| geneid | 989 |
|---|---|
| ensemblid | ENSG00000122545.22 |
| hgncid | 1717 |
| symbol | SEPTIN7 |
| name | septin 7 |
| refseq_nuc | NM_001788.6 |
| refseq_prot | NP_001779.3 |
| ensembl_nuc | ENST00000350320.11 |
| ensembl_prot | ENSP00000344868.8 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 35801057 |
| end | 35907110 |
| strand | + |
| ver | v1.2 |
| region | chr7:35801057-35907110 |
| region5000 | chr7:35796057-35912110 |
| regionname0 | SEPTIN7_chr7_35801057_35907110 |
| regionname5000 | SEPTIN7_chr7_35796057_35912110 |
| 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 | 437 | 345 | 91 | 60 | 154 | 10 | 28 | 118 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0002 | 0/0 | 437 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1314 | 334 | 89 | 58 | 148 | 10 | 27 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| c0002 | 0/0 | 1314 | 9 | 1 | 2 | 6 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| c0003 | 0/0 | 1314 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| c0004 | 0/0 | 1314 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| c0005 | 0/0 | 1314 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| 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 | 2970 | 95 | 10 | 32 | 37 | 4 | 11 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0002 | 0/0 | 2969 | 76 | 29 | 6 | 38 | 1 | 2 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0003 | 0/0 | 2969 | 36 | 2 | 8 | 17 | 4 | 5 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0004 | 1/0 | 2971 | 16 | 15 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0005 | 0/0 | 2970 | 15 | 5 | 4 | 0 | 0 | 6 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0006 | 0/0 | 2970 | 12 | 1 | 0 | 11 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0007 | 0/0 | 2970 | 9 | 1 | 1 | 6 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0008 | 0/0 | 2971 | 9 | 9 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0009 | 0/0 | 2970 | 9 | 0 | 0 | 9 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0010 | 0/0 | 2970 | 8 | 0 | 1 | 7 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0011 | 0/0 | 2970 | 8 | 8 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0012 | 0/0 | 2970 | 8 | 0 | 0 | 8 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0013 | 0/0 | 2970 | 6 | 5 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0014 | 0/0 | 2969 | 4 | 0 | 0 | 4 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0015 | 0/0 | 2971 | 3 | 0 | 1 | 2 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0016 | 0/0 | 2970 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0017 | 0/0 | 2969 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0018 | 0/0 | 2969 | 2 | 0 | 1 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0019 | 0/0 | 2970 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0020 | 0/0 | 2970 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0021 | 0/0 | 2970 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0022 | 0/0 | 2971 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0023 | 0/0 | 2969 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0024 | 0/0 | 2971 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0025 | 0/0 | 2969 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0026 | 0/0 | 2971 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0027 | 0/0 | 2969 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0028 | 0/0 | 2970 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0029 | 0/0 | 2969 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0030 | 0/0 | 2969 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0031 | 0/0 | 2969 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0032 | 0/0 | 2969 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0033 | 0/0 | 2970 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0034 | 0/0 | 2970 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0035 | 0/0 | 2970 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0036 | 0/0 | 2970 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0037 | 0/0 | 2970 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0038 | 0/0 | 2970 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| t0039 | 0/0 | 2970 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| 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 | 0 | 3 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0331 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| g0337 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1314 | 334 | 89 | 58 | 148 | 10 | 27 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0002 | 0/0 | 1314 | 9 | 1 | 2 | 6 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0003 | 0/0 | 1314 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0004 | 0/0 | 1314 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0002c0005 | 0/0 | 1314 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4283 | 86 | 9 | 30 | 31 | 4 | 11 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0002 | 0/0 | 4282 | 74 | 28 | 6 | 38 | 1 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0003 | 0/0 | 4282 | 36 | 2 | 8 | 17 | 4 | 5 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0004 | 1/0 | 4284 | 16 | 15 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0005 | 0/0 | 4283 | 15 | 5 | 4 | 0 | 0 | 6 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0006 | 0/0 | 4283 | 12 | 1 | 0 | 11 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0007 | 0/0 | 4283 | 9 | 1 | 1 | 6 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0008 | 0/0 | 4284 | 9 | 9 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0009 | 0/0 | 4283 | 9 | 0 | 0 | 9 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0010 | 0/0 | 4283 | 8 | 0 | 1 | 7 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0011 | 0/0 | 4283 | 8 | 8 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0012 | 0/0 | 4283 | 8 | 0 | 0 | 8 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0013 | 0/0 | 4283 | 5 | 4 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0014 | 0/0 | 4282 | 4 | 0 | 0 | 4 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0015 | 0/0 | 4284 | 3 | 0 | 1 | 2 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0016 | 0/0 | 4283 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0017 | 0/0 | 4282 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0018 | 0/0 | 4282 | 2 | 0 | 1 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0019 | 0/0 | 4283 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0020 | 0/0 | 4283 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0021 | 0/0 | 4283 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0022 | 0/0 | 4284 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0023 | 0/0 | 4282 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0024 | 0/0 | 4284 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0025 | 0/0 | 4282 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0026 | 0/0 | 4284 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0027 | 0/0 | 4282 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0028 | 0/0 | 4283 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0029 | 0/0 | 4282 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0030 | 0/0 | 4282 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0031 | 0/0 | 4282 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0032 | 0/0 | 4282 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0033 | 0/0 | 4283 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0034 | 0/0 | 4283 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0035 | 0/0 | 4283 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0036 | 0/0 | 4283 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0037 | 0/0 | 4283 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0038 | 0/0 | 4283 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0001t0039 | 0/0 | 4283 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0002t0001 | 0/0 | 4283 | 9 | 1 | 2 | 6 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0003t0002 | 0/0 | 4282 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0001c0004t0013 | 0/0 | 4283 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| a0002c0005t0002 | 0/0 | 4282 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | copy fasta | chr7 | 35796057 | 35912110 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0331 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0004g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0004g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0004g0337 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0005g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0005g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0005g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0005g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0005g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0005g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0005g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0005g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0005g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0005g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0006g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0006g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0006g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0006g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0006g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0006g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0006g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0006g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0006g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0007g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0007g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0007g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0007g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0007g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0007g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0007g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0007g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0008g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0008g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0008g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0008g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0008g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0008g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0008g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0008g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0008g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0009g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0009g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0009g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0009g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0009g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0009g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0009g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0009g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0009g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0010g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0010g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0010g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0010g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0010g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0010g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0010g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0010g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0011g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0011g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0011g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0011g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0011g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0011g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0011g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0012g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0012g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0012g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0012g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0012g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0012g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0012g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0012g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0013g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0013g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0013g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0013g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0013g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0014g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0014g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0014g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0014g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0015g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0015g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0015g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0016g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0016g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0016g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0017g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0017g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0018g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0018g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0019g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0019g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0020g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0021g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0021g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0022g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0022g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0023g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0024g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0025g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0026g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0027g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0028g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0029g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0030g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0031g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0032g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0033g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0034g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0035g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0036g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0037g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0038g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0039g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0002t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0002t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0004t0013g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0002c0005t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0101 | EUR | GBR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0249 | EUR | GBR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0294 | EUR | GBR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0166 | EUR | GBR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | CHS | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | CHS | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | CHS | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | CHS | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | CHS | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | CHS | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00597 | hp2 | a0001 | c0001 | t0033 | g0061 | EAS | CHS | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00609 | hp1 | a0001 | c0001 | t0012 | g0234 | EAS | CHS | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | CHS | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0334 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0112 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | CHS | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00738 | hp1 | a0001 | c0001 | t0005 | g0202 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00741 | hp1 | a0001 | c0001 | t0007 | g0117 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01081 | hp1 | a0001 | c0001 | t0026 | g0204 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01081 | hp2 | a0001 | c0001 | t0023 | g0089 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0332 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0094 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0102 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0333 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0169 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01255 | hp1 | a0001 | c0001 | t0013 | g0044 | AMR | CLM | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01255 | hp2 | a0001 | c0001 | t0005 | g0197 | AMR | CLM | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01257 | hp1 | a0001 | c0001 | t0020 | g0007 | AMR | CLM | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0335 | AMR | CLM | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01258 | hp1 | a0001 | c0001 | t0020 | g0007 | AMR | CLM | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | CLM | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0090 | AMR | CLM | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | CLM | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | CLM | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01433 | hp2 | a0001 | c0001 | t0030 | g0107 | AMR | CLM | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0026 | EUR | IBS | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0265 | EUR | IBS | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0232 | EUR | IBS | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0027 | EUR | IBS | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0221 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01884 | hp2 | a0001 | c0001 | t0013 | g0047 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01891 | hp1 | a0001 | c0001 | t0013 | g0048 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0203 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01934 | hp1 | a0001 | c0001 | t0010 | g0307 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0093 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0091 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01981 | hp2 | a0001 | c0001 | t0005 | g0209 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0012 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0336 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | KHV | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02055 | hp1 | a0001 | c0001 | t0019 | g0311 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0179 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | KHV | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | KHV | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | KHV | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02080 | hp2 | a0001 | c0001 | t0017 | g0210 | EAS | KHV | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | KHV | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02083 | hp2 | a0001 | c0001 | t0009 | g0275 | EAS | KHV | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | KHV | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02129 | hp2 | a0001 | c0001 | t0016 | g0268 | EAS | KHV | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | KHV | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02132 | hp2 | a0001 | c0001 | t0032 | g0158 | EAS | KHV | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02135 | hp1 | a0001 | c0001 | t0014 | g0165 | EAS | KHV | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02155 | hp1 | a0001 | c0001 | t0014 | g0129 | EAS | CDX | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02155 | hp2 | a0001 | c0001 | t0021 | g0059 | EAS | CDX | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02165 | hp1 | a0001 | c0001 | t0014 | g0130 | EAS | CDX | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | CDX | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0198 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0173 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02280 | hp2 | a0001 | c0001 | t0011 | g0070 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0115 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02293 | hp2 | a0001 | c0001 | t0015 | g0260 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02300 | hp1 | a0001 | c0001 | t0018 | g0121 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02451 | hp1 | a0001 | c0001 | t0011 | g0069 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0313 | SAS | PJL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0219 | SAS | PJL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02615 | hp2 | a0001 | c0001 | t0011 | g0067 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0017 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0095 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0174 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02683 | hp1 | a0001 | c0001 | t0007 | g0136 | SAS | PJL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0312 | SAS | PJL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0096 | SAS | PJL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0214 | SAS | PJL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0310 | SAS | PJL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02809 | hp1 | a0001 | c0001 | t0008 | g0022 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0199 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0171 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02886 | hp2 | a0001 | c0001 | t0008 | g0020 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02895 | hp1 | a0001 | c0001 | t0008 | g0023 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02896 | hp2 | a0001 | c0001 | t0008 | g0018 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02897 | hp2 | a0001 | c0001 | t0008 | g0019 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0178 | AFR | ESN | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0175 | AFR | ESN | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0200 | AFR | ESN | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0108 | AFR | ESN | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ESN | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | ESN | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0220 | AFR | ESN | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0015 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03098 | hp2 | a0001 | c0001 | t0011 | g0065 | AFR | MSL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03130 | hp1 | a0001 | c0001 | t0011 | g0003 | AFR | ESN | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0176 | AFR | ESN | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03139 | hp1 | a0001 | c0001 | t0013 | g0045 | AFR | ESN | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | ESN | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03195 | hp1 | a0002 | c0005 | t0002 | g0104 | AFR | ESN | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | ESN | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | MSL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03209 | hp2 | a0001 | c0001 | t0007 | g0037 | AFR | MSL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | MSL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0205 | SAS | PJL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | MSL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0016 | AFR | MSL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03486 | hp1 | a0001 | c0001 | t0022 | g0195 | AFR | MSL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0172 | AFR | MSL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ESN | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03516 | hp2 | a0001 | c0001 | t0011 | g0068 | AFR | ESN | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03540 | hp2 | a0001 | c0001 | t0019 | g0266 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | MSL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03669 | hp2 | a0001 | c0001 | t0037 | g0206 | SAS | PJL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03704 | hp1 | a0001 | c0003 | t0002 | g0085 | SAS | PJL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0099 | SAS | PJL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0097 | SAS | BEB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | BEB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0192 | SAS | BEB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03942 | hp2 | a0001 | c0001 | t0034 | g0267 | SAS | BEB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG04115 | hp1 | a0001 | c0001 | t0031 | g0167 | SAS | STU | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | STU | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0100 | SAS | STU | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG04199 | hp2 | a0001 | c0001 | t0005 | g0207 | SAS | STU | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0208 | SAS | STU | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | STU | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18522 | hp1 | a0001 | c0001 | t0011 | g0003 | AFR | YRI | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | YRI | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18612 | hp1 | a0001 | c0001 | t0025 | g0168 | EAS | CHB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CHB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | CHB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18906 | hp1 | a0001 | c0001 | t0008 | g0021 | AFR | YRI | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18906 | hp2 | a0001 | c0001 | t0029 | g0036 | AFR | YRI | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18940 | hp1 | a0001 | c0001 | t0028 | g0053 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18942 | hp1 | a0001 | c0001 | t0009 | g0322 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18942 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18944 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18948 | hp1 | a0001 | c0001 | t0010 | g0259 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18948 | hp2 | a0001 | c0001 | t0014 | g0105 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18949 | hp1 | a0001 | c0001 | t0018 | g0103 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0303 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18951 | hp1 | a0001 | c0001 | t0006 | g0055 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18952 | hp1 | a0001 | c0001 | t0007 | g0164 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18952 | hp2 | a0001 | c0001 | t0012 | g0257 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18956 | hp1 | a0001 | c0001 | t0007 | g0131 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18957 | hp2 | a0001 | c0001 | t0009 | g0296 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18960 | hp1 | a0001 | c0001 | t0006 | g0024 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18961 | hp1 | a0001 | c0001 | t0016 | g0077 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18968 | hp1 | a0001 | c0001 | t0027 | g0145 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18969 | hp1 | a0001 | c0001 | t0036 | g0201 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18970 | hp1 | a0001 | c0001 | t0006 | g0054 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18970 | hp2 | a0001 | c0001 | t0012 | g0233 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18972 | hp1 | a0001 | c0001 | t0015 | g0051 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0302 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18975 | hp2 | a0001 | c0001 | t0012 | g0064 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18978 | hp1 | a0001 | c0001 | t0015 | g0277 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18978 | hp2 | a0001 | c0001 | t0006 | g0060 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18979 | hp2 | a0001 | c0001 | t0006 | g0052 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0301 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18991 | hp2 | a0001 | c0001 | t0007 | g0157 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18992 | hp1 | a0001 | c0001 | t0012 | g0228 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0305 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18995 | hp1 | a0001 | c0001 | t0016 | g0328 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18995 | hp2 | a0001 | c0001 | t0017 | g0217 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18997 | hp1 | a0001 | c0001 | t0010 | g0241 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18997 | hp2 | a0001 | c0001 | t0006 | g0066 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19001 | hp1 | a0001 | c0001 | t0006 | g0057 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19001 | hp2 | a0001 | c0001 | t0009 | g0230 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19004 | hp2 | a0001 | c0001 | t0009 | g0264 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19006 | hp1 | a0001 | c0001 | t0012 | g0063 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19007 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19009 | hp2 | a0001 | c0001 | t0006 | g0056 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19010 | hp1 | a0001 | c0001 | t0012 | g0263 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19030 | hp1 | a0001 | c0001 | t0011 | g0072 | AFR | LWK | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | LWK | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19043 | hp1 | a0001 | c0004 | t0013 | g0043 | AFR | LWK | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19043 | hp2 | a0001 | c0001 | t0024 | g0177 | AFR | LWK | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19057 | hp2 | a0001 | c0001 | t0035 | g0227 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19059 | hp1 | a0001 | c0001 | t0007 | g0147 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19059 | hp2 | a0001 | c0001 | t0009 | g0299 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19060 | hp1 | a0001 | c0001 | t0009 | g0300 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19062 | hp2 | a0001 | c0001 | t0012 | g0062 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19064 | hp2 | a0001 | c0001 | t0007 | g0132 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19067 | hp1 | a0001 | c0001 | t0009 | g0242 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19067 | hp2 | a0001 | c0001 | t0007 | g0163 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19072 | hp2 | a0001 | c0001 | t0010 | g0330 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19075 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19076 | hp2 | a0001 | c0001 | t0010 | g0329 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19078 | hp2 | a0001 | c0001 | t0010 | g0238 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19081 | hp1 | a0001 | c0001 | t0021 | g0050 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19084 | hp1 | a0001 | c0001 | t0009 | g0327 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19085 | hp2 | a0001 | c0001 | t0010 | g0262 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19090 | hp1 | a0001 | c0001 | t0010 | g0306 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA20129 | hp1 | a0001 | c0001 | t0013 | g0046 | AFR | ASW | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | ASW | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA20805 | hp1 | a0001 | c0001 | t0039 | g0196 | EUR | TSI | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0092 | EUR | TSI | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA20905 | hp1 | a0001 | c0001 | t0005 | g0010 | SAS | GIH | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | GIH | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | CLM | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | CLM | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0193 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02486 | hp2 | a0001 | c0001 | t0038 | g0170 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03471 | hp1 | a0001 | c0001 | t0022 | g0194 | AFR | MSL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | MSL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | USA | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0058 | AFR | USA | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | USA | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | USA | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0098 | AFR | LWK | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | LWK | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0331 | REF | REF | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0337 | REF | REF | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:35801229
|
C | G | 1 | a0002 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.20C>G | p.Ser7Cys | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/14 | 173/4284 | 20/1314 | 7/437 | chr7 | 35801229 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:35801233
|
T | A | 1 | a0001c0003 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.24T>A | p.Ala8Ala | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/14 | 177/4284 | 24/1314 | 8/437 | chr7 | 35801233 | ||
| chr7:35903153
|
C | T | 1 | a0001c0002 | 9 | HG00408.hp2 HG01952.hp2 HG02004.hp1 others(6): Show |
synonymous_variant | LOW | c.1212C>T | p.Phe404Phe | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 13/14 | 1365/4284 | 1212/1314 | 404/437 | chr7 | 35903153 | ||
| chr7:35904290
|
T | C | 1 | a0001c0004 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.1311T>C | p.Phe437Phe | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 1464/4284 | 1311/1314 | 437/437 | chr7 | 35904290 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:35801107
|
A | C | 2 | a0001c0001t0022a0001c0001t0039 | 3 | HG03471.hp1 HG03486.hp1 NA20805.hp1 |
5_prime_UTR_variant | MODIFIER | c.-103A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/14 | 103 | chr7 | 35801107 | |||||
| chr7:35801198
|
G | A | 1 | a0001c0001t0023 | 1 | HG01081.hp2 | 5_prime_UTR_variant | MODIFIER | c.-12G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/14 | 12 | chr7 | 35801198 | |||||
| chr7:35904342
|
T | A | 1 | a0001c0001t0024 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*49T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 49 | chr7 | 35904342 | |||||
| chr7:35904593
|
T | C | 1 | a0001c0001t0025 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*300T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 300 | chr7 | 35904593 | |||||
| chr7:35904636
|
C | T | 1 | a0001c0001t0014 | 4 | HG02135.hp1 HG02155.hp1 HG02165.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*343C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 343 | chr7 | 35904636 | |||||
| chr7:35904805
|
GA | G | 36 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(33): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*524delA | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 524 | INFO_REALIGN_3_PRIME | chr7 | 35904805 | ||||
| chr7:35904895
|
T | C | 1 | a0001c0001t0027 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*602T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 602 | chr7 | 35904895 | |||||
| chr7:35905147
|
C | G | 1 | a0001c0001t0016 | 3 | HG02129.hp2 NA18961.hp1 NA18995.hp1 |
3_prime_UTR_variant | MODIFIER | c.*854C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 854 | chr7 | 35905147 | |||||
| chr7:35905363
|
G | A | 1 | a0001c0001t0017 | 2 | HG02080.hp2 NA18995.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1070G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 1070 | chr7 | 35905363 | |||||
| chr7:35905495
|
C | T | 1 | a0001c0001t0021 | 2 | HG02155.hp2 NA19081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1202C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 1202 | chr7 | 35905495 | |||||
| chr7:35905522
|
AT | A | 15 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(12): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*1239delT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 1239 | INFO_REALIGN_3_PRIME | chr7 | 35905522 | ||||
| chr7:35905529
|
T | C | 1 | a0001c0001t0028 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1236T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 1236 | chr7 | 35905529 | |||||
| chr7:35905571
|
T | G | 1 | a0001c0001t0029 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1278T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 1278 | chr7 | 35905571 | |||||
| chr7:35905574
|
G | A | 21 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(18): Show | 158 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*1281G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 1281 | chr7 | 35905574 | |||||
| chr7:35905592
|
T | C | 32 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(29): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
3_prime_UTR_variant | MODIFIER | c.*1299T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 1299 | chr7 | 35905592 | |||||
| chr7:35905737
|
C | T | 1 | a0001c0001t0018 | 2 | HG02300.hp1 NA18949.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1444C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 1444 | chr7 | 35905737 | |||||
| chr7:35905802
|
G | A | 3 | a0001c0001t0003a0001c0001t0017a0001c0001t0023 | 39 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1509G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 1509 | chr7 | 35905802 | |||||
| chr7:35905811
|
A | G | 2 | a0001c0001t0009a0001c0001t0035 | 10 | HG02083.hp2 NA18942.hp1 NA18957.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1518A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 1518 | chr7 | 35905811 | |||||
| chr7:35905825
|
T | G | 1 | a0001c0001t0036 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1532T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 1532 | chr7 | 35905825 | |||||
| chr7:35905866
|
A | T | 4 | a0001c0001t0009a0001c0001t0012a0001c0001t0016others(1): Show | 21 | HG00609.hp1 HG02083.hp2 HG02129.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1573A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 1573 | chr7 | 35905866 | |||||
| chr7:35906106
|
C | T | 1 | a0001c0001t0011 | 8 | HG02280.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1813C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 1813 | chr7 | 35906106 | |||||
| chr7:35906243
|
C | G | 6 | a0001c0001t0006a0001c0001t0013a0001c0001t0021others(3): Show | 22 | HG00597.hp2 HG01255.hp1 HG01884.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1950C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 1950 | chr7 | 35906243 | |||||
| chr7:35906325
|
A | G | 1 | a0001c0001t0034 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2032A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 2032 | chr7 | 35906325 | |||||
| chr7:35906357
|
T | C | 1 | a0001c0001t0019 | 2 | HG02055.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2064T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 2064 | chr7 | 35906357 | |||||
| chr7:35906411
|
G | A | 6 | a0001c0001t0006a0001c0001t0013a0001c0001t0021others(3): Show | 22 | HG00597.hp2 HG01255.hp1 HG01884.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2118G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 2118 | chr7 | 35906411 | |||||
| chr7:35906494
|
T | C | 4 | a0001c0001t0006a0001c0001t0021a0001c0001t0028others(1): Show | 16 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2201T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 2201 | chr7 | 35906494 | |||||
| chr7:35906499
|
A | C | 1 | a0001c0001t0020 | 2 | HG01257.hp1 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2206A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 2206 | chr7 | 35906499 | |||||
| chr7:35906612
|
G | A | 1 | a0001c0001t0035 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2319G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 2319 | chr7 | 35906612 | |||||
| chr7:35906643
|
T | C | 5 | a0001c0001t0005a0001c0001t0020a0001c0001t0026others(2): Show | 20 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2350T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 2350 | chr7 | 35906643 | |||||
| chr7:35906649
|
A | G | 1 | a0001c0001t0010 | 8 | HG01934.hp1 NA18948.hp1 NA18997.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2356A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 2356 | chr7 | 35906649 | |||||
| chr7:35906660
|
C | T | 1 | a0001c0001t0032 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2367C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 2367 | chr7 | 35906660 | |||||
| chr7:35906680
|
G | A | 1 | a0001c0001t0030 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2387G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 2387 | chr7 | 35906680 | |||||
| chr7:35906711
|
T | C | 1 | a0001c0001t0037 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2418T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 2418 | chr7 | 35906711 | |||||
| chr7:35906743
|
C | G | 1 | a0001c0001t0033 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2450C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 2450 | chr7 | 35906743 | |||||
| chr7:35906818
|
T | G | 1 | a0001c0001t0031 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2525T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 2525 | chr7 | 35906818 | |||||
| chr7:35906999
|
T | G | 1 | a0001c0001t0008 | 9 | HG02622.hp1 HG02809.hp1 HG02886.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2706T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 2706 | chr7 | 35906999 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:35801288
|
G | GC | 336 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(333): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.61+18_61+19insC | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35801288 | ||||||
| chr7:35801464
|
G | A | 1 | a0001c0001t0004g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.61+194G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35801464 | ||||||
| chr7:35801488
|
G | A | 1 | a0001c0001t0005g0010 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.61+218G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35801488 | ||||||
| chr7:35801490
|
G | A | 4 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(1): Show | 4 | HG00408.hp2 HG01952.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+220G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35801490 | ||||||
| chr7:35801647
|
T | G | 216 | a0001c0001t0001g0049a0001c0001t0001g0180a0001c0001t0001g0181others(213): Show | 224 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.61+377T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35801647 | ||||||
| chr7:35801669
|
G | C | 9 | a0001c0001t0008g0015a0001c0001t0008g0016a0001c0001t0008g0017others(6): Show | 9 | HG02622.hp1 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.61+399G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35801669 | ||||||
| chr7:35801687
|
G | C | 150 | a0001c0001t0001g0049a0001c0001t0002g0004a0001c0001t0002g0025others(147): Show | 155 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.61+417G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35801687 | ||||||
| chr7:35802127
|
G | A | 1 | a0001c0001t0006g0024 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.61+857G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35802127 | ||||||
| chr7:35802276
|
A | G | 43 | a0001c0001t0003g0005a0001c0001t0003g0183a0001c0001t0003g0184others(40): Show | 46 | HG00438.hp1 HG00673.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.61+1006A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35802276 | ||||||
| chr7:35802379
|
T | A | 10 | a0001c0001t0003g0005a0001c0001t0003g0183a0001c0001t0003g0184others(7): Show | 11 | HG00438.hp1 HG00673.hp1 NA18954.hp2 others(8): Show |
intron_variant | MODIFIER | c.61+1109T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35802379 | ||||||
| chr7:35802398
|
T | G | 1 | a0001c0001t0002g0025 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.61+1128T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35802398 | ||||||
| chr7:35802455
|
C | G | 1 | a0001c0001t0002g0025 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.61+1185C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35802455 | ||||||
| chr7:35802567
|
A | C | 2 | a0001c0001t0005g0220a0001c0001t0005g0221 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.61+1297A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35802567 | ||||||
| chr7:35802577
|
A | G | 1 | a0001c0001t0005g0219 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.61+1307A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35802577 | ||||||
| chr7:35802647
|
G | C | 2 | a0001c0001t0003g0026a0001c0001t0003g0027 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.61+1377G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35802647 | ||||||
| chr7:35802694
|
A | G | 1 | a0001c0001t0003g0169 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.61+1424A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35802694 | ||||||
| chr7:35802720
|
G | C | 2 | a0001c0001t0005g0220a0001c0001t0005g0221 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.61+1450G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35802720 | ||||||
| chr7:35802814
|
G | C | 5 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG00438.hp2 HG01346.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+1544G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35802814 | ||||||
| chr7:35802816
|
G | A | 46 | a0001c0001t0004g0002a0001c0001t0004g0006a0001c0001t0004g0009others(43): Show | 49 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(46): Show |
intron_variant | MODIFIER | c.61+1546G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35802816 | ||||||
| chr7:35802829
|
G | C | 1 | a0001c0001t0035g0227 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.61+1559G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35802829 | ||||||
| chr7:35803044
|
T | C | 3 | a0001c0001t0002g0029a0001c0001t0002g0030a0001c0001t0002g0031 | 3 | HG02486.hp1 HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.61+1774T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35803044 | ||||||
| chr7:35803114
|
A | G | 123 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(120): Show | 125 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.61+1844A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35803114 | ||||||
| chr7:35803453
|
A | T | 1 | a0001c0001t0003g0191 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.61+2183A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35803453 | ||||||
| chr7:35803550
|
G | A | 1 | a0001c0001t0038g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.61+2280G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35803550 | ||||||
| chr7:35803710
|
A | ACAAAACT others(307): Show |
1 | a0001c0001t0025g0168 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.61+2451_61+2452ins others(314): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35803710 | |||||
| chr7:35803846
|
C | T | 2 | a0001c0001t0005g0220a0001c0001t0005g0221 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.61+2576C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35803846 | ||||||
| chr7:35803880
|
T | C | 11 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034others(8): Show | 11 | HG01109.hp1 HG02258.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.61+2610T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35803880 | ||||||
| chr7:35804029
|
C | T | 1 | a0001c0001t0001g0336 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.61+2759C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35804029 | ||||||
| chr7:35804275
|
A | G | 1 | a0001c0001t0031g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.61+3005A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35804275 | ||||||
| chr7:35804760
|
A | G | 1 | a0001c0001t0001g0335 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.61+3490A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35804760 | ||||||
| chr7:35804835
|
G | GT | 37 | a0001c0001t0001g0324a0001c0001t0001g0325a0001c0001t0001g0326others(34): Show | 40 | HG00438.hp1 HG01099.hp1 HG01123.hp1 others(37): Show |
intron_variant | MODIFIER | c.61+3583dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35804835 | |||||
| chr7:35804835
|
G | GTT | 13 | a0001c0001t0002g0166a0001c0001t0005g0010a0001c0001t0005g0202others(10): Show | 13 | HG00140.hp2 HG00738.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.61+3582_61+3583dup others(2): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35804835 | |||||
| chr7:35804835
|
G | T | 28 | a0001c0001t0001g0331a0001c0001t0001g0332a0001c0001t0001g0333others(25): Show | 29 | HG00642.hp1 HG01099.hp2 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.61+3565G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35804835 | ||||||
| chr7:35804867
|
G | A | 1 | a0001c0001t0011g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.61+3597G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35804867 | ||||||
| chr7:35805070
|
C | T | 1 | a0001c0001t0011g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.61+3800C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35805070 | ||||||
| chr7:35805177
|
C | T | 3 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0004g0009 | 3 | HG02109.hp1 HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.61+3907C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35805177 | ||||||
| chr7:35805230
|
A | C | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.61+3960A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35805230 | ||||||
| chr7:35805843
|
A | C | 1 | a0001c0001t0001g0323 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.61+4573A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35805843 | ||||||
| chr7:35806012
|
T | C | 1 | a0001c0001t0002g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.61+4742T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35806012 | ||||||
| chr7:35806038
|
C | G | 1 | a0001c0001t0032g0158 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.61+4768C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35806038 | ||||||
| chr7:35806103
|
G | T | 1 | a0001c0001t0009g0322 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.61+4833G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35806103 | ||||||
| chr7:35806105
|
G | C | 1 | a0001c0001t0001g0331 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.61+4835G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35806105 | ||||||
| chr7:35806125
|
G | T | 7 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0001t0002g0153others(4): Show | 7 | HG00609.hp2 NA18951.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.61+4855G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35806125 | ||||||
| chr7:35806237
|
T | C | 1 | a0001c0001t0002g0166 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.61+4967T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35806237 | ||||||
| chr7:35806290
|
T | C | 1 | a0001c0001t0012g0228 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.61+5020T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35806290 | ||||||
| chr7:35806350
|
T | G | 6 | a0001c0001t0013g0044a0001c0001t0013g0045a0001c0001t0013g0046others(3): Show | 6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.61+5080T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35806350 | ||||||
| chr7:35806478
|
G | A | 1 | a0001c0001t0005g0192 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.61+5208G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35806478 | ||||||
| chr7:35806498
|
A | G | 119 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(116): Show | 121 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.61+5228A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35806498 | ||||||
| chr7:35806517
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.61+5247G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35806517 | ||||||
| chr7:35806648
|
A | G | 4 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+5378A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35806648 | ||||||
| chr7:35807173
|
T | C | 2 | a0001c0001t0003g0026a0001c0001t0003g0027 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.61+5903T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35807173 | ||||||
| chr7:35807186
|
C | CT | 44 | a0001c0001t0001g0321a0001c0001t0002g0123a0001c0001t0002g0124others(41): Show | 44 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.61+5931dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35807186 | |||||
| chr7:35807237
|
T | C | 2 | a0001c0001t0005g0220a0001c0001t0005g0221 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.61+5967T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35807237 | ||||||
| chr7:35807269
|
C | T | 47 | a0001c0001t0002g0071a0001c0001t0004g0002a0001c0001t0004g0006others(44): Show | 50 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(47): Show |
intron_variant | MODIFIER | c.61+5999C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35807269 | ||||||
| chr7:35807278
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.61+6008G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35807278 | ||||||
| chr7:35807309
|
G | A | 21 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(18): Show | 23 | HG00597.hp2 HG01255.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.61+6039G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35807309 | ||||||
| chr7:35807313
|
A | G | 1 | a0001c0001t0003g0169 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.61+6043A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35807313 | ||||||
| chr7:35807351
|
AT | A | 174 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(171): Show | 179 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.61+6110delT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35807351 | |||||
| chr7:35807351
|
ATT | A | 124 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0002g0004others(121): Show | 128 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.61+6109_61+6110del others(2): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35807351 | |||||
| chr7:35807351
|
ATTT | A | 14 | a0001c0001t0002g0025a0001c0001t0002g0078a0001c0001t0002g0079others(11): Show | 14 | HG02129.hp1 HG02896.hp1 HG03239.hp1 others(11): Show |
intron_variant | MODIFIER | c.61+6108_61+6110del others(3): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35807351 | |||||
| chr7:35807400
|
C | T | 1 | a0001c0001t0003g0216 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.61+6130C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35807400 | ||||||
| chr7:35807431
|
G | A | 133 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(130): Show | 135 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.61+6161G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35807431 | ||||||
| chr7:35807436
|
G | A | 25 | a0001c0001t0002g0071a0001c0001t0004g0002a0001c0001t0004g0006others(22): Show | 27 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.61+6166G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35807436 | ||||||
| chr7:35807525
|
C | T | 10 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0118others(7): Show | 11 | HG00733.hp2 HG00741.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.61+6255C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35807525 | ||||||
| chr7:35807606
|
G | A | 154 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(151): Show | 158 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.61+6336G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35807606 | ||||||
| chr7:35807643
|
G | A | 24 | a0001c0001t0004g0002a0001c0001t0004g0006a0001c0001t0004g0009others(21): Show | 26 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.61+6373G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35807643 | ||||||
| chr7:35807861
|
G | T | 13 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0202others(10): Show | 14 | HG00738.hp1 HG01081.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.61+6591G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35807861 | ||||||
| chr7:35808095
|
G | A | 3 | a0001c0001t0002g0029a0001c0001t0002g0030a0001c0001t0002g0031 | 3 | HG02486.hp1 HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.61+6825G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35808095 | ||||||
| chr7:35808099
|
A | G | 201 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(198): Show | 208 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.61+6829A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35808099 | ||||||
| chr7:35808113
|
A | G | 201 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(198): Show | 208 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.61+6843A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35808113 | ||||||
| chr7:35808210
|
TCTTA | T | 13 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0202others(10): Show | 14 | HG00738.hp1 HG01081.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.61+6944_61+6947del others(4): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35808210 | |||||
| chr7:35808377
|
T | C | 154 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(151): Show | 158 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.61+7107T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35808377 | ||||||
| chr7:35808709
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.61+7439G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35808709 | ||||||
| chr7:35808720
|
C | G | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.61+7450C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35808720 | ||||||
| chr7:35808802
|
A | G | 5 | a0001c0001t0002g0035a0001c0001t0002g0038a0001c0001t0002g0039others(2): Show | 5 | HG01109.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+7532A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35808802 | ||||||
| chr7:35808941
|
A | G | 1 | a0001c0001t0003g0115 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.61+7671A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35808941 | ||||||
| chr7:35808975
|
G | A | 1 | a0001c0001t0008g0016 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.61+7705G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35808975 | ||||||
| chr7:35808988
|
A | G | 1 | a0001c0001t0031g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.61+7718A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35808988 | ||||||
| chr7:35809227
|
G | A | 3 | a0001c0001t0012g0062a0001c0001t0012g0063a0001c0001t0012g0064 | 3 | NA18975.hp2 NA19006.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.61+7957G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35809227 | ||||||
| chr7:35809378
|
A | G | 1 | a0001c0001t0002g0025 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.61+8108A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35809378 | ||||||
| chr7:35809643
|
G | A | 2 | a0001c0001t0022g0194a0001c0001t0022g0195 | 2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.61+8373G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35809643 | ||||||
| chr7:35809706
|
A | G | 3 | a0001c0001t0002g0073a0001c0001t0002g0113a0001c0001t0002g0114 | 3 | HG02559.hp2 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.61+8436A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35809706 | ||||||
| chr7:35809869
|
A | G | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.61+8599A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35809869 | ||||||
| chr7:35809983
|
A | T | 1 | a0001c0001t0001g0309 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.61+8713A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35809983 | ||||||
| chr7:35810044
|
T | C | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.61+8774T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35810044 | ||||||
| chr7:35810448
|
C | T | 7 | a0001c0001t0002g0071a0001c0001t0013g0044a0001c0001t0013g0045others(4): Show | 7 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.61+9178C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35810448 | ||||||
| chr7:35810569
|
C | T | 1 | a0001c0001t0020g0007 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.61+9299C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35810569 | ||||||
| chr7:35810612
|
C | T | 133 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(130): Show | 135 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.61+9342C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35810612 | ||||||
| chr7:35810735
|
T | C | 15 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(12): Show | 17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.61+9465T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35810735 | ||||||
| chr7:35810771
|
G | GT | 12 | a0001c0001t0001g0226a0001c0001t0001g0308a0001c0001t0003g0112others(9): Show | 12 | HG00438.hp2 HG00642.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.61+9514dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35810771 | |||||
| chr7:35810923
|
C | T | 5 | a0001c0002t0001g0301a0001c0002t0001g0302a0001c0002t0001g0303others(2): Show | 5 | NA18949.hp2 NA18974.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+9653C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35810923 | ||||||
| chr7:35810958
|
G | A | 4 | a0001c0001t0012g0062a0001c0001t0012g0063a0001c0001t0012g0064others(1): Show | 4 | NA18970.hp2 NA18975.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+9688G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35810958 | ||||||
| chr7:35811096
|
G | A | 22 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0197others(19): Show | 23 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.61+9826G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35811096 | ||||||
| chr7:35811224
|
A | G | 1 | a0001c0001t0038g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.61+9954A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35811224 | ||||||
| chr7:35811275
|
C | T | 1 | a0001c0001t0004g0193 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.61+10005C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35811275 | ||||||
| chr7:35811288
|
G | A | 1 | a0001c0001t0009g0230 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.61+10018G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35811288 | ||||||
| chr7:35811628
|
G | T | 202 | a0001c0001t0001g0181a0001c0001t0002g0004a0001c0001t0002g0025others(199): Show | 209 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.61+10358G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35811628 | ||||||
| chr7:35811639
|
C | T | 1 | a0001c0001t0009g0230 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.61+10369C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35811639 | ||||||
| chr7:35811707
|
T | C | 38 | a0001c0001t0003g0005a0001c0001t0003g0026a0001c0001t0003g0027others(35): Show | 39 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.61+10437T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35811707 | ||||||
| chr7:35811730
|
T | G | 3 | a0001c0001t0004g0171a0001c0001t0004g0178a0001c0001t0004g0179 | 3 | HG02055.hp2 HG02886.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.61+10460T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35811730 | ||||||
| chr7:35812104
|
C | G | 2 | a0001c0001t0009g0299a0001c0001t0009g0300 | 2 | NA19059.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.61+10834C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35812104 | ||||||
| chr7:35812128
|
CA | C | 183 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(180): Show | 190 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.61+10872delA | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35812128 | |||||
| chr7:35812142
|
A | C | 9 | a0001c0001t0003g0214a0001c0001t0004g0172a0001c0001t0013g0044others(6): Show | 9 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.61+10872A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35812142 | ||||||
| chr7:35812143
|
C | A | 11 | a0001c0001t0001g0181a0001c0001t0003g0214a0001c0001t0004g0172others(8): Show | 11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.61+10873C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35812143 | ||||||
| chr7:35812153
|
A | C | 2 | a0001c0001t0002g0030a0001c0001t0002g0031 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.61+10883A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35812153 | ||||||
| chr7:35812336
|
T | C | 1 | a0001c0001t0015g0051 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.61+11066T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35812336 | ||||||
| chr7:35812343
|
T | A | 1 | a0001c0001t0015g0051 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.61+11073T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35812343 | ||||||
| chr7:35812418
|
A | T | 1 | a0001c0001t0018g0103 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.61+11148A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35812418 | ||||||
| chr7:35812452
|
T | C | 1 | a0001c0002t0001g0011 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.61+11182T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35812452 | ||||||
| chr7:35812481
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.61+11211A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35812481 | ||||||
| chr7:35812686
|
C | T | 1 | a0001c0001t0015g0051 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.61+11416C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35812686 | ||||||
| chr7:35812687
|
T | C | 1 | a0001c0001t0015g0051 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.61+11417T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35812687 | ||||||
| chr7:35812755
|
A | T | 1 | a0001c0001t0015g0051 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.61+11485A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35812755 | ||||||
| chr7:35813017
|
G | A | 1 | a0001c0001t0012g0234 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.61+11747G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35813017 | ||||||
| chr7:35813282
|
T | TAAAAACT others(289): Show |
1 | a0001c0004t0013g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.61+12025_61+12026i others(298): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35813282 | |||||
| chr7:35813311
|
C | T | 1 | a0001c0001t0008g0023 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.61+12041C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35813311 | ||||||
| chr7:35813341
|
A | G | 1 | a0001c0001t0001g0320 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.61+12071A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35813341 | ||||||
| chr7:35813385
|
C | T | 4 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(1): Show | 4 | HG00408.hp2 HG01952.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+12115C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35813385 | ||||||
| chr7:35813398
|
A | G | 1 | a0001c0001t0037g0206 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.61+12128A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35813398 | ||||||
| chr7:35813830
|
A | T | 1 | a0001c0001t0005g0205 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.61+12560A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35813830 | ||||||
| chr7:35813875
|
G | A | 1 | a0001c0001t0011g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.61+12605G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35813875 | ||||||
| chr7:35814006
|
A | C | 1 | a0001c0001t0015g0051 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.61+12736A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35814006 | ||||||
| chr7:35814012
|
A | C | 1 | a0001c0001t0015g0051 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.61+12742A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35814012 | ||||||
| chr7:35814055
|
T | TAAAAGTT others(196): Show |
1 | a0001c0001t0005g0200 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.61+12802_61+12803i others(205): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35814055 | |||||
| chr7:35814055
|
T | TAAAAGTT others(197): Show |
6 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(3): Show | 6 | HG01255.hp2 HG02257.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.61+12802_61+12803i others(206): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35814055 | |||||
| chr7:35814055
|
T | TAAAAGTT others(198): Show |
14 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0202others(11): Show | 15 | HG00738.hp1 HG01081.hp1 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.61+12802_61+12803i others(207): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35814055 | |||||
| chr7:35814055
|
T | TAAAAGTT others(199): Show |
1 | a0001c0001t0005g0207 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.61+12802_61+12803i others(208): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35814055 | |||||
| chr7:35814120
|
G | A | 9 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(6): Show | 9 | HG00408.hp2 HG01952.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.61+12850G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35814120 | ||||||
| chr7:35814340
|
A | T | 3 | a0001c0001t0002g0074a0001c0001t0002g0075a0001c0001t0002g0076 | 3 | HG01243.hp2 HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.61+13070A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35814340 | ||||||
| chr7:35814355
|
T | A | 1 | a0001c0001t0015g0051 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.61+13085T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35814355 | ||||||
| chr7:35814368
|
T | C | 1 | a0001c0001t0023g0089 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.61+13098T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35814368 | ||||||
| chr7:35814428
|
T | G | 1 | a0001c0001t0002g0125 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.61+13158T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35814428 | ||||||
| chr7:35814487
|
G | GT | 134 | a0001c0001t0001g0298a0001c0001t0002g0004a0001c0001t0002g0025others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.61+13224dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35814487 | |||||
| chr7:35814627
|
G | GGTGATTT others(8): Show |
1 | a0001c0001t0038g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.61+13358_61+13372d others(17): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35814627 | |||||
| chr7:35814792
|
G | C | 1 | a0001c0001t0002g0126 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.61+13522G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35814792 | ||||||
| chr7:35814902
|
A | G | 202 | a0001c0001t0001g0298a0001c0001t0002g0004a0001c0001t0002g0025others(199): Show | 209 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.61+13632A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35814902 | ||||||
| chr7:35814930
|
T | G | 18 | a0001c0001t0003g0005a0001c0001t0003g0183a0001c0001t0003g0184others(15): Show | 19 | HG00438.hp1 HG00673.hp1 HG02074.hp1 others(16): Show |
intron_variant | MODIFIER | c.61+13660T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35814930 | ||||||
| chr7:35814955
|
A | G | 1 | a0001c0001t0024g0177 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.61+13685A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35814955 | ||||||
| chr7:35814974
|
C | CA | 59 | a0001c0001t0001g0049a0001c0001t0001g0181a0001c0001t0001g0182others(56): Show | 62 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.61+13730dupA | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35814974 | |||||
| chr7:35814974
|
C | CAA | 6 | a0001c0001t0003g0090a0001c0001t0003g0215a0001c0001t0003g0216others(3): Show | 6 | HG01358.hp1 HG02080.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.61+13729_61+13730d others(4): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35814974 | |||||
| chr7:35814974
|
CA | C | 14 | a0001c0001t0002g0039a0001c0001t0003g0101a0001c0001t0003g0102others(11): Show | 14 | HG00099.hp1 HG01167.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.61+13730delA | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35814974 | |||||
| chr7:35814976
|
A | C | 1 | a0001c0001t0001g0297 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.61+13706A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35814976 | ||||||
| chr7:35815108
|
C | G | 10 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0293others(7): Show | 10 | HG00140.hp1 HG01074.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.61+13838C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35815108 | ||||||
| chr7:35815129
|
T | A | 1 | a0001c0001t0001g0325 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.61+13859T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35815129 | ||||||
| chr7:35815244
|
T | G | 2 | a0001c0002t0001g0012a0001c0002t0001g0013 | 2 | HG01952.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.61+13974T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35815244 | ||||||
| chr7:35815381
|
G | T | 1 | a0001c0001t0002g0076 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.61+14111G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35815381 | ||||||
| chr7:35815822
|
T | G | 1 | a0001c0001t0001g0235 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.61+14552T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35815822 | ||||||
| chr7:35816030
|
A | G | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.61+14760A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35816030 | ||||||
| chr7:35816190
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.61+14920C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35816190 | ||||||
| chr7:35816322
|
A | G | 5 | a0001c0001t0002g0035a0001c0001t0002g0038a0001c0001t0002g0039others(2): Show | 5 | HG01109.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+15052A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35816322 | ||||||
| chr7:35816400
|
T | A | 1 | a0001c0001t0004g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.62-15092T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35816400 | ||||||
| chr7:35816473
|
G | A | 336 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(333): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.62-15019G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35816473 | ||||||
| chr7:35816729
|
G | T | 133 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(130): Show | 135 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.62-14763G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35816729 | ||||||
| chr7:35816746
|
C | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0317 | 2 | NA18973.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.62-14746C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35816746 | ||||||
| chr7:35817008
|
GT | G | 16 | a0001c0001t0001g0222a0001c0001t0006g0001a0001c0001t0006g0024others(13): Show | 18 | HG00597.hp2 HG01943.hp2 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.62-14470delT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35817008 | |||||
| chr7:35817021
|
T | TTTACGTT others(5): Show |
1 | a0001c0001t0009g0242 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.62-14470_62-14469i others(14): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35817021 | |||||
| chr7:35817024
|
C | G | 1 | a0001c0001t0009g0242 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.62-14468C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35817024 | ||||||
| chr7:35817126
|
T | C | 1 | a0001c0001t0022g0194 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.62-14366T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35817126 | ||||||
| chr7:35817186
|
A | G | 15 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(12): Show | 17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.62-14306A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35817186 | ||||||
| chr7:35817201
|
TTTTTGAT others(3): Show |
T | 8 | a0001c0001t0001g0182a0001c0001t0011g0003a0001c0001t0011g0065others(5): Show | 9 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.62-14284_62-14275d others(12): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35817201 | |||||
| chr7:35817252
|
T | G | 1 | a0001c0001t0011g0067 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.62-14240T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35817252 | ||||||
| chr7:35817269
|
A | G | 1 | a0001c0001t0010g0241 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.62-14223A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35817269 | ||||||
| chr7:35817315
|
A | G | 1 | a0001c0001t0001g0288 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.62-14177A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35817315 | ||||||
| chr7:35817317
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.62-14175T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35817317 | ||||||
| chr7:35817499
|
C | T | 1 | a0001c0001t0002g0162 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.62-13993C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35817499 | ||||||
| chr7:35817536
|
C | T | 1 | a0001c0001t0012g0233 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.62-13956C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35817536 | ||||||
| chr7:35817571
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.62-13921A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35817571 | ||||||
| chr7:35817589
|
G | A | 1 | a0001c0001t0002g0116 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.62-13903G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35817589 | ||||||
| chr7:35817609
|
A | T | 2 | a0001c0001t0002g0125a0001c0001t0002g0146 | 2 | NA18941.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.62-13883A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35817609 | ||||||
| chr7:35817615
|
A | G | 37 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0197others(34): Show | 40 | HG00597.hp2 HG00738.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.62-13877A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35817615 | ||||||
| chr7:35817928
|
A | T | 3 | a0001c0001t0002g0074a0001c0001t0002g0075a0001c0001t0002g0076 | 3 | HG01243.hp2 HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.62-13564A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35817928 | ||||||
| chr7:35818006
|
C | T | 1 | a0001c0001t0014g0165 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.62-13486C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35818006 | ||||||
| chr7:35818094
|
A | G | 1 | a0001c0001t0027g0145 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.62-13398A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35818094 | ||||||
| chr7:35818460
|
A | C | 2 | a0001c0001t0003g0091a0001c0001t0003g0115 | 2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.62-13032A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35818460 | ||||||
| chr7:35818577
|
G | A | 9 | a0001c0001t0001g0049a0001c0001t0001g0182a0001c0001t0011g0003others(6): Show | 10 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.62-12915G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35818577 | ||||||
| chr7:35818769
|
T | A | 1 | a0001c0001t0020g0007 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.62-12723T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35818769 | ||||||
| chr7:35818798
|
A | G | 1 | a0001c0001t0001g0316 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.62-12694A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35818798 | ||||||
| chr7:35818884
|
G | A | 3 | a0001c0001t0001g0236a0001c0001t0001g0243a0001c0001t0001g0244 | 3 | NA18979.hp1 NA18991.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.62-12608G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35818884 | ||||||
| chr7:35819054
|
G | A | 211 | a0001c0001t0001g0049a0001c0001t0001g0181a0001c0001t0001g0182others(208): Show | 219 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.62-12438G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35819054 | ||||||
| chr7:35819071
|
A | G | 8 | a0001c0001t0002g0128a0001c0001t0002g0140a0001c0001t0002g0141others(5): Show | 8 | HG00558.hp1 HG00597.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.62-12421A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35819071 | ||||||
| chr7:35819109
|
C | T | 15 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(12): Show | 17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.62-12383C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35819109 | ||||||
| chr7:35819137
|
G | A | 1 | a0001c0001t0031g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.62-12355G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35819137 | ||||||
| chr7:35819399
|
C | T | 2 | a0001c0001t0001g0222a0001c0001t0001g0225 | 2 | HG01346.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.62-12093C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35819399 | ||||||
| chr7:35819409
|
T | A | 201 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(198): Show | 208 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.62-12083T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35819409 | ||||||
| chr7:35819460
|
AGTTGGTT others(6): Show |
A | 2 | a0001c0001t0002g0041a0001c0001t0002g0042 | 2 | HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.62-12027_62-12015d others(15): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35819460 | |||||
| chr7:35819496
|
T | A | 1 | a0001c0001t0002g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.62-11996T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35819496 | ||||||
| chr7:35819521
|
G | A | 201 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(198): Show | 208 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.62-11971G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35819521 | ||||||
| chr7:35819535
|
G | A | 1 | a0001c0001t0004g0174 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.62-11957G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35819535 | ||||||
| chr7:35819629
|
C | T | 2 | a0001c0001t0004g0173a0001c0001t0004g0176 | 2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.62-11863C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35819629 | ||||||
| chr7:35819704
|
A | G | 2 | a0001c0001t0005g0220a0001c0001t0005g0221 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.62-11788A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35819704 | ||||||
| chr7:35819756
|
C | G | 1 | a0001c0001t0001g0287 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.62-11736C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35819756 | ||||||
| chr7:35819867
|
C | T | 2 | a0001c0001t0004g0002a0001c0001t0004g0028 | 3 | HG02615.hp1 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.62-11625C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35819867 | ||||||
| chr7:35820051
|
A | G | 122 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.62-11441A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35820051 | ||||||
| chr7:35820082
|
C | T | 211 | a0001c0001t0001g0049a0001c0001t0001g0181a0001c0001t0001g0182others(208): Show | 219 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.62-11410C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35820082 | ||||||
| chr7:35820570
|
T | A | 2 | a0001c0001t0002g0041a0001c0001t0002g0042 | 2 | HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.62-10922T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35820570 | ||||||
| chr7:35820619
|
T | C | 47 | a0001c0001t0002g0071a0001c0001t0004g0002a0001c0001t0004g0006others(44): Show | 50 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(47): Show |
intron_variant | MODIFIER | c.62-10873T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35820619 | ||||||
| chr7:35820657
|
A | G | 1 | a0001c0001t0012g0233 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.62-10835A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35820657 | ||||||
| chr7:35820755
|
GT | G | 6 | a0001c0001t0013g0044a0001c0001t0013g0045a0001c0001t0013g0046others(3): Show | 6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-10729delT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35820755 | |||||
| chr7:35820756
|
T | G | 6 | a0001c0001t0004g0171a0001c0001t0004g0173a0001c0001t0004g0174others(3): Show | 6 | HG02055.hp2 HG02258.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.62-10736T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35820756 | ||||||
| chr7:35820949
|
A | G | 176 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(173): Show | 181 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.62-10543A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35820949 | ||||||
| chr7:35821066
|
G | GT | 132 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(129): Show | 134 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.62-10419dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35821066 | |||||
| chr7:35821106
|
G | A | 1 | a0001c0001t0011g0068 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.62-10386G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35821106 | ||||||
| chr7:35821154
|
C | G | 176 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(173): Show | 181 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.62-10338C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35821154 | ||||||
| chr7:35821247
|
G | A | 1 | a0001c0001t0002g0074 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.62-10245G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35821247 | ||||||
| chr7:35821352
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.62-10140C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35821352 | ||||||
| chr7:35821399
|
A | G | 2 | a0001c0001t0003g0090a0001c0001t0023g0089 | 2 | HG01081.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.62-10093A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35821399 | ||||||
| chr7:35821749
|
C | A | 1 | a0001c0001t0001g0245 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.62-9743C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35821749 | ||||||
| chr7:35821765
|
A | T | 11 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034others(8): Show | 11 | HG01109.hp1 HG02258.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.62-9727A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35821765 | ||||||
| chr7:35821952
|
G | A | 1 | a0002c0005t0002g0104 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.62-9540G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35821952 | ||||||
| chr7:35821959
|
C | T | 1 | a0001c0002t0001g0303 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.62-9533C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35821959 | ||||||
| chr7:35822061
|
C | T | 6 | a0001c0001t0013g0044a0001c0001t0013g0045a0001c0001t0013g0046others(3): Show | 6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-9431C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35822061 | ||||||
| chr7:35822189
|
C | T | 133 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(130): Show | 135 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.62-9303C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35822189 | ||||||
| chr7:35822512
|
C | T | 15 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(12): Show | 17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.62-8980C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35822512 | ||||||
| chr7:35822534
|
G | A | 154 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(151): Show | 158 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.62-8958G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35822534 | ||||||
| chr7:35822610
|
C | T | 2 | a0001c0001t0021g0050a0001c0001t0021g0059 | 2 | HG02155.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.62-8882C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35822610 | ||||||
| chr7:35822699
|
G | A | 211 | a0001c0001t0001g0049a0001c0001t0001g0181a0001c0001t0001g0182others(208): Show | 219 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.62-8793G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35822699 | ||||||
| chr7:35822745
|
C | A | 15 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(12): Show | 17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.62-8747C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35822745 | ||||||
| chr7:35823359
|
G | A | 1 | a0001c0001t0002g0152 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.62-8133G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35823359 | ||||||
| chr7:35823448
|
G | T | 22 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0197others(19): Show | 23 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.62-8044G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35823448 | ||||||
| chr7:35823491
|
G | A | 1 | a0001c0001t0031g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.62-8001G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35823491 | ||||||
| chr7:35823624
|
C | T | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0315 | 3 | HG00735.hp2 HG00741.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.62-7868C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35823624 | ||||||
| chr7:35823861
|
C | CT | 7 | a0001c0001t0003g0215a0001c0001t0004g0171a0001c0001t0004g0173others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.62-7622dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35823861 | |||||
| chr7:35823869
|
T | G | 3 | a0001c0001t0014g0105a0001c0001t0014g0129a0001c0001t0014g0130 | 3 | HG02155.hp1 HG02165.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.62-7623T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35823869 | ||||||
| chr7:35823870
|
T | G | 81 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(78): Show | 82 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.62-7622T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35823870 | ||||||
| chr7:35824037
|
C | T | 1 | a0001c0001t0002g0128 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.62-7455C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35824037 | ||||||
| chr7:35824068
|
T | C | 9 | a0001c0001t0001g0049a0001c0001t0001g0182a0001c0001t0011g0003others(6): Show | 10 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.62-7424T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35824068 | ||||||
| chr7:35824596
|
A | G | 1 | a0001c0002t0001g0014 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.62-6896A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35824596 | ||||||
| chr7:35824684
|
C | G | 1 | a0001c0001t0002g0111 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.62-6808C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35824684 | ||||||
| chr7:35824751
|
G | A | 1 | a0001c0001t0002g0032 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.62-6741G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35824751 | ||||||
| chr7:35825319
|
A | G | 1 | a0001c0001t0004g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.62-6173A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35825319 | ||||||
| chr7:35825442
|
A | T | 9 | a0001c0001t0002g0088a0001c0001t0002g0128a0001c0001t0002g0140others(6): Show | 9 | HG00558.hp1 HG00597.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.62-6050A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35825442 | ||||||
| chr7:35825626
|
C | T | 3 | a0001c0001t0002g0029a0001c0001t0002g0030a0001c0001t0002g0031 | 3 | HG02486.hp1 HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.62-5866C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35825626 | ||||||
| chr7:35825678
|
A | G | 2 | a0001c0001t0002g0138a0001c0001t0002g0139 | 2 | HG02071.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.62-5814A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35825678 | ||||||
| chr7:35825967
|
G | C | 1 | a0001c0001t0002g0078 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.62-5525G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35825967 | ||||||
| chr7:35826409
|
A | T | 8 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0004g0171others(5): Show | 8 | HG00673.hp2 HG02055.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.62-5083A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35826409 | ||||||
| chr7:35826416
|
A | T | 2 | a0001c0001t0005g0220a0001c0001t0005g0221 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.62-5076A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35826416 | ||||||
| chr7:35826512
|
T | C | 201 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(198): Show | 208 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.62-4980T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35826512 | ||||||
| chr7:35826555
|
T | A | 2 | a0001c0001t0003g0026a0001c0001t0003g0027 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.62-4937T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35826555 | ||||||
| chr7:35826765
|
C | T | 6 | a0001c0001t0004g0171a0001c0001t0004g0173a0001c0001t0004g0174others(3): Show | 6 | HG02055.hp2 HG02258.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.62-4727C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35826765 | ||||||
| chr7:35826766
|
T | G | 43 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0197others(40): Show | 46 | HG00597.hp2 HG00738.hp1 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.62-4726T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35826766 | ||||||
| chr7:35826828
|
T | C | 201 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(198): Show | 208 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.62-4664T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35826828 | ||||||
| chr7:35826901
|
C | T | 1 | a0001c0001t0005g0209 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.62-4591C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35826901 | ||||||
| chr7:35827024
|
C | T | 11 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034others(8): Show | 11 | HG01109.hp1 HG02258.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.62-4468C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35827024 | ||||||
| chr7:35827070
|
C | T | 1 | a0001c0001t0026g0204 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.62-4422C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35827070 | ||||||
| chr7:35827187
|
T | A | 1 | a0001c0001t0001g0309 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.62-4305T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35827187 | ||||||
| chr7:35827321
|
G | GT | 201 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(198): Show | 208 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.62-4169dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35827321 | |||||
| chr7:35827525
|
C | T | 6 | a0001c0001t0013g0044a0001c0001t0013g0045a0001c0001t0013g0046others(3): Show | 6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-3967C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35827525 | ||||||
| chr7:35827552
|
G | A | 22 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0197others(19): Show | 23 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.62-3940G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35827552 | ||||||
| chr7:35827567
|
T | C | 2 | a0001c0001t0002g0118a0001c0001t0007g0117 | 2 | HG00733.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.62-3925T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35827567 | ||||||
| chr7:35827687
|
C | T | 1 | a0001c0001t0002g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.62-3805C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35827687 | ||||||
| chr7:35827796
|
A | T | 1 | a0001c0001t0002g0025 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.62-3696A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35827796 | ||||||
| chr7:35827891
|
T | C | 1 | a0001c0001t0038g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.62-3601T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35827891 | ||||||
| chr7:35827987
|
A | G | 2 | a0001c0001t0005g0220a0001c0001t0005g0221 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.62-3505A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35827987 | ||||||
| chr7:35828058
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.62-3434C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35828058 | ||||||
| chr7:35828252
|
T | G | 46 | a0001c0001t0004g0002a0001c0001t0004g0006a0001c0001t0004g0009others(43): Show | 49 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(46): Show |
intron_variant | MODIFIER | c.62-3240T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35828252 | ||||||
| chr7:35828265
|
C | G | 1 | a0001c0001t0002g0144 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.62-3227C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35828265 | ||||||
| chr7:35828400
|
A | T | 1 | a0001c0001t0004g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.62-3092A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35828400 | ||||||
| chr7:35828454
|
C | T | 1 | a0001c0001t0038g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.62-3038C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35828454 | ||||||
| chr7:35828545
|
A | G | 1 | a0001c0001t0003g0213 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.62-2947A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35828545 | ||||||
| chr7:35828676
|
C | T | 2 | a0001c0001t0001g0308a0001c0001t0010g0307 | 2 | HG01358.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.62-2816C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35828676 | ||||||
| chr7:35828712
|
C | T | 1 | a0001c0001t0003g0188 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.62-2780C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35828712 | ||||||
| chr7:35828821
|
C | T | 2 | a0001c0001t0002g0041a0001c0001t0002g0042 | 2 | HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.62-2671C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35828821 | ||||||
| chr7:35828836
|
C | G | 38 | a0001c0001t0003g0005a0001c0001t0003g0026a0001c0001t0003g0027others(35): Show | 39 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.62-2656C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35828836 | ||||||
| chr7:35828873
|
G | T | 1 | a0001c0001t0002g0155 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.62-2619G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35828873 | ||||||
| chr7:35829086
|
C | T | 1 | a0001c0001t0002g0149 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.62-2406C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35829086 | ||||||
| chr7:35829128
|
C | CT | 47 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0222others(44): Show | 51 | HG00438.hp2 HG00738.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.62-2340dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | |||||
| chr7:35829128
|
C | CTTTT | 10 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034others(7): Show | 10 | HG01109.hp1 HG02258.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.62-2343_62-2340dup others(4): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | |||||
| chr7:35829128
|
C | CTTTTT | 10 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0080others(7): Show | 10 | HG01433.hp2 HG02895.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.62-2344_62-2340dup others(5): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | |||||
| chr7:35829128
|
C | CTTTTTT | 48 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0073others(45): Show | 50 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.62-2345_62-2340dup others(6): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | |||||
| chr7:35829128
|
C | CTTTTTTT | 31 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0078others(28): Show | 31 | HG00558.hp1 HG00597.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.62-2346_62-2340dup others(7): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | |||||
| chr7:35829128
|
C | CTTTTTTT others(1): Show |
10 | a0001c0001t0002g0074a0001c0001t0002g0075a0001c0001t0002g0088others(7): Show | 10 | HG00733.hp2 HG01175.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.62-2347_62-2340dup others(8): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | |||||
| chr7:35829128
|
C | CTTTTTTT others(3): Show |
7 | a0001c0001t0002g0087a0001c0001t0002g0109a0001c0001t0002g0110others(4): Show | 7 | HG00099.hp1 HG01081.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.62-2349_62-2340dup others(10): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | |||||
| chr7:35829128
|
C | CTTTTTTT others(4): Show |
3 | a0001c0001t0003g0094a0001c0001t0003g0095a0001c0001t0003g0115 | 3 | HG01106.hp1 HG02293.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.62-2350_62-2340dup others(11): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | |||||
| chr7:35829128
|
C | CTTTTTTT others(5): Show |
4 | a0001c0001t0003g0096a0001c0001t0003g0097a0001c0001t0003g0102others(1): Show | 4 | HG00642.hp2 HG01167.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-2351_62-2340dup others(12): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | |||||
| chr7:35829128
|
C | CTTTTTTT others(6): Show |
3 | a0001c0001t0003g0098a0001c0001t0003g0169a0001c0001t0003g0214 | 3 | HG01192.hp2 HG02738.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.62-2352_62-2340dup others(13): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | |||||
| chr7:35829128
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0003g0091 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.62-2353_62-2340dup others(14): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | |||||
| chr7:35829128
|
C | CTTTTTTT others(8): Show |
2 | a0001c0001t0003g0099a0001c0001t0003g0100 | 2 | HG03704.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.62-2354_62-2340dup others(15): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | |||||
| chr7:35829128
|
C | CTTTTTTT others(15): Show |
1 | a0001c0001t0003g0026 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.62-2361_62-2340dup others(22): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | |||||
| chr7:35829128
|
C | CTTTTTTT others(16): Show |
1 | a0001c0001t0003g0027 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.62-2362_62-2340dup others(23): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | |||||
| chr7:35829128
|
CT | C | 8 | a0001c0001t0001g0182a0001c0001t0001g0247a0001c0001t0001g0248others(5): Show | 8 | HG00099.hp2 HG01099.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.62-2340delT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | |||||
| chr7:35829128
|
CTT | C | 15 | a0001c0001t0002g0029a0001c0001t0004g0173a0001c0001t0004g0174others(12): Show | 15 | HG02258.hp2 HG02572.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.62-2341_62-2340del others(2): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | |||||
| chr7:35829128
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0246 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.62-2349_62-2340del others(10): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | |||||
| chr7:35829257
|
A | T | 134 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.62-2235A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35829257 | ||||||
| chr7:35829328
|
G | C | 7 | a0001c0001t0011g0003a0001c0001t0011g0065a0001c0001t0011g0067others(4): Show | 8 | HG02280.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.62-2164G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35829328 | ||||||
| chr7:35829380
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.62-2112A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35829380 | ||||||
| chr7:35829394
|
G | A | 3 | a0001c0001t0003g0211a0001c0001t0003g0212a0001c0001t0003g0215 | 3 | NA19060.hp2 NA19068.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.62-2098G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35829394 | ||||||
| chr7:35829502
|
C | G | 1 | a0001c0001t0004g0002 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.62-1990C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35829502 | ||||||
| chr7:35829545
|
A | T | 1 | a0001c0001t0004g0002 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.62-1947A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35829545 | ||||||
| chr7:35829742
|
A | G | 2 | a0001c0001t0002g0041a0001c0001t0002g0042 | 2 | HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.62-1750A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35829742 | ||||||
| chr7:35829911
|
G | T | 1 | a0001c0001t0003g0216 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.62-1581G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35829911 | ||||||
| chr7:35829916
|
G | A | 1 | a0001c0001t0001g0309 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.62-1576G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35829916 | ||||||
| chr7:35829925
|
C | T | 4 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-1567C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35829925 | ||||||
| chr7:35829936
|
C | T | 6 | a0001c0001t0013g0044a0001c0001t0013g0045a0001c0001t0013g0046others(3): Show | 6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-1556C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35829936 | ||||||
| chr7:35830042
|
C | T | 40 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(37): Show | 40 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.62-1450C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35830042 | ||||||
| chr7:35830043
|
G | A | 24 | a0001c0001t0004g0002a0001c0001t0004g0006a0001c0001t0004g0009others(21): Show | 26 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.62-1449G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35830043 | ||||||
| chr7:35830241
|
T | A | 201 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(198): Show | 208 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.62-1251T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35830241 | ||||||
| chr7:35830337
|
A | T | 1 | a0001c0001t0030g0107 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.62-1155A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35830337 | ||||||
| chr7:35830447
|
G | T | 2 | a0001c0001t0001g0231a0001c0001t0001g0279 | 2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.62-1045G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35830447 | ||||||
| chr7:35830613
|
GTCATGGA others(12): Show |
G | 1 | a0001c0003t0002g0085 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.62-877_62-859delCA others(17): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35830613 | |||||
| chr7:35830732
|
T | G | 1 | a0001c0001t0002g0119 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.62-760T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35830732 | ||||||
| chr7:35830776
|
T | G | 134 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.62-716T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35830776 | ||||||
| chr7:35830903
|
A | G | 1 | a0001c0001t0003g0214 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.62-589A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35830903 | ||||||
| chr7:35831190
|
G | A | 1 | a0001c0001t0003g0094 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.62-302G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35831190 | ||||||
| chr7:35831448
|
G | A | 1 | a0001c0001t0004g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.62-44G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35831448 | ||||||
| chr7:35831616
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.66+120C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 2/13 | chr7 | 35831616 | ||||||
| chr7:35832038
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.66+542A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 2/13 | chr7 | 35832038 | ||||||
| chr7:35832098
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.66+602C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 2/13 | chr7 | 35832098 | ||||||
| chr7:35832124
|
A | C | 6 | a0001c0001t0003g0005a0001c0001t0003g0185a0001c0001t0003g0186others(3): Show | 7 | NA18954.hp2 NA18956.hp2 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.66+628A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 2/13 | chr7 | 35832124 | ||||||
| chr7:35832246
|
G | T | 2 | a0001c0001t0002g0108a0001c0001t0002g0110 | 2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.67-552G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 2/13 | chr7 | 35832246 | ||||||
| chr7:35832276
|
A | G | 2 | a0001c0001t0002g0125a0001c0001t0002g0146 | 2 | NA18941.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.67-522A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 2/13 | chr7 | 35832276 | ||||||
| chr7:35832424
|
T | G | 6 | a0001c0001t0013g0044a0001c0001t0013g0045a0001c0001t0013g0046others(3): Show | 6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-374T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 2/13 | chr7 | 35832424 | ||||||
| chr7:35832527
|
A | G | 1 | a0001c0001t0001g0316 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.67-271A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 2/13 | chr7 | 35832527 | ||||||
| chr7:35832941
|
G | A | 22 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0197others(19): Show | 23 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.169+41G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35832941 | ||||||
| chr7:35832994
|
T | C | 1 | a0001c0001t0007g0136 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.169+94T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35832994 | ||||||
| chr7:35833082
|
C | T | 1 | a0001c0001t0005g0199 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.169+182C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35833082 | ||||||
| chr7:35833089
|
T | C | 1 | a0001c0001t0003g0169 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.169+189T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35833089 | ||||||
| chr7:35833207
|
C | T | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.169+307C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35833207 | ||||||
| chr7:35833318
|
A | C | 2 | a0001c0001t0005g0198a0001c0001t0005g0200 | 2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.169+418A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35833318 | ||||||
| chr7:35833337
|
C | G | 1 | a0001c0001t0001g0316 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.169+437C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35833337 | ||||||
| chr7:35833444
|
T | C | 1 | a0001c0001t0001g0288 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.169+544T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35833444 | ||||||
| chr7:35833503
|
A | G | 2 | a0001c0001t0002g0071a0001c0001t0002g0143 | 2 | HG02132.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.169+603A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35833503 | ||||||
| chr7:35833695
|
A | G | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.169+795A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35833695 | ||||||
| chr7:35833773
|
C | A | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.169+873C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35833773 | ||||||
| chr7:35833930
|
G | A | 133 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(130): Show | 135 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.169+1030G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35833930 | ||||||
| chr7:35833973
|
A | T | 1 | a0001c0001t0001g0290 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.169+1073A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35833973 | ||||||
| chr7:35834113
|
G | A | 9 | a0001c0001t0008g0015a0001c0001t0008g0016a0001c0001t0008g0017others(6): Show | 9 | HG02622.hp1 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.169+1213G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35834113 | ||||||
| chr7:35834231
|
A | G | 6 | a0001c0001t0013g0044a0001c0001t0013g0045a0001c0001t0013g0046others(3): Show | 6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.169+1331A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35834231 | ||||||
| chr7:35834492
|
A | C | 1 | a0001c0001t0002g0143 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.169+1592A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35834492 | ||||||
| chr7:35834519
|
A | G | 1 | a0001c0001t0039g0196 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.169+1619A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35834519 | ||||||
| chr7:35834633
|
A | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0278 | 2 | HG00558.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.169+1733A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35834633 | ||||||
| chr7:35834650
|
T | C | 3 | a0001c0001t0022g0194a0001c0001t0022g0195a0001c0001t0039g0196 | 3 | HG03471.hp1 HG03486.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.169+1750T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35834650 | ||||||
| chr7:35834660
|
G | T | 18 | a0001c0001t0003g0005a0001c0001t0003g0183a0001c0001t0003g0184others(15): Show | 19 | HG00438.hp1 HG00673.hp1 HG02074.hp1 others(16): Show |
intron_variant | MODIFIER | c.169+1760G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35834660 | ||||||
| chr7:35834681
|
A | G | 1 | a0001c0001t0002g0110 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.169+1781A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35834681 | ||||||
| chr7:35834701
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.169+1801A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35834701 | ||||||
| chr7:35834706
|
CACTT | C | 7 | a0001c0001t0006g0001a0001c0001t0006g0052a0001c0001t0006g0054others(4): Show | 9 | NA18942.hp2 NA18944.hp2 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.169+1810_169+1813d others(6): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35834706 | |||||
| chr7:35834855
|
T | G | 1 | a0001c0001t0010g0329 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.169+1955T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35834855 | ||||||
| chr7:35834886
|
A | C | 6 | a0001c0001t0013g0044a0001c0001t0013g0045a0001c0001t0013g0046others(3): Show | 6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.169+1986A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35834886 | ||||||
| chr7:35834946
|
T | C | 1 | a0001c0001t0021g0059 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.169+2046T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35834946 | ||||||
| chr7:35835181
|
G | C | 1 | a0001c0001t0001g0312 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.169+2281G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35835181 | ||||||
| chr7:35835318
|
C | G | 212 | a0001c0001t0001g0049a0001c0001t0001g0181a0001c0001t0001g0182others(209): Show | 220 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.169+2418C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35835318 | ||||||
| chr7:35835379
|
T | C | 3 | a0001c0001t0004g0171a0001c0001t0004g0178a0001c0001t0004g0179 | 3 | HG02055.hp2 HG02886.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.169+2479T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35835379 | ||||||
| chr7:35835893
|
TG | T | 3 | a0001c0001t0003g0211a0001c0001t0003g0212a0001c0001t0003g0215 | 3 | NA19060.hp2 NA19068.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.169+2994delG | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35835893 | ||||||
| chr7:35835904
|
A | G | 1 | a0001c0001t0001g0235 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.169+3004A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35835904 | ||||||
| chr7:35836211
|
C | G | 1 | a0001c0001t0003g0101 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.169+3311C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35836211 | ||||||
| chr7:35836286
|
A | G | 1 | a0001c0001t0005g0203 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.169+3386A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35836286 | ||||||
| chr7:35836699
|
G | C | 4 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+3799G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35836699 | ||||||
| chr7:35836885
|
A | G | 4 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+3985A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35836885 | ||||||
| chr7:35836933
|
GTAACT | G | 6 | a0001c0001t0013g0044a0001c0001t0013g0045a0001c0001t0013g0046others(3): Show | 6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.169+4039_169+4043d others(7): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35836933 | |||||
| chr7:35837062
|
A | G | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.169+4162A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35837062 | ||||||
| chr7:35837419
|
CAGGAT | C | 8 | a0001c0001t0002g0128a0001c0001t0002g0140a0001c0001t0002g0141others(5): Show | 8 | HG00558.hp1 HG00597.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.169+4522_169+4526d others(7): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35837419 | |||||
| chr7:35837507
|
GAAT | G | 6 | a0001c0001t0013g0044a0001c0001t0013g0045a0001c0001t0013g0046others(3): Show | 6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.169+4613_169+4615d others(5): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35837507 | |||||
| chr7:35837764
|
C | G | 2 | a0001c0001t0005g0220a0001c0001t0005g0221 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.169+4864C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35837764 | ||||||
| chr7:35837791
|
G | A | 2 | a0001c0001t0005g0220a0001c0001t0005g0221 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.169+4891G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35837791 | ||||||
| chr7:35837831
|
A | G | 4 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(1): Show | 4 | HG00408.hp2 HG01952.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+4931A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35837831 | ||||||
| chr7:35837930
|
G | T | 2 | a0001c0001t0001g0282a0001c0001t0001g0297 | 2 | HG00733.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.169+5030G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35837930 | ||||||
| chr7:35837980
|
C | T | 8 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(5): Show | 10 | NA18942.hp2 NA18944.hp2 NA18951.hp1 others(7): Show |
intron_variant | MODIFIER | c.169+5080C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35837980 | ||||||
| chr7:35838031
|
C | T | 7 | a0001c0001t0002g0029a0001c0001t0002g0030a0001c0001t0002g0031others(4): Show | 7 | HG01433.hp2 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.169+5131C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838031 | ||||||
| chr7:35838240
|
C | A | 88 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(85): Show | 91 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.169+5340C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838240 | ||||||
| chr7:35838244
|
C | A | 34 | a0001c0001t0001g0049a0001c0001t0001g0240a0001c0001t0001g0245others(31): Show | 35 | HG00558.hp2 HG01081.hp1 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.169+5344C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838244 | ||||||
| chr7:35838244
|
C | T | 1 | a0001c0001t0002g0111 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.169+5344C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838244 | ||||||
| chr7:35838248
|
C | A | 14 | a0001c0001t0001g0240a0001c0001t0001g0245a0001c0001t0004g0006others(11): Show | 15 | HG01346.hp1 HG02071.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.169+5348C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838248 | ||||||
| chr7:35838252
|
C | A | 2 | a0001c0001t0004g0172a0001c0001t0004g0175 | 2 | HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.169+5352C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838252 | ||||||
| chr7:35838256
|
C | A | 1 | a0001c0001t0004g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.169+5356C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838256 | ||||||
| chr7:35838274
|
TTCCTTCC others(53): Show |
T | 1 | a0001c0001t0002g0035 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.169+5378_169+5437d others(62): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838274 | |||||
| chr7:35838278
|
TTCCTTCC others(41): Show |
T | 1 | a0001c0001t0003g0093 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.169+5382_169+5429d others(50): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838278 | |||||
| chr7:35838278
|
TTCCTTCC others(45): Show |
T | 4 | a0001c0001t0002g0040a0001c0001t0002g0140a0001c0001t0002g0150others(1): Show | 4 | HG02622.hp2 NA18954.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+5382_169+5433d others(54): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838278 | |||||
| chr7:35838278
|
TTCCTTCC others(49): Show |
T | 7 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0038others(4): Show | 7 | HG02258.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.169+5382_169+5437d others(58): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838278 | |||||
| chr7:35838282
|
TTCCTTCC others(37): Show |
T | 4 | a0001c0001t0002g0073a0001c0001t0002g0159a0001c0001t0002g0161others(1): Show | 4 | HG00140.hp2 HG01099.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+5386_169+5429d others(46): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838282 | |||||
| chr7:35838282
|
TTCCTTCC others(41): Show |
T | 7 | a0001c0001t0002g0082a0001c0001t0002g0148a0001c0001t0002g0153others(4): Show | 7 | HG01952.hp1 HG02155.hp1 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.169+5386_169+5433d others(50): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838282 | |||||
| chr7:35838282
|
TTCCTTCC others(45): Show |
T | 23 | a0001c0001t0002g0071a0001c0001t0002g0122a0001c0001t0002g0126others(20): Show | 23 | HG00597.hp1 HG02027.hp1 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.169+5386_169+5437d others(54): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838282 | |||||
| chr7:35838284
|
CCTTCCTT others(72): Show |
C | 4 | a0001c0001t0002g0081a0001c0001t0002g0106a0001c0001t0030g0107others(1): Show | 4 | HG01433.hp2 HG02896.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+5386_169+5464d others(81): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838284 | |||||
| chr7:35838286
|
TTCCTTCC others(25): Show |
T | 1 | a0001c0001t0001g0332 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.169+5390_169+5421d others(34): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838286 | |||||
| chr7:35838286
|
TTCCTTCC others(29): Show |
T | 2 | a0001c0001t0002g0113a0001c0001t0002g0114 | 2 | HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.169+5390_169+5425d others(38): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838286 | |||||
| chr7:35838286
|
TTCCTTCC others(33): Show |
T | 2 | a0001c0001t0001g0181a0001c0001t0002g0162 | 2 | HG01175.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.169+5390_169+5429d others(42): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838286 | |||||
| chr7:35838286
|
TTCCTTCC others(37): Show |
T | 6 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0001t0002g0154others(3): Show | 6 | HG00609.hp2 NA18973.hp1 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.169+5390_169+5433d others(46): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838286 | |||||
| chr7:35838286
|
TTCCTTCC others(41): Show |
T | 31 | a0001c0001t0002g0004a0001c0001t0002g0029a0001c0001t0002g0030others(28): Show | 33 | HG00558.hp1 HG01243.hp2 HG02129.hp1 others(30): Show |
intron_variant | MODIFIER | c.169+5390_169+5437d others(50): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838286 | |||||
| chr7:35838286
|
TTCCTTCC others(45): Show |
T | 1 | a0001c0001t0002g0160 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.169+5390_169+5441d others(54): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838286 | |||||
| chr7:35838290
|
TTCCTTCC others(17): Show |
T | 1 | a0001c0001t0001g0325 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.169+5394_169+5417d others(26): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838290 | |||||
| chr7:35838290
|
TTCCTTCC others(25): Show |
T | 5 | a0001c0001t0003g0211a0001c0001t0003g0212a0001c0001t0003g0215others(2): Show | 5 | HG02922.hp2 NA18952.hp2 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.169+5394_169+5425d others(34): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838290 | |||||
| chr7:35838290
|
TTCCTTCC others(29): Show |
T | 2 | a0001c0001t0001g0180a0001c0001t0001g0258 | 2 | HG03710.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.169+5394_169+5429d others(38): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838290 | |||||
| chr7:35838290
|
TTCCTTCC others(33): Show |
T | 12 | a0001c0001t0003g0026a0001c0001t0003g0027a0001c0001t0003g0090others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.169+5394_169+5433d others(42): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838290 | |||||
| chr7:35838290
|
TTCCTTCC others(37): Show |
T | 37 | a0001c0001t0001g0182a0001c0001t0002g0025a0001c0001t0002g0108others(34): Show | 39 | HG00408.hp1 HG00438.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.169+5394_169+5437d others(46): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838290 | |||||
| chr7:35838290
|
TTCCTTCC others(41): Show |
T | 1 | a0001c0001t0039g0196 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.169+5394_169+5441d others(50): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838290 | |||||
| chr7:35838290
|
TTCCTTCC others(45): Show |
T | 1 | a0001c0001t0008g0015 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.169+5394_169+5445d others(54): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838290 | |||||
| chr7:35838294
|
TTCCTTCC others(13): Show |
T | 3 | a0001c0001t0010g0259a0001c0001t0010g0306a0001c0001t0010g0329 | 3 | NA18948.hp1 NA19076.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.169+5398_169+5417d others(22): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838294 | |||||
| chr7:35838294
|
TTCCTTCC others(17): Show |
T | 7 | a0001c0001t0001g0237a0001c0001t0001g0249a0001c0001t0001g0310others(4): Show | 7 | HG00099.hp2 HG00408.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.169+5398_169+5421d others(26): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838294 | |||||
| chr7:35838294
|
TTCCTTCC others(21): Show |
T | 6 | a0001c0001t0001g0280a0001c0001t0004g0002a0001c0001t0004g0028others(3): Show | 7 | HG02109.hp2 HG02486.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.169+5398_169+5425d others(30): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838294 | |||||
| chr7:35838294
|
TTCCTTCC others(25): Show |
T | 11 | a0001c0001t0001g0224a0001c0001t0001g0247a0001c0001t0001g0261others(8): Show | 11 | HG01255.hp2 HG02080.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.169+5398_169+5429d others(34): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838294 | |||||
| chr7:35838294
|
TTCCTTCC others(29): Show |
T | 4 | a0001c0001t0002g0120a0001c0001t0003g0097a0001c0001t0023g0089others(1): Show | 4 | HG01081.hp2 HG02451.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+5398_169+5433d others(38): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838294 | |||||
| chr7:35838294
|
TTCCTTCC others(33): Show |
T | 11 | a0001c0001t0002g0078a0001c0001t0002g0116a0001c0001t0002g0118others(8): Show | 11 | HG00733.hp2 HG01884.hp2 NA18522.hp2 others(8): Show |
intron_variant | MODIFIER | c.169+5398_169+5437d others(42): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838294 | |||||
| chr7:35838294
|
TTCCTTCC others(37): Show |
T | 2 | a0001c0001t0022g0194a0001c0001t0022g0195 | 2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.169+5398_169+5441d others(46): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838294 | |||||
| chr7:35838294
|
TTCCTTCC others(41): Show |
T | 3 | a0001c0001t0001g0252a0001c0001t0013g0046a0001c0001t0013g0048 | 3 | HG01891.hp1 NA19077.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.169+5398_169+5445d others(50): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838294 | |||||
| chr7:35838294
|
TTCCTTCC others(45): Show |
T | 1 | a0001c0001t0013g0045 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.169+5398_169+5449d others(54): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838294 | |||||
| chr7:35838294
|
TTCCTTCC others(49): Show |
T | 2 | a0001c0001t0012g0228a0001c0002t0001g0305 | 2 | NA18992.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.169+5398_169+5453d others(58): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838294 | |||||
| chr7:35838298
|
TTCCTTCC others(5): Show |
T | 3 | a0001c0001t0001g0285a0001c0001t0001g0315a0001c0001t0010g0238 | 3 | HG00735.hp2 HG00741.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.169+5402_169+5413d others(14): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838298 | |||||
| chr7:35838298
|
TTCCTTCC others(9): Show |
T | 4 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0010g0241others(1): Show | 4 | HG00642.hp1 HG01167.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+5402_169+5417d others(18): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838298 | |||||
| chr7:35838298
|
TTCCTTCC others(13): Show |
T | 6 | a0001c0001t0001g0290a0001c0001t0001g0318a0001c0001t0001g0319others(3): Show | 6 | HG01106.hp2 HG01978.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.169+5402_169+5421d others(22): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838298 | |||||
| chr7:35838298
|
TTCCTTCC others(17): Show |
T | 4 | a0001c0001t0001g0250a0001c0001t0001g0286a0001c0002t0001g0012others(1): Show | 4 | HG01192.hp1 HG01952.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+5402_169+5425d others(26): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838298 | |||||
| chr7:35838298
|
TTCCTTCC others(21): Show |
T | 21 | a0001c0001t0001g0008a0001c0001t0001g0222a0001c0001t0001g0223others(18): Show | 22 | HG00438.hp2 HG00609.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.169+5402_169+5429d others(30): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838298 | |||||
| chr7:35838298
|
TTCCTTCC others(25): Show |
T | 1 | a0001c0001t0001g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.169+5402_169+5433d others(34): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838298 | |||||
| chr7:35838298
|
TTCCTTCC others(29): Show |
T | 11 | a0001c0001t0001g0316a0001c0001t0006g0001a0001c0001t0006g0024others(8): Show | 13 | HG00597.hp2 HG02155.hp2 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.169+5402_169+5437d others(38): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838298 | |||||
| chr7:35838298
|
TTCCTTCC others(33): Show |
T | 4 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0287others(1): Show | 5 | HG00673.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+5402_169+5441d others(42): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838298 | |||||
| chr7:35838298
|
TTCCTTCC others(37): Show |
T | 2 | a0001c0001t0001g0232a0001c0001t0001g0326 | 2 | HG01517.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.169+5402_169+5445d others(46): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838298 | |||||
| chr7:35838302
|
T | C | 15 | a0001c0001t0004g0009a0001c0001t0004g0173a0001c0001t0004g0176others(12): Show | 15 | HG00738.hp1 HG01081.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.169+5402T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838302 | ||||||
| chr7:35838302
|
TTCCCTCC others(5): Show |
T | 9 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0009g0242others(6): Show | 9 | HG00140.hp1 HG01934.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.169+5454_169+5465d others(14): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838302 | |||||
| chr7:35838302
|
TTCCCTCC others(9): Show |
T | 19 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(16): Show | 19 | HG00741.hp1 HG01074.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.169+5450_169+5465d others(18): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838302 | |||||
| chr7:35838302
|
TTCCCTCC others(13): Show |
T | 3 | a0001c0001t0001g0251a0001c0001t0001g0279a0001c0001t0009g0230 | 3 | HG02559.hp1 HG04204.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.169+5446_169+5465d others(22): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838302 | |||||
| chr7:35838302
|
TTCCCTCC others(17): Show |
T | 9 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0240others(6): Show | 9 | HG00558.hp2 HG02071.hp2 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.169+5442_169+5465d others(26): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838302 | |||||
| chr7:35838302
|
TTCCCTCC others(21): Show |
T | 2 | a0001c0001t0001g0231a0001c0001t0003g0095 | 2 | HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.169+5438_169+5465d others(30): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838302 | |||||
| chr7:35838302
|
TTCCCTCC others(25): Show |
T | 3 | a0001c0001t0001g0321a0001c0001t0016g0077a0001c0001t0021g0050 | 3 | HG02027.hp2 NA18961.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.169+5434_169+5465d others(34): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838302 | |||||
| chr7:35838302
|
TTCCCTCC others(33): Show |
T | 1 | a0001c0001t0001g0256 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.169+5426_169+5465d others(42): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838302 | |||||
| chr7:35838306
|
C | T | 3 | a0001c0001t0004g0179a0001c0001t0005g0220a0001c0001t0005g0221 | 3 | HG01884.hp1 HG02055.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.169+5406C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838306 | ||||||
| chr7:35838308
|
CCCTCCCT others(48): Show |
C | 2 | a0001c0001t0019g0266a0001c0001t0019g0311 | 2 | HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.169+5436_169+5490d others(57): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838308 | |||||
| chr7:35838310
|
C | T | 1 | a0001c0001t0005g0221 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.169+5410C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838310 | ||||||
| chr7:35838314
|
C | T | 1 | a0001c0001t0009g0296 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.169+5414C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838314 | ||||||
| chr7:35838316
|
CCCTCCCT others(40): Show |
C | 1 | a0001c0001t0013g0044 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.169+5444_169+5490d others(49): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838316 | |||||
| chr7:35838318
|
C | T | 7 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0009g0242others(4): Show | 7 | HG00140.hp1 HG01981.hp1 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.169+5418C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838318 | ||||||
| chr7:35838319
|
TCCCTCCC others(22): Show |
T | 11 | a0001c0001t0004g0171a0001c0001t0005g0010a0001c0001t0005g0192others(8): Show | 11 | HG00738.hp1 HG01081.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.169+5422_169+5450d others(31): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838319 | |||||
| chr7:35838322
|
C | T | 2 | a0001c0001t0001g0276a0001c0001t0007g0117 | 2 | HG00741.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.169+5422C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838322 | ||||||
| chr7:35838323
|
TCCCTCCC others(18): Show |
T | 8 | a0001c0001t0004g0009a0001c0001t0004g0173a0001c0001t0004g0176others(5): Show | 8 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.169+5426_169+5450d others(27): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838323 | |||||
| chr7:35838326
|
C | T | 2 | a0001c0001t0001g0279a0001c0001t0007g0117 | 2 | HG00741.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.169+5426C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838326 | ||||||
| chr7:35838327
|
TCCCTCCC others(6): Show |
T | 1 | a0001c0001t0005g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.169+5430_169+5442d others(15): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838327 | |||||
| chr7:35838327
|
TCCCTCCC others(14): Show |
T | 2 | a0001c0001t0004g0172a0001c0001t0024g0177 | 2 | HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.169+5430_169+5450d others(23): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838327 | |||||
| chr7:35838330
|
C | T | 3 | a0001c0001t0001g0235a0001c0001t0001g0279a0001c0001t0007g0117 | 3 | HG00741.hp1 HG02135.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.169+5430C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838330 | ||||||
| chr7:35838331
|
TCCCTCCC others(10): Show |
T | 1 | a0001c0001t0005g0221 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.169+5434_169+5450d others(19): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838331 | |||||
| chr7:35838334
|
C | T | 4 | a0001c0001t0001g0231a0001c0001t0001g0279a0001c0001t0003g0095others(1): Show | 4 | HG00741.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+5434C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838334 | ||||||
| chr7:35838335
|
TCCCTCCC others(10): Show |
T | 1 | a0001c0001t0001g0274 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.169+5438_169+5454d others(19): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838335 | |||||
| chr7:35838340
|
CCCTCCCT others(16): Show |
C | 1 | a0001c0001t0001g0239 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.169+5466_169+5488d others(25): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838340 | |||||
| chr7:35838347
|
TC | T | 10 | a0001c0001t0004g0002a0001c0001t0004g0006a0001c0001t0004g0028others(7): Show | 12 | HG01255.hp2 HG02109.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.169+5450delC | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838347 | |||||
| chr7:35838358
|
C | A | 15 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(12): Show | 17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.169+5458C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838358 | ||||||
| chr7:35838360
|
CCCT | C | 6 | a0001c0001t0002g0148a0001c0001t0002g0160a0001c0001t0005g0220others(3): Show | 6 | HG01891.hp1 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.169+5466_169+5468d others(5): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838360 | |||||
| chr7:35838362
|
C | T | 49 | a0001c0001t0002g0159a0001c0001t0002g0161a0001c0001t0002g0162others(46): Show | 52 | HG00140.hp2 HG00738.hp1 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.169+5462C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838362 | ||||||
| chr7:35838363
|
T | C | 49 | a0001c0001t0002g0159a0001c0001t0002g0161a0001c0001t0002g0162others(46): Show | 52 | HG00140.hp2 HG00738.hp1 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.169+5463T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838363 | ||||||
| chr7:35838366
|
T | C | 1 | a0001c0001t0001g0274 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.169+5466T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838366 | ||||||
| chr7:35838370
|
TC | T | 3 | a0001c0001t0022g0194a0001c0001t0022g0195a0001c0001t0039g0196 | 3 | HG03471.hp1 HG03486.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.169+5473delC | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838370 | |||||
| chr7:35838425
|
A | G | 2 | a0001c0001t0022g0194a0001c0001t0022g0195 | 2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.169+5525A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838425 | ||||||
| chr7:35838482
|
C | G | 1 | a0001c0001t0005g0192 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.169+5582C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838482 | ||||||
| chr7:35838828
|
C | T | 133 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(130): Show | 135 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.169+5928C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838828 | ||||||
| chr7:35838986
|
A | G | 1 | a0001c0001t0002g0114 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.169+6086A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838986 | ||||||
| chr7:35838988
|
A | G | 1 | a0001c0002t0001g0014 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.169+6088A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838988 | ||||||
| chr7:35839301
|
A | G | 1 | a0001c0002t0001g0304 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.169+6401A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35839301 | ||||||
| chr7:35839321
|
T | C | 211 | a0001c0001t0001g0049a0001c0001t0001g0181a0001c0001t0001g0182others(208): Show | 219 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.169+6421T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35839321 | ||||||
| chr7:35839340
|
G | T | 1 | a0001c0001t0001g0323 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.169+6440G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35839340 | ||||||
| chr7:35839460
|
G | A | 21 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(18): Show | 23 | HG00597.hp2 HG01255.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.169+6560G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35839460 | ||||||
| chr7:35839523
|
T | TTTATG | 195 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(192): Show | 201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.169+6663_169+6667d others(7): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35839523 | |||||
| chr7:35839523
|
T | TTTATGTT others(3): Show |
67 | a0001c0001t0001g0247a0001c0001t0001g0249a0001c0001t0001g0269others(64): Show | 69 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.169+6658_169+6667d others(12): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35839523 | |||||
| chr7:35839523
|
T | TTTATGTT others(8): Show |
11 | a0001c0001t0001g0231a0001c0001t0001g0240a0001c0001t0001g0279others(8): Show | 11 | HG00099.hp1 HG00741.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.169+6653_169+6667d others(17): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35839523 | |||||
| chr7:35839523
|
T | TTTATGTT others(13): Show |
1 | a0001c0001t0003g0092 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.169+6648_169+6667d others(22): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35839523 | |||||
| chr7:35839523
|
T | TTTATGTT others(18): Show |
1 | a0001c0001t0002g0118 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.169+6643_169+6667d others(27): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35839523 | |||||
| chr7:35839523
|
TTTATG | T | 6 | a0001c0001t0001g0289a0001c0001t0002g0159a0001c0001t0002g0162others(3): Show | 6 | HG01123.hp2 HG01175.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.169+6663_169+6667d others(7): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35839523 | |||||
| chr7:35839523
|
TTTATGTT others(3): Show |
T | 22 | a0001c0001t0004g0175a0001c0001t0005g0010a0001c0001t0005g0192others(19): Show | 23 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.169+6658_169+6667d others(12): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35839523 | |||||
| chr7:35839566
|
A | ATGTTATG others(6): Show |
1 | a0001c0003t0002g0085 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.169+6667_169+6668i others(15): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35839566 | |||||
| chr7:35839568
|
T | A | 1 | a0001c0003t0002g0085 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.169+6668T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35839568 | ||||||
| chr7:35839575
|
A | G | 8 | a0001c0001t0001g0272a0001c0001t0010g0238a0001c0001t0010g0241others(5): Show | 8 | HG01934.hp2 NA18948.hp1 NA18997.hp1 others(5): Show |
intron_variant | MODIFIER | c.169+6675A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35839575 | ||||||
| chr7:35839677
|
C | G | 1 | a0001c0001t0015g0051 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.169+6777C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35839677 | ||||||
| chr7:35839803
|
T | C | 1 | a0001c0001t0036g0201 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.169+6903T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35839803 | ||||||
| chr7:35839805
|
G | A | 1 | a0001c0001t0004g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.169+6905G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35839805 | ||||||
| chr7:35839989
|
T | A | 202 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(199): Show | 209 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.169+7089T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35839989 | ||||||
| chr7:35840070
|
G | A | 5 | a0001c0001t0005g0202a0001c0001t0005g0203a0001c0001t0005g0208others(2): Show | 6 | HG00738.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.169+7170G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35840070 | ||||||
| chr7:35840136
|
C | A | 3 | a0001c0001t0022g0194a0001c0001t0022g0195a0001c0001t0039g0196 | 3 | HG03471.hp1 HG03486.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.169+7236C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35840136 | ||||||
| chr7:35840188
|
T | TCCCCCTT others(7): Show |
3 | a0001c0001t0022g0194a0001c0001t0022g0195a0001c0001t0039g0196 | 3 | HG03471.hp1 HG03486.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.169+7296_169+7309d others(16): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35840188 | |||||
| chr7:35840200
|
C | CTCCCCCC others(15): Show |
1 | a0001c0001t0001g0181 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.169+7320_169+7341d others(24): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35840200 | |||||
| chr7:35840220
|
C | G | 1 | a0001c0001t0036g0201 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.169+7320C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35840220 | ||||||
| chr7:35840486
|
C | T | 1 | a0001c0001t0003g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.169+7586C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35840486 | ||||||
| chr7:35840540
|
A | G | 1 | a0001c0001t0037g0206 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.169+7640A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35840540 | ||||||
| chr7:35840570
|
G | A | 21 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(18): Show | 23 | HG00597.hp2 HG01255.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.169+7670G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35840570 | ||||||
| chr7:35840605
|
C | T | 1 | a0001c0001t0002g0074 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.169+7705C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35840605 | ||||||
| chr7:35841059
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.169+8159A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35841059 | ||||||
| chr7:35841086
|
C | T | 202 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(199): Show | 209 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.169+8186C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35841086 | ||||||
| chr7:35841093
|
C | T | 4 | a0001c0001t0001g0331a0001c0001t0001g0332a0001c0001t0001g0333others(1): Show | 4 | HG00642.hp1 HG01099.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+8193C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35841093 | ||||||
| chr7:35841105
|
T | A | 1 | a0001c0001t0004g0193 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.169+8205T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35841105 | ||||||
| chr7:35841222
|
C | T | 1 | a0001c0001t0005g0207 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.169+8322C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35841222 | ||||||
| chr7:35841404
|
A | T | 1 | a0001c0001t0005g0010 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.169+8504A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35841404 | ||||||
| chr7:35841424
|
T | C | 15 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(12): Show | 17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.169+8524T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35841424 | ||||||
| chr7:35841657
|
A | G | 2 | a0001c0001t0003g0092a0001c0001t0003g0101 | 2 | HG00099.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.169+8757A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35841657 | ||||||
| chr7:35841724
|
G | A | 1 | a0001c0001t0003g0115 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.169+8824G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35841724 | ||||||
| chr7:35842032
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.169+9132G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35842032 | ||||||
| chr7:35842064
|
A | G | 1 | a0001c0001t0002g0075 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.169+9164A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35842064 | ||||||
| chr7:35842348
|
G | GA | 147 | a0001c0001t0001g0270a0001c0001t0001g0282a0001c0001t0001g0310others(144): Show | 152 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.169+9460dupA | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35842348 | |||||
| chr7:35842348
|
G | GAA | 15 | a0001c0001t0002g0080a0001c0001t0002g0082a0001c0001t0002g0128others(12): Show | 15 | HG00597.hp1 HG00609.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.169+9459_169+9460d others(4): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35842348 | |||||
| chr7:35842360
|
A | C | 1 | a0001c0001t0016g0077 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.169+9460A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35842360 | ||||||
| chr7:35842486
|
A | C | 1 | a0001c0001t0001g0181 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.169+9586A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35842486 | ||||||
| chr7:35842556
|
A | T | 1 | a0001c0001t0011g0067 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.169+9656A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35842556 | ||||||
| chr7:35842577
|
T | G | 2 | a0001c0001t0004g0002a0001c0001t0004g0028 | 3 | HG02615.hp1 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.169+9677T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35842577 | ||||||
| chr7:35842640
|
T | C | 1 | a0001c0001t0012g0234 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.169+9740T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35842640 | ||||||
| chr7:35842671
|
G | A | 6 | a0001c0001t0003g0005a0001c0001t0003g0185a0001c0001t0003g0186others(3): Show | 7 | NA18954.hp2 NA18956.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.169+9771G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35842671 | ||||||
| chr7:35842819
|
A | G | 4 | a0001c0001t0002g0082a0001c0001t0002g0122a0001c0001t0015g0277others(1): Show | 4 | NA18612.hp1 NA18940.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+9919A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35842819 | ||||||
| chr7:35842837
|
C | T | 24 | a0001c0001t0004g0002a0001c0001t0004g0006a0001c0001t0004g0009others(21): Show | 26 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.169+9937C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35842837 | ||||||
| chr7:35843049
|
C | T | 4 | a0001c0001t0001g0252a0001c0001t0001g0256a0001c0001t0001g0309others(1): Show | 4 | NA18966.hp2 NA18968.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+10149C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35843049 | ||||||
| chr7:35843369
|
C | T | 135 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(132): Show | 137 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.169+10469C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35843369 | ||||||
| chr7:35843434
|
T | C | 135 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(132): Show | 137 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.169+10534T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35843434 | ||||||
| chr7:35843452
|
G | A | 1 | a0001c0001t0006g0055 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.169+10552G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35843452 | ||||||
| chr7:35843583
|
C | T | 22 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0197others(19): Show | 23 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.169+10683C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35843583 | ||||||
| chr7:35843687
|
A | G | 15 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(12): Show | 17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.169+10787A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35843687 | ||||||
| chr7:35843791
|
C | T | 156 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(153): Show | 160 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.169+10891C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35843791 | ||||||
| chr7:35844030
|
C | G | 1 | a0001c0001t0009g0275 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.169+11130C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35844030 | ||||||
| chr7:35844233
|
G | A | 9 | a0001c0001t0001g0049a0001c0001t0001g0182a0001c0001t0011g0003others(6): Show | 10 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.169+11333G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35844233 | ||||||
| chr7:35844524
|
A | G | 1 | a0001c0001t0007g0147 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.169+11624A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35844524 | ||||||
| chr7:35844607
|
CT | C | 211 | a0001c0001t0001g0049a0001c0001t0001g0181a0001c0001t0001g0182others(208): Show | 219 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.169+11717delT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35844607 | |||||
| chr7:35844623
|
G | C | 1 | a0001c0001t0001g0254 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.169+11723G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35844623 | ||||||
| chr7:35844686
|
G | A | 133 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(130): Show | 135 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.169+11786G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35844686 | ||||||
| chr7:35844747
|
C | T | 2 | a0001c0001t0005g0220a0001c0001t0005g0221 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.169+11847C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35844747 | ||||||
| chr7:35844852
|
C | T | 13 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0202others(10): Show | 14 | HG00738.hp1 HG01081.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.169+11952C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35844852 | ||||||
| chr7:35844931
|
C | A | 1 | a0001c0001t0002g0025 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.169+12031C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35844931 | ||||||
| chr7:35845149
|
C | A | 15 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(12): Show | 17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.169+12249C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35845149 | ||||||
| chr7:35845172
|
G | A | 22 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0197others(19): Show | 23 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.169+12272G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35845172 | ||||||
| chr7:35845387
|
G | A | 155 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(152): Show | 159 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.169+12487G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35845387 | ||||||
| chr7:35845544
|
G | A | 21 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(18): Show | 23 | HG00597.hp2 HG01255.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.169+12644G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35845544 | ||||||
| chr7:35845567
|
C | T | 21 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(18): Show | 23 | HG00597.hp2 HG01255.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.169+12667C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35845567 | ||||||
| chr7:35845580
|
T | C | 19 | a0001c0001t0001g0272a0001c0001t0001g0291a0001c0001t0001g0292others(16): Show | 19 | HG00140.hp1 HG01074.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.169+12680T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35845580 | ||||||
| chr7:35845775
|
A | G | 2 | a0001c0001t0004g0006a0001c0001t0004g0193 | 3 | HG02109.hp2 HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.169+12875A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35845775 | ||||||
| chr7:35845847
|
G | C | 1 | a0001c0001t0002g0159 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.169+12947G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35845847 | ||||||
| chr7:35845962
|
G | GT | 24 | a0001c0001t0004g0006a0001c0001t0004g0193a0001c0001t0005g0010others(21): Show | 26 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.169+13072dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35845962 | |||||
| chr7:35845964
|
T | C | 135 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(132): Show | 137 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.169+13064T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35845964 | ||||||
| chr7:35845986
|
T | C | 2 | a0001c0001t0002g0004a0001c0001t0002g0119 | 3 | HG02976.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.169+13086T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35845986 | ||||||
| chr7:35846008
|
T | C | 1 | a0001c0001t0003g0191 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.169+13108T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35846008 | ||||||
| chr7:35846145
|
T | C | 2 | a0001c0001t0002g0106a0002c0005t0002g0104 | 2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.169+13245T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35846145 | ||||||
| chr7:35846173
|
T | C | 1 | a0001c0001t0002g0125 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.169+13273T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35846173 | ||||||
| chr7:35846359
|
T | C | 21 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(18): Show | 23 | HG00597.hp2 HG01255.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.169+13459T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35846359 | ||||||
| chr7:35846647
|
C | T | 134 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.169+13747C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35846647 | ||||||
| chr7:35846718
|
T | G | 1 | a0001c0001t0038g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.169+13818T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35846718 | ||||||
| chr7:35846806
|
C | G | 2 | a0001c0001t0002g0108a0001c0001t0002g0110 | 2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.169+13906C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35846806 | ||||||
| chr7:35846936
|
A | G | 1 | a0001c0001t0002g0086 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.169+14036A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35846936 | ||||||
| chr7:35846993
|
A | G | 24 | a0001c0001t0004g0002a0001c0001t0004g0006a0001c0001t0004g0009others(21): Show | 26 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.169+14093A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35846993 | ||||||
| chr7:35847081
|
GTC | G | 18 | a0001c0001t0002g0025a0001c0001t0002g0078a0001c0001t0002g0079others(15): Show | 18 | HG02300.hp1 HG03239.hp1 HG03704.hp2 others(15): Show |
intron_variant | MODIFIER | c.169+14185_169+1418 others(6): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35847081 | |||||
| chr7:35847120
|
A | T | 1 | a0001c0001t0038g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.169+14220A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35847120 | ||||||
| chr7:35847122
|
A | C | 1 | a0001c0001t0038g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.169+14222A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35847122 | ||||||
| chr7:35847173
|
C | CA | 24 | a0001c0001t0004g0002a0001c0001t0004g0006a0001c0001t0004g0009others(21): Show | 26 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.169+14274dupA | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35847173 | |||||
| chr7:35847178
|
G | A | 9 | a0001c0001t0001g0049a0001c0001t0001g0182a0001c0001t0011g0003others(6): Show | 10 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.169+14278G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35847178 | ||||||
| chr7:35847239
|
C | T | 1 | a0001c0001t0004g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.169+14339C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35847239 | ||||||
| chr7:35847252
|
G | A | 1 | a0001c0001t0009g0275 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.169+14352G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35847252 | ||||||
| chr7:35847532
|
ATTAT | A | 134 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.169+14639_169+1464 others(8): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35847532 | |||||
| chr7:35847974
|
G | T | 2 | a0001c0001t0002g0113a0001c0001t0002g0114 | 2 | HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.169+15074G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35847974 | ||||||
| chr7:35848099
|
C | A | 1 | a0001c0001t0001g0245 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.169+15199C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35848099 | ||||||
| chr7:35848138
|
G | A | 24 | a0001c0001t0004g0002a0001c0001t0004g0006a0001c0001t0004g0009others(21): Show | 26 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.169+15238G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35848138 | ||||||
| chr7:35848146
|
C | T | 6 | a0001c0001t0013g0044a0001c0001t0013g0045a0001c0001t0013g0046others(3): Show | 6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.169+15246C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35848146 | ||||||
| chr7:35848159
|
A | G | 9 | a0001c0001t0001g0049a0001c0001t0001g0182a0001c0001t0011g0003others(6): Show | 10 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.169+15259A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35848159 | ||||||
| chr7:35848287
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.170-15265A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35848287 | ||||||
| chr7:35848337
|
G | A | 3 | a0001c0001t0002g0074a0001c0001t0002g0075a0001c0001t0002g0076 | 3 | HG01243.hp2 HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.170-15215G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35848337 | ||||||
| chr7:35848424
|
T | C | 156 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(153): Show | 160 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.170-15128T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35848424 | ||||||
| chr7:35848481
|
A | G | 15 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(12): Show | 17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.170-15071A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35848481 | ||||||
| chr7:35848505
|
C | G | 1 | a0001c0001t0001g0181 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.170-15047C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35848505 | ||||||
| chr7:35848505
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.170-15047C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35848505 | ||||||
| chr7:35848514
|
C | G | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.170-15038C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35848514 | ||||||
| chr7:35848612
|
T | G | 1 | a0001c0001t0010g0259 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.170-14940T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35848612 | ||||||
| chr7:35848905
|
G | T | 2 | a0001c0001t0005g0220a0001c0001t0005g0221 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.170-14647G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35848905 | ||||||
| chr7:35848925
|
T | C | 1 | a0001c0001t0004g0028 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.170-14627T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35848925 | ||||||
| chr7:35849098
|
T | C | 3 | a0001c0001t0002g0159a0001c0001t0002g0162a0001c0001t0002g0166 | 3 | HG00140.hp2 HG01123.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.170-14454T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35849098 | ||||||
| chr7:35849278
|
G | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0317 | 2 | NA18973.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.170-14274G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35849278 | ||||||
| chr7:35849286
|
C | T | 2 | a0001c0001t0001g0232a0001c0001t0001g0265 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.170-14266C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35849286 | ||||||
| chr7:35849460
|
G | A | 1 | a0001c0001t0002g0029 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.170-14092G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35849460 | ||||||
| chr7:35849488
|
C | T | 4 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.170-14064C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35849488 | ||||||
| chr7:35849531
|
A | G | 135 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(132): Show | 137 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.170-14021A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35849531 | ||||||
| chr7:35849791
|
A | C | 7 | a0001c0001t0011g0003a0001c0001t0011g0065a0001c0001t0011g0067others(4): Show | 8 | HG02280.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.170-13761A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35849791 | ||||||
| chr7:35849910
|
C | G | 2 | a0001c0001t0002g0041a0001c0001t0002g0042 | 2 | HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.170-13642C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35849910 | ||||||
| chr7:35850076
|
A | G | 22 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0197others(19): Show | 23 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.170-13476A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35850076 | ||||||
| chr7:35850181
|
A | G | 2 | a0001c0001t0004g0171a0001c0001t0004g0179 | 2 | HG02055.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.170-13371A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35850181 | ||||||
| chr7:35850434
|
C | T | 4 | a0001c0001t0012g0062a0001c0001t0012g0063a0001c0001t0012g0064others(1): Show | 4 | NA18970.hp2 NA18975.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-13118C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35850434 | ||||||
| chr7:35850438
|
T | C | 1 | a0001c0001t0003g0098 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.170-13114T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35850438 | ||||||
| chr7:35850804
|
C | A | 1 | a0001c0001t0002g0160 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.170-12748C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35850804 | ||||||
| chr7:35851066
|
A | C | 1 | a0001c0001t0003g0098 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.170-12486A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35851066 | ||||||
| chr7:35851107
|
G | A | 3 | a0001c0001t0002g0074a0001c0001t0002g0075a0001c0001t0002g0076 | 3 | HG01243.hp2 HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.170-12445G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35851107 | ||||||
| chr7:35851158
|
A | G | 5 | a0001c0001t0001g0231a0001c0001t0001g0239a0001c0001t0001g0276others(2): Show | 5 | HG01123.hp1 HG01891.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.170-12394A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35851158 | ||||||
| chr7:35851264
|
A | C | 2 | a0001c0001t0003g0100a0001c0003t0002g0085 | 2 | HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.170-12288A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35851264 | ||||||
| chr7:35851299
|
T | C | 7 | a0001c0001t0001g0291a0001c0001t0001g0293a0001c0001t0001g0294others(4): Show | 7 | HG00140.hp1 HG01074.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.170-12253T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35851299 | ||||||
| chr7:35851339
|
C | A | 1 | a0001c0001t0002g0079 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.170-12213C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35851339 | ||||||
| chr7:35851413
|
G | A | 212 | a0001c0001t0001g0049a0001c0001t0001g0181a0001c0001t0001g0182others(209): Show | 220 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.170-12139G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35851413 | ||||||
| chr7:35851429
|
G | A | 1 | a0001c0001t0002g0149 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.170-12123G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35851429 | ||||||
| chr7:35851501
|
A | G | 15 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(12): Show | 17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.170-12051A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35851501 | ||||||
| chr7:35851788
|
T | G | 1 | a0001c0001t0003g0097 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.170-11764T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35851788 | ||||||
| chr7:35851791
|
A | G | 1 | a0001c0001t0001g0294 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.170-11761A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35851791 | ||||||
| chr7:35851975
|
C | A | 2 | a0001c0001t0022g0194a0001c0001t0022g0195 | 2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.170-11577C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35851975 | ||||||
| chr7:35852017
|
G | A | 3 | a0001c0001t0004g0171a0001c0001t0004g0178a0001c0001t0004g0179 | 3 | HG02055.hp2 HG02886.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.170-11535G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35852017 | ||||||
| chr7:35852283
|
G | A | 202 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(199): Show | 209 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.170-11269G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35852283 | ||||||
| chr7:35852339
|
T | G | 1 | a0001c0002t0001g0305 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.170-11213T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35852339 | ||||||
| chr7:35852340
|
A | G | 1 | a0001c0001t0002g0025 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.170-11212A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35852340 | ||||||
| chr7:35852522
|
A | G | 1 | a0001c0001t0031g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.170-11030A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35852522 | ||||||
| chr7:35852587
|
C | T | 1 | a0001c0001t0005g0205 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.170-10965C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35852587 | ||||||
| chr7:35852808
|
A | G | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.170-10744A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35852808 | ||||||
| chr7:35853129
|
A | G | 5 | a0001c0001t0002g0035a0001c0001t0002g0038a0001c0001t0002g0039others(2): Show | 5 | HG01109.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.170-10423A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35853129 | ||||||
| chr7:35853198
|
G | A | 1 | a0001c0001t0003g0094 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.170-10354G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35853198 | ||||||
| chr7:35853298
|
C | T | 22 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0197others(19): Show | 23 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.170-10254C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35853298 | ||||||
| chr7:35853696
|
T | G | 1 | a0001c0001t0004g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.170-9856T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35853696 | ||||||
| chr7:35853898
|
C | T | 1 | a0001c0001t0001g0326 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.170-9654C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35853898 | ||||||
| chr7:35854006
|
T | C | 12 | a0001c0001t0001g0229a0001c0001t0001g0235a0001c0001t0001g0236others(9): Show | 12 | HG00558.hp2 HG00673.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.170-9546T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35854006 | ||||||
| chr7:35854061
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.170-9491A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35854061 | ||||||
| chr7:35854237
|
A | G | 3 | a0001c0001t0001g0236a0001c0001t0001g0243a0001c0001t0001g0244 | 3 | NA18979.hp1 NA18991.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.170-9315A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35854237 | ||||||
| chr7:35854629
|
C | A | 134 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.170-8923C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35854629 | ||||||
| chr7:35854793
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.170-8759A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35854793 | ||||||
| chr7:35855003
|
A | G | 1 | a0001c0001t0037g0206 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.170-8549A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35855003 | ||||||
| chr7:35855127
|
C | T | 201 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(198): Show | 208 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.170-8425C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35855127 | ||||||
| chr7:35855203
|
A | G | 15 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(12): Show | 17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.170-8349A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35855203 | ||||||
| chr7:35855322
|
C | T | 15 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(12): Show | 17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.170-8230C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35855322 | ||||||
| chr7:35855323
|
G | A | 4 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-8229G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35855323 | ||||||
| chr7:35855946
|
G | C | 313 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(310): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.170-7606G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35855946 | ||||||
| chr7:35856077
|
C | A | 1 | a0001c0001t0036g0201 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.170-7475C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35856077 | ||||||
| chr7:35856574
|
G | A | 289 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(286): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.170-6978G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35856574 | ||||||
| chr7:35856625
|
A | G | 1 | a0001c0001t0002g0025 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.170-6927A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35856625 | ||||||
| chr7:35856686
|
G | A | 133 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(130): Show | 135 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.170-6866G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35856686 | ||||||
| chr7:35856696
|
C | G | 1 | a0001c0001t0014g0165 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.170-6856C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35856696 | ||||||
| chr7:35856759
|
G | A | 13 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0202others(10): Show | 14 | HG00738.hp1 HG01081.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.170-6793G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35856759 | ||||||
| chr7:35856907
|
A | G | 22 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0197others(19): Show | 23 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.170-6645A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35856907 | ||||||
| chr7:35857339
|
G | A | 1 | a0001c0001t0001g0325 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.170-6213G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35857339 | ||||||
| chr7:35857600
|
G | A | 312 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(309): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.170-5952G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35857600 | ||||||
| chr7:35858017
|
A | T | 1 | a0001c0001t0001g0323 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.170-5535A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35858017 | ||||||
| chr7:35858145
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.170-5407A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35858145 | ||||||
| chr7:35858345
|
A | G | 133 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(130): Show | 135 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.170-5207A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35858345 | ||||||
| chr7:35858395
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.170-5157C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35858395 | ||||||
| chr7:35858419
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.170-5133G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35858419 | ||||||
| chr7:35858441
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.170-5111C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35858441 | ||||||
| chr7:35858509
|
C | T | 3 | a0001c0001t0002g0073a0001c0001t0002g0113a0001c0001t0002g0114 | 3 | HG02559.hp2 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.170-5043C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35858509 | ||||||
| chr7:35858577
|
A | G | 6 | a0001c0001t0013g0044a0001c0001t0013g0045a0001c0001t0013g0046others(3): Show | 6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.170-4975A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35858577 | ||||||
| chr7:35858633
|
C | T | 1 | a0001c0001t0034g0267 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.170-4919C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35858633 | ||||||
| chr7:35858643
|
C | T | 1 | a0001c0001t0002g0150 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.170-4909C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35858643 | ||||||
| chr7:35858681
|
C | CT | 20 | a0001c0001t0002g0108a0001c0001t0002g0110a0001c0001t0005g0010others(17): Show | 21 | HG00738.hp1 HG01081.hp1 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.170-4855dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35858681 | |||||
| chr7:35858738
|
A | G | 37 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0197others(34): Show | 40 | HG00597.hp2 HG00738.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.170-4814A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35858738 | ||||||
| chr7:35858872
|
G | A | 1 | a0001c0001t0002g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.170-4680G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35858872 | ||||||
| chr7:35859014
|
G | A | 1 | a0001c0001t0020g0007 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.170-4538G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35859014 | ||||||
| chr7:35859081
|
C | T | 3 | a0001c0001t0002g0073a0001c0001t0002g0113a0001c0001t0002g0114 | 3 | HG02559.hp2 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.170-4471C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35859081 | ||||||
| chr7:35859125
|
A | G | 3 | a0001c0001t0022g0194a0001c0001t0022g0195a0001c0001t0039g0196 | 3 | HG03471.hp1 HG03486.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.170-4427A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35859125 | ||||||
| chr7:35859145
|
A | G | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.170-4407A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35859145 | ||||||
| chr7:35859180
|
G | A | 134 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(131): Show | 136 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.170-4372G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35859180 | ||||||
| chr7:35859217
|
T | C | 4 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.170-4335T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35859217 | ||||||
| chr7:35859565
|
C | G | 1 | a0001c0001t0010g0238 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.170-3987C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35859565 | ||||||
| chr7:35860074
|
T | C | 22 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0197others(19): Show | 23 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.170-3478T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35860074 | ||||||
| chr7:35860096
|
A | G | 6 | a0001c0001t0003g0005a0001c0001t0003g0185a0001c0001t0003g0186others(3): Show | 7 | NA18954.hp2 NA18956.hp2 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.170-3456A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35860096 | ||||||
| chr7:35860114
|
C | CT | 16 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(13): Show | 18 | HG00597.hp2 HG02155.hp2 HG03098.hp2 others(15): Show |
intron_variant | MODIFIER | c.170-3427dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35860114 | |||||
| chr7:35860200
|
T | G | 1 | a0001c0001t0004g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.170-3352T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35860200 | ||||||
| chr7:35860494
|
C | T | 133 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(130): Show | 135 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.170-3058C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35860494 | ||||||
| chr7:35860534
|
G | A | 1 | a0001c0001t0012g0263 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.170-3018G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35860534 | ||||||
| chr7:35860778
|
G | C | 5 | a0001c0001t0004g0006a0001c0001t0004g0009a0001c0001t0004g0172others(2): Show | 6 | HG02109.hp1 HG02109.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.170-2774G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35860778 | ||||||
| chr7:35860944
|
C | T | 1 | a0001c0001t0001g0317 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.170-2608C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35860944 | ||||||
| chr7:35860970
|
A | G | 1 | a0001c0001t0029g0036 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.170-2582A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35860970 | ||||||
| chr7:35861096
|
T | C | 1 | a0001c0001t0013g0047 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.170-2456T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35861096 | ||||||
| chr7:35861264
|
C | T | 4 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.170-2288C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35861264 | ||||||
| chr7:35861470
|
C | T | 1 | a0001c0001t0017g0217 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.170-2082C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35861470 | ||||||
| chr7:35861539
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.170-2013G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35861539 | ||||||
| chr7:35861542
|
C | T | 1 | a0001c0001t0002g0109 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.170-2010C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35861542 | ||||||
| chr7:35861627
|
A | G | 1 | a0001c0001t0002g0074 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.170-1925A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35861627 | ||||||
| chr7:35861659
|
A | C | 15 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(12): Show | 17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.170-1893A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35861659 | ||||||
| chr7:35861666
|
A | G | 1 | a0001c0001t0039g0196 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.170-1886A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35861666 | ||||||
| chr7:35861773
|
T | G | 1 | a0001c0001t0003g0213 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.170-1779T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35861773 | ||||||
| chr7:35861806
|
G | T | 2 | a0001c0001t0001g0308a0001c0001t0010g0307 | 2 | HG01358.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.170-1746G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35861806 | ||||||
| chr7:35861880
|
G | A | 133 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(130): Show | 135 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.170-1672G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35861880 | ||||||
| chr7:35861914
|
C | T | 133 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(130): Show | 135 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.170-1638C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35861914 | ||||||
| chr7:35862074
|
A | G | 1 | a0001c0001t0038g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.170-1478A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35862074 | ||||||
| chr7:35862239
|
C | G | 5 | a0001c0001t0013g0044a0001c0001t0013g0045a0001c0001t0013g0046others(2): Show | 5 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.170-1313C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35862239 | ||||||
| chr7:35862427
|
A | G | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.170-1125A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35862427 | ||||||
| chr7:35862545
|
T | A | 1 | a0001c0001t0021g0050 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.170-1007T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35862545 | ||||||
| chr7:35862717
|
A | T | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.170-835A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35862717 | ||||||
| chr7:35862838
|
T | C | 3 | a0001c0001t0002g0073a0001c0001t0002g0113a0001c0001t0002g0114 | 3 | HG02559.hp2 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.170-714T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35862838 | ||||||
| chr7:35862900
|
CAA | C | 11 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034others(8): Show | 11 | HG01109.hp1 HG02258.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.170-647_170-646del others(2): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35862900 | |||||
| chr7:35862989
|
A | C | 13 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0202others(10): Show | 14 | HG00738.hp1 HG01081.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.170-563A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35862989 | ||||||
| chr7:35863152
|
A | G | 1 | a0001c0001t0001g0245 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.170-400A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35863152 | ||||||
| chr7:35863239
|
A | AT | 125 | a0001c0001t0001g0008a0001c0001t0001g0180a0001c0001t0001g0222others(122): Show | 126 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.170-307dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35863239 | |||||
| chr7:35863512
|
G | C | 1 | a0001c0001t0002g0159 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.170-40G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35863512 | ||||||
| chr7:35863688
|
G | A | 13 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0202others(10): Show | 14 | HG00738.hp1 HG01081.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.276+30G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35863688 | ||||||
| chr7:35863808
|
A | T | 21 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(18): Show | 23 | HG00597.hp2 HG01255.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.276+150A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35863808 | ||||||
| chr7:35864278
|
A | G | 1 | a0001c0001t0004g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.276+620A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35864278 | ||||||
| chr7:35864424
|
T | C | 312 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(309): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.276+766T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35864424 | ||||||
| chr7:35864664
|
G | GCTA | 176 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(173): Show | 181 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.276+1007_276+1009d others(5): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 35864664 | |||||
| chr7:35864770
|
A | G | 135 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(132): Show | 137 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.276+1112A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35864770 | ||||||
| chr7:35864838
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.276+1180G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35864838 | ||||||
| chr7:35864991
|
T | G | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.276+1333T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35864991 | ||||||
| chr7:35865023
|
A | AT | 45 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0197others(42): Show | 48 | HG00597.hp2 HG00738.hp1 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.276+1379dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 35865023 | |||||
| chr7:35865077
|
A | G | 1 | a0001c0001t0002g0159 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.276+1419A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35865077 | ||||||
| chr7:35865100
|
C | G | 1 | a0001c0001t0038g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.276+1442C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35865100 | ||||||
| chr7:35865207
|
T | C | 1 | a0001c0001t0004g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.276+1549T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35865207 | ||||||
| chr7:35865282
|
C | G | 2 | a0001c0001t0003g0183a0001c0001t0003g0191 | 2 | NA19072.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.276+1624C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35865282 | ||||||
| chr7:35865297
|
G | A | 1 | a0001c0001t0002g0161 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.276+1639G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35865297 | ||||||
| chr7:35865322
|
C | A | 135 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(132): Show | 137 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.276+1664C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35865322 | ||||||
| chr7:35865427
|
A | C | 6 | a0001c0001t0013g0044a0001c0001t0013g0045a0001c0001t0013g0046others(3): Show | 6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.276+1769A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35865427 | ||||||
| chr7:35865453
|
T | C | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.276+1795T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35865453 | ||||||
| chr7:35865471
|
T | A | 3 | a0001c0001t0002g0073a0001c0001t0002g0113a0001c0001t0002g0114 | 3 | HG02559.hp2 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.276+1813T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35865471 | ||||||
| chr7:35865498
|
G | C | 2 | a0001c0001t0001g0283a0001c0001t0001g0284 | 2 | HG00673.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.276+1840G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35865498 | ||||||
| chr7:35865626
|
T | C | 4 | a0001c0001t0001g0008a0001c0001t0001g0253a0001c0001t0001g0282others(1): Show | 5 | HG00733.hp1 HG00738.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.276+1968T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35865626 | ||||||
| chr7:35865850
|
C | A | 1 | a0001c0001t0004g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.276+2192C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35865850 | ||||||
| chr7:35865944
|
C | T | 1 | a0001c0001t0002g0108 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.276+2286C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35865944 | ||||||
| chr7:35866021
|
A | G | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.276+2363A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35866021 | ||||||
| chr7:35866023
|
G | C | 3 | a0001c0001t0022g0194a0001c0001t0022g0195a0001c0001t0039g0196 | 3 | HG03471.hp1 HG03486.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.276+2365G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35866023 | ||||||
| chr7:35866155
|
C | A | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.276+2497C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35866155 | ||||||
| chr7:35866201
|
C | G | 5 | a0001c0001t0003g0005a0001c0001t0003g0185a0001c0001t0003g0186others(2): Show | 6 | NA18954.hp2 NA18956.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.276+2543C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35866201 | ||||||
| chr7:35866379
|
C | G | 1 | a0001c0001t0003g0169 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.276+2721C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35866379 | ||||||
| chr7:35866807
|
C | T | 1 | a0001c0001t0001g0325 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.276+3149C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35866807 | ||||||
| chr7:35866874
|
C | A | 15 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(12): Show | 17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.276+3216C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35866874 | ||||||
| chr7:35866907
|
T | C | 135 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(132): Show | 137 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.276+3249T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35866907 | ||||||
| chr7:35867448
|
C | G | 15 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(12): Show | 17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.276+3790C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35867448 | ||||||
| chr7:35867560
|
G | A | 1 | a0001c0001t0002g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.276+3902G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35867560 | ||||||
| chr7:35867617
|
C | T | 2 | a0001c0001t0001g0308a0001c0001t0010g0307 | 2 | HG01358.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.276+3959C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35867617 | ||||||
| chr7:35867673
|
T | C | 1 | a0001c0001t0004g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.276+4015T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35867673 | ||||||
| chr7:35867851
|
A | T | 312 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(309): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.276+4193A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35867851 | ||||||
| chr7:35867977
|
A | G | 1 | a0001c0001t0004g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.276+4319A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35867977 | ||||||
| chr7:35867984
|
T | C | 1 | a0001c0001t0008g0020 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.276+4326T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35867984 | ||||||
| chr7:35868019
|
C | T | 2 | a0001c0001t0005g0220a0001c0001t0005g0221 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.276+4361C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35868019 | ||||||
| chr7:35868020
|
G | A | 15 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(12): Show | 17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.276+4362G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35868020 | ||||||
| chr7:35868253
|
A | G | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.277-4413A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35868253 | ||||||
| chr7:35868331
|
G | A | 260 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0231others(257): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.277-4335G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35868331 | ||||||
| chr7:35868331
|
G | C | 51 | a0001c0001t0001g0008a0001c0001t0001g0180a0001c0001t0001g0222others(48): Show | 52 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.277-4335G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35868331 | ||||||
| chr7:35868551
|
C | G | 37 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0197others(34): Show | 40 | HG00597.hp2 HG00738.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.277-4115C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35868551 | ||||||
| chr7:35868745
|
G | C | 13 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0202others(10): Show | 14 | HG00738.hp1 HG01081.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.277-3921G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35868745 | ||||||
| chr7:35868791
|
A | G | 1 | a0001c0001t0001g0336 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.277-3875A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35868791 | ||||||
| chr7:35869123
|
A | G | 134 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.277-3543A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35869123 | ||||||
| chr7:35869187
|
T | C | 312 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(309): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.277-3479T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35869187 | ||||||
| chr7:35869198
|
A | G | 1 | a0001c0001t0002g0144 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.277-3468A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35869198 | ||||||
| chr7:35869265
|
G | A | 125 | a0001c0001t0001g0008a0001c0001t0001g0180a0001c0001t0001g0222others(122): Show | 126 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.277-3401G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35869265 | ||||||
| chr7:35869293
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.277-3373G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35869293 | ||||||
| chr7:35869324
|
A | G | 8 | a0001c0001t0001g0182a0001c0001t0011g0003a0001c0001t0011g0065others(5): Show | 9 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.277-3342A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35869324 | ||||||
| chr7:35869796
|
A | G | 2 | a0001c0001t0018g0103a0001c0001t0018g0121 | 2 | HG02300.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.277-2870A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35869796 | ||||||
| chr7:35869959
|
G | A | 1 | a0001c0001t0021g0050 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.277-2707G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35869959 | ||||||
| chr7:35870037
|
A | T | 2 | a0001c0001t0002g0030a0001c0001t0002g0031 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.277-2629A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35870037 | ||||||
| chr7:35870091
|
A | G | 177 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(174): Show | 182 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.277-2575A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35870091 | ||||||
| chr7:35870093
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.277-2573G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35870093 | ||||||
| chr7:35870374
|
T | C | 1 | a0001c0001t0015g0051 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.277-2292T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35870374 | ||||||
| chr7:35870479
|
C | G | 40 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(37): Show | 40 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.277-2187C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35870479 | ||||||
| chr7:35870618
|
A | G | 2 | a0001c0001t0001g0282a0001c0001t0001g0297 | 2 | HG00733.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.277-2048A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35870618 | ||||||
| chr7:35870713
|
C | T | 5 | a0001c0001t0004g0006a0001c0001t0004g0009a0001c0001t0004g0172others(2): Show | 6 | HG02109.hp1 HG02109.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.277-1953C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35870713 | ||||||
| chr7:35870743
|
C | A | 1 | a0001c0001t0002g0032 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.277-1923C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35870743 | ||||||
| chr7:35870823
|
T | TA | 11 | a0001c0001t0001g0049a0001c0001t0001g0243a0001c0001t0001g0270others(8): Show | 11 | HG01074.hp1 HG01109.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.277-1822dupA | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 35870823 | |||||
| chr7:35870823
|
T | TAA | 18 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0197others(15): Show | 19 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.277-1823_277-1822d others(4): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 35870823 | |||||
| chr7:35870823
|
TA | T | 7 | a0001c0001t0002g0134a0001c0001t0002g0141a0001c0001t0003g0218others(4): Show | 7 | HG02135.hp1 HG02155.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.277-1822delA | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 35870823 | |||||
| chr7:35870823
|
TAA | T | 111 | a0001c0001t0002g0004a0001c0001t0002g0029a0001c0001t0002g0030others(108): Show | 113 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.277-1823_277-1822d others(4): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 35870823 | |||||
| chr7:35870823
|
TAAA | T | 18 | a0001c0001t0002g0025a0001c0001t0002g0078a0001c0001t0002g0079others(15): Show | 18 | HG00741.hp1 HG01943.hp1 HG02300.hp1 others(15): Show |
intron_variant | MODIFIER | c.277-1824_277-1822d others(5): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 35870823 | |||||
| chr7:35870871
|
C | T | 2 | a0001c0001t0003g0091a0001c0001t0003g0115 | 2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.277-1795C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35870871 | ||||||
| chr7:35870912
|
T | C | 3 | a0001c0001t0022g0194a0001c0001t0022g0195a0001c0001t0039g0196 | 3 | HG03471.hp1 HG03486.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.277-1754T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35870912 | ||||||
| chr7:35870939
|
A | G | 126 | a0001c0001t0001g0008a0001c0001t0001g0180a0001c0001t0001g0222others(123): Show | 127 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.277-1727A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35870939 | ||||||
| chr7:35871086
|
T | G | 136 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(133): Show | 138 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.277-1580T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35871086 | ||||||
| chr7:35871105
|
T | C | 9 | a0001c0001t0008g0015a0001c0001t0008g0016a0001c0001t0008g0017others(6): Show | 9 | HG02622.hp1 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.277-1561T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35871105 | ||||||
| chr7:35871197
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.277-1469C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35871197 | ||||||
| chr7:35871199
|
T | C | 6 | a0001c0001t0013g0044a0001c0001t0013g0045a0001c0001t0013g0046others(3): Show | 6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.277-1467T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35871199 | ||||||
| chr7:35871218
|
C | T | 22 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0197others(19): Show | 23 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.277-1448C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35871218 | ||||||
| chr7:35871348
|
G | A | 1 | a0001c0001t0002g0149 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.277-1318G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35871348 | ||||||
| chr7:35871485
|
A | G | 1 | a0001c0001t0002g0142 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.277-1181A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35871485 | ||||||
| chr7:35871554
|
T | G | 1 | a0001c0001t0003g0112 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.277-1112T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35871554 | ||||||
| chr7:35871835
|
G | A | 1 | a0001c0001t0013g0045 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.277-831G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35871835 | ||||||
| chr7:35871854
|
T | C | 6 | a0001c0001t0013g0044a0001c0001t0013g0045a0001c0001t0013g0046others(3): Show | 6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.277-812T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35871854 | ||||||
| chr7:35871999
|
G | T | 3 | a0001c0001t0002g0073a0001c0001t0002g0113a0001c0001t0002g0114 | 3 | HG02559.hp2 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.277-667G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35871999 | ||||||
| chr7:35872129
|
A | G | 12 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034others(9): Show | 12 | HG01109.hp1 HG02258.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.277-537A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35872129 | ||||||
| chr7:35872254
|
A | T | 1 | a0001c0001t0003g0097 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.277-412A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35872254 | ||||||
| chr7:35872500
|
A | G | 22 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0197others(19): Show | 23 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.277-166A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35872500 | ||||||
| chr7:35872991
|
A | T | 15 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0202others(12): Show | 16 | HG00738.hp1 HG01081.hp1 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.377+225A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 5/13 | chr7 | 35872991 | ||||||
| chr7:35873027
|
A | G | 136 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(133): Show | 138 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.377+261A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 5/13 | chr7 | 35873027 | ||||||
| chr7:35873083
|
T | C | 313 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(310): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.377+317T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 5/13 | chr7 | 35873083 | ||||||
| chr7:35873116
|
A | G | 4 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.377+350A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 5/13 | chr7 | 35873116 | ||||||
| chr7:35873391
|
G | A | 4 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.378-250G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 5/13 | chr7 | 35873391 | ||||||
| chr7:35873424
|
C | T | 134 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.378-217C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 5/13 | chr7 | 35873424 | ||||||
| chr7:35873503
|
A | G | 134 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.378-138A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 5/13 | chr7 | 35873503 | ||||||
| chr7:35873563
|
C | T | 1 | a0001c0001t0006g0058 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.378-78C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 5/13 | chr7 | 35873563 | ||||||
| chr7:35873952
|
T | C | 134 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.512+177T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35873952 | ||||||
| chr7:35873954
|
A | G | 134 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.512+179A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35873954 | ||||||
| chr7:35874201
|
A | G | 1 | a0001c0001t0009g0264 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.512+426A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35874201 | ||||||
| chr7:35874439
|
T | C | 154 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(151): Show | 158 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.512+664T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35874439 | ||||||
| chr7:35874454
|
A | T | 5 | a0001c0001t0001g0231a0001c0001t0001g0239a0001c0001t0001g0276others(2): Show | 5 | HG01123.hp1 HG01891.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.512+679A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35874454 | ||||||
| chr7:35874463
|
G | A | 312 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(309): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.512+688G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35874463 | ||||||
| chr7:35874615
|
G | T | 13 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0202others(10): Show | 14 | HG00738.hp1 HG01081.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.512+840G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35874615 | ||||||
| chr7:35874652
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.512+877A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35874652 | ||||||
| chr7:35874673
|
T | C | 2 | a0001c0001t0002g0083a0001c0003t0002g0085 | 2 | HG03239.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.512+898T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35874673 | ||||||
| chr7:35874760
|
A | T | 1 | a0001c0001t0001g0256 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.512+985A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35874760 | ||||||
| chr7:35875106
|
T | C | 2 | a0001c0001t0022g0194a0001c0001t0022g0195 | 2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.512+1331T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35875106 | ||||||
| chr7:35875770
|
T | TATAC | 6 | a0001c0001t0002g0035a0001c0001t0002g0038a0001c0001t0002g0039others(3): Show | 6 | HG01109.hp1 HG01934.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.512+2017_512+2020d others(6): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr7 | 35875770 | |||||
| chr7:35875955
|
C | A | 2 | a0001c0001t0005g0220a0001c0001t0005g0221 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.512+2180C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35875955 | ||||||
| chr7:35876121
|
A | G | 1 | a0001c0004t0013g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.512+2346A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35876121 | ||||||
| chr7:35876265
|
CTTG | C | 12 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034others(9): Show | 12 | HG01109.hp1 HG02258.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.512+2493_512+2495d others(5): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr7 | 35876265 | |||||
| chr7:35876411
|
ATT | A | 4 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.512+2638_512+2639d others(4): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr7 | 35876411 | |||||
| chr7:35876483
|
A | G | 2 | a0001c0001t0005g0220a0001c0001t0005g0221 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.512+2708A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35876483 | ||||||
| chr7:35876576
|
G | A | 3 | a0001c0001t0022g0194a0001c0001t0022g0195a0001c0001t0039g0196 | 3 | HG03471.hp1 HG03486.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.512+2801G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35876576 | ||||||
| chr7:35876588
|
A | C | 1 | a0001c0001t0009g0275 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.512+2813A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35876588 | ||||||
| chr7:35876621
|
C | G | 1 | a0001c0001t0002g0160 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.512+2846C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35876621 | ||||||
| chr7:35876864
|
G | T | 1 | a0001c0001t0001g0247 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.513-2959G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35876864 | ||||||
| chr7:35876949
|
A | G | 1 | a0001c0001t0026g0204 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.513-2874A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35876949 | ||||||
| chr7:35876977
|
A | C | 1 | a0001c0001t0011g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.513-2846A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35876977 | ||||||
| chr7:35876977
|
A | G | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.513-2846A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35876977 | ||||||
| chr7:35877231
|
T | C | 1 | a0001c0001t0003g0214 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.513-2592T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35877231 | ||||||
| chr7:35877289
|
G | A | 7 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0001t0002g0153others(4): Show | 7 | HG00609.hp2 NA18951.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.513-2534G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35877289 | ||||||
| chr7:35877299
|
A | G | 136 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(133): Show | 138 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.513-2524A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35877299 | ||||||
| chr7:35877540
|
T | G | 1 | a0001c0001t0001g0298 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.513-2283T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35877540 | ||||||
| chr7:35877814
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.513-2009A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35877814 | ||||||
| chr7:35877879
|
A | C | 2 | a0001c0001t0002g0108a0001c0001t0002g0110 | 2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.513-1944A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35877879 | ||||||
| chr7:35878294
|
G | A | 1 | a0001c0002t0001g0302 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.513-1529G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35878294 | ||||||
| chr7:35878315
|
G | GC | 3 | a0001c0001t0002g0073a0001c0001t0002g0113a0001c0001t0002g0114 | 3 | HG02559.hp2 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.513-1508_513-1507i others(3): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35878315 | ||||||
| chr7:35878316
|
T | C | 3 | a0001c0001t0002g0073a0001c0001t0002g0113a0001c0001t0002g0114 | 3 | HG02559.hp2 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.513-1507T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35878316 | ||||||
| chr7:35878317
|
A | T | 3 | a0001c0001t0002g0073a0001c0001t0002g0113a0001c0001t0002g0114 | 3 | HG02559.hp2 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.513-1506A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35878317 | ||||||
| chr7:35878320
|
A | G | 3 | a0001c0001t0002g0073a0001c0001t0002g0113a0001c0001t0002g0114 | 3 | HG02559.hp2 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.513-1503A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35878320 | ||||||
| chr7:35878797
|
A | G | 136 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(133): Show | 138 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.513-1026A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35878797 | ||||||
| chr7:35878847
|
C | T | 336 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(333): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.513-976C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35878847 | ||||||
| chr7:35878943
|
G | T | 1 | a0001c0001t0002g0160 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.513-880G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35878943 | ||||||
| chr7:35878986
|
C | T | 2 | a0001c0001t0005g0198a0001c0001t0005g0200 | 2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.513-837C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35878986 | ||||||
| chr7:35878993
|
G | T | 1 | a0001c0001t0002g0122 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.513-830G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35878993 | ||||||
| chr7:35879130
|
G | C | 1 | a0001c0001t0005g0219 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.513-693G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35879130 | ||||||
| chr7:35879150
|
C | T | 1 | a0001c0001t0002g0149 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.513-673C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35879150 | ||||||
| chr7:35879305
|
G | A | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0315 | 3 | HG00735.hp2 HG00741.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.513-518G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35879305 | ||||||
| chr7:35879333
|
A | G | 1 | a0001c0001t0019g0266 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.513-490A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35879333 | ||||||
| chr7:35879456
|
G | T | 3 | a0001c0001t0010g0306a0001c0001t0010g0329a0001c0001t0010g0330 | 3 | NA19072.hp2 NA19076.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.513-367G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35879456 | ||||||
| chr7:35879458
|
A | T | 3 | a0001c0001t0010g0306a0001c0001t0010g0329a0001c0001t0010g0330 | 3 | NA19072.hp2 NA19076.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.513-365A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35879458 | ||||||
| chr7:35879490
|
T | TA | 8 | a0001c0001t0005g0198a0001c0001t0005g0199a0001c0001t0005g0200others(5): Show | 8 | HG00738.hp1 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.513-320dupA | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr7 | 35879490 | |||||
| chr7:35879490
|
TA | T | 284 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(281): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.513-320delA | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr7 | 35879490 | |||||
| chr7:35879789
|
T | G | 20 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(17): Show | 22 | HG00597.hp2 HG01255.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.513-34T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35879789 | ||||||
| chr7:35879976
|
G | A | 20 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(17): Show | 22 | HG00597.hp2 HG01255.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.630+36G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35879976 | ||||||
| chr7:35880131
|
G | C | 134 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.630+191G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35880131 | ||||||
| chr7:35880165
|
T | C | 1 | a0001c0001t0003g0169 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.630+225T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35880165 | ||||||
| chr7:35880179
|
A | ATTTTCTT | 134 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.630+249_630+255dup others(7): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 35880179 | |||||
| chr7:35880186
|
T | C | 1 | a0001c0001t0009g0300 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.630+246T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35880186 | ||||||
| chr7:35880198
|
CTTTTCTT others(8): Show |
C | 14 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(11): Show | 16 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(13): Show |
intron_variant | MODIFIER | c.630+278_630+292del others(15): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 35880198 | |||||
| chr7:35880223
|
C | CT | 19 | a0001c0001t0001g0229a0001c0001t0001g0236a0001c0001t0001g0243others(16): Show | 19 | HG00735.hp1 HG01884.hp1 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.630+303dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 35880223 | |||||
| chr7:35880223
|
CT | C | 147 | a0001c0001t0001g0008a0001c0001t0001g0181a0001c0001t0001g0249others(144): Show | 151 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.630+303delT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 35880223 | |||||
| chr7:35880223
|
CTT | C | 7 | a0001c0001t0002g0038a0001c0001t0002g0071a0001c0001t0002g0119others(4): Show | 7 | HG02165.hp1 HG02723.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.630+302_630+303del others(2): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 35880223 | |||||
| chr7:35880223
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0008g0015 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.630+291_630+303del others(13): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 35880223 | |||||
| chr7:35880227
|
T | C | 1 | a0001c0001t0006g0058 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.630+287T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35880227 | ||||||
| chr7:35880228
|
T | C | 1 | a0001c0001t0020g0007 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.630+288T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35880228 | ||||||
| chr7:35880229
|
T | C | 1 | a0001c0001t0002g0087 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.630+289T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35880229 | ||||||
| chr7:35880352
|
C | T | 1 | a0001c0001t0003g0100 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.630+412C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35880352 | ||||||
| chr7:35880422
|
T | C | 4 | a0001c0001t0003g0092a0001c0001t0003g0101a0001c0001t0003g0169others(1): Show | 4 | HG00099.hp1 HG01192.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.630+482T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35880422 | ||||||
| chr7:35880660
|
T | A | 136 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(133): Show | 138 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.630+720T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35880660 | ||||||
| chr7:35880701
|
G | A | 6 | a0001c0001t0013g0044a0001c0001t0013g0045a0001c0001t0013g0046others(3): Show | 6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.630+761G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35880701 | ||||||
| chr7:35880769
|
A | C | 2 | a0001c0001t0004g0173a0001c0001t0004g0176 | 2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.630+829A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35880769 | ||||||
| chr7:35880932
|
C | A | 4 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.630+992C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35880932 | ||||||
| chr7:35881145
|
T | C | 134 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.630+1205T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35881145 | ||||||
| chr7:35881157
|
A | G | 3 | a0001c0001t0022g0194a0001c0001t0022g0195a0001c0001t0039g0196 | 3 | HG03471.hp1 HG03486.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.630+1217A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35881157 | ||||||
| chr7:35881512
|
T | A | 1 | a0001c0001t0038g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.631-972T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35881512 | ||||||
| chr7:35881525
|
G | A | 6 | a0001c0001t0013g0044a0001c0001t0013g0045a0001c0001t0013g0046others(3): Show | 6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.631-959G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35881525 | ||||||
| chr7:35881702
|
G | A | 1 | a0001c0002t0001g0012 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.631-782G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35881702 | ||||||
| chr7:35881768
|
G | A | 136 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(133): Show | 138 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.631-716G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35881768 | ||||||
| chr7:35881939
|
A | T | 1 | a0001c0001t0001g0182 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.631-545A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35881939 | ||||||
| chr7:35881970
|
G | A | 2 | a0001c0001t0001g0282a0001c0001t0001g0297 | 2 | HG00733.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.631-514G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35881970 | ||||||
| chr7:35882030
|
A | C | 1 | a0001c0002t0001g0305 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.631-454A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35882030 | ||||||
| chr7:35882160
|
A | T | 134 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.631-324A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35882160 | ||||||
| chr7:35882302
|
T | TA | 52 | a0001c0001t0001g0181a0001c0001t0001g0250a0001c0001t0002g0032others(49): Show | 53 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.631-168dupA | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 35882302 | |||||
| chr7:35882302
|
TA | T | 9 | a0001c0001t0001g0274a0001c0001t0005g0203a0001c0001t0006g0001others(6): Show | 11 | HG01258.hp2 HG01928.hp1 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.631-168delA | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 35882302 | |||||
| chr7:35882353
|
G | C | 1 | a0001c0001t0036g0201 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.631-131G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35882353 | ||||||
| chr7:35882448
|
A | G | 1 | a0001c0001t0005g0197 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.631-36A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35882448 | ||||||
| chr7:35882598
|
C | T | 1 | a0001c0001t0038g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.723+22C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 8/13 | chr7 | 35882598 | ||||||
| chr7:35882599
|
G | A | 1 | a0001c0001t0004g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.723+23G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 8/13 | chr7 | 35882599 | ||||||
| chr7:35882652
|
A | C | 1 | a0001c0001t0001g0181 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.723+76A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 8/13 | chr7 | 35882652 | ||||||
| chr7:35882876
|
G | T | 5 | a0001c0001t0001g0008a0001c0001t0001g0245a0001c0001t0001g0253others(2): Show | 6 | HG00733.hp1 HG00738.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.723+300G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 8/13 | chr7 | 35882876 | ||||||
| chr7:35882979
|
G | A | 3 | a0001c0001t0004g0173a0001c0001t0004g0174a0001c0001t0004g0176 | 3 | HG02258.hp2 HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.723+403G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 8/13 | chr7 | 35882979 | ||||||
| chr7:35883139
|
A | G | 15 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0202others(12): Show | 16 | HG00738.hp1 HG01081.hp1 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.723+563A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 8/13 | chr7 | 35883139 | ||||||
| chr7:35883235
|
T | C | 22 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0197others(19): Show | 23 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.724-656T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 8/13 | chr7 | 35883235 | ||||||
| chr7:35883283
|
G | C | 1 | a0001c0001t0038g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.724-608G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 8/13 | chr7 | 35883283 | ||||||
| chr7:35883393
|
A | G | 1 | a0001c0001t0002g0111 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.724-498A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 8/13 | chr7 | 35883393 | ||||||
| chr7:35883786
|
A | AT | 131 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(128): Show | 133 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.724-91dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 35883786 | |||||
| chr7:35883786
|
A | ATT | 8 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0315others(5): Show | 8 | HG00642.hp1 HG00735.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.724-92_724-91dupTT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 35883786 | |||||
| chr7:35883786
|
AT | A | 21 | a0001c0001t0005g0207a0001c0001t0006g0001a0001c0001t0006g0024others(18): Show | 23 | HG00597.hp2 HG01255.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.724-91delT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 35883786 | |||||
| chr7:35883831
|
T | A | 6 | a0001c0001t0013g0044a0001c0001t0013g0045a0001c0001t0013g0046others(3): Show | 6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.724-60T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 8/13 | chr7 | 35883831 | ||||||
| chr7:35884050
|
T | G | 3 | a0001c0001t0004g0006a0001c0001t0004g0009a0001c0001t0004g0193 | 4 | HG02109.hp1 HG02109.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.820+63T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | chr7 | 35884050 | ||||||
| chr7:35884066
|
G | A | 6 | a0001c0001t0013g0044a0001c0001t0013g0045a0001c0001t0013g0046others(3): Show | 6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.820+79G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | chr7 | 35884066 | ||||||
| chr7:35884132
|
T | C | 7 | a0001c0001t0011g0003a0001c0001t0011g0065a0001c0001t0011g0067others(4): Show | 8 | HG02280.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.820+145T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | chr7 | 35884132 | ||||||
| chr7:35884191
|
A | G | 6 | a0001c0001t0013g0044a0001c0001t0013g0045a0001c0001t0013g0046others(3): Show | 6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.820+204A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | chr7 | 35884191 | ||||||
| chr7:35884236
|
A | G | 1 | a0001c0001t0002g0074 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.820+249A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | chr7 | 35884236 | ||||||
| chr7:35884283
|
G | A | 136 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(133): Show | 138 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.820+296G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | chr7 | 35884283 | ||||||
| chr7:35884357
|
A | C | 2 | a0001c0001t0002g0156a0001c0001t0007g0157 | 2 | NA18991.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.820+370A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | chr7 | 35884357 | ||||||
| chr7:35884370
|
G | A | 3 | a0001c0001t0022g0194a0001c0001t0022g0195a0001c0001t0039g0196 | 3 | HG03471.hp1 HG03486.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.820+383G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | chr7 | 35884370 | ||||||
| chr7:35884546
|
A | G | 136 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(133): Show | 138 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.820+559A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | chr7 | 35884546 | ||||||
| chr7:35884592
|
T | C | 1 | a0001c0001t0002g0075 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.820+605T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | chr7 | 35884592 | ||||||
| chr7:35884788
|
GT | G | 2 | a0001c0001t0004g0002a0001c0001t0004g0028 | 3 | HG02615.hp1 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.820+807delT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 35884788 | |||||
| chr7:35884892
|
A | C | 2 | a0001c0001t0006g0057a0001c0001t0028g0053 | 2 | NA18940.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.820+905A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | chr7 | 35884892 | ||||||
| chr7:35885010
|
T | C | 1 | a0001c0001t0010g0241 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.821-818T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | chr7 | 35885010 | ||||||
| chr7:35885020
|
GT | G | 20 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(17): Show | 22 | HG00597.hp2 HG01255.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.821-797delT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 35885020 | |||||
| chr7:35885231
|
T | C | 1 | a0001c0001t0001g0281 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.821-597T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | chr7 | 35885231 | ||||||
| chr7:35885550
|
A | T | 1 | a0001c0001t0003g0216 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.821-278A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | chr7 | 35885550 | ||||||
| chr7:35885732
|
C | T | 1 | a0001c0001t0002g0082 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.821-96C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | chr7 | 35885732 | ||||||
| chr7:35885807
|
C | T | 1 | a0001c0001t0038g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.821-21C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | chr7 | 35885807 | ||||||
| chr7:35885890
|
G | A | 40 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(37): Show | 40 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.872+11G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35885890 | ||||||
| chr7:35885953
|
G | A | 2 | a0001c0001t0002g0108a0001c0001t0002g0110 | 2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.872+74G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35885953 | ||||||
| chr7:35886009
|
A | G | 42 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0197others(39): Show | 45 | HG00597.hp2 HG00738.hp1 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.872+130A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35886009 | ||||||
| chr7:35886037
|
A | G | 1 | a0001c0001t0001g0229 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.872+158A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35886037 | ||||||
| chr7:35886055
|
C | G | 2 | a0001c0001t0005g0220a0001c0001t0005g0221 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.872+176C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35886055 | ||||||
| chr7:35886135
|
A | G | 6 | a0001c0001t0013g0044a0001c0001t0013g0045a0001c0001t0013g0046others(3): Show | 6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.872+256A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35886135 | ||||||
| chr7:35886157
|
A | C | 3 | a0001c0001t0004g0173a0001c0001t0004g0174a0001c0001t0004g0176 | 3 | HG02258.hp2 HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.872+278A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35886157 | ||||||
| chr7:35886169
|
C | A | 6 | a0001c0001t0013g0044a0001c0001t0013g0045a0001c0001t0013g0046others(3): Show | 6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.872+290C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35886169 | ||||||
| chr7:35886248
|
T | C | 1 | a0001c0001t0005g0208 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.872+369T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35886248 | ||||||
| chr7:35886268
|
G | A | 134 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.872+389G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35886268 | ||||||
| chr7:35886433
|
T | TG | 313 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(310): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.872+555dupG | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr7 | 35886433 | |||||
| chr7:35886509
|
C | T | 2 | a0001c0001t0002g0125a0001c0001t0002g0146 | 2 | NA18941.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.872+630C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35886509 | ||||||
| chr7:35886532
|
A | G | 135 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(132): Show | 137 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.872+653A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35886532 | ||||||
| chr7:35886742
|
CTT | C | 3 | a0001c0001t0002g0029a0001c0001t0002g0030a0001c0001t0002g0031 | 3 | HG02486.hp1 HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.872+866_872+867del others(2): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr7 | 35886742 | |||||
| chr7:35886786
|
G | A | 1 | a0001c0001t0031g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.872+907G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35886786 | ||||||
| chr7:35886975
|
T | A | 72 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0237others(69): Show | 72 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.872+1096T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35886975 | ||||||
| chr7:35887161
|
A | G | 1 | a0001c0001t0004g0178 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.872+1282A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35887161 | ||||||
| chr7:35887190
|
A | G | 1 | a0001c0001t0002g0082 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.872+1311A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35887190 | ||||||
| chr7:35887315
|
C | T | 1 | a0001c0001t0005g0207 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.872+1436C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35887315 | ||||||
| chr7:35887413
|
G | A | 2 | a0001c0001t0004g0002a0001c0001t0004g0028 | 3 | HG02615.hp1 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.872+1534G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35887413 | ||||||
| chr7:35887432
|
C | T | 7 | a0001c0001t0011g0003a0001c0001t0011g0065a0001c0001t0011g0067others(4): Show | 8 | HG02280.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.872+1553C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35887432 | ||||||
| chr7:35887509
|
A | G | 312 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(309): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.872+1630A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35887509 | ||||||
| chr7:35887622
|
C | A | 3 | a0001c0001t0002g0140a0001c0001t0002g0150a0001c0001t0027g0145 | 3 | NA18954.hp1 NA18968.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.872+1743C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35887622 | ||||||
| chr7:35887622
|
C | G | 2 | a0001c0001t0003g0091a0001c0001t0003g0115 | 2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.872+1743C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35887622 | ||||||
| chr7:35887622
|
C | T | 21 | a0001c0001t0002g0004a0001c0001t0002g0116a0001c0001t0002g0118others(18): Show | 24 | HG00597.hp2 HG00733.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.872+1743C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35887622 | ||||||
| chr7:35887775
|
A | C | 134 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.872+1896A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35887775 | ||||||
| chr7:35887823
|
T | A | 1 | a0001c0001t0036g0201 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.872+1944T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35887823 | ||||||
| chr7:35887847
|
A | G | 3 | a0001c0001t0004g0173a0001c0001t0004g0174a0001c0001t0004g0176 | 3 | HG02258.hp2 HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.872+1968A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35887847 | ||||||
| chr7:35888033
|
G | A | 3 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0226 | 3 | HG00438.hp2 NA18944.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.872+2154G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35888033 | ||||||
| chr7:35888091
|
G | T | 20 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(17): Show | 22 | HG00597.hp2 HG01255.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.872+2212G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35888091 | ||||||
| chr7:35888203
|
CTA | C | 3 | a0001c0001t0022g0194a0001c0001t0022g0195a0001c0001t0039g0196 | 3 | HG03471.hp1 HG03486.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.872+2326_872+2327d others(4): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr7 | 35888203 | |||||
| chr7:35888227
|
T | G | 1 | a0001c0001t0018g0103 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.872+2348T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35888227 | ||||||
| chr7:35888488
|
GA | G | 3 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034 | 3 | HG02258.hp1 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.873-2179delA | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35888488 | ||||||
| chr7:35888491
|
T | G | 3 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034 | 3 | HG02258.hp1 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.873-2177T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35888491 | ||||||
| chr7:35888492
|
T | A | 3 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034 | 3 | HG02258.hp1 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.873-2176T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35888492 | ||||||
| chr7:35888494
|
T | G | 3 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034 | 3 | HG02258.hp1 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.873-2174T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35888494 | ||||||
| chr7:35888645
|
C | G | 6 | a0001c0001t0013g0044a0001c0001t0013g0045a0001c0001t0013g0046others(3): Show | 6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.873-2023C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35888645 | ||||||
| chr7:35888649
|
G | A | 29 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(26): Show | 31 | HG00597.hp2 HG01255.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.873-2019G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35888649 | ||||||
| chr7:35888665
|
C | G | 134 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.873-2003C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35888665 | ||||||
| chr7:35888783
|
G | A | 2 | a0001c0001t0004g0002a0001c0001t0004g0028 | 3 | HG02615.hp1 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.873-1885G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35888783 | ||||||
| chr7:35888823
|
C | CA | 225 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(222): Show | 230 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(227): Show |
intron_variant | MODIFIER | c.873-1823dupA | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr7 | 35888823 | |||||
| chr7:35888823
|
C | CAA | 55 | a0001c0001t0001g0182a0001c0001t0001g0222a0001c0001t0001g0223others(52): Show | 56 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.873-1824_873-1823d others(4): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr7 | 35888823 | |||||
| chr7:35888823
|
C | CAAA | 8 | a0001c0001t0002g0126a0001c0001t0002g0134a0001c0001t0011g0068others(5): Show | 8 | HG00609.hp1 HG02083.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.873-1825_873-1823d others(5): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr7 | 35888823 | |||||
| chr7:35888888
|
G | A | 1 | a0001c0001t0013g0047 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.873-1780G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35888888 | ||||||
| chr7:35888941
|
A | G | 134 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.873-1727A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35888941 | ||||||
| chr7:35888960
|
G | C | 5 | a0001c0001t0003g0090a0001c0001t0003g0093a0001c0001t0003g0098others(2): Show | 5 | HG00642.hp2 HG01081.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.873-1708G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35888960 | ||||||
| chr7:35889035
|
T | G | 42 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0197others(39): Show | 45 | HG00597.hp2 HG00738.hp1 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.873-1633T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35889035 | ||||||
| chr7:35889068
|
T | A | 136 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(133): Show | 138 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.873-1600T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35889068 | ||||||
| chr7:35889170
|
G | A | 14 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(11): Show | 16 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(13): Show |
intron_variant | MODIFIER | c.873-1498G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35889170 | ||||||
| chr7:35889235
|
T | G | 9 | a0001c0001t0001g0049a0001c0001t0001g0182a0001c0001t0011g0003others(6): Show | 10 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.873-1433T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35889235 | ||||||
| chr7:35889315
|
C | T | 14 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0052others(11): Show | 16 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(13): Show |
intron_variant | MODIFIER | c.873-1353C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35889315 | ||||||
| chr7:35889349
|
A | T | 3 | a0001c0001t0022g0194a0001c0001t0022g0195a0001c0001t0039g0196 | 3 | HG03471.hp1 HG03486.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.873-1319A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35889349 | ||||||
| chr7:35889378
|
A | G | 6 | a0001c0001t0013g0044a0001c0001t0013g0045a0001c0001t0013g0046others(3): Show | 6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.873-1290A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35889378 | ||||||
| chr7:35889548
|
T | A | 6 | a0001c0001t0002g0111a0001c0001t0002g0159a0001c0001t0002g0160others(3): Show | 6 | HG00140.hp2 HG01099.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.873-1120T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35889548 | ||||||
| chr7:35889690
|
C | T | 3 | a0001c0001t0008g0016a0001c0001t0008g0020a0001c0001t0008g0021 | 3 | HG02886.hp2 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.873-978C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35889690 | ||||||
| chr7:35889700
|
C | A | 1 | a0001c0001t0002g0151 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.873-968C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35889700 | ||||||
| chr7:35889764
|
G | A | 1 | a0001c0001t0010g0329 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.873-904G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35889764 | ||||||
| chr7:35890170
|
A | G | 1 | a0001c0001t0002g0151 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.873-498A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35890170 | ||||||
| chr7:35890583
|
A | C | 1 | a0001c0001t0005g0192 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.873-85A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35890583 | ||||||
| chr7:35890650
|
G | T | 134 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.873-18G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35890650 | ||||||
| chr7:35890827
|
A | C | 134 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.998+34A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35890827 | ||||||
| chr7:35890833
|
G | A | 1 | a0001c0001t0002g0111 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.998+40G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35890833 | ||||||
| chr7:35890944
|
T | A | 2 | a0001c0001t0022g0194a0001c0001t0022g0195 | 2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.998+151T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35890944 | ||||||
| chr7:35890959
|
C | T | 134 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.998+166C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35890959 | ||||||
| chr7:35891099
|
A | C | 2 | a0001c0001t0005g0192a0001c0001t0005g0205 | 2 | HG03239.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.998+306A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35891099 | ||||||
| chr7:35891189
|
G | A | 2 | a0001c0001t0022g0194a0001c0001t0022g0195 | 2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.998+396G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35891189 | ||||||
| chr7:35891205
|
T | G | 312 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(309): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.998+412T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35891205 | ||||||
| chr7:35891208
|
G | A | 1 | a0001c0001t0005g0207 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.998+415G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35891208 | ||||||
| chr7:35891291
|
C | T | 1 | a0001c0001t0004g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.998+498C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35891291 | ||||||
| chr7:35891367
|
C | CAT | 6 | a0001c0001t0013g0044a0001c0001t0013g0045a0001c0001t0013g0046others(3): Show | 6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.998+576_998+577dup others(2): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 35891367 | |||||
| chr7:35891762
|
C | G | 1 | a0001c0001t0001g0258 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.998+969C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35891762 | ||||||
| chr7:35891884
|
T | C | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0315 | 3 | HG00735.hp2 HG00741.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.998+1091T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35891884 | ||||||
| chr7:35892213
|
T | C | 42 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0197others(39): Show | 45 | HG00597.hp2 HG00738.hp1 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.998+1420T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35892213 | ||||||
| chr7:35892267
|
T | C | 1 | a0001c0001t0038g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.998+1474T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35892267 | ||||||
| chr7:35892306
|
C | G | 1 | a0001c0001t0002g0138 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.998+1513C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35892306 | ||||||
| chr7:35892337
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.998+1544A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35892337 | ||||||
| chr7:35892656
|
G | T | 126 | a0001c0001t0001g0008a0001c0001t0001g0180a0001c0001t0001g0222others(123): Show | 127 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.998+1863G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35892656 | ||||||
| chr7:35892730
|
G | C | 1 | a0001c0001t0001g0235 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.998+1937G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35892730 | ||||||
| chr7:35892763
|
G | GA | 134 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.998+1974dupA | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 35892763 | |||||
| chr7:35892879
|
G | C | 9 | a0001c0001t0008g0015a0001c0001t0008g0016a0001c0001t0008g0017others(6): Show | 9 | HG02622.hp1 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.998+2086G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35892879 | ||||||
| chr7:35892931
|
G | A | 13 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0202others(10): Show | 14 | HG00738.hp1 HG01081.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.998+2138G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35892931 | ||||||
| chr7:35893234
|
T | TCC | 312 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(309): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.998+2441_998+2442i others(4): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35893234 | ||||||
| chr7:35893539
|
C | T | 6 | a0001c0001t0013g0044a0001c0001t0013g0045a0001c0001t0013g0046others(3): Show | 6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.998+2746C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35893539 | ||||||
| chr7:35893609
|
G | C | 1 | a0001c0001t0001g0235 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.998+2816G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35893609 | ||||||
| chr7:35893760
|
T | C | 5 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0274others(2): Show | 5 | HG01074.hp1 HG01243.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.998+2967T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35893760 | ||||||
| chr7:35893868
|
G | A | 2 | a0001c0001t0001g0232a0001c0001t0001g0265 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.998+3075G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35893868 | ||||||
| chr7:35894125
|
CT | C | 167 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(164): Show | 170 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.998+3349delT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 35894125 | |||||
| chr7:35894125
|
CTT | C | 136 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(133): Show | 138 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.998+3348_998+3349d others(4): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 35894125 | |||||
| chr7:35894227
|
G | T | 1 | a0001c0001t0004g0179 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.998+3434G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35894227 | ||||||
| chr7:35894252
|
T | C | 126 | a0001c0001t0001g0008a0001c0001t0001g0180a0001c0001t0001g0222others(123): Show | 127 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.998+3459T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35894252 | ||||||
| chr7:35894343
|
C | A | 134 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.998+3550C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35894343 | ||||||
| chr7:35894389
|
A | G | 1 | a0001c0001t0012g0257 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.998+3596A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35894389 | ||||||
| chr7:35894664
|
T | G | 2 | a0001c0001t0021g0050a0001c0001t0021g0059 | 2 | HG02155.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.999-3584T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35894664 | ||||||
| chr7:35894702
|
G | A | 1 | a0001c0001t0003g0189 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.999-3546G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35894702 | ||||||
| chr7:35894726
|
A | G | 1 | a0001c0001t0009g0275 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.999-3522A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35894726 | ||||||
| chr7:35894928
|
A | T | 1 | a0001c0001t0001g0181 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.999-3320A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35894928 | ||||||
| chr7:35895481
|
A | T | 6 | a0001c0001t0013g0044a0001c0001t0013g0045a0001c0001t0013g0046others(3): Show | 6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.999-2767A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35895481 | ||||||
| chr7:35895792
|
T | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0317 | 2 | NA18973.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.999-2456T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35895792 | ||||||
| chr7:35895864
|
A | G | 1 | a0001c0001t0001g0274 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.999-2384A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35895864 | ||||||
| chr7:35895884
|
C | T | 1 | a0001c0001t0005g0205 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.999-2364C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35895884 | ||||||
| chr7:35895888
|
G | A | 136 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(133): Show | 138 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.999-2360G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35895888 | ||||||
| chr7:35895998
|
A | G | 22 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0197others(19): Show | 23 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.999-2250A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35895998 | ||||||
| chr7:35896037
|
G | C | 313 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(310): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.999-2211G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35896037 | ||||||
| chr7:35896055
|
T | C | 289 | a0001c0001t0001g0008a0001c0001t0001g0180a0001c0001t0001g0181others(286): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.999-2193T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35896055 | ||||||
| chr7:35896058
|
C | T | 8 | a0001c0001t0001g0182a0001c0001t0011g0003a0001c0001t0011g0065others(5): Show | 9 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.999-2190C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35896058 | ||||||
| chr7:35896075
|
C | T | 1 | a0001c0001t0001g0318 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.999-2173C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35896075 | ||||||
| chr7:35896142
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.999-2106C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35896142 | ||||||
| chr7:35896342
|
G | T | 1 | a0001c0001t0001g0291 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.999-1906G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35896342 | ||||||
| chr7:35896388
|
C | G | 2 | a0001c0001t0001g0250a0001c0001t0001g0251 | 2 | HG03669.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.999-1860C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35896388 | ||||||
| chr7:35896450
|
A | G | 1 | a0001c0001t0003g0214 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.999-1798A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35896450 | ||||||
| chr7:35896595
|
T | C | 2 | a0001c0001t0021g0050a0001c0001t0021g0059 | 2 | HG02155.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.999-1653T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35896595 | ||||||
| chr7:35896970
|
C | T | 1 | a0001c0001t0001g0288 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.999-1278C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35896970 | ||||||
| chr7:35897088
|
C | T | 1 | a0001c0001t0002g0142 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.999-1160C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35897088 | ||||||
| chr7:35897150
|
A | T | 12 | a0001c0001t0001g0049a0001c0001t0001g0182a0001c0001t0010g0238others(9): Show | 12 | HG01934.hp1 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.999-1098A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35897150 | ||||||
| chr7:35897189
|
A | T | 1 | a0001c0001t0001g0295 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.999-1059A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35897189 | ||||||
| chr7:35897509
|
AT | A | 27 | a0001c0001t0002g0073a0001c0001t0002g0113a0001c0001t0002g0114others(24): Show | 29 | HG00597.hp2 HG01255.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.999-728delT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 35897509 | |||||
| chr7:35897588
|
G | T | 2 | a0001c0001t0006g0057a0001c0001t0028g0053 | 2 | NA18940.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.999-660G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35897588 | ||||||
| chr7:35897640
|
C | T | 4 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.999-608C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35897640 | ||||||
| chr7:35897698
|
T | C | 1 | a0001c0001t0008g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.999-550T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35897698 | ||||||
| chr7:35897916
|
A | AT | 41 | a0001c0001t0005g0010a0001c0001t0005g0197a0001c0001t0005g0198others(38): Show | 44 | HG00597.hp2 HG00738.hp1 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.999-331dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 35897916 | |||||
| chr7:35897983
|
A | AT | 134 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.999-258dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 35897983 | |||||
| chr7:35898515
|
C | T | 1 | a0001c0001t0001g0248 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1134+132C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35898515 | ||||||
| chr7:35898597
|
T | G | 4 | a0001c0001t0002g0081a0001c0001t0002g0106a0001c0001t0030g0107others(1): Show | 4 | HG01433.hp2 HG02896.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1134+214T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35898597 | ||||||
| chr7:35898714
|
A | T | 1 | a0001c0001t0002g0110 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1134+331A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35898714 | ||||||
| chr7:35898798
|
A | G | 2 | a0001c0001t0019g0266a0001c0001t0019g0311 | 2 | HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1134+415A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35898798 | ||||||
| chr7:35898970
|
A | G | 134 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.1134+587A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35898970 | ||||||
| chr7:35898987
|
C | T | 290 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(287): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1134+604C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35898987 | ||||||
| chr7:35899210
|
G | C | 22 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0197others(19): Show | 23 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.1134+827G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35899210 | ||||||
| chr7:35899281
|
C | T | 136 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(133): Show | 138 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.1134+898C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35899281 | ||||||
| chr7:35899399
|
G | A | 6 | a0001c0001t0013g0044a0001c0001t0013g0045a0001c0001t0013g0046others(3): Show | 6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1134+1016G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35899399 | ||||||
| chr7:35899420
|
A | G | 2 | a0001c0001t0002g0108a0001c0001t0002g0110 | 2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1134+1037A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35899420 | ||||||
| chr7:35899536
|
A | G | 4 | a0001c0001t0002g0081a0001c0001t0002g0106a0001c0001t0030g0107others(1): Show | 4 | HG01433.hp2 HG02896.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1134+1153A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35899536 | ||||||
| chr7:35899551
|
A | G | 1 | a0001c0001t0007g0163 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1134+1168A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35899551 | ||||||
| chr7:35899557
|
A | G | 1 | a0001c0001t0002g0123 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1134+1174A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35899557 | ||||||
| chr7:35899711
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1134+1328A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35899711 | ||||||
| chr7:35899751
|
G | T | 136 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(133): Show | 138 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.1134+1368G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35899751 | ||||||
| chr7:35899808
|
T | G | 4 | a0001c0002t0001g0011a0001c0002t0001g0012a0001c0002t0001g0013others(1): Show | 4 | HG00408.hp2 HG01952.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.1134+1425T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35899808 | ||||||
| chr7:35899813
|
G | T | 1 | a0001c0001t0002g0166 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1134+1430G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35899813 | ||||||
| chr7:35899894
|
A | G | 1 | a0001c0001t0002g0151 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1134+1511A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35899894 | ||||||
| chr7:35900037
|
AT | A | 3 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034 | 3 | HG02258.hp1 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1134+1656delT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 35900037 | |||||
| chr7:35900042
|
T | C | 2 | a0001c0001t0005g0220a0001c0001t0005g0221 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1134+1659T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35900042 | ||||||
| chr7:35900105
|
G | C | 134 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.1134+1722G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35900105 | ||||||
| chr7:35900588
|
G | A | 1 | a0001c0001t0003g0169 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1134+2205G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35900588 | ||||||
| chr7:35900696
|
A | G | 136 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(133): Show | 138 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.1134+2313A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35900696 | ||||||
| chr7:35900752
|
C | T | 4 | a0001c0001t0002g0159a0001c0001t0002g0161a0001c0001t0002g0162others(1): Show | 4 | HG00140.hp2 HG01099.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.1135-2324C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35900752 | ||||||
| chr7:35900817
|
A | C | 4 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1135-2259A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35900817 | ||||||
| chr7:35901063
|
C | A | 1 | a0001c0001t0004g0174 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1135-2013C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35901063 | ||||||
| chr7:35901266
|
A | G | 1 | a0001c0001t0005g0197 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1135-1810A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35901266 | ||||||
| chr7:35901619
|
C | T | 1 | a0001c0001t0001g0256 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1135-1457C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35901619 | ||||||
| chr7:35901670
|
G | A | 42 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0197others(39): Show | 45 | HG00597.hp2 HG00738.hp1 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.1135-1406G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35901670 | ||||||
| chr7:35901853
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1135-1223C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35901853 | ||||||
| chr7:35901856
|
T | G | 19 | a0001c0001t0003g0026a0001c0001t0003g0027a0001c0001t0003g0090others(16): Show | 19 | HG00099.hp1 HG00642.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.1135-1220T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35901856 | ||||||
| chr7:35902030
|
T | A | 1 | a0001c0001t0009g0242 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1135-1046T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35902030 | ||||||
| chr7:35902368
|
A | G | 1 | a0001c0001t0004g0193 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1135-708A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35902368 | ||||||
| chr7:35902376
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1135-700A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35902376 | ||||||
| chr7:35902472
|
G | C | 1 | a0001c0001t0004g0002 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1135-604G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35902472 | ||||||
| chr7:35902710
|
G | A | 1 | a0001c0001t0003g0189 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1135-366G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35902710 | ||||||
| chr7:35902840
|
CT | C | 282 | a0001c0001t0001g0008a0001c0001t0001g0049a0001c0001t0001g0180others(279): Show | 288 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.1135-223delT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 35902840 | |||||
| chr7:35902855
|
C | A | 13 | a0001c0001t0005g0010a0001c0001t0005g0192a0001c0001t0005g0202others(10): Show | 14 | HG00738.hp1 HG01081.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1135-221C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35902855 | ||||||
| chr7:35902894
|
G | C | 1 | a0001c0001t0005g0203 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1135-182G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35902894 | ||||||
| chr7:35902895
|
G | A | 2 | a0001c0001t0002g0124a0001c0001t0002g0135 | 2 | NA18961.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1135-181G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35902895 | ||||||
| chr7:35902895
|
G | C | 1 | a0001c0001t0005g0203 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1135-181G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35902895 | ||||||
| chr7:35903018
|
A | G | 4 | a0001c0001t0002g0078a0001c0001t0002g0084a0001c0001t0002g0087others(1): Show | 4 | NA18957.hp1 NA18960.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.1135-58A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35903018 | ||||||
| chr7:35903019
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1135-57T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35903019 | ||||||
| chr7:35903374
|
A | G | 9 | a0001c0001t0001g0049a0001c0001t0001g0182a0001c0001t0011g0003others(6): Show | 10 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1274+159A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 13/13 | chr7 | 35903374 | ||||||
| chr7:35903395
|
TAGC | T | 126 | a0001c0001t0001g0008a0001c0001t0001g0180a0001c0001t0001g0222others(123): Show | 127 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1274+183_1274+185d others(5): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 35903395 | |||||
| chr7:35903443
|
T | C | 1 | a0001c0001t0001g0290 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1274+228T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 13/13 | chr7 | 35903443 | ||||||
| chr7:35903457
|
C | T | 4 | a0001c0001t0005g0197a0001c0001t0005g0198a0001c0001t0005g0199others(1): Show | 4 | HG01255.hp2 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1274+242C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 13/13 | chr7 | 35903457 | ||||||
| chr7:35903510
|
C | G | 38 | a0001c0001t0003g0005a0001c0001t0003g0026a0001c0001t0003g0027others(35): Show | 39 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1274+295C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 13/13 | chr7 | 35903510 | ||||||
| chr7:35903817
|
G | A | 1 | a0001c0001t0003g0214 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1275-437G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 13/13 | chr7 | 35903817 | ||||||
| chr7:35903837
|
A | C | 134 | a0001c0001t0002g0004a0001c0001t0002g0025a0001c0001t0002g0029others(131): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.1275-417A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 13/13 | chr7 | 35903837 |