| geneid | 831 |
|---|---|
| ensemblid | ENSG00000153113.24 |
| hgncid | 1515 |
| symbol | CAST |
| name | calpastatin |
| refseq_nuc | NM_001750.7 |
| refseq_prot | NP_001741.4 |
| ensembl_nuc | ENST00000675179.1 |
| ensembl_prot | ENSP00000501872.1 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 96662376 |
| end | 96774683 |
| strand | + |
| ver | v1.2 |
| region | chr5:96662376-96774683 |
| region5000 | chr5:96657376-96779683 |
| regionname0 | CAST_chr5_96662376_96774683 |
| regionname5000 | CAST_chr5_96657376_96779683 |
| 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 | 791 | 238 | 45 | 36 | 116 | 14 | 25 | 96 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0002 | 0/0 | 791 | 91 | 25 | 23 | 26 | 2 | 15 | 23 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0003 | 0/0 | 791 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0004 | 0/0 | 791 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0005 | 0/0 | 791 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0006 | 0/0 | 791 | 4 | 0 | 2 | 2 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0007 | 0/0 | 791 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0008 | 0/0 | 791 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0009 | 0/0 | 791 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0010 | 0/0 | 791 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0011 | 0/0 | 791 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0012 | 0/0 | 791 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0013 | 0/0 | 791 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0014 | 0/0 | 791 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 2376 | 166 | 30 | 24 | 83 | 11 | 17 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| c0002 | 0/1 | 2376 | 54 | 2 | 9 | 33 | 3 | 6 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| c0003 | 0/0 | 2376 | 48 | 5 | 14 | 19 | 2 | 8 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| c0004 | 0/0 | 2376 | 32 | 15 | 6 | 7 | 0 | 4 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| c0005 | 0/0 | 2376 | 7 | 7 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| c0006 | 0/0 | 2376 | 7 | 2 | 3 | 0 | 0 | 2 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| c0007 | 0/0 | 2376 | 6 | 5 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| c0008 | 0/0 | 2376 | 4 | 3 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| c0009 | 0/0 | 2376 | 4 | 0 | 2 | 2 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| c0010 | 0/0 | 2376 | 4 | 3 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| c0011 | 0/0 | 2376 | 3 | 2 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| c0012 | 0/0 | 2376 | 3 | 2 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| c0013 | 0/0 | 2376 | 2 | 2 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| c0014 | 0/0 | 2376 | 2 | 2 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| c0015 | 0/0 | 2376 | 2 | 0 | 0 | 0 | 0 | 2 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| c0016 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| c0017 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| c0018 | 0/0 | 2376 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| c0019 | 0/0 | 2376 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| c0020 | 0/0 | 2376 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| c0021 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| c0022 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| c0023 | 0/0 | 2376 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| c0024 | 0/0 | 2376 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| c0025 | 0/0 | 2376 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| c0026 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| c0027 | 0/0 | 2376 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| c0028 | 0/0 | 2376 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| c0029 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 2115 | 143 | 27 | 19 | 77 | 5 | 14 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| t0002 | 1/0 | 2115 | 89 | 23 | 9 | 45 | 1 | 10 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| t0003 | 0/0 | 2115 | 52 | 6 | 20 | 16 | 2 | 8 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| t0004 | 0/0 | 2115 | 14 | 0 | 6 | 0 | 4 | 4 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| t0005 | 0/0 | 2116 | 7 | 7 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| t0006 | 0/0 | 2117 | 6 | 0 | 2 | 0 | 4 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| t0007 | 0/0 | 2116 | 5 | 5 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| t0008 | 0/0 | 2116 | 5 | 0 | 2 | 3 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| t0009 | 0/0 | 2119 | 5 | 5 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| t0010 | 0/0 | 2115 | 5 | 1 | 2 | 0 | 0 | 2 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| t0011 | 0/0 | 2115 | 4 | 3 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| t0012 | 0/0 | 2116 | 3 | 0 | 0 | 0 | 0 | 3 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| t0013 | 0/0 | 2116 | 3 | 3 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| t0014 | 0/0 | 2123 | 3 | 2 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| t0015 | 0/0 | 2117 | 3 | 0 | 0 | 3 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| t0016 | 0/0 | 2115 | 2 | 0 | 2 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| t0017 | 0/0 | 2115 | 2 | 0 | 0 | 2 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| t0018 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| t0019 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| t0020 | 0/0 | 2115 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| t0021 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| t0022 | 0/0 | 2115 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| t0023 | 0/0 | 2115 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| t0024 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| 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 | 3 | 0 | 1 | 2 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0220 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0287 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2376 | 166 | 30 | 24 | 83 | 11 | 17 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0002 | 0/1 | 2376 | 54 | 2 | 9 | 33 | 3 | 6 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0005 | 0/0 | 2376 | 7 | 7 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0011 | 0/0 | 2376 | 3 | 2 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0012 | 0/0 | 2376 | 3 | 2 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0017 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0018 | 0/0 | 2376 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0020 | 0/0 | 2376 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0021 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0028 | 0/0 | 2376 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0002c0003 | 0/0 | 2376 | 48 | 5 | 14 | 19 | 2 | 8 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0002c0004 | 0/0 | 2376 | 32 | 15 | 6 | 7 | 0 | 4 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0002c0006 | 0/0 | 2376 | 7 | 2 | 3 | 0 | 0 | 2 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0002c0013 | 0/0 | 2376 | 2 | 2 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0002c0022 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0002c0024 | 0/0 | 2376 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0003c0007 | 0/0 | 2376 | 6 | 5 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0004c0008 | 0/0 | 2376 | 4 | 3 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0004c0029 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0005c0010 | 0/0 | 2376 | 4 | 3 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0006c0009 | 0/0 | 2376 | 4 | 0 | 2 | 2 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0007c0015 | 0/0 | 2376 | 2 | 0 | 0 | 0 | 0 | 2 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0008c0014 | 0/0 | 2376 | 2 | 2 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0009c0023 | 0/0 | 2376 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0010c0016 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0011c0026 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0012c0025 | 0/0 | 2376 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0013c0019 | 0/0 | 2376 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0014c0027 | 0/0 | 2376 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4490 | 63 | 9 | 8 | 41 | 2 | 3 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0001t0002 | 1/0 | 4490 | 70 | 14 | 5 | 40 | 1 | 9 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0001t0003 | 0/0 | 4490 | 2 | 2 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0001t0004 | 0/0 | 4490 | 13 | 0 | 6 | 0 | 4 | 3 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0001t0006 | 0/0 | 4492 | 6 | 0 | 2 | 0 | 4 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0001t0007 | 0/0 | 4491 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0001t0008 | 0/0 | 4491 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0001t0009 | 0/0 | 4494 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0001t0010 | 0/0 | 4490 | 3 | 1 | 1 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0001t0016 | 0/0 | 4490 | 2 | 0 | 2 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0001t0018 | 0/0 | 4490 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0001t0019 | 0/0 | 4490 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0001t0022 | 0/0 | 4490 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0001t0023 | 0/0 | 4490 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0002t0001 | 0/1 | 4490 | 48 | 2 | 8 | 28 | 3 | 6 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0002t0002 | 0/0 | 4490 | 2 | 0 | 1 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0002t0003 | 0/0 | 4490 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0002t0017 | 0/0 | 4490 | 2 | 0 | 0 | 2 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0002t0020 | 0/0 | 4490 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0005t0001 | 0/0 | 4490 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0005t0007 | 0/0 | 4491 | 3 | 3 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0005t0009 | 0/0 | 4494 | 3 | 3 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0011t0002 | 0/0 | 4490 | 3 | 2 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0012t0001 | 0/0 | 4490 | 2 | 2 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0012t0012 | 0/0 | 4491 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0017t0001 | 0/0 | 4490 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0018t0010 | 0/0 | 4490 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0020t0004 | 0/0 | 4490 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0021t0009 | 0/0 | 4494 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0001c0028t0001 | 0/0 | 4490 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0002c0003t0001 | 0/0 | 4490 | 4 | 2 | 1 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0002c0003t0002 | 0/0 | 4490 | 5 | 0 | 1 | 4 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0002c0003t0003 | 0/0 | 4490 | 35 | 3 | 12 | 12 | 2 | 6 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0002c0003t0010 | 0/0 | 4490 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0002c0003t0015 | 0/0 | 4492 | 3 | 0 | 0 | 3 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0002c0004t0001 | 0/0 | 4490 | 13 | 4 | 1 | 5 | 0 | 3 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0002c0004t0002 | 0/0 | 4490 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0002c0004t0003 | 0/0 | 4490 | 8 | 1 | 5 | 2 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0002c0004t0005 | 0/0 | 4491 | 7 | 7 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0002c0004t0013 | 0/0 | 4491 | 2 | 2 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0002c0004t0021 | 0/0 | 4490 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0002c0006t0001 | 0/0 | 4490 | 2 | 2 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0002c0006t0003 | 0/0 | 4490 | 5 | 0 | 3 | 0 | 0 | 2 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0002c0013t0001 | 0/0 | 4490 | 2 | 2 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0002c0022t0013 | 0/0 | 4491 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0002c0024t0001 | 0/0 | 4490 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0003c0007t0002 | 0/0 | 4490 | 6 | 5 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0004c0008t0007 | 0/0 | 4491 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0004c0008t0011 | 0/0 | 4490 | 3 | 2 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0004c0029t0001 | 0/0 | 4490 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0005c0010t0014 | 0/0 | 4498 | 3 | 2 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0005c0010t0024 | 0/0 | 4490 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0006c0009t0008 | 0/0 | 4491 | 4 | 0 | 2 | 2 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0007c0015t0012 | 0/0 | 4491 | 2 | 0 | 0 | 0 | 0 | 2 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0008c0014t0002 | 0/0 | 4490 | 2 | 2 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0009c0023t0003 | 0/0 | 4490 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0010c0016t0011 | 0/0 | 4490 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0011c0026t0001 | 0/0 | 4490 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0012c0025t0001 | 0/0 | 4490 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0013c0019t0001 | 0/0 | 4490 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| a0014c0027t0001 | 0/0 | 4490 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | copy fasta | chr5 | 96657376 | 96779683 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0287 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0004g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0006g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0006g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0006g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0006g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0006g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0007g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0008g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0009g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0010g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0010g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0010g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0016g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0018g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0019g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0022g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0001t0023g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0220 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0017g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0017g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0002t0020g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0005t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0005t0007g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0005t0007g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0005t0007g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0005t0009g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0005t0009g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0011t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0011t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0011t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0012t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0012t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0012t0012g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0017t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0018t0010g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0020t0004g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0021t0009g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0001c0028t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0010g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0003t0015g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0004t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0004t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0004t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0004t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0004t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0004t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0004t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0004t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0004t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0004t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0004t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0004t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0004t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0004t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0004t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0004t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0004t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0004t0003g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0004t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0004t0003g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0004t0003g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0004t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0004t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0004t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0004t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0004t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0004t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0004t0005g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0004t0013g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0004t0013g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0004t0021g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0006t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0006t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0006t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0006t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0006t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0006t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0006t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0013t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0013t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0022t0013g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0002c0024t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0003c0007t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0003c0007t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0003c0007t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0003c0007t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0003c0007t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0003c0007t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0004c0008t0007g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0004c0008t0011g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0004c0008t0011g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0004c0008t0011g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0004c0029t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0005c0010t0014g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0005c0010t0014g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0005c0010t0014g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0005c0010t0024g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0006c0009t0008g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0006c0009t0008g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0006c0009t0008g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0006c0009t0008g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0007c0015t0012g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0007c0015t0012g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0008c0014t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0008c0014t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0009c0023t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0010c0016t0011g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0011c0026t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0012c0025t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0013c0019t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| a0014c0027t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG00099 | hp2 | a0002 | c0003 | t0003 | g0333 | EUR | GBR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0250 | EUR | GBR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG00140 | hp2 | a0001 | c0001 | t0006 | g0279 | EUR | GBR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0267 | EUR | FIN | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG00280 | hp2 | a0001 | c0001 | t0006 | g0010 | EUR | FIN | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0095 | EUR | FIN | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0307 | EUR | FIN | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | CHS | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0203 | EAS | CHS | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | CHS | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG00609 | hp1 | a0002 | c0003 | t0003 | g0309 | EAS | CHS | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | CHS | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG00621 | hp2 | a0001 | c0002 | t0020 | g0161 | EAS | CHS | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG00639 | hp1 | a0002 | c0006 | t0003 | g0213 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG00639 | hp2 | a0002 | c0003 | t0003 | g0327 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG00642 | hp2 | a0002 | c0003 | t0002 | g0276 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG00735 | hp1 | a0001 | c0001 | t0006 | g0093 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG00735 | hp2 | a0002 | c0003 | t0003 | g0324 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG00738 | hp1 | a0006 | c0009 | t0008 | g0139 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG00741 | hp1 | a0001 | c0011 | t0002 | g0102 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG00741 | hp2 | a0002 | c0004 | t0003 | g0299 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0199 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01069 | hp2 | a0002 | c0003 | t0003 | g0338 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0285 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01070 | hp2 | a0002 | c0004 | t0003 | g0298 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0269 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0229 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01074 | hp1 | a0002 | c0003 | t0003 | g0281 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0337 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0272 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01081 | hp2 | a0002 | c0004 | t0003 | g0297 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0249 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01099 | hp2 | a0002 | c0003 | t0003 | g0339 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0266 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01109 | hp1 | a0004 | c0008 | t0011 | g0238 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01109 | hp2 | a0005 | c0010 | t0014 | g0131 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01167 | hp2 | a0002 | c0006 | t0003 | g0212 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01168 | hp1 | a0001 | c0001 | t0016 | g0004 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01168 | hp2 | a0002 | c0003 | t0003 | g0314 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01169 | hp1 | a0001 | c0001 | t0016 | g0004 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01169 | hp2 | a0002 | c0006 | t0003 | g0201 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0247 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01175 | hp2 | a0002 | c0003 | t0001 | g0335 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01192 | hp1 | a0002 | c0003 | t0003 | g0320 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0135 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01243 | hp1 | a0002 | c0004 | t0003 | g0260 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0301 | AMR | PUR | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01255 | hp1 | a0003 | c0007 | t0002 | g0050 | AMR | CLM | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | CLM | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01257 | hp2 | a0002 | c0003 | t0003 | g0016 | AMR | CLM | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01258 | hp1 | a0001 | c0001 | t0006 | g0094 | AMR | CLM | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01258 | hp2 | a0002 | c0003 | t0003 | g0016 | AMR | CLM | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01346 | hp1 | a0002 | c0004 | t0001 | g0283 | AMR | CLM | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01361 | hp1 | a0001 | c0001 | t0010 | g0028 | AMR | CLM | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0012 | EUR | IBS | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0132 | EUR | IBS | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0014 | EUR | IBS | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01516 | hp2 | a0002 | c0003 | t0003 | g0268 | EUR | IBS | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0012 | EUR | IBS | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0014 | EUR | IBS | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01891 | hp1 | a0003 | c0007 | t0002 | g0254 | AFR | ACB | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01891 | hp2 | a0002 | c0004 | t0021 | g0233 | AFR | ACB | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0133 | AMR | PEL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01934 | hp2 | a0002 | c0003 | t0003 | g0331 | AMR | PEL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01943 | hp1 | a0002 | c0003 | t0003 | g0321 | AMR | PEL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0248 | AMR | PEL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01981 | hp1 | a0006 | c0009 | t0008 | g0142 | AMR | PEL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01981 | hp2 | a0001 | c0028 | t0001 | g0230 | AMR | PEL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02004 | hp1 | a0002 | c0003 | t0003 | g0326 | AMR | PEL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0228 | AMR | PEL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | KHV | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02015 | hp2 | a0006 | c0009 | t0008 | g0141 | EAS | KHV | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02055 | hp1 | a0011 | c0026 | t0001 | g0017 | AFR | ACB | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02055 | hp2 | a0003 | c0007 | t0002 | g0020 | AFR | ACB | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | KHV | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | KHV | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | KHV | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02083 | hp1 | a0009 | c0023 | t0003 | g0039 | EAS | KHV | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0197 | EAS | KHV | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | KHV | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | KHV | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | KHV | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0227 | AMR | PEL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02155 | hp1 | a0006 | c0009 | t0008 | g0140 | EAS | CDX | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02155 | hp2 | a0002 | c0003 | t0003 | g0319 | EAS | CDX | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02257 | hp1 | a0001 | c0001 | t0019 | g0332 | AFR | ACB | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02257 | hp2 | a0002 | c0003 | t0003 | g0271 | AFR | ACB | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | ACB | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02258 | hp2 | a0002 | c0003 | t0003 | g0330 | AFR | ACB | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0262 | AFR | ACB | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02280 | hp2 | a0002 | c0004 | t0005 | g0190 | AFR | ACB | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0304 | AMR | PEL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02293 | hp2 | a0002 | c0004 | t0003 | g0300 | AMR | PEL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02451 | hp2 | a0002 | c0004 | t0005 | g0031 | AFR | ACB | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0257 | AFR | GWD | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02572 | hp2 | a0002 | c0004 | t0001 | g0116 | AFR | GWD | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02602 | hp1 | a0001 | c0012 | t0012 | g0270 | SAS | PJL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02602 | hp2 | a0002 | c0004 | t0001 | g0282 | SAS | PJL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02615 | hp1 | a0001 | c0005 | t0009 | g0007 | AFR | GWD | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02615 | hp2 | a0002 | c0003 | t0003 | g0311 | AFR | GWD | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02622 | hp1 | a0002 | c0013 | t0001 | g0234 | AFR | GWD | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02622 | hp2 | a0004 | c0008 | t0011 | g0236 | AFR | GWD | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02630 | hp1 | a0004 | c0029 | t0001 | g0187 | AFR | GWD | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02647 | hp1 | a0002 | c0004 | t0003 | g0124 | AFR | GWD | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02647 | hp2 | a0001 | c0005 | t0009 | g0007 | AFR | GWD | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0246 | SAS | PJL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02683 | hp2 | a0002 | c0003 | t0003 | g0306 | SAS | PJL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02698 | hp1 | a0002 | c0003 | t0003 | g0305 | SAS | PJL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0164 | SAS | PJL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0223 | AFR | GWD | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | GWD | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0264 | AFR | GWD | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02723 | hp2 | a0005 | c0010 | t0024 | g0042 | AFR | GWD | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02738 | hp1 | a0007 | c0015 | t0012 | g0137 | SAS | PJL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02738 | hp2 | a0002 | c0003 | t0003 | g0310 | SAS | PJL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | GWD | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02809 | hp2 | a0002 | c0004 | t0001 | g0101 | AFR | GWD | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02886 | hp1 | a0002 | c0013 | t0001 | g0191 | AFR | GWD | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0231 | AFR | GWD | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02895 | hp1 | a0002 | c0003 | t0001 | g0240 | AFR | GWD | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0255 | AFR | GWD | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02897 | hp1 | a0002 | c0003 | t0001 | g0239 | AFR | GWD | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02922 | hp1 | a0008 | c0014 | t0002 | g0110 | AFR | ESN | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02922 | hp2 | a0005 | c0010 | t0014 | g0044 | AFR | ESN | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02970 | hp1 | a0001 | c0012 | t0001 | g0328 | AFR | ESN | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02970 | hp2 | a0005 | c0010 | t0014 | g0043 | AFR | ESN | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02976 | hp2 | a0002 | c0004 | t0013 | g0259 | AFR | ESN | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03017 | hp1 | a0001 | c0001 | t0010 | g0023 | SAS | PJL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0163 | SAS | PJL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03041 | hp1 | a0003 | c0007 | t0002 | g0112 | AFR | GWD | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0256 | AFR | MSL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03098 | hp2 | a0002 | c0006 | t0001 | g0040 | AFR | MSL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03209 | hp1 | a0003 | c0007 | t0002 | g0252 | AFR | MSL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | MSL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03225 | hp1 | a0002 | c0004 | t0001 | g0120 | AFR | MSL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03225 | hp2 | a0002 | c0006 | t0001 | g0041 | AFR | MSL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03453 | hp1 | a0001 | c0012 | t0001 | g0329 | AFR | MSL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03453 | hp2 | a0001 | c0001 | t0010 | g0038 | AFR | MSL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03486 | hp1 | a0001 | c0001 | t0009 | g0336 | AFR | MSL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03486 | hp2 | a0004 | c0008 | t0011 | g0037 | AFR | MSL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0226 | SAS | PJL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03490 | hp2 | a0002 | c0003 | t0003 | g0278 | SAS | PJL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03491 | hp2 | a0002 | c0006 | t0003 | g0237 | SAS | PJL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03492 | hp1 | a0002 | c0006 | t0003 | g0232 | SAS | PJL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03492 | hp2 | a0002 | c0003 | t0003 | g0275 | SAS | PJL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03516 | hp1 | a0001 | c0005 | t0009 | g0189 | AFR | ESN | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03516 | hp2 | a0001 | c0011 | t0002 | g0104 | AFR | ESN | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03540 | hp2 | a0001 | c0021 | t0009 | g0035 | AFR | GWD | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03579 | hp1 | a0001 | c0005 | t0001 | g0244 | AFR | MSL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0096 | SAS | PJL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0207 | SAS | PJL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0092 | SAS | PJL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03669 | hp2 | a0001 | c0020 | t0004 | g0022 | SAS | PJL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03704 | hp1 | a0001 | c0001 | t0023 | g0208 | SAS | PJL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | PJL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03710 | hp2 | a0002 | c0003 | t0001 | g0334 | SAS | PJL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03831 | hp1 | a0007 | c0015 | t0012 | g0138 | SAS | BEB | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03831 | hp2 | a0002 | c0003 | t0010 | g0284 | SAS | BEB | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0245 | SAS | BEB | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0211 | SAS | BEB | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0136 | SAS | BEB | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03942 | hp1 | a0002 | c0003 | t0003 | g0021 | SAS | BEB | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03942 | hp2 | a0002 | c0004 | t0001 | g0115 | SAS | BEB | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG04115 | hp1 | a0002 | c0004 | t0001 | g0126 | SAS | STU | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0125 | SAS | STU | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG04184 | hp1 | a0002 | c0024 | t0001 | g0225 | SAS | BEB | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG04184 | hp2 | a0002 | c0004 | t0002 | g0144 | SAS | BEB | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0277 | SAS | STU | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | STU | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0134 | SAS | STU | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0077 | SAS | STU | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0210 | SAS | STU | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0224 | SAS | STU | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18522 | hp1 | a0002 | c0004 | t0005 | g0030 | AFR | YRI | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | YRI | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18612 | hp1 | a0002 | c0003 | t0003 | g0340 | EAS | CHB | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | CHB | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18906 | hp1 | a0001 | c0005 | t0007 | g0251 | AFR | YRI | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | YRI | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18939 | hp1 | a0014 | c0027 | t0001 | g0221 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18942 | hp1 | a0002 | c0003 | t0015 | g0002 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18946 | hp1 | a0002 | c0003 | t0003 | g0308 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18949 | hp2 | a0002 | c0003 | t0002 | g0291 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18954 | hp2 | a0001 | c0002 | t0003 | g0204 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18956 | hp1 | a0002 | c0003 | t0003 | g0316 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18959 | hp1 | a0002 | c0003 | t0003 | g0317 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18963 | hp1 | a0002 | c0003 | t0003 | g0325 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18970 | hp1 | a0002 | c0003 | t0015 | g0002 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18970 | hp2 | a0001 | c0002 | t0017 | g0195 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18973 | hp2 | a0002 | c0003 | t0002 | g0294 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18974 | hp1 | a0001 | c0001 | t0008 | g0323 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18982 | hp2 | a0002 | c0004 | t0003 | g0006 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18984 | hp2 | a0002 | c0004 | t0001 | g0113 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18988 | hp1 | a0002 | c0003 | t0003 | g0015 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18991 | hp1 | a0002 | c0004 | t0001 | g0047 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0303 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18994 | hp1 | a0002 | c0003 | t0002 | g0289 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18995 | hp1 | a0002 | c0003 | t0003 | g0015 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18997 | hp2 | a0002 | c0003 | t0003 | g0174 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19001 | hp2 | a0002 | c0003 | t0002 | g0296 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19002 | hp1 | a0002 | c0004 | t0001 | g0048 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19002 | hp2 | a0002 | c0003 | t0015 | g0002 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19004 | hp1 | a0002 | c0004 | t0003 | g0006 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19005 | hp2 | a0002 | c0003 | t0003 | g0312 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0288 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19006 | hp2 | a0001 | c0001 | t0022 | g0182 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19009 | hp2 | a0001 | c0002 | t0017 | g0219 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19010 | hp1 | a0002 | c0004 | t0001 | g0053 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19011 | hp2 | a0002 | c0003 | t0003 | g0100 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19030 | hp1 | a0002 | c0004 | t0013 | g0258 | AFR | LWK | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19030 | hp2 | a0001 | c0011 | t0002 | g0103 | AFR | LWK | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19043 | hp1 | a0002 | c0004 | t0005 | g0027 | AFR | LWK | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | LWK | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0302 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19074 | hp1 | a0002 | c0004 | t0001 | g0049 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19086 | hp1 | a0012 | c0025 | t0001 | g0019 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19090 | hp2 | a0013 | c0019 | t0001 | g0114 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19240 | hp1 | a0002 | c0022 | t0013 | g0188 | AFR | YRI | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA19240 | hp2 | a0002 | c0004 | t0005 | g0105 | AFR | YRI | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA20129 | hp1 | a0008 | c0014 | t0002 | g0111 | AFR | ASW | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA20129 | hp2 | a0001 | c0005 | t0007 | g0242 | AFR | ASW | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA20805 | hp1 | a0001 | c0001 | t0006 | g0273 | EUR | TSI | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA20805 | hp2 | a0001 | c0001 | t0006 | g0010 | EUR | TSI | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | CLM | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG01123 | hp2 | a0001 | c0018 | t0010 | g0029 | AMR | CLM | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02109 | hp1 | a0001 | c0001 | t0018 | g0274 | AFR | ACB | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | ACB | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02486 | hp1 | a0002 | c0004 | t0001 | g0117 | AFR | ACB | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | ACB | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02559 | hp1 | a0002 | c0004 | t0005 | g0033 | AFR | ACB | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG02559 | hp2 | a0001 | c0005 | t0007 | g0243 | AFR | ACB | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03471 | hp1 | a0004 | c0008 | t0007 | g0061 | AFR | MSL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG03471 | hp2 | a0003 | c0007 | t0002 | g0313 | AFR | MSL | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG06807 | hp1 | a0002 | c0004 | t0005 | g0032 | AFR | USA | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0280 | AFR | USA | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | USA | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | USA | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA21309 | hp1 | a0010 | c0016 | t0011 | g0026 | AFR | LWK | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| NA21309 | hp2 | a0001 | c0017 | t0001 | g0025 | AFR | LWK | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0220 | REF | REF | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0287 | REF | REF | CAST_chr5_96657376_96779683 | CAST | chr5 | 96657376 | 96779683 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:96730817
|
G | T | 1 | a0009 | 1 | HG02083.hp1 | missense_variant | MODERATE | c.587G>T | p.Ser196Ile | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/32 | 634/4490 | 587/2376 | 196/791 | chr5 | 96730817 | ||
| chr5:96737924
|
A | G | 1 | a0007 | 2 | HG02738.hp1 HG03831.hp1 |
missense_variant | MODERATE | c.775A>G | p.Thr259Ala | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 11/32 | 822/4490 | 775/2376 | 259/791 | chr5 | 96737924 | ||
| chr5:96741272
|
A | C | 2 | a0006a0007 | 6 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(3): Show |
missense_variant | MODERATE | c.925A>C | p.Ile309Leu | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 14/32 | 972/4490 | 925/2376 | 309/791 | chr5 | 96741272 | ||
| chr5:96742709
|
C | A | 1 | a0010 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1153C>A | p.Gln385Lys | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/32 | 1200/4490 | 1153/2376 | 385/791 | chr5 | 96742709 | ||
| chr5:96746348
|
G | C | 1 | a0003 | 6 | HG01255.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
missense_variant | MODERATE | c.1207G>C | p.Ala403Pro | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 17/32 | 1254/4490 | 1207/2376 | 403/791 | chr5 | 96746348 | ||
| chr5:96746383
|
T | A | 1 | a0010 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1242T>A | p.Asp414Glu | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 17/32 | 1289/4490 | 1242/2376 | 414/791 | chr5 | 96746383 | ||
| chr5:96746421
|
C | T | 1 | a0014 | 1 | NA18939.hp1 | missense_variant | MODERATE | c.1280C>T | p.Ala427Val | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 17/32 | 1327/4490 | 1280/2376 | 427/791 | chr5 | 96746421 | ||
| chr5:96746424
|
C | T | 1 | a0008 | 2 | HG02922.hp1 NA20129.hp1 |
missense_variant&splice_region_variant | MODERATE | c.1283C>T | p.Thr428Met | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 17/32 | 1330/4490 | 1283/2376 | 428/791 | chr5 | 96746424 | ||
| chr5:96748567
|
G | T | 1 | a0011 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.1382G>T | p.Arg461Leu | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 19/32 | 1429/4490 | 1382/2376 | 461/791 | chr5 | 96748567 | ||
| chr5:96750630
|
G | C | 3 | a0002a0009a0013 | 93 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(90): Show |
missense_variant | MODERATE | c.1472G>C | p.Cys491Ser | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/32 | 1519/4490 | 1472/2376 | 491/791 | chr5 | 96750630 | ||
| chr5:96754680
|
G | A | 1 | a0010 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1649G>A | p.Arg550His | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 22/32 | 1696/4490 | 1649/2376 | 550/791 | chr5 | 96754680 | ||
| chr5:96762275
|
A | G | 1 | a0005 | 4 | HG01109.hp2 HG02723.hp2 HG02922.hp2 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.1835A>G | p.Lys612Arg | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 25/32 | 1882/4490 | 1835/2376 | 612/791 | chr5 | 96762275 | ||
| chr5:96762299
|
C | T | 1 | a0004 | 5 | HG01109.hp1 HG02622.hp2 HG02630.hp1 others(2): Show |
missense_variant | MODERATE | c.1859C>T | p.Ala620Val | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 25/32 | 1906/4490 | 1859/2376 | 620/791 | chr5 | 96762299 | ||
| chr5:96765225
|
G | A | 1 | a0013 | 1 | NA19090.hp2 | missense_variant | MODERATE | c.1937G>A | p.Ser646Asn | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 26/32 | 1984/4490 | 1937/2376 | 646/791 | chr5 | 96765225 | ||
| chr5:96767459
|
A | G | 1 | a0012 | 1 | NA19086.hp1 | missense_variant | MODERATE | c.2152A>G | p.Thr718Ala | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 28/32 | 2199/4490 | 2152/2376 | 718/791 | chr5 | 96767459 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:96675556
|
C | T | 1 | a0004c0029 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.93C>T | p.Thr31Thr | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/32 | 140/4490 | 93/2376 | 31/791 | chr5 | 96675556 | ||
| chr5:96695853
|
C | T | 1 | a0001c0028 | 1 | HG01981.hp2 | synonymous_variant | LOW | c.156C>T | p.Leu52Leu | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/32 | 203/4490 | 156/2376 | 52/791 | chr5 | 96695853 | ||
| chr5:96695865
|
A | G | 8 | a0001c0002a0001c0028a0002c0006others(5): Show | 70 | HG00140.hp1 HG00544.hp1 HG00621.hp2 others(67): Show |
synonymous_variant | LOW | c.168A>G | p.Gln56Gln | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/32 | 215/4490 | 168/2376 | 56/791 | chr5 | 96695865 | ||
| chr5:96736204
|
G | T | 3 | a0001c0005a0002c0022a0004c0029 | 9 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(6): Show |
synonymous_variant | LOW | c.663G>T | p.Val221Val | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 10/32 | 710/4490 | 663/2376 | 221/791 | chr5 | 96736204 | ||
| chr5:96736234
|
G | A | 1 | a0001c0011 | 3 | HG00741.hp1 HG03516.hp2 NA19030.hp2 |
synonymous_variant | LOW | c.693G>A | p.Ser231Ser | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 10/32 | 740/4490 | 693/2376 | 231/791 | chr5 | 96736234 | ||
| chr5:96740783
|
G | A | 4 | a0001c0012a0002c0003a0002c0024others(1): Show | 53 | HG00099.hp2 HG00609.hp1 HG00639.hp2 others(50): Show |
splice_region_variant&synonymous_variant | LOW | c.918G>A | p.Ser306Ser | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 13/32 | 965/4490 | 918/2376 | 306/791 | chr5 | 96740783 | ||
| chr5:96741274
|
A | T | 1 | a0001c0021 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.927A>T | p.Ile309Ile | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 14/32 | 974/4490 | 927/2376 | 309/791 | chr5 | 96741274 | ||
| chr5:96741325
|
G | A | 1 | a0001c0017 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.978G>A | p.Ser326Ser | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 14/32 | 1025/4490 | 978/2376 | 326/791 | chr5 | 96741325 | ||
| chr5:96742690
|
G | A | 1 | a0001c0018 | 1 | HG01123.hp2 | synonymous_variant | LOW | c.1134G>A | p.Ser378Ser | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/32 | 1181/4490 | 1134/2376 | 378/791 | chr5 | 96742690 | ||
| chr5:96766070
|
A | G | 1 | a0010c0016 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.2055A>G | p.Glu685Glu | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 27/32 | 2102/4490 | 2055/2376 | 685/791 | chr5 | 96766070 | ||
| chr5:96766118
|
C | T | 1 | a0001c0020 | 1 | HG03669.hp2 | synonymous_variant | LOW | c.2103C>T | p.Tyr701Tyr | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 27/32 | 2150/4490 | 2103/2376 | 701/791 | chr5 | 96766118 | ||
| chr5:96767912
|
T | G | 1 | a0002c0013 | 2 | HG02622.hp1 HG02886.hp1 |
synonymous_variant | LOW | c.2181T>G | p.Pro727Pro | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 29/32 | 2228/4490 | 2181/2376 | 727/791 | chr5 | 96767912 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:96772997
|
T | C | 4 | a0001c0001t0004a0001c0001t0016a0001c0001t0018others(1): Show | 17 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*381T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 32/32 | 1318 | chr5 | 96772997 | |||||
| chr5:96773290
|
C | CA | 3 | a0001c0001t0007a0001c0005t0007a0004c0008t0007 | 5 | HG02559.hp2 HG02896.hp2 HG03471.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*675dupA | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 32/32 | 1613 | INFO_REALIGN_3_PRIME | chr5 | 96773290 | ||||
| chr5:96773375
|
C | T | 1 | a0005c0010t0024 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*759C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 32/32 | 1696 | chr5 | 96773375 | |||||
| chr5:96773376
|
G | A | 4 | a0001c0001t0008a0001c0012t0012a0006c0009t0008others(1): Show | 8 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*760G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 32/32 | 1697 | chr5 | 96773376 | |||||
| chr5:96773380
|
A | G | 1 | a0001c0001t0023 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*764A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 32/32 | 1701 | chr5 | 96773380 | |||||
| chr5:96773473
|
T | C | 2 | a0002c0004t0013a0002c0022t0013 | 3 | HG02976.hp2 NA19030.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*857T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 32/32 | 1794 | chr5 | 96773473 | |||||
| chr5:96773501
|
T | C | 5 | a0001c0001t0004a0001c0001t0016a0001c0001t0018others(2): Show | 18 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*885T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 32/32 | 1822 | chr5 | 96773501 | |||||
| chr5:96773540
|
G | A | 20 | a0001c0001t0003a0001c0001t0008a0001c0001t0009others(17): Show | 78 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*924G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 32/32 | 1861 | chr5 | 96773540 | |||||
| chr5:96773601
|
T | TTA | 2 | a0001c0001t0006a0002c0003t0015 | 9 | HG00140.hp2 HG00280.hp2 HG00735.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*997_*998dupAT | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 32/32 | 1936 | INFO_REALIGN_3_PRIME | chr5 | 96773601 | ||||
| chr5:96773782
|
T | G | 1 | a0001c0001t0018 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1166T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 32/32 | 2103 | chr5 | 96773782 | |||||
| chr5:96773830
|
T | C | 1 | a0001c0002t0020 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1214T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 32/32 | 2151 | chr5 | 96773830 | |||||
| chr5:96773881
|
T | C | 2 | a0002c0004t0013a0002c0022t0013 | 3 | HG02976.hp2 NA19030.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1265T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 32/32 | 2202 | chr5 | 96773881 | |||||
| chr5:96773906
|
G | A | 6 | a0001c0001t0003a0001c0002t0003a0002c0003t0003others(3): Show | 52 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1290G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 32/32 | 2227 | chr5 | 96773906 | |||||
| chr5:96773965
|
C | CAAAT | 1 | a0005c0010t0014 | 3 | HG01109.hp2 HG02922.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1351_*1354dupAATA | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 32/32 | 2292 | INFO_REALIGN_3_PRIME | chr5 | 96773965 | ||||
| chr5:96774029
|
A | G | 1 | a0001c0001t0022 | 1 | NA19006.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1413A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 32/32 | 2350 | chr5 | 96774029 | |||||
| chr5:96774068
|
A | C | 1 | a0002c0004t0021 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1452A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 32/32 | 2389 | chr5 | 96774068 | |||||
| chr5:96774135
|
A | AT | 9 | a0001c0001t0008a0001c0001t0010a0001c0012t0012others(6): Show | 16 | HG00738.hp1 HG01123.hp2 HG01361.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1522dupT | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 32/32 | 2460 | INFO_REALIGN_3_PRIME | chr5 | 96774135 | ||||
| chr5:96774157
|
C | T | 1 | a0001c0002t0017 | 2 | NA18970.hp2 NA19009.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1541C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 32/32 | 2478 | chr5 | 96774157 | |||||
| chr5:96774179
|
G | GA | 1 | a0002c0004t0005 | 7 | HG02280.hp2 HG02451.hp2 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1568dupA | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 32/32 | 2506 | INFO_REALIGN_3_PRIME | chr5 | 96774179 | ||||
| chr5:96774231
|
T | G | 52 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(49): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
3_prime_UTR_variant | MODIFIER | c.*1615T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 32/32 | 2552 | chr5 | 96774231 | |||||
| chr5:96774253
|
G | GTATC | 4 | a0001c0001t0009a0001c0005t0009a0001c0021t0009others(1): Show | 8 | HG01109.hp2 HG02615.hp1 HG02647.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1639_*1642dupATCT | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 32/32 | 2580 | INFO_REALIGN_3_PRIME | chr5 | 96774253 | ||||
| chr5:96774297
|
TA | T | 3 | a0001c0001t0010a0001c0018t0010a0002c0003t0010 | 5 | HG01123.hp2 HG01361.hp1 HG03017.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1684delA | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 32/32 | 2621 | INFO_REALIGN_3_PRIME | chr5 | 96774297 | ||||
| chr5:96774360
|
T | A | 2 | a0001c0001t0008a0006c0009t0008 | 5 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1744T>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 32/32 | 2681 | chr5 | 96774360 | |||||
| chr5:96774507
|
A | T | 6 | a0001c0001t0003a0001c0002t0003a0002c0003t0003others(3): Show | 52 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1891A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 32/32 | 2828 | chr5 | 96774507 | |||||
| chr5:96774610
|
C | T | 1 | a0001c0001t0016 | 2 | HG01168.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1994C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 32/32 | 2931 | chr5 | 96774610 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:96662536
|
T | A | 1 | a0011c0026t0001g0017 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.75+39T>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96662536 | ||||||
| chr5:96662536
|
T | TG | 4 | a0001c0001t0001g0018a0002c0003t0003g0021a0003c0007t0002g0020others(1): Show | 4 | HG02055.hp2 HG03942.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+43dupG | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96662536 | |||||
| chr5:96662643
|
G | A | 1 | a0001c0020t0004g0022 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.75+146G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96662643 | ||||||
| chr5:96662653
|
G | GGCAGGTG others(3): Show |
6 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(3): Show | 6 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+165_75+166insAG others(8): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96662653 | |||||
| chr5:96662653
|
G | GGCAGGTG others(13): Show |
116 | a0001c0001t0001g0024a0001c0001t0001g0051a0001c0001t0001g0063others(113): Show | 118 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.75+165_75+166insAG others(18): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96662653 | |||||
| chr5:96662653
|
G | GGCAGGTG others(3): Show |
121 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(118): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.75+167_75+176dupGC others(8): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96662653 | |||||
| chr5:96662683
|
C | T | 1 | a0001c0005t0007g0251 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.75+186C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96662683 | ||||||
| chr5:96662687
|
C | T | 6 | a0001c0001t0004g0132a0001c0001t0004g0133a0001c0001t0004g0134others(3): Show | 7 | HG01168.hp1 HG01169.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+190C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96662687 | ||||||
| chr5:96662768
|
G | A | 15 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(12): Show | 16 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.75+271G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96662768 | ||||||
| chr5:96662795
|
G | C | 1 | a0001c0001t0010g0023 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.75+298G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96662795 | ||||||
| chr5:96662810
|
A | G | 7 | a0001c0002t0001g0012a0001c0002t0001g0245a0001c0002t0001g0246others(4): Show | 8 | HG00140.hp1 HG01099.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+313A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96662810 | ||||||
| chr5:96662817
|
C | G | 1 | a0005c0010t0014g0131 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.75+320C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96662817 | ||||||
| chr5:96662920
|
C | T | 3 | a0001c0005t0001g0244a0001c0005t0007g0242a0001c0005t0007g0243 | 3 | HG02559.hp2 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.75+423C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96662920 | ||||||
| chr5:96662990
|
C | T | 1 | a0001c0001t0016g0004 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.75+493C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96662990 | ||||||
| chr5:96663070
|
C | G | 15 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(12): Show | 16 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.75+573C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96663070 | ||||||
| chr5:96663175
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+678G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96663175 | ||||||
| chr5:96663181
|
T | G | 1 | a0001c0001t0001g0265 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.75+684T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96663181 | ||||||
| chr5:96663458
|
C | T | 2 | a0001c0001t0002g0130a0001c0002t0001g0241 | 2 | HG00621.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.75+961C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96663458 | ||||||
| chr5:96663477
|
A | G | 2 | a0002c0003t0001g0239a0002c0003t0001g0240 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.75+980A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96663477 | ||||||
| chr5:96663505
|
T | A | 1 | a0003c0007t0002g0252 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.75+1008T>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96663505 | ||||||
| chr5:96663565
|
A | G | 1 | a0001c0001t0016g0004 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.75+1068A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96663565 | ||||||
| chr5:96663675
|
A | G | 1 | a0004c0008t0011g0238 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.75+1178A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96663675 | ||||||
| chr5:96663822
|
A | G | 316 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(313): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.75+1325A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96663822 | ||||||
| chr5:96663939
|
C | CA | 36 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0143others(33): Show | 39 | HG00423.hp1 HG00621.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.75+1459dupA | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96663939 | |||||
| chr5:96663939
|
C | CAA | 7 | a0001c0001t0004g0132a0001c0001t0004g0133a0001c0001t0004g0134others(4): Show | 8 | HG01168.hp1 HG01169.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+1458_75+1459dup others(2): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96663939 | |||||
| chr5:96663939
|
CA | C | 17 | a0001c0001t0001g0261a0001c0001t0001g0263a0001c0001t0002g0013others(14): Show | 18 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.75+1459delA | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96663939 | |||||
| chr5:96663939
|
CAAA | C | 17 | a0001c0001t0002g0034a0001c0001t0002g0036a0001c0001t0010g0028others(14): Show | 17 | HG01123.hp2 HG01361.hp1 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.75+1457_75+1459del others(3): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96663939 | |||||
| chr5:96663939
|
CAAAA | C | 92 | a0001c0001t0001g0024a0001c0001t0001g0051a0001c0001t0001g0063others(89): Show | 93 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.75+1456_75+1459del others(4): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96663939 | |||||
| chr5:96664291
|
C | T | 15 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(12): Show | 16 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.75+1794C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96664291 | ||||||
| chr5:96664299
|
G | T | 1 | a0004c0008t0011g0236 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.75+1802G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96664299 | ||||||
| chr5:96664318
|
CAT | C | 15 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(12): Show | 16 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.75+1826_75+1827del others(2): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96664318 | |||||
| chr5:96664354
|
AAT | A | 6 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(3): Show | 6 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+1862_75+1863del others(2): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96664354 | |||||
| chr5:96664357
|
A | G | 1 | a0001c0002t0001g0235 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.75+1860A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96664357 | ||||||
| chr5:96664382
|
TGTGCATA others(11): Show |
T | 1 | a0004c0008t0011g0238 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.75+1886_75+1903del others(18): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96664382 | ||||||
| chr5:96664400
|
A | AAT | 3 | a0001c0001t0001g0162a0001c0002t0001g0163a0001c0002t0001g0164 | 3 | HG02698.hp2 HG03017.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.75+1916_75+1917dup others(2): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96664400 | |||||
| chr5:96664400
|
AAT | A | 126 | a0001c0001t0001g0051a0001c0001t0001g0063a0001c0001t0001g0064others(123): Show | 128 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(125): Show |
intron_variant | MODIFIER | c.75+1916_75+1917del others(2): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96664400 | |||||
| chr5:96664400
|
AATAT | A | 7 | a0001c0001t0004g0132a0001c0001t0004g0133a0001c0001t0004g0134others(4): Show | 8 | HG01168.hp1 HG01169.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+1914_75+1917del others(4): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96664400 | |||||
| chr5:96664402
|
T | A | 1 | a0004c0008t0011g0238 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.75+1905T>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96664402 | ||||||
| chr5:96664412
|
TATGC | T | 4 | a0001c0001t0001g0024a0001c0001t0001g0127a0001c0001t0001g0129others(1): Show | 4 | HG02451.hp1 HG02976.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+1917_75+1920del others(4): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96664412 | |||||
| chr5:96664417
|
A | G | 4 | a0001c0001t0001g0024a0001c0001t0001g0127a0001c0001t0001g0129others(1): Show | 4 | HG02451.hp1 HG02976.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+1920A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96664417 | ||||||
| chr5:96664528
|
T | C | 1 | a0004c0008t0011g0236 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.75+2031T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96664528 | ||||||
| chr5:96664565
|
G | A | 138 | a0001c0001t0001g0024a0001c0001t0001g0051a0001c0001t0001g0063others(135): Show | 141 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(138): Show |
intron_variant | MODIFIER | c.75+2068G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96664565 | ||||||
| chr5:96664759
|
A | G | 15 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(12): Show | 16 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.75+2262A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96664759 | ||||||
| chr5:96664903
|
A | G | 3 | a0001c0001t0001g0011a0001c0001t0006g0010a0004c0008t0011g0238 | 5 | HG00099.hp1 HG00280.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+2406A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96664903 | ||||||
| chr5:96664954
|
A | C | 15 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(12): Show | 16 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.75+2457A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96664954 | ||||||
| chr5:96665091
|
C | A | 263 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(260): Show | 275 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.75+2594C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96665091 | ||||||
| chr5:96665104
|
C | T | 15 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(12): Show | 16 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.75+2607C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96665104 | ||||||
| chr5:96665188
|
A | G | 15 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(12): Show | 16 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.75+2691A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96665188 | ||||||
| chr5:96665243
|
A | G | 94 | a0001c0001t0001g0024a0001c0001t0001g0051a0001c0001t0001g0063others(91): Show | 95 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.75+2746A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96665243 | ||||||
| chr5:96665295
|
A | G | 3 | a0001c0001t0002g0337a0002c0003t0003g0338a0002c0003t0003g0339 | 3 | HG01069.hp2 HG01074.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.75+2798A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96665295 | ||||||
| chr5:96665333
|
T | G | 1 | a0001c0001t0002g0045 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.75+2836T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96665333 | ||||||
| chr5:96665360
|
T | C | 1 | a0010c0016t0011g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.75+2863T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96665360 | ||||||
| chr5:96665532
|
T | C | 1 | a0001c0001t0002g0046 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.75+3035T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96665532 | ||||||
| chr5:96665550
|
A | G | 1 | a0002c0003t0002g0296 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.75+3053A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96665550 | ||||||
| chr5:96665725
|
A | AAC | 13 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(10): Show | 14 | HG00280.hp1 HG01106.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.75+3244_75+3245dup others(2): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96665725 | |||||
| chr5:96665725
|
A | AACAC | 4 | a0001c0001t0007g0255a0003c0007t0002g0020a0003c0007t0002g0252others(1): Show | 4 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+3242_75+3245dup others(4): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96665725 | |||||
| chr5:96665735
|
C | G | 1 | a0004c0008t0011g0236 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.75+3238C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96665735 | ||||||
| chr5:96665741
|
CATACACA others(13): Show |
C | 6 | a0001c0001t0004g0132a0001c0001t0004g0133a0001c0001t0004g0134others(3): Show | 7 | HG01168.hp1 HG01169.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+3250_75+3269del others(20): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96665741 | |||||
| chr5:96665743
|
T | TAC | 3 | a0002c0004t0001g0047a0002c0004t0001g0048a0002c0004t0001g0049 | 3 | NA18991.hp1 NA19002.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.75+3262_75+3263dup others(2): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96665743 | |||||
| chr5:96665783
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.75+3286T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96665783 | ||||||
| chr5:96665818
|
A | G | 6 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(3): Show | 6 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+3321A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96665818 | ||||||
| chr5:96665906
|
CTGTA | C | 15 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(12): Show | 16 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.75+3414_75+3417del others(4): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96665906 | |||||
| chr5:96665985
|
C | T | 1 | a0010c0016t0011g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.75+3488C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96665985 | ||||||
| chr5:96666138
|
G | A | 116 | a0001c0001t0001g0024a0001c0001t0001g0051a0001c0001t0001g0063others(113): Show | 118 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.75+3641G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96666138 | ||||||
| chr5:96666183
|
G | T | 5 | a0002c0006t0001g0040a0002c0006t0001g0041a0005c0010t0014g0043others(2): Show | 5 | HG02723.hp2 HG02922.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+3686G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96666183 | ||||||
| chr5:96666255
|
T | TACACACA others(3): Show |
1 | a0002c0004t0001g0126 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.75+3759_75+3760ins others(10): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96666255 | |||||
| chr5:96666257
|
A | AAC | 4 | a0002c0003t0001g0239a0002c0003t0001g0240a0002c0003t0003g0305others(1): Show | 4 | HG02698.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+3781_75+3782dup others(2): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96666257 | |||||
| chr5:96666257
|
A | AACAC | 4 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(1): Show | 4 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+3779_75+3782dup others(4): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96666257 | |||||
| chr5:96666257
|
A | AACACAC | 75 | a0001c0001t0001g0123a0001c0001t0002g0209a0001c0001t0002g0210others(72): Show | 79 | HG00140.hp1 HG00544.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.75+3777_75+3782dup others(6): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96666257 | |||||
| chr5:96666257
|
A | AACACACA others(1): Show |
87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(84): Show | 93 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.75+3775_75+3782dup others(8): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96666257 | |||||
| chr5:96666257
|
A | AACACACA others(3): Show |
26 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0166others(23): Show | 27 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.75+3773_75+3782dup others(10): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96666257 | |||||
| chr5:96666257
|
A | AACACACA others(5): Show |
60 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0068others(57): Show | 61 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.75+3771_75+3782dup others(12): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96666257 | |||||
| chr5:96666257
|
A | AACACACA others(7): Show |
5 | a0001c0001t0001g0051a0003c0007t0002g0050a0005c0010t0014g0043others(2): Show | 5 | HG01109.hp2 HG01255.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+3769_75+3782dup others(14): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96666257 | |||||
| chr5:96666257
|
A | AACACACA others(11): Show |
1 | a0010c0016t0011g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.75+3765_75+3782dup others(18): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96666257 | |||||
| chr5:96666257
|
A | ACACACAC others(4): Show |
1 | a0001c0001t0002g0125 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.75+3760_75+3761ins others(11): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96666257 | ||||||
| chr5:96666257
|
A | C | 1 | a0002c0004t0001g0126 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.75+3760A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96666257 | ||||||
| chr5:96666279
|
C | CACACACA others(3): Show |
1 | a0002c0004t0001g0049 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.75+3782_75+3783ins others(10): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96666279 | ||||||
| chr5:96666316
|
A | G | 116 | a0001c0001t0001g0024a0001c0001t0001g0051a0001c0001t0001g0063others(113): Show | 118 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.75+3819A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96666316 | ||||||
| chr5:96666354
|
T | C | 1 | a0001c0002t0001g0186 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.75+3857T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96666354 | ||||||
| chr5:96666573
|
C | G | 1 | a0001c0001t0001g0185 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.75+4076C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96666573 | ||||||
| chr5:96666854
|
G | C | 4 | a0001c0001t0001g0051a0002c0004t0001g0101a0003c0007t0002g0050others(1): Show | 4 | HG01109.hp2 HG01255.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+4357G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96666854 | ||||||
| chr5:96666904
|
ACTACT | A | 9 | a0001c0005t0001g0244a0001c0005t0007g0242a0001c0005t0007g0243others(6): Show | 10 | HG02280.hp2 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.75+4411_75+4415del others(5): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96666904 | |||||
| chr5:96667355
|
C | T | 1 | a0001c0001t0010g0038 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.75+4858C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96667355 | ||||||
| chr5:96667371
|
C | T | 11 | a0001c0001t0004g0132a0001c0001t0004g0133a0001c0001t0004g0134others(8): Show | 12 | HG01168.hp1 HG01169.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.75+4874C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96667371 | ||||||
| chr5:96667445
|
T | G | 119 | a0001c0001t0001g0024a0001c0001t0001g0051a0001c0001t0001g0063others(116): Show | 121 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.75+4948T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96667445 | ||||||
| chr5:96667456
|
C | A | 1 | a0002c0013t0001g0191 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.75+4959C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96667456 | ||||||
| chr5:96667475
|
A | T | 11 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(8): Show | 12 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.75+4978A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96667475 | ||||||
| chr5:96667575
|
A | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(260): Show | 275 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.75+5078A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96667575 | ||||||
| chr5:96667695
|
A | C | 4 | a0002c0004t0003g0297a0002c0004t0003g0298a0002c0004t0003g0299others(1): Show | 4 | HG00741.hp2 HG01070.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+5198A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96667695 | ||||||
| chr5:96667743
|
GT | G | 340 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(337): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.75+5248delT | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96667743 | |||||
| chr5:96667753
|
G | A | 9 | a0001c0005t0001g0244a0001c0005t0007g0242a0001c0005t0007g0243others(6): Show | 10 | HG02280.hp2 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.75+5256G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96667753 | ||||||
| chr5:96667972
|
A | G | 8 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(5): Show | 8 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+5475A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96667972 | ||||||
| chr5:96667994
|
G | A | 1 | a0001c0001t0002g0052 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.75+5497G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96667994 | ||||||
| chr5:96668010
|
G | A | 3 | a0001c0002t0001g0192a0001c0002t0001g0193a0001c0002t0001g0194 | 3 | NA18948.hp1 NA18984.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.75+5513G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96668010 | ||||||
| chr5:96668081
|
A | G | 6 | a0001c0001t0004g0132a0001c0001t0004g0133a0001c0001t0004g0134others(3): Show | 7 | HG01168.hp1 HG01169.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+5584A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96668081 | ||||||
| chr5:96668122
|
C | T | 1 | a0011c0026t0001g0017 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.75+5625C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96668122 | ||||||
| chr5:96668150
|
G | GCA | 6 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(3): Show | 6 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+5675_75+5676dup others(2): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96668150 | |||||
| chr5:96668150
|
GCA | G | 255 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(252): Show | 267 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.75+5675_75+5676del others(2): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96668150 | |||||
| chr5:96668159
|
C | T | 1 | a0001c0001t0002g0099 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.75+5662C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96668159 | ||||||
| chr5:96668172
|
A | C | 4 | a0001c0001t0007g0255a0003c0007t0002g0020a0003c0007t0002g0252others(1): Show | 4 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+5675A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96668172 | ||||||
| chr5:96668302
|
G | A | 2 | a0001c0001t0001g0307a0002c0003t0003g0306 | 2 | HG00323.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.75+5805G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96668302 | ||||||
| chr5:96668304
|
T | C | 6 | a0001c0001t0001g0005a0001c0001t0001g0168a0001c0001t0001g0169others(3): Show | 7 | HG00609.hp2 NA18950.hp2 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+5807T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96668304 | ||||||
| chr5:96668469
|
C | T | 68 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0211others(65): Show | 71 | HG00140.hp1 HG00544.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.75+5972C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96668469 | ||||||
| chr5:96668570
|
T | C | 11 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(8): Show | 12 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.75+6073T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96668570 | ||||||
| chr5:96668633
|
T | G | 6 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(3): Show | 6 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+6136T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96668633 | ||||||
| chr5:96668640
|
C | T | 2 | a0002c0003t0001g0334a0002c0003t0001g0335 | 2 | HG01175.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.75+6143C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96668640 | ||||||
| chr5:96668659
|
T | C | 108 | a0001c0001t0001g0024a0001c0001t0001g0051a0001c0001t0001g0063others(105): Show | 109 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.75+6162T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96668659 | ||||||
| chr5:96668675
|
G | A | 1 | a0001c0001t0009g0336 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.75+6178G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96668675 | ||||||
| chr5:96668809
|
T | TA | 50 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(47): Show | 56 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.75+6324dupA | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96668809 | |||||
| chr5:96668809
|
TA | T | 137 | a0001c0001t0001g0024a0001c0001t0001g0051a0001c0001t0001g0063others(134): Show | 140 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(137): Show |
intron_variant | MODIFIER | c.75+6324delA | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96668809 | |||||
| chr5:96669133
|
A | G | 1 | a0004c0008t0011g0238 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.76-6406A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96669133 | ||||||
| chr5:96669468
|
T | G | 2 | a0001c0001t0001g0307a0002c0003t0003g0306 | 2 | HG00323.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.76-6071T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96669468 | ||||||
| chr5:96669476
|
A | C | 6 | a0001c0001t0004g0132a0001c0001t0004g0133a0001c0001t0004g0134others(3): Show | 7 | HG01168.hp1 HG01169.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.76-6063A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96669476 | ||||||
| chr5:96669548
|
G | A | 11 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(8): Show | 12 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-5991G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96669548 | ||||||
| chr5:96669881
|
T | C | 11 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(8): Show | 12 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-5658T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96669881 | ||||||
| chr5:96669899
|
A | G | 4 | a0002c0004t0003g0297a0002c0004t0003g0298a0002c0004t0003g0299others(1): Show | 4 | HG00741.hp2 HG01070.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-5640A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96669899 | ||||||
| chr5:96669913
|
A | C | 136 | a0001c0001t0001g0024a0001c0001t0001g0051a0001c0001t0001g0063others(133): Show | 139 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(136): Show |
intron_variant | MODIFIER | c.76-5626A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96669913 | ||||||
| chr5:96670135
|
C | A | 1 | a0002c0004t0001g0113 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.76-5404C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96670135 | ||||||
| chr5:96670717
|
C | T | 1 | a0001c0001t0004g0014 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.76-4822C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96670717 | ||||||
| chr5:96670782
|
C | T | 11 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(8): Show | 12 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-4757C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96670782 | ||||||
| chr5:96670792
|
G | A | 3 | a0001c0001t0010g0028a0001c0001t0010g0038a0001c0018t0010g0029 | 3 | HG01123.hp2 HG01361.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.76-4747G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96670792 | ||||||
| chr5:96670819
|
T | C | 1 | a0002c0003t0003g0268 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.76-4720T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96670819 | ||||||
| chr5:96670960
|
T | C | 1 | a0001c0002t0017g0195 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.76-4579T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96670960 | ||||||
| chr5:96670962
|
G | A | 1 | a0004c0008t0011g0236 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.76-4577G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96670962 | ||||||
| chr5:96670992
|
T | G | 3 | a0001c0011t0002g0102a0001c0011t0002g0103a0001c0011t0002g0104 | 3 | HG00741.hp1 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.76-4547T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96670992 | ||||||
| chr5:96671371
|
T | C | 11 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(8): Show | 12 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-4168T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96671371 | ||||||
| chr5:96671607
|
T | G | 209 | a0001c0001t0001g0024a0001c0001t0001g0051a0001c0001t0001g0063others(206): Show | 215 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(212): Show |
intron_variant | MODIFIER | c.76-3932T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96671607 | ||||||
| chr5:96671624
|
T | C | 1 | a0004c0008t0011g0238 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.76-3915T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96671624 | ||||||
| chr5:96671715
|
T | G | 6 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(3): Show | 6 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-3824T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96671715 | ||||||
| chr5:96671791
|
C | T | 1 | a0001c0002t0001g0231 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.76-3748C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96671791 | ||||||
| chr5:96671837
|
C | G | 1 | a0001c0001t0001g0286 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.76-3702C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96671837 | ||||||
| chr5:96672048
|
C | G | 2 | a0001c0001t0001g0123a0002c0004t0003g0124 | 2 | HG00738.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.76-3491C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96672048 | ||||||
| chr5:96672109
|
G | C | 9 | a0001c0005t0001g0244a0001c0005t0007g0242a0001c0005t0007g0243others(6): Show | 10 | HG02280.hp2 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-3430G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96672109 | ||||||
| chr5:96672229
|
G | GTC | 10 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0253others(7): Show | 10 | HG01243.hp1 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-3292_76-3291dup others(2): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96672229 | |||||
| chr5:96672286
|
A | G | 7 | a0002c0006t0001g0040a0002c0006t0001g0041a0005c0010t0014g0043others(4): Show | 7 | HG01109.hp2 HG02723.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.76-3253A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96672286 | ||||||
| chr5:96672334
|
G | A | 11 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(8): Show | 12 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-3205G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96672334 | ||||||
| chr5:96672586
|
A | G | 1 | a0004c0008t0011g0238 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.76-2953A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96672586 | ||||||
| chr5:96672615
|
A | G | 11 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(8): Show | 12 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-2924A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96672615 | ||||||
| chr5:96672656
|
A | G | 264 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(261): Show | 276 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.76-2883A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96672656 | ||||||
| chr5:96672706
|
C | CA | 39 | a0001c0001t0001g0051a0001c0001t0001g0097a0001c0001t0001g0109others(36): Show | 40 | HG00323.hp1 HG00609.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.76-2810dupA | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96672706 | |||||
| chr5:96672706
|
C | CAA | 113 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(110): Show | 119 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.76-2811_76-2810dup others(2): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96672706 | |||||
| chr5:96672706
|
C | CAAA | 10 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0160others(7): Show | 10 | HG02135.hp2 HG02148.hp1 HG04184.hp2 others(7): Show |
intron_variant | MODIFIER | c.76-2812_76-2810dup others(3): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96672706 | |||||
| chr5:96672706
|
CA | C | 30 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(27): Show | 32 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.76-2810delA | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96672706 | |||||
| chr5:96672706
|
CAAAAAAA others(4): Show |
C | 2 | a0002c0003t0001g0239a0002c0003t0001g0240 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.76-2820_76-2810del others(11): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96672706 | |||||
| chr5:96672895
|
AAAGTTGT others(6): Show |
A | 20 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(17): Show | 21 | HG01243.hp1 HG02280.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.76-2627_76-2615del others(13): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96672895 | |||||
| chr5:96673067
|
T | A | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(189): Show | 201 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.76-2472T>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96673067 | ||||||
| chr5:96673425
|
T | C | 1 | a0004c0008t0011g0236 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.76-2114T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96673425 | ||||||
| chr5:96673544
|
T | C | 1 | a0004c0008t0011g0238 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.76-1995T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96673544 | ||||||
| chr5:96673640
|
C | G | 1 | a0001c0001t0001g0108 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.76-1899C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96673640 | ||||||
| chr5:96673647
|
A | C | 1 | a0001c0001t0002g0226 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.76-1892A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96673647 | ||||||
| chr5:96673988
|
G | A | 4 | a0001c0001t0001g0261a0001c0001t0001g0263a0001c0001t0002g0262others(1): Show | 4 | HG01243.hp1 HG02280.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-1551G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96673988 | ||||||
| chr5:96674051
|
T | C | 1 | a0004c0008t0011g0238 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.76-1488T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96674051 | ||||||
| chr5:96674260
|
T | C | 1 | a0001c0001t0001g0146 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.76-1279T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96674260 | ||||||
| chr5:96674408
|
CATTTTAT others(6): Show |
C | 1 | a0001c0002t0002g0301 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.76-1127_76-1115del others(13): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 96674408 | |||||
| chr5:96674416
|
A | G | 11 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(8): Show | 12 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-1123A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96674416 | ||||||
| chr5:96674442
|
G | A | 3 | a0001c0001t0004g0014a0001c0001t0004g0269a0001c0001t0004g0285 | 4 | HG01070.hp1 HG01071.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-1097G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96674442 | ||||||
| chr5:96674480
|
G | A | 1 | a0001c0002t0001g0198 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.76-1059G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96674480 | ||||||
| chr5:96674508
|
C | T | 1 | a0004c0008t0011g0236 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.76-1031C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96674508 | ||||||
| chr5:96674584
|
A | G | 1 | a0002c0003t0003g0268 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.76-955A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96674584 | ||||||
| chr5:96674619
|
C | T | 1 | a0002c0024t0001g0225 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.76-920C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96674619 | ||||||
| chr5:96674770
|
A | G | 47 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0068others(44): Show | 48 | HG00423.hp2 HG00621.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.76-769A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96674770 | ||||||
| chr5:96675069
|
A | G | 1 | a0002c0013t0001g0191 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.76-470A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96675069 | ||||||
| chr5:96675236
|
G | A | 4 | a0001c0001t0001g0143a0001c0001t0001g0149a0001c0001t0002g0147others(1): Show | 4 | HG02080.hp1 NA19000.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-303G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96675236 | ||||||
| chr5:96675319
|
T | C | 7 | a0001c0001t0004g0132a0001c0001t0004g0133a0001c0001t0004g0134others(4): Show | 8 | HG01168.hp1 HG01169.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.76-220T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96675319 | ||||||
| chr5:96675339
|
T | G | 7 | a0001c0001t0002g0034a0001c0021t0009g0035a0002c0004t0005g0027others(4): Show | 7 | HG02451.hp2 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-200T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96675339 | ||||||
| chr5:96675440
|
G | A | 6 | a0001c0002t0001g0199a0001c0002t0001g0227a0001c0002t0001g0228others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-99G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 1/31 | chr5 | 96675440 | ||||||
| chr5:96675698
|
C | T | 6 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(3): Show | 6 | HG01243.hp1 HG02280.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.138+97C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96675698 | ||||||
| chr5:96675774
|
A | T | 1 | a0001c0017t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.138+173A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96675774 | ||||||
| chr5:96676009
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.138+408A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96676009 | ||||||
| chr5:96676254
|
A | G | 1 | a0010c0016t0011g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.138+653A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96676254 | ||||||
| chr5:96676281
|
A | T | 1 | a0010c0016t0011g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.138+680A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96676281 | ||||||
| chr5:96676380
|
T | A | 1 | a0002c0003t0003g0268 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.138+779T>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96676380 | ||||||
| chr5:96676387
|
A | G | 2 | a0001c0002t0001g0198a0001c0002t0001g0235 | 2 | NA18983.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.138+786A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96676387 | ||||||
| chr5:96676627
|
C | G | 1 | a0004c0008t0011g0236 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.138+1026C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96676627 | ||||||
| chr5:96676713
|
C | T | 4 | a0001c0001t0002g0092a0001c0001t0002g0125a0001c0001t0006g0093others(1): Show | 4 | HG00735.hp1 HG01258.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.138+1112C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96676713 | ||||||
| chr5:96676725
|
A | G | 6 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(3): Show | 6 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.138+1124A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96676725 | ||||||
| chr5:96676727
|
A | C | 11 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(8): Show | 12 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.138+1126A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96676727 | ||||||
| chr5:96676728
|
AC | A | 17 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(14): Show | 18 | HG00738.hp1 HG01243.hp1 HG01981.hp1 others(15): Show |
intron_variant | MODIFIER | c.138+1129delC | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96676728 | |||||
| chr5:96676729
|
C | A | 250 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(247): Show | 261 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.138+1128C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96676729 | ||||||
| chr5:96676776
|
C | A | 1 | a0004c0008t0011g0238 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.138+1175C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96676776 | ||||||
| chr5:96676782
|
C | T | 1 | a0002c0003t0002g0296 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.138+1181C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96676782 | ||||||
| chr5:96676881
|
C | T | 11 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(8): Show | 12 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.138+1280C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96676881 | ||||||
| chr5:96676954
|
T | C | 11 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(8): Show | 12 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.138+1353T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96676954 | ||||||
| chr5:96676980
|
G | A | 9 | a0001c0005t0001g0244a0001c0005t0007g0242a0001c0005t0007g0243others(6): Show | 10 | HG02280.hp2 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.138+1379G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96676980 | ||||||
| chr5:96677049
|
A | G | 6 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(3): Show | 6 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.138+1448A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96677049 | ||||||
| chr5:96677190
|
C | A | 17 | a0001c0001t0001g0051a0001c0001t0001g0109a0001c0001t0007g0255others(14): Show | 17 | HG01109.hp2 HG01255.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.138+1589C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96677190 | ||||||
| chr5:96677293
|
C | T | 1 | a0004c0008t0007g0061 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.138+1692C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96677293 | ||||||
| chr5:96677328
|
C | G | 1 | a0002c0004t0003g0300 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.138+1727C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96677328 | ||||||
| chr5:96677333
|
C | T | 6 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(3): Show | 6 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.138+1732C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96677333 | ||||||
| chr5:96677357
|
A | G | 6 | a0001c0001t0004g0132a0001c0001t0004g0133a0001c0001t0004g0134others(3): Show | 7 | HG01168.hp1 HG01169.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.138+1756A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96677357 | ||||||
| chr5:96677376
|
G | A | 2 | a0002c0003t0001g0239a0002c0003t0001g0240 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.138+1775G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96677376 | ||||||
| chr5:96677415
|
G | C | 6 | a0001c0001t0004g0132a0001c0001t0004g0133a0001c0001t0004g0134others(3): Show | 7 | HG01168.hp1 HG01169.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.138+1814G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96677415 | ||||||
| chr5:96677571
|
C | T | 44 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(41): Show | 49 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.138+1970C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96677571 | ||||||
| chr5:96677621
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.138+2020C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96677621 | ||||||
| chr5:96677622
|
G | A | 1 | a0001c0001t0002g0036 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.138+2021G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96677622 | ||||||
| chr5:96677737
|
G | C | 119 | a0001c0001t0001g0024a0001c0001t0001g0051a0001c0001t0001g0063others(116): Show | 121 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.138+2136G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96677737 | ||||||
| chr5:96677745
|
G | C | 9 | a0001c0005t0001g0244a0001c0005t0007g0242a0001c0005t0007g0243others(6): Show | 10 | HG02280.hp2 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.138+2144G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96677745 | ||||||
| chr5:96678012
|
G | C | 1 | a0001c0001t0010g0028 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.138+2411G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96678012 | ||||||
| chr5:96678227
|
C | T | 106 | a0001c0001t0001g0024a0001c0001t0001g0051a0001c0001t0001g0063others(103): Show | 107 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.138+2626C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96678227 | ||||||
| chr5:96678288
|
C | G | 1 | a0004c0008t0011g0037 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.138+2687C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96678288 | ||||||
| chr5:96678360
|
T | C | 11 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(8): Show | 12 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.138+2759T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96678360 | ||||||
| chr5:96678462
|
G | A | 1 | a0001c0012t0012g0270 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.138+2861G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96678462 | ||||||
| chr5:96678532
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.138+2931G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96678532 | ||||||
| chr5:96678597
|
C | A | 6 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(3): Show | 6 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.138+2996C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96678597 | ||||||
| chr5:96678629
|
G | A | 1 | a0004c0008t0011g0238 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.138+3028G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96678629 | ||||||
| chr5:96678716
|
G | A | 1 | a0002c0013t0001g0191 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.138+3115G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96678716 | ||||||
| chr5:96678772
|
G | A | 11 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(8): Show | 12 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.138+3171G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96678772 | ||||||
| chr5:96678772
|
G | T | 1 | a0004c0008t0011g0238 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.138+3171G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96678772 | ||||||
| chr5:96678977
|
G | C | 1 | a0001c0002t0001g0200 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.138+3376G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96678977 | ||||||
| chr5:96678979
|
A | G | 131 | a0001c0001t0001g0024a0001c0001t0001g0051a0001c0001t0001g0063others(128): Show | 134 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(131): Show |
intron_variant | MODIFIER | c.138+3378A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96678979 | ||||||
| chr5:96679094
|
C | CG | 11 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(8): Show | 12 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.138+3494dupG | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96679094 | |||||
| chr5:96679121
|
A | G | 45 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(42): Show | 50 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.138+3520A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96679121 | ||||||
| chr5:96679134
|
T | C | 264 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(261): Show | 276 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.138+3533T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96679134 | ||||||
| chr5:96679254
|
A | G | 3 | a0001c0001t0002g0034a0001c0001t0002g0036a0004c0008t0011g0037 | 3 | HG02486.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.138+3653A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96679254 | ||||||
| chr5:96679353
|
T | C | 78 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0211others(75): Show | 81 | HG00140.hp1 HG00544.hp1 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.138+3752T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96679353 | ||||||
| chr5:96679356
|
C | A | 3 | a0001c0001t0002g0034a0001c0001t0002g0036a0004c0008t0011g0037 | 3 | HG02486.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.138+3755C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96679356 | ||||||
| chr5:96679495
|
C | T | 1 | a0004c0008t0011g0236 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.138+3894C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96679495 | ||||||
| chr5:96679513
|
G | A | 1 | a0001c0017t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.138+3912G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96679513 | ||||||
| chr5:96679565
|
G | C | 4 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(1): Show | 4 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+3964G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96679565 | ||||||
| chr5:96679585
|
CAGAG | C | 3 | a0003c0007t0002g0112a0008c0014t0002g0110a0008c0014t0002g0111 | 3 | HG02922.hp1 HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.138+3987_138+3990d others(6): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96679585 | |||||
| chr5:96679881
|
C | G | 11 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(8): Show | 12 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.138+4280C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96679881 | ||||||
| chr5:96679926
|
A | T | 264 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(261): Show | 276 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.138+4325A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96679926 | ||||||
| chr5:96680209
|
CGTGGTCG others(5): Show |
C | 2 | a0007c0015t0012g0137a0007c0015t0012g0138 | 2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.138+4613_138+4624d others(14): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96680209 | |||||
| chr5:96680260
|
C | A | 1 | a0004c0008t0011g0238 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.138+4659C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96680260 | ||||||
| chr5:96680354
|
C | CA | 15 | a0001c0001t0001g0265a0001c0001t0001g0315a0001c0001t0002g0290others(12): Show | 15 | HG01070.hp1 HG01106.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.138+4778dupA | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96680354 | |||||
| chr5:96680354
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0002g0036a0002c0004t0001g0120 | 2 | HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.138+4769_138+4778d others(12): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96680354 | |||||
| chr5:96680354
|
C | CAAAAAAA others(4): Show |
26 | a0001c0001t0001g0024a0001c0001t0001g0079a0001c0001t0001g0082others(23): Show | 26 | HG02451.hp1 HG02976.hp1 HG03017.hp1 others(23): Show |
intron_variant | MODIFIER | c.138+4768_138+4778d others(13): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96680354 | |||||
| chr5:96680354
|
C | CAAAAAAA others(5): Show |
23 | a0001c0001t0001g0068a0001c0001t0002g0003a0001c0001t0002g0055others(20): Show | 24 | HG00621.hp1 HG02074.hp1 HG02083.hp1 others(21): Show |
intron_variant | MODIFIER | c.138+4767_138+4778d others(14): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96680354 | |||||
| chr5:96680354
|
C | CAAAAAAA others(6): Show |
10 | a0001c0001t0002g0046a0001c0001t0002g0052a0001c0001t0002g0066others(7): Show | 10 | HG00642.hp1 HG00741.hp1 HG03654.hp1 others(7): Show |
intron_variant | MODIFIER | c.138+4766_138+4778d others(15): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96680354 | |||||
| chr5:96680354
|
C | CAAAAAAA others(7): Show |
3 | a0001c0001t0002g0065a0001c0001t0010g0028a0001c0001t0010g0038 | 3 | HG01361.hp1 HG02080.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.138+4765_138+4778d others(16): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96680354 | |||||
| chr5:96680354
|
C | CAAAAAAA others(8): Show |
5 | a0001c0001t0001g0051a0001c0001t0001g0064a0001c0001t0002g0054others(2): Show | 5 | HG00323.hp1 HG01255.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+4764_138+4778d others(17): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96680354 | |||||
| chr5:96680354
|
C | CAAAAAAA others(9): Show |
3 | a0001c0001t0001g0063a0001c0001t0001g0127a0001c0001t0002g0059 | 3 | HG00423.hp2 HG02258.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.138+4763_138+4778d others(18): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96680354 | |||||
| chr5:96680354
|
C | CAAAAAAA others(10): Show |
2 | a0001c0001t0002g0058a0001c0001t0002g0062 | 2 | HG02717.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.138+4762_138+4778d others(19): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96680354 | |||||
| chr5:96680354
|
C | CAAAAAAA others(11): Show |
2 | a0001c0001t0002g0057a0002c0004t0001g0101 | 2 | HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.138+4761_138+4778d others(20): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96680354 | |||||
| chr5:96680354
|
C | CAAAAAAA others(12): Show |
3 | a0001c0001t0001g0109a0008c0014t0002g0110a0008c0014t0002g0111 | 3 | HG02895.hp2 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.138+4760_138+4778d others(21): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96680354 | |||||
| chr5:96680354
|
C | CAAAAAAA others(13): Show |
1 | a0004c0029t0001g0187 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.138+4759_138+4778d others(22): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96680354 | |||||
| chr5:96680354
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0002g0056 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.138+4758_138+4778d others(23): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96680354 | |||||
| chr5:96680354
|
C | CAAAAAAA others(16): Show |
1 | a0001c0018t0010g0029 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.138+4756_138+4778d others(25): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96680354 | |||||
| chr5:96680354
|
C | CAAAAAAA others(22): Show |
1 | a0004c0008t0007g0061 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.138+4778_138+4779i others(31): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96680354 | |||||
| chr5:96680370
|
AAAAAAAA others(6): Show |
A | 10 | a0001c0001t0001g0261a0001c0001t0001g0263a0001c0001t0002g0262others(7): Show | 11 | HG01168.hp1 HG01169.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.138+4772_138+4784d others(15): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96680370 | |||||
| chr5:96680372
|
AAAAAAAA others(4): Show |
A | 1 | a0003c0007t0002g0112 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.138+4774_138+4784d others(13): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96680372 | |||||
| chr5:96680373
|
AAAAAAAG others(3): Show |
A | 1 | a0001c0017t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.138+4775_138+4784d others(12): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96680373 | |||||
| chr5:96680377
|
AAAG | A | 5 | a0001c0005t0009g0007a0001c0005t0009g0189a0002c0004t0005g0190others(2): Show | 6 | HG02280.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.138+4788_138+4790d others(5): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96680377 | |||||
| chr5:96680377
|
AAAGAAG | A | 9 | a0001c0001t0001g0108a0001c0001t0001g0253a0001c0001t0002g0091others(6): Show | 9 | HG01257.hp1 HG01361.hp2 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.138+4785_138+4790d others(8): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96680377 | |||||
| chr5:96680378
|
AAG | A | 62 | a0001c0001t0001g0158a0001c0001t0002g0209a0001c0001t0002g0210others(59): Show | 65 | HG00140.hp1 HG00621.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.138+4779_138+4780d others(4): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96680378 | |||||
| chr5:96680378
|
AAGAAG | A | 7 | a0001c0001t0002g0013a0001c0001t0002g0045a0006c0009t0008g0139others(4): Show | 8 | HG00738.hp1 HG01106.hp2 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.138+4779_138+4783d others(7): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96680378 | |||||
| chr5:96680379
|
AG | A | 53 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(50): Show | 58 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.138+4779delG | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96680379 | ||||||
| chr5:96680380
|
G | A | 109 | a0001c0001t0001g0024a0001c0001t0001g0051a0001c0001t0001g0063others(106): Show | 110 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.138+4779G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96680380 | ||||||
| chr5:96680383
|
G | A | 98 | a0001c0001t0001g0024a0001c0001t0001g0051a0001c0001t0001g0063others(95): Show | 99 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.138+4782G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96680383 | ||||||
| chr5:96680463
|
G | A | 7 | a0001c0001t0004g0132a0001c0001t0004g0133a0001c0001t0004g0134others(4): Show | 8 | HG01168.hp1 HG01169.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.138+4862G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96680463 | ||||||
| chr5:96680576
|
G | A | 6 | a0001c0001t0004g0132a0001c0001t0004g0133a0001c0001t0004g0134others(3): Show | 7 | HG01168.hp1 HG01169.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.138+4975G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96680576 | ||||||
| chr5:96680622
|
T | TA | 11 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(8): Show | 12 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.138+5028dupA | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96680622 | |||||
| chr5:96680645
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.138+5044G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96680645 | ||||||
| chr5:96680758
|
T | A | 1 | a0001c0017t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.138+5157T>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96680758 | ||||||
| chr5:96680773
|
G | A | 113 | a0001c0001t0001g0024a0001c0001t0001g0051a0001c0001t0001g0063others(110): Show | 115 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(112): Show |
intron_variant | MODIFIER | c.138+5172G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96680773 | ||||||
| chr5:96680865
|
A | G | 83 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0001g0064others(80): Show | 84 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.138+5264A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96680865 | ||||||
| chr5:96680912
|
C | T | 99 | a0001c0001t0001g0024a0001c0001t0001g0051a0001c0001t0001g0063others(96): Show | 100 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.138+5311C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96680912 | ||||||
| chr5:96680913
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.138+5312A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96680913 | ||||||
| chr5:96680977
|
G | A | 1 | a0001c0002t0017g0195 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.138+5376G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96680977 | ||||||
| chr5:96680999
|
C | T | 2 | a0001c0001t0002g0092a0001c0001t0002g0125 | 2 | HG03669.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.138+5398C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96680999 | ||||||
| chr5:96681196
|
G | A | 6 | a0002c0003t0003g0015a0002c0003t0003g0100a0002c0003t0003g0308others(3): Show | 7 | NA18946.hp1 NA18956.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+5595G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96681196 | ||||||
| chr5:96681302
|
A | G | 1 | a0001c0002t0003g0204 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.138+5701A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96681302 | ||||||
| chr5:96681393
|
T | C | 2 | a0002c0006t0003g0232a0002c0006t0003g0237 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.138+5792T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96681393 | ||||||
| chr5:96681491
|
T | A | 9 | a0001c0005t0001g0244a0001c0005t0007g0242a0001c0005t0007g0243others(6): Show | 10 | HG02280.hp2 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.138+5890T>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96681491 | ||||||
| chr5:96681625
|
T | C | 1 | a0001c0001t0010g0038 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.138+6024T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96681625 | ||||||
| chr5:96681655
|
C | T | 1 | a0010c0016t0011g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.138+6054C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96681655 | ||||||
| chr5:96681732
|
C | CA | 19 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(16): Show | 19 | HG01192.hp2 HG01515.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.138+6152dupA | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96681732 | |||||
| chr5:96681732
|
C | CAA | 7 | a0001c0001t0002g0013a0001c0001t0002g0264a0001c0001t0003g0257others(4): Show | 8 | HG01243.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.138+6151_138+6152d others(4): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96681732 | |||||
| chr5:96681732
|
CA | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(140): Show | 152 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.138+6152delA | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96681732 | |||||
| chr5:96681784
|
G | A | 1 | a0001c0002t0001g0207 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.138+6183G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96681784 | ||||||
| chr5:96681850
|
GT | G | 3 | a0003c0007t0002g0112a0008c0014t0002g0110a0008c0014t0002g0111 | 3 | HG02922.hp1 HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.138+6252delT | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96681850 | |||||
| chr5:96681896
|
C | G | 9 | a0001c0005t0001g0244a0001c0005t0007g0242a0001c0005t0007g0243others(6): Show | 10 | HG02280.hp2 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.138+6295C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96681896 | ||||||
| chr5:96681906
|
A | G | 78 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0211others(75): Show | 81 | HG00140.hp1 HG00544.hp1 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.138+6305A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96681906 | ||||||
| chr5:96681962
|
T | TGA | 107 | a0001c0001t0001g0024a0001c0001t0001g0051a0001c0001t0001g0063others(104): Show | 109 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.138+6372_138+6373d others(4): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96681962 | |||||
| chr5:96682155
|
C | T | 11 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(8): Show | 12 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.138+6554C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96682155 | ||||||
| chr5:96682252
|
C | T | 125 | a0001c0001t0001g0024a0001c0001t0001g0051a0001c0001t0001g0063others(122): Show | 128 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(125): Show |
intron_variant | MODIFIER | c.138+6651C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96682252 | ||||||
| chr5:96682362
|
C | G | 123 | a0001c0001t0001g0024a0001c0001t0001g0051a0001c0001t0001g0063others(120): Show | 126 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(123): Show |
intron_variant | MODIFIER | c.138+6761C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96682362 | ||||||
| chr5:96682474
|
A | G | 6 | a0002c0006t0001g0040a0002c0006t0001g0041a0005c0010t0014g0043others(3): Show | 6 | HG01109.hp2 HG02723.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.138+6873A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96682474 | ||||||
| chr5:96682484
|
C | G | 1 | a0001c0001t0002g0076 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.138+6883C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96682484 | ||||||
| chr5:96682500
|
C | G | 11 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(8): Show | 12 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.138+6899C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96682500 | ||||||
| chr5:96682571
|
A | G | 11 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(8): Show | 12 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.138+6970A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96682571 | ||||||
| chr5:96682601
|
G | A | 11 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(8): Show | 12 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.138+7000G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96682601 | ||||||
| chr5:96682848
|
C | A | 4 | a0001c0005t0001g0244a0001c0005t0007g0242a0001c0005t0007g0243others(1): Show | 4 | HG02559.hp2 HG03579.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.138+7247C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96682848 | ||||||
| chr5:96682963
|
G | A | 2 | a0007c0015t0012g0137a0007c0015t0012g0138 | 2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.138+7362G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96682963 | ||||||
| chr5:96683095
|
G | A | 1 | a0002c0004t0005g0030 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.138+7494G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96683095 | ||||||
| chr5:96683218
|
T | C | 45 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(42): Show | 50 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.138+7617T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96683218 | ||||||
| chr5:96683267
|
A | G | 1 | a0004c0008t0011g0238 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.138+7666A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96683267 | ||||||
| chr5:96683389
|
C | T | 4 | a0001c0001t0002g0013a0002c0004t0013g0258a0002c0004t0013g0259others(1): Show | 5 | HG02896.hp1 HG02897.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+7788C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96683389 | ||||||
| chr5:96683416
|
T | C | 3 | a0001c0001t0002g0337a0002c0003t0003g0338a0002c0003t0003g0339 | 3 | HG01069.hp2 HG01074.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.138+7815T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96683416 | ||||||
| chr5:96683754
|
G | A | 45 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(42): Show | 50 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.138+8153G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96683754 | ||||||
| chr5:96684369
|
G | A | 8 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(5): Show | 8 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.138+8768G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96684369 | ||||||
| chr5:96684373
|
T | C | 45 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(42): Show | 50 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.138+8772T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96684373 | ||||||
| chr5:96684374
|
G | T | 2 | a0001c0001t0001g0011a0001c0001t0006g0010 | 4 | HG00099.hp1 HG00280.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+8773G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96684374 | ||||||
| chr5:96684549
|
A | G | 2 | a0007c0015t0012g0137a0007c0015t0012g0138 | 2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.138+8948A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96684549 | ||||||
| chr5:96684565
|
C | CT | 16 | a0001c0001t0001g0011a0001c0001t0001g0051a0001c0001t0001g0109others(13): Show | 17 | HG00099.hp1 HG01074.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.138+8979dupT | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96684565 | |||||
| chr5:96684636
|
C | T | 2 | a0001c0001t0002g0036a0004c0008t0011g0037 | 2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.138+9035C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96684636 | ||||||
| chr5:96684708
|
G | A | 6 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(3): Show | 6 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.138+9107G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96684708 | ||||||
| chr5:96684767
|
G | A | 7 | a0001c0001t0002g0034a0001c0021t0009g0035a0002c0004t0005g0027others(4): Show | 7 | HG02451.hp2 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+9166G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96684767 | ||||||
| chr5:96684837
|
T | C | 2 | a0005c0010t0014g0043a0005c0010t0014g0044 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.138+9236T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96684837 | ||||||
| chr5:96684860
|
A | G | 1 | a0004c0029t0001g0187 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.138+9259A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96684860 | ||||||
| chr5:96684977
|
ATGT | A | 168 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(165): Show | 176 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.138+9380_138+9382d others(5): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96684977 | |||||
| chr5:96684984
|
A | G | 3 | a0001c0001t0002g0013a0002c0004t0013g0258a0002c0004t0013g0259 | 4 | HG02896.hp1 HG02897.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+9383A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96684984 | ||||||
| chr5:96685049
|
AAT | A | 8 | a0001c0001t0002g0034a0001c0001t0002g0056a0001c0021t0009g0035others(5): Show | 8 | HG02451.hp2 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.138+9460_138+9461d others(4): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96685049 | |||||
| chr5:96685095
|
A | G | 1 | a0001c0001t0002g0075 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.138+9494A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96685095 | ||||||
| chr5:96685171
|
G | A | 316 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(313): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.138+9570G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96685171 | ||||||
| chr5:96685259
|
A | G | 1 | a0001c0001t0002g0075 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.138+9658A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96685259 | ||||||
| chr5:96685589
|
A | G | 53 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0068others(50): Show | 54 | HG00423.hp2 HG00621.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.138+9988A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96685589 | ||||||
| chr5:96685636
|
A | C | 1 | a0005c0010t0014g0131 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.138+10035A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96685636 | ||||||
| chr5:96685774
|
A | C | 1 | a0001c0017t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.139-10062A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96685774 | ||||||
| chr5:96685882
|
A | G | 1 | a0002c0003t0003g0331 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.139-9954A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96685882 | ||||||
| chr5:96686036
|
T | C | 1 | a0002c0003t0003g0174 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.139-9800T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96686036 | ||||||
| chr5:96686169
|
CT | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(164): Show | 175 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.139-9657delT | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96686169 | |||||
| chr5:96686179
|
T | C | 1 | a0004c0008t0011g0238 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.139-9657T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96686179 | ||||||
| chr5:96686181
|
A | T | 1 | a0004c0008t0007g0061 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.139-9655A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96686181 | ||||||
| chr5:96686224
|
A | G | 1 | a0001c0002t0001g0250 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.139-9612A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96686224 | ||||||
| chr5:96686416
|
A | G | 1 | a0004c0008t0011g0238 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.139-9420A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96686416 | ||||||
| chr5:96686566
|
C | T | 1 | a0002c0004t0005g0190 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.139-9270C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96686566 | ||||||
| chr5:96686859
|
A | C | 6 | a0001c0001t0004g0132a0001c0001t0004g0133a0001c0001t0004g0134others(3): Show | 7 | HG01168.hp1 HG01169.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.139-8977A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96686859 | ||||||
| chr5:96686963
|
G | A | 1 | a0001c0017t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.139-8873G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96686963 | ||||||
| chr5:96687185
|
G | A | 2 | a0007c0015t0012g0137a0007c0015t0012g0138 | 2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.139-8651G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96687185 | ||||||
| chr5:96687767
|
T | C | 1 | a0004c0008t0011g0238 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.139-8069T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96687767 | ||||||
| chr5:96687882
|
A | G | 6 | a0001c0001t0004g0132a0001c0001t0004g0133a0001c0001t0004g0134others(3): Show | 7 | HG01168.hp1 HG01169.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.139-7954A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96687882 | ||||||
| chr5:96687973
|
G | T | 8 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(5): Show | 8 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.139-7863G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96687973 | ||||||
| chr5:96687997
|
G | A | 10 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(7): Show | 10 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-7839G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96687997 | ||||||
| chr5:96688178
|
A | G | 18 | a0001c0001t0002g0034a0001c0005t0001g0244a0001c0005t0007g0242others(15): Show | 19 | HG02280.hp2 HG02451.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.139-7658A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96688178 | ||||||
| chr5:96688259
|
A | G | 6 | a0001c0001t0004g0132a0001c0001t0004g0133a0001c0001t0004g0134others(3): Show | 7 | HG01168.hp1 HG01169.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.139-7577A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96688259 | ||||||
| chr5:96688465
|
A | C | 1 | a0004c0008t0011g0236 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.139-7371A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96688465 | ||||||
| chr5:96688474
|
T | C | 45 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(42): Show | 50 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.139-7362T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96688474 | ||||||
| chr5:96688529
|
C | T | 4 | a0001c0001t0001g0261a0001c0001t0001g0263a0001c0001t0002g0262others(1): Show | 4 | HG01243.hp1 HG02280.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-7307C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96688529 | ||||||
| chr5:96688533
|
G | A | 3 | a0001c0001t0002g0013a0002c0004t0013g0258a0002c0004t0013g0259 | 4 | HG02896.hp1 HG02897.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-7303G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96688533 | ||||||
| chr5:96688769
|
G | A | 264 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(261): Show | 276 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.139-7067G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96688769 | ||||||
| chr5:96688904
|
G | C | 3 | a0001c0001t0002g0013a0002c0004t0013g0258a0002c0004t0013g0259 | 4 | HG02896.hp1 HG02897.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-6932G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96688904 | ||||||
| chr5:96689004
|
G | A | 2 | a0001c0001t0002g0036a0004c0008t0011g0037 | 2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.139-6832G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96689004 | ||||||
| chr5:96689009
|
G | A | 45 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(42): Show | 50 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.139-6827G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96689009 | ||||||
| chr5:96689027
|
C | CAT | 174 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(171): Show | 182 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.139-6809_139-6808i others(4): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96689027 | ||||||
| chr5:96689060
|
G | C | 6 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(3): Show | 6 | HG01243.hp1 HG02280.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-6776G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96689060 | ||||||
| chr5:96689177
|
A | G | 1 | a0001c0001t0002g0074 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.139-6659A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96689177 | ||||||
| chr5:96689184
|
C | T | 1 | a0004c0008t0011g0238 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.139-6652C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96689184 | ||||||
| chr5:96689186
|
A | G | 4 | a0001c0001t0001g0108a0001c0001t0002g0045a0001c0001t0002g0106others(1): Show | 4 | HG01106.hp2 HG01257.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-6650A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96689186 | ||||||
| chr5:96689241
|
A | T | 1 | a0001c0002t0002g0301 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.139-6595A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96689241 | ||||||
| chr5:96689264
|
C | A | 1 | a0003c0007t0002g0313 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.139-6572C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96689264 | ||||||
| chr5:96689365
|
A | G | 9 | a0001c0001t0002g0062a0001c0001t0002g0072a0001c0001t0002g0073others(6): Show | 9 | HG02015.hp1 NA18957.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.139-6471A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96689365 | ||||||
| chr5:96689545
|
A | T | 175 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(172): Show | 183 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.139-6291A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96689545 | ||||||
| chr5:96689560
|
A | G | 2 | a0002c0003t0001g0239a0002c0003t0001g0240 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.139-6276A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96689560 | ||||||
| chr5:96689679
|
A | G | 3 | a0001c0001t0002g0034a0001c0001t0002g0036a0004c0008t0011g0037 | 3 | HG02486.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.139-6157A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96689679 | ||||||
| chr5:96689745
|
G | T | 8 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(5): Show | 8 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.139-6091G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96689745 | ||||||
| chr5:96689789
|
G | A | 1 | a0001c0001t0001g0318 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.139-6047G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96689789 | ||||||
| chr5:96689841
|
T | C | 2 | a0001c0001t0001g0123a0002c0004t0003g0124 | 2 | HG00738.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.139-5995T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96689841 | ||||||
| chr5:96689953
|
A | G | 1 | a0002c0013t0001g0191 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.139-5883A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96689953 | ||||||
| chr5:96689980
|
G | C | 4 | a0002c0004t0001g0047a0002c0004t0001g0048a0002c0004t0001g0049others(1): Show | 4 | NA18991.hp1 NA19002.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-5856G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96689980 | ||||||
| chr5:96690143
|
A | G | 85 | a0001c0001t0001g0024a0001c0001t0001g0063a0001c0001t0001g0064others(82): Show | 86 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.139-5693A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96690143 | ||||||
| chr5:96690144
|
C | G | 4 | a0001c0012t0001g0328a0001c0012t0001g0329a0002c0003t0003g0311others(1): Show | 4 | HG02258.hp2 HG02615.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-5692C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96690144 | ||||||
| chr5:96690240
|
A | AT | 6 | a0001c0001t0001g0108a0001c0001t0002g0045a0001c0001t0002g0095others(3): Show | 6 | HG00323.hp1 HG01106.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-5587dupT | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96690240 | |||||
| chr5:96690274
|
C | G | 3 | a0001c0001t0002g0034a0001c0001t0002g0036a0004c0008t0011g0037 | 3 | HG02486.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.139-5562C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96690274 | ||||||
| chr5:96690289
|
T | C | 6 | a0001c0001t0004g0132a0001c0001t0004g0133a0001c0001t0004g0134others(3): Show | 7 | HG01168.hp1 HG01169.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.139-5547T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96690289 | ||||||
| chr5:96690334
|
C | T | 14 | a0001c0001t0001g0118a0001c0001t0002g0119a0001c0001t0010g0023others(11): Show | 14 | HG02486.hp1 HG02572.hp2 HG03017.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-5502C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96690334 | ||||||
| chr5:96690335
|
G | A | 1 | a0001c0002t0001g0184 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.139-5501G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96690335 | ||||||
| chr5:96690380
|
C | T | 1 | a0001c0002t0001g0194 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.139-5456C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96690380 | ||||||
| chr5:96690381
|
G | T | 97 | a0001c0001t0001g0024a0001c0001t0001g0051a0001c0001t0001g0063others(94): Show | 98 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.139-5455G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96690381 | ||||||
| chr5:96690560
|
A | G | 45 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(42): Show | 50 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.139-5276A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96690560 | ||||||
| chr5:96690735
|
G | A | 5 | a0001c0001t0001g0108a0001c0001t0002g0045a0001c0001t0002g0106others(2): Show | 5 | HG01106.hp2 HG01257.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-5101G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96690735 | ||||||
| chr5:96690774
|
A | C | 3 | a0001c0001t0002g0034a0001c0001t0002g0036a0004c0008t0011g0037 | 3 | HG02486.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.139-5062A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96690774 | ||||||
| chr5:96690775
|
C | T | 3 | a0001c0001t0002g0034a0001c0001t0002g0036a0004c0008t0011g0037 | 3 | HG02486.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.139-5061C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96690775 | ||||||
| chr5:96690918
|
T | C | 45 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(42): Show | 50 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.139-4918T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96690918 | ||||||
| chr5:96690995
|
T | C | 2 | a0001c0001t0001g0265a0001c0001t0001g0318 | 2 | HG02074.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.139-4841T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96690995 | ||||||
| chr5:96691019
|
C | G | 1 | a0001c0001t0002g0226 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.139-4817C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96691019 | ||||||
| chr5:96691200
|
C | T | 9 | a0001c0005t0001g0244a0001c0005t0007g0242a0001c0005t0007g0243others(6): Show | 10 | HG02280.hp2 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-4636C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96691200 | ||||||
| chr5:96691281
|
A | G | 8 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(5): Show | 8 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.139-4555A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96691281 | ||||||
| chr5:96691366
|
C | CT | 45 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(42): Show | 50 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.139-4468dupT | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96691366 | |||||
| chr5:96691533
|
G | A | 4 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(1): Show | 4 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-4303G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96691533 | ||||||
| chr5:96691548
|
G | T | 103 | a0001c0001t0001g0024a0001c0001t0001g0051a0001c0001t0001g0063others(100): Show | 104 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(101): Show |
intron_variant | MODIFIER | c.139-4288G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96691548 | ||||||
| chr5:96691592
|
C | G | 2 | a0001c0001t0001g0123a0002c0004t0003g0124 | 2 | HG00738.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.139-4244C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96691592 | ||||||
| chr5:96691832
|
T | C | 7 | a0001c0001t0002g0034a0001c0021t0009g0035a0002c0004t0005g0027others(4): Show | 7 | HG02451.hp2 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-4004T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96691832 | ||||||
| chr5:96691838
|
G | C | 1 | a0002c0004t0001g0116 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.139-3998G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96691838 | ||||||
| chr5:96691889
|
C | G | 1 | a0001c0001t0002g0295 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.139-3947C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96691889 | ||||||
| chr5:96691933
|
C | T | 6 | a0001c0001t0004g0132a0001c0001t0004g0133a0001c0001t0004g0134others(3): Show | 7 | HG01168.hp1 HG01169.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.139-3903C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96691933 | ||||||
| chr5:96691971
|
C | T | 4 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(1): Show | 4 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-3865C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96691971 | ||||||
| chr5:96691980
|
A | G | 1 | a0001c0001t0002g0046 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.139-3856A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96691980 | ||||||
| chr5:96691996
|
A | G | 6 | a0001c0001t0004g0132a0001c0001t0004g0133a0001c0001t0004g0134others(3): Show | 7 | HG01168.hp1 HG01169.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.139-3840A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96691996 | ||||||
| chr5:96692045
|
C | A | 1 | a0002c0004t0005g0027 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.139-3791C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96692045 | ||||||
| chr5:96692126
|
G | A | 8 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(5): Show | 8 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.139-3710G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96692126 | ||||||
| chr5:96692273
|
C | T | 2 | a0007c0015t0012g0137a0007c0015t0012g0138 | 2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.139-3563C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96692273 | ||||||
| chr5:96692606
|
A | G | 4 | a0001c0005t0001g0244a0001c0005t0007g0242a0001c0005t0007g0243others(1): Show | 4 | HG02559.hp2 HG03579.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-3230A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96692606 | ||||||
| chr5:96692646
|
T | G | 3 | a0001c0001t0009g0336a0002c0004t0021g0233a0002c0013t0001g0234 | 3 | HG01891.hp2 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.139-3190T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96692646 | ||||||
| chr5:96692724
|
C | T | 8 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(5): Show | 8 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.139-3112C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96692724 | ||||||
| chr5:96692731
|
A | T | 2 | a0007c0015t0012g0137a0007c0015t0012g0138 | 2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.139-3105A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96692731 | ||||||
| chr5:96693138
|
A | G | 1 | a0001c0001t0002g0013 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.139-2698A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96693138 | ||||||
| chr5:96693150
|
C | T | 1 | a0001c0002t0001g0224 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.139-2686C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96693150 | ||||||
| chr5:96693156
|
A | G | 162 | a0001c0001t0001g0109a0001c0001t0001g0265a0001c0001t0001g0286others(159): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.139-2680A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96693156 | ||||||
| chr5:96693168
|
T | C | 1 | a0001c0001t0004g0272 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.139-2668T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96693168 | ||||||
| chr5:96693229
|
C | G | 9 | a0001c0005t0001g0244a0001c0005t0007g0242a0001c0005t0007g0243others(6): Show | 10 | HG02280.hp2 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-2607C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96693229 | ||||||
| chr5:96693264
|
G | A | 67 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0012others(64): Show | 70 | HG00140.hp1 HG00544.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.139-2572G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96693264 | ||||||
| chr5:96693278
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.139-2558C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96693278 | ||||||
| chr5:96693284
|
G | A | 1 | a0001c0001t0009g0336 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.139-2552G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96693284 | ||||||
| chr5:96693312
|
A | C | 8 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(5): Show | 8 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.139-2524A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96693312 | ||||||
| chr5:96693609
|
G | T | 1 | a0001c0002t0003g0204 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.139-2227G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96693609 | ||||||
| chr5:96693889
|
T | C | 1 | a0002c0004t0005g0031 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.139-1947T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96693889 | ||||||
| chr5:96693916
|
CTATT | C | 45 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(42): Show | 50 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.139-1915_139-1912d others(6): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr5 | 96693916 | |||||
| chr5:96693990
|
G | A | 3 | a0001c0001t0002g0013a0002c0004t0013g0258a0002c0004t0013g0259 | 4 | HG02896.hp1 HG02897.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-1846G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96693990 | ||||||
| chr5:96694062
|
T | A | 8 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(5): Show | 8 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.139-1774T>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96694062 | ||||||
| chr5:96694127
|
A | T | 6 | a0001c0001t0004g0132a0001c0001t0004g0133a0001c0001t0004g0134others(3): Show | 7 | HG01168.hp1 HG01169.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.139-1709A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96694127 | ||||||
| chr5:96694141
|
C | A | 67 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0012others(64): Show | 70 | HG00140.hp1 HG00544.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.139-1695C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96694141 | ||||||
| chr5:96694491
|
C | T | 13 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(10): Show | 14 | HG01109.hp1 HG01243.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-1345C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96694491 | ||||||
| chr5:96694501
|
T | C | 1 | a0001c0001t0002g0062 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.139-1335T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96694501 | ||||||
| chr5:96694634
|
A | C | 5 | a0002c0004t0005g0027a0002c0004t0005g0030a0002c0004t0005g0031others(2): Show | 5 | HG02451.hp2 HG02559.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-1202A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96694634 | ||||||
| chr5:96694654
|
C | A | 3 | a0001c0001t0002g0013a0002c0004t0013g0258a0002c0004t0013g0259 | 4 | HG02896.hp1 HG02897.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-1182C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96694654 | ||||||
| chr5:96694747
|
C | A | 2 | a0001c0001t0001g0175a0001c0001t0001g0185 | 2 | NA19091.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.139-1089C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96694747 | ||||||
| chr5:96695039
|
C | T | 9 | a0001c0005t0001g0244a0001c0005t0007g0242a0001c0005t0007g0243others(6): Show | 10 | HG02280.hp2 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-797C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96695039 | ||||||
| chr5:96695040
|
C | G | 67 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0012others(64): Show | 70 | HG00140.hp1 HG00544.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.139-796C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96695040 | ||||||
| chr5:96695166
|
A | T | 1 | a0001c0002t0001g0231 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.139-670A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96695166 | ||||||
| chr5:96695261
|
G | T | 1 | a0001c0001t0001g0123 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.139-575G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96695261 | ||||||
| chr5:96695290
|
A | G | 1 | a0004c0029t0001g0187 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.139-546A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96695290 | ||||||
| chr5:96695554
|
G | A | 2 | a0001c0001t0002g0209a0001c0001t0023g0208 | 2 | HG01123.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.139-282G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96695554 | ||||||
| chr5:96695582
|
A | G | 71 | a0001c0001t0001g0265a0001c0001t0001g0307a0001c0001t0001g0315others(68): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.139-254A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96695582 | ||||||
| chr5:96695683
|
C | T | 8 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(5): Show | 8 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.139-153C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 2/31 | chr5 | 96695683 | ||||||
| chr5:96695972
|
G | C | 3 | a0001c0001t0002g0013a0002c0004t0013g0258a0002c0004t0013g0259 | 4 | HG02896.hp1 HG02897.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.210+65G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96695972 | ||||||
| chr5:96696123
|
G | T | 67 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0012others(64): Show | 70 | HG00140.hp1 HG00544.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.210+216G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96696123 | ||||||
| chr5:96696271
|
C | T | 8 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(5): Show | 8 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.210+364C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96696271 | ||||||
| chr5:96696391
|
G | A | 70 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(67): Show | 77 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.210+484G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96696391 | ||||||
| chr5:96696470
|
T | C | 3 | a0001c0001t0009g0336a0002c0004t0021g0233a0002c0013t0001g0234 | 3 | HG01891.hp2 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.210+563T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96696470 | ||||||
| chr5:96696606
|
G | GCAGGAGG others(5): Show |
1 | a0001c0001t0002g0095 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.210+712_210+723dup others(12): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 96696606 | |||||
| chr5:96696660
|
G | A | 6 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(3): Show | 6 | HG01243.hp1 HG02280.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.210+753G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96696660 | ||||||
| chr5:96696686
|
T | TAAAAAAA others(3): Show |
9 | a0001c0001t0002g0013a0001c0002t0001g0184a0001c0002t0001g0194others(6): Show | 10 | HG01099.hp1 HG02896.hp1 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.210+783_210+792dup others(10): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 96696686 | |||||
| chr5:96696686
|
T | TAAAAAAA others(4): Show |
63 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0012others(60): Show | 66 | HG00140.hp1 HG00544.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.210+782_210+792dup others(11): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 96696686 | |||||
| chr5:96696686
|
T | TAAAAAAA others(5): Show |
12 | a0001c0001t0004g0132a0001c0001t0004g0133a0001c0001t0004g0134others(9): Show | 13 | HG00621.hp2 HG01168.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.210+781_210+792dup others(12): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 96696686 | |||||
| chr5:96696686
|
T | TAAAAAAA others(6): Show |
3 | a0001c0001t0001g0157a0001c0001t0001g0181a0002c0013t0001g0191 | 3 | HG00558.hp1 HG01167.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.210+780_210+792dup others(13): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 96696686 | |||||
| chr5:96696686
|
T | TAAAAAAA others(7): Show |
54 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(51): Show | 60 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.210+792_210+793ins others(14): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 96696686 | |||||
| chr5:96696686
|
T | TAAAAAAA others(8): Show |
51 | a0001c0001t0001g0151a0001c0001t0001g0170a0001c0001t0001g0173others(48): Show | 54 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.210+792_210+793ins others(15): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 96696686 | |||||
| chr5:96696686
|
T | TAAAAAAA others(9): Show |
20 | a0001c0001t0001g0143a0001c0001t0001g0263a0001c0001t0002g0262others(17): Show | 21 | HG00140.hp2 HG00609.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.210+792_210+793ins others(16): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 96696686 | |||||
| chr5:96696686
|
T | TAAAAAAA others(10): Show |
14 | a0001c0001t0001g0261a0001c0001t0004g0014a0001c0001t0004g0266others(11): Show | 15 | HG00280.hp1 HG00642.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.210+792_210+793ins others(17): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 96696686 | |||||
| chr5:96696686
|
T | TAAAAAAA others(11): Show |
1 | a0002c0003t0003g0021 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.210+792_210+793ins others(18): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 96696686 | |||||
| chr5:96696723
|
A | G | 336 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(333): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.210+816A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96696723 | ||||||
| chr5:96696726
|
C | T | 6 | a0001c0001t0004g0132a0001c0001t0004g0133a0001c0001t0004g0134others(3): Show | 7 | HG01168.hp1 HG01169.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.210+819C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96696726 | ||||||
| chr5:96697038
|
C | T | 1 | a0001c0001t0002g0264 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.210+1131C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96697038 | ||||||
| chr5:96697039
|
G | A | 1 | a0001c0001t0006g0093 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.210+1132G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96697039 | ||||||
| chr5:96697093
|
G | A | 1 | a0010c0016t0011g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.210+1186G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96697093 | ||||||
| chr5:96697185
|
G | A | 3 | a0001c0001t0001g0286a0002c0004t0001g0282a0002c0004t0001g0283 | 3 | HG01346.hp1 HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.210+1278G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96697185 | ||||||
| chr5:96697280
|
A | G | 1 | a0001c0001t0002g0060 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.210+1373A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96697280 | ||||||
| chr5:96697292
|
CT | C | 5 | a0001c0001t0002g0013a0001c0017t0001g0025a0002c0004t0013g0258others(2): Show | 6 | HG01109.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+1395delT | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 96697292 | |||||
| chr5:96697475
|
T | G | 67 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0012others(64): Show | 70 | HG00140.hp1 HG00544.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.210+1568T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96697475 | ||||||
| chr5:96697499
|
T | C | 9 | a0001c0005t0001g0244a0001c0005t0007g0242a0001c0005t0007g0243others(6): Show | 10 | HG02280.hp2 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.210+1592T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96697499 | ||||||
| chr5:96697774
|
G | A | 6 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(3): Show | 6 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+1867G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96697774 | ||||||
| chr5:96697987
|
A | G | 7 | a0001c0001t0002g0034a0001c0021t0009g0035a0002c0004t0005g0027others(4): Show | 7 | HG02451.hp2 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.210+2080A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96697987 | ||||||
| chr5:96698118
|
T | G | 1 | a0001c0001t0010g0038 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.210+2211T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96698118 | ||||||
| chr5:96698166
|
C | T | 56 | a0001c0001t0001g0265a0001c0001t0001g0307a0001c0001t0001g0315others(53): Show | 60 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.210+2259C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96698166 | ||||||
| chr5:96698258
|
G | T | 1 | a0001c0001t0001g0315 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.210+2351G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96698258 | ||||||
| chr5:96698555
|
G | A | 1 | a0004c0008t0011g0236 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.210+2648G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96698555 | ||||||
| chr5:96698587
|
T | C | 7 | a0001c0001t0002g0034a0001c0021t0009g0035a0002c0004t0005g0027others(4): Show | 7 | HG02451.hp2 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.210+2680T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96698587 | ||||||
| chr5:96698623
|
C | T | 1 | a0001c0017t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.210+2716C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96698623 | ||||||
| chr5:96698676
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.210+2769T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96698676 | ||||||
| chr5:96698704
|
T | C | 3 | a0001c0001t0001g0024a0001c0001t0001g0127a0001c0001t0001g0129 | 3 | HG02451.hp1 HG02976.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.210+2797T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96698704 | ||||||
| chr5:96698808
|
T | C | 4 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(1): Show | 4 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.210+2901T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96698808 | ||||||
| chr5:96698915
|
G | A | 3 | a0001c0001t0002g0013a0002c0004t0013g0258a0002c0004t0013g0259 | 4 | HG02896.hp1 HG02897.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.210+3008G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96698915 | ||||||
| chr5:96699028
|
T | C | 2 | a0007c0015t0012g0137a0007c0015t0012g0138 | 2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.210+3121T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96699028 | ||||||
| chr5:96699078
|
T | C | 1 | a0002c0004t0005g0031 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.210+3171T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96699078 | ||||||
| chr5:96699170
|
C | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(42): Show | 50 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.210+3263C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96699170 | ||||||
| chr5:96699221
|
A | G | 1 | a0001c0001t0009g0336 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.210+3314A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96699221 | ||||||
| chr5:96699310
|
A | C | 2 | a0007c0015t0012g0137a0007c0015t0012g0138 | 2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.210+3403A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96699310 | ||||||
| chr5:96699401
|
C | T | 6 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(3): Show | 6 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+3494C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96699401 | ||||||
| chr5:96699921
|
G | A | 1 | a0001c0001t0002g0095 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.210+4014G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96699921 | ||||||
| chr5:96699995
|
G | A | 3 | a0001c0001t0002g0013a0002c0004t0013g0258a0002c0004t0013g0259 | 4 | HG02896.hp1 HG02897.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.210+4088G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96699995 | ||||||
| chr5:96700214
|
G | A | 1 | a0010c0016t0011g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.210+4307G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96700214 | ||||||
| chr5:96700415
|
C | G | 8 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(5): Show | 8 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.210+4508C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96700415 | ||||||
| chr5:96700460
|
A | C | 6 | a0002c0006t0001g0040a0002c0006t0001g0041a0005c0010t0014g0043others(3): Show | 6 | HG01109.hp2 HG02723.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+4553A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96700460 | ||||||
| chr5:96700607
|
G | C | 21 | a0001c0001t0004g0014a0001c0001t0004g0132a0001c0001t0004g0133others(18): Show | 23 | HG00280.hp1 HG00642.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.210+4700G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96700607 | ||||||
| chr5:96700664
|
G | A | 1 | a0001c0002t0001g0193 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.210+4757G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96700664 | ||||||
| chr5:96700694
|
T | C | 1 | a0001c0001t0002g0045 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.210+4787T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96700694 | ||||||
| chr5:96700737
|
C | T | 1 | a0002c0003t0010g0284 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.210+4830C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96700737 | ||||||
| chr5:96700923
|
C | T | 1 | a0001c0028t0001g0230 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.210+5016C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96700923 | ||||||
| chr5:96700931
|
A | T | 2 | a0002c0004t0021g0233a0002c0013t0001g0234 | 2 | HG01891.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.210+5024A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96700931 | ||||||
| chr5:96700932
|
T | A | 15 | a0001c0001t0001g0108a0001c0001t0002g0036a0001c0001t0002g0045others(12): Show | 15 | HG00323.hp1 HG01106.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.210+5025T>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96700932 | ||||||
| chr5:96700989
|
T | C | 6 | a0001c0002t0001g0199a0001c0002t0001g0227a0001c0002t0001g0228others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+5082T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96700989 | ||||||
| chr5:96701082
|
C | T | 2 | a0001c0017t0001g0025a0004c0008t0011g0238 | 2 | HG01109.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.210+5175C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96701082 | ||||||
| chr5:96701428
|
A | G | 3 | a0001c0001t0001g0051a0008c0014t0002g0110a0008c0014t0002g0111 | 3 | HG02922.hp1 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.210+5521A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96701428 | ||||||
| chr5:96701441
|
TTTTTAAA others(8): Show |
T | 1 | a0002c0003t0003g0174 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.210+5535_210+5549d others(17): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96701441 | ||||||
| chr5:96701470
|
T | G | 1 | a0002c0003t0003g0174 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.210+5563T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96701470 | ||||||
| chr5:96701487
|
A | T | 1 | a0002c0003t0003g0174 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.210+5580A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96701487 | ||||||
| chr5:96701489
|
G | T | 1 | a0002c0003t0003g0174 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.210+5582G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96701489 | ||||||
| chr5:96701494
|
A | G | 1 | a0002c0003t0003g0174 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.210+5587A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96701494 | ||||||
| chr5:96701495
|
T | A | 1 | a0002c0003t0003g0174 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.210+5588T>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96701495 | ||||||
| chr5:96701496
|
A | G | 1 | a0002c0003t0003g0174 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.210+5589A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96701496 | ||||||
| chr5:96701505
|
A | G | 1 | a0002c0003t0003g0174 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.210+5598A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96701505 | ||||||
| chr5:96701516
|
A | AAAG | 3 | a0001c0001t0009g0336a0002c0004t0021g0233a0002c0013t0001g0234 | 3 | HG01891.hp2 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.210+5610_210+5611i others(5): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 96701516 | |||||
| chr5:96701525
|
T | G | 1 | a0002c0003t0003g0174 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.210+5618T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96701525 | ||||||
| chr5:96701575
|
T | G | 1 | a0002c0003t0003g0174 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.210+5668T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96701575 | ||||||
| chr5:96701576
|
G | C | 1 | a0002c0003t0003g0174 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.210+5669G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96701576 | ||||||
| chr5:96701577
|
G | A | 1 | a0002c0003t0003g0174 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.210+5670G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96701577 | ||||||
| chr5:96701590
|
A | G | 1 | a0002c0003t0003g0174 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.210+5683A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96701590 | ||||||
| chr5:96701591
|
G | A | 1 | a0002c0003t0003g0174 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.210+5684G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96701591 | ||||||
| chr5:96701616
|
C | G | 1 | a0002c0003t0003g0174 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.210+5709C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96701616 | ||||||
| chr5:96701676
|
A | T | 1 | a0002c0003t0003g0174 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.210+5769A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96701676 | ||||||
| chr5:96701688
|
G | C | 1 | a0002c0003t0003g0174 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.210+5781G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96701688 | ||||||
| chr5:96701704
|
C | T | 1 | a0002c0003t0003g0174 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.210+5797C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96701704 | ||||||
| chr5:96701706
|
G | C | 1 | a0002c0003t0003g0174 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.210+5799G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96701706 | ||||||
| chr5:96701715
|
G | T | 1 | a0002c0003t0003g0174 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.210+5808G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96701715 | ||||||
| chr5:96701764
|
G | C | 1 | a0002c0003t0003g0174 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.210+5857G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96701764 | ||||||
| chr5:96701805
|
C | CA | 28 | a0001c0001t0002g0077a0001c0001t0004g0014a0001c0001t0004g0132others(25): Show | 30 | HG00280.hp1 HG00642.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.210+5913dupA | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 96701805 | |||||
| chr5:96701805
|
C | CAA | 48 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(45): Show | 54 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.210+5912_210+5913d others(4): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 96701805 | |||||
| chr5:96702163
|
T | C | 9 | a0001c0001t0002g0290a0001c0001t0002g0292a0001c0001t0002g0293others(6): Show | 11 | HG00423.hp1 NA18942.hp1 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.210+6256T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96702163 | ||||||
| chr5:96702174
|
T | C | 1 | a0001c0001t0010g0028 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.210+6267T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96702174 | ||||||
| chr5:96702323
|
A | G | 3 | a0001c0001t0009g0336a0002c0004t0021g0233a0002c0013t0001g0234 | 3 | HG01891.hp2 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.210+6416A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96702323 | ||||||
| chr5:96702488
|
A | C | 1 | a0001c0001t0001g0145 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.210+6581A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96702488 | ||||||
| chr5:96702781
|
G | A | 6 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(3): Show | 6 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+6874G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96702781 | ||||||
| chr5:96702971
|
G | A | 24 | a0001c0001t0002g0013a0001c0001t0004g0014a0001c0001t0004g0132others(21): Show | 27 | HG00280.hp1 HG00642.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.210+7064G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96702971 | ||||||
| chr5:96703111
|
A | G | 45 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(42): Show | 50 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.210+7204A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96703111 | ||||||
| chr5:96703113
|
T | G | 45 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(42): Show | 50 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.210+7206T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96703113 | ||||||
| chr5:96703114
|
C | A | 45 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(42): Show | 50 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.210+7207C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96703114 | ||||||
| chr5:96703205
|
TGTGGCCC others(7): Show |
T | 2 | a0001c0017t0001g0025a0004c0008t0011g0238 | 2 | HG01109.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.210+7307_210+7320d others(16): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 96703205 | |||||
| chr5:96703215
|
TACAAGTG others(7): Show |
T | 5 | a0001c0001t0001g0005a0001c0001t0001g0127a0001c0001t0001g0129others(2): Show | 6 | HG02451.hp1 HG03579.hp2 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+7334_210+7347d others(16): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 96703215 | |||||
| chr5:96703321
|
T | C | 113 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(110): Show | 121 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.210+7414T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96703321 | ||||||
| chr5:96703327
|
C | T | 64 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0068others(61): Show | 65 | HG00423.hp2 HG00621.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.210+7420C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96703327 | ||||||
| chr5:96703338
|
G | C | 7 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(4): Show | 7 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.210+7431G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96703338 | ||||||
| chr5:96703627
|
T | C | 1 | a0001c0001t0001g0315 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.210+7720T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96703627 | ||||||
| chr5:96703702
|
C | G | 7 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(4): Show | 7 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.210+7795C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96703702 | ||||||
| chr5:96703827
|
G | T | 2 | a0001c0001t0001g0123a0002c0004t0003g0124 | 2 | HG00738.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.210+7920G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96703827 | ||||||
| chr5:96703872
|
A | G | 9 | a0001c0005t0001g0244a0001c0005t0007g0242a0001c0005t0007g0243others(6): Show | 10 | HG02280.hp2 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.210+7965A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96703872 | ||||||
| chr5:96703912
|
T | A | 7 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(4): Show | 7 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.210+8005T>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96703912 | ||||||
| chr5:96704085
|
G | A | 9 | a0001c0005t0001g0244a0001c0005t0007g0242a0001c0005t0007g0243others(6): Show | 10 | HG02280.hp2 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.210+8178G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96704085 | ||||||
| chr5:96704088
|
G | T | 1 | a0001c0001t0002g0295 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.210+8181G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96704088 | ||||||
| chr5:96704191
|
G | T | 1 | a0002c0004t0001g0283 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.210+8284G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96704191 | ||||||
| chr5:96704197
|
G | A | 2 | a0001c0017t0001g0025a0004c0008t0011g0238 | 2 | HG01109.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.210+8290G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96704197 | ||||||
| chr5:96704316
|
G | A | 1 | a0001c0001t0016g0004 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.210+8409G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96704316 | ||||||
| chr5:96704418
|
C | A | 26 | a0001c0001t0002g0013a0001c0001t0004g0014a0001c0001t0004g0132others(23): Show | 29 | HG00280.hp1 HG00642.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.210+8511C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96704418 | ||||||
| chr5:96704631
|
A | G | 3 | a0001c0011t0002g0102a0001c0011t0002g0103a0001c0011t0002g0104 | 3 | HG00741.hp1 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.210+8724A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96704631 | ||||||
| chr5:96704663
|
A | G | 1 | a0001c0001t0004g0277 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.210+8756A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96704663 | ||||||
| chr5:96704709
|
T | C | 7 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(4): Show | 7 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.210+8802T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96704709 | ||||||
| chr5:96704822
|
A | T | 1 | a0001c0001t0001g0307 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.210+8915A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96704822 | ||||||
| chr5:96704933
|
G | A | 63 | a0001c0001t0001g0265a0001c0001t0001g0307a0001c0001t0001g0315others(60): Show | 67 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.210+9026G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96704933 | ||||||
| chr5:96705026
|
C | G | 41 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(38): Show | 44 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.210+9119C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96705026 | ||||||
| chr5:96705194
|
A | G | 1 | a0010c0016t0011g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.210+9287A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96705194 | ||||||
| chr5:96705208
|
A | G | 6 | a0002c0006t0001g0040a0002c0006t0001g0041a0005c0010t0014g0043others(3): Show | 6 | HG01109.hp2 HG02723.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+9301A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96705208 | ||||||
| chr5:96705318
|
A | G | 1 | a0002c0004t0001g0113 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.210+9411A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96705318 | ||||||
| chr5:96705499
|
G | C | 1 | a0010c0016t0011g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.210+9592G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96705499 | ||||||
| chr5:96705508
|
A | G | 1 | a0001c0002t0001g0245 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.210+9601A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96705508 | ||||||
| chr5:96705546
|
G | C | 1 | a0001c0001t0002g0095 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.210+9639G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96705546 | ||||||
| chr5:96705634
|
A | G | 2 | a0002c0004t0021g0233a0002c0013t0001g0234 | 2 | HG01891.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.210+9727A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96705634 | ||||||
| chr5:96705790
|
G | A | 7 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(4): Show | 7 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.210+9883G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96705790 | ||||||
| chr5:96705896
|
C | G | 1 | a0001c0001t0001g0127 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.210+9989C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96705896 | ||||||
| chr5:96705959
|
C | T | 1 | a0001c0002t0001g0223 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.210+10052C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96705959 | ||||||
| chr5:96706067
|
T | C | 8 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(5): Show | 8 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.210+10160T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96706067 | ||||||
| chr5:96706075
|
C | A | 7 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(4): Show | 7 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.210+10168C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96706075 | ||||||
| chr5:96706391
|
T | C | 26 | a0001c0001t0002g0013a0001c0001t0004g0014a0001c0001t0004g0132others(23): Show | 29 | HG00280.hp1 HG00642.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.210+10484T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96706391 | ||||||
| chr5:96706475
|
G | A | 8 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(5): Show | 8 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.210+10568G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96706475 | ||||||
| chr5:96706598
|
T | C | 2 | a0002c0003t0003g0316a0002c0003t0003g0317 | 2 | NA18956.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.210+10691T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96706598 | ||||||
| chr5:96706616
|
G | A | 3 | a0001c0001t0002g0013a0002c0004t0013g0258a0002c0004t0013g0259 | 4 | HG02896.hp1 HG02897.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.210+10709G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96706616 | ||||||
| chr5:96706833
|
T | C | 1 | a0001c0002t0001g0231 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.210+10926T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96706833 | ||||||
| chr5:96706959
|
C | T | 1 | a0010c0016t0011g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.210+11052C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96706959 | ||||||
| chr5:96707024
|
C | G | 1 | a0001c0002t0001g0224 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.210+11117C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96707024 | ||||||
| chr5:96707024
|
C | T | 1 | a0010c0016t0011g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.210+11117C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96707024 | ||||||
| chr5:96707106
|
A | G | 1 | a0001c0001t0006g0279 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.210+11199A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96707106 | ||||||
| chr5:96707136
|
A | G | 117 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(114): Show | 125 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.210+11229A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96707136 | ||||||
| chr5:96707298
|
A | G | 1 | a0011c0026t0001g0017 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.210+11391A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96707298 | ||||||
| chr5:96707392
|
C | CT | 26 | a0001c0001t0002g0013a0001c0001t0004g0014a0001c0001t0004g0132others(23): Show | 29 | HG00280.hp1 HG00642.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.210+11497dupT | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 96707392 | |||||
| chr5:96707430
|
G | A | 1 | a0001c0001t0006g0279 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.210+11523G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96707430 | ||||||
| chr5:96707593
|
G | T | 21 | a0001c0001t0004g0014a0001c0001t0004g0132a0001c0001t0004g0133others(18): Show | 23 | HG00280.hp1 HG00642.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.210+11686G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96707593 | ||||||
| chr5:96707631
|
C | T | 1 | a0002c0013t0001g0191 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.210+11724C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96707631 | ||||||
| chr5:96707670
|
T | A | 9 | a0001c0005t0001g0244a0001c0005t0007g0242a0001c0005t0007g0243others(6): Show | 10 | HG02280.hp2 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.210+11763T>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96707670 | ||||||
| chr5:96707716
|
T | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(156): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.210+11809T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96707716 | ||||||
| chr5:96707771
|
T | C | 2 | a0007c0015t0012g0137a0007c0015t0012g0138 | 2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.210+11864T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96707771 | ||||||
| chr5:96707798
|
G | GT | 6 | a0001c0001t0002g0073a0001c0001t0002g0086a0001c0001t0002g0087others(3): Show | 6 | HG02015.hp1 NA18957.hp1 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.210+11892dupT | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 96707798 | |||||
| chr5:96707862
|
C | CTAGGATA others(8): Show |
7 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(4): Show | 7 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.210+11955_210+1195 others(19): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96707862 | ||||||
| chr5:96707862
|
C | T | 3 | a0001c0001t0002g0013a0002c0004t0013g0258a0002c0004t0013g0259 | 4 | HG02896.hp1 HG02897.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.210+11955C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96707862 | ||||||
| chr5:96708210
|
T | A | 7 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(4): Show | 7 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.210+12303T>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96708210 | ||||||
| chr5:96708297
|
A | G | 2 | a0001c0001t0001g0168a0001c0001t0001g0170 | 2 | NA18950.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.210+12390A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96708297 | ||||||
| chr5:96708356
|
G | C | 336 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(333): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.210+12449G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96708356 | ||||||
| chr5:96708411
|
G | T | 6 | a0001c0002t0001g0199a0001c0002t0001g0227a0001c0002t0001g0228others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+12504G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96708411 | ||||||
| chr5:96708597
|
C | G | 2 | a0002c0004t0021g0233a0002c0013t0001g0234 | 2 | HG01891.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.210+12690C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96708597 | ||||||
| chr5:96708763
|
T | C | 1 | a0001c0001t0002g0077 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.210+12856T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96708763 | ||||||
| chr5:96708808
|
A | C | 1 | a0002c0003t0003g0320 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.210+12901A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96708808 | ||||||
| chr5:96708977
|
G | A | 34 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(31): Show | 37 | HG00280.hp1 HG00642.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.210+13070G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96708977 | ||||||
| chr5:96709008
|
C | G | 3 | a0001c0011t0002g0102a0001c0011t0002g0103a0001c0011t0002g0104 | 3 | HG00741.hp1 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.210+13101C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96709008 | ||||||
| chr5:96709064
|
G | A | 1 | a0001c0005t0007g0251 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.210+13157G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96709064 | ||||||
| chr5:96709210
|
A | G | 41 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(38): Show | 44 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.210+13303A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96709210 | ||||||
| chr5:96709286
|
G | A | 7 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(4): Show | 7 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.211-13353G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96709286 | ||||||
| chr5:96709390
|
C | T | 1 | a0002c0004t0001g0282 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.211-13249C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96709390 | ||||||
| chr5:96709433
|
G | T | 340 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(337): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.211-13206G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96709433 | ||||||
| chr5:96709633
|
C | T | 6 | a0001c0021t0009g0035a0002c0004t0005g0027a0002c0004t0005g0030others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.211-13006C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96709633 | ||||||
| chr5:96709636
|
GCTTAT | G | 7 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(4): Show | 7 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.211-12996_211-1299 others(9): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 96709636 | |||||
| chr5:96709719
|
C | T | 1 | a0002c0004t0005g0027 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.211-12920C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96709719 | ||||||
| chr5:96709761
|
TA | T | 4 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(1): Show | 4 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-12877delA | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96709761 | ||||||
| chr5:96709846
|
T | C | 7 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(4): Show | 7 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.211-12793T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96709846 | ||||||
| chr5:96709881
|
G | A | 1 | a0010c0016t0011g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.211-12758G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96709881 | ||||||
| chr5:96709988
|
G | A | 1 | a0001c0001t0002g0078 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.211-12651G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96709988 | ||||||
| chr5:96710007
|
A | G | 6 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(3): Show | 6 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.211-12632A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96710007 | ||||||
| chr5:96710321
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.211-12318T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96710321 | ||||||
| chr5:96710327
|
TC | T | 7 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(4): Show | 7 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.211-12310delC | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 96710327 | |||||
| chr5:96710335
|
A | C | 184 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(181): Show | 195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.211-12304A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96710335 | ||||||
| chr5:96710342
|
A | G | 1 | a0001c0002t0001g0198 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.211-12297A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96710342 | ||||||
| chr5:96710346
|
C | G | 1 | a0002c0004t0001g0101 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.211-12293C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96710346 | ||||||
| chr5:96710349
|
A | G | 7 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(4): Show | 7 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.211-12290A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96710349 | ||||||
| chr5:96710571
|
C | T | 1 | a0011c0026t0001g0017 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.211-12068C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96710571 | ||||||
| chr5:96710715
|
G | A | 1 | a0010c0016t0011g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.211-11924G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96710715 | ||||||
| chr5:96710736
|
G | T | 3 | a0001c0001t0004g0014a0001c0001t0004g0269a0001c0001t0004g0285 | 4 | HG01070.hp1 HG01071.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-11903G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96710736 | ||||||
| chr5:96710868
|
T | TA | 19 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(16): Show | 19 | HG01243.hp1 HG02280.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.211-11759dupA | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 96710868 | |||||
| chr5:96710868
|
TA | T | 7 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(4): Show | 7 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.211-11759delA | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 96710868 | |||||
| chr5:96711081
|
C | T | 7 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(4): Show | 7 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.211-11558C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96711081 | ||||||
| chr5:96711120
|
T | G | 7 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(4): Show | 7 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.211-11519T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96711120 | ||||||
| chr5:96711150
|
T | G | 7 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(4): Show | 7 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.211-11489T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96711150 | ||||||
| chr5:96711208
|
A | G | 26 | a0001c0001t0002g0013a0001c0001t0004g0014a0001c0001t0004g0132others(23): Show | 29 | HG00280.hp1 HG00642.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.211-11431A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96711208 | ||||||
| chr5:96711260
|
G | A | 1 | a0001c0001t0002g0290 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.211-11379G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96711260 | ||||||
| chr5:96711404
|
G | A | 2 | a0001c0002t0001g0186a0001c0018t0010g0029 | 2 | HG01123.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.211-11235G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96711404 | ||||||
| chr5:96711425
|
T | C | 1 | a0006c0009t0008g0140 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.211-11214T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96711425 | ||||||
| chr5:96711533
|
T | C | 7 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(4): Show | 7 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.211-11106T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96711533 | ||||||
| chr5:96711667
|
T | C | 7 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(4): Show | 7 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.211-10972T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96711667 | ||||||
| chr5:96711750
|
T | G | 2 | a0007c0015t0012g0137a0007c0015t0012g0138 | 2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.211-10889T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96711750 | ||||||
| chr5:96711807
|
T | C | 7 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(4): Show | 7 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.211-10832T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96711807 | ||||||
| chr5:96711810
|
G | T | 7 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(4): Show | 7 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.211-10829G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96711810 | ||||||
| chr5:96711970
|
A | ATTG | 7 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(4): Show | 7 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.211-10667_211-1066 others(7): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 96711970 | |||||
| chr5:96711983
|
T | C | 7 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(4): Show | 7 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.211-10656T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96711983 | ||||||
| chr5:96712008
|
C | T | 2 | a0002c0003t0003g0326a0002c0003t0003g0327 | 2 | HG00639.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.211-10631C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96712008 | ||||||
| chr5:96712032
|
C | A | 1 | a0010c0016t0011g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.211-10607C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96712032 | ||||||
| chr5:96712070
|
T | C | 2 | a0002c0003t0003g0321a0002c0003t0003g0333 | 2 | HG00099.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.211-10569T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96712070 | ||||||
| chr5:96712307
|
C | A | 1 | a0002c0003t0002g0291 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.211-10332C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96712307 | ||||||
| chr5:96712317
|
C | G | 1 | a0010c0016t0011g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.211-10322C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96712317 | ||||||
| chr5:96712320
|
TTTTTC | T | 10 | a0001c0001t0002g0290a0001c0001t0002g0292a0001c0001t0002g0293others(7): Show | 12 | HG00423.hp1 HG02738.hp1 NA18942.hp1 others(9): Show |
intron_variant | MODIFIER | c.211-10304_211-1030 others(9): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 96712320 | |||||
| chr5:96712400
|
C | T | 2 | a0002c0004t0021g0233a0002c0013t0001g0234 | 2 | HG01891.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.211-10239C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96712400 | ||||||
| chr5:96712556
|
T | G | 3 | a0001c0001t0001g0068a0001c0001t0001g0079a0001c0001t0001g0097 | 3 | NA18946.hp2 NA18974.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.211-10083T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96712556 | ||||||
| chr5:96712632
|
A | G | 42 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(39): Show | 45 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.211-10007A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96712632 | ||||||
| chr5:96712727
|
C | T | 2 | a0002c0004t0021g0233a0002c0013t0001g0234 | 2 | HG01891.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.211-9912C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96712727 | ||||||
| chr5:96712761
|
TCC | T | 7 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(4): Show | 7 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.211-9875_211-9874d others(4): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 96712761 | |||||
| chr5:96712900
|
T | C | 33 | a0001c0001t0002g0013a0001c0001t0004g0014a0001c0001t0004g0132others(30): Show | 36 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.211-9739T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96712900 | ||||||
| chr5:96712995
|
A | G | 2 | a0001c0017t0001g0025a0004c0008t0011g0238 | 2 | HG01109.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.211-9644A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96712995 | ||||||
| chr5:96713010
|
G | A | 33 | a0001c0001t0002g0013a0001c0001t0004g0014a0001c0001t0004g0132others(30): Show | 36 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.211-9629G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96713010 | ||||||
| chr5:96713053
|
C | G | 1 | a0002c0003t0003g0016 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.211-9586C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96713053 | ||||||
| chr5:96713133
|
C | CT | 129 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(126): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.211-9489dupT | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 96713133 | |||||
| chr5:96713133
|
C | CTT | 16 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(13): Show | 17 | HG00738.hp1 HG01243.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.211-9490_211-9489d others(4): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 96713133 | |||||
| chr5:96713226
|
A | G | 33 | a0001c0001t0002g0013a0001c0001t0004g0014a0001c0001t0004g0132others(30): Show | 36 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.211-9413A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96713226 | ||||||
| chr5:96713239
|
C | T | 21 | a0001c0001t0004g0014a0001c0001t0004g0132a0001c0001t0004g0133others(18): Show | 23 | HG00280.hp1 HG00642.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.211-9400C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96713239 | ||||||
| chr5:96713281
|
G | T | 4 | a0002c0006t0001g0040a0002c0006t0001g0041a0005c0010t0014g0131others(1): Show | 4 | HG01109.hp2 HG02723.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-9358G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96713281 | ||||||
| chr5:96713515
|
A | G | 2 | a0001c0017t0001g0025a0004c0008t0011g0238 | 2 | HG01109.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.211-9124A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96713515 | ||||||
| chr5:96713836
|
G | T | 4 | a0002c0003t0003g0015a0002c0003t0003g0100a0002c0003t0003g0308others(1): Show | 5 | NA18946.hp1 NA18988.hp1 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.211-8803G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96713836 | ||||||
| chr5:96713939
|
C | A | 1 | a0001c0001t0001g0153 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.211-8700C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96713939 | ||||||
| chr5:96713989
|
C | G | 1 | a0001c0001t0001g0153 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.211-8650C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96713989 | ||||||
| chr5:96714026
|
G | T | 2 | a0001c0002t0001g0302a0001c0002t0001g0303 | 2 | NA18993.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.211-8613G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96714026 | ||||||
| chr5:96714366
|
G | A | 9 | a0001c0001t0002g0290a0001c0001t0002g0292a0001c0001t0002g0293others(6): Show | 11 | HG00423.hp1 NA18942.hp1 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.211-8273G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96714366 | ||||||
| chr5:96714737
|
GCT | G | 4 | a0001c0001t0007g0255a0003c0007t0002g0020a0003c0007t0002g0252others(1): Show | 4 | HG01891.hp1 HG02055.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-7901_211-7900d others(4): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96714737 | ||||||
| chr5:96714975
|
A | AG | 117 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(114): Show | 125 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.211-7663dupG | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 96714975 | |||||
| chr5:96715332
|
C | T | 3 | a0001c0001t0001g0051a0008c0014t0002g0110a0008c0014t0002g0111 | 3 | HG02922.hp1 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.211-7307C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96715332 | ||||||
| chr5:96715345
|
C | A | 1 | a0002c0004t0001g0282 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.211-7294C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96715345 | ||||||
| chr5:96715348
|
G | A | 1 | a0001c0001t0002g0210 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.211-7291G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96715348 | ||||||
| chr5:96715407
|
T | C | 6 | a0002c0006t0001g0040a0002c0006t0001g0041a0005c0010t0014g0043others(3): Show | 6 | HG01109.hp2 HG02723.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.211-7232T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96715407 | ||||||
| chr5:96715599
|
A | T | 1 | a0001c0002t0002g0301 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.211-7040A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96715599 | ||||||
| chr5:96715923
|
T | C | 7 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(4): Show | 7 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.211-6716T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96715923 | ||||||
| chr5:96715962
|
T | C | 2 | a0005c0010t0014g0043a0005c0010t0014g0044 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.211-6677T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96715962 | ||||||
| chr5:96716163
|
C | T | 2 | a0001c0002t0001g0163a0001c0002t0001g0164 | 2 | HG02698.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.211-6476C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96716163 | ||||||
| chr5:96716286
|
T | G | 67 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0012others(64): Show | 70 | HG00140.hp1 HG00544.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.211-6353T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96716286 | ||||||
| chr5:96716346
|
C | T | 76 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0068others(73): Show | 77 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.211-6293C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96716346 | ||||||
| chr5:96716566
|
T | C | 2 | a0002c0003t0001g0239a0002c0003t0001g0240 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.211-6073T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96716566 | ||||||
| chr5:96716717
|
T | A | 1 | a0002c0003t0001g0334 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.211-5922T>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96716717 | ||||||
| chr5:96716806
|
C | T | 340 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(337): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.211-5833C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96716806 | ||||||
| chr5:96716815
|
T | C | 1 | a0001c0001t0006g0010 | 2 | HG00280.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.211-5824T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96716815 | ||||||
| chr5:96717004
|
T | G | 1 | a0002c0013t0001g0191 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.211-5635T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96717004 | ||||||
| chr5:96717146
|
T | G | 21 | a0001c0001t0004g0014a0001c0001t0004g0132a0001c0001t0004g0133others(18): Show | 23 | HG00280.hp1 HG00642.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.211-5493T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96717146 | ||||||
| chr5:96717399
|
T | C | 1 | a0002c0013t0001g0191 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.211-5240T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96717399 | ||||||
| chr5:96717592
|
G | A | 1 | a0001c0001t0001g0176 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.211-5047G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96717592 | ||||||
| chr5:96717640
|
T | C | 82 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(79): Show | 87 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.211-4999T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96717640 | ||||||
| chr5:96717773
|
G | C | 1 | a0001c0001t0004g0136 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.211-4866G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96717773 | ||||||
| chr5:96717901
|
C | A | 115 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(112): Show | 123 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.211-4738C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96717901 | ||||||
| chr5:96718149
|
T | C | 26 | a0001c0001t0002g0013a0001c0001t0004g0014a0001c0001t0004g0132others(23): Show | 29 | HG00280.hp1 HG00642.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.211-4490T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96718149 | ||||||
| chr5:96718417
|
G | A | 2 | a0001c0001t0002g0066a0001c0001t0002g0096 | 2 | HG00642.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.211-4222G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96718417 | ||||||
| chr5:96718479
|
C | A | 8 | a0001c0005t0001g0244a0001c0005t0007g0242a0001c0005t0007g0243others(5): Show | 9 | HG02280.hp2 HG02559.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.211-4160C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96718479 | ||||||
| chr5:96718494
|
C | T | 2 | a0007c0015t0012g0137a0007c0015t0012g0138 | 2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.211-4145C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96718494 | ||||||
| chr5:96718545
|
T | TA | 20 | a0001c0001t0004g0014a0001c0001t0004g0132a0001c0001t0004g0133others(17): Show | 22 | HG00280.hp1 HG00642.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.211-4083dupA | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 96718545 | |||||
| chr5:96718552
|
A | T | 4 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(1): Show | 4 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-4087A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96718552 | ||||||
| chr5:96718637
|
C | T | 1 | a0002c0013t0001g0191 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.211-4002C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96718637 | ||||||
| chr5:96718654
|
C | G | 6 | a0002c0006t0001g0040a0002c0006t0001g0041a0005c0010t0014g0043others(3): Show | 6 | HG01109.hp2 HG02723.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.211-3985C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96718654 | ||||||
| chr5:96718683
|
T | C | 7 | a0001c0001t0007g0255a0002c0004t0001g0101a0003c0007t0002g0020others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.211-3956T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96718683 | ||||||
| chr5:96718691
|
A | C | 57 | a0001c0001t0001g0265a0001c0001t0001g0307a0001c0001t0001g0315others(54): Show | 61 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.211-3948A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96718691 | ||||||
| chr5:96718919
|
G | A | 1 | a0003c0007t0002g0112 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.211-3720G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96718919 | ||||||
| chr5:96718934
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.211-3705C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96718934 | ||||||
| chr5:96718945
|
A | C | 1 | a0002c0013t0001g0191 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.211-3694A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96718945 | ||||||
| chr5:96718956
|
G | A | 8 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(5): Show | 8 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.211-3683G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96718956 | ||||||
| chr5:96718981
|
C | G | 4 | a0002c0004t0001g0047a0002c0004t0001g0048a0002c0004t0001g0049others(1): Show | 4 | NA18991.hp1 NA19002.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-3658C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96718981 | ||||||
| chr5:96719093
|
C | A | 6 | a0001c0021t0009g0035a0002c0004t0005g0027a0002c0004t0005g0030others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.211-3546C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96719093 | ||||||
| chr5:96719114
|
G | A | 3 | a0002c0004t0005g0030a0002c0004t0005g0032a0002c0004t0005g0033 | 3 | HG02559.hp1 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.211-3525G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96719114 | ||||||
| chr5:96719133
|
C | T | 133 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0263others(130): Show | 140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.211-3506C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96719133 | ||||||
| chr5:96719443
|
G | A | 6 | a0001c0021t0009g0035a0002c0004t0005g0027a0002c0004t0005g0030others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.211-3196G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96719443 | ||||||
| chr5:96719698
|
G | A | 4 | a0001c0001t0002g0092a0001c0001t0002g0125a0001c0001t0006g0093others(1): Show | 4 | HG00735.hp1 HG01258.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-2941G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96719698 | ||||||
| chr5:96719739
|
G | A | 2 | a0002c0006t0001g0040a0002c0006t0001g0041 | 2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.211-2900G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96719739 | ||||||
| chr5:96719766
|
G | A | 101 | a0001c0001t0001g0253a0001c0001t0001g0265a0001c0001t0001g0315others(98): Show | 107 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.211-2873G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96719766 | ||||||
| chr5:96719772
|
A | C | 54 | a0001c0001t0001g0307a0001c0001t0002g0280a0001c0001t0002g0290others(51): Show | 58 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.211-2867A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96719772 | ||||||
| chr5:96719858
|
G | A | 6 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0058others(3): Show | 6 | HG02258.hp1 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.211-2781G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96719858 | ||||||
| chr5:96720170
|
A | G | 23 | a0001c0001t0001g0024a0001c0001t0001g0118a0001c0001t0001g0127others(20): Show | 23 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.211-2469A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96720170 | ||||||
| chr5:96720221
|
A | G | 9 | a0001c0005t0001g0244a0001c0005t0007g0242a0001c0005t0007g0243others(6): Show | 10 | HG02055.hp2 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.211-2418A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96720221 | ||||||
| chr5:96720227
|
T | A | 1 | a0002c0013t0001g0191 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.211-2412T>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96720227 | ||||||
| chr5:96720300
|
C | A | 67 | a0001c0001t0001g0154a0001c0001t0001g0265a0001c0001t0001g0286others(64): Show | 70 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.211-2339C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96720300 | ||||||
| chr5:96720305
|
T | G | 2 | a0002c0003t0003g0331a0003c0007t0002g0313 | 2 | HG01934.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.211-2334T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96720305 | ||||||
| chr5:96720370
|
A | C | 4 | a0001c0001t0002g0057a0001c0001t0002g0058a0001c0001t0002g0059others(1): Show | 4 | HG02258.hp1 HG02630.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-2269A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96720370 | ||||||
| chr5:96720415
|
G | T | 60 | a0001c0001t0002g0280a0001c0001t0002g0337a0001c0011t0002g0102others(57): Show | 64 | HG00099.hp2 HG00609.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.211-2224G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96720415 | ||||||
| chr5:96720507
|
C | T | 1 | a0001c0001t0002g0209 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.211-2132C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96720507 | ||||||
| chr5:96720636
|
C | T | 2 | a0001c0012t0012g0270a0010c0016t0011g0026 | 2 | HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.211-2003C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96720636 | ||||||
| chr5:96720648
|
T | C | 1 | a0011c0026t0001g0017 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.211-1991T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96720648 | ||||||
| chr5:96720655
|
C | G | 48 | a0001c0012t0001g0328a0001c0012t0001g0329a0001c0012t0012g0270others(45): Show | 52 | HG00099.hp2 HG00609.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.211-1984C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96720655 | ||||||
| chr5:96720669
|
G | C | 17 | a0001c0001t0004g0014a0001c0001t0004g0132a0001c0001t0004g0133others(14): Show | 19 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.211-1970G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96720669 | ||||||
| chr5:96720756
|
A | C | 1 | a0001c0001t0001g0165 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.211-1883A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96720756 | ||||||
| chr5:96720826
|
T | G | 1 | a0002c0003t0003g0339 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.211-1813T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96720826 | ||||||
| chr5:96720909
|
A | T | 2 | a0001c0002t0001g0012a0001c0002t0001g0248 | 3 | HG01515.hp1 HG01517.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.211-1730A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96720909 | ||||||
| chr5:96720964
|
C | G | 9 | a0001c0011t0002g0102a0001c0011t0002g0103a0001c0011t0002g0104others(6): Show | 9 | HG00738.hp1 HG00741.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.211-1675C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96720964 | ||||||
| chr5:96721295
|
C | CT | 3 | a0001c0001t0002g0013a0002c0004t0013g0258a0002c0004t0013g0259 | 4 | HG02896.hp1 HG02897.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-1343dupT | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 96721295 | |||||
| chr5:96721609
|
G | A | 67 | a0001c0001t0001g0169a0001c0001t0001g0265a0001c0001t0001g0286others(64): Show | 70 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.211-1030G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96721609 | ||||||
| chr5:96721867
|
G | C | 85 | a0001c0001t0001g0169a0001c0001t0001g0253a0001c0001t0001g0265others(82): Show | 88 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.211-772G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96721867 | ||||||
| chr5:96721938
|
T | G | 2 | a0001c0002t0001g0196a0001c0002t0001g0214 | 2 | NA18972.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.211-701T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96721938 | ||||||
| chr5:96721977
|
C | G | 1 | a0002c0004t0001g0053 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.211-662C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96721977 | ||||||
| chr5:96722014
|
C | T | 9 | a0001c0011t0002g0102a0001c0011t0002g0103a0001c0011t0002g0104others(6): Show | 9 | HG00738.hp1 HG00741.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.211-625C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96722014 | ||||||
| chr5:96722052
|
T | C | 1 | a0001c0017t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.211-587T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96722052 | ||||||
| chr5:96722178
|
G | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(204): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.211-461G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96722178 | ||||||
| chr5:96722187
|
C | T | 49 | a0001c0012t0001g0328a0001c0012t0001g0329a0001c0012t0012g0270others(46): Show | 53 | HG00099.hp2 HG00609.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.211-452C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96722187 | ||||||
| chr5:96722216
|
C | T | 1 | a0003c0007t0002g0050 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.211-423C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96722216 | ||||||
| chr5:96722380
|
G | T | 1 | a0002c0013t0001g0191 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.211-259G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96722380 | ||||||
| chr5:96722436
|
TAGC | T | 81 | a0001c0001t0001g0169a0001c0001t0001g0265a0001c0001t0001g0286others(78): Show | 85 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.211-200_211-198del others(3): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 96722436 | |||||
| chr5:96722604
|
G | A | 2 | a0001c0001t0003g0256a0001c0001t0003g0257 | 2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.211-35G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 3/31 | chr5 | 96722604 | ||||||
| chr5:96722778
|
A | G | 9 | a0001c0011t0002g0102a0001c0011t0002g0103a0001c0011t0002g0104others(6): Show | 9 | HG00738.hp1 HG00741.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.270+80A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96722778 | ||||||
| chr5:96722780
|
G | A | 1 | a0002c0003t0003g0321 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.270+82G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96722780 | ||||||
| chr5:96722896
|
A | C | 1 | a0001c0001t0002g0128 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.270+198A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96722896 | ||||||
| chr5:96722913
|
A | G | 6 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(3): Show | 6 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.270+215A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96722913 | ||||||
| chr5:96722934
|
G | GTTGTT | 42 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(39): Show | 47 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.270+260_270+264dup others(5): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr5 | 96722934 | |||||
| chr5:96722934
|
G | GTTGTTTT others(3): Show |
2 | a0001c0001t0001g0150a0001c0001t0001g0158 | 2 | NA18959.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.270+255_270+264dup others(10): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr5 | 96722934 | |||||
| chr5:96722934
|
GTTGTTTT others(3): Show |
G | 1 | a0002c0003t0003g0326 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.270+255_270+264del others(10): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr5 | 96722934 | |||||
| chr5:96723077
|
G | A | 1 | a0001c0001t0002g0095 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.270+379G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96723077 | ||||||
| chr5:96723116
|
T | TTTCGTTT others(1): Show |
8 | a0001c0005t0001g0244a0001c0005t0007g0242a0001c0005t0007g0243others(5): Show | 9 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.270+420_270+421ins others(8): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr5 | 96723116 | |||||
| chr5:96723139
|
T | C | 1 | a0002c0004t0001g0053 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.270+441T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96723139 | ||||||
| chr5:96723157
|
G | T | 46 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(43): Show | 51 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.270+459G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96723157 | ||||||
| chr5:96723197
|
C | T | 155 | a0001c0001t0001g0109a0001c0001t0001g0169a0001c0001t0001g0253others(152): Show | 163 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.270+499C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96723197 | ||||||
| chr5:96723206
|
C | A | 1 | a0001c0001t0001g0143 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.270+508C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96723206 | ||||||
| chr5:96723225
|
A | G | 1 | a0001c0017t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.270+527A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96723225 | ||||||
| chr5:96723399
|
G | T | 87 | a0001c0001t0001g0169a0001c0001t0001g0265a0001c0001t0001g0286others(84): Show | 91 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.270+701G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96723399 | ||||||
| chr5:96723402
|
C | T | 235 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(232): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.270+704C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96723402 | ||||||
| chr5:96723571
|
T | A | 1 | a0011c0026t0001g0017 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.270+873T>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96723571 | ||||||
| chr5:96723646
|
C | T | 1 | a0006c0009t0008g0141 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.270+948C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96723646 | ||||||
| chr5:96724010
|
C | G | 5 | a0001c0001t0001g0024a0001c0001t0001g0127a0001c0001t0001g0129others(2): Show | 5 | HG02451.hp1 HG02976.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.270+1312C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96724010 | ||||||
| chr5:96724028
|
C | T | 1 | a0001c0001t0002g0091 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.270+1330C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96724028 | ||||||
| chr5:96724141
|
G | A | 1 | a0001c0002t0001g0215 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.270+1443G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96724141 | ||||||
| chr5:96724186
|
C | CT | 57 | a0001c0001t0001g0253a0001c0001t0002g0262a0001c0001t0003g0256others(54): Show | 61 | HG00099.hp2 HG00609.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.270+1497dupT | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr5 | 96724186 | |||||
| chr5:96724191
|
T | C | 17 | a0001c0001t0004g0014a0001c0001t0004g0132a0001c0001t0004g0133others(14): Show | 19 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.270+1493T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96724191 | ||||||
| chr5:96724248
|
A | T | 4 | a0001c0001t0002g0055a0001c0001t0002g0071a0001c0001t0002g0083others(1): Show | 4 | HG02135.hp2 NA18977.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.270+1550A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96724248 | ||||||
| chr5:96724429
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.270+1731C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96724429 | ||||||
| chr5:96724440
|
C | A | 1 | a0001c0002t0001g0163 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.270+1742C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96724440 | ||||||
| chr5:96724538
|
G | T | 4 | a0002c0004t0003g0297a0002c0004t0003g0298a0002c0004t0003g0299others(1): Show | 4 | HG00741.hp2 HG01070.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+1840G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96724538 | ||||||
| chr5:96724541
|
C | G | 2 | a0001c0001t0001g0166a0001c0001t0001g0167 | 2 | NA18967.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.270+1843C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96724541 | ||||||
| chr5:96724558
|
T | C | 161 | a0001c0001t0001g0109a0001c0001t0001g0169a0001c0001t0001g0253others(158): Show | 169 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.270+1860T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96724558 | ||||||
| chr5:96724602
|
G | A | 17 | a0001c0001t0004g0014a0001c0001t0004g0132a0001c0001t0004g0133others(14): Show | 19 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.270+1904G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96724602 | ||||||
| chr5:96724610
|
C | T | 2 | a0002c0004t0001g0101a0004c0008t0011g0238 | 2 | HG01109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.270+1912C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96724610 | ||||||
| chr5:96724651
|
C | T | 17 | a0001c0001t0004g0014a0001c0001t0004g0132a0001c0001t0004g0133others(14): Show | 19 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.270+1953C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96724651 | ||||||
| chr5:96724824
|
AAAAT | A | 223 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(220): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.271-1943_271-1940d others(6): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr5 | 96724824 | |||||
| chr5:96724874
|
C | A | 3 | a0001c0011t0002g0102a0001c0011t0002g0103a0001c0011t0002g0104 | 3 | HG00741.hp1 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.271-1920C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96724874 | ||||||
| chr5:96724888
|
A | G | 48 | a0001c0012t0001g0328a0001c0012t0001g0329a0001c0012t0012g0270others(45): Show | 52 | HG00099.hp2 HG00609.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.271-1906A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96724888 | ||||||
| chr5:96725034
|
T | C | 17 | a0001c0001t0004g0014a0001c0001t0004g0132a0001c0001t0004g0133others(14): Show | 19 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.271-1760T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96725034 | ||||||
| chr5:96725124
|
G | T | 5 | a0001c0012t0001g0328a0001c0012t0001g0329a0002c0003t0003g0016others(2): Show | 6 | HG01257.hp2 HG01258.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.271-1670G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96725124 | ||||||
| chr5:96725379
|
G | A | 1 | a0001c0001t0002g0226 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.271-1415G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96725379 | ||||||
| chr5:96725476
|
C | G | 9 | a0001c0011t0002g0102a0001c0011t0002g0103a0001c0011t0002g0104others(6): Show | 9 | HG00738.hp1 HG00741.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.271-1318C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96725476 | ||||||
| chr5:96725616
|
T | C | 43 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(40): Show | 48 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.271-1178T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96725616 | ||||||
| chr5:96725860
|
T | C | 1 | a0001c0001t0006g0273 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.271-934T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96725860 | ||||||
| chr5:96725924
|
A | C | 1 | a0001c0001t0010g0028 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.271-870A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96725924 | ||||||
| chr5:96725995
|
C | T | 50 | a0001c0012t0001g0328a0001c0012t0001g0329a0001c0012t0012g0270others(47): Show | 54 | HG00099.hp2 HG00609.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.271-799C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96725995 | ||||||
| chr5:96726232
|
GTACT | G | 8 | a0001c0001t0009g0336a0002c0004t0005g0027a0002c0004t0005g0030others(5): Show | 8 | HG01891.hp2 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.271-556_271-553del others(4): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr5 | 96726232 | |||||
| chr5:96726345
|
C | T | 1 | a0002c0004t0001g0101 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.271-449C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96726345 | ||||||
| chr5:96726526
|
G | A | 1 | a0002c0003t0003g0314 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.271-268G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96726526 | ||||||
| chr5:96726632
|
G | C | 8 | a0001c0005t0001g0244a0001c0005t0007g0242a0001c0005t0007g0243others(5): Show | 9 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.271-162G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96726632 | ||||||
| chr5:96726751
|
C | T | 1 | a0001c0001t0009g0336 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.271-43C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 4/31 | chr5 | 96726751 | ||||||
| chr5:96726913
|
C | T | 15 | a0001c0001t0004g0014a0001c0001t0004g0133a0001c0001t0004g0134others(12): Show | 17 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.336+54C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 5/31 | chr5 | 96726913 | ||||||
| chr5:96726914
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0006g0010 | 4 | HG00099.hp1 HG00280.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.336+55G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 5/31 | chr5 | 96726914 | ||||||
| chr5:96727253
|
T | C | 55 | a0001c0001t0001g0253a0001c0001t0002g0262a0001c0001t0003g0256others(52): Show | 59 | HG00099.hp2 HG00609.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.337-236T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 5/31 | chr5 | 96727253 | ||||||
| chr5:96727539
|
T | C | 1 | a0002c0003t0003g0340 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.378+9T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 6/31 | chr5 | 96727539 | ||||||
| chr5:96727711
|
G | A | 9 | a0001c0011t0002g0102a0001c0011t0002g0103a0001c0011t0002g0104others(6): Show | 9 | HG00738.hp1 HG00741.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.378+181G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 6/31 | chr5 | 96727711 | ||||||
| chr5:96727791
|
T | C | 1 | a0001c0001t0002g0280 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.378+261T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 6/31 | chr5 | 96727791 | ||||||
| chr5:96727798
|
A | G | 55 | a0001c0001t0001g0253a0001c0001t0002g0262a0001c0001t0003g0256others(52): Show | 59 | HG00099.hp2 HG00609.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.378+268A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 6/31 | chr5 | 96727798 | ||||||
| chr5:96727884
|
A | G | 4 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(1): Show | 4 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+354A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 6/31 | chr5 | 96727884 | ||||||
| chr5:96727932
|
T | C | 1 | a0001c0001t0001g0286 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.378+402T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 6/31 | chr5 | 96727932 | ||||||
| chr5:96727974
|
G | A | 8 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0058others(5): Show | 8 | HG02258.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.378+444G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 6/31 | chr5 | 96727974 | ||||||
| chr5:96727992
|
T | A | 1 | a0001c0001t0001g0322 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.378+462T>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 6/31 | chr5 | 96727992 | ||||||
| chr5:96728016
|
A | C | 1 | a0001c0001t0001g0123 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.378+486A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 6/31 | chr5 | 96728016 | ||||||
| chr5:96728020
|
G | A | 48 | a0001c0012t0001g0328a0001c0012t0001g0329a0001c0012t0012g0270others(45): Show | 52 | HG00099.hp2 HG00609.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.378+490G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 6/31 | chr5 | 96728020 | ||||||
| chr5:96728084
|
A | G | 9 | a0001c0001t0001g0109a0001c0001t0007g0255a0002c0004t0005g0190others(6): Show | 9 | HG01255.hp1 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.378+554A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 6/31 | chr5 | 96728084 | ||||||
| chr5:96728170
|
C | G | 73 | a0001c0001t0001g0169a0001c0001t0001g0265a0001c0001t0001g0286others(70): Show | 76 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.378+640C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 6/31 | chr5 | 96728170 | ||||||
| chr5:96728364
|
A | G | 1 | a0001c0001t0002g0209 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.379-789A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 6/31 | chr5 | 96728364 | ||||||
| chr5:96728473
|
G | GT | 22 | a0001c0001t0001g0143a0001c0001t0001g0154a0001c0001t0001g0173others(19): Show | 22 | HG00642.hp1 HG02015.hp1 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.379-665dupT | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr5 | 96728473 | |||||
| chr5:96728473
|
G | GTT | 8 | a0001c0001t0002g0089a0001c0011t0002g0102a0001c0011t0002g0103others(5): Show | 8 | HG00738.hp1 HG00741.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.379-666_379-665dup others(2): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr5 | 96728473 | |||||
| chr5:96728473
|
GT | G | 73 | a0001c0001t0001g0109a0001c0001t0001g0253a0001c0001t0002g0262others(70): Show | 78 | HG00099.hp2 HG00609.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.379-665delT | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr5 | 96728473 | |||||
| chr5:96728567
|
C | T | 17 | a0001c0001t0004g0014a0001c0001t0004g0132a0001c0001t0004g0133others(14): Show | 19 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.379-586C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 6/31 | chr5 | 96728567 | ||||||
| chr5:96728575
|
C | T | 9 | a0001c0011t0002g0102a0001c0011t0002g0103a0001c0011t0002g0104others(6): Show | 9 | HG00738.hp1 HG00741.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.379-578C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 6/31 | chr5 | 96728575 | ||||||
| chr5:96728622
|
A | G | 52 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(49): Show | 57 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.379-531A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 6/31 | chr5 | 96728622 | ||||||
| chr5:96728654
|
T | C | 1 | a0002c0004t0001g0101 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.379-499T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 6/31 | chr5 | 96728654 | ||||||
| chr5:96728670
|
G | A | 1 | a0001c0002t0001g0214 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.379-483G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 6/31 | chr5 | 96728670 | ||||||
| chr5:96728697
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.379-456T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 6/31 | chr5 | 96728697 | ||||||
| chr5:96728799
|
G | A | 9 | a0001c0011t0002g0102a0001c0011t0002g0103a0001c0011t0002g0104others(6): Show | 9 | HG00738.hp1 HG00741.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.379-354G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 6/31 | chr5 | 96728799 | ||||||
| chr5:96728804
|
G | A | 1 | a0002c0003t0003g0324 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.379-349G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 6/31 | chr5 | 96728804 | ||||||
| chr5:96728929
|
A | C | 73 | a0001c0001t0001g0169a0001c0001t0001g0265a0001c0001t0001g0286others(70): Show | 76 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.379-224A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 6/31 | chr5 | 96728929 | ||||||
| chr5:96728966
|
A | G | 4 | a0001c0001t0002g0057a0001c0001t0002g0058a0001c0001t0002g0059others(1): Show | 4 | HG02258.hp1 HG02630.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.379-187A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 6/31 | chr5 | 96728966 | ||||||
| chr5:96728992
|
T | G | 3 | a0001c0011t0002g0102a0001c0011t0002g0103a0001c0011t0002g0104 | 3 | HG00741.hp1 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.379-161T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 6/31 | chr5 | 96728992 | ||||||
| chr5:96729011
|
A | T | 73 | a0001c0001t0001g0169a0001c0001t0001g0265a0001c0001t0001g0286others(70): Show | 76 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.379-142A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 6/31 | chr5 | 96729011 | ||||||
| chr5:96729458
|
C | A | 4 | a0001c0005t0001g0244a0001c0005t0007g0242a0001c0005t0007g0243others(1): Show | 4 | HG02559.hp2 HG03579.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-154C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 7/31 | chr5 | 96729458 | ||||||
| chr5:96729508
|
A | T | 4 | a0001c0005t0001g0244a0001c0005t0007g0242a0001c0005t0007g0243others(1): Show | 4 | HG02559.hp2 HG03579.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-104A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 7/31 | chr5 | 96729508 | ||||||
| chr5:96729774
|
A | G | 3 | a0001c0011t0002g0102a0001c0011t0002g0103a0001c0011t0002g0104 | 3 | HG00741.hp1 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.549+49A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 8/31 | chr5 | 96729774 | ||||||
| chr5:96729789
|
G | C | 2 | a0002c0003t0003g0316a0002c0003t0003g0317 | 2 | NA18956.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.549+64G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 8/31 | chr5 | 96729789 | ||||||
| chr5:96729932
|
A | G | 17 | a0001c0001t0004g0014a0001c0001t0004g0132a0001c0001t0004g0133others(14): Show | 19 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.549+207A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 8/31 | chr5 | 96729932 | ||||||
| chr5:96729958
|
C | T | 9 | a0001c0001t0001g0109a0001c0001t0007g0255a0002c0004t0005g0190others(6): Show | 9 | HG01255.hp1 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.549+233C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 8/31 | chr5 | 96729958 | ||||||
| chr5:96730023
|
A | ACAGCAGA others(11): Show |
10 | a0001c0012t0001g0328a0001c0012t0001g0329a0002c0003t0002g0289others(7): Show | 13 | HG01257.hp2 HG01258.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.549+301_549+302ins others(18): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 8/31 | INFO_REALIGN_3_PRIME | chr5 | 96730023 | |||||
| chr5:96730027
|
G | A | 10 | a0001c0012t0001g0328a0001c0012t0001g0329a0002c0003t0002g0289others(7): Show | 13 | HG01257.hp2 HG01258.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.549+302G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 8/31 | chr5 | 96730027 | ||||||
| chr5:96730237
|
A | G | 4 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0261others(1): Show | 4 | HG02451.hp1 HG03579.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.549+512A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 8/31 | chr5 | 96730237 | ||||||
| chr5:96730265
|
G | C | 4 | a0001c0001t0001g0253a0001c0001t0002g0262a0002c0004t0003g0124others(1): Show | 4 | HG01243.hp1 HG02280.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.550-515G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 8/31 | chr5 | 96730265 | ||||||
| chr5:96730516
|
C | G | 1 | a0001c0002t0001g0247 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.550-264C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 8/31 | chr5 | 96730516 | ||||||
| chr5:96730633
|
C | T | 3 | a0001c0011t0002g0102a0001c0011t0002g0103a0001c0011t0002g0104 | 3 | HG00741.hp1 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.550-147C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 8/31 | chr5 | 96730633 | ||||||
| chr5:96730662
|
C | A | 17 | a0001c0001t0004g0014a0001c0001t0004g0132a0001c0001t0004g0133others(14): Show | 19 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.550-118C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 8/31 | chr5 | 96730662 | ||||||
| chr5:96730872
|
C | G | 17 | a0001c0001t0004g0014a0001c0001t0004g0132a0001c0001t0004g0133others(14): Show | 19 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.630+12C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96730872 | ||||||
| chr5:96730885
|
A | G | 1 | a0010c0016t0011g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.630+25A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96730885 | ||||||
| chr5:96730897
|
G | A | 1 | a0006c0009t0008g0141 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.630+37G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96730897 | ||||||
| chr5:96730948
|
C | T | 223 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(220): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.630+88C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96730948 | ||||||
| chr5:96731324
|
A | G | 2 | a0001c0001t0001g0143a0001c0001t0001g0149 | 2 | NA19000.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.630+464A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96731324 | ||||||
| chr5:96731426
|
TCTACCCA others(5): Show |
T | 16 | a0001c0001t0004g0014a0001c0001t0004g0132a0001c0001t0004g0133others(13): Show | 18 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.630+567_630+578del others(12): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96731426 | ||||||
| chr5:96731442
|
T | C | 1 | a0001c0001t0002g0054 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.630+582T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96731442 | ||||||
| chr5:96731463
|
A | C | 1 | a0002c0003t0003g0310 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.630+603A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96731463 | ||||||
| chr5:96731473
|
G | GT | 30 | a0001c0001t0001g0109a0001c0001t0002g0088a0001c0001t0002g0089others(27): Show | 31 | HG00423.hp1 HG00741.hp1 HG01934.hp2 others(28): Show |
intron_variant | MODIFIER | c.630+630dupT | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr5 | 96731473 | |||||
| chr5:96731473
|
G | GTT | 12 | a0001c0001t0002g0073a0001c0001t0007g0255a0002c0004t0005g0190others(9): Show | 12 | HG00738.hp1 HG01255.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.630+629_630+630dup others(2): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr5 | 96731473 | |||||
| chr5:96731473
|
GT | G | 40 | a0001c0001t0001g0167a0001c0001t0001g0173a0001c0001t0001g0253others(37): Show | 42 | HG00323.hp1 HG00609.hp1 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.630+630delT | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr5 | 96731473 | |||||
| chr5:96731473
|
GTT | G | 60 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(57): Show | 67 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.630+629_630+630del others(2): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr5 | 96731473 | |||||
| chr5:96731512
|
T | G | 17 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0145others(14): Show | 18 | HG01167.hp1 HG01255.hp2 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.630+652T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96731512 | ||||||
| chr5:96731636
|
A | G | 8 | a0001c0005t0001g0244a0001c0005t0007g0242a0001c0005t0007g0243others(5): Show | 9 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.630+776A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96731636 | ||||||
| chr5:96731678
|
G | A | 16 | a0001c0001t0004g0014a0001c0001t0004g0132a0001c0001t0004g0133others(13): Show | 18 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.630+818G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96731678 | ||||||
| chr5:96731729
|
A | G | 1 | a0002c0013t0001g0191 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.630+869A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96731729 | ||||||
| chr5:96731731
|
G | C | 235 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(232): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.630+871G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96731731 | ||||||
| chr5:96731748
|
C | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(44): Show | 52 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.630+888C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96731748 | ||||||
| chr5:96731749
|
G | A | 9 | a0001c0001t0001g0109a0001c0001t0007g0255a0002c0004t0005g0190others(6): Show | 9 | HG01255.hp1 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.630+889G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96731749 | ||||||
| chr5:96731771
|
C | T | 4 | a0001c0001t0002g0070a0001c0001t0002g0077a0001c0001t0002g0092others(1): Show | 4 | HG03491.hp1 HG03669.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.630+911C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96731771 | ||||||
| chr5:96731784
|
A | G | 14 | a0001c0001t0001g0118a0002c0004t0001g0047a0002c0004t0001g0048others(11): Show | 14 | HG01346.hp1 HG02486.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.630+924A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96731784 | ||||||
| chr5:96731803
|
T | C | 86 | a0001c0001t0001g0169a0001c0001t0001g0253a0001c0001t0001g0265others(83): Show | 89 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.630+943T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96731803 | ||||||
| chr5:96731925
|
G | A | 3 | a0001c0001t0002g0013a0002c0004t0013g0258a0002c0004t0013g0259 | 4 | HG02896.hp1 HG02897.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.630+1065G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96731925 | ||||||
| chr5:96732006
|
T | G | 9 | a0001c0001t0001g0109a0001c0001t0007g0255a0002c0004t0005g0190others(6): Show | 9 | HG01255.hp1 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.630+1146T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96732006 | ||||||
| chr5:96732021
|
A | C | 1 | a0010c0016t0011g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.630+1161A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96732021 | ||||||
| chr5:96732037
|
C | G | 1 | a0011c0026t0001g0017 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.630+1177C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96732037 | ||||||
| chr5:96732072
|
C | T | 82 | a0001c0001t0001g0169a0001c0001t0001g0265a0001c0001t0001g0286others(79): Show | 86 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.630+1212C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96732072 | ||||||
| chr5:96732092
|
G | T | 235 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(232): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.630+1232G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96732092 | ||||||
| chr5:96732108
|
CA | C | 7 | a0002c0004t0005g0027a0002c0004t0005g0030a0002c0004t0005g0031others(4): Show | 7 | HG01891.hp2 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.630+1249delA | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96732108 | ||||||
| chr5:96732281
|
T | C | 2 | a0007c0015t0012g0137a0007c0015t0012g0138 | 2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.630+1421T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96732281 | ||||||
| chr5:96732329
|
C | T | 1 | a0001c0001t0002g0209 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.630+1469C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96732329 | ||||||
| chr5:96732354
|
G | C | 1 | a0002c0004t0001g0113 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.630+1494G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96732354 | ||||||
| chr5:96732500
|
T | G | 5 | a0001c0001t0001g0024a0001c0001t0001g0127a0001c0001t0001g0129others(2): Show | 5 | HG02451.hp1 HG02976.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.630+1640T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96732500 | ||||||
| chr5:96732531
|
G | T | 223 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(220): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.630+1671G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96732531 | ||||||
| chr5:96732627
|
A | G | 3 | a0001c0001t0002g0013a0002c0004t0013g0258a0002c0004t0013g0259 | 4 | HG02896.hp1 HG02897.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.630+1767A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96732627 | ||||||
| chr5:96732710
|
G | A | 16 | a0001c0001t0004g0014a0001c0001t0004g0132a0001c0001t0004g0133others(13): Show | 18 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.630+1850G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96732710 | ||||||
| chr5:96732807
|
C | T | 1 | a0001c0002t0001g0227 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.630+1947C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96732807 | ||||||
| chr5:96732830
|
A | T | 1 | a0002c0003t0003g0314 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.630+1970A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96732830 | ||||||
| chr5:96733022
|
G | GT | 8 | a0001c0005t0001g0244a0001c0005t0007g0242a0001c0005t0007g0243others(5): Show | 9 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.630+2163dupT | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr5 | 96733022 | |||||
| chr5:96733063
|
T | C | 161 | a0001c0001t0001g0109a0001c0001t0001g0169a0001c0001t0001g0253others(158): Show | 169 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.630+2203T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96733063 | ||||||
| chr5:96733428
|
T | G | 1 | a0002c0003t0001g0334 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.630+2568T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96733428 | ||||||
| chr5:96733543
|
G | A | 1 | a0001c0021t0009g0035 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.631-2629G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96733543 | ||||||
| chr5:96733591
|
G | A | 14 | a0001c0001t0001g0051a0001c0001t0001g0108a0001c0001t0002g0036others(11): Show | 14 | HG00323.hp1 HG01074.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.631-2581G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96733591 | ||||||
| chr5:96733676
|
A | G | 223 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(220): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.631-2496A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96733676 | ||||||
| chr5:96733781
|
G | T | 2 | a0007c0015t0012g0137a0007c0015t0012g0138 | 2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.631-2391G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96733781 | ||||||
| chr5:96733817
|
C | T | 9 | a0001c0011t0002g0102a0001c0011t0002g0103a0001c0011t0002g0104others(6): Show | 9 | HG00738.hp1 HG00741.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.631-2355C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96733817 | ||||||
| chr5:96733957
|
G | C | 9 | a0001c0011t0002g0102a0001c0011t0002g0103a0001c0011t0002g0104others(6): Show | 9 | HG00738.hp1 HG00741.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.631-2215G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96733957 | ||||||
| chr5:96733973
|
A | G | 1 | a0002c0004t0001g0282 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.631-2199A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96733973 | ||||||
| chr5:96733975
|
T | G | 9 | a0001c0011t0002g0102a0001c0011t0002g0103a0001c0011t0002g0104others(6): Show | 9 | HG00738.hp1 HG00741.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.631-2197T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96733975 | ||||||
| chr5:96734180
|
G | A | 1 | a0002c0003t0003g0314 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.631-1992G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96734180 | ||||||
| chr5:96734224
|
G | A | 1 | a0001c0002t0002g0301 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.631-1948G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96734224 | ||||||
| chr5:96734227
|
A | C | 2 | a0001c0001t0001g0143a0001c0001t0001g0149 | 2 | NA19000.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.631-1945A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96734227 | ||||||
| chr5:96734345
|
C | T | 9 | a0001c0001t0001g0109a0001c0001t0007g0255a0002c0004t0005g0190others(6): Show | 9 | HG01255.hp1 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.631-1827C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96734345 | ||||||
| chr5:96734501
|
T | C | 161 | a0001c0001t0001g0109a0001c0001t0001g0169a0001c0001t0001g0253others(158): Show | 169 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.631-1671T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96734501 | ||||||
| chr5:96734545
|
A | T | 9 | a0001c0011t0002g0102a0001c0011t0002g0103a0001c0011t0002g0104others(6): Show | 9 | HG00738.hp1 HG00741.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.631-1627A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96734545 | ||||||
| chr5:96734616
|
G | A | 8 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0058others(5): Show | 8 | HG02258.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.631-1556G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96734616 | ||||||
| chr5:96734623
|
G | A | 9 | a0001c0001t0001g0109a0001c0001t0007g0255a0002c0004t0005g0190others(6): Show | 9 | HG01255.hp1 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.631-1549G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96734623 | ||||||
| chr5:96735005
|
G | A | 1 | a0002c0013t0001g0191 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.631-1167G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96735005 | ||||||
| chr5:96735216
|
T | G | 1 | a0010c0016t0011g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.631-956T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96735216 | ||||||
| chr5:96735278
|
A | G | 235 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(232): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.631-894A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96735278 | ||||||
| chr5:96735293
|
T | C | 1 | a0001c0002t0001g0008 | 2 | NA18964.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.631-879T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96735293 | ||||||
| chr5:96735322
|
C | T | 84 | a0001c0001t0001g0169a0001c0001t0001g0265a0001c0001t0001g0286others(81): Show | 88 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.631-850C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96735322 | ||||||
| chr5:96735375
|
C | T | 2 | a0001c0002t0001g0183a0012c0025t0001g0019 | 2 | NA19000.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.631-797C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96735375 | ||||||
| chr5:96735490
|
T | C | 54 | a0001c0001t0001g0253a0001c0001t0002g0262a0001c0001t0003g0256others(51): Show | 58 | HG00099.hp2 HG00609.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.631-682T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96735490 | ||||||
| chr5:96735533
|
A | G | 3 | a0001c0011t0002g0102a0001c0011t0002g0103a0001c0011t0002g0104 | 3 | HG00741.hp1 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.631-639A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96735533 | ||||||
| chr5:96735589
|
G | A | 9 | a0001c0001t0001g0109a0001c0001t0007g0255a0002c0004t0005g0190others(6): Show | 9 | HG01255.hp1 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.631-583G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96735589 | ||||||
| chr5:96735596
|
A | G | 3 | a0001c0001t0002g0013a0002c0004t0013g0258a0002c0004t0013g0259 | 4 | HG02896.hp1 HG02897.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.631-576A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96735596 | ||||||
| chr5:96735832
|
G | A | 46 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(43): Show | 51 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.631-340G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96735832 | ||||||
| chr5:96736076
|
A | G | 48 | a0001c0012t0001g0328a0001c0012t0001g0329a0001c0012t0012g0270others(45): Show | 52 | HG00099.hp2 HG00609.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.631-96A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96736076 | ||||||
| chr5:96736137
|
A | G | 9 | a0001c0011t0002g0102a0001c0011t0002g0103a0001c0011t0002g0104others(6): Show | 9 | HG00738.hp1 HG00741.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.631-35A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 9/31 | chr5 | 96736137 | ||||||
| chr5:96736453
|
A | T | 49 | a0001c0012t0001g0328a0001c0012t0001g0329a0001c0012t0012g0270others(46): Show | 53 | HG00099.hp2 HG00609.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.699+213A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 10/31 | chr5 | 96736453 | ||||||
| chr5:96736458
|
AAAAC | A | 49 | a0001c0012t0001g0328a0001c0012t0001g0329a0001c0012t0012g0270others(46): Show | 53 | HG00099.hp2 HG00609.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.699+227_699+230del others(4): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 10/31 | INFO_REALIGN_3_PRIME | chr5 | 96736458 | |||||
| chr5:96736462
|
C | A | 1 | a0001c0001t0002g0060 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.699+222C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 10/31 | chr5 | 96736462 | ||||||
| chr5:96736490
|
G | A | 3 | a0001c0001t0002g0262a0002c0004t0003g0124a0002c0004t0003g0260 | 3 | HG01243.hp1 HG02280.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.699+250G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 10/31 | chr5 | 96736490 | ||||||
| chr5:96736602
|
A | C | 1 | a0002c0004t0005g0030 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.699+362A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 10/31 | chr5 | 96736602 | ||||||
| chr5:96736614
|
A | G | 1 | a0010c0016t0011g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.699+374A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 10/31 | chr5 | 96736614 | ||||||
| chr5:96736676
|
CA | C | 58 | a0001c0011t0002g0102a0001c0011t0002g0103a0001c0011t0002g0104others(55): Show | 62 | HG00099.hp2 HG00609.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.699+446delA | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 10/31 | INFO_REALIGN_3_PRIME | chr5 | 96736676 | |||||
| chr5:96736691
|
A | G | 1 | a0001c0002t0001g0164 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.699+451A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 10/31 | chr5 | 96736691 | ||||||
| chr5:96736744
|
T | C | 1 | a0002c0003t0003g0016 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.699+504T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 10/31 | chr5 | 96736744 | ||||||
| chr5:96736817
|
C | CT | 4 | a0001c0005t0009g0007a0001c0005t0009g0189a0002c0022t0013g0188others(1): Show | 5 | HG02615.hp1 HG02630.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.699+579dupT | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 10/31 | INFO_REALIGN_3_PRIME | chr5 | 96736817 | |||||
| chr5:96736851
|
G | GTTATAAA others(23): Show |
1 | a0001c0001t0002g0065 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.699+622_699+651dup others(30): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 10/31 | INFO_REALIGN_3_PRIME | chr5 | 96736851 | |||||
| chr5:96736928
|
G | A | 3 | a0001c0011t0002g0102a0001c0011t0002g0103a0001c0011t0002g0104 | 3 | HG00741.hp1 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.699+688G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 10/31 | chr5 | 96736928 | ||||||
| chr5:96736994
|
G | C | 1 | a0001c0001t0004g0014 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.699+754G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 10/31 | chr5 | 96736994 | ||||||
| chr5:96737322
|
C | A | 40 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(37): Show | 45 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.700-527C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 10/31 | chr5 | 96737322 | ||||||
| chr5:96737322
|
C | CA | 96 | a0001c0001t0001g0169a0001c0001t0001g0173a0001c0001t0001g0176others(93): Show | 100 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.700-518dupA | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 10/31 | INFO_REALIGN_3_PRIME | chr5 | 96737322 | |||||
| chr5:96737325
|
A | C | 1 | a0010c0016t0011g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.700-524A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 10/31 | chr5 | 96737325 | ||||||
| chr5:96737333
|
A | G | 9 | a0001c0001t0001g0109a0001c0001t0007g0255a0002c0004t0005g0190others(6): Show | 9 | HG01255.hp1 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.700-516A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 10/31 | chr5 | 96737333 | ||||||
| chr5:96737373
|
A | C | 9 | a0001c0011t0002g0102a0001c0011t0002g0103a0001c0011t0002g0104others(6): Show | 9 | HG00738.hp1 HG00741.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.700-476A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 10/31 | chr5 | 96737373 | ||||||
| chr5:96737756
|
G | T | 1 | a0002c0003t0010g0284 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.700-93G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 10/31 | chr5 | 96737756 | ||||||
| chr5:96738195
|
G | A | 1 | a0002c0022t0013g0188 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.798+248G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 11/31 | chr5 | 96738195 | ||||||
| chr5:96738309
|
G | A | 86 | a0001c0001t0001g0169a0001c0001t0001g0253a0001c0001t0001g0265others(83): Show | 89 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.798+362G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 11/31 | chr5 | 96738309 | ||||||
| chr5:96738357
|
A | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(45): Show | 53 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.798+410A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 11/31 | chr5 | 96738357 | ||||||
| chr5:96738443
|
A | G | 17 | a0001c0001t0004g0014a0001c0001t0004g0132a0001c0001t0004g0133others(14): Show | 19 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.798+496A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 11/31 | chr5 | 96738443 | ||||||
| chr5:96738634
|
T | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(45): Show | 53 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.798+687T>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 11/31 | chr5 | 96738634 | ||||||
| chr5:96738670
|
C | G | 1 | a0005c0010t0014g0131 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.798+723C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 11/31 | chr5 | 96738670 | ||||||
| chr5:96738731
|
A | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(105): Show | 117 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.798+784A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 11/31 | chr5 | 96738731 | ||||||
| chr5:96738836
|
G | A | 9 | a0001c0001t0001g0109a0001c0001t0007g0255a0002c0004t0005g0190others(6): Show | 9 | HG01255.hp1 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.798+889G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 11/31 | chr5 | 96738836 | ||||||
| chr5:96738840
|
C | T | 2 | a0002c0003t0003g0271a0002c0003t0003g0320 | 2 | HG01192.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.798+893C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 11/31 | chr5 | 96738840 | ||||||
| chr5:96738871
|
G | A | 7 | a0002c0004t0005g0027a0002c0004t0005g0030a0002c0004t0005g0031others(4): Show | 7 | HG01891.hp2 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.798+924G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 11/31 | chr5 | 96738871 | ||||||
| chr5:96738935
|
C | CA | 52 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(49): Show | 58 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.798+1005dupA | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr5 | 96738935 | |||||
| chr5:96738935
|
CA | C | 69 | a0001c0001t0001g0169a0001c0001t0001g0265a0001c0001t0001g0286others(66): Show | 72 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.798+1005delA | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr5 | 96738935 | |||||
| chr5:96738951
|
A | G | 1 | a0010c0016t0011g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.798+1004A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 11/31 | chr5 | 96738951 | ||||||
| chr5:96738987
|
A | G | 2 | a0001c0001t0002g0147a0001c0001t0002g0148 | 2 | HG02080.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.798+1040A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 11/31 | chr5 | 96738987 | ||||||
| chr5:96739089
|
G | A | 1 | a0002c0003t0003g0016 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.799-949G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 11/31 | chr5 | 96739089 | ||||||
| chr5:96739485
|
A | T | 2 | a0001c0002t0001g0199a0001c0002t0001g0229 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.799-553A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 11/31 | chr5 | 96739485 | ||||||
| chr5:96739546
|
G | A | 2 | a0007c0015t0012g0137a0007c0015t0012g0138 | 2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.799-492G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 11/31 | chr5 | 96739546 | ||||||
| chr5:96739559
|
T | C | 15 | a0001c0001t0001g0109a0001c0001t0007g0255a0002c0004t0005g0190others(12): Show | 15 | HG01109.hp2 HG01255.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.799-479T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 11/31 | chr5 | 96739559 | ||||||
| chr5:96739768
|
G | T | 2 | a0001c0001t0003g0256a0001c0001t0003g0257 | 2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.799-270G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 11/31 | chr5 | 96739768 | ||||||
| chr5:96740437
|
C | G | 1 | a0001c0001t0009g0336 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.880-308C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 12/31 | chr5 | 96740437 | ||||||
| chr5:96740496
|
C | T | 1 | a0001c0001t0009g0336 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.880-249C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 12/31 | chr5 | 96740496 | ||||||
| chr5:96740521
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.880-224G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 12/31 | chr5 | 96740521 | ||||||
| chr5:96740537
|
T | A | 1 | a0002c0003t0003g0321 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.880-208T>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 12/31 | chr5 | 96740537 | ||||||
| chr5:96740637
|
T | C | 1 | a0002c0003t0003g0305 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.880-108T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 12/31 | chr5 | 96740637 | ||||||
| chr5:96740690
|
G | T | 8 | a0001c0005t0001g0244a0001c0005t0007g0242a0001c0005t0007g0243others(5): Show | 9 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.880-55G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 12/31 | chr5 | 96740690 | ||||||
| chr5:96740924
|
A | T | 2 | a0007c0015t0012g0137a0007c0015t0012g0138 | 2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.918+141A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 13/31 | chr5 | 96740924 | ||||||
| chr5:96741132
|
A | T | 7 | a0001c0001t0001g0253a0001c0001t0002g0262a0001c0001t0003g0256others(4): Show | 7 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.919-134A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 13/31 | chr5 | 96741132 | ||||||
| chr5:96741173
|
G | A | 2 | a0007c0015t0012g0137a0007c0015t0012g0138 | 2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.919-93G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 13/31 | chr5 | 96741173 | ||||||
| chr5:96741880
|
C | T | 1 | a0002c0003t0003g0268 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1098+300C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 15/31 | chr5 | 96741880 | ||||||
| chr5:96741987
|
T | C | 1 | a0006c0009t0008g0141 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1098+407T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 15/31 | chr5 | 96741987 | ||||||
| chr5:96741999
|
G | A | 6 | a0006c0009t0008g0139a0006c0009t0008g0140a0006c0009t0008g0141others(3): Show | 6 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.1098+419G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 15/31 | chr5 | 96741999 | ||||||
| chr5:96742042
|
T | C | 1 | a0001c0021t0009g0035 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1098+462T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 15/31 | chr5 | 96742042 | ||||||
| chr5:96742213
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1099-442C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 15/31 | chr5 | 96742213 | ||||||
| chr5:96742236
|
A | G | 17 | a0001c0001t0004g0014a0001c0001t0004g0132a0001c0001t0004g0133others(14): Show | 19 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.1099-419A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 15/31 | chr5 | 96742236 | ||||||
| chr5:96742264
|
A | T | 17 | a0001c0001t0004g0014a0001c0001t0004g0132a0001c0001t0004g0133others(14): Show | 19 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.1099-391A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 15/31 | chr5 | 96742264 | ||||||
| chr5:96742339
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1099-316C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 15/31 | chr5 | 96742339 | ||||||
| chr5:96742346
|
T | G | 12 | a0001c0001t0002g0013a0001c0001t0002g0057a0001c0002t0001g0223others(9): Show | 13 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.1099-309T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 15/31 | chr5 | 96742346 | ||||||
| chr5:96742347
|
T | G | 6 | a0001c0001t0001g0253a0001c0001t0002g0262a0001c0001t0003g0256others(3): Show | 6 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099-308T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 15/31 | chr5 | 96742347 | ||||||
| chr5:96742434
|
G | A | 3 | a0001c0001t0001g0169a0001c0002t0001g0200a0001c0002t0001g0216 | 3 | NA18945.hp2 NA18949.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1099-221G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 15/31 | chr5 | 96742434 | ||||||
| chr5:96742510
|
G | T | 2 | a0002c0003t0001g0239a0002c0003t0001g0240 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1099-145G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 15/31 | chr5 | 96742510 | ||||||
| chr5:96742605
|
G | A | 223 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(220): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.1099-50G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 15/31 | chr5 | 96742605 | ||||||
| chr5:96742633
|
C | G | 17 | a0001c0001t0004g0014a0001c0001t0004g0132a0001c0001t0004g0133others(14): Show | 19 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.1099-22C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 15/31 | chr5 | 96742633 | ||||||
| chr5:96742809
|
C | A | 6 | a0001c0001t0002g0290a0001c0001t0002g0292a0001c0001t0002g0293others(3): Show | 6 | HG00423.hp1 NA18954.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.1200+53C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96742809 | ||||||
| chr5:96742838
|
C | T | 12 | a0001c0012t0012g0270a0002c0003t0003g0015a0002c0003t0003g0100others(9): Show | 13 | HG01891.hp2 HG02451.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1200+82C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96742838 | ||||||
| chr5:96742927
|
A | G | 2 | a0001c0001t0001g0143a0001c0001t0001g0149 | 2 | NA19000.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1200+171A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96742927 | ||||||
| chr5:96742966
|
A | G | 1 | a0001c0001t0002g0295 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1200+210A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96742966 | ||||||
| chr5:96742998
|
A | G | 17 | a0001c0001t0004g0014a0001c0001t0004g0132a0001c0001t0004g0133others(14): Show | 19 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.1200+242A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96742998 | ||||||
| chr5:96743138
|
GAAGATCC others(20): Show |
G | 1 | a0002c0004t0001g0126 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1200+388_1200+414d others(29): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr5 | 96743138 | |||||
| chr5:96743272
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1200+516T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96743272 | ||||||
| chr5:96743323
|
C | G | 223 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(220): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.1200+567C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96743323 | ||||||
| chr5:96743471
|
C | T | 10 | a0001c0001t0001g0109a0001c0001t0001g0123a0001c0001t0007g0255others(7): Show | 10 | HG00738.hp2 HG01255.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.1200+715C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96743471 | ||||||
| chr5:96743683
|
C | T | 72 | a0001c0001t0001g0169a0001c0001t0001g0253a0001c0001t0001g0265others(69): Show | 75 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.1200+927C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96743683 | ||||||
| chr5:96743698
|
C | T | 176 | a0001c0001t0001g0123a0001c0001t0001g0169a0001c0001t0001g0173others(173): Show | 186 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.1200+942C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96743698 | ||||||
| chr5:96743730
|
G | A | 3 | a0001c0002t0001g0184a0001c0002t0001g0198a0001c0002t0001g0235 | 3 | NA18983.hp1 NA18990.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1200+974G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96743730 | ||||||
| chr5:96743814
|
C | T | 1 | a0002c0004t0005g0027 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1200+1058C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96743814 | ||||||
| chr5:96743843
|
C | T | 1 | a0001c0002t0001g0196 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1200+1087C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96743843 | ||||||
| chr5:96743866
|
G | A | 2 | a0005c0010t0014g0043a0005c0010t0014g0044 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1200+1110G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96743866 | ||||||
| chr5:96743922
|
C | G | 3 | a0001c0001t0002g0013a0002c0004t0013g0258a0002c0004t0013g0259 | 4 | HG02896.hp1 HG02897.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1200+1166C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96743922 | ||||||
| chr5:96743942
|
C | T | 1 | a0002c0003t0003g0268 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1200+1186C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96743942 | ||||||
| chr5:96744119
|
A | G | 1 | a0002c0004t0003g0260 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1200+1363A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96744119 | ||||||
| chr5:96744240
|
C | T | 1 | a0001c0002t0020g0161 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1200+1484C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96744240 | ||||||
| chr5:96744282
|
A | G | 4 | a0001c0001t0009g0336a0002c0004t0005g0027a0002c0013t0001g0234others(1): Show | 4 | HG02622.hp1 HG03486.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1200+1526A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96744282 | ||||||
| chr5:96744340
|
G | A | 3 | a0001c0001t0001g0143a0001c0001t0001g0149a0001c0001t0002g0083 | 3 | NA18977.hp2 NA19000.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1200+1584G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96744340 | ||||||
| chr5:96744479
|
G | A | 1 | a0007c0015t0012g0138 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1200+1723G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96744479 | ||||||
| chr5:96744687
|
T | G | 3 | a0002c0004t0013g0258a0002c0004t0013g0259a0002c0022t0013g0188 | 3 | HG02976.hp2 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1201-1655T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96744687 | ||||||
| chr5:96744764
|
C | T | 225 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(222): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1201-1578C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96744764 | ||||||
| chr5:96744780
|
C | A | 13 | a0001c0001t0004g0014a0001c0001t0004g0133a0001c0001t0004g0134others(10): Show | 15 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1201-1562C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96744780 | ||||||
| chr5:96744869
|
C | T | 1 | a0001c0002t0001g0227 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1201-1473C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96744869 | ||||||
| chr5:96744974
|
T | C | 3 | a0001c0001t0002g0076a0001c0001t0002g0080a0001c0001t0002g0130 | 3 | HG00621.hp1 HG02074.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.1201-1368T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96744974 | ||||||
| chr5:96745104
|
G | A | 2 | a0002c0013t0001g0191a0002c0013t0001g0234 | 2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1201-1238G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96745104 | ||||||
| chr5:96745162
|
T | A | 8 | a0001c0001t0002g0036a0001c0001t0003g0256a0001c0001t0003g0257others(5): Show | 8 | HG01109.hp1 HG02572.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1201-1180T>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96745162 | ||||||
| chr5:96745179
|
A | G | 113 | a0001c0001t0001g0068a0001c0001t0001g0079a0001c0001t0001g0097others(110): Show | 115 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.1201-1163A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96745179 | ||||||
| chr5:96745230
|
C | T | 110 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0034others(107): Show | 112 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1201-1112C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96745230 | ||||||
| chr5:96745400
|
T | G | 3 | a0001c0001t0002g0077a0001c0001t0002g0092a0001c0001t0002g0125 | 3 | HG03669.hp1 HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1201-942T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96745400 | ||||||
| chr5:96745821
|
G | A | 3 | a0001c0001t0007g0255a0001c0005t0007g0242a0002c0004t0021g0233 | 3 | HG01891.hp2 HG02896.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1201-521G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96745821 | ||||||
| chr5:96745995
|
T | C | 2 | a0001c0001t0002g0045a0001c0001t0002g0106 | 2 | HG01106.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1201-347T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96745995 | ||||||
| chr5:96746121
|
G | T | 28 | a0002c0003t0001g0239a0002c0003t0001g0240a0002c0003t0001g0334others(25): Show | 28 | HG01175.hp2 HG01346.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1201-221G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96746121 | ||||||
| chr5:96746286
|
T | C | 2 | a0001c0005t0009g0007a0001c0005t0009g0189 | 3 | HG02615.hp1 HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1201-56T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 16/31 | chr5 | 96746286 | ||||||
| chr5:96746431
|
T | G | 1 | a0001c0021t0009g0035 | 1 | HG03540.hp2 | splice_region_variant&intron_variant | LOW | c.1284+6T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 17/31 | chr5 | 96746431 | ||||||
| chr5:96746697
|
C | T | 322 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(319): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.1284+272C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 17/31 | chr5 | 96746697 | ||||||
| chr5:96746729
|
T | C | 55 | a0002c0003t0002g0276a0002c0003t0002g0289a0002c0003t0002g0291others(52): Show | 60 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.1284+304T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 17/31 | chr5 | 96746729 | ||||||
| chr5:96746790
|
C | T | 331 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(328): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.1284+365C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 17/31 | chr5 | 96746790 | ||||||
| chr5:96746927
|
T | A | 323 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(320): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.1285-418T>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 17/31 | chr5 | 96746927 | ||||||
| chr5:96746948
|
T | G | 1 | a0001c0002t0002g0301 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1285-397T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 17/31 | chr5 | 96746948 | ||||||
| chr5:96746976
|
A | C | 262 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(259): Show | 274 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.1285-369A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 17/31 | chr5 | 96746976 | ||||||
| chr5:96747254
|
T | C | 1 | a0004c0029t0001g0187 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1285-91T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 17/31 | chr5 | 96747254 | ||||||
| chr5:96747443
|
G | A | 2 | a0002c0004t0003g0124a0002c0004t0003g0260 | 2 | HG01243.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1332+51G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 18/31 | chr5 | 96747443 | ||||||
| chr5:96747634
|
C | T | 17 | a0001c0001t0001g0109a0001c0001t0002g0036a0001c0001t0003g0256others(14): Show | 17 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1332+242C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 18/31 | chr5 | 96747634 | ||||||
| chr5:96747638
|
A | T | 52 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(49): Show | 56 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.1332+246A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 18/31 | chr5 | 96747638 | ||||||
| chr5:96747775
|
C | T | 1 | a0001c0017t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1332+383C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 18/31 | chr5 | 96747775 | ||||||
| chr5:96748080
|
G | A | 8 | a0001c0001t0008g0323a0001c0012t0012g0270a0006c0009t0008g0139others(5): Show | 8 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.1333-438G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 18/31 | chr5 | 96748080 | ||||||
| chr5:96748104
|
C | T | 3 | a0002c0004t0013g0258a0002c0004t0013g0259a0002c0022t0013g0188 | 3 | HG02976.hp2 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1333-414C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 18/31 | chr5 | 96748104 | ||||||
| chr5:96748196
|
A | T | 2 | a0002c0013t0001g0191a0002c0013t0001g0234 | 2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1333-322A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 18/31 | chr5 | 96748196 | ||||||
| chr5:96748514
|
A | G | 1 | a0001c0002t0002g0202 | 1 | NA18963.hp2 | splice_region_variant&intron_variant | LOW | c.1333-4A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 18/31 | chr5 | 96748514 | ||||||
| chr5:96748727
|
G | A | 28 | a0002c0003t0001g0239a0002c0003t0001g0240a0002c0003t0001g0334others(25): Show | 28 | HG01175.hp2 HG01346.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1428+114G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 19/31 | chr5 | 96748727 | ||||||
| chr5:96749072
|
C | A | 55 | a0002c0003t0002g0276a0002c0003t0002g0289a0002c0003t0002g0291others(52): Show | 60 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.1428+459C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 19/31 | chr5 | 96749072 | ||||||
| chr5:96749122
|
C | T | 1 | a0002c0003t0003g0325 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1428+509C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 19/31 | chr5 | 96749122 | ||||||
| chr5:96749244
|
T | G | 28 | a0002c0003t0001g0239a0002c0003t0001g0240a0002c0003t0001g0334others(25): Show | 28 | HG01175.hp2 HG01346.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1428+631T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 19/31 | chr5 | 96749244 | ||||||
| chr5:96749268
|
T | A | 3 | a0002c0004t0013g0258a0002c0004t0013g0259a0002c0022t0013g0188 | 3 | HG02976.hp2 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1428+655T>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 19/31 | chr5 | 96749268 | ||||||
| chr5:96749362
|
T | G | 2 | a0001c0001t0002g0092a0001c0001t0002g0125 | 2 | HG03669.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1428+749T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 19/31 | chr5 | 96749362 | ||||||
| chr5:96749432
|
A | C | 1 | a0001c0001t0002g0066 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1428+819A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 19/31 | chr5 | 96749432 | ||||||
| chr5:96749455
|
T | C | 1 | a0001c0001t0002g0077 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1428+842T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 19/31 | chr5 | 96749455 | ||||||
| chr5:96749531
|
C | T | 114 | a0001c0001t0001g0109a0001c0001t0002g0036a0001c0001t0003g0256others(111): Show | 119 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(116): Show |
intron_variant | MODIFIER | c.1428+918C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 19/31 | chr5 | 96749531 | ||||||
| chr5:96749659
|
G | A | 1 | a0001c0001t0002g0058 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1429-928G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 19/31 | chr5 | 96749659 | ||||||
| chr5:96749719
|
G | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(141): Show | 154 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.1429-868G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 19/31 | chr5 | 96749719 | ||||||
| chr5:96749752
|
G | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0170 | 2 | NA18950.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1429-835G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 19/31 | chr5 | 96749752 | ||||||
| chr5:96749898
|
T | C | 3 | a0002c0004t0013g0258a0002c0004t0013g0259a0002c0022t0013g0188 | 3 | HG02976.hp2 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1429-689T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 19/31 | chr5 | 96749898 | ||||||
| chr5:96749905
|
C | T | 8 | a0001c0001t0008g0323a0001c0012t0012g0270a0006c0009t0008g0139others(5): Show | 8 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.1429-682C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 19/31 | chr5 | 96749905 | ||||||
| chr5:96749924
|
G | T | 1 | a0001c0001t0002g0290 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1429-663G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 19/31 | chr5 | 96749924 | ||||||
| chr5:96749925
|
T | G | 1 | a0001c0001t0001g0024 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1429-662T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 19/31 | chr5 | 96749925 | ||||||
| chr5:96749932
|
T | G | 1 | a0001c0001t0002g0290 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1429-655T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 19/31 | chr5 | 96749932 | ||||||
| chr5:96749954
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1429-633T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 19/31 | chr5 | 96749954 | ||||||
| chr5:96749968
|
C | A | 2 | a0002c0013t0001g0191a0002c0013t0001g0234 | 2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1429-619C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 19/31 | chr5 | 96749968 | ||||||
| chr5:96749999
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1429-588G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 19/31 | chr5 | 96749999 | ||||||
| chr5:96750030
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1429-557T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 19/31 | chr5 | 96750030 | ||||||
| chr5:96750198
|
G | A | 2 | a0002c0013t0001g0191a0002c0013t0001g0234 | 2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1429-389G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 19/31 | chr5 | 96750198 | ||||||
| chr5:96750205
|
T | C | 4 | a0001c0001t0001g0068a0001c0001t0001g0079a0001c0001t0001g0097others(1): Show | 4 | NA18946.hp2 NA18957.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.1429-382T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 19/31 | chr5 | 96750205 | ||||||
| chr5:96750346
|
A | G | 1 | a0010c0016t0011g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1429-241A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 19/31 | chr5 | 96750346 | ||||||
| chr5:96750358
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1429-229C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 19/31 | chr5 | 96750358 | ||||||
| chr5:96750379
|
A | C | 2 | a0001c0001t0009g0336a0001c0021t0009g0035 | 2 | HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1429-208A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 19/31 | chr5 | 96750379 | ||||||
| chr5:96750427
|
A | C | 1 | a0007c0015t0012g0137 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1429-160A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 19/31 | chr5 | 96750427 | ||||||
| chr5:96750528
|
C | T | 5 | a0004c0008t0007g0061a0004c0008t0011g0037a0004c0008t0011g0236others(2): Show | 5 | HG01109.hp1 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1429-59C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 19/31 | chr5 | 96750528 | ||||||
| chr5:96750829
|
T | C | 1 | a0001c0001t0002g0078 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1524+147T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96750829 | ||||||
| chr5:96750847
|
G | A | 1 | a0001c0001t0010g0028 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1524+165G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96750847 | ||||||
| chr5:96750914
|
C | G | 15 | a0002c0003t0001g0334a0002c0003t0001g0335a0002c0004t0001g0047others(12): Show | 15 | HG01175.hp2 HG01346.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.1524+232C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96750914 | ||||||
| chr5:96750986
|
G | A | 58 | a0002c0003t0002g0276a0002c0003t0002g0289a0002c0003t0002g0291others(55): Show | 63 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.1524+304G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96750986 | ||||||
| chr5:96751003
|
C | T | 1 | a0002c0003t0003g0333 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1524+321C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96751003 | ||||||
| chr5:96751138
|
T | C | 2 | a0002c0013t0001g0191a0002c0013t0001g0234 | 2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1524+456T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96751138 | ||||||
| chr5:96751211
|
G | GT | 73 | a0001c0001t0001g0024a0001c0001t0001g0051a0001c0001t0001g0064others(70): Show | 76 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1524+537dupT | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | INFO_REALIGN_3_PRIME | chr5 | 96751211 | |||||
| chr5:96751311
|
T | A | 57 | a0002c0003t0002g0289a0002c0003t0002g0291a0002c0003t0002g0294others(54): Show | 62 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.1524+629T>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96751311 | ||||||
| chr5:96751763
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1524+1081G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96751763 | ||||||
| chr5:96751906
|
G | A | 1 | a0010c0016t0011g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1524+1224G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96751906 | ||||||
| chr5:96752248
|
T | G | 8 | a0001c0001t0002g0036a0001c0001t0003g0256a0001c0001t0003g0257others(5): Show | 8 | HG01109.hp1 HG02572.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1524+1566T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96752248 | ||||||
| chr5:96752495
|
T | G | 1 | a0001c0001t0001g0064 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1525-1565T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96752495 | ||||||
| chr5:96752539
|
AAACCTCA others(5): Show |
A | 10 | a0001c0001t0002g0045a0001c0001t0002g0057a0001c0001t0002g0060others(7): Show | 10 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.1525-1508_1525-149 others(16): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | INFO_REALIGN_3_PRIME | chr5 | 96752539 | |||||
| chr5:96752550
|
ATAACCTC others(6): Show |
A | 20 | a0001c0001t0001g0079a0001c0001t0001g0160a0001c0001t0001g0169others(17): Show | 21 | HG01257.hp1 HG02109.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1525-1508_1525-149 others(17): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | INFO_REALIGN_3_PRIME | chr5 | 96752550 | |||||
| chr5:96752550
|
ATAACCTC others(7): Show |
A | 55 | a0001c0001t0001g0005a0001c0001t0001g0063a0001c0001t0001g0068others(52): Show | 58 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1525-1508_1525-149 others(18): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | INFO_REALIGN_3_PRIME | chr5 | 96752550 | |||||
| chr5:96752550
|
ATAACCTC others(8): Show |
A | 123 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0018others(120): Show | 132 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.1525-1508_1525-149 others(19): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | INFO_REALIGN_3_PRIME | chr5 | 96752550 | |||||
| chr5:96752550
|
ATAACCTC others(9): Show |
A | 24 | a0001c0001t0001g0108a0001c0001t0001g0118a0001c0001t0004g0014others(21): Show | 27 | HG00280.hp1 HG01069.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.1525-1508_1525-149 others(20): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | INFO_REALIGN_3_PRIME | chr5 | 96752550 | |||||
| chr5:96752550
|
ATAACCTC others(10): Show |
A | 3 | a0001c0001t0004g0269a0001c0001t0004g0285a0001c0017t0001g0025 | 3 | HG01070.hp1 HG01071.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1525-1508_1525-149 others(21): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | INFO_REALIGN_3_PRIME | chr5 | 96752550 | |||||
| chr5:96752550
|
ATAACCTC others(11): Show |
A | 1 | a0002c0004t0001g0126 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1525-1508_1525-149 others(22): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | INFO_REALIGN_3_PRIME | chr5 | 96752550 | |||||
| chr5:96752550
|
ATAACCTC others(12): Show |
A | 2 | a0002c0004t0001g0053a0002c0006t0001g0041 | 2 | HG03225.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1525-1508_1525-149 others(23): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | INFO_REALIGN_3_PRIME | chr5 | 96752550 | |||||
| chr5:96752550
|
ATAACCTC others(13): Show |
A | 25 | a0002c0003t0001g0240a0002c0003t0001g0334a0002c0003t0001g0335others(22): Show | 25 | HG01175.hp2 HG01346.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.1525-1508_1525-148 others(24): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | INFO_REALIGN_3_PRIME | chr5 | 96752550 | |||||
| chr5:96752550
|
ATAACCTC others(14): Show |
A | 7 | a0001c0001t0003g0256a0002c0003t0001g0239a0004c0008t0007g0061others(4): Show | 7 | HG01109.hp1 HG02622.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1525-1508_1525-148 others(25): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | INFO_REALIGN_3_PRIME | chr5 | 96752550 | |||||
| chr5:96752550
|
ATAACCTC others(15): Show |
A | 9 | a0001c0001t0001g0109a0001c0001t0003g0257a0001c0001t0010g0023others(6): Show | 9 | HG01123.hp2 HG01361.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1525-1508_1525-148 others(26): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | INFO_REALIGN_3_PRIME | chr5 | 96752550 | |||||
| chr5:96752550
|
ATAACCTC others(16): Show |
A | 2 | a0001c0001t0002g0036a0005c0010t0014g0131 | 2 | HG01109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1525-1508_1525-148 others(27): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | INFO_REALIGN_3_PRIME | chr5 | 96752550 | |||||
| chr5:96752551
|
TAACCTCA others(3): Show |
T | 2 | a0001c0011t0002g0104a0003c0007t0002g0254 | 2 | HG01891.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1525-1507_1525-149 others(14): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | INFO_REALIGN_3_PRIME | chr5 | 96752551 | |||||
| chr5:96752551
|
TAACCTCA others(4): Show |
T | 3 | a0001c0001t0002g0034a0001c0002t0002g0301a0002c0013t0001g0191 | 3 | HG01243.hp2 HG02486.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1525-1508_1525-149 others(15): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96752551 | ||||||
| chr5:96752561
|
G | T | 2 | a0003c0007t0002g0020a0003c0007t0002g0252 | 2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1525-1499G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96752561 | ||||||
| chr5:96752562
|
A | T | 4 | a0001c0011t0002g0104a0003c0007t0002g0020a0003c0007t0002g0252others(1): Show | 4 | HG01891.hp1 HG02055.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525-1498A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96752562 | ||||||
| chr5:96752562
|
AT | A | 28 | a0001c0001t0002g0052a0001c0001t0002g0054a0001c0001t0002g0055others(25): Show | 28 | HG00140.hp2 HG00621.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.1525-1466delT | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | INFO_REALIGN_3_PRIME | chr5 | 96752562 | |||||
| chr5:96752592
|
T | C | 1 | a0001c0001t0001g0064 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1525-1468T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96752592 | ||||||
| chr5:96752814
|
T | C | 4 | a0001c0001t0007g0255a0001c0005t0001g0244a0001c0005t0007g0242others(1): Show | 4 | HG02559.hp2 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525-1246T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96752814 | ||||||
| chr5:96752914
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1525-1146A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96752914 | ||||||
| chr5:96752921
|
A | G | 4 | a0005c0010t0014g0043a0005c0010t0014g0044a0005c0010t0014g0131others(1): Show | 4 | HG01109.hp2 HG02723.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1525-1139A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96752921 | ||||||
| chr5:96752961
|
T | TAC | 80 | a0001c0001t0001g0265a0001c0001t0001g0315a0001c0001t0001g0322others(77): Show | 84 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1525-1070_1525-106 others(6): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | INFO_REALIGN_3_PRIME | chr5 | 96752961 | |||||
| chr5:96752961
|
T | TACAC | 20 | a0001c0001t0001g0064a0001c0001t0001g0082a0002c0003t0001g0239others(17): Show | 21 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.1525-1072_1525-106 others(8): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | INFO_REALIGN_3_PRIME | chr5 | 96752961 | |||||
| chr5:96752961
|
T | TACACAC | 7 | a0002c0004t0001g0101a0002c0004t0001g0113a0002c0004t0005g0030others(4): Show | 7 | HG02622.hp1 HG02809.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1525-1074_1525-106 others(10): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | INFO_REALIGN_3_PRIME | chr5 | 96752961 | |||||
| chr5:96752961
|
T | TACACACA others(3): Show |
15 | a0001c0001t0001g0108a0001c0001t0004g0014a0001c0001t0004g0132others(12): Show | 17 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1525-1078_1525-106 others(14): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | INFO_REALIGN_3_PRIME | chr5 | 96752961 | |||||
| chr5:96752961
|
T | TACACACA others(5): Show |
2 | a0001c0001t0004g0133a0001c0001t0019g0332 | 2 | HG01934.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1525-1080_1525-106 others(16): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | INFO_REALIGN_3_PRIME | chr5 | 96752961 | |||||
| chr5:96752961
|
TAC | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(53): Show | 61 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.1525-1070_1525-106 others(6): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | INFO_REALIGN_3_PRIME | chr5 | 96752961 | |||||
| chr5:96752961
|
TACAC | T | 3 | a0001c0001t0002g0036a0001c0001t0003g0256a0001c0001t0003g0257 | 3 | HG02572.hp1 HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1525-1072_1525-106 others(8): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | INFO_REALIGN_3_PRIME | chr5 | 96752961 | |||||
| chr5:96752973
|
C | A | 1 | a0001c0001t0010g0023 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1525-1087C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96752973 | ||||||
| chr5:96752998
|
AT | A | 34 | a0002c0003t0001g0239a0002c0003t0001g0240a0002c0003t0001g0334others(31): Show | 34 | HG01109.hp1 HG01175.hp2 HG01346.hp1 others(31): Show |
intron_variant | MODIFIER | c.1525-1049delT | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | INFO_REALIGN_3_PRIME | chr5 | 96752998 | |||||
| chr5:96753034
|
T | C | 1 | a0002c0003t0003g0016 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1525-1026T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96753034 | ||||||
| chr5:96753120
|
A | AG | 5 | a0001c0001t0001g0109a0001c0001t0010g0023a0001c0001t0010g0028others(2): Show | 5 | HG01123.hp2 HG01361.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525-938dupG | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | INFO_REALIGN_3_PRIME | chr5 | 96753120 | |||||
| chr5:96753146
|
A | G | 17 | a0001c0001t0001g0108a0001c0001t0004g0014a0001c0001t0004g0132others(14): Show | 19 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.1525-914A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96753146 | ||||||
| chr5:96753174
|
T | C | 1 | a0001c0001t0002g0098 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1525-886T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96753174 | ||||||
| chr5:96753299
|
C | T | 15 | a0002c0003t0001g0334a0002c0003t0001g0335a0002c0004t0001g0047others(12): Show | 15 | HG01175.hp2 HG01346.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.1525-761C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96753299 | ||||||
| chr5:96753332
|
C | T | 1 | a0002c0004t0021g0233 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1525-728C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96753332 | ||||||
| chr5:96753342
|
T | C | 56 | a0002c0003t0002g0289a0002c0003t0002g0291a0002c0003t0002g0294others(53): Show | 59 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1525-718T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96753342 | ||||||
| chr5:96753363
|
A | C | 53 | a0002c0003t0002g0289a0002c0003t0002g0291a0002c0003t0002g0294others(50): Show | 56 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.1525-697A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96753363 | ||||||
| chr5:96753407
|
G | A | 257 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(254): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1525-653G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96753407 | ||||||
| chr5:96753491
|
A | G | 2 | a0005c0010t0014g0131a0005c0010t0024g0042 | 2 | HG01109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1525-569A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96753491 | ||||||
| chr5:96753658
|
G | C | 2 | a0001c0001t0009g0336a0001c0021t0009g0035 | 2 | HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1525-402G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96753658 | ||||||
| chr5:96753732
|
C | T | 1 | a0007c0015t0012g0138 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1525-328C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96753732 | ||||||
| chr5:96753749
|
G | T | 2 | a0001c0001t0009g0336a0001c0021t0009g0035 | 2 | HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1525-311G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96753749 | ||||||
| chr5:96753750
|
G | T | 2 | a0001c0001t0009g0336a0001c0021t0009g0035 | 2 | HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1525-310G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96753750 | ||||||
| chr5:96753807
|
C | T | 29 | a0001c0001t0002g0264a0002c0003t0001g0239a0002c0003t0001g0240others(26): Show | 29 | HG01175.hp2 HG01346.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1525-253C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96753807 | ||||||
| chr5:96753823
|
G | A | 4 | a0001c0001t0002g0045a0001c0001t0002g0106a0001c0001t0002g0107others(1): Show | 4 | HG00642.hp2 HG01106.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525-237G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96753823 | ||||||
| chr5:96753874
|
A | G | 1 | a0002c0003t0003g0316 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1525-186A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96753874 | ||||||
| chr5:96753935
|
C | G | 20 | a0001c0001t0001g0109a0001c0001t0002g0036a0001c0001t0003g0256others(17): Show | 20 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.1525-125C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96753935 | ||||||
| chr5:96753954
|
G | A | 259 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(256): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.1525-106G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96753954 | ||||||
| chr5:96754015
|
G | A | 8 | a0001c0001t0008g0323a0001c0012t0012g0270a0006c0009t0008g0139others(5): Show | 8 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.1525-45G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 20/31 | chr5 | 96754015 | ||||||
| chr5:96754272
|
A | G | 147 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(144): Show | 157 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1626+111A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 21/31 | chr5 | 96754272 | ||||||
| chr5:96754802
|
C | T | 1 | a0001c0002t0002g0301 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1710+61C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 22/31 | chr5 | 96754802 | ||||||
| chr5:96755122
|
C | T | 1 | a0001c0001t0010g0028 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1710+381C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 22/31 | chr5 | 96755122 | ||||||
| chr5:96755234
|
G | A | 52 | a0002c0003t0002g0289a0002c0003t0002g0291a0002c0003t0002g0294others(49): Show | 55 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.1710+493G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 22/31 | chr5 | 96755234 | ||||||
| chr5:96755325
|
C | T | 8 | a0001c0001t0008g0323a0001c0012t0012g0270a0006c0009t0008g0139others(5): Show | 8 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.1710+584C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 22/31 | chr5 | 96755325 | ||||||
| chr5:96755347
|
G | T | 2 | a0001c0002t0001g0217a0001c0002t0003g0204 | 2 | NA18954.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1710+606G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 22/31 | chr5 | 96755347 | ||||||
| chr5:96755558
|
A | G | 1 | a0001c0001t0001g0253 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1710+817A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 22/31 | chr5 | 96755558 | ||||||
| chr5:96755631
|
A | G | 1 | a0001c0012t0001g0329 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1710+890A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 22/31 | chr5 | 96755631 | ||||||
| chr5:96755898
|
G | C | 8 | a0001c0001t0008g0323a0001c0012t0012g0270a0006c0009t0008g0139others(5): Show | 8 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.1710+1157G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 22/31 | chr5 | 96755898 | ||||||
| chr5:96756132
|
C | G | 1 | a0005c0010t0024g0042 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1711-1312C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 22/31 | chr5 | 96756132 | ||||||
| chr5:96756221
|
C | T | 17 | a0001c0001t0001g0108a0001c0001t0004g0014a0001c0001t0004g0132others(14): Show | 19 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.1711-1223C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 22/31 | chr5 | 96756221 | ||||||
| chr5:96756222
|
G | A | 56 | a0002c0003t0002g0289a0002c0003t0002g0291a0002c0003t0002g0294others(53): Show | 59 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1711-1222G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 22/31 | chr5 | 96756222 | ||||||
| chr5:96756269
|
C | T | 2 | a0002c0013t0001g0191a0002c0013t0001g0234 | 2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1711-1175C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 22/31 | chr5 | 96756269 | ||||||
| chr5:96756284
|
A | G | 28 | a0002c0003t0001g0239a0002c0003t0001g0240a0002c0003t0001g0334others(25): Show | 28 | HG01175.hp2 HG01346.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1711-1160A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 22/31 | chr5 | 96756284 | ||||||
| chr5:96756380
|
T | C | 1 | a0007c0015t0012g0138 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1711-1064T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 22/31 | chr5 | 96756380 | ||||||
| chr5:96756382
|
A | G | 1 | a0003c0007t0002g0050 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1711-1062A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 22/31 | chr5 | 96756382 | ||||||
| chr5:96756499
|
T | G | 2 | a0001c0005t0001g0244a0001c0005t0007g0243 | 2 | HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1711-945T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 22/31 | chr5 | 96756499 | ||||||
| chr5:96756570
|
C | G | 17 | a0001c0001t0001g0108a0001c0001t0004g0014a0001c0001t0004g0132others(14): Show | 19 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.1711-874C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 22/31 | chr5 | 96756570 | ||||||
| chr5:96756640
|
C | T | 3 | a0001c0001t0004g0014a0001c0001t0004g0269a0001c0001t0004g0285 | 4 | HG01070.hp1 HG01071.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1711-804C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 22/31 | chr5 | 96756640 | ||||||
| chr5:96756658
|
A | G | 5 | a0001c0001t0008g0323a0006c0009t0008g0139a0006c0009t0008g0140others(2): Show | 5 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.1711-786A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 22/31 | chr5 | 96756658 | ||||||
| chr5:96756820
|
G | A | 29 | a0001c0001t0001g0108a0002c0003t0001g0239a0002c0003t0001g0240others(26): Show | 29 | HG01175.hp2 HG01346.hp1 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.1711-624G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 22/31 | chr5 | 96756820 | ||||||
| chr5:96757039
|
T | A | 1 | a0001c0012t0012g0270 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1711-405T>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 22/31 | chr5 | 96757039 | ||||||
| chr5:96757054
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1711-390C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 22/31 | chr5 | 96757054 | ||||||
| chr5:96757132
|
C | T | 1 | a0001c0001t0001g0155 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1711-312C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 22/31 | chr5 | 96757132 | ||||||
| chr5:96757228
|
C | T | 3 | a0002c0004t0013g0258a0002c0004t0013g0259a0002c0022t0013g0188 | 3 | HG02976.hp2 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1711-216C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 22/31 | chr5 | 96757228 | ||||||
| chr5:96757286
|
A | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(255): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1711-158A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 22/31 | chr5 | 96757286 | ||||||
| chr5:96757307
|
C | T | 29 | a0001c0001t0001g0108a0002c0003t0001g0239a0002c0003t0001g0240others(26): Show | 29 | HG01175.hp2 HG01346.hp1 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.1711-137C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 22/31 | chr5 | 96757307 | ||||||
| chr5:96757434
|
C | T | 29 | a0001c0001t0001g0108a0002c0003t0001g0239a0002c0003t0001g0240others(26): Show | 29 | HG01175.hp2 HG01346.hp1 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.1711-10C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 22/31 | chr5 | 96757434 | ||||||
| chr5:96757518
|
G | A | 143 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(140): Show | 153 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1761+24G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 23/31 | chr5 | 96757518 | ||||||
| chr5:96757685
|
T | C | 29 | a0001c0001t0001g0108a0002c0003t0001g0239a0002c0003t0001g0240others(26): Show | 29 | HG01175.hp2 HG01346.hp1 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.1833+31T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96757685 | ||||||
| chr5:96757687
|
G | GT | 59 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(56): Show | 64 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1833+49dupT | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | INFO_REALIGN_3_PRIME | chr5 | 96757687 | |||||
| chr5:96757703
|
T | C | 7 | a0001c0012t0012g0270a0006c0009t0008g0139a0006c0009t0008g0140others(4): Show | 7 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.1833+49T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96757703 | ||||||
| chr5:96757737
|
C | T | 128 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(125): Show | 138 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1833+83C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96757737 | ||||||
| chr5:96757759
|
T | G | 1 | a0002c0003t0003g0174 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1833+105T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96757759 | ||||||
| chr5:96757768
|
G | A | 7 | a0004c0008t0007g0061a0004c0008t0011g0037a0004c0008t0011g0236others(4): Show | 7 | HG01109.hp1 HG02622.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1833+114G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96757768 | ||||||
| chr5:96757879
|
C | T | 2 | a0001c0001t0002g0055a0001c0001t0002g0083 | 2 | HG02135.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.1833+225C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96757879 | ||||||
| chr5:96757935
|
C | T | 1 | a0010c0016t0011g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1833+281C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96757935 | ||||||
| chr5:96758164
|
A | G | 5 | a0001c0001t0008g0323a0006c0009t0008g0139a0006c0009t0008g0140others(2): Show | 5 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.1833+510A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96758164 | ||||||
| chr5:96758359
|
G | C | 1 | a0001c0002t0001g0194 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1833+705G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96758359 | ||||||
| chr5:96758675
|
G | C | 29 | a0001c0001t0001g0108a0002c0003t0001g0239a0002c0003t0001g0240others(26): Show | 29 | HG01175.hp2 HG01346.hp1 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.1833+1021G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96758675 | ||||||
| chr5:96758990
|
T | G | 240 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(237): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.1833+1336T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96758990 | ||||||
| chr5:96759066
|
C | A | 1 | a0001c0001t0002g0122 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1833+1412C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96759066 | ||||||
| chr5:96759124
|
A | G | 3 | a0003c0007t0002g0050a0003c0007t0002g0112a0003c0007t0002g0313 | 3 | HG01255.hp1 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1833+1470A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96759124 | ||||||
| chr5:96759203
|
T | C | 3 | a0002c0004t0013g0258a0002c0004t0013g0259a0002c0022t0013g0188 | 3 | HG02976.hp2 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1833+1549T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96759203 | ||||||
| chr5:96759269
|
A | C | 6 | a0001c0001t0001g0109a0001c0001t0010g0023a0001c0001t0010g0028others(3): Show | 6 | HG01123.hp2 HG01361.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1833+1615A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96759269 | ||||||
| chr5:96759464
|
T | C | 2 | a0002c0013t0001g0191a0002c0013t0001g0234 | 2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1833+1810T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96759464 | ||||||
| chr5:96759477
|
C | T | 1 | a0001c0002t0001g0231 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1833+1823C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96759477 | ||||||
| chr5:96759700
|
A | T | 4 | a0001c0001t0004g0132a0001c0001t0004g0134a0001c0001t0004g0135others(1): Show | 4 | HG01192.hp2 HG01515.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1833+2046A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96759700 | ||||||
| chr5:96759754
|
T | C | 1 | a0001c0002t0001g0203 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1833+2100T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96759754 | ||||||
| chr5:96759789
|
A | G | 1 | a0001c0001t0010g0038 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1833+2135A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96759789 | ||||||
| chr5:96759874
|
A | G | 6 | a0002c0003t0003g0015a0002c0003t0003g0100a0002c0003t0003g0308others(3): Show | 7 | NA18946.hp1 NA18956.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.1833+2220A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96759874 | ||||||
| chr5:96759972
|
G | A | 2 | a0002c0013t0001g0191a0002c0013t0001g0234 | 2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1834-2302G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96759972 | ||||||
| chr5:96760120
|
A | G | 4 | a0002c0003t0001g0239a0002c0003t0001g0240a0002c0006t0001g0040others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1834-2154A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96760120 | ||||||
| chr5:96760343
|
A | G | 2 | a0005c0010t0014g0043a0005c0010t0014g0044 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1834-1931A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96760343 | ||||||
| chr5:96760412
|
C | T | 2 | a0001c0001t0002g0099a0001c0001t0002g0119 | 2 | NA18939.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.1834-1862C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96760412 | ||||||
| chr5:96760426
|
G | A | 5 | a0001c0001t0001g0109a0001c0001t0010g0023a0001c0001t0010g0028others(2): Show | 5 | HG01123.hp2 HG01361.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1834-1848G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96760426 | ||||||
| chr5:96760485
|
G | T | 55 | a0002c0003t0002g0289a0002c0003t0002g0291a0002c0003t0002g0294others(52): Show | 58 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.1834-1789G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96760485 | ||||||
| chr5:96760510
|
C | A | 1 | a0001c0001t0002g0046 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1834-1764C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96760510 | ||||||
| chr5:96760515
|
C | G | 128 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(125): Show | 138 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1834-1759C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96760515 | ||||||
| chr5:96760760
|
C | T | 29 | a0001c0001t0001g0108a0002c0003t0001g0239a0002c0003t0001g0240others(26): Show | 29 | HG01175.hp2 HG01346.hp1 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.1834-1514C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96760760 | ||||||
| chr5:96760960
|
A | G | 5 | a0004c0008t0007g0061a0004c0008t0011g0037a0004c0008t0011g0236others(2): Show | 5 | HG01109.hp1 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1834-1314A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96760960 | ||||||
| chr5:96761124
|
A | G | 86 | a0001c0001t0001g0108a0002c0003t0001g0239a0002c0003t0001g0240others(83): Show | 89 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.1834-1150A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96761124 | ||||||
| chr5:96761220
|
T | A | 1 | a0001c0002t0001g0303 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1834-1054T>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96761220 | ||||||
| chr5:96761269
|
A | G | 2 | a0002c0013t0001g0191a0002c0013t0001g0234 | 2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1834-1005A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96761269 | ||||||
| chr5:96761370
|
A | G | 2 | a0002c0013t0001g0191a0002c0013t0001g0234 | 2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1834-904A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96761370 | ||||||
| chr5:96761559
|
A | G | 1 | a0004c0029t0001g0187 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1834-715A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96761559 | ||||||
| chr5:96761901
|
A | G | 2 | a0002c0013t0001g0191a0002c0013t0001g0234 | 2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1834-373A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96761901 | ||||||
| chr5:96762014
|
C | T | 4 | a0005c0010t0014g0043a0005c0010t0014g0044a0005c0010t0014g0131others(1): Show | 4 | HG01109.hp2 HG02723.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1834-260C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96762014 | ||||||
| chr5:96762144
|
T | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(47): Show | 54 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.1834-130T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96762144 | ||||||
| chr5:96762191
|
T | G | 146 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(143): Show | 156 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.1834-83T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 24/31 | chr5 | 96762191 | ||||||
| chr5:96762412
|
G | A | 5 | a0001c0001t0001g0064a0001c0001t0001g0082a0001c0001t0001g0178others(2): Show | 5 | HG03834.hp1 NA18983.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.1932+40G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 25/31 | chr5 | 96762412 | ||||||
| chr5:96762418
|
A | C | 2 | a0001c0002t0001g0215a0001c0002t0001g0222 | 2 | NA18944.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1932+46A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 25/31 | chr5 | 96762418 | ||||||
| chr5:96762439
|
C | T | 4 | a0002c0004t0001g0047a0002c0004t0001g0048a0002c0004t0001g0049others(1): Show | 4 | NA18991.hp1 NA19002.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.1932+67C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 25/31 | chr5 | 96762439 | ||||||
| chr5:96762440
|
G | A | 9 | a0004c0008t0007g0061a0004c0008t0011g0037a0004c0008t0011g0236others(6): Show | 9 | HG01109.hp1 HG01109.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1932+68G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 25/31 | chr5 | 96762440 | ||||||
| chr5:96762510
|
G | A | 146 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(143): Show | 156 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.1932+138G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 25/31 | chr5 | 96762510 | ||||||
| chr5:96762557
|
A | G | 1 | a0001c0017t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1932+185A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 25/31 | chr5 | 96762557 | ||||||
| chr5:96762848
|
A | G | 2 | a0002c0006t0003g0232a0002c0006t0003g0237 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1932+476A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 25/31 | chr5 | 96762848 | ||||||
| chr5:96763045
|
G | T | 16 | a0001c0001t0001g0108a0002c0003t0001g0334a0002c0003t0001g0335others(13): Show | 16 | HG01175.hp2 HG01346.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.1932+673G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 25/31 | chr5 | 96763045 | ||||||
| chr5:96763054
|
C | T | 29 | a0001c0001t0001g0108a0002c0003t0001g0239a0002c0003t0001g0240others(26): Show | 29 | HG01175.hp2 HG01346.hp1 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.1932+682C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 25/31 | chr5 | 96763054 | ||||||
| chr5:96763136
|
T | C | 1 | a0001c0021t0009g0035 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1932+764T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 25/31 | chr5 | 96763136 | ||||||
| chr5:96763274
|
C | T | 2 | a0001c0001t0001g0051a0001c0002t0001g0223 | 2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1932+902C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 25/31 | chr5 | 96763274 | ||||||
| chr5:96763425
|
G | A | 3 | a0001c0001t0003g0256a0001c0001t0003g0257a0010c0016t0011g0026 | 3 | HG02572.hp1 HG03098.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1932+1053G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 25/31 | chr5 | 96763425 | ||||||
| chr5:96763561
|
A | G | 16 | a0001c0001t0004g0014a0001c0001t0004g0132a0001c0001t0004g0133others(13): Show | 18 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1932+1189A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 25/31 | chr5 | 96763561 | ||||||
| chr5:96763892
|
A | T | 3 | a0001c0001t0003g0256a0001c0001t0003g0257a0010c0016t0011g0026 | 3 | HG02572.hp1 HG03098.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1933-1329A>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 25/31 | chr5 | 96763892 | ||||||
| chr5:96763963
|
C | CA | 99 | a0001c0001t0001g0108a0001c0001t0002g0036a0001c0001t0003g0256others(96): Show | 102 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.1933-1247dupA | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr5 | 96763963 | |||||
| chr5:96764068
|
C | T | 3 | a0001c0001t0003g0256a0001c0001t0003g0257a0010c0016t0011g0026 | 3 | HG02572.hp1 HG03098.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1933-1153C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 25/31 | chr5 | 96764068 | ||||||
| chr5:96764187
|
A | G | 1 | a0008c0014t0002g0111 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1933-1034A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 25/31 | chr5 | 96764187 | ||||||
| chr5:96764254
|
C | T | 111 | a0001c0001t0001g0108a0001c0001t0002g0036a0001c0001t0003g0256others(108): Show | 114 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(111): Show |
intron_variant | MODIFIER | c.1933-967C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 25/31 | chr5 | 96764254 | ||||||
| chr5:96764578
|
A | C | 29 | a0001c0001t0001g0108a0002c0003t0001g0239a0002c0003t0001g0240others(26): Show | 29 | HG01175.hp2 HG01346.hp1 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.1933-643A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 25/31 | chr5 | 96764578 | ||||||
| chr5:96764940
|
C | A | 3 | a0001c0001t0003g0256a0001c0001t0003g0257a0010c0016t0011g0026 | 3 | HG02572.hp1 HG03098.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1933-281C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 25/31 | chr5 | 96764940 | ||||||
| chr5:96765007
|
A | G | 2 | a0002c0003t0003g0311a0002c0003t0003g0330 | 2 | HG02258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1933-214A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 25/31 | chr5 | 96765007 | ||||||
| chr5:96765038
|
TCTC | T | 29 | a0001c0001t0001g0108a0002c0003t0001g0239a0002c0003t0001g0240others(26): Show | 29 | HG01175.hp2 HG01346.hp1 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.1933-180_1933-178d others(5): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr5 | 96765038 | |||||
| chr5:96765060
|
G | C | 108 | a0001c0001t0001g0108a0001c0001t0002g0036a0001c0001t0003g0256others(105): Show | 111 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.1933-161G>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 25/31 | chr5 | 96765060 | ||||||
| chr5:96765197
|
A | C | 1 | a0001c0001t0001g0315 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1933-24A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 25/31 | chr5 | 96765197 | ||||||
| chr5:96765218
|
C | T | 3 | a0001c0001t0003g0256a0001c0001t0003g0257a0010c0016t0011g0026 | 3 | HG02572.hp1 HG03098.hp1 NA21309.hp1 |
splice_region_variant&intron_variant | LOW | c.1933-3C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 25/31 | chr5 | 96765218 | ||||||
| chr5:96765327
|
T | TA | 11 | a0001c0001t0002g0034a0001c0001t0002g0055a0001c0001t0002g0060others(8): Show | 11 | HG01123.hp1 HG01891.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.2037+28dupA | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 26/31 | INFO_REALIGN_3_PRIME | chr5 | 96765327 | |||||
| chr5:96765327
|
TA | T | 34 | a0001c0001t0001g0063a0001c0001t0001g0177a0001c0001t0002g0045others(31): Show | 36 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.2037+28delA | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 26/31 | INFO_REALIGN_3_PRIME | chr5 | 96765327 | |||||
| chr5:96765327
|
TAA | T | 125 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(122): Show | 132 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.2037+27_2037+28del others(2): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 26/31 | INFO_REALIGN_3_PRIME | chr5 | 96765327 | |||||
| chr5:96765327
|
TAAA | T | 92 | a0001c0001t0001g0024a0001c0001t0001g0051a0001c0001t0001g0064others(89): Show | 98 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.2037+26_2037+28del others(3): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 26/31 | INFO_REALIGN_3_PRIME | chr5 | 96765327 | |||||
| chr5:96765327
|
TAAAA | T | 6 | a0001c0001t0001g0185a0001c0001t0008g0323a0006c0009t0008g0139others(3): Show | 6 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.2037+25_2037+28del others(4): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 26/31 | INFO_REALIGN_3_PRIME | chr5 | 96765327 | |||||
| chr5:96765340
|
A | G | 1 | a0002c0004t0001g0115 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2037+15A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 26/31 | chr5 | 96765340 | ||||||
| chr5:96765362
|
T | TA | 256 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(253): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.2037+38dupA | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 26/31 | INFO_REALIGN_3_PRIME | chr5 | 96765362 | |||||
| chr5:96765379
|
T | A | 1 | a0001c0002t0001g0197 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2037+54T>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 26/31 | chr5 | 96765379 | ||||||
| chr5:96765516
|
A | G | 52 | a0002c0003t0002g0289a0002c0003t0002g0291a0002c0003t0002g0294others(49): Show | 55 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.2037+191A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 26/31 | chr5 | 96765516 | ||||||
| chr5:96765522
|
G | A | 52 | a0002c0003t0002g0289a0002c0003t0002g0291a0002c0003t0002g0294others(49): Show | 55 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.2037+197G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 26/31 | chr5 | 96765522 | ||||||
| chr5:96765525
|
G | T | 3 | a0001c0001t0002g0292a0001c0001t0002g0293a0001c0001t0002g0295 | 3 | HG00423.hp1 NA18979.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.2037+200G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 26/31 | chr5 | 96765525 | ||||||
| chr5:96765814
|
AATAT | A | 52 | a0002c0003t0002g0289a0002c0003t0002g0291a0002c0003t0002g0294others(49): Show | 55 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.2038-237_2038-234d others(6): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 26/31 | INFO_REALIGN_3_PRIME | chr5 | 96765814 | |||||
| chr5:96766203
|
C | T | 1 | a0001c0002t0001g0220 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2130+58C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 27/31 | chr5 | 96766203 | ||||||
| chr5:96766240
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(206): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.2130+95A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 27/31 | chr5 | 96766240 | ||||||
| chr5:96766255
|
C | T | 111 | a0001c0001t0001g0108a0001c0001t0002g0036a0001c0001t0003g0256others(108): Show | 114 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(111): Show |
intron_variant | MODIFIER | c.2130+110C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 27/31 | chr5 | 96766255 | ||||||
| chr5:96766289
|
C | T | 7 | a0002c0004t0005g0027a0002c0004t0005g0030a0002c0004t0005g0031others(4): Show | 7 | HG02280.hp2 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.2130+144C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 27/31 | chr5 | 96766289 | ||||||
| chr5:96766545
|
G | T | 1 | a0010c0016t0011g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2130+400G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 27/31 | chr5 | 96766545 | ||||||
| chr5:96766733
|
C | A | 6 | a0003c0007t0002g0020a0003c0007t0002g0050a0003c0007t0002g0112others(3): Show | 6 | HG01255.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.2130+588C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 27/31 | chr5 | 96766733 | ||||||
| chr5:96766871
|
TG | T | 128 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(125): Show | 138 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.2131-565delG | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 27/31 | INFO_REALIGN_3_PRIME | chr5 | 96766871 | |||||
| chr5:96767117
|
C | G | 8 | a0001c0001t0008g0323a0001c0012t0012g0270a0006c0009t0008g0139others(5): Show | 8 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.2131-321C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 27/31 | chr5 | 96767117 | ||||||
| chr5:96767222
|
C | T | 5 | a0004c0008t0007g0061a0004c0008t0011g0037a0004c0008t0011g0236others(2): Show | 5 | HG01109.hp1 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2131-216C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 27/31 | chr5 | 96767222 | ||||||
| chr5:96767366
|
T | G | 1 | a0001c0001t0002g0078 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2131-72T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 27/31 | chr5 | 96767366 | ||||||
| chr5:96767372
|
C | T | 1 | a0001c0021t0009g0035 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2131-66C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 27/31 | chr5 | 96767372 | ||||||
| chr5:96767406
|
A | G | 29 | a0001c0001t0001g0108a0002c0003t0001g0239a0002c0003t0001g0240others(26): Show | 29 | HG01175.hp2 HG01346.hp1 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.2131-32A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 27/31 | chr5 | 96767406 | ||||||
| chr5:96767606
|
T | C | 1 | a0002c0003t0003g0268 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2175+124T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 28/31 | chr5 | 96767606 | ||||||
| chr5:96767648
|
C | T | 80 | a0001c0001t0002g0036a0001c0001t0003g0256a0001c0001t0003g0257others(77): Show | 83 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.2175+166C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 28/31 | chr5 | 96767648 | ||||||
| chr5:96767754
|
A | G | 1 | a0002c0003t0002g0291 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2176-153A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 28/31 | chr5 | 96767754 | ||||||
| chr5:96767788
|
TGTCA | T | 3 | a0002c0004t0013g0258a0002c0004t0013g0259a0002c0022t0013g0188 | 3 | HG02976.hp2 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2176-112_2176-109d others(6): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 28/31 | INFO_REALIGN_3_PRIME | chr5 | 96767788 | |||||
| chr5:96767885
|
G | A | 5 | a0001c0001t0002g0036a0001c0001t0010g0023a0001c0001t0010g0028others(2): Show | 5 | HG01123.hp2 HG01361.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.2176-22G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 28/31 | chr5 | 96767885 | ||||||
| chr5:96768095
|
C | G | 29 | a0001c0001t0001g0108a0002c0003t0001g0239a0002c0003t0001g0240others(26): Show | 29 | HG01175.hp2 HG01346.hp1 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.2268+96C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 29/31 | chr5 | 96768095 | ||||||
| chr5:96768258
|
A | AT | 5 | a0004c0008t0007g0061a0004c0008t0011g0037a0004c0008t0011g0236others(2): Show | 5 | HG01109.hp1 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2268+266dupT | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr5 | 96768258 | |||||
| chr5:96768354
|
G | T | 1 | a0001c0001t0001g0108 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2268+355G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 29/31 | chr5 | 96768354 | ||||||
| chr5:96768440
|
GAAGAA | G | 3 | a0001c0001t0003g0256a0001c0001t0003g0257a0010c0016t0011g0026 | 3 | HG02572.hp1 HG03098.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2268+449_2268+453d others(7): Show |
CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr5 | 96768440 | |||||
| chr5:96768778
|
G | A | 29 | a0001c0001t0001g0108a0002c0003t0001g0239a0002c0003t0001g0240others(26): Show | 29 | HG01175.hp2 HG01346.hp1 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.2268+779G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 29/31 | chr5 | 96768778 | ||||||
| chr5:96768790
|
G | A | 1 | a0002c0004t0001g0053 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2268+791G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 29/31 | chr5 | 96768790 | ||||||
| chr5:96769063
|
T | G | 1 | a0001c0001t0002g0036 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2268+1064T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 29/31 | chr5 | 96769063 | ||||||
| chr5:96769131
|
G | A | 110 | a0001c0001t0001g0108a0001c0001t0002g0036a0001c0001t0003g0256others(107): Show | 113 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(110): Show |
intron_variant | MODIFIER | c.2268+1132G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 29/31 | chr5 | 96769131 | ||||||
| chr5:96769132
|
A | C | 2 | a0008c0014t0002g0110a0008c0014t0002g0111 | 2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2268+1133A>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 29/31 | chr5 | 96769132 | ||||||
| chr5:96769191
|
C | T | 1 | a0002c0003t0003g0016 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2268+1192C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 29/31 | chr5 | 96769191 | ||||||
| chr5:96769247
|
A | G | 1 | a0001c0021t0009g0035 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2268+1248A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 29/31 | chr5 | 96769247 | ||||||
| chr5:96769339
|
C | T | 110 | a0001c0001t0001g0108a0001c0001t0002g0036a0001c0001t0003g0256others(107): Show | 113 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(110): Show |
intron_variant | MODIFIER | c.2269-1192C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 29/31 | chr5 | 96769339 | ||||||
| chr5:96769387
|
T | G | 2 | a0002c0003t0003g0327a0004c0008t0011g0238 | 2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.2269-1144T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 29/31 | chr5 | 96769387 | ||||||
| chr5:96769396
|
G | GT | 7 | a0001c0001t0002g0095a0001c0001t0002g0280a0001c0001t0002g0337others(4): Show | 7 | HG00323.hp1 HG01074.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2269-1122dupT | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr5 | 96769396 | |||||
| chr5:96769396
|
GT | G | 69 | a0001c0001t0002g0036a0001c0001t0003g0256a0001c0001t0003g0257others(66): Show | 72 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.2269-1122delT | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr5 | 96769396 | |||||
| chr5:96769439
|
T | G | 1 | a0001c0001t0004g0132 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2269-1092T>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 29/31 | chr5 | 96769439 | ||||||
| chr5:96769514
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2269-1017A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 29/31 | chr5 | 96769514 | ||||||
| chr5:96769599
|
C | A | 1 | a0001c0001t0001g0051 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2269-932C>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 29/31 | chr5 | 96769599 | ||||||
| chr5:96769918
|
G | T | 4 | a0005c0010t0014g0043a0005c0010t0014g0044a0005c0010t0014g0131others(1): Show | 4 | HG01109.hp2 HG02723.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2269-613G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 29/31 | chr5 | 96769918 | ||||||
| chr5:96770221
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2269-310C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 29/31 | chr5 | 96770221 | ||||||
| chr5:96770222
|
G | A | 110 | a0001c0001t0001g0108a0001c0001t0002g0036a0001c0001t0003g0256others(107): Show | 113 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(110): Show |
intron_variant | MODIFIER | c.2269-309G>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 29/31 | chr5 | 96770222 | ||||||
| chr5:96770234
|
C | T | 1 | a0001c0002t0001g0303 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2269-297C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 29/31 | chr5 | 96770234 | ||||||
| chr5:96770274
|
G | T | 8 | a0001c0001t0008g0323a0001c0012t0012g0270a0006c0009t0008g0139others(5): Show | 8 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.2269-257G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 29/31 | chr5 | 96770274 | ||||||
| chr5:96770392
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2269-139A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 29/31 | chr5 | 96770392 | ||||||
| chr5:96770407
|
A | G | 1 | a0001c0001t0001g0011 | 2 | HG00099.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.2269-124A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 29/31 | chr5 | 96770407 | ||||||
| chr5:96770836
|
C | T | 5 | a0001c0001t0001g0064a0001c0001t0001g0082a0001c0001t0001g0178others(2): Show | 5 | HG03834.hp1 NA18983.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.2340+234C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 30/31 | chr5 | 96770836 | ||||||
| chr5:96771121
|
C | T | 1 | a0001c0002t0001g0207 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2340+519C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 30/31 | chr5 | 96771121 | ||||||
| chr5:96771154
|
A | G | 1 | a0010c0016t0011g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2341-490A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 30/31 | chr5 | 96771154 | ||||||
| chr5:96771156
|
A | G | 4 | a0004c0008t0007g0061a0004c0008t0011g0037a0004c0008t0011g0236others(1): Show | 4 | HG01109.hp1 HG02622.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2341-488A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 30/31 | chr5 | 96771156 | ||||||
| chr5:96771195
|
T | A | 126 | a0001c0001t0001g0108a0001c0001t0002g0036a0001c0001t0003g0256others(123): Show | 131 | HG00099.hp2 HG00280.hp1 HG00609.hp1 others(128): Show |
intron_variant | MODIFIER | c.2341-449T>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 30/31 | chr5 | 96771195 | ||||||
| chr5:96771212
|
C | T | 8 | a0001c0001t0008g0323a0001c0012t0012g0270a0006c0009t0008g0139others(5): Show | 8 | HG00738.hp1 HG01981.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.2341-432C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 30/31 | chr5 | 96771212 | ||||||
| chr5:96771234
|
C | T | 1 | a0001c0001t0019g0332 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2341-410C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 30/31 | chr5 | 96771234 | ||||||
| chr5:96771301
|
A | G | 16 | a0001c0001t0004g0014a0001c0001t0004g0132a0001c0001t0004g0133others(13): Show | 18 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.2341-343A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 30/31 | chr5 | 96771301 | ||||||
| chr5:96771318
|
C | T | 12 | a0001c0001t0002g0036a0001c0001t0010g0023a0001c0001t0010g0038others(9): Show | 12 | HG01109.hp1 HG01109.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.2341-326C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 30/31 | chr5 | 96771318 | ||||||
| chr5:96771498
|
G | T | 279 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(276): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.2341-146G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 30/31 | chr5 | 96771498 | ||||||
| chr5:96771502
|
C | G | 1 | a0001c0001t0002g0262 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2341-142C>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 30/31 | chr5 | 96771502 | ||||||
| chr5:96772070
|
C | T | 110 | a0001c0001t0001g0108a0001c0001t0002g0036a0001c0001t0003g0256others(107): Show | 113 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(110): Show |
intron_variant | MODIFIER | c.*23+368C>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 31/31 | chr5 | 96772070 | ||||||
| chr5:96772097
|
A | G | 16 | a0001c0001t0004g0014a0001c0001t0004g0132a0001c0001t0004g0133others(13): Show | 18 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.*23+395A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 31/31 | chr5 | 96772097 | ||||||
| chr5:96772103
|
G | T | 3 | a0002c0004t0005g0030a0002c0004t0005g0032a0002c0004t0005g0033 | 3 | HG02559.hp1 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.*23+401G>T | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 31/31 | chr5 | 96772103 | ||||||
| chr5:96772342
|
T | A | 1 | a0001c0005t0009g0007 | 2 | HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.*24-298T>A | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 31/31 | chr5 | 96772342 | ||||||
| chr5:96772434
|
GA | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(255): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.*24-200delA | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr5 | 96772434 | |||||
| chr5:96772555
|
T | C | 1 | a0001c0002t0020g0161 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.*24-85T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 31/31 | chr5 | 96772555 | ||||||
| chr5:96772600
|
A | G | 1 | a0001c0001t0002g0036 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.*24-40A>G | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 31/31 | chr5 | 96772600 | ||||||
| chr5:96772601
|
T | C | 1 | a0001c0017t0001g0025 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.*24-39T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 31/31 | chr5 | 96772601 | ||||||
| chr5:96772610
|
T | C | 1 | a0001c0002t0001g0184 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.*24-30T>C | CAST | ENSG00000153113.24 | transcript | ENST00000675179.1 | protein_coding | 31/31 | chr5 | 96772610 |