/19 | 2623/3875 | 2259/2856 | 753/951 | chr9 | 133569422 | ||
| chr9:133569476
|
A | G | 29 | a0001c0001a0001c0006a0001c0007others(26): Show | 83 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
synonymous_variant | LOW | c.2313A>G | p.Val771Val | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 16/19 | 2677/3875 | 2313/2856 | 771/951 | chr9 | 133569476 | ||
| chr9:133569488
|
C | G | 5 | a0001c0008a0001c0012a0001c0015others(2): Show | 11 | HG00438.hp2 HG00544.hp1 HG01257.hp2 others(8): Show |
synonymous_variant | LOW | c.2325C>G | p.Ser775Ser | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 16/19 | 2689/3875 | 2325/2856 | 775/951 | chr9 | 133569488 | ||
| chr9:133570351
|
C | T | 2 | a0001c0020a0001c0031 | 2 | HG01261.hp2 HG01433.hp2 |
synonymous_variant | LOW | c.2436C>T | p.Arg812Arg | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/19 | 2800/3875 | 2436/2856 | 812/951 | chr9 | 133570351 | ||
| chr9:133570435
|
C | T | 1 | a0001c0031 | 1 | HG01261.hp2 | synonymous_variant | LOW | c.2520C>T | p.Ala840Ala | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/19 | 2884/3875 | 2520/2856 | 840/951 | chr9 | 133570435 | ||
| chr9:133570495
|
C | T | 1 | a0001c0028 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.2580C>T | p.Ser860Ser | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/19 | 2944/3875 | 2580/2856 | 860/951 | chr9 | 133570495 | ||
| chr9:133573863
|
G | A | 6 | a0001c0007a0001c0022a0001c0026others(3): Show | 12 | HG00323.hp2 HG01255.hp1 HG01261.hp1 others(9): Show |
synonymous_variant | LOW | c.2613G>A | p.Val871Val | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 18/19 | 2977/3875 | 2613/2856 | 871/951 | chr9 | 133573863 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:133534739
|
G | C | 1 | a0001c0001t0007 | 1 | HG02647.hp1 | 5_prime_UTR_variant | MODIFIER | c.-329G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 1/19 | 1974 | chr9 | 133534739 | |||||
| chr9:133534773
|
G | A | 1 | a0001c0006t0008 | 1 | HG03041.hp1 | 5_prime_UTR_variant | MODIFIER | c.-295G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 1/19 | 1940 | chr9 | 133534773 | |||||
| chr9:133534857
|
G | C | 1 | a0001c0001t0009 | 1 | HG02809.hp1 | 5_prime_UTR_variant | MODIFIER | c.-211G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 1/19 | 1856 | chr9 | 133534857 | |||||
| chr9:133534872
|
C | T | 1 | a0001c0021t0016 | 1 | HG02896.hp2 | 5_prime_UTR_variant | MODIFIER | c.-196C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 1/19 | 1841 | chr9 | 133534872 | |||||
| chr9:133536674
|
G | A | 1 | a0002c0002t0010 | 1 | HG02056.hp1 | 5_prime_UTR_variant | MODIFIER | c.-39G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 2/19 | 39 | chr9 | 133536674 | |||||
| chr9:133574956
|
G | A | 6 | a0001c0006t0005a0001c0006t0008a0001c0020t0012others(3): Show | 7 | HG01261.hp2 HG01433.hp2 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*92G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 19/19 | 92 | chr9 | 133574956 | |||||
| chr9:133575022
|
G | A | 33 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(30): Show | 73 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*158G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 19/19 | 158 | chr9 | 133575022 | |||||
| chr9:133575081
|
G | T | 1 | a0001c0020t0012 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*217G>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 19/19 | 217 | chr9 | 133575081 | |||||
| chr9:133575116
|
C | T | 2 | a0001c0001t0004a0001c0001t0009 | 7 | HG02109.hp1 HG02622.hp1 HG02809.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*252C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 19/19 | 252 | chr9 | 133575116 | |||||
| chr9:133575149
|
GC | G | 18 | a0001c0001t0002a0001c0003t0002a0001c0005t0002others(15): Show | 47 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*291delC | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 19/19 | 291 | INFO_REALIGN_3_PRIME | chr9 | 133575149 | ||||
| chr9:133575228
|
C | T | 1 | a0001c0033t0015 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*364C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 19/19 | 364 | chr9 | 133575228 | |||||
| chr9:133575240
|
G | A | 2 | a0001c0020t0012a0001c0031t0011 | 2 | HG01261.hp2 HG01433.hp2 |
3_prime_UTR_variant | MODIFIER | c.*376G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 19/19 | 376 | chr9 | 133575240 | |||||
| chr9:133575288
|
G | T | 2 | a0001c0006t0006a0001c0019t0006 | 2 | HG01255.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*424G>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 19/19 | 424 | chr9 | 133575288 | |||||
| chr9:133575347
|
A | C | 1 | a0001c0001t0014 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*483A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 19/19 | 483 | chr9 | 133575347 | |||||
| chr9:133575459
|
G | A | 1 | a0007c0030t0013 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*595G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 19/19 | 595 | chr9 | 133575459 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:133535371
|
G | A | 1 | a0001c0001t0009g0001 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-151+454G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 1/18 | chr9 | 133535371 | ||||||
| chr9:133535376
|
TG | T | 17 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(14): Show | 17 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(14): Show |
intron_variant | MODIFIER | c.-151+465delG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr9 | 133535376 | |||||
| chr9:133535441
|
C | T | 66 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(63): Show | 66 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.-151+524C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 1/18 | chr9 | 133535441 | ||||||
| chr9:133535444
|
C | G | 23 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0138others(20): Show | 23 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.-151+527C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 1/18 | chr9 | 133535444 | ||||||
| chr9:133536042
|
T | C | 17 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(14): Show | 17 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(14): Show |
intron_variant | MODIFIER | c.-150-521T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 1/18 | chr9 | 133536042 | ||||||
| chr9:133536200
|
A | T | 50 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0138others(47): Show | 50 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.-150-363A>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 1/18 | chr9 | 133536200 | ||||||
| chr9:133536303
|
G | A | 50 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0138others(47): Show | 50 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.-150-260G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 1/18 | chr9 | 133536303 | ||||||
| chr9:133536322
|
C | G | 4 | a0001c0001t0001g0078a0001c0001t0004g0079a0001c0006t0001g0080others(1): Show | 4 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-150-241C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 1/18 | chr9 | 133536322 | ||||||
| chr9:133536322
|
C | T | 1 | a0001c0024t0005g0126 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-150-241C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 1/18 | chr9 | 133536322 | ||||||
| chr9:133536463
|
C | A | 1 | a0002c0002t0003g0019 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-150-100C>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 1/18 | chr9 | 133536463 | ||||||
| chr9:133536484
|
A | C | 89 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.-150-79A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 1/18 | chr9 | 133536484 | ||||||
| chr9:133536945
|
G | T | 35 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(32): Show | 35 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.90+143G>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 2/18 | chr9 | 133536945 | ||||||
| chr9:133536965
|
G | A | 1 | a0001c0001t0009g0001 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.90+163G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 2/18 | chr9 | 133536965 | ||||||
| chr9:133537093
|
C | T | 1 | a0001c0001t0003g0077 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.90+291C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 2/18 | chr9 | 133537093 | ||||||
| chr9:133537223
|
T | A | 48 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0138others(45): Show | 48 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(45): Show |
intron_variant | MODIFIER | c.91-182T>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 2/18 | chr9 | 133537223 | ||||||
| chr9:133537293
|
G | C | 2 | a0003c0036t0001g0113a0003c0037t0001g0114 | 2 | HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.91-112G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 2/18 | chr9 | 133537293 | ||||||
| chr9:133537784
|
G | C | 1 | a0002c0002t0002g0002 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.233+237G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 3/18 | chr9 | 133537784 | ||||||
| chr9:133538011
|
T | C | 2 | a0001c0001t0007g0112a0001c0024t0005g0126 | 2 | HG02647.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.234-338T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 3/18 | chr9 | 133538011 | ||||||
| chr9:133538440
|
G | T | 21 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(18): Show | 21 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(18): Show |
intron_variant | MODIFIER | c.309+16G>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | chr9 | 133538440 | ||||||
| chr9:133538583
|
C | A | 1 | a0002c0004t0003g0082 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.309+159C>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | chr9 | 133538583 | ||||||
| chr9:133538632
|
T | C | 87 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.309+208T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | chr9 | 133538632 | ||||||
| chr9:133538673
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.309+249G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | chr9 | 133538673 | ||||||
| chr9:133538814
|
G | C | 86 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.309+390G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | chr9 | 133538814 | ||||||
| chr9:133538893
|
A | G | 5 | a0001c0001t0001g0120a0001c0001t0014g0118a0001c0019t0006g0117others(2): Show | 5 | HG02145.hp1 HG02922.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.309+469A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | chr9 | 133538893 | ||||||
| chr9:133538927
|
A | T | 2 | a0001c0006t0001g0103a0001c0006t0001g0104 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.309+503A>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | chr9 | 133538927 | ||||||
| chr9:133538995
|
C | A | 1 | a0001c0001t0001g0023 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.309+571C>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | chr9 | 133538995 | ||||||
| chr9:133539102
|
C | T | 1 | a0001c0015t0002g0148 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.310-669C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | chr9 | 133539102 | ||||||
| chr9:133539210
|
G | A | 1 | a0001c0008t0002g0024 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.310-561G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | chr9 | 133539210 | ||||||
| chr9:133539270
|
A | G | 1 | a0001c0003t0002g0076 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.310-501A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | chr9 | 133539270 | ||||||
| chr9:133539377
|
C | T | 1 | a0001c0010t0002g0075 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.310-394C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | chr9 | 133539377 | ||||||
| chr9:133539394
|
C | T | 139 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(136): Show | 139 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.310-377C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | chr9 | 133539394 | ||||||
| chr9:133539435
|
G | A | 1 | a0001c0003t0002g0033 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.310-336G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | chr9 | 133539435 | ||||||
| chr9:133539444
|
G | A | 1 | a0001c0031t0011g0004 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.310-327G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | chr9 | 133539444 | ||||||
| chr9:133539463
|
C | T | 2 | a0001c0006t0001g0111a0001c0006t0008g0074 | 2 | HG02109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.310-308C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | chr9 | 133539463 | ||||||
| chr9:133539540
|
G | C | 2 | a0001c0005t0002g0085a0001c0024t0005g0126 | 2 | HG03239.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.310-231G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | chr9 | 133539540 | ||||||
| chr9:133539547
|
T | G | 1 | a0001c0035t0003g0020 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.310-224T>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | chr9 | 133539547 | ||||||
| chr9:133539572
|
T | C | 98 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.310-199T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | chr9 | 133539572 | ||||||
| chr9:133539601
|
C | T | 1 | a0002c0002t0003g0102 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.310-170C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | chr9 | 133539601 | ||||||
| chr9:133539602
|
A | G | 107 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(104): Show | 107 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.310-169A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | chr9 | 133539602 | ||||||
| chr9:133539646
|
C | G | 2 | a0001c0005t0002g0064a0002c0004t0003g0063 | 2 | HG00621.hp1 HG00621.hp2 |
intron_variant | MODIFIER | c.310-125C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | chr9 | 133539646 | ||||||
| chr9:133539653
|
A | ACGGCTGT others(2): Show |
11 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0132others(8): Show | 11 | HG01192.hp2 HG01255.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.310-93_310-85dupTC others(7): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 133539653 | |||||
| chr9:133539653
|
A | ACGGCTGT others(11): Show |
22 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0004g0079others(19): Show | 22 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(19): Show |
intron_variant | MODIFIER | c.310-102_310-85dupT others(17): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 133539653 | |||||
| chr9:133539653
|
A | ACGGCTGT others(20): Show |
35 | a0001c0001t0001g0052a0001c0001t0001g0130a0001c0001t0001g0138others(32): Show | 35 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.310-111_310-85dupT others(26): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 133539653 | |||||
| chr9:133539653
|
A | ACGGCTGT others(29): Show |
42 | a0001c0001t0001g0012a0001c0001t0001g0056a0001c0001t0001g0122others(39): Show | 42 | HG00140.hp1 HG00323.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.310-85_310-84insTC others(34): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 133539653 | |||||
| chr9:133539653
|
A | ACGGCTGT others(38): Show |
16 | a0001c0001t0001g0013a0001c0001t0001g0120a0001c0001t0009g0001others(13): Show | 16 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(13): Show |
intron_variant | MODIFIER | c.310-85_310-84insTC others(43): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 133539653 | |||||
| chr9:133539653
|
A | ACGGCTGT others(47): Show |
5 | a0001c0001t0001g0078a0001c0001t0001g0115a0001c0001t0014g0118others(2): Show | 5 | HG00323.hp2 HG00609.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.310-85_310-84insTC others(52): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 133539653 | |||||
| chr9:133539653
|
A | ACGGCTGT others(56): Show |
3 | a0001c0006t0001g0103a0001c0006t0001g0104a0001c0006t0005g0125 | 3 | HG01070.hp1 HG01071.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.310-85_310-84insTC others(61): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 133539653 | |||||
| chr9:133539653
|
A | ACGGCTGT others(65): Show |
2 | a0002c0002t0003g0096a0002c0002t0003g0101 | 2 | HG01433.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.310-85_310-84insTC others(70): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 133539653 | |||||
| chr9:133539653
|
A | ACGGCTGT others(83): Show |
1 | a0001c0011t0001g0062 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.310-85_310-84insTC others(88): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 133539653 | |||||
| chr9:133539653
|
A | ACGGCTGT others(65): Show |
1 | a0002c0002t0003g0021 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.310-85_310-84insTC others(70): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 133539653 | |||||
| chr9:133539653
|
A | ATGGCTGT others(20): Show |
1 | a0002c0009t0001g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.310-118_310-117ins others(27): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | chr9 | 133539653 | ||||||
| chr9:133539653
|
ACGGCTGT others(2): Show |
A | 2 | a0001c0001t0004g0150a0002c0009t0001g0149 | 2 | HG03453.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.310-93_310-85delTC others(7): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | 133539653 | |||||
| chr9:133539762
|
G | A | 1 | a0001c0003t0002g0097 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.310-9G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 4/18 | chr9 | 133539762 | ||||||
| chr9:133539920
|
T | A | 74 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(71): Show | 74 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.412+47T>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 5/18 | chr9 | 133539920 | ||||||
| chr9:133540118
|
C | G | 19 | a0001c0001t0001g0025a0001c0001t0001g0115a0001c0001t0001g0138others(16): Show | 19 | HG00140.hp1 HG00140.hp2 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.412+245C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 5/18 | chr9 | 133540118 | ||||||
| chr9:133540191
|
G | A | 1 | a0001c0006t0005g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.412+318G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 5/18 | chr9 | 133540191 | ||||||
| chr9:133540239
|
T | C | 6 | a0001c0003t0002g0133a0001c0008t0002g0090a0002c0002t0002g0046others(3): Show | 6 | HG00438.hp1 HG02083.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.413-359T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 5/18 | chr9 | 133540239 | ||||||
| chr9:133540282
|
G | A | 2 | a0001c0005t0002g0145a0001c0020t0012g0005 | 2 | HG00140.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.413-316G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 5/18 | chr9 | 133540282 | ||||||
| chr9:133540399
|
G | A | 8 | a0001c0001t0001g0146a0001c0008t0002g0024a0001c0010t0001g0084others(5): Show | 8 | HG00609.hp1 HG01975.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.413-199G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 5/18 | chr9 | 133540399 | ||||||
| chr9:133540549
|
G | A | 1 | a0001c0007t0001g0073 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.413-49G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 5/18 | chr9 | 133540549 | ||||||
| chr9:133540563
|
C | T | 2 | a0001c0006t0005g0125a0001c0006t0008g0074 | 2 | HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.413-35C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 5/18 | chr9 | 133540563 | ||||||
| chr9:133540843
|
C | A | 9 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0115others(6): Show | 9 | HG00140.hp2 HG01433.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.559-35C>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 6/18 | chr9 | 133540843 | ||||||
| chr9:133541015
|
C | T | 1 | a0001c0007t0001g0060 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.682+14C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133541015 | ||||||
| chr9:133541087
|
T | G | 5 | a0001c0005t0002g0145a0001c0007t0001g0060a0001c0020t0012g0005others(2): Show | 5 | HG00140.hp2 HG01433.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.682+86T>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133541087 | ||||||
| chr9:133541292
|
C | CT | 11 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(8): Show | 11 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.682+305dupT | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr9 | 133541292 | |||||
| chr9:133541292
|
C | CTTT | 5 | a0001c0005t0002g0145a0001c0007t0001g0060a0001c0020t0012g0005others(2): Show | 5 | HG00140.hp2 HG01433.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.682+303_682+305dup others(3): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr9 | 133541292 | |||||
| chr9:133541530
|
C | A | 25 | a0001c0001t0001g0023a0001c0001t0001g0115a0001c0001t0001g0120others(22): Show | 25 | HG00099.hp1 HG00140.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.682+529C>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133541530 | ||||||
| chr9:133541579
|
A | G | 1 | a0001c0003t0002g0076 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.682+578A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133541579 | ||||||
| chr9:133541603
|
A | G | 27 | a0001c0001t0001g0023a0001c0001t0001g0115a0001c0001t0001g0120others(24): Show | 27 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(24): Show |
intron_variant | MODIFIER | c.682+602A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133541603 | ||||||
| chr9:133541636
|
C | G | 18 | a0001c0001t0001g0078a0001c0005t0001g0127a0001c0005t0002g0050others(15): Show | 18 | HG00323.hp2 HG01070.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.682+635C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133541636 | ||||||
| chr9:133541703
|
C | T | 3 | a0001c0005t0002g0145a0001c0020t0012g0005a0002c0002t0003g0030 | 3 | HG00099.hp2 HG00140.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.682+702C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133541703 | ||||||
| chr9:133541735
|
C | T | 18 | a0001c0001t0001g0078a0001c0005t0001g0127a0001c0005t0002g0050others(15): Show | 18 | HG00323.hp2 HG01070.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.682+734C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133541735 | ||||||
| chr9:133541785
|
G | A | 5 | a0001c0019t0006g0117a0002c0004t0001g0106a0002c0004t0003g0063others(2): Show | 5 | HG00621.hp2 HG02451.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.682+784G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133541785 | ||||||
| chr9:133541811
|
C | G | 1 | a0001c0005t0002g0143 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.682+810C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133541811 | ||||||
| chr9:133541816
|
A | T | 26 | a0001c0001t0001g0023a0001c0001t0001g0115a0001c0001t0001g0120others(23): Show | 26 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(23): Show |
intron_variant | MODIFIER | c.682+815A>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133541816 | ||||||
| chr9:133541969
|
A | G | 6 | a0001c0005t0002g0145a0001c0007t0001g0060a0001c0020t0012g0005others(3): Show | 6 | HG00099.hp2 HG00140.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.682+968A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133541969 | ||||||
| chr9:133542086
|
C | T | 25 | a0001c0001t0001g0023a0001c0001t0001g0115a0001c0001t0001g0120others(22): Show | 25 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(22): Show |
intron_variant | MODIFIER | c.682+1085C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133542086 | ||||||
| chr9:133542155
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.682+1154G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133542155 | ||||||
| chr9:133542168
|
C | G | 26 | a0001c0001t0001g0023a0001c0001t0001g0115a0001c0001t0001g0120others(23): Show | 26 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(23): Show |
intron_variant | MODIFIER | c.682+1167C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133542168 | ||||||
| chr9:133542232
|
C | T | 3 | a0001c0005t0002g0145a0001c0020t0012g0005a0002c0002t0003g0030 | 3 | HG00099.hp2 HG00140.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.682+1231C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133542232 | ||||||
| chr9:133542238
|
G | A | 26 | a0001c0001t0001g0023a0001c0001t0001g0115a0001c0001t0001g0120others(23): Show | 26 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(23): Show |
intron_variant | MODIFIER | c.682+1237G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133542238 | ||||||
| chr9:133542267
|
A | G | 12 | a0001c0001t0001g0023a0001c0001t0001g0115a0001c0001t0001g0146others(9): Show | 12 | HG00099.hp1 HG01884.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.682+1266A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133542267 | ||||||
| chr9:133542327
|
C | A | 3 | a0001c0007t0001g0060a0002c0002t0003g0095a0002c0002t0003g0099 | 3 | HG01515.hp2 NA18612.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.682+1326C>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133542327 | ||||||
| chr9:133542446
|
C | T | 1 | a0001c0003t0002g0107 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.682+1445C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133542446 | ||||||
| chr9:133542537
|
A | C | 111 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.682+1536A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133542537 | ||||||
| chr9:133542548
|
A | G | 6 | a0001c0001t0001g0120a0001c0001t0004g0150a0001c0001t0007g0112others(3): Show | 6 | HG02145.hp1 HG02647.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.682+1547A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133542548 | ||||||
| chr9:133542779
|
G | A | 14 | a0001c0001t0001g0025a0001c0001t0001g0138a0001c0010t0001g0084others(11): Show | 14 | HG00140.hp1 HG00438.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.683-1691G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133542779 | ||||||
| chr9:133542954
|
A | AT | 6 | a0001c0005t0002g0145a0001c0007t0001g0060a0001c0020t0012g0005others(3): Show | 6 | HG00099.hp2 HG00140.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.683-1505dupT | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr9 | 133542954 | |||||
| chr9:133543024
|
C | G | 1 | a0002c0002t0003g0065 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.683-1446C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133543024 | ||||||
| chr9:133543127
|
A | T | 3 | a0001c0001t0001g0132a0001c0001t0003g0077a0002c0002t0003g0053 | 3 | HG02615.hp1 HG02896.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.683-1343A>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133543127 | ||||||
| chr9:133543127
|
AT | A | 14 | a0001c0001t0001g0025a0001c0001t0001g0138a0001c0010t0001g0084others(11): Show | 14 | HG00140.hp1 HG00438.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.683-1338delT | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr9 | 133543127 | |||||
| chr9:133543251
|
A | G | 59 | a0001c0001t0001g0025a0001c0001t0001g0043a0001c0001t0001g0052others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.683-1219A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133543251 | ||||||
| chr9:133543315
|
A | G | 1 | a0002c0002t0010g0039 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.683-1155A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133543315 | ||||||
| chr9:133543440
|
C | T | 1 | a0002c0002t0003g0102 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.683-1030C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133543440 | ||||||
| chr9:133543498
|
T | C | 108 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.683-972T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133543498 | ||||||
| chr9:133543547
|
T | C | 53 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(50): Show | 53 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(50): Show |
intron_variant | MODIFIER | c.683-923T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133543547 | ||||||
| chr9:133543620
|
T | C | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.683-850T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133543620 | ||||||
| chr9:133543658
|
C | T | 1 | a0001c0022t0001g0059 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.683-812C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133543658 | ||||||
| chr9:133543677
|
A | G | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.683-793A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133543677 | ||||||
| chr9:133543687
|
G | A | 1 | a0001c0023t0001g0119 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.683-783G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133543687 | ||||||
| chr9:133543694
|
C | A | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.683-776C>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133543694 | ||||||
| chr9:133543719
|
C | T | 56 | a0001c0001t0001g0025a0001c0001t0001g0043a0001c0001t0001g0052others(53): Show | 56 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.683-751C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133543719 | ||||||
| chr9:133543754
|
G | A | 100 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0043others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.683-716G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133543754 | ||||||
| chr9:133543767
|
T | C | 50 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(47): Show | 50 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(47): Show |
intron_variant | MODIFIER | c.683-703T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133543767 | ||||||
| chr9:133543821
|
T | C | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.683-649T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133543821 | ||||||
| chr9:133543908
|
A | T | 15 | a0001c0001t0001g0025a0001c0001t0001g0138a0001c0005t0002g0064others(12): Show | 15 | HG00140.hp1 HG00438.hp2 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.683-562A>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133543908 | ||||||
| chr9:133543924
|
G | T | 1 | a0002c0004t0003g0068 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.683-546G>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133543924 | ||||||
| chr9:133544042
|
T | G | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.683-428T>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133544042 | ||||||
| chr9:133544054
|
T | C | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.683-416T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133544054 | ||||||
| chr9:133544057
|
A | G | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.683-413A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133544057 | ||||||
| chr9:133544160
|
G | C | 2 | a0001c0006t0005g0125a0001c0006t0008g0074 | 2 | HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.683-310G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133544160 | ||||||
| chr9:133544200
|
C | T | 1 | a0001c0021t0016g0129 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.683-270C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133544200 | ||||||
| chr9:133544245
|
T | C | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.683-225T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133544245 | ||||||
| chr9:133544282
|
G | C | 55 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(52): Show | 55 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(52): Show |
intron_variant | MODIFIER | c.683-188G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133544282 | ||||||
| chr9:133544298
|
A | G | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.683-172A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133544298 | ||||||
| chr9:133544335
|
A | G | 55 | a0001c0001t0001g0025a0001c0001t0001g0043a0001c0001t0001g0052others(52): Show | 55 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.683-135A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133544335 | ||||||
| chr9:133544407
|
C | T | 54 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(51): Show |
intron_variant | MODIFIER | c.683-63C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133544407 | ||||||
| chr9:133544458
|
T | G | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.683-12T>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 7/18 | chr9 | 133544458 | ||||||
| chr9:133544602
|
G | A | 2 | a0001c0001t0004g0150a0001c0001t0014g0118 | 2 | HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.763+52G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133544602 | ||||||
| chr9:133544623
|
G | A | 2 | a0001c0006t0005g0125a0001c0006t0008g0074 | 2 | HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.763+73G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133544623 | ||||||
| chr9:133544732
|
C | T | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.763+182C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133544732 | ||||||
| chr9:133544863
|
C | T | 2 | a0002c0002t0003g0151a0002c0002t0003g0152 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.763+313C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133544863 | ||||||
| chr9:133544864
|
G | A | 2 | a0001c0001t0001g0132a0001c0001t0003g0077 | 2 | HG02896.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.763+314G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133544864 | ||||||
| chr9:133544980
|
C | T | 1 | a0002c0009t0001g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.763+430C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133544980 | ||||||
| chr9:133544984
|
C | CTGA | 7 | a0001c0005t0002g0145a0001c0007t0001g0060a0001c0020t0012g0005others(4): Show | 7 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(4): Show |
intron_variant | MODIFIER | c.763+437_763+439dup others(3): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr9 | 133544984 | |||||
| chr9:133545177
|
G | A | 1 | a0002c0004t0003g0047 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.763+627G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133545177 | ||||||
| chr9:133545182
|
G | A | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.763+632G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133545182 | ||||||
| chr9:133545183
|
C | A | 3 | a0002c0004t0001g0051a0002c0004t0003g0063a0006c0017t0002g0031 | 3 | HG00609.hp1 HG00621.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.763+633C>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133545183 | ||||||
| chr9:133545183
|
C | T | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.763+633C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133545183 | ||||||
| chr9:133545249
|
C | G | 5 | a0001c0007t0001g0032a0001c0007t0001g0042a0001c0007t0001g0073others(2): Show | 5 | HG01255.hp1 HG01261.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.763+699C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133545249 | ||||||
| chr9:133545262
|
T | C | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.763+712T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133545262 | ||||||
| chr9:133545284
|
G | A | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.763+734G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133545284 | ||||||
| chr9:133545287
|
C | T | 3 | a0001c0001t0001g0132a0001c0001t0003g0077a0002c0002t0003g0053 | 3 | HG02615.hp1 HG02896.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.763+737C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133545287 | ||||||
| chr9:133545403
|
G | A | 55 | a0001c0001t0001g0025a0001c0001t0001g0043a0001c0001t0001g0052others(52): Show | 55 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.763+853G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133545403 | ||||||
| chr9:133545461
|
C | T | 1 | a0001c0035t0003g0020 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.763+911C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133545461 | ||||||
| chr9:133545583
|
A | G | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.763+1033A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133545583 | ||||||
| chr9:133545607
|
G | A | 2 | a0001c0005t0001g0127a0001c0007t0001g0147 | 2 | HG00323.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.763+1057G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133545607 | ||||||
| chr9:133545802
|
G | A | 7 | a0001c0010t0002g0075a0001c0011t0001g0007a0001c0011t0001g0029others(4): Show | 7 | HG00140.hp1 HG00738.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.764-1236G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133545802 | ||||||
| chr9:133545810
|
C | T | 6 | a0001c0001t0001g0120a0001c0001t0004g0150a0001c0001t0007g0112others(3): Show | 6 | HG02145.hp1 HG02647.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.764-1228C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133545810 | ||||||
| chr9:133545948
|
G | A | 2 | a0001c0006t0005g0125a0001c0006t0008g0074 | 2 | HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.764-1090G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133545948 | ||||||
| chr9:133546063
|
T | G | 40 | a0001c0001t0001g0025a0001c0001t0001g0043a0001c0001t0001g0052others(37): Show | 40 | HG00438.hp1 HG00609.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.764-975T>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133546063 | ||||||
| chr9:133546109
|
A | G | 54 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(51): Show |
intron_variant | MODIFIER | c.764-929A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133546109 | ||||||
| chr9:133546111
|
C | T | 1 | a0002c0002t0003g0022 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.764-927C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133546111 | ||||||
| chr9:133546126
|
G | A | 2 | a0001c0006t0005g0125a0001c0006t0008g0074 | 2 | HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.764-912G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133546126 | ||||||
| chr9:133546192
|
T | C | 54 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(51): Show |
intron_variant | MODIFIER | c.764-846T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133546192 | ||||||
| chr9:133546215
|
T | A | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.764-823T>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133546215 | ||||||
| chr9:133546370
|
A | G | 122 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.764-668A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133546370 | ||||||
| chr9:133546422
|
C | T | 54 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(51): Show |
intron_variant | MODIFIER | c.764-616C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133546422 | ||||||
| chr9:133546423
|
G | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0130 | 2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.764-615G>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133546423 | ||||||
| chr9:133546445
|
C | T | 1 | a0001c0008t0002g0024 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.764-593C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133546445 | ||||||
| chr9:133546624
|
C | G | 4 | a0001c0005t0002g0145a0001c0020t0012g0005a0002c0002t0003g0030others(1): Show | 4 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(1): Show |
intron_variant | MODIFIER | c.764-414C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133546624 | ||||||
| chr9:133546636
|
C | T | 2 | a0001c0001t0001g0078a0001c0026t0001g0123 | 2 | HG02559.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.764-402C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133546636 | ||||||
| chr9:133546663
|
C | T | 19 | a0001c0001t0001g0122a0001c0001t0001g0130a0001c0005t0001g0127others(16): Show | 19 | HG00323.hp2 HG01070.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.764-375C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133546663 | ||||||
| chr9:133546891
|
G | C | 12 | a0001c0010t0001g0084a0001c0010t0002g0075a0001c0010t0002g0088others(9): Show | 12 | HG00140.hp1 HG00438.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.764-147G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133546891 | ||||||
| chr9:133546919
|
C | T | 52 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(49): Show | 52 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(49): Show |
intron_variant | MODIFIER | c.764-119C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133546919 | ||||||
| chr9:133547015
|
G | A | 1 | a0002c0018t0003g0110 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.764-23G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 8/18 | chr9 | 133547015 | ||||||
| chr9:133547224
|
C | T | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.939+11C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133547224 | ||||||
| chr9:133547260
|
T | C | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.939+47T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133547260 | ||||||
| chr9:133547304
|
G | A | 2 | a0001c0006t0005g0125a0001c0006t0008g0074 | 2 | HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.939+91G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133547304 | ||||||
| chr9:133547332
|
C | T | 12 | a0001c0010t0001g0084a0001c0010t0002g0075a0001c0010t0002g0088others(9): Show | 12 | HG00140.hp1 HG00438.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.939+119C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133547332 | ||||||
| chr9:133547434
|
C | T | 1 | a0002c0002t0003g0121 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.939+221C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133547434 | ||||||
| chr9:133547476
|
C | T | 40 | a0001c0001t0001g0025a0001c0001t0001g0043a0001c0001t0001g0052others(37): Show | 40 | HG00438.hp1 HG00609.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.939+263C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133547476 | ||||||
| chr9:133547512
|
A | T | 6 | a0001c0001t0001g0120a0001c0001t0004g0150a0001c0001t0007g0112others(3): Show | 6 | HG02145.hp1 HG02647.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.939+299A>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133547512 | ||||||
| chr9:133547516
|
A | G | 4 | a0001c0005t0002g0145a0001c0020t0012g0005a0002c0002t0003g0030others(1): Show | 4 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(1): Show |
intron_variant | MODIFIER | c.939+303A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133547516 | ||||||
| chr9:133547548
|
C | G | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.939+335C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133547548 | ||||||
| chr9:133547589
|
C | T | 1 | a0001c0008t0002g0105 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.939+376C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133547589 | ||||||
| chr9:133547598
|
C | T | 3 | a0001c0003t0002g0054a0001c0003t0002g0097a0001c0003t0003g0003 | 3 | HG01192.hp1 HG01257.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.939+385C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133547598 | ||||||
| chr9:133547682
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0115 | 2 | HG01884.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.939+469G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133547682 | ||||||
| chr9:133547708
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.939+495G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133547708 | ||||||
| chr9:133547724
|
C | G | 2 | a0001c0001t0001g0078a0001c0026t0001g0123 | 2 | HG02559.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.939+511C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133547724 | ||||||
| chr9:133547746
|
C | G | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.939+533C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133547746 | ||||||
| chr9:133547858
|
G | A | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.939+645G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133547858 | ||||||
| chr9:133547866
|
G | A | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.939+653G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133547866 | ||||||
| chr9:133547889
|
A | G | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.939+676A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133547889 | ||||||
| chr9:133547919
|
C | A | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.939+706C>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133547919 | ||||||
| chr9:133547931
|
G | C | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.939+718G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133547931 | ||||||
| chr9:133547939
|
G | A | 1 | a0002c0029t0003g0011 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.939+726G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133547939 | ||||||
| chr9:133547958
|
G | A | 2 | a0001c0001t0001g0078a0001c0026t0001g0123 | 2 | HG02559.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.939+745G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133547958 | ||||||
| chr9:133548008
|
A | T | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.939+795A>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133548008 | ||||||
| chr9:133548072
|
T | A | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.939+859T>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133548072 | ||||||
| chr9:133548087
|
A | G | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.939+874A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133548087 | ||||||
| chr9:133548121
|
G | A | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.939+908G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133548121 | ||||||
| chr9:133548140
|
T | C | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.939+927T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133548140 | ||||||
| chr9:133548377
|
G | A | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.939+1164G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133548377 | ||||||
| chr9:133548410
|
G | A | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.939+1197G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133548410 | ||||||
| chr9:133548459
|
G | A | 12 | a0001c0010t0001g0084a0001c0010t0002g0075a0001c0010t0002g0088others(9): Show | 12 | HG00140.hp1 HG00438.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.939+1246G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133548459 | ||||||
| chr9:133548513
|
A | G | 120 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.939+1300A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133548513 | ||||||
| chr9:133548553
|
A | G | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.939+1340A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133548553 | ||||||
| chr9:133548587
|
A | G | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.939+1374A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133548587 | ||||||
| chr9:133548640
|
C | T | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.939+1427C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133548640 | ||||||
| chr9:133548672
|
A | G | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.939+1459A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133548672 | ||||||
| chr9:133548713
|
C | G | 3 | a0001c0001t0001g0132a0001c0001t0003g0077a0002c0002t0003g0053 | 3 | HG02615.hp1 HG02896.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.939+1500C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133548713 | ||||||
| chr9:133548780
|
G | A | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.939+1567G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133548780 | ||||||
| chr9:133548782
|
A | G | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.939+1569A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133548782 | ||||||
| chr9:133548830
|
A | G | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.939+1617A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133548830 | ||||||
| chr9:133548831
|
G | A | 1 | a0001c0007t0001g0073 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.939+1618G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133548831 | ||||||
| chr9:133548845
|
T | C | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.939+1632T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133548845 | ||||||
| chr9:133548900
|
T | C | 1 | a0001c0013t0001g0108 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.939+1687T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133548900 | ||||||
| chr9:133548979
|
TCACAGTT others(317): Show |
T | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.939+1782_939+2105d others(2): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr9 | 133548979 | |||||
| chr9:133549236
|
C | A | 1 | a0001c0003t0003g0091 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.939+2023C>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133549236 | ||||||
| chr9:133549247
|
G | C | 1 | a0001c0013t0001g0108 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.939+2034G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133549247 | ||||||
| chr9:133549409
|
A | G | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.939+2196A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133549409 | ||||||
| chr9:133549437
|
C | T | 1 | a0001c0013t0001g0108 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.939+2224C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133549437 | ||||||
| chr9:133549541
|
CTTTT | C | 9 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.939+2347_939+2350d others(6): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr9 | 133549541 | |||||
| chr9:133549541
|
CTTTTT | C | 57 | a0001c0001t0001g0120a0001c0001t0001g0122a0001c0001t0001g0130others(54): Show | 57 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(54): Show |
intron_variant | MODIFIER | c.939+2346_939+2350d others(7): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr9 | 133549541 | |||||
| chr9:133549541
|
CTTTTTT | C | 39 | a0001c0001t0001g0025a0001c0001t0001g0043a0001c0001t0001g0052others(36): Show | 39 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.939+2345_939+2350d others(8): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr9 | 133549541 | |||||
| chr9:133549604
|
C | T | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.939+2391C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133549604 | ||||||
| chr9:133549656
|
A | AT | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.939+2445dupT | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr9 | 133549656 | |||||
| chr9:133549709
|
A | G | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.939+2496A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133549709 | ||||||
| chr9:133549805
|
T | C | 1 | a0001c0005t0002g0144 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.939+2592T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133549805 | ||||||
| chr9:133549815
|
G | A | 39 | a0001c0001t0001g0025a0001c0001t0001g0043a0001c0001t0001g0052others(36): Show | 39 | HG00438.hp1 HG00609.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.939+2602G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133549815 | ||||||
| chr9:133550039
|
A | C | 13 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(10): Show | 13 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.939+2826A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133550039 | ||||||
| chr9:133550050
|
C | A | 25 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(22): Show | 25 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(22): Show |
intron_variant | MODIFIER | c.939+2837C>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133550050 | ||||||
| chr9:133550072
|
A | T | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.939+2859A>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133550072 | ||||||
| chr9:133550339
|
G | C | 78 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(75): Show | 78 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.939+3126G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133550339 | ||||||
| chr9:133550486
|
A | G | 78 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(75): Show | 78 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.939+3273A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133550486 | ||||||
| chr9:133550639
|
G | A | 8 | a0001c0001t0001g0146a0001c0005t0003g0014a0001c0006t0005g0137others(5): Show | 8 | HG00099.hp1 HG01884.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.939+3426G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133550639 | ||||||
| chr9:133550692
|
C | CTCCA | 62 | a0001c0001t0001g0025a0001c0001t0001g0043a0001c0001t0001g0052others(59): Show | 62 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.939+3479_939+3480i others(6): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133550692 | ||||||
| chr9:133550778
|
C | T | 78 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(75): Show | 78 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.939+3565C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133550778 | ||||||
| chr9:133550823
|
T | A | 109 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.940-3534T>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133550823 | ||||||
| chr9:133550900
|
T | G | 78 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(75): Show | 78 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.940-3457T>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133550900 | ||||||
| chr9:133551282
|
C | T | 1 | a0001c0022t0001g0059 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.940-3075C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133551282 | ||||||
| chr9:133551296
|
G | GAC | 11 | a0001c0005t0001g0127a0001c0006t0001g0080a0001c0006t0001g0128others(8): Show | 11 | HG00323.hp2 HG01943.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.940-3061_940-3060i others(4): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133551296 | ||||||
| chr9:133551296
|
G | GACC | 6 | a0001c0001t0001g0122a0001c0001t0001g0130a0001c0006t0001g0081others(3): Show | 6 | HG01255.hp1 HG01255.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.940-3061_940-3060i others(5): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133551296 | ||||||
| chr9:133551297
|
C | A | 12 | a0001c0010t0001g0084a0001c0010t0002g0075a0001c0010t0002g0088others(9): Show | 12 | HG00140.hp1 HG00438.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.940-3060C>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133551297 | ||||||
| chr9:133551304
|
A | ACC | 12 | a0001c0010t0001g0084a0001c0010t0002g0075a0001c0010t0002g0088others(9): Show | 12 | HG00140.hp1 HG00438.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.940-3052_940-3051i others(4): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr9 | 133551304 | |||||
| chr9:133551304
|
A | C | 19 | a0001c0001t0001g0122a0001c0001t0001g0130a0001c0005t0001g0127others(16): Show | 19 | HG00323.hp2 HG01070.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.940-3053A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133551304 | ||||||
| chr9:133551306
|
A | C | 31 | a0001c0001t0001g0122a0001c0001t0001g0130a0001c0005t0001g0127others(28): Show | 31 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.940-3051A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133551306 | ||||||
| chr9:133551441
|
C | T | 3 | a0001c0001t0001g0132a0001c0001t0003g0077a0002c0002t0003g0053 | 3 | HG02615.hp1 HG02896.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.940-2916C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133551441 | ||||||
| chr9:133551481
|
C | T | 34 | a0001c0001t0001g0025a0001c0001t0001g0043a0001c0001t0001g0052others(31): Show | 34 | HG00438.hp1 HG00609.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.940-2876C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133551481 | ||||||
| chr9:133551512
|
G | A | 31 | a0001c0001t0001g0122a0001c0001t0001g0130a0001c0005t0001g0127others(28): Show | 31 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.940-2845G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133551512 | ||||||
| chr9:133551599
|
A | G | 31 | a0001c0001t0001g0122a0001c0001t0001g0130a0001c0005t0001g0127others(28): Show | 31 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.940-2758A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133551599 | ||||||
| chr9:133551812
|
C | CT | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0078others(12): Show | 15 | HG00738.hp2 HG01192.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.940-2519dupT | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr9 | 133551812 | |||||
| chr9:133551812
|
CT | C | 40 | a0001c0001t0001g0025a0001c0001t0001g0052a0001c0001t0001g0138others(37): Show | 40 | HG00099.hp1 HG00609.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.940-2519delT | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr9 | 133551812 | |||||
| chr9:133551812
|
CTT | C | 9 | a0001c0001t0001g0132a0001c0001t0003g0077a0001c0005t0002g0145others(6): Show | 9 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(6): Show |
intron_variant | MODIFIER | c.940-2520_940-2519d others(4): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr9 | 133551812 | |||||
| chr9:133551812
|
CTTTTTTT others(6): Show |
C | 30 | a0001c0001t0001g0122a0001c0001t0001g0130a0001c0005t0001g0127others(27): Show | 30 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.940-2531_940-2519d others(15): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr9 | 133551812 | |||||
| chr9:133551812
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0015t0002g0148 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.940-2532_940-2519d others(16): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr9 | 133551812 | |||||
| chr9:133551836
|
T | G | 31 | a0001c0001t0001g0122a0001c0001t0001g0130a0001c0005t0001g0127others(28): Show | 31 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.940-2521T>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133551836 | ||||||
| chr9:133551922
|
T | C | 101 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.940-2435T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133551922 | ||||||
| chr9:133551997
|
T | A | 31 | a0001c0001t0001g0122a0001c0001t0001g0130a0001c0005t0001g0127others(28): Show | 31 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.940-2360T>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133551997 | ||||||
| chr9:133552005
|
C | T | 31 | a0001c0001t0001g0122a0001c0001t0001g0130a0001c0005t0001g0127others(28): Show | 31 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.940-2352C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133552005 | ||||||
| chr9:133552037
|
C | G | 34 | a0001c0001t0001g0025a0001c0001t0001g0043a0001c0001t0001g0052others(31): Show | 34 | HG00438.hp1 HG00609.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.940-2320C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133552037 | ||||||
| chr9:133552278
|
C | T | 1 | a0002c0002t0003g0099 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.940-2079C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133552278 | ||||||
| chr9:133552332
|
GTTGAATC | G | 12 | a0001c0010t0001g0084a0001c0010t0002g0075a0001c0010t0002g0088others(9): Show | 12 | HG00140.hp1 HG00438.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.940-2023_940-2017d others(9): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr9 | 133552332 | |||||
| chr9:133552387
|
T | C | 39 | a0001c0001t0001g0078a0001c0001t0001g0122a0001c0001t0001g0130others(36): Show | 39 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.940-1970T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133552387 | ||||||
| chr9:133552826
|
T | TTTAGGTC others(6): Show |
1 | a0001c0015t0002g0148 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.940-1529_940-1517d others(15): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr9 | 133552826 | |||||
| chr9:133552873
|
A | T | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0056 | 3 | HG00738.hp2 HG01192.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.940-1484A>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133552873 | ||||||
| chr9:133552894
|
A | G | 1 | a0006c0017t0002g0031 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.940-1463A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133552894 | ||||||
| chr9:133552909
|
C | T | 1 | a0002c0004t0003g0093 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.940-1448C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133552909 | ||||||
| chr9:133552910
|
G | T | 1 | a0001c0001t0001g0132 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.940-1447G>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133552910 | ||||||
| chr9:133552938
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.940-1419C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133552938 | ||||||
| chr9:133553090
|
G | A | 1 | a0001c0011t0001g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.940-1267G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133553090 | ||||||
| chr9:133553137
|
C | T | 6 | a0001c0013t0001g0108a0001c0019t0006g0117a0002c0004t0001g0051others(3): Show | 6 | HG00609.hp1 HG00621.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.940-1220C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133553137 | ||||||
| chr9:133553201
|
T | G | 1 | a0001c0001t0001g0078 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.940-1156T>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133553201 | ||||||
| chr9:133553366
|
C | T | 96 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(93): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.940-991C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133553366 | ||||||
| chr9:133553395
|
G | T | 6 | a0001c0001t0001g0040a0001c0001t0001g0056a0001c0005t0003g0070others(3): Show | 6 | HG00738.hp2 HG02080.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.940-962G>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133553395 | ||||||
| chr9:133553417
|
A | C | 13 | a0001c0001t0001g0023a0001c0001t0001g0115a0001c0001t0001g0122others(10): Show | 13 | HG00140.hp1 HG00738.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.940-940A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133553417 | ||||||
| chr9:133553609
|
G | A | 8 | a0001c0001t0001g0122a0001c0001t0001g0130a0001c0001t0004g0006others(5): Show | 8 | HG01496.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.940-748G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133553609 | ||||||
| chr9:133553617
|
C | G | 22 | a0001c0001t0001g0052a0001c0001t0007g0112a0001c0005t0002g0050others(19): Show | 22 | HG00621.hp2 HG01070.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.940-740C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133553617 | ||||||
| chr9:133553778
|
G | C | 7 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0056others(4): Show | 7 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(4): Show |
intron_variant | MODIFIER | c.940-579G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133553778 | ||||||
| chr9:133554044
|
G | A | 3 | a0001c0005t0002g0050a0001c0006t0001g0103a0001c0006t0001g0104 | 3 | HG01070.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.940-313G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133554044 | ||||||
| chr9:133554049
|
C | T | 15 | a0001c0005t0001g0127a0001c0006t0001g0080a0001c0006t0001g0081others(12): Show | 15 | HG01070.hp1 HG01071.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.940-308C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133554049 | ||||||
| chr9:133554206
|
G | A | 1 | a0002c0002t0003g0030 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.940-151G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 9/18 | chr9 | 133554206 | ||||||
| chr9:133555253
|
A | G | 20 | a0001c0001t0001g0023a0001c0001t0001g0078a0001c0001t0001g0115others(17): Show | 20 | HG00140.hp1 HG00738.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.1277-305A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 10/18 | chr9 | 133555253 | ||||||
| chr9:133555301
|
C | G | 25 | a0001c0005t0001g0127a0001c0006t0001g0080a0001c0006t0001g0081others(22): Show | 25 | HG00323.hp2 HG01070.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.1277-257C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 10/18 | chr9 | 133555301 | ||||||
| chr9:133555344
|
G | A | 1 | a0001c0033t0015g0135 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1277-214G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 10/18 | chr9 | 133555344 | ||||||
| chr9:133555378
|
A | G | 37 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(34): Show | 37 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.1277-180A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 10/18 | chr9 | 133555378 | ||||||
| chr9:133555444
|
C | T | 1 | a0001c0020t0012g0005 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1277-114C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 10/18 | chr9 | 133555444 | ||||||
| chr9:133555985
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1649+55C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133555985 | ||||||
| chr9:133556067
|
C | T | 1 | a0001c0007t0001g0147 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1649+137C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133556067 | ||||||
| chr9:133556188
|
A | G | 1 | a0002c0002t0003g0134 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1649+258A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133556188 | ||||||
| chr9:133556204
|
G | T | 1 | a0002c0002t0003g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1649+274G>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133556204 | ||||||
| chr9:133556242
|
C | A | 3 | a0002c0002t0002g0027a0002c0002t0002g0028a0002c0002t0003g0121 | 3 | HG02056.hp2 HG02080.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1649+312C>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133556242 | ||||||
| chr9:133556276
|
A | G | 1 | a0001c0035t0003g0020 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1649+346A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133556276 | ||||||
| chr9:133556387
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1649+457C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133556387 | ||||||
| chr9:133556558
|
G | A | 13 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(10): Show | 13 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1649+628G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133556558 | ||||||
| chr9:133556587
|
A | G | 1 | a0001c0003t0002g0133 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1649+657A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133556587 | ||||||
| chr9:133556734
|
C | T | 1 | a0002c0002t0003g0121 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1649+804C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133556734 | ||||||
| chr9:133556788
|
T | G | 79 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(76): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.1649+858T>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133556788 | ||||||
| chr9:133556823
|
C | A | 7 | a0001c0005t0003g0014a0001c0008t0002g0090a0001c0008t0002g0105others(4): Show | 7 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(4): Show |
intron_variant | MODIFIER | c.1649+893C>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133556823 | ||||||
| chr9:133556903
|
T | A | 1 | a0001c0006t0008g0074 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1649+973T>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133556903 | ||||||
| chr9:133557062
|
C | T | 1 | a0001c0007t0001g0147 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1649+1132C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133557062 | ||||||
| chr9:133557075
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1649+1145G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133557075 | ||||||
| chr9:133557211
|
C | T | 7 | a0001c0005t0003g0014a0001c0008t0002g0090a0001c0008t0002g0105others(4): Show | 7 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(4): Show |
intron_variant | MODIFIER | c.1649+1281C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133557211 | ||||||
| chr9:133557510
|
G | C | 16 | a0001c0006t0001g0080a0001c0006t0001g0081a0001c0006t0001g0103others(13): Show | 16 | HG01070.hp1 HG01071.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.1649+1580G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133557510 | ||||||
| chr9:133557631
|
G | T | 11 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(8): Show | 11 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.1649+1701G>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133557631 | ||||||
| chr9:133557816
|
G | A | 3 | a0002c0009t0001g0016a0002c0009t0001g0124a0002c0009t0001g0149 | 3 | HG02451.hp1 HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1649+1886G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133557816 | ||||||
| chr9:133557843
|
G | A | 7 | a0001c0005t0003g0014a0001c0008t0002g0090a0001c0008t0002g0105others(4): Show | 7 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(4): Show |
intron_variant | MODIFIER | c.1649+1913G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133557843 | ||||||
| chr9:133557950
|
C | T | 4 | a0002c0002t0003g0053a0002c0009t0001g0016a0002c0009t0001g0124others(1): Show | 4 | HG02451.hp1 HG02615.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1649+2020C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133557950 | ||||||
| chr9:133557954
|
C | T | 30 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0043others(27): Show | 30 | HG00140.hp1 HG00738.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.1649+2024C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133557954 | ||||||
| chr9:133557957
|
GGGGGCTT others(17): Show |
G | 30 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0043others(27): Show | 30 | HG00140.hp1 HG00738.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.1649+2031_1649+205 others(28): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr9 | 133557957 | |||||
| chr9:133558110
|
C | G | 12 | a0001c0006t0001g0080a0001c0006t0001g0081a0001c0006t0001g0103others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.1649+2180C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133558110 | ||||||
| chr9:133558115
|
C | T | 34 | a0001c0003t0003g0003a0001c0003t0003g0091a0001c0008t0002g0024others(31): Show | 34 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.1649+2185C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133558115 | ||||||
| chr9:133558237
|
A | G | 1 | a0001c0026t0001g0123 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1649+2307A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133558237 | ||||||
| chr9:133558376
|
A | G | 8 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(5): Show | 8 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1649+2446A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133558376 | ||||||
| chr9:133558429
|
CAGAAAAG others(22): Show |
C | 1 | a0001c0013t0001g0108 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1649+2500_1649+252 others(33): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133558429 | ||||||
| chr9:133558476
|
C | T | 1 | a0001c0007t0001g0042 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1649+2546C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133558476 | ||||||
| chr9:133558534
|
G | A | 1 | a0002c0004t0003g0094 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1649+2604G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133558534 | ||||||
| chr9:133558534
|
G | C | 1 | a0002c0002t0003g0019 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1649+2604G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133558534 | ||||||
| chr9:133559040
|
A | G | 27 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(24): Show | 27 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.1650-2158A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133559040 | ||||||
| chr9:133559215
|
G | T | 1 | a0002c0002t0003g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1650-1983G>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133559215 | ||||||
| chr9:133559322
|
G | C | 23 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(20): Show | 23 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.1650-1876G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133559322 | ||||||
| chr9:133559351
|
A | AT | 11 | a0001c0001t0007g0112a0001c0005t0002g0085a0001c0015t0002g0148others(8): Show | 11 | HG00438.hp2 HG00621.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.1650-1831dupT | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr9 | 133559351 | |||||
| chr9:133559351
|
AT | A | 9 | a0001c0001t0004g0006a0001c0001t0004g0009a0001c0001t0004g0018others(6): Show | 9 | HG01070.hp2 HG02109.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1650-1831delT | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr9 | 133559351 | |||||
| chr9:133559351
|
ATTT | A | 21 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(18): Show | 21 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.1650-1833_1650-183 others(7): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr9 | 133559351 | |||||
| chr9:133559396
|
T | C | 1 | a0001c0007t0001g0142 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1650-1802T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133559396 | ||||||
| chr9:133559430
|
G | A | 1 | a0006c0017t0002g0031 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1650-1768G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133559430 | ||||||
| chr9:133559510
|
A | AT | 30 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(27): Show | 30 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.1650-1673dupT | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr9 | 133559510 | |||||
| chr9:133559604
|
G | A | 1 | a0002c0004t0003g0044 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1650-1594G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133559604 | ||||||
| chr9:133559686
|
G | A | 80 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(77): Show | 80 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.1650-1512G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133559686 | ||||||
| chr9:133559808
|
G | A | 30 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0043others(27): Show | 30 | HG00140.hp1 HG00738.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.1650-1390G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133559808 | ||||||
| chr9:133559825
|
T | C | 1 | a0002c0002t0003g0096 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1650-1373T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133559825 | ||||||
| chr9:133560058
|
C | A | 1 | a0002c0002t0010g0039 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1650-1140C>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133560058 | ||||||
| chr9:133560208
|
G | A | 74 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(71): Show | 74 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1650-990G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133560208 | ||||||
| chr9:133560265
|
A | G | 42 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(39): Show | 42 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1650-933A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133560265 | ||||||
| chr9:133560310
|
G | A | 1 | a0001c0005t0002g0145 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1650-888G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133560310 | ||||||
| chr9:133560383
|
GGCGTCCC others(5): Show |
G | 1 | a0001c0012t0002g0139 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1650-814_1650-803d others(14): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133560383 | ||||||
| chr9:133560388
|
C | T | 1 | a0002c0002t0010g0039 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1650-810C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133560388 | ||||||
| chr9:133560411
|
G | T | 1 | a0002c0002t0002g0046 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1650-787G>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133560411 | ||||||
| chr9:133560573
|
C | T | 2 | a0001c0001t0004g0006a0001c0001t0004g0009 | 2 | HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1650-625C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133560573 | ||||||
| chr9:133560588
|
G | A | 2 | a0001c0019t0006g0117a0001c0035t0003g0020 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1650-610G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133560588 | ||||||
| chr9:133560755
|
G | A | 2 | a0001c0019t0006g0117a0001c0035t0003g0020 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1650-443G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133560755 | ||||||
| chr9:133560808
|
C | T | 1 | a0001c0016t0001g0087 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1650-390C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133560808 | ||||||
| chr9:133560822
|
A | T | 1 | a0002c0002t0010g0039 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1650-376A>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133560822 | ||||||
| chr9:133561003
|
C | T | 1 | a0001c0020t0012g0005 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1650-195C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133561003 | ||||||
| chr9:133561049
|
A | G | 2 | a0001c0001t0001g0043a0001c0001t0007g0112 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1650-149A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133561049 | ||||||
| chr9:133561098
|
G | A | 1 | a0002c0002t0003g0021 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1650-100G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 11/18 | chr9 | 133561098 | ||||||
| chr9:133561321
|
A | G | 30 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0043others(27): Show | 30 | HG00140.hp1 HG00738.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.1747+26A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133561321 | ||||||
| chr9:133561397
|
C | G | 3 | a0001c0027t0001g0010a0001c0028t0001g0116a0003c0037t0001g0114 | 3 | HG02280.hp2 HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1747+102C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133561397 | ||||||
| chr9:133561431
|
T | G | 2 | a0001c0006t0001g0103a0001c0006t0001g0104 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1747+136T>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133561431 | ||||||
| chr9:133561432
|
TG | T | 3 | a0001c0022t0001g0059a0002c0002t0003g0095a0002c0002t0003g0152 | 3 | HG01515.hp2 HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1747+142delG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133561432 | |||||
| chr9:133561457
|
T | C | 1 | a0002c0009t0001g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1747+162T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133561457 | ||||||
| chr9:133561506
|
G | A | 2 | a0001c0020t0012g0005a0001c0031t0011g0004 | 2 | HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1747+211G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133561506 | ||||||
| chr9:133561513
|
TC | T | 10 | a0001c0001t0003g0077a0001c0007t0001g0032a0001c0007t0001g0042others(7): Show | 10 | HG00323.hp2 HG01255.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1747+220delC | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133561513 | |||||
| chr9:133561650
|
T | C | 70 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(67): Show | 70 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.1747+355T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133561650 | ||||||
| chr9:133561792
|
T | G | 66 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(63): Show | 66 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.1747+497T>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133561792 | ||||||
| chr9:133561922
|
T | C | 1 | a0001c0001t0007g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1747+627T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133561922 | ||||||
| chr9:133561923
|
C | T | 1 | a0001c0001t0007g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1747+628C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133561923 | ||||||
| chr9:133561927
|
T | C | 1 | a0001c0001t0007g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1747+632T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133561927 | ||||||
| chr9:133561927
|
T | G | 29 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0043others(26): Show | 29 | HG00140.hp1 HG00738.hp1 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.1747+632T>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133561927 | ||||||
| chr9:133561963
|
T | G | 32 | a0001c0003t0001g0140a0001c0003t0002g0033a0001c0003t0002g0049others(29): Show | 32 | HG00140.hp2 HG00438.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.1747+668T>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133561963 | ||||||
| chr9:133562015
|
C | A | 1 | a0001c0001t0003g0077 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1747+720C>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562015 | ||||||
| chr9:133562063
|
G | A | 30 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0043others(27): Show | 30 | HG00140.hp1 HG00738.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.1747+768G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562063 | ||||||
| chr9:133562382
|
C | T | 1 | a0001c0003t0002g0107 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1747+1087C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562382 | ||||||
| chr9:133562444
|
C | T | 73 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(70): Show | 73 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.1747+1149C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562444 | ||||||
| chr9:133562482
|
C | G | 2 | a0001c0020t0012g0005a0001c0031t0011g0004 | 2 | HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1747+1187C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562482 | ||||||
| chr9:133562489
|
C | G | 71 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(68): Show | 71 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.1747+1194C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562489 | ||||||
| chr9:133562489
|
C | T | 2 | a0001c0019t0006g0117a0001c0035t0003g0020 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1747+1194C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562489 | ||||||
| chr9:133562492
|
C | G | 1 | a0001c0001t0007g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1747+1197C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562492 | ||||||
| chr9:133562507
|
C | CG | 2 | a0001c0003t0002g0057a0002c0002t0002g0046 | 2 | HG00438.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1747+1213dupG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133562507 | |||||
| chr9:133562509
|
T | C | 1 | a0001c0006t0001g0128 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1747+1214T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562509 | ||||||
| chr9:133562510
|
G | A | 8 | a0001c0007t0001g0032a0001c0007t0001g0042a0001c0007t0001g0060others(5): Show | 8 | HG00323.hp2 HG01255.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1747+1215G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562510 | ||||||
| chr9:133562530
|
GGCTGGGC others(38): Show |
G | 30 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0052others(27): Show | 30 | HG00140.hp1 HG00738.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.1747+1280_1747+132 others(49): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133562530 | |||||
| chr9:133562539
|
C | A | 42 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(39): Show | 42 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1747+1244C>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562539 | ||||||
| chr9:133562542
|
CTCGCACC others(37): Show |
C | 1 | a0001c0006t0005g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1747+1248_1747+129 others(48): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562542 | ||||||
| chr9:133562554
|
T | C | 1 | a0001c0006t0001g0128 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1747+1259T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562554 | ||||||
| chr9:133562566
|
C | T | 2 | a0002c0002t0003g0151a0002c0002t0003g0152 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1747+1271C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562566 | ||||||
| chr9:133562567
|
GGGCACCC others(37): Show |
G | 1 | a0001c0001t0001g0122 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1747+1275_1747+131 others(48): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133562567 | |||||
| chr9:133562572
|
CCCTGCTG others(37): Show |
C | 1 | a0001c0001t0001g0043 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1747+1280_1747+132 others(48): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133562572 | |||||
| chr9:133562575
|
T | G | 48 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(45): Show | 48 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.1747+1280T>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562575 | ||||||
| chr9:133562584
|
C | A | 30 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0052others(27): Show | 30 | HG00140.hp1 HG00738.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.1747+1289C>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562584 | ||||||
| chr9:133562603
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1747+1308C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562603 | ||||||
| chr9:133562612
|
GGGCACCC others(37): Show |
G | 2 | a0001c0001t0004g0035a0001c0001t0007g0112 | 2 | HG02647.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1747+1320_1747+136 others(48): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133562612 | |||||
| chr9:133562623
|
T | TG | 3 | a0001c0005t0003g0070a0001c0006t0001g0128a0001c0006t0005g0137 | 3 | HG02300.hp1 HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1747+1331dupG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133562623 | |||||
| chr9:133562632
|
T | C | 79 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(76): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.1747+1337T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562632 | ||||||
| chr9:133562668
|
T | G | 2 | a0001c0019t0006g0117a0001c0035t0003g0020 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1747+1373T>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562668 | ||||||
| chr9:133562673
|
A | C | 2 | a0001c0019t0006g0117a0001c0035t0003g0020 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1747+1378A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562673 | ||||||
| chr9:133562687
|
G | T | 2 | a0001c0020t0012g0005a0001c0031t0011g0004 | 2 | HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1747+1392G>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562687 | ||||||
| chr9:133562689
|
GGGCGGCG others(81): Show |
G | 1 | a0001c0008t0002g0105 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1747+1397_1747+148 others(92): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133562689 | |||||
| chr9:133562700
|
T | C | 12 | a0001c0001t0001g0122a0001c0001t0001g0130a0001c0001t0004g0006others(9): Show | 12 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1747+1405T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562700 | ||||||
| chr9:133562710
|
A | G | 2 | a0001c0019t0006g0117a0001c0035t0003g0020 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1747+1415A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562710 | ||||||
| chr9:133562729
|
G | A | 1 | a0001c0007t0001g0142 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1747+1434G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562729 | ||||||
| chr9:133562731
|
CGTGGGCG others(37): Show |
C | 1 | a0002c0018t0003g0110 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1747+1502_1747+154 others(48): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133562731 | |||||
| chr9:133562754
|
G | A | 2 | a0001c0019t0006g0117a0001c0035t0003g0020 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1747+1459G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562754 | ||||||
| chr9:133562767
|
C | T | 26 | a0001c0003t0001g0140a0001c0003t0002g0033a0001c0003t0002g0049others(23): Show | 26 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.1747+1472C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562767 | ||||||
| chr9:133562767
|
CGCACCGC others(127): Show |
C | 1 | a0001c0007t0001g0060 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1747+1546_1747+167 others(4): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133562767 | |||||
| chr9:133562775
|
T | C | 47 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(44): Show | 47 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.1747+1480T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562775 | ||||||
| chr9:133562817
|
G | A | 1 | a0002c0004t0001g0106 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1747+1522G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562817 | ||||||
| chr9:133562819
|
T | C | 42 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(39): Show | 42 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.1747+1524T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562819 | ||||||
| chr9:133562838
|
AC | A | 3 | a0001c0008t0002g0105a0001c0019t0006g0117a0001c0035t0003g0020 | 3 | HG02280.hp1 HG02922.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1747+1546delC | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133562838 | |||||
| chr9:133562862
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1747+1567G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562862 | ||||||
| chr9:133562864
|
T | C | 26 | a0001c0005t0001g0127a0001c0006t0001g0080a0001c0006t0001g0081others(23): Show | 26 | HG00323.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1747+1569T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562864 | ||||||
| chr9:133562870
|
A | C | 2 | a0001c0019t0006g0117a0001c0035t0003g0020 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1747+1575A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562870 | ||||||
| chr9:133562874
|
G | A | 3 | a0002c0009t0001g0016a0002c0009t0001g0124a0002c0009t0001g0149 | 3 | HG02451.hp1 HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1747+1579G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562874 | ||||||
| chr9:133562875
|
TGGTGGGC others(37): Show |
T | 1 | a0001c0013t0001g0108 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1747+1581_1747+162 others(48): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562875 | ||||||
| chr9:133562884
|
CCCGGCTT others(37): Show |
C | 4 | a0001c0001t0001g0132a0001c0019t0006g0117a0001c0031t0011g0004others(1): Show | 4 | HG01261.hp2 HG02280.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1747+1606_1747+164 others(48): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133562884 | |||||
| chr9:133562901
|
T | C | 72 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(69): Show | 72 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.1747+1606T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562901 | ||||||
| chr9:133562909
|
T | C | 2 | a0001c0007t0001g0060a0004c0014t0002g0098 | 2 | HG01257.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1747+1614T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562909 | ||||||
| chr9:133562928
|
A | AC | 4 | a0001c0001t0001g0043a0001c0001t0007g0112a0001c0001t0014g0118others(1): Show | 4 | HG02572.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1747+1635dupC | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133562928 | |||||
| chr9:133562930
|
C | CT | 27 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0052others(24): Show | 27 | HG00140.hp1 HG00738.hp1 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.1747+1635_1747+163 others(5): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562930 | ||||||
| chr9:133562930
|
C | G | 1 | a0001c0006t0005g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1747+1635C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562930 | ||||||
| chr9:133562930
|
CGGCTTGG others(38): Show |
C | 1 | a0001c0006t0001g0111 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1747+1680_1747+172 others(49): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133562930 | |||||
| chr9:133562931
|
G | A | 2 | a0001c0006t0001g0103a0001c0006t0001g0104 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1747+1636G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562931 | ||||||
| chr9:133562931
|
G | C | 1 | a0001c0006t0005g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1747+1636G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562931 | ||||||
| chr9:133562946
|
GCACCGCT others(37): Show |
G | 1 | a0001c0001t0003g0077 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1747+1652_1747+169 others(48): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562946 | ||||||
| chr9:133562950
|
C | T | 1 | a0002c0004t0003g0068 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1747+1655C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562950 | ||||||
| chr9:133562974
|
CT | C | 2 | a0001c0001t0001g0132a0001c0013t0001g0108 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1747+1680delT | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562974 | ||||||
| chr9:133562991
|
G | T | 1 | a0001c0001t0004g0006 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1747+1696G>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133562991 | ||||||
| chr9:133563068
|
G | T | 2 | a0001c0019t0006g0117a0001c0035t0003g0020 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1747+1773G>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563068 | ||||||
| chr9:133563087
|
C | T | 2 | a0001c0006t0001g0080a0001c0006t0001g0081 | 2 | HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1747+1792C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563087 | ||||||
| chr9:133563093
|
A | G | 1 | a0001c0032t0005g0100 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1747+1798A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563093 | ||||||
| chr9:133563118
|
C | T | 2 | a0001c0019t0006g0117a0001c0035t0003g0020 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1747+1823C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563118 | ||||||
| chr9:133563271
|
TG | T | 2 | a0002c0002t0003g0095a0002c0002t0003g0102 | 2 | HG00280.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1747+1978delG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563271 | |||||
| chr9:133563296
|
TC | T | 2 | a0001c0003t0002g0107a0002c0002t0003g0102 | 2 | HG00280.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1747+2003delC | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563296 | |||||
| chr9:133563330
|
G | A | 23 | a0001c0006t0001g0080a0001c0006t0001g0081a0001c0006t0001g0103others(20): Show | 23 | HG00323.hp2 HG01070.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.1747+2035G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563330 | ||||||
| chr9:133563331
|
TG | T | 3 | a0001c0007t0001g0147a0002c0002t0003g0102a0004c0014t0002g0098 | 3 | HG00280.hp1 HG00323.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.1747+2040delG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563331 | |||||
| chr9:133563334
|
G | C | 1 | a0001c0006t0005g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1747+2039G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563334 | ||||||
| chr9:133563422
|
T | TG | 3 | a0001c0003t0002g0057a0001c0006t0001g0128a0002c0002t0003g0066 | 3 | HG02129.hp1 HG02132.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1747+2130dupG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563422 | |||||
| chr9:133563434
|
GTAAGTGT others(21): Show |
G | 3 | a0002c0009t0001g0016a0002c0009t0001g0124a0002c0009t0001g0149 | 3 | HG02451.hp1 HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1747+2148_1747+217 others(32): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563434 | |||||
| chr9:133563560
|
C | CG | 2 | a0001c0013t0001g0108a0003c0036t0001g0113 | 2 | HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1747+2265_1747+226 others(5): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563560 | ||||||
| chr9:133563561
|
A | G | 77 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.1747+2266A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563561 | ||||||
| chr9:133563562
|
A | G | 2 | a0001c0013t0001g0108a0003c0036t0001g0113 | 2 | HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1747+2267A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563562 | ||||||
| chr9:133563603
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1747+2308G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563603 | ||||||
| chr9:133563604
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1747+2309A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563604 | ||||||
| chr9:133563661
|
T | TC | 2 | a0001c0001t0003g0077a0002c0002t0003g0065 | 2 | HG02896.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.1747+2367dupC | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563661 | |||||
| chr9:133563674
|
GC | G | 3 | a0001c0001t0001g0132a0001c0003t0002g0107a0002c0002t0003g0134 | 3 | HG02976.hp1 HG03710.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1747+2382delC | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563674 | |||||
| chr9:133563712
|
GA | G | 2 | a0001c0003t0002g0049a0001c0006t0008g0074 | 2 | HG02602.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1747+2420delA | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563712 | |||||
| chr9:133563751
|
T | G | 1 | a0001c0001t0001g0132 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1747+2456T>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563751 | ||||||
| chr9:133563772
|
TG | T | 2 | a0001c0007t0001g0147a0002c0002t0003g0099 | 2 | HG00323.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.1747+2479delG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563772 | |||||
| chr9:133563814
|
AG | A | 3 | a0001c0003t0001g0140a0002c0002t0003g0022a0002c0002t0003g0151 | 3 | HG01884.hp1 HG03834.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.1747+2524delG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563814 | |||||
| chr9:133563818
|
G | GA | 2 | a0001c0001t0001g0132a0002c0002t0003g0102 | 2 | HG00280.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1747+2523_1747+252 others(5): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563818 | ||||||
| chr9:133563818
|
G | GGAGGGAG others(21): Show |
1 | a0002c0004t0003g0082 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1747+2526_1747+252 others(32): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563818 | |||||
| chr9:133563818
|
GGAGA | G | 10 | a0001c0001t0001g0120a0001c0001t0004g0006a0001c0001t0004g0009others(7): Show | 10 | HG00140.hp2 HG01433.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1747+2545_1747+254 others(8): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563818 | |||||
| chr9:133563819
|
GAGA | G | 2 | a0001c0001t0001g0043a0001c0001t0014g0118 | 2 | HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1747+2525_1747+252 others(7): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563819 | ||||||
| chr9:133563819
|
GAGAGAGA others(8): Show |
G | 2 | a0001c0008t0002g0105a0001c0012t0002g0048 | 2 | HG00544.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1747+2525_1747+253 others(19): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563819 | ||||||
| chr9:133563826
|
AGAGAGAG others(11): Show |
A | 1 | a0001c0008t0002g0090 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1747+2549_1747+256 others(22): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563826 | |||||
| chr9:133563828
|
AGAGAGAG others(9): Show |
A | 2 | a0001c0012t0002g0139a0001c0015t0002g0072 | 2 | NA18612.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.1747+2549_1747+256 others(20): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563828 | |||||
| chr9:133563836
|
A | G | 1 | a0001c0031t0011g0004 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1747+2541A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563836 | ||||||
| chr9:133563836
|
AGAGAGAG others(1): Show |
A | 50 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(47): Show | 50 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.1747+2549_1747+255 others(12): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563836 | |||||
| chr9:133563838
|
AGAGAGG | A | 2 | a0001c0007t0001g0032a0001c0007t0001g0142 | 2 | HG03492.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1747+2549_1747+255 others(10): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563838 | |||||
| chr9:133563840
|
A | G | 1 | a0002c0002t0002g0002 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1747+2545A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563840 | ||||||
| chr9:133563842
|
A | AG | 3 | a0001c0006t0001g0111a0002c0002t0003g0134a0002c0004t0003g0044 | 3 | HG02109.hp2 HG02165.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1747+2550dupG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563842 | |||||
| chr9:133563842
|
A | G | 1 | a0002c0002t0003g0102 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1747+2547A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563842 | ||||||
| chr9:133563844
|
G | A | 5 | a0001c0006t0005g0137a0001c0008t0002g0105a0001c0012t0002g0048others(2): Show | 5 | HG00438.hp2 HG00544.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.1747+2549G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563844 | ||||||
| chr9:133563844
|
G | GA | 2 | a0002c0002t0002g0028a0002c0002t0003g0102 | 2 | HG00280.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.1747+2549_1747+255 others(5): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563844 | ||||||
| chr9:133563844
|
G | GGA | 6 | a0001c0003t0002g0054a0001c0003t0003g0091a0001c0013t0001g0108others(3): Show | 6 | HG01192.hp1 HG02300.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1747+2567_1747+256 others(6): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563844 | |||||
| chr9:133563846
|
A | G | 1 | a0001c0007t0001g0032 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1747+2551A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563846 | ||||||
| chr9:133563848
|
A | G | 52 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(49): Show | 52 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.1747+2553A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563848 | ||||||
| chr9:133563852
|
A | G | 1 | a0001c0031t0011g0004 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1747+2557A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563852 | ||||||
| chr9:133563857
|
GA | G | 2 | a0001c0001t0014g0118a0001c0006t0005g0137 | 2 | HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1747+2563delA | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563857 | ||||||
| chr9:133563858
|
AGAGAG | A | 2 | a0001c0001t0004g0006a0001c0001t0004g0150 | 2 | HG03130.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1747+2565_1747+256 others(9): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563858 | |||||
| chr9:133563859
|
GA | G | 2 | a0002c0002t0003g0151a0004c0014t0002g0098 | 2 | HG01257.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1747+2565delA | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563859 | ||||||
| chr9:133563859
|
GAGA | G | 2 | a0001c0001t0004g0009a0003c0036t0001g0113 | 2 | HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1747+2565_1747+256 others(7): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563859 | ||||||
| chr9:133563859
|
GAGAGGGA others(8): Show |
G | 1 | a0001c0015t0002g0148 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1747+2565_1747+257 others(19): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563859 | ||||||
| chr9:133563860
|
A | G | 3 | a0001c0007t0001g0060a0001c0032t0005g0100a0004c0014t0002g0034 | 3 | HG02559.hp1 HG04228.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1747+2565A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563860 | ||||||
| chr9:133563862
|
A | G | 2 | a0001c0001t0001g0120a0002c0002t0002g0028 | 2 | HG02056.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1747+2567A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563862 | ||||||
| chr9:133563864
|
G | A | 7 | a0001c0001t0001g0120a0001c0006t0005g0137a0001c0031t0011g0004others(4): Show | 7 | HG01261.hp2 HG02056.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1747+2569G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563864 | ||||||
| chr9:133563864
|
G | GA | 2 | a0002c0004t0003g0094a0004c0014t0002g0098 | 2 | HG01257.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1747+2569_1747+257 others(5): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563864 | ||||||
| chr9:133563864
|
G | GGA | 3 | a0001c0001t0001g0132a0001c0005t0002g0064a0002c0004t0003g0038 | 3 | HG00621.hp1 HG02273.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1747+2589_1747+259 others(6): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563864 | |||||
| chr9:133563865
|
G | A | 1 | a0001c0001t0003g0077 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1747+2570G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563865 | ||||||
| chr9:133563866
|
A | G | 3 | a0001c0001t0003g0077a0001c0001t0004g0150a0002c0004t0003g0082 | 3 | HG02896.hp1 HG03453.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1747+2571A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563866 | ||||||
| chr9:133563870
|
A | G | 1 | a0001c0031t0011g0004 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1747+2575A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563870 | ||||||
| chr9:133563872
|
A | AGAGAGAG others(27): Show |
1 | a0002c0002t0010g0039 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1747+2610_1747+261 others(38): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563872 | |||||
| chr9:133563874
|
A | G | 1 | a0001c0006t0005g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1747+2579A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563874 | ||||||
| chr9:133563875
|
G | A | 1 | a0001c0006t0005g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1747+2580G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563875 | ||||||
| chr9:133563881
|
GAGA | G | 2 | a0001c0020t0012g0005a0004c0014t0002g0034 | 2 | HG01433.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1747+2587_1747+258 others(7): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563881 | ||||||
| chr9:133563883
|
GA | G | 3 | a0001c0001t0001g0120a0001c0006t0005g0137a0001c0032t0005g0100 | 3 | HG02145.hp1 HG02559.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1747+2589delA | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563883 | ||||||
| chr9:133563884
|
A | G | 24 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0052others(21): Show | 24 | HG00140.hp1 HG00738.hp1 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.1747+2589A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563884 | ||||||
| chr9:133563886
|
G | A | 24 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0052others(21): Show | 24 | HG00140.hp1 HG00738.hp1 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.1747+2591G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563886 | ||||||
| chr9:133563886
|
G | GA | 3 | a0001c0001t0003g0077a0001c0026t0001g0123a0002c0002t0003g0151 | 3 | HG01884.hp1 HG02559.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1747+2591_1747+259 others(5): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563886 | ||||||
| chr9:133563886
|
G | T | 1 | a0001c0006t0005g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1747+2591G>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563886 | ||||||
| chr9:133563888
|
A | G | 1 | a0002c0002t0003g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1747+2593A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563888 | ||||||
| chr9:133563897
|
G | A | 1 | a0001c0006t0005g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1747+2602G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563897 | ||||||
| chr9:133563898
|
A | G | 2 | a0001c0006t0005g0137a0001c0020t0012g0005 | 2 | HG01433.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1747+2603A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563898 | ||||||
| chr9:133563899
|
G | A | 25 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0052others(22): Show | 25 | HG00140.hp1 HG00738.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.1747+2604G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563899 | ||||||
| chr9:133563899
|
G | GA | 2 | a0001c0007t0001g0147a0004c0014t0002g0098 | 2 | HG00323.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.1747+2606dupA | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563899 | |||||
| chr9:133563901
|
A | AAG | 31 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(28): Show | 31 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.1747+2606_1747+260 others(6): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563901 | ||||||
| chr9:133563901
|
A | AAGG | 2 | a0001c0006t0001g0128a0001c0031t0011g0004 | 2 | HG01261.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1747+2606_1747+260 others(7): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563901 | ||||||
| chr9:133563901
|
A | G | 28 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0052others(25): Show | 28 | HG00140.hp1 HG00438.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1747+2606A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563901 | ||||||
| chr9:133563901
|
AGGGGAGA others(5): Show |
A | 1 | a0001c0001t0004g0150 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1747+2607_1747+261 others(16): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563901 | ||||||
| chr9:133563902
|
G | A | 7 | a0001c0003t0002g0049a0001c0007t0001g0142a0001c0020t0012g0005others(4): Show | 7 | HG01433.hp2 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1747+2607G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563902 | ||||||
| chr9:133563904
|
GGAGAGAG others(11): Show |
G | 1 | a0001c0003t0002g0054 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1747+2623_1747+264 others(22): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563904 | |||||
| chr9:133563904
|
GGAGAGAG others(13): Show |
G | 25 | a0001c0001t0003g0077a0001c0003t0001g0140a0001c0003t0002g0033others(22): Show | 25 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.1747+2655_1747+267 others(24): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563904 | |||||
| chr9:133563905
|
GAGAGAGA others(12): Show |
G | 2 | a0001c0005t0002g0064a0006c0017t0002g0031 | 2 | HG00609.hp1 HG00621.hp1 |
intron_variant | MODIFIER | c.1747+2611_1747+262 others(23): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563905 | ||||||
| chr9:133563906
|
A | G | 13 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(10): Show | 13 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1747+2611A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563906 | ||||||
| chr9:133563908
|
AGAGAGAG others(3): Show |
A | 1 | a0001c0007t0001g0142 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1747+2623_1747+263 others(14): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563908 | |||||
| chr9:133563916
|
A | G | 2 | a0001c0001t0004g0150a0001c0006t0005g0137 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1747+2621A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563916 | ||||||
| chr9:133563917
|
GGGAGAGA others(12): Show |
G | 1 | a0001c0005t0003g0070 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1747+2625_1747+264 others(23): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563917 | |||||
| chr9:133563918
|
G | A | 4 | a0001c0020t0012g0005a0001c0027t0001g0010a0001c0028t0001g0116others(1): Show | 4 | HG01433.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1747+2623G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563918 | ||||||
| chr9:133563919
|
G | A | 1 | a0001c0020t0012g0005 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1747+2624G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563919 | ||||||
| chr9:133563920
|
A | G | 3 | a0001c0027t0001g0010a0001c0028t0001g0116a0003c0037t0001g0114 | 3 | HG02280.hp2 HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1747+2625A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563920 | ||||||
| chr9:133563920
|
AGAGAGAG others(11): Show |
A | 1 | a0001c0001t0001g0132 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1747+2643_1747+266 others(22): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563920 | |||||
| chr9:133563922
|
A | G | 1 | a0001c0020t0012g0005 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1747+2627A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563922 | ||||||
| chr9:133563924
|
A | G | 1 | a0001c0020t0012g0005 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1747+2629A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563924 | ||||||
| chr9:133563924
|
AGAGAGAG others(7): Show |
A | 5 | a0001c0001t0001g0023a0001c0001t0001g0146a0001c0011t0001g0029others(2): Show | 5 | HG00140.hp1 HG00738.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1747+2643_1747+265 others(18): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563924 | |||||
| chr9:133563926
|
AGAGAGAG others(5): Show |
A | 1 | a0001c0001t0002g0017 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1747+2643_1747+265 others(16): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563926 | |||||
| chr9:133563928
|
AGAGAGAG others(3): Show |
A | 1 | a0001c0001t0001g0025 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1747+2643_1747+265 others(14): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563928 | |||||
| chr9:133563932
|
A | G | 2 | a0001c0001t0004g0150a0001c0007t0001g0142 | 2 | HG03453.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1747+2637A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563932 | ||||||
| chr9:133563935
|
GAGGGAGA others(4): Show |
G | 1 | a0001c0001t0014g0118 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1747+2641_1747+265 others(15): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563935 | ||||||
| chr9:133563936
|
A | G | 1 | a0001c0031t0011g0004 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1747+2641A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563936 | ||||||
| chr9:133563936
|
AGG | A | 8 | a0001c0001t0001g0130a0001c0001t0004g0006a0001c0001t0004g0009others(5): Show | 8 | HG00099.hp1 HG02109.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1747+2643_1747+264 others(6): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563936 | |||||
| chr9:133563938
|
G | A | 25 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(22): Show | 25 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.1747+2643G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563938 | ||||||
| chr9:133563939
|
G | A | 1 | a0004c0014t0002g0034 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1747+2644G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563939 | ||||||
| chr9:133563939
|
GAGAGAGA others(4): Show |
G | 1 | a0002c0002t0003g0071 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1747+2645_1747+265 others(15): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563939 | ||||||
| chr9:133563939
|
GAGAGAGA others(6): Show |
G | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1747+2645_1747+265 others(17): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563939 | ||||||
| chr9:133563940
|
A | G | 21 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(18): Show | 21 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1747+2645A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563940 | ||||||
| chr9:133563941
|
G | A | 1 | a0002c0002t0002g0028 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1747+2646G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563941 | ||||||
| chr9:133563942
|
A | G | 10 | a0001c0001t0001g0130a0001c0001t0004g0006a0001c0001t0004g0009others(7): Show | 10 | HG00099.hp1 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1747+2647A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563942 | ||||||
| chr9:133563942
|
AGAGAGAG others(9): Show |
A | 7 | a0001c0008t0002g0090a0001c0008t0002g0105a0001c0012t0002g0139others(4): Show | 7 | HG02129.hp2 HG02280.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1747+2659_1747+267 others(20): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563942 | |||||
| chr9:133563944
|
AGAGAGAG others(7): Show |
A | 2 | a0001c0006t0001g0081a0001c0012t0002g0048 | 2 | HG00544.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1747+2661_1747+267 others(18): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563944 | |||||
| chr9:133563946
|
AGAGAGAG others(17): Show |
A | 2 | a0001c0019t0006g0117a0001c0035t0003g0020 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1747+2663_1747+268 others(28): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563946 | |||||
| chr9:133563948
|
AGAGAGAG others(3): Show |
A | 1 | a0004c0014t0002g0034 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1747+2663_1747+267 others(14): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563948 | |||||
| chr9:133563950
|
A | G | 3 | a0001c0001t0001g0043a0001c0003t0003g0055a0001c0006t0001g0111 | 3 | HG01496.hp1 HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1747+2655A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563950 | ||||||
| chr9:133563951
|
GAGAGAGG others(6): Show |
G | 1 | a0001c0015t0002g0148 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1747+2657_1747+266 others(17): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563951 | ||||||
| chr9:133563952
|
A | G | 4 | a0001c0001t0001g0025a0001c0001t0001g0078a0001c0001t0007g0112others(1): Show | 4 | HG02647.hp1 HG02970.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1747+2657A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563952 | ||||||
| chr9:133563953
|
GAGAGGGA others(8): Show |
G | 1 | a0001c0008t0002g0024 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1747+2659_1747+267 others(19): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563953 | ||||||
| chr9:133563954
|
A | G | 21 | a0001c0001t0001g0023a0001c0001t0001g0115a0001c0001t0001g0146others(18): Show | 21 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.1747+2659A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563954 | ||||||
| chr9:133563954
|
AGAGGGAG others(8): Show |
A | 1 | a0001c0007t0001g0073 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1747+2661_1747+267 others(19): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563954 | |||||
| chr9:133563958
|
G | A | 31 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0043others(28): Show | 31 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1747+2663G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563958 | ||||||
| chr9:133563961
|
GAGAGAGA others(4): Show |
G | 1 | a0001c0010t0002g0075 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1747+2667_1747+267 others(15): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563961 | ||||||
| chr9:133563963
|
GAGAGAGG others(4): Show |
G | 1 | a0003c0036t0001g0113 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1747+2669_1747+267 others(15): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563963 | ||||||
| chr9:133563967
|
GAGGGAGA others(12): Show |
G | 1 | a0001c0003t0003g0055 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1747+2673_1747+269 others(23): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563967 | ||||||
| chr9:133563970
|
G | A | 42 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(39): Show | 42 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.1747+2675G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563970 | ||||||
| chr9:133563972
|
A | G | 11 | a0001c0006t0001g0080a0001c0006t0001g0104a0001c0006t0006g0109others(8): Show | 11 | HG00323.hp2 HG01071.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.1747+2677A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563972 | ||||||
| chr9:133563974
|
A | G | 3 | a0001c0006t0008g0074a0001c0019t0006g0117a0001c0035t0003g0020 | 3 | HG02280.hp1 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1747+2679A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563974 | ||||||
| chr9:133563976
|
A | G | 13 | a0001c0001t0001g0052a0001c0001t0001g0120a0001c0001t0001g0130others(10): Show | 13 | HG01496.hp2 HG01943.hp2 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.1747+2681A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563976 | ||||||
| chr9:133563978
|
A | G | 6 | a0001c0001t0004g0009a0001c0005t0003g0014a0001c0006t0005g0125others(3): Show | 6 | HG00099.hp1 HG02559.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1747+2683A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563978 | ||||||
| chr9:133563980
|
A | G | 9 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1747+2685A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563980 | ||||||
| chr9:133563981
|
GAGAGAGG others(4): Show |
G | 1 | a0001c0003t0002g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1747+2687_1747+269 others(15): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563981 | ||||||
| chr9:133563982
|
A | G | 2 | a0001c0001t0004g0006a0001c0001t0004g0079 | 2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1747+2687A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563982 | ||||||
| chr9:133563983
|
G | A | 1 | a0001c0001t0014g0118 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1747+2688G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563983 | ||||||
| chr9:133563984
|
A | G | 2 | a0001c0001t0014g0118a0001c0007t0001g0032 | 2 | HG02970.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1747+2689A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563984 | ||||||
| chr9:133563985
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1747+2690G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563985 | ||||||
| chr9:133563986
|
A | AGAGAAAG others(1): Show |
8 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(5): Show | 8 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1747+2692_1747+269 others(12): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563986 | |||||
| chr9:133563986
|
A | G | 2 | a0001c0031t0011g0004a0002c0002t0003g0099 | 2 | HG01261.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.1747+2691A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563986 | ||||||
| chr9:133563988
|
G | A | 25 | a0001c0001t0001g0052a0001c0001t0001g0120a0001c0001t0001g0122others(22): Show | 25 | HG00099.hp1 HG01496.hp2 HG01943.hp2 others(22): Show |
intron_variant | MODIFIER | c.1747+2693G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563988 | ||||||
| chr9:133563989
|
G | A | 2 | a0001c0001t0014g0118a0001c0006t0008g0074 | 2 | HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1747+2694G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563989 | ||||||
| chr9:133563990
|
A | G | 15 | a0001c0001t0001g0078a0001c0001t0014g0118a0001c0006t0001g0080others(12): Show | 15 | HG00323.hp2 HG01070.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1747+2695A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563990 | ||||||
| chr9:133563991
|
G | A | 11 | a0001c0001t0001g0052a0001c0001t0001g0120a0001c0001t0001g0130others(8): Show | 11 | HG01496.hp2 HG01943.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1747+2696G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563991 | ||||||
| chr9:133563992
|
A | G | 2 | a0001c0006t0001g0128a0001c0006t0008g0074 | 2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1747+2697A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563992 | ||||||
| chr9:133563992
|
AGAGAGAG others(6): Show |
A | 13 | a0001c0001t0001g0078a0001c0006t0001g0080a0001c0006t0001g0103others(10): Show | 13 | HG00323.hp2 HG01070.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.1747+2708_1747+272 others(17): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563992 | |||||
| chr9:133563993
|
G | A | 5 | a0001c0001t0004g0009a0001c0005t0003g0014a0001c0006t0005g0125others(2): Show | 5 | HG00099.hp1 HG02559.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1747+2698G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563993 | ||||||
| chr9:133563994
|
A | G | 14 | a0001c0001t0001g0052a0001c0001t0001g0120a0001c0001t0001g0130others(11): Show | 14 | HG01496.hp2 HG01943.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1747+2699A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563994 | ||||||
| chr9:133563994
|
AGAGAGAG others(4): Show |
A | 1 | a0004c0014t0002g0098 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1747+2708_1747+271 others(15): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563994 | |||||
| chr9:133563995
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1747+2700G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563995 | ||||||
| chr9:133563996
|
A | G | 17 | a0001c0001t0001g0052a0001c0001t0001g0120a0001c0001t0001g0130others(14): Show | 17 | HG00099.hp1 HG01496.hp2 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.1747+2701A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563996 | ||||||
| chr9:133563997
|
G | A | 2 | a0001c0001t0004g0006a0001c0001t0004g0079 | 2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1747+2702G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563997 | ||||||
| chr9:133563998
|
A | G | 6 | a0001c0001t0001g0122a0001c0001t0004g0009a0001c0005t0003g0014others(3): Show | 6 | HG00099.hp1 HG02145.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1747+2703A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133563998 | ||||||
| chr9:133563998
|
AGAGAAGG | A | 13 | a0001c0001t0001g0052a0001c0001t0001g0120a0001c0001t0001g0130others(10): Show | 13 | HG01496.hp2 HG01943.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1747+2708_1747+271 others(11): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133563998 | |||||
| chr9:133564000
|
A | G | 4 | a0001c0001t0001g0122a0001c0001t0004g0006a0001c0001t0004g0079others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1747+2705A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564000 | ||||||
| chr9:133564000
|
AGAAGG | A | 2 | a0001c0001t0004g0009a0001c0006t0008g0074 | 2 | HG03041.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1747+2708_1747+271 others(9): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564000 | |||||
| chr9:133564001
|
G | GGGAGAGA others(2): Show |
8 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(5): Show | 8 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1747+2706_1747+270 others(13): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564001 | ||||||
| chr9:133564001
|
GA | G | 2 | a0001c0001t0014g0118a0001c0007t0001g0142 | 2 | HG02970.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1747+2708delA | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564001 | |||||
| chr9:133564002
|
A | AG | 3 | a0001c0027t0001g0010a0001c0028t0001g0116a0003c0037t0001g0114 | 3 | HG02280.hp2 HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1747+2707_1747+270 others(5): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564002 | ||||||
| chr9:133564002
|
A | AGAGAGAG others(64): Show |
1 | a0001c0031t0011g0004 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1747+2707_1747+270 others(75): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564002 | ||||||
| chr9:133564002
|
A | G | 11 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(8): Show | 11 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.1747+2707A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564002 | ||||||
| chr9:133564002
|
AAGG | A | 5 | a0001c0001t0001g0122a0001c0005t0003g0014a0001c0006t0005g0125others(2): Show | 5 | HG00099.hp1 HG02145.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1747+2708_1747+271 others(7): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564002 | ||||||
| chr9:133564003
|
A | AAGG | 9 | a0001c0001t0001g0023a0001c0001t0001g0115a0001c0001t0001g0146others(6): Show | 9 | HG00140.hp1 HG01433.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.1747+2708_1747+270 others(7): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564003 | ||||||
| chr9:133564003
|
A | AAGGGG | 3 | a0001c0001t0001g0043a0001c0001t0007g0112a0003c0036t0001g0113 | 3 | HG02572.hp1 HG02647.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1747+2708_1747+270 others(9): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564003 | ||||||
| chr9:133564003
|
A | G | 9 | a0001c0001t0004g0079a0001c0006t0001g0081a0001c0006t0001g0111others(6): Show | 9 | HG01261.hp1 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1747+2708A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564003 | ||||||
| chr9:133564004
|
G | A | 1 | a0001c0011t0001g0062 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1747+2709G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564004 | ||||||
| chr9:133564005
|
G | A | 16 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(13): Show | 16 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1747+2710G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564005 | ||||||
| chr9:133564005
|
G | GGGA | 4 | a0001c0006t0001g0081a0001c0007t0001g0073a0001c0008t0002g0024others(1): Show | 4 | HG01261.hp1 HG02622.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1747+2711_1747+271 others(7): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564005 | |||||
| chr9:133564005
|
GGA | G | 3 | a0001c0012t0002g0048a0001c0012t0002g0139a0001c0015t0002g0072 | 3 | HG00544.hp1 NA18612.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.1747+2729_1747+273 others(6): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564005 | |||||
| chr9:133564005
|
GGAGA | G | 3 | a0001c0001t0001g0132a0001c0013t0001g0108a0002c0002t0003g0036 | 3 | HG02015.hp2 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1747+2727_1747+273 others(8): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564005 | |||||
| chr9:133564006
|
GA | G | 3 | a0001c0008t0002g0090a0001c0008t0002g0105a0001c0011t0001g0062 | 3 | HG00738.hp1 HG02129.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1747+2712delA | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564006 | ||||||
| chr9:133564007
|
A | G | 1 | a0001c0007t0001g0142 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1747+2712A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564007 | ||||||
| chr9:133564009
|
A | G | 5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0056others(2): Show | 5 | HG00738.hp1 HG00738.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.1747+2714A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564009 | ||||||
| chr9:133564011
|
A | G | 5 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG00280.hp2 HG00323.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.1747+2716A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564011 | ||||||
| chr9:133564014
|
G | C | 1 | a0001c0006t0001g0111 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1747+2719G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564014 | ||||||
| chr9:133564023
|
AG | A | 2 | a0001c0015t0002g0148a0004c0014t0002g0098 | 2 | HG00438.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.1747+2729delG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564023 | ||||||
| chr9:133564024
|
G | A | 1 | a0001c0031t0011g0004 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1747+2729G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564024 | ||||||
| chr9:133564027
|
A | AG | 7 | a0001c0003t0002g0069a0001c0007t0001g0142a0001c0008t0002g0024others(4): Show | 7 | HG01515.hp1 HG02083.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1747+2737dupG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564027 | |||||
| chr9:133564027
|
A | G | 4 | a0001c0003t0002g0049a0001c0006t0001g0128a0001c0015t0002g0148others(1): Show | 4 | HG00438.hp2 HG01257.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.1747+2732A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564027 | ||||||
| chr9:133564031
|
G | GGA | 9 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1747+2743_1747+274 others(6): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564031 | |||||
| chr9:133564040
|
C | G | 9 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1747+2745C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564040 | ||||||
| chr9:133564053
|
A | AG | 4 | a0001c0001t0001g0122a0001c0005t0002g0064a0002c0002t0002g0046others(1): Show | 4 | HG00438.hp1 HG00621.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.1747+2763dupG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564053 | |||||
| chr9:133564075
|
AG | A | 3 | a0001c0006t0001g0111a0002c0002t0002g0027a0002c0002t0010g0039 | 3 | HG02056.hp1 HG02080.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1747+2783delG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564075 | |||||
| chr9:133564077
|
GGA | G | 20 | a0001c0006t0001g0080a0001c0006t0001g0081a0001c0006t0001g0103others(17): Show | 20 | HG00323.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1747+2796_1747+279 others(6): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564077 | |||||
| chr9:133564078
|
G | GGGAGAGA others(11): Show |
1 | a0001c0020t0012g0005 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1747+2783_1747+278 others(22): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564078 | ||||||
| chr9:133564081
|
A | G | 1 | a0001c0020t0012g0005 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1747+2786A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564081 | ||||||
| chr9:133564091
|
A | AG | 3 | a0001c0001t0001g0132a0001c0011t0001g0007a0001c0012t0002g0048 | 3 | HG00544.hp1 HG01496.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1747+2799dupG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564091 | |||||
| chr9:133564091
|
A | G | 4 | a0001c0006t0001g0128a0001c0027t0001g0010a0001c0028t0001g0116others(1): Show | 4 | HG02280.hp2 HG02723.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1747+2796A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564091 | ||||||
| chr9:133564093
|
G | A | 1 | a0001c0032t0005g0100 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1747+2798G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564093 | ||||||
| chr9:133564093
|
GGA | G | 3 | a0001c0001t0001g0052a0001c0033t0015g0135a0002c0029t0003g0011 | 3 | HG02080.hp1 HG02451.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1747+2815_1747+281 others(6): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564093 | |||||
| chr9:133564095
|
A | G | 20 | a0001c0006t0001g0080a0001c0006t0001g0081a0001c0006t0001g0103others(17): Show | 20 | HG00323.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1747+2800A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564095 | ||||||
| chr9:133564095
|
A | T | 1 | a0001c0003t0002g0049 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1747+2800A>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564095 | ||||||
| chr9:133564098
|
G | A | 1 | a0001c0032t0005g0100 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1747+2803G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564098 | ||||||
| chr9:133564100
|
G | A | 1 | a0001c0032t0005g0100 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1747+2805G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564100 | ||||||
| chr9:133564103
|
A | G | 1 | a0001c0032t0005g0100 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1747+2808A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564103 | ||||||
| chr9:133564105
|
A | G | 1 | a0001c0032t0005g0100 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1747+2810A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564105 | ||||||
| chr9:133564108
|
GAGAA | G | 3 | a0001c0027t0001g0010a0001c0028t0001g0116a0003c0037t0001g0114 | 3 | HG02280.hp2 HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1747+2815_1747+281 others(8): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564108 | |||||
| chr9:133564112
|
A | G | 1 | a0001c0032t0005g0100 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1747+2817A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564112 | ||||||
| chr9:133564114
|
A | G | 1 | a0001c0032t0005g0100 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1747+2819A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564114 | ||||||
| chr9:133564115
|
A | G | 23 | a0001c0006t0001g0080a0001c0006t0001g0081a0001c0006t0001g0103others(20): Show | 23 | HG00323.hp2 HG01070.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.1747+2820A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564115 | ||||||
| chr9:133564116
|
G | A | 3 | a0001c0027t0001g0010a0001c0028t0001g0116a0003c0037t0001g0114 | 3 | HG02280.hp2 HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1748-2820G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564116 | ||||||
| chr9:133564117
|
G | A | 1 | a0001c0032t0005g0100 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1748-2819G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564117 | ||||||
| chr9:133564117
|
GGGGAGA | G | 3 | a0002c0009t0001g0016a0002c0009t0001g0124a0002c0009t0001g0149 | 3 | HG02451.hp1 HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1748-2817_1748-281 others(10): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564117 | |||||
| chr9:133564119
|
G | A | 21 | a0001c0006t0001g0080a0001c0006t0001g0081a0001c0006t0001g0103others(18): Show | 21 | HG00323.hp2 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1748-2817G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564119 | ||||||
| chr9:133564119
|
G | GGA | 6 | a0001c0005t0003g0070a0001c0013t0001g0108a0002c0002t0002g0002others(3): Show | 6 | HG02056.hp1 HG02155.hp1 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.1748-2796_1748-279 others(6): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564119 | |||||
| chr9:133564120
|
GA | G | 3 | a0001c0008t0002g0090a0001c0008t0002g0105a0002c0002t0002g0046 | 3 | HG00438.hp1 HG02129.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1748-2815delA | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564120 | ||||||
| chr9:133564124
|
G | A | 1 | a0001c0032t0005g0100 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1748-2812G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564124 | ||||||
| chr9:133564125
|
A | G | 1 | a0001c0032t0005g0100 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1748-2811A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564125 | ||||||
| chr9:133564134
|
G | C | 1 | a0001c0032t0005g0100 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1748-2802G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564134 | ||||||
| chr9:133564134
|
G | GAGAAGGA others(7): Show |
7 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0056others(4): Show | 7 | HG00099.hp1 HG00738.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.1748-2799_1748-279 others(18): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564134 | |||||
| chr9:133564137
|
AGAGAAAG others(1): Show |
A | 5 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG00280.hp2 HG00323.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.1748-2797_1748-279 others(12): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564137 | |||||
| chr9:133564143
|
A | G | 2 | a0001c0005t0003g0070a0001c0012t0002g0048 | 2 | HG00544.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1748-2793A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564143 | ||||||
| chr9:133564143
|
AG | A | 4 | a0001c0006t0001g0111a0001c0007t0001g0147a0002c0002t0003g0121others(1): Show | 4 | HG00323.hp2 HG02109.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1748-2788delG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564143 | |||||
| chr9:133564144
|
G | A | 2 | a0001c0015t0002g0148a0002c0002t0003g0053 | 2 | HG00438.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1748-2792G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564144 | ||||||
| chr9:133564146
|
G | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | HG00280.hp2 HG00323.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.1748-2790G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564146 | ||||||
| chr9:133564147
|
G | A | 8 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0056others(5): Show | 8 | HG00099.hp1 HG00738.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.1748-2789G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564147 | ||||||
| chr9:133564154
|
G | A | 8 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0056others(5): Show | 8 | HG00099.hp1 HG00738.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.1748-2782G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564154 | ||||||
| chr9:133564156
|
C | G | 8 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0056others(5): Show | 8 | HG00099.hp1 HG00738.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.1748-2780C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564156 | ||||||
| chr9:133564156
|
CAG | C | 4 | a0002c0002t0003g0053a0002c0009t0001g0016a0002c0009t0001g0124others(1): Show | 4 | HG02451.hp1 HG02615.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1748-2774_1748-277 others(6): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564156 | |||||
| chr9:133564164
|
A | C | 1 | a0002c0002t0003g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1748-2772A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564164 | ||||||
| chr9:133564164
|
A | G | 8 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0056others(5): Show | 8 | HG00099.hp1 HG00738.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.1748-2772A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564164 | ||||||
| chr9:133564166
|
GGGAGAGA others(6): Show |
G | 1 | a0001c0007t0001g0147 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1748-2768_1748-275 others(17): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564166 | |||||
| chr9:133564169
|
A | G | 1 | a0002c0002t0003g0021 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1748-2767A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564169 | ||||||
| chr9:133564170
|
G | GAGAGAA | 10 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(7): Show | 10 | HG00280.hp2 HG00323.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.1748-2761_1748-276 others(10): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564170 | |||||
| chr9:133564170
|
G | GAGAGAGA others(77): Show |
1 | a0001c0020t0012g0005 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1748-2758_1748-275 others(88): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564170 | |||||
| chr9:133564171
|
AGAGAGAG others(5): Show |
A | 23 | a0001c0006t0001g0080a0001c0006t0001g0081a0001c0006t0001g0103others(20): Show | 23 | HG01070.hp1 HG01071.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.1748-2753_1748-274 others(16): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564171 | |||||
| chr9:133564172
|
G | GAGAA | 21 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0052others(18): Show | 21 | HG00140.hp1 HG00738.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1748-2761_1748-276 others(8): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564172 | |||||
| chr9:133564175
|
A | T | 1 | a0001c0001t0014g0118 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1748-2761A>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564175 | ||||||
| chr9:133564176
|
G | A | 2 | a0001c0001t0001g0120a0001c0031t0011g0004 | 2 | HG01261.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1748-2760G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564176 | ||||||
| chr9:133564183
|
G | A | 26 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0052others(23): Show | 26 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.1748-2753G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564183 | ||||||
| chr9:133564185
|
A | G | 22 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0052others(19): Show | 22 | HG00140.hp1 HG00738.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1748-2751A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564185 | ||||||
| chr9:133564187
|
A | G | 1 | a0001c0001t0004g0018 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1748-2749A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564187 | ||||||
| chr9:133564188
|
G | A | 24 | a0001c0006t0001g0080a0001c0006t0001g0081a0001c0006t0001g0103others(21): Show | 24 | HG00323.hp2 HG01070.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.1748-2748G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564188 | ||||||
| chr9:133564189
|
A | G | 1 | a0001c0031t0011g0004 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1748-2747A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564189 | ||||||
| chr9:133564196
|
GA | G | 4 | a0001c0001t0001g0043a0001c0001t0001g0078a0001c0011t0001g0007others(1): Show | 4 | HG01496.hp2 HG02572.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1748-2739delA | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564196 | ||||||
| chr9:133564197
|
A | G | 1 | a0001c0016t0001g0087 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1748-2739A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564197 | ||||||
| chr9:133564199
|
G | A | 5 | a0001c0001t0001g0078a0001c0001t0004g0018a0001c0011t0001g0007others(2): Show | 5 | HG01261.hp2 HG01496.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1748-2737G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564199 | ||||||
| chr9:133564201
|
A | G | 1 | a0001c0001t0004g0018 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1748-2735A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564201 | ||||||
| chr9:133564201
|
A | T | 1 | a0001c0006t0005g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1748-2735A>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564201 | ||||||
| chr9:133564205
|
A | G | 1 | a0001c0031t0011g0004 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1748-2731A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564205 | ||||||
| chr9:133564211
|
AG | A | 4 | a0001c0001t0007g0112a0001c0006t0001g0111a0001c0032t0005g0100others(1): Show | 4 | HG02056.hp2 HG02109.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1748-2722delG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564211 | |||||
| chr9:133564213
|
G | A | 1 | a0001c0031t0011g0004 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1748-2723G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564213 | ||||||
| chr9:133564219
|
G | A | 1 | a0001c0001t0014g0118 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1748-2717G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564219 | ||||||
| chr9:133564224
|
GAGAGGGA others(4): Show |
G | 1 | a0001c0001t0014g0118 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1748-2711_1748-270 others(15): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564224 | ||||||
| chr9:133564233
|
A | T | 1 | a0001c0003t0002g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1748-2703A>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564233 | ||||||
| chr9:133564242
|
GA | G | 3 | a0001c0006t0001g0111a0001c0006t0005g0137a0001c0016t0001g0087 | 3 | HG02109.hp2 HG02723.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1748-2691delA | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564242 | |||||
| chr9:133564243
|
AAAGAGGG others(4): Show |
A | 1 | a0001c0001t0014g0118 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1748-2691_1748-268 others(15): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564243 | |||||
| chr9:133564244
|
A | G | 1 | a0001c0001t0007g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1748-2692A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564244 | ||||||
| chr9:133564247
|
A | AG | 3 | a0001c0001t0004g0079a0001c0003t0002g0107a0001c0005t0003g0070 | 3 | HG02109.hp1 HG02300.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1748-2686dupG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564247 | |||||
| chr9:133564249
|
G | T | 1 | a0001c0006t0005g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1748-2687G>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564249 | ||||||
| chr9:133564259
|
A | AG | 3 | a0001c0005t0003g0070a0001c0020t0012g0005a0002c0004t0003g0093 | 3 | HG01433.hp2 HG02300.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1748-2674dupG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564259 | |||||
| chr9:133564261
|
GGA | G | 24 | a0001c0001t0002g0017a0001c0006t0001g0080a0001c0006t0001g0081others(21): Show | 24 | HG01070.hp1 HG01071.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1748-2664_1748-266 others(6): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564261 | |||||
| chr9:133564270
|
G | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1748-2666G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564270 | ||||||
| chr9:133564274
|
A | G | 7 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1748-2662A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564274 | ||||||
| chr9:133564275
|
A | G | 7 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1748-2661A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564275 | ||||||
| chr9:133564279
|
G | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1748-2657G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564279 | ||||||
| chr9:133564280
|
G | A | 1 | a0001c0006t0001g0111 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1748-2656G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564280 | ||||||
| chr9:133564281
|
A | G | 1 | a0001c0006t0001g0111 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1748-2655A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564281 | ||||||
| chr9:133564281
|
AGAGAGAG others(3): Show |
A | 1 | a0001c0019t0006g0117 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1748-2635_1748-262 others(14): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564281 | |||||
| chr9:133564284
|
G | C | 1 | a0001c0006t0001g0128 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1748-2652G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564284 | ||||||
| chr9:133564287
|
A | G | 7 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1748-2649A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564287 | ||||||
| chr9:133564288
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1748-2648G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564288 | ||||||
| chr9:133564291
|
G | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1748-2645G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564291 | ||||||
| chr9:133564291
|
G | GGAGA | 54 | a0001c0001t0001g0025a0001c0001t0001g0043a0001c0001t0001g0052others(51): Show | 54 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.1748-2639_1748-263 others(8): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564291 | |||||
| chr9:133564295
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1748-2641A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564295 | ||||||
| chr9:133564297
|
AGAGGGAG others(19): Show |
A | 1 | a0001c0001t0001g0078 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1748-2635_1748-261 others(30): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564297 | |||||
| chr9:133564300
|
G | A | 1 | a0001c0001t0014g0118 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1748-2636G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564300 | ||||||
| chr9:133564301
|
G | A | 4 | a0001c0001t0001g0041a0001c0006t0005g0137a0001c0020t0012g0005others(1): Show | 4 | HG01192.hp2 HG01433.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1748-2635G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564301 | ||||||
| chr9:133564302
|
G | A | 1 | a0001c0001t0014g0118 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1748-2634G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564302 | ||||||
| chr9:133564302
|
G | GAAAGAGA others(25): Show |
1 | a0002c0009t0001g0124 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1748-2633_1748-263 others(36): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564302 | |||||
| chr9:133564303
|
A | G | 1 | a0001c0031t0011g0004 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1748-2633A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564303 | ||||||
| chr9:133564305
|
A | G | 1 | a0001c0006t0005g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1748-2631A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564305 | ||||||
| chr9:133564307
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1748-2629A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564307 | ||||||
| chr9:133564307
|
A | T | 1 | a0001c0001t0003g0077 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1748-2629A>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564307 | ||||||
| chr9:133564311
|
A | G | 1 | a0002c0009t0001g0124 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1748-2625A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564311 | ||||||
| chr9:133564313
|
A | AG | 2 | a0001c0016t0001g0087a0002c0002t0003g0065 | 2 | HG02723.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.1748-2623_1748-262 others(5): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564313 | ||||||
| chr9:133564314
|
A | AAGAGAGA others(35): Show |
1 | a0002c0009t0001g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1748-2603_1748-256 others(46): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564314 | |||||
| chr9:133564314
|
A | G | 3 | a0001c0001t0001g0041a0001c0001t0007g0112a0002c0009t0001g0124 | 3 | HG01192.hp2 HG02451.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1748-2622A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564314 | ||||||
| chr9:133564321
|
A | AG | 3 | a0001c0013t0001g0108a0001c0015t0002g0148a0002c0002t0002g0027 | 3 | HG00438.hp2 HG02080.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1748-2612dupG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564321 | |||||
| chr9:133564321
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1748-2615A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564321 | ||||||
| chr9:133564323
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1748-2613G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564323 | ||||||
| chr9:133564323
|
G | GGA | 35 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(32): Show |
intron_variant | MODIFIER | c.1748-2604_1748-260 others(6): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564323 | |||||
| chr9:133564324
|
G | A | 1 | a0001c0001t0014g0118 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1748-2612G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564324 | ||||||
| chr9:133564325
|
A | G | 1 | a0001c0005t0003g0070 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1748-2611A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564325 | ||||||
| chr9:133564330
|
GAGAA | G | 2 | a0001c0012t0002g0139a0005c0034t0003g0037 | 2 | HG01975.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.1748-2602_1748-259 others(8): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564330 | |||||
| chr9:133564331
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1748-2605A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564331 | ||||||
| chr9:133564334
|
A | G | 27 | a0001c0001t0001g0078a0001c0001t0007g0112a0001c0001t0014g0118others(24): Show | 27 | HG00323.hp2 HG01070.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1748-2602A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564334 | ||||||
| chr9:133564336
|
G | A | 22 | a0001c0006t0001g0080a0001c0006t0001g0081a0001c0006t0001g0103others(19): Show | 22 | HG00323.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1748-2600G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564336 | ||||||
| chr9:133564343
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1748-2593A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564343 | ||||||
| chr9:133564344
|
A | G | 3 | a0001c0001t0001g0041a0001c0001t0007g0112a0001c0006t0001g0111 | 3 | HG01192.hp2 HG02109.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1748-2592A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564344 | ||||||
| chr9:133564345
|
A | G | 2 | a0001c0001t0007g0112a0002c0002t0003g0151 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1748-2591A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564345 | ||||||
| chr9:133564353
|
G | A | 3 | a0001c0001t0001g0041a0001c0001t0004g0018a0001c0001t0007g0112 | 3 | HG01192.hp2 HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1748-2583G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564353 | ||||||
| chr9:133564353
|
GGA | G | 3 | a0001c0005t0003g0014a0001c0006t0005g0137a0002c0002t0003g0151 | 3 | HG00099.hp1 HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1748-2573_1748-257 others(6): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564353 | |||||
| chr9:133564354
|
G | A | 1 | a0001c0001t0004g0018 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1748-2582G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564354 | ||||||
| chr9:133564355
|
AGAGAGAG others(3): Show |
A | 6 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0040others(3): Show | 6 | HG00280.hp2 HG00738.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.1748-2551_1748-254 others(14): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564355 | |||||
| chr9:133564355
|
AGAGAGAG others(13): Show |
A | 1 | a0001c0011t0001g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1748-2561_1748-254 others(24): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564355 | |||||
| chr9:133564356
|
G | A | 2 | a0001c0001t0001g0041a0001c0006t0005g0125 | 2 | HG01192.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1748-2580G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564356 | ||||||
| chr9:133564358
|
GA | G | 2 | a0001c0001t0007g0112a0001c0032t0005g0100 | 2 | HG02559.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1748-2577delA | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564358 | ||||||
| chr9:133564361
|
AGAGGGAG others(6): Show |
A | 1 | a0001c0006t0008g0074 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1748-2573_1748-256 others(17): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564361 | |||||
| chr9:133564363
|
AGGGAGAG others(4): Show |
A | 1 | a0002c0002t0003g0095 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1748-2570_1748-256 others(15): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564363 | |||||
| chr9:133564365
|
G | A | 4 | a0001c0001t0001g0041a0001c0001t0001g0078a0001c0001t0007g0112others(1): Show | 4 | HG01192.hp2 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1748-2571G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564365 | ||||||
| chr9:133564365
|
G | GGAGAGAG others(25): Show |
1 | a0002c0009t0001g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1748-2562_1748-256 others(36): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564365 | |||||
| chr9:133564365
|
GGA | G | 3 | a0001c0001t0001g0132a0001c0001t0003g0077a0001c0035t0003g0020 | 3 | HG02280.hp1 HG02896.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1748-2563_1748-256 others(6): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564365 | |||||
| chr9:133564365
|
GGAGAGAG others(15): Show |
G | 26 | a0001c0001t0001g0012a0001c0001t0001g0023a0001c0001t0001g0025others(23): Show | 26 | HG00140.hp1 HG00323.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.1748-2551_1748-253 others(26): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564365 | |||||
| chr9:133564366
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0078 | 2 | HG01192.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1748-2570G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564366 | ||||||
| chr9:133564371
|
AGAGGGAG others(7): Show |
A | 1 | a0001c0019t0006g0117 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1748-2561_1748-254 others(18): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564371 | |||||
| chr9:133564373
|
A | G | 1 | a0001c0013t0001g0108 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1748-2563A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564373 | ||||||
| chr9:133564373
|
AG | A | 3 | a0001c0001t0004g0018a0001c0006t0005g0137a0002c0002t0003g0099 | 3 | HG02622.hp1 NA18612.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1748-2560delG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564373 | |||||
| chr9:133564375
|
G | A | 3 | a0001c0001t0001g0078a0001c0001t0007g0112a0001c0013t0001g0108 | 3 | HG02647.hp1 HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1748-2561G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564375 | ||||||
| chr9:133564375
|
G | GGAGAGAG others(5): Show |
3 | a0002c0002t0003g0022a0002c0002t0003g0071a0002c0002t0003g0096 | 3 | HG02155.hp1 HG02155.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1748-2493_1748-248 others(16): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564375 | |||||
| chr9:133564375
|
GGAGAGAG others(5): Show |
G | 2 | a0001c0006t0001g0128a0001c0028t0001g0116 | 2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1748-2493_1748-248 others(16): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564375 | |||||
| chr9:133564376
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1748-2560G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564376 | ||||||
| chr9:133564385
|
G | A | 2 | a0001c0001t0001g0041a0001c0006t0005g0137 | 2 | HG01192.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1748-2551G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564385 | ||||||
| chr9:133564387
|
A | G | 2 | a0001c0001t0001g0041a0001c0019t0006g0117 | 2 | HG01192.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1748-2549A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564387 | ||||||
| chr9:133564397
|
GGAGA | G | 27 | a0001c0003t0001g0140a0001c0003t0002g0049a0001c0003t0002g0057others(24): Show | 27 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.1748-2531_1748-252 others(8): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564397 | |||||
| chr9:133564397
|
GGAGAGAG others(9): Show |
G | 3 | a0001c0003t0002g0033a0001c0003t0002g0054a0001c0005t0003g0070 | 3 | HG01192.hp1 HG02300.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.1748-2531_1748-251 others(20): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564397 | |||||
| chr9:133564409
|
GGAGAGAG others(9): Show |
G | 1 | a0002c0002t0002g0046 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1748-2519_1748-250 others(20): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564409 | |||||
| chr9:133564411
|
A | AGAGAGAG others(3): Show |
5 | a0001c0008t0002g0105a0001c0012t0002g0048a0001c0012t0002g0139others(2): Show | 5 | HG00438.hp2 HG00544.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.1748-2515_1748-250 others(14): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564411 | |||||
| chr9:133564415
|
A | T | 1 | a0001c0006t0005g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1748-2521A>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564415 | ||||||
| chr9:133564419
|
A | AGGGAGAG others(4): Show |
1 | a0001c0008t0002g0090 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1748-2516_1748-250 others(15): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564419 | |||||
| chr9:133564419
|
AG | A | 3 | a0001c0001t0007g0112a0001c0007t0001g0147a0002c0002t0003g0095 | 3 | HG00323.hp2 HG01515.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1748-2514delG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564419 | |||||
| chr9:133564421
|
G | A | 1 | a0001c0001t0003g0077 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1748-2515G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564421 | ||||||
| chr9:133564421
|
GGA | G | 25 | a0001c0003t0002g0049a0001c0003t0002g0057a0001c0003t0002g0061others(22): Show | 25 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.1748-2505_1748-250 others(6): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564421 | |||||
| chr9:133564423
|
A | G | 1 | a0001c0005t0002g0064 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1748-2513A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564423 | ||||||
| chr9:133564427
|
A | G | 1 | a0001c0006t0001g0111 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1748-2509A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564427 | ||||||
| chr9:133564429
|
A | T | 1 | a0001c0006t0005g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1748-2507A>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564429 | ||||||
| chr9:133564431
|
A | T | 1 | a0001c0032t0005g0100 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1748-2505A>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564431 | ||||||
| chr9:133564432
|
GGGAGAGA others(4): Show |
G | 1 | a0002c0004t0003g0044 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1748-2501_1748-249 others(15): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564432 | |||||
| chr9:133564433
|
G | A | 2 | a0001c0006t0001g0111a0001c0006t0005g0137 | 2 | HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1748-2503G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564433 | ||||||
| chr9:133564433
|
GGA | G | 3 | a0001c0003t0002g0033a0001c0003t0002g0054a0001c0005t0003g0070 | 3 | HG01192.hp1 HG02300.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.1748-2493_1748-249 others(6): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564433 | |||||
| chr9:133564437
|
A | G | 1 | a0001c0006t0001g0111 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1748-2499A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564437 | ||||||
| chr9:133564439
|
A | G | 1 | a0001c0006t0005g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1748-2497A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564439 | ||||||
| chr9:133564440
|
G | A | 1 | a0001c0006t0005g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1748-2496G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564440 | ||||||
| chr9:133564441
|
A | G | 2 | a0001c0020t0012g0005a0001c0031t0011g0004 | 2 | HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1748-2495A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564441 | ||||||
| chr9:133564443
|
A | G | 34 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0040others(31): Show | 34 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.1748-2493A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564443 | ||||||
| chr9:133564445
|
G | A | 37 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0040others(34): Show | 37 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.1748-2491G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564445 | ||||||
| chr9:133564451
|
A | G | 34 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0040others(31): Show | 34 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.1748-2485A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564451 | ||||||
| chr9:133564453
|
A | G | 3 | a0001c0001t0014g0118a0001c0020t0012g0005a0001c0031t0011g0004 | 3 | HG01261.hp2 HG01433.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1748-2483A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564453 | ||||||
| chr9:133564453
|
AG | A | 3 | a0002c0002t0002g0028a0002c0002t0003g0065a0002c0004t0003g0063 | 3 | HG00621.hp2 HG02056.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.1748-2480delG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564453 | |||||
| chr9:133564455
|
G | A | 11 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0040others(8): Show | 11 | HG00280.hp2 HG00738.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.1748-2481G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564455 | ||||||
| chr9:133564455
|
GGAGAGAG others(7): Show |
G | 1 | a0002c0002t0003g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1748-2461_1748-244 others(18): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564455 | |||||
| chr9:133564461
|
A | G | 1 | a0001c0001t0014g0118 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1748-2475A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564461 | ||||||
| chr9:133564461
|
AG | A | 3 | a0001c0001t0001g0120a0001c0001t0003g0077a0002c0002t0002g0027 | 3 | HG02080.hp2 HG02145.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1748-2472delG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564461 | |||||
| chr9:133564462
|
G | A | 1 | a0001c0001t0014g0118 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1748-2474G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564462 | ||||||
| chr9:133564463
|
G | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0040others(4): Show | 7 | HG00280.hp2 HG00738.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.1748-2473G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564463 | ||||||
| chr9:133564465
|
A | G | 7 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0040others(4): Show | 7 | HG00280.hp2 HG00738.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.1748-2471A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564465 | ||||||
| chr9:133564465
|
AGAGAGAG others(5): Show |
A | 26 | a0001c0003t0001g0140a0001c0003t0002g0049a0001c0003t0002g0057others(23): Show | 26 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.1748-2454_1748-244 others(16): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564465 | |||||
| chr9:133564467
|
A | AGAGG | 2 | a0001c0020t0012g0005a0001c0031t0011g0004 | 2 | HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1748-2466_1748-246 others(8): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564467 | |||||
| chr9:133564467
|
A | G | 3 | a0001c0003t0002g0033a0001c0003t0002g0054a0001c0005t0003g0070 | 3 | HG01192.hp1 HG02300.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.1748-2469A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564467 | ||||||
| chr9:133564475
|
A | G | 3 | a0001c0003t0002g0033a0001c0003t0002g0054a0001c0005t0003g0070 | 3 | HG01192.hp1 HG02300.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.1748-2461A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564475 | ||||||
| chr9:133564477
|
G | A | 2 | a0001c0003t0002g0033a0001c0003t0002g0054 | 2 | HG01192.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.1748-2459G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564477 | ||||||
| chr9:133564479
|
A | G | 1 | a0001c0006t0005g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1748-2457A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564479 | ||||||
| chr9:133564480
|
GAGAGAGA others(7): Show |
G | 1 | a0001c0005t0002g0144 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1748-2449_1748-243 others(18): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564480 | |||||
| chr9:133564481
|
A | T | 1 | a0001c0006t0005g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1748-2455A>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564481 | ||||||
| chr9:133564482
|
G | C | 7 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0040others(4): Show | 7 | HG00280.hp2 HG00738.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.1748-2454G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564482 | ||||||
| chr9:133564486
|
GAGGGAGA others(34): Show |
G | 1 | a0001c0001t0014g0118 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1748-2449_1748-240 others(45): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564486 | ||||||
| chr9:133564490
|
GAGAC | G | 7 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0040others(4): Show | 7 | HG00280.hp2 HG00738.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.1748-2442_1748-243 others(8): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564490 | |||||
| chr9:133564494
|
C | CAGAGAGG others(1): Show |
27 | a0001c0001t0001g0012a0001c0001t0001g0041a0001c0005t0003g0014others(24): Show | 27 | HG00099.hp1 HG00323.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1748-2435_1748-242 others(12): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564494 | |||||
| chr9:133564494
|
C | CAGGG | 26 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0043others(23): Show | 26 | HG00140.hp1 HG00738.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.1748-2440_1748-243 others(8): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564494 | |||||
| chr9:133564494
|
C | G | 1 | a0001c0001t0007g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1748-2442C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564494 | ||||||
| chr9:133564496
|
G | C | 1 | a0001c0005t0002g0144 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1748-2440G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564496 | ||||||
| chr9:133564499
|
A | T | 1 | a0001c0006t0005g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1748-2437A>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564499 | ||||||
| chr9:133564507
|
A | G | 1 | a0001c0005t0003g0070 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1748-2429A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564507 | ||||||
| chr9:133564507
|
AGAGAGG | A | 29 | a0001c0003t0001g0140a0001c0003t0002g0033a0001c0003t0002g0049others(26): Show | 29 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.1748-2417_1748-241 others(10): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564507 | |||||
| chr9:133564509
|
A | G | 3 | a0001c0001t0007g0112a0001c0006t0001g0103a0004c0014t0002g0098 | 3 | HG01070.hp1 HG01257.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1748-2427A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564509 | ||||||
| chr9:133564513
|
G | A | 5 | a0001c0001t0004g0079a0001c0001t0007g0112a0001c0005t0003g0070others(2): Show | 5 | HG01257.hp2 HG01515.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1748-2423G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564513 | ||||||
| chr9:133564513
|
G | GGAGGGAG others(3): Show |
1 | a0001c0012t0002g0139 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1748-2420_1748-241 others(14): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564513 | |||||
| chr9:133564518
|
G | GAGGAGAG others(5): Show |
1 | a0004c0014t0002g0098 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1748-2418_1748-241 others(16): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564518 | ||||||
| chr9:133564519
|
G | A | 2 | a0001c0012t0002g0139a0002c0002t0003g0095 | 2 | HG01515.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.1748-2417G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564519 | ||||||
| chr9:133564521
|
A | C | 1 | a0001c0012t0002g0139 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1748-2415A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564521 | ||||||
| chr9:133564524
|
GA | G | 2 | a0002c0002t0003g0053a0003c0036t0001g0113 | 2 | HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1748-2411delA | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564524 | ||||||
| chr9:133564529
|
A | G | 1 | a0001c0001t0007g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1748-2407A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564529 | ||||||
| chr9:133564531
|
A | AG | 2 | a0001c0001t0001g0132a0002c0002t0003g0151 | 2 | HG01884.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1748-2404dupG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564531 | |||||
| chr9:133564534
|
C | G | 2 | a0001c0001t0007g0112a0002c0002t0003g0053 | 2 | HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1748-2402C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564534 | ||||||
| chr9:133564536
|
G | C | 1 | a0002c0002t0003g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1748-2400G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564536 | ||||||
| chr9:133564539
|
AG | A | 3 | a0001c0003t0002g0049a0001c0003t0003g0091a0001c0012t0002g0048 | 3 | HG00544.hp1 HG02602.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.1748-2394delG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564539 | |||||
| chr9:133564541
|
G | A | 1 | a0001c0001t0007g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1748-2395G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564541 | ||||||
| chr9:133564541
|
GGAGAGAG others(11): Show |
G | 2 | a0002c0002t0003g0151a0002c0002t0003g0152 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1748-2372_1748-235 others(22): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564541 | |||||
| chr9:133564543
|
A | AG | 2 | a0001c0001t0007g0112a0001c0013t0001g0108 | 2 | HG02647.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1748-2392dupG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564543 | |||||
| chr9:133564547
|
AG | A | 5 | a0001c0001t0004g0150a0002c0002t0003g0095a0002c0004t0003g0063others(2): Show | 5 | HG00621.hp2 HG01257.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.1748-2386delG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564547 | |||||
| chr9:133564549
|
G | A | 1 | a0001c0001t0007g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1748-2387G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564549 | ||||||
| chr9:133564553
|
AG | A | 4 | a0001c0003t0001g0140a0001c0012t0002g0139a0002c0002t0002g0027others(1): Show | 4 | HG02080.hp2 HG02647.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.1748-2380delG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564553 | |||||
| chr9:133564559
|
A | G | 1 | a0001c0008t0002g0024 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1748-2377A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564559 | ||||||
| chr9:133564566
|
G | GA | 2 | a0001c0003t0002g0107a0004c0014t0002g0098 | 2 | HG01257.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1748-2370_1748-236 others(5): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564566 | ||||||
| chr9:133564571
|
AG | A | 5 | a0001c0001t0001g0120a0001c0006t0005g0137a0001c0007t0001g0060others(2): Show | 5 | HG02056.hp2 HG02145.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1748-2362delG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564571 | |||||
| chr9:133564572
|
G | A | 1 | a0001c0001t0014g0118 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1748-2364G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564572 | ||||||
| chr9:133564573
|
G | A | 2 | a0001c0001t0007g0112a0001c0026t0001g0123 | 2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1748-2363G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564573 | ||||||
| chr9:133564577
|
A | G | 1 | a0001c0001t0007g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1748-2359A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564577 | ||||||
| chr9:133564580
|
GA | G | 2 | a0001c0006t0001g0103a0001c0012t0002g0139 | 2 | HG01070.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.1748-2354delA | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564580 | |||||
| chr9:133564581
|
A | AG | 2 | a0001c0001t0004g0150a0004c0014t0002g0098 | 2 | HG01257.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1748-2355_1748-235 others(5): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564581 | ||||||
| chr9:133564582
|
A | G | 2 | a0001c0001t0007g0112a0002c0004t0001g0051 | 2 | HG02647.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.1748-2354A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564582 | ||||||
| chr9:133564582
|
AGGAGAGA others(7): Show |
A | 1 | a0001c0032t0005g0100 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1748-2343_1748-233 others(18): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564582 | |||||
| chr9:133564583
|
G | A | 1 | a0002c0004t0001g0051 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1748-2353G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564583 | ||||||
| chr9:133564583
|
GGA | G | 6 | a0001c0008t0002g0024a0001c0008t0002g0045a0001c0025t0002g0089others(3): Show | 6 | HG02280.hp1 HG03654.hp2 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1748-2343_1748-234 others(6): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564583 | |||||
| chr9:133564583
|
GGAGAGAG others(23): Show |
G | 1 | a0001c0005t0003g0014 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1748-2339_1748-231 others(34): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564583 | |||||
| chr9:133564585
|
A | AG | 2 | a0002c0004t0003g0082a0004c0014t0002g0098 | 2 | HG01257.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1748-2350dupG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564585 | |||||
| chr9:133564593
|
AG | A | 3 | a0001c0003t0003g0091a0001c0006t0001g0103a0002c0002t0010g0039 | 3 | HG01070.hp1 HG02056.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.1748-2338delG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564593 | |||||
| chr9:133564595
|
G | A | 1 | a0001c0001t0007g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1748-2341G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564595 | ||||||
| chr9:133564595
|
GGGGAGAG others(7): Show |
G | 1 | a0001c0006t0005g0125 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1748-2339_1748-232 others(18): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564595 | |||||
| chr9:133564596
|
GGGAGAGA others(8): Show |
G | 1 | a0001c0001t0014g0118 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1748-2338_1748-232 others(19): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564596 | |||||
| chr9:133564597
|
G | A | 1 | a0001c0006t0005g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1748-2339G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564597 | ||||||
| chr9:133564597
|
G | GGAGAGAG others(11): Show |
5 | a0002c0002t0003g0022a0002c0002t0003g0030a0002c0002t0003g0036others(2): Show | 5 | HG00099.hp2 HG02015.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.1748-2313_1748-229 others(22): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564597 | |||||
| chr9:133564597
|
GGAGAGAG others(7): Show |
G | 22 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0052others(19): Show | 22 | HG00140.hp1 HG00738.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1748-2329_1748-231 others(18): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564597 | |||||
| chr9:133564598
|
GA | G | 2 | a0001c0001t0007g0112a0001c0033t0015g0135 | 2 | HG02080.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1748-2337delA | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564598 | ||||||
| chr9:133564598
|
GAGAGAGA others(6): Show |
G | 1 | a0001c0031t0011g0004 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1748-2337_1748-232 others(17): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564598 | ||||||
| chr9:133564599
|
AGAGAGAG others(1): Show |
A | 6 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0040others(3): Show | 6 | HG00280.hp2 HG00738.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1748-2329_1748-232 others(12): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564599 | |||||
| chr9:133564600
|
GAGAGAGG others(6): Show |
G | 1 | a0001c0006t0005g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1748-2335_1748-232 others(17): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564600 | ||||||
| chr9:133564603
|
AGAGG | A | 3 | a0001c0001t0001g0043a0001c0001t0004g0150a0001c0023t0001g0119 | 3 | HG02572.hp1 HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1748-2329_1748-232 others(8): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564603 | |||||
| chr9:133564605
|
A | AGGAGAGA others(11): Show |
1 | a0002c0002t0003g0065 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1748-2329_1748-232 others(22): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564605 | |||||
| chr9:133564607
|
G | A | 4 | a0001c0001t0007g0112a0001c0011t0001g0007a0001c0033t0015g0135others(1): Show | 4 | HG01496.hp2 HG02080.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1748-2329G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564607 | ||||||
| chr9:133564608
|
G | A | 1 | a0002c0002t0003g0065 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1748-2328G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564608 | ||||||
| chr9:133564609
|
A | AGGGAGAG others(55): Show |
1 | a0001c0011t0001g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1748-2326_1748-232 others(66): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564609 | |||||
| chr9:133564611
|
A | G | 2 | a0001c0001t0007g0112a0003c0036t0001g0113 | 2 | HG02647.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1748-2325A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564611 | ||||||
| chr9:133564613
|
A | G | 2 | a0001c0001t0004g0079a0001c0033t0015g0135 | 2 | HG02080.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1748-2323A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564613 | ||||||
| chr9:133564615
|
A | G | 4 | a0001c0001t0001g0043a0001c0001t0004g0150a0001c0001t0007g0112others(1): Show | 4 | HG02572.hp1 HG02647.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1748-2321A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564615 | ||||||
| chr9:133564619
|
A | G | 6 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0040others(3): Show | 6 | HG00280.hp2 HG00738.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1748-2317A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564619 | ||||||
| chr9:133564621
|
A | G | 1 | a0001c0011t0001g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1748-2315A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564621 | ||||||
| chr9:133564623
|
A | G | 2 | a0001c0005t0003g0070a0001c0032t0005g0100 | 2 | HG02300.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1748-2313A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564623 | ||||||
| chr9:133564625
|
G | A | 12 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0040others(9): Show | 12 | HG00280.hp2 HG00738.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.1748-2311G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564625 | ||||||
| chr9:133564625
|
G | GGA | 35 | a0001c0001t0001g0132a0001c0001t0003g0077a0001c0003t0002g0033others(32): Show | 35 | HG00140.hp2 HG00438.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.1748-2297_1748-229 others(6): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564625 | |||||
| chr9:133564629
|
A | G | 1 | a0001c0011t0001g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1748-2307A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564629 | ||||||
| chr9:133564629
|
A | T | 1 | a0001c0001t0004g0079 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1748-2307A>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564629 | ||||||
| chr9:133564629
|
AGAGAGAG others(5): Show |
A | 1 | a0001c0001t0001g0012 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1748-2299_1748-228 others(16): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564629 | |||||
| chr9:133564631
|
A | G | 2 | a0001c0001t0004g0079a0001c0033t0015g0135 | 2 | HG02080.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1748-2305A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564631 | ||||||
| chr9:133564634
|
GAGA | G | 2 | a0001c0001t0007g0112a0001c0016t0001g0087 | 2 | HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1748-2301_1748-229 others(7): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564634 | ||||||
| chr9:133564634
|
GAGAGAGG others(6): Show |
G | 1 | a0001c0001t0004g0150 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1748-2301_1748-228 others(17): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564634 | ||||||
| chr9:133564635
|
A | C | 1 | a0002c0002t0003g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1748-2301A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564635 | ||||||
| chr9:133564635
|
A | G | 20 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0052others(17): Show | 20 | HG00140.hp1 HG00738.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1748-2301A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564635 | ||||||
| chr9:133564635
|
AGAGAGG | A | 22 | a0001c0006t0001g0080a0001c0006t0001g0104a0001c0006t0001g0128others(19): Show | 22 | HG00323.hp2 HG01071.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.1748-2295_1748-229 others(10): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564635 | |||||
| chr9:133564635
|
AGAGAGGG others(6): Show |
A | 1 | a0001c0023t0001g0119 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1748-2299_1748-228 others(17): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564635 | |||||
| chr9:133564637
|
A | G | 8 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0040others(5): Show | 8 | HG00280.hp2 HG00738.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.1748-2299A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564637 | ||||||
| chr9:133564637
|
AGAGG | A | 2 | a0001c0006t0001g0081a0004c0014t0002g0034 | 2 | HG02622.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1748-2295_1748-229 others(8): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564637 | |||||
| chr9:133564639
|
AGG | A | 20 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0052others(17): Show | 20 | HG00140.hp1 HG00738.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1748-2295_1748-229 others(6): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564639 | |||||
| chr9:133564640
|
G | GGGAGAGA others(6): Show |
1 | a0001c0003t0003g0091 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1748-2288_1748-228 others(17): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564640 | |||||
| chr9:133564641
|
G | A | 11 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0040others(8): Show | 11 | HG00280.hp2 HG00738.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.1748-2295G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564641 | ||||||
| chr9:133564641
|
G | C | 1 | a0001c0001t0001g0122 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1748-2295G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564641 | ||||||
| chr9:133564641
|
G | GGAGAGAG others(29): Show |
1 | a0001c0031t0011g0004 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1748-2288_1748-228 others(40): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564641 | |||||
| chr9:133564647
|
A | G | 1 | a0001c0006t0001g0081 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1748-2289A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564647 | ||||||
| chr9:133564648
|
G | A | 2 | a0001c0006t0005g0137a0001c0033t0015g0135 | 2 | HG02080.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1748-2288G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564648 | ||||||
| chr9:133564649
|
G | A | 2 | a0001c0001t0007g0112a0001c0006t0001g0081 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1748-2287G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564649 | ||||||
| chr9:133564651
|
A | T | 1 | a0001c0001t0007g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1748-2285A>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564651 | ||||||
| chr9:133564655
|
AG | A | 4 | a0001c0001t0004g0079a0001c0006t0008g0074a0001c0021t0016g0129others(1): Show | 4 | HG02109.hp1 HG02615.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1748-2278delG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564655 | |||||
| chr9:133564656
|
G | A | 1 | a0001c0006t0001g0103 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1748-2280G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564656 | ||||||
| chr9:133564657
|
G | A | 1 | a0001c0005t0003g0014 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1748-2279G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564657 | ||||||
| chr9:133564661
|
A | G | 1 | a0001c0005t0003g0014 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1748-2275A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564661 | ||||||
| chr9:133564667
|
AG | A | 6 | a0001c0001t0003g0077a0001c0006t0001g0081a0001c0006t0001g0103others(3): Show | 6 | HG00280.hp1 HG01070.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1748-2266delG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564667 | |||||
| chr9:133564673
|
A | G | 1 | a0001c0006t0001g0103 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1748-2263A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564673 | ||||||
| chr9:133564673
|
AG | A | 3 | a0001c0001t0004g0079a0001c0003t0003g0091a0002c0002t0003g0053 | 3 | HG02109.hp1 HG02615.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.1748-2260delG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564673 | |||||
| chr9:133564675
|
G | A | 1 | a0001c0006t0001g0103 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1748-2261G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564675 | ||||||
| chr9:133564685
|
A | G | 1 | a0001c0026t0001g0123 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1748-2251A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564685 | ||||||
| chr9:133564687
|
G | A | 1 | a0001c0026t0001g0123 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1748-2249G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564687 | ||||||
| chr9:133564689
|
A | AG | 2 | a0001c0001t0001g0120a0001c0001t0001g0122 | 2 | HG02145.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1748-2246dupG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564689 | |||||
| chr9:133564690
|
GA | G | 2 | a0001c0001t0001g0078a0001c0005t0003g0070 | 2 | HG02300.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1748-2245delA | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564690 | ||||||
| chr9:133564691
|
AG | A | 3 | a0001c0006t0005g0137a0001c0023t0001g0119a0002c0004t0003g0063 | 3 | HG00621.hp2 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1748-2242delG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564691 | |||||
| chr9:133564692
|
G | T | 1 | a0001c0001t0001g0078 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1748-2244G>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564692 | ||||||
| chr9:133564693
|
G | GGA | 3 | a0001c0003t0002g0057a0001c0006t0005g0125a0001c0010t0002g0075 | 3 | HG01515.hp1 HG02129.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1748-2232_1748-223 others(6): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564693 | |||||
| chr9:133564694
|
G | A | 22 | a0001c0006t0001g0080a0001c0006t0001g0081a0001c0006t0001g0103others(19): Show | 22 | HG00323.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1748-2242G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564694 | ||||||
| chr9:133564697
|
A | C | 2 | a0001c0001t0001g0122a0001c0001t0004g0079 | 2 | HG02109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1748-2239A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564697 | ||||||
| chr9:133564698
|
G | T | 1 | a0001c0001t0004g0079 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1748-2238G>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564698 | ||||||
| chr9:133564699
|
A | C | 1 | a0001c0001t0004g0079 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1748-2237A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564699 | ||||||
| chr9:133564701
|
A | C | 1 | a0001c0001t0004g0079 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1748-2235A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564701 | ||||||
| chr9:133564705
|
A | C | 1 | a0001c0001t0004g0079 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1748-2231A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564705 | ||||||
| chr9:133564706
|
A | C | 1 | a0001c0001t0004g0079 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1748-2230A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564706 | ||||||
| chr9:133564709
|
A | C | 1 | a0001c0001t0004g0079 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1748-2227A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564709 | ||||||
| chr9:133564710
|
G | T | 1 | a0001c0001t0004g0079 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1748-2226G>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564710 | ||||||
| chr9:133564711
|
A | C | 1 | a0001c0001t0004g0079 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1748-2225A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564711 | ||||||
| chr9:133564713
|
A | C | 1 | a0001c0001t0004g0079 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1748-2223A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564713 | ||||||
| chr9:133564717
|
A | C | 1 | a0001c0001t0004g0079 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1748-2219A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564717 | ||||||
| chr9:133564718
|
G | GC | 2 | a0001c0001t0004g0079a0001c0006t0005g0137 | 2 | HG02109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1748-2218_1748-221 others(5): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564718 | ||||||
| chr9:133564719
|
A | T | 1 | a0001c0001t0004g0079 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1748-2217A>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564719 | ||||||
| chr9:133564722
|
G | A | 1 | a0001c0001t0004g0079 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1748-2214G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564722 | ||||||
| chr9:133564723
|
T | A | 1 | a0001c0010t0002g0075 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1748-2213T>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564723 | ||||||
| chr9:133564723
|
T | TC | 2 | a0001c0032t0005g0100a0002c0002t0003g0102 | 2 | HG00280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1748-2213_1748-221 others(5): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564723 | ||||||
| chr9:133564723
|
TGA | T | 2 | a0001c0003t0002g0057a0002c0004t0003g0047 | 2 | HG02129.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1748-2198_1748-219 others(6): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564723 | |||||
| chr9:133564725
|
A | C | 1 | a0001c0001t0004g0079 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1748-2211A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564725 | ||||||
| chr9:133564727
|
A | C | 1 | a0001c0001t0004g0079 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1748-2209A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564727 | ||||||
| chr9:133564733
|
A | C | 1 | a0001c0001t0001g0078 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1748-2203A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564733 | ||||||
| chr9:133564737
|
A | C | 1 | a0001c0001t0004g0079 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1748-2199A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564737 | ||||||
| chr9:133564741
|
AG | A | 4 | a0001c0001t0004g0079a0001c0007t0001g0147a0002c0002t0003g0102others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1748-2192delG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564741 | |||||
| chr9:133564750
|
A | C | 1 | a0001c0001t0004g0079 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1748-2186A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564750 | ||||||
| chr9:133564758
|
G | C | 1 | a0001c0001t0004g0079 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1748-2178G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564758 | ||||||
| chr9:133564761
|
A | T | 1 | a0001c0001t0004g0079 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1748-2175A>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564761 | ||||||
| chr9:133564792
|
TG | T | 3 | a0001c0012t0002g0048a0001c0023t0001g0119a0001c0032t0005g0100 | 3 | HG00544.hp1 HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1748-2142delG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564792 | |||||
| chr9:133564844
|
T | TC | 3 | a0001c0012t0002g0048a0002c0004t0003g0093a0003c0036t0001g0113 | 3 | HG00544.hp1 HG02647.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1748-2090dupC | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564844 | |||||
| chr9:133564850
|
C | A | 1 | a0001c0006t0005g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1748-2086C>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564850 | ||||||
| chr9:133564854
|
T | A | 1 | a0001c0032t0005g0100 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1748-2082T>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564854 | ||||||
| chr9:133564883
|
C | T | 1 | a0001c0006t0005g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1748-2053C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564883 | ||||||
| chr9:133564895
|
T | A | 1 | a0001c0001t0004g0079 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1748-2041T>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564895 | ||||||
| chr9:133564966
|
G | A | 2 | a0001c0020t0012g0005a0001c0031t0011g0004 | 2 | HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1748-1970G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133564966 | ||||||
| chr9:133564976
|
GT | G | 3 | a0001c0032t0005g0100a0002c0002t0003g0053a0002c0002t0003g0095 | 3 | HG01515.hp2 HG02559.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1748-1955delT | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133564976 | |||||
| chr9:133565050
|
G | A | 1 | a0001c0013t0001g0108 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1748-1886G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565050 | ||||||
| chr9:133565051
|
G | C | 1 | a0001c0013t0001g0108 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1748-1885G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565051 | ||||||
| chr9:133565052
|
T | A | 1 | a0001c0013t0001g0108 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1748-1884T>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565052 | ||||||
| chr9:133565056
|
A | C | 1 | a0001c0013t0001g0108 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1748-1880A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565056 | ||||||
| chr9:133565057
|
G | T | 1 | a0001c0013t0001g0108 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1748-1879G>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565057 | ||||||
| chr9:133565058
|
G | C | 1 | a0001c0013t0001g0108 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1748-1878G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565058 | ||||||
| chr9:133565060
|
G | A | 1 | a0001c0013t0001g0108 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1748-1876G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565060 | ||||||
| chr9:133565061
|
G | T | 1 | a0001c0013t0001g0108 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1748-1875G>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565061 | ||||||
| chr9:133565062
|
A | C | 1 | a0001c0013t0001g0108 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1748-1874A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565062 | ||||||
| chr9:133565065
|
T | A | 1 | a0001c0013t0001g0108 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1748-1871T>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565065 | ||||||
| chr9:133565102
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1748-1834A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565102 | ||||||
| chr9:133565112
|
A | C | 1 | a0002c0002t0003g0030 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1748-1824A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565112 | ||||||
| chr9:133565142
|
T | C | 1 | a0001c0005t0003g0070 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1748-1794T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565142 | ||||||
| chr9:133565145
|
C | T | 1 | a0001c0005t0003g0070 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1748-1791C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565145 | ||||||
| chr9:133565146
|
T | C | 1 | a0001c0005t0003g0070 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1748-1790T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565146 | ||||||
| chr9:133565175
|
AG | A | 3 | a0002c0002t0003g0021a0002c0002t0003g0065a0002c0002t0003g0102 | 3 | HG00280.hp1 HG02165.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.1748-1756delG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133565175 | |||||
| chr9:133565192
|
C | A | 1 | a0001c0006t0005g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1748-1744C>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565192 | ||||||
| chr9:133565211
|
C | A | 1 | a0001c0006t0005g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1748-1725C>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565211 | ||||||
| chr9:133565228
|
G | GA | 4 | a0001c0020t0012g0005a0002c0004t0001g0106a0002c0004t0003g0044others(1): Show | 4 | HG01433.hp2 HG02165.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1748-1702dupA | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133565228 | |||||
| chr9:133565276
|
C | A | 1 | a0001c0005t0003g0070 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1748-1660C>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565276 | ||||||
| chr9:133565293
|
T | G | 1 | a0001c0003t0002g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1748-1643T>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565293 | ||||||
| chr9:133565355
|
G | A | 1 | a0001c0016t0001g0087 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1748-1581G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565355 | ||||||
| chr9:133565356
|
A | T | 1 | a0001c0016t0001g0087 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1748-1580A>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565356 | ||||||
| chr9:133565434
|
A | G | 2 | a0001c0006t0001g0080a0001c0006t0001g0081 | 2 | HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1748-1502A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565434 | ||||||
| chr9:133565457
|
G | A | 8 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(5): Show | 8 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1748-1479G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565457 | ||||||
| chr9:133565469
|
G | GC | 3 | a0001c0001t0001g0043a0001c0003t0002g0054a0001c0010t0002g0075 | 3 | HG01192.hp1 HG01515.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1748-1463dupC | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133565469 | |||||
| chr9:133565497
|
G | A | 26 | a0001c0003t0001g0140a0001c0003t0002g0033a0001c0003t0002g0049others(23): Show | 26 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.1748-1439G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565497 | ||||||
| chr9:133565506
|
A | G | 54 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0043others(51): Show | 54 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.1748-1430A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565506 | ||||||
| chr9:133565547
|
G | T | 1 | a0001c0007t0001g0073 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1748-1389G>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565547 | ||||||
| chr9:133565574
|
C | A | 1 | a0001c0013t0001g0108 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1748-1362C>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565574 | ||||||
| chr9:133565615
|
G | GA | 3 | a0001c0001t0001g0122a0002c0002t0003g0065a0002c0002t0003g0121 | 3 | HG02145.hp2 NA18951.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1748-1315dupA | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133565615 | |||||
| chr9:133565646
|
TC | T | 3 | a0001c0010t0002g0075a0002c0002t0002g0027a0002c0002t0003g0065 | 3 | HG01515.hp1 HG02080.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.1748-1287delC | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133565646 | |||||
| chr9:133565724
|
C | G | 1 | a0001c0006t0005g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1748-1212C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565724 | ||||||
| chr9:133565725
|
G | C | 1 | a0001c0006t0005g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1748-1211G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565725 | ||||||
| chr9:133565742
|
A | G | 30 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0043others(27): Show | 30 | HG00140.hp1 HG00738.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.1748-1194A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565742 | ||||||
| chr9:133565819
|
G | C | 1 | a0001c0001t0001g0043 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1748-1117G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565819 | ||||||
| chr9:133565820
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1748-1116C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565820 | ||||||
| chr9:133565821
|
T | G | 1 | a0001c0001t0001g0043 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1748-1115T>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565821 | ||||||
| chr9:133565838
|
G | A | 1 | a0001c0003t0002g0049 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1748-1098G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565838 | ||||||
| chr9:133565839
|
C | CCA | 41 | a0001c0001t0001g0008a0001c0001t0001g0078a0001c0001t0004g0006others(38): Show | 41 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.1748-1062_1748-106 others(6): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133565839 | |||||
| chr9:133565839
|
C | CCACA | 14 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0040others(11): Show | 14 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.1748-1064_1748-106 others(8): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133565839 | |||||
| chr9:133565839
|
C | CCACACA | 14 | a0001c0001t0001g0052a0001c0001t0001g0120a0001c0001t0001g0138others(11): Show | 14 | HG01070.hp1 HG01257.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1748-1066_1748-106 others(10): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133565839 | |||||
| chr9:133565839
|
C | CCACACAC others(1): Show |
2 | a0001c0001t0001g0025a0001c0006t0006g0109 | 2 | HG01255.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1748-1068_1748-106 others(12): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133565839 | |||||
| chr9:133565839
|
C | CCACACAC others(5): Show |
1 | a0001c0025t0002g0089 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1748-1072_1748-106 others(16): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133565839 | |||||
| chr9:133565839
|
CCA | C | 4 | a0001c0001t0001g0132a0002c0002t0003g0095a0002c0004t0001g0106others(1): Show | 4 | HG01515.hp2 HG02040.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1748-1062_1748-106 others(6): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133565839 | |||||
| chr9:133565839
|
CCACA | C | 6 | a0002c0002t0002g0028a0002c0002t0003g0019a0002c0002t0003g0121others(3): Show | 6 | HG01071.hp1 HG02056.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.1748-1064_1748-106 others(8): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133565839 | |||||
| chr9:133565874
|
C | CACACACA others(1): Show |
2 | a0001c0006t0005g0125a0001c0006t0008g0074 | 2 | HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1748-1061_1748-106 others(12): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133565874 | |||||
| chr9:133565874
|
C | T | 1 | a0001c0006t0005g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1748-1062C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565874 | ||||||
| chr9:133565875
|
A | ACAG | 2 | a0001c0005t0003g0070a0001c0010t0002g0075 | 2 | HG01515.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1748-1061_1748-106 others(7): Show |
ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565875 | ||||||
| chr9:133565876
|
G | C | 2 | a0001c0005t0003g0070a0001c0010t0002g0075 | 2 | HG01515.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1748-1060G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565876 | ||||||
| chr9:133565995
|
G | A | 2 | a0001c0020t0012g0005a0001c0031t0011g0004 | 2 | HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1748-941G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565995 | ||||||
| chr9:133565996
|
G | T | 1 | a0001c0003t0002g0054 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1748-940G>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133565996 | ||||||
| chr9:133566033
|
T | A | 1 | a0002c0009t0001g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1748-903T>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133566033 | ||||||
| chr9:133566074
|
GC | G | 2 | a0001c0003t0002g0054a0001c0010t0002g0075 | 2 | HG01192.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1748-860delC | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133566074 | |||||
| chr9:133566112
|
C | CG | 3 | a0001c0001t0004g0018a0001c0015t0002g0148a0002c0002t0003g0102 | 3 | HG00280.hp1 HG00438.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1748-820dupG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133566112 | |||||
| chr9:133566225
|
T | G | 2 | a0001c0020t0012g0005a0001c0031t0011g0004 | 2 | HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1748-711T>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133566225 | ||||||
| chr9:133566334
|
G | A | 17 | a0001c0006t0001g0080a0001c0006t0001g0081a0001c0006t0001g0103others(14): Show | 17 | HG00438.hp2 HG00544.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.1748-602G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133566334 | ||||||
| chr9:133566364
|
C | T | 1 | a0001c0031t0011g0004 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1748-572C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133566364 | ||||||
| chr9:133566368
|
G | A | 1 | a0002c0002t0003g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1748-568G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133566368 | ||||||
| chr9:133566369
|
A | G | 1 | a0002c0002t0003g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1748-567A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133566369 | ||||||
| chr9:133566422
|
C | A | 1 | a0002c0002t0003g0021 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1748-514C>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133566422 | ||||||
| chr9:133566507
|
C | G | 1 | a0001c0031t0011g0004 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1748-429C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133566507 | ||||||
| chr9:133566508
|
G | A | 1 | a0001c0031t0011g0004 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1748-428G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133566508 | ||||||
| chr9:133566510
|
A | C | 1 | a0001c0031t0011g0004 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1748-426A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133566510 | ||||||
| chr9:133566539
|
C | T | 2 | a0001c0020t0012g0005a0001c0031t0011g0004 | 2 | HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1748-397C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133566539 | ||||||
| chr9:133566727
|
C | CG | 3 | a0001c0005t0001g0127a0002c0004t0003g0093a0002c0029t0003g0011 | 3 | HG02602.hp1 HG04199.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1748-205dupG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | 133566727 | |||||
| chr9:133566801
|
G | C | 7 | a0001c0005t0003g0014a0001c0006t0005g0125a0001c0006t0005g0137others(4): Show | 7 | HG00099.hp1 HG01261.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.1748-135G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133566801 | ||||||
| chr9:133566935
|
G | T | 1 | a0001c0021t0016g0129 | 1 | HG02896.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.1748-1G>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 12/18 | chr9 | 133566935 | ||||||
| chr9:133567096
|
G | A | 1 | a0001c0001t0007g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1874+34G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 13/18 | chr9 | 133567096 | ||||||
| chr9:133567097
|
G | A | 2 | a0001c0005t0002g0085a0001c0010t0002g0075 | 2 | HG01515.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1874+35G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 13/18 | chr9 | 133567097 | ||||||
| chr9:133567099
|
A | C | 1 | a0001c0001t0001g0052 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1874+37A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 13/18 | chr9 | 133567099 | ||||||
| chr9:133567152
|
G | A | 1 | a0001c0012t0002g0139 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1874+90G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 13/18 | chr9 | 133567152 | ||||||
| chr9:133567164
|
C | T | 4 | a0001c0001t0001g0132a0001c0001t0003g0077a0001c0006t0001g0111others(1): Show | 4 | HG02109.hp2 HG02809.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1874+102C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 13/18 | chr9 | 133567164 | ||||||
| chr9:133567256
|
C | T | 8 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(5): Show | 8 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1874+194C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 13/18 | chr9 | 133567256 | ||||||
| chr9:133567276
|
C | T | 2 | a0001c0006t0001g0080a0001c0006t0001g0081 | 2 | HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1874+214C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 13/18 | chr9 | 133567276 | ||||||
| chr9:133567444
|
G | A | 5 | a0001c0005t0003g0014a0001c0006t0005g0125a0001c0006t0005g0137others(2): Show | 5 | HG00099.hp1 HG02559.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1874+382G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 13/18 | chr9 | 133567444 | ||||||
| chr9:133567542
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1874+480T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 13/18 | chr9 | 133567542 | ||||||
| chr9:133567839
|
G | A | 1 | a0001c0001t0002g0017 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1875-434G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 13/18 | chr9 | 133567839 | ||||||
| chr9:133567845
|
A | G | 81 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(78): Show | 81 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.1875-428A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 13/18 | chr9 | 133567845 | ||||||
| chr9:133568010
|
C | T | 5 | a0001c0005t0003g0014a0001c0006t0005g0125a0001c0006t0005g0137others(2): Show | 5 | HG00099.hp1 HG02559.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1875-263C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 13/18 | chr9 | 133568010 | ||||||
| chr9:133568028
|
G | A | 5 | a0001c0005t0003g0014a0001c0006t0005g0125a0001c0006t0005g0137others(2): Show | 5 | HG00099.hp1 HG02559.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1875-245G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 13/18 | chr9 | 133568028 | ||||||
| chr9:133568035
|
C | T | 4 | a0001c0003t0003g0055a0002c0004t0003g0038a0002c0004t0003g0047others(1): Show | 4 | HG01496.hp1 HG01975.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.1875-238C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 13/18 | chr9 | 133568035 | ||||||
| chr9:133568548
|
G | A | 4 | a0001c0006t0005g0125a0001c0006t0005g0137a0001c0006t0008g0074others(1): Show | 4 | HG02559.hp1 HG02615.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2089-55G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 14/18 | chr9 | 133568548 | ||||||
| chr9:133568577
|
C | T | 1 | a0001c0020t0012g0005 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2089-26C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 14/18 | chr9 | 133568577 | ||||||
| chr9:133568974
|
T | C | 5 | a0001c0006t0005g0125a0001c0006t0005g0137a0001c0006t0008g0074others(2): Show | 5 | HG02559.hp1 HG02615.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2244+216T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 15/18 | chr9 | 133568974 | ||||||
| chr9:133569102
|
T | C | 1 | a0001c0013t0001g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2245-306T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 15/18 | chr9 | 133569102 | ||||||
| chr9:133569143
|
G | A | 27 | a0001c0007t0001g0032a0001c0007t0001g0042a0001c0007t0001g0060others(24): Show | 27 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.2245-265G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 15/18 | chr9 | 133569143 | ||||||
| chr9:133569599
|
G | A | 1 | a0001c0008t0002g0105 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2415+21G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 16/18 | chr9 | 133569599 | ||||||
| chr9:133569624
|
G | A | 3 | a0002c0009t0001g0016a0002c0009t0001g0124a0002c0009t0001g0149 | 3 | HG02451.hp1 HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2415+46G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 16/18 | chr9 | 133569624 | ||||||
| chr9:133569879
|
G | C | 1 | a0001c0022t0001g0059 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2415+301G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 16/18 | chr9 | 133569879 | ||||||
| chr9:133569907
|
G | T | 1 | a0001c0003t0002g0133 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2415+329G>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 16/18 | chr9 | 133569907 | ||||||
| chr9:133570210
|
A | G | 6 | a0001c0008t0002g0090a0001c0008t0002g0105a0001c0012t0002g0048others(3): Show | 6 | HG00438.hp2 HG00544.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.2416-121A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 16/18 | chr9 | 133570210 | ||||||
| chr9:133570234
|
T | C | 1 | a0002c0004t0001g0106 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2416-97T>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 16/18 | chr9 | 133570234 | ||||||
| chr9:133570247
|
G | A | 1 | a0002c0002t0003g0101 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2416-84G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 16/18 | chr9 | 133570247 | ||||||
| chr9:133570322
|
C | T | 4 | a0001c0001t0001g0132a0001c0001t0003g0077a0001c0006t0001g0111others(1): Show | 4 | HG02109.hp2 HG02809.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2416-9C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 16/18 | chr9 | 133570322 | ||||||
| chr9:133570574
|
C | T | 35 | a0001c0006t0005g0125a0001c0006t0005g0137a0001c0006t0008g0074others(32): Show | 35 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.2592+67C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133570574 | ||||||
| chr9:133570584
|
C | G | 3 | a0001c0001t0001g0122a0001c0001t0001g0130a0001c0013t0001g0015 | 3 | HG02145.hp2 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2592+77C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133570584 | ||||||
| chr9:133570765
|
C | G | 1 | a0001c0031t0011g0004 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2592+258C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133570765 | ||||||
| chr9:133570825
|
C | T | 35 | a0001c0006t0005g0125a0001c0006t0005g0137a0001c0006t0008g0074others(32): Show | 35 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.2592+318C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133570825 | ||||||
| chr9:133570837
|
A | C | 2 | a0001c0006t0005g0125a0001c0006t0008g0074 | 2 | HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2592+330A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133570837 | ||||||
| chr9:133570916
|
G | A | 1 | a0002c0004t0001g0106 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2592+409G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133570916 | ||||||
| chr9:133570935
|
A | G | 10 | a0001c0001t0001g0025a0001c0001t0001g0043a0001c0001t0001g0052others(7): Show | 10 | HG01943.hp2 HG02145.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.2592+428A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133570935 | ||||||
| chr9:133570970
|
C | G | 1 | a0001c0006t0008g0074 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2592+463C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133570970 | ||||||
| chr9:133571020
|
G | T | 8 | a0001c0006t0005g0125a0001c0006t0005g0137a0001c0006t0008g0074others(5): Show | 8 | HG02451.hp1 HG02559.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2592+513G>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133571020 | ||||||
| chr9:133571063
|
G | A | 1 | a0001c0006t0006g0109 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2592+556G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133571063 | ||||||
| chr9:133571158
|
C | G | 3 | a0002c0009t0001g0016a0002c0009t0001g0124a0002c0009t0001g0149 | 3 | HG02451.hp1 HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2592+651C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133571158 | ||||||
| chr9:133571291
|
G | C | 1 | a0002c0029t0003g0011 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2592+784G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133571291 | ||||||
| chr9:133571319
|
A | C | 85 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(82): Show | 85 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.2592+812A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133571319 | ||||||
| chr9:133571737
|
A | G | 1 | a0001c0011t0001g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2592+1230A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133571737 | ||||||
| chr9:133571835
|
C | G | 1 | a0001c0020t0012g0005 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2592+1328C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133571835 | ||||||
| chr9:133572132
|
C | T | 112 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(109): Show | 112 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.2592+1625C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133572132 | ||||||
| chr9:133572188
|
C | G | 10 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(7): Show | 10 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.2593-1655C>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133572188 | ||||||
| chr9:133572236
|
A | G | 43 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0043others(40): Show | 43 | HG00140.hp1 HG00738.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.2593-1607A>G | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133572236 | ||||||
| chr9:133572256
|
A | C | 2 | a0001c0020t0012g0005a0001c0031t0011g0004 | 2 | HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.2593-1587A>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133572256 | ||||||
| chr9:133572321
|
G | C | 12 | a0001c0007t0001g0032a0001c0007t0001g0042a0001c0007t0001g0060others(9): Show | 12 | HG00323.hp2 HG01255.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.2593-1522G>C | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133572321 | ||||||
| chr9:133572410
|
G | A | 5 | a0001c0006t0005g0125a0001c0006t0005g0137a0001c0006t0008g0074others(2): Show | 5 | HG02559.hp1 HG02615.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2593-1433G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133572410 | ||||||
| chr9:133572532
|
G | T | 10 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(7): Show | 10 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.2593-1311G>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133572532 | ||||||
| chr9:133572547
|
G | T | 2 | a0001c0024t0005g0126a0001c0032t0005g0100 | 2 | HG02559.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2593-1296G>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133572547 | ||||||
| chr9:133572725
|
G | A | 11 | a0001c0008t0002g0024a0001c0008t0002g0045a0001c0008t0002g0090others(8): Show | 11 | HG00438.hp2 HG00544.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2593-1118G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133572725 | ||||||
| chr9:133572962
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2593-881G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133572962 | ||||||
| chr9:133573082
|
TG | T | 38 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0043others(35): Show | 38 | HG00140.hp1 HG00738.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.2593-760delG | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133573082 | ||||||
| chr9:133573200
|
G | A | 10 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(7): Show | 10 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.2593-643G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133573200 | ||||||
| chr9:133573340
|
G | A | 2 | a0001c0006t0006g0109a0001c0019t0006g0117 | 2 | HG01255.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2593-503G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133573340 | ||||||
| chr9:133573487
|
G | A | 2 | a0001c0006t0005g0125a0001c0006t0008g0074 | 2 | HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2593-356G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133573487 | ||||||
| chr9:133573494
|
G | A | 1 | a0002c0004t0001g0106 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2593-349G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133573494 | ||||||
| chr9:133573516
|
G | T | 69 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(66): Show | 69 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.2593-327G>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133573516 | ||||||
| chr9:133573728
|
G | A | 73 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0043others(70): Show | 73 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.2593-115G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133573728 | ||||||
| chr9:133573731
|
C | T | 1 | a0002c0002t0003g0066 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2593-112C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 17/18 | chr9 | 133573731 | ||||||
| chr9:133574207
|
G | A | 5 | a0001c0001t0001g0078a0001c0003t0001g0140a0001c0005t0001g0127others(2): Show | 5 | HG02040.hp2 HG02602.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2737+220G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 18/18 | chr9 | 133574207 | ||||||
| chr9:133574320
|
C | T | 28 | a0001c0001t0002g0017a0001c0003t0002g0033a0001c0003t0002g0049others(25): Show | 28 | HG00140.hp2 HG00597.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.2737+333C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 18/18 | chr9 | 133574320 | ||||||
| chr9:133574344
|
G | A | 3 | a0002c0009t0001g0016a0002c0009t0001g0124a0002c0009t0001g0149 | 3 | HG02451.hp1 HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2737+357G>A | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 18/18 | chr9 | 133574344 | ||||||
| chr9:133574450
|
C | T | 1 | a0001c0003t0002g0049 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2738-296C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 18/18 | chr9 | 133574450 | ||||||
| chr9:133574681
|
C | T | 43 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0043others(40): Show | 43 | HG00140.hp1 HG00738.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.2738-65C>T | ADAMTSL2 | ENSG00000197859.11 | transcript | ENST00000651351.2 | protein_coding | 18/18 | chr9 | 133574681 |