| geneid | 122481 |
|---|---|
| ensemblid | ENSG00000140057.9 |
| hgncid | 20091 |
| symbol | AK7 |
| name | adenylate kinase 7 |
| refseq_nuc | NM_152327.5 |
| refseq_prot | NP_689540.2 |
| ensembl_nuc | ENST00000267584.9 |
| ensembl_prot | ENSP00000267584.4 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 96392128 |
| end | 96489427 |
| strand | + |
| ver | v1.2 |
| region | chr14:96392128-96489427 |
| region5000 | chr14:96387128-96494427 |
| regionname0 | AK7_chr14_96392128_96489427 |
| regionname5000 | AK7_chr14_96387128_96494427 |
| 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 | 0/1 | 723 | 205 | 55 | 41 | 69 | 14 | 25 | 53 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0002 | 0/0 | 723 | 64 | 17 | 11 | 27 | 0 | 9 | 22 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0003 | 1/0 | 723 | 22 | 2 | 6 | 6 | 2 | 5 | 4 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0004 | 0/0 | 723 | 12 | 10 | 2 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0005 | 0/0 | 723 | 3 | 0 | 0 | 1 | 0 | 2 | 1 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0006 | 0/0 | 723 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0007 | 0/0 | 723 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0008 | 0/0 | 723 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0009 | 0/0 | 723 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0010 | 0/0 | 723 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0011 | 0/0 | 723 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0012 | 0/0 | 723 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0013 | 0/0 | 723 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2172 | 197 | 51 | 40 | 67 | 14 | 24 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| c0002 | 0/0 | 2172 | 62 | 16 | 11 | 27 | 0 | 8 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| c0003 | 1/0 | 2172 | 14 | 0 | 6 | 0 | 2 | 5 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| c0004 | 0/0 | 2172 | 12 | 10 | 2 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| c0005 | 0/0 | 2172 | 6 | 0 | 0 | 6 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| c0006 | 0/0 | 2172 | 4 | 4 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| c0007 | 0/0 | 2172 | 4 | 0 | 1 | 2 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| c0008 | 0/0 | 2172 | 2 | 0 | 0 | 0 | 0 | 2 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| c0009 | 0/0 | 2172 | 2 | 2 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| c0010 | 0/0 | 2172 | 2 | 0 | 0 | 2 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| c0011 | 0/0 | 2172 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| c0012 | 0/0 | 2172 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| c0013 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| c0014 | 0/0 | 2172 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| c0015 | 0/0 | 2172 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| c0016 | 0/0 | 2172 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| c0017 | 0/0 | 2172 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| c0018 | 0/0 | 2172 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| c0019 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| c0020 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| c0021 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| 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 | 1111 | 196 | 40 | 49 | 72 | 9 | 25 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| t0002 | 1/0 | 1112 | 84 | 31 | 9 | 23 | 7 | 13 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| t0003 | 0/0 | 1112 | 14 | 0 | 1 | 9 | 0 | 4 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| t0004 | 0/0 | 1110 | 6 | 2 | 1 | 3 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| t0005 | 0/0 | 1112 | 5 | 4 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| t0006 | 0/0 | 1112 | 4 | 4 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| t0007 | 0/0 | 1109 | 3 | 2 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| t0008 | 0/0 | 1112 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| t0009 | 0/0 | 1111 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| t0010 | 0/0 | 1111 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| t0011 | 0/0 | 1112 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0018 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0174 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2172 | 197 | 51 | 40 | 67 | 14 | 24 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0001c0006 | 0/0 | 2172 | 4 | 4 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0001c0007 | 0/0 | 2172 | 4 | 0 | 1 | 2 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0002c0002 | 0/0 | 2172 | 62 | 16 | 11 | 27 | 0 | 8 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0002c0014 | 0/0 | 2172 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0002c0016 | 0/0 | 2172 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0003c0003 | 1/0 | 2172 | 14 | 0 | 6 | 0 | 2 | 5 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0003c0005 | 0/0 | 2172 | 6 | 0 | 0 | 6 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0003c0009 | 0/0 | 2172 | 2 | 2 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0004c0004 | 0/0 | 2172 | 12 | 10 | 2 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0005c0008 | 0/0 | 2172 | 2 | 0 | 0 | 0 | 0 | 2 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0005c0013 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0006c0010 | 0/0 | 2172 | 2 | 0 | 0 | 2 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0006c0021 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0007c0012 | 0/0 | 2172 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0008c0015 | 0/0 | 2172 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0009c0011 | 0/0 | 2172 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0010c0020 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0011c0019 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0012c0018 | 0/0 | 2172 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0013c0017 | 0/0 | 2172 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3282 | 138 | 25 | 33 | 55 | 9 | 15 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0001c0001t0002 | 0/0 | 3283 | 46 | 19 | 4 | 9 | 5 | 9 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0001c0001t0004 | 0/0 | 3281 | 4 | 1 | 1 | 2 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0001c0001t0005 | 0/0 | 3283 | 3 | 2 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0001c0001t0006 | 0/0 | 3283 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0001c0001t0007 | 0/0 | 3280 | 2 | 1 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0001c0001t0008 | 0/0 | 3283 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0001c0001t0009 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0001c0001t0010 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0001c0006t0001 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0001c0006t0002 | 0/0 | 3283 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0001c0006t0004 | 0/0 | 3281 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0001c0006t0006 | 0/0 | 3283 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0001c0007t0003 | 0/0 | 3283 | 4 | 0 | 1 | 2 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0002c0002t0001 | 0/0 | 3282 | 37 | 7 | 8 | 14 | 0 | 8 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0002c0002t0002 | 0/0 | 3283 | 20 | 5 | 3 | 12 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0002c0002t0004 | 0/0 | 3281 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0002c0002t0005 | 0/0 | 3283 | 2 | 2 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0002c0002t0007 | 0/0 | 3280 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0002c0002t0011 | 0/0 | 3283 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0002c0014t0003 | 0/0 | 3283 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0002c0016t0002 | 0/0 | 3283 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0003c0003t0001 | 0/0 | 3282 | 6 | 0 | 5 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0003c0003t0002 | 1/0 | 3283 | 8 | 0 | 1 | 0 | 2 | 4 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0003c0005t0003 | 0/0 | 3283 | 6 | 0 | 0 | 6 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0003c0009t0002 | 0/0 | 3283 | 2 | 2 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0004c0004t0001 | 0/0 | 3282 | 9 | 7 | 2 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0004c0004t0002 | 0/0 | 3283 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0004c0004t0006 | 0/0 | 3283 | 2 | 2 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0005c0008t0003 | 0/0 | 3283 | 2 | 0 | 0 | 0 | 0 | 2 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0005c0013t0002 | 0/0 | 3283 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0006c0010t0001 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0006c0010t0002 | 0/0 | 3283 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0006c0021t0003 | 0/0 | 3283 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0007c0012t0002 | 0/0 | 3283 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0008c0015t0002 | 0/0 | 3283 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0009c0011t0002 | 0/0 | 3283 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0010c0020t0001 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0011c0019t0001 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0012c0018t0001 | 0/0 | 3282 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| a0013c0017t0001 | 0/0 | 3282 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | copy fasta | chr14 | 96387128 | 96494427 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0018 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0005g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0005g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0006g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0007g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0007g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0008g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0009g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0001t0010g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0006t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0006t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0006t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0006t0006g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0007t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0007t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0007t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0001c0007t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0007g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0002t0011g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0014t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0002c0016t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0003c0003t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0003c0003t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0003c0003t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0003c0003t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0003c0003t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0003c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0003c0003t0002g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0003c0003t0002g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0003c0003t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0003c0003t0002g0174 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0003c0003t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0003c0003t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0003c0003t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0003c0003t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0003c0005t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0003c0005t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0003c0005t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0003c0005t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0003c0005t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0003c0005t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0003c0009t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0003c0009t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0004c0004t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0004c0004t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0004c0004t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0004c0004t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0004c0004t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0004c0004t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0004c0004t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0004c0004t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0004c0004t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0004c0004t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0004c0004t0006g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0004c0004t0006g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0005c0008t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0005c0008t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0005c0013t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0006c0010t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0006c0010t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0006c0021t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0007c0012t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0008c0015t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0009c0011t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0010c0020t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0011c0019t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0012c0018t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| a0013c0017t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0137 | EUR | GBR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | GBR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | FIN | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0121 | EUR | FIN | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG00323 | hp1 | a0003 | c0003 | t0002 | g0263 | EUR | FIN | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0189 | EUR | FIN | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG00423 | hp1 | a0003 | c0005 | t0003 | g0211 | EAS | CHS | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0175 | EAS | CHS | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG00621 | hp1 | a0006 | c0010 | t0002 | g0085 | EAS | CHS | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG00639 | hp1 | a0001 | c0001 | t0007 | g0243 | AMR | PUR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0149 | AMR | PUR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG00642 | hp2 | a0004 | c0004 | t0001 | g0070 | AMR | PUR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG00733 | hp2 | a0013 | c0017 | t0001 | g0316 | AMR | PUR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0267 | AMR | PUR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0302 | AMR | PUR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | PUR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0116 | AMR | PUR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0265 | AMR | PUR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0268 | AMR | PUR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0047 | AMR | PUR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0046 | AMR | PUR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01255 | hp1 | a0004 | c0004 | t0001 | g0155 | AMR | CLM | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0180 | AMR | CLM | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0183 | AMR | CLM | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01261 | hp1 | a0003 | c0003 | t0002 | g0033 | AMR | CLM | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01261 | hp2 | a0008 | c0015 | t0002 | g0244 | AMR | CLM | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | CLM | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01358 | hp2 | a0003 | c0003 | t0001 | g0101 | AMR | CLM | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0128 | AMR | CLM | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01433 | hp2 | a0003 | c0003 | t0001 | g0090 | AMR | CLM | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01496 | hp1 | a0003 | c0003 | t0001 | g0042 | AMR | CLM | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01496 | hp2 | a0002 | c0002 | t0002 | g0245 | AMR | CLM | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0222 | EUR | IBS | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0083 | EUR | IBS | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0126 | EUR | IBS | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0076 | EUR | IBS | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0082 | EUR | IBS | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0123 | EUR | IBS | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0310 | AFR | ACB | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | ACB | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01978 | hp1 | a0003 | c0003 | t0001 | g0080 | AMR | PEL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0095 | AMR | PEL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0275 | AMR | PEL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG01981 | hp2 | a0003 | c0003 | t0001 | g0110 | AMR | PEL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | KHV | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | KHV | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | ACB | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02074 | hp1 | a0001 | c0007 | t0003 | g0191 | EAS | KHV | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0225 | EAS | KHV | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0202 | EAS | KHV | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02145 | hp1 | a0002 | c0002 | t0002 | g0306 | AFR | ACB | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02145 | hp2 | a0004 | c0004 | t0001 | g0164 | AFR | ACB | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CDX | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02155 | hp2 | a0003 | c0005 | t0003 | g0212 | EAS | CDX | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CDX | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | CDX | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02257 | hp1 | a0002 | c0002 | t0005 | g0063 | AFR | ACB | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02300 | hp2 | a0001 | c0007 | t0003 | g0119 | AMR | PEL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02451 | hp2 | a0009 | c0011 | t0002 | g0007 | AFR | ACB | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02572 | hp1 | a0004 | c0004 | t0001 | g0293 | AFR | GWD | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | GWD | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0135 | SAS | PJL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0276 | SAS | PJL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | GWD | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0152 | AFR | GWD | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02647 | hp1 | a0002 | c0002 | t0011 | g0254 | AFR | GWD | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0203 | SAS | PJL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02683 | hp2 | a0005 | c0008 | t0003 | g0074 | SAS | PJL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02698 | hp1 | a0005 | c0008 | t0003 | g0274 | SAS | PJL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0315 | SAS | PJL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0288 | AFR | GWD | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | GWD | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0305 | AFR | GWD | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02723 | hp2 | a0004 | c0004 | t0001 | g0151 | AFR | GWD | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02735 | hp1 | a0003 | c0003 | t0002 | g0003 | SAS | PJL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0248 | SAS | PJL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02818 | hp1 | a0002 | c0002 | t0002 | g0169 | AFR | GWD | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0162 | AFR | GWD | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02886 | hp1 | a0001 | c0001 | t0007 | g0287 | AFR | GWD | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0308 | AFR | GWD | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02895 | hp1 | a0004 | c0004 | t0006 | g0148 | AFR | GWD | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02895 | hp2 | a0004 | c0004 | t0001 | g0170 | AFR | GWD | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02896 | hp1 | a0004 | c0004 | t0006 | g0168 | AFR | GWD | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02896 | hp2 | a0001 | c0001 | t0010 | g0260 | AFR | GWD | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0258 | AFR | GWD | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02897 | hp2 | a0004 | c0004 | t0002 | g0147 | AFR | GWD | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | ESN | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02970 | hp2 | a0003 | c0009 | t0002 | g0166 | AFR | ESN | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | ESN | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02976 | hp2 | a0003 | c0009 | t0002 | g0165 | AFR | ESN | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0242 | SAS | PJL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0206 | SAS | PJL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0271 | AFR | GWD | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03041 | hp2 | a0001 | c0006 | t0004 | g0010 | AFR | GWD | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | MSL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0235 | AFR | MSL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03130 | hp1 | a0001 | c0001 | t0008 | g0279 | AFR | ESN | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0167 | AFR | ESN | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0012 | AFR | ESN | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0066 | AFR | ESN | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0286 | AFR | ESN | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03209 | hp1 | a0001 | c0006 | t0001 | g0008 | AFR | MSL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03209 | hp2 | a0001 | c0006 | t0006 | g0009 | AFR | MSL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | MSL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | MSL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03239 | hp1 | a0003 | c0003 | t0002 | g0004 | SAS | PJL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03453 | hp2 | a0002 | c0002 | t0002 | g0297 | AFR | MSL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0161 | AFR | MSL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0256 | AFR | MSL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0053 | SAS | PJL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0220 | SAS | PJL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0054 | SAS | PJL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0221 | SAS | PJL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03516 | hp2 | a0002 | c0016 | t0002 | g0013 | AFR | ESN | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03540 | hp1 | a0002 | c0002 | t0002 | g0146 | AFR | GWD | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0312 | AFR | GWD | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03579 | hp1 | a0004 | c0004 | t0001 | g0153 | AFR | MSL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03579 | hp2 | a0002 | c0002 | t0005 | g0059 | AFR | MSL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03669 | hp1 | a0012 | c0018 | t0001 | g0111 | SAS | PJL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0228 | SAS | PJL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0057 | SAS | STU | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03710 | hp2 | a0003 | c0003 | t0001 | g0226 | SAS | PJL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0040 | SAS | BEB | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0253 | SAS | BEB | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | BEB | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0073 | SAS | BEB | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG04115 | hp1 | a0001 | c0007 | t0003 | g0044 | SAS | STU | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | STU | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG04199 | hp1 | a0003 | c0003 | t0002 | g0255 | SAS | STU | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0303 | SAS | STU | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | STU | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG04204 | hp2 | a0002 | c0014 | t0003 | g0058 | SAS | STU | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | STU | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | STU | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | YRI | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | YRI | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18941 | hp1 | a0005 | c0013 | t0002 | g0102 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18946 | hp2 | a0001 | c0007 | t0003 | g0181 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0092 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18951 | hp1 | a0011 | c0019 | t0001 | g0262 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18960 | hp2 | a0006 | c0010 | t0001 | g0049 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18961 | hp2 | a0002 | c0002 | t0002 | g0178 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18967 | hp1 | a0003 | c0005 | t0003 | g0172 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0231 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18983 | hp2 | a0003 | c0005 | t0003 | g0030 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18985 | hp1 | a0003 | c0005 | t0003 | g0024 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18990 | hp2 | a0002 | c0002 | t0002 | g0200 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19005 | hp1 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0280 | AFR | LWK | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | LWK | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | LWK | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19064 | hp1 | a0001 | c0001 | t0009 | g0187 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19064 | hp2 | a0006 | c0021 | t0003 | g0314 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0050 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0198 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19070 | hp2 | a0002 | c0002 | t0004 | g0020 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19072 | hp1 | a0003 | c0005 | t0003 | g0120 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19072 | hp2 | a0001 | c0001 | t0004 | g0216 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19081 | hp1 | a0010 | c0020 | t0001 | g0192 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0051 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19091 | hp2 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | YRI | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0285 | AFR | YRI | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0065 | AFR | ASW | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA20129 | hp2 | a0004 | c0004 | t0001 | g0154 | AFR | ASW | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA20752 | hp1 | a0003 | c0003 | t0002 | g0234 | EUR | TSI | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0290 | EUR | TSI | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | TSI | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0182 | EUR | TSI | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA20905 | hp1 | a0003 | c0003 | t0002 | g0259 | SAS | GIH | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | GIH | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02109 | hp1 | a0002 | c0002 | t0007 | g0298 | AFR | ACB | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | ACB | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02486 | hp1 | a0001 | c0006 | t0002 | g0011 | AFR | ACB | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | ACB | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG02559 | hp2 | a0004 | c0004 | t0001 | g0156 | AFR | ACB | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | MSL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | MSL | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | USA | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| HG06807 | hp2 | a0007 | c0012 | t0002 | g0142 | AFR | USA | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | USA | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0307 | AFR | USA | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0018 | REF | REF | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| homoSapiens_grch38 | hp1 | a0003 | c0003 | t0002 | g0174 | REF | REF | AK7_chr14_96387128_96494427 | AK7 | chr14 | 96387128 | 96494427 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:96398254
|
G | C | 1 | a0007 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.285G>C | p.Glu95Asp | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/18 | 312/3283 | 285/2172 | 95/723 | chr14 | 96398254 | ||
| chr14:96404767
|
G | A | 4 | a0002a0004a0005others(1): Show | 80 | HG00544.hp2 HG00621.hp2 HG00642.hp1 others(77): Show |
missense_variant | MODERATE | c.305G>A | p.Arg102Gln | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/18 | 332/3283 | 305/2172 | 102/723 | chr14 | 96404767 | ||
| chr14:96408898
|
T | C | 1 | a0013 | 1 | HG00733.hp2 | missense_variant | MODERATE | c.455T>C | p.Leu152Pro | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/18 | 482/3283 | 455/2172 | 152/723 | chr14 | 96408898 | ||
| chr14:96456401
|
A | G | 2 | a0004a0009 | 13 | HG00642.hp2 HG01255.hp1 HG02145.hp2 others(10): Show |
missense_variant | MODERATE | c.1153A>G | p.Lys385Glu | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 11/18 | 1180/3283 | 1153/2172 | 385/723 | chr14 | 96456401 | ||
| chr14:96456415
|
C | G | 10 | a0001a0002a0004others(7): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
missense_variant | MODERATE | c.1167C>G | p.Asn389Lys | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 11/18 | 1194/3283 | 1167/2172 | 389/723 | chr14 | 96456415 | ||
| chr14:96456429
|
A | G | 1 | a0006 | 3 | HG00621.hp1 NA18960.hp2 NA19064.hp2 |
missense_variant | MODERATE | c.1181A>G | p.His394Arg | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 11/18 | 1208/3283 | 1181/2172 | 394/723 | chr14 | 96456429 | ||
| chr14:96478470
|
G | A | 1 | a0012 | 1 | HG03669.hp1 | missense_variant | MODERATE | c.1561G>A | p.Val521Ile | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/18 | 1588/3283 | 1561/2172 | 521/723 | chr14 | 96478470 | ||
| chr14:96478506
|
G | A | 1 | a0011 | 1 | NA18951.hp1 | missense_variant | MODERATE | c.1597G>A | p.Glu533Lys | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/18 | 1624/3283 | 1597/2172 | 533/723 | chr14 | 96478506 | ||
| chr14:96478651
|
C | T | 1 | a0008 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.1742C>T | p.Pro581Leu | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/18 | 1769/3283 | 1742/2172 | 581/723 | chr14 | 96478651 | ||
| chr14:96483181
|
G | A | 1 | a0010 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1936G>A | p.Val646Met | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/18 | 1963/3283 | 1936/2172 | 646/723 | chr14 | 96483181 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:96392205
|
C | A | 2 | a0001c0006a0009c0011 | 5 | HG02451.hp2 HG02486.hp1 HG03041.hp2 others(2): Show |
synonymous_variant | LOW | c.51C>A | p.Thr17Thr | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/18 | 78/3283 | 51/2172 | 17/723 | chr14 | 96392205 | ||
| chr14:96471488
|
C | T | 2 | a0002c0016a0003c0009 | 3 | HG02970.hp2 HG02976.hp2 HG03516.hp2 |
synonymous_variant | LOW | c.1368C>T | p.Asp456Asp | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 13/18 | 1395/3283 | 1368/2172 | 456/723 | chr14 | 96471488 | ||
| chr14:96478541
|
G | A | 5 | a0001c0007a0002c0014a0003c0005others(2): Show | 14 | HG00423.hp1 HG02074.hp1 HG02155.hp2 others(11): Show |
synonymous_variant | LOW | c.1632G>A | p.Ala544Ala | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/18 | 1659/3283 | 1632/2172 | 544/723 | chr14 | 96478541 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:96392130
|
C | T | 1 | a0002c0002t0011 | 1 | HG02647.hp1 | 5_prime_UTR_variant | MODIFIER | c.-25C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/18 | 25 | chr14 | 96392130 | |||||
| chr14:96488480
|
T | C | 1 | a0001c0001t0008 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*137T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 18/18 | 137 | chr14 | 96488480 | |||||
| chr14:96488515
|
TAA | T | 2 | a0001c0001t0007a0002c0002t0007 | 3 | HG00639.hp1 HG02109.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*175_*176delAA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 18/18 | 175 | INFO_REALIGN_3_PRIME | chr14 | 96488515 | ||||
| chr14:96488725
|
T | G | 1 | a0001c0001t0009 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*382T>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 18/18 | 382 | chr14 | 96488725 | |||||
| chr14:96488779
|
T | G | 3 | a0001c0001t0006a0001c0006t0006a0004c0004t0006 | 4 | HG02895.hp1 HG02896.hp1 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*436T>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 18/18 | 436 | chr14 | 96488779 | |||||
| chr14:96488824
|
CT | C | 14 | a0001c0001t0001a0001c0001t0007a0001c0001t0009others(11): Show | 201 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(198): Show |
3_prime_UTR_variant | MODIFIER | c.*500delT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 18/18 | 500 | INFO_REALIGN_3_PRIME | chr14 | 96488824 | ||||
| chr14:96488824
|
CTT | C | 3 | a0001c0001t0004a0001c0006t0004a0002c0002t0004 | 6 | HG01167.hp2 HG03041.hp1 HG03041.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*499_*500delTT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 18/18 | 499 | INFO_REALIGN_3_PRIME | chr14 | 96488824 | ||||
| chr14:96488854
|
A | G | 5 | a0001c0007t0003a0002c0014t0003a0003c0005t0003others(2): Show | 14 | HG00423.hp1 HG02074.hp1 HG02155.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*511A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 18/18 | 511 | chr14 | 96488854 | |||||
| chr14:96488895
|
C | T | 1 | a0001c0001t0008 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*552C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 18/18 | 552 | chr14 | 96488895 | |||||
| chr14:96489235
|
A | G | 5 | a0001c0007t0003a0002c0014t0003a0003c0005t0003others(2): Show | 14 | HG00423.hp1 HG02074.hp1 HG02155.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*892A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 18/18 | 892 | chr14 | 96489235 | |||||
| chr14:96489404
|
A | G | 3 | a0001c0001t0005a0001c0001t0010a0002c0002t0005 | 6 | HG01109.hp1 HG02257.hp1 HG02896.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1061A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 18/18 | 1061 | chr14 | 96489404 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:96392330
|
A | G | 84 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0238others(81): Show | 84 | HG00323.hp1 HG00609.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.105+71A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96392330 | ||||||
| chr14:96392415
|
G | A | 14 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(11): Show | 14 | HG00621.hp2 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.105+156G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96392415 | ||||||
| chr14:96392440
|
T | A | 157 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.105+181T>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96392440 | ||||||
| chr14:96392580
|
A | C | 1 | a0001c0001t0001g0014 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.105+321A>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96392580 | ||||||
| chr14:96392669
|
AT | A | 255 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(252): Show | 255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.105+422delT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr14 | 96392669 | |||||
| chr14:96392820
|
G | A | 6 | a0001c0001t0001g0005a0001c0001t0001g0015a0002c0002t0002g0001others(3): Show | 6 | HG00621.hp2 HG02083.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.105+561G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96392820 | ||||||
| chr14:96392829
|
A | AT | 12 | a0001c0001t0001g0150a0001c0001t0002g0145a0002c0002t0001g0152others(9): Show | 12 | HG00642.hp1 HG01255.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.105+576dupT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr14 | 96392829 | |||||
| chr14:96392883
|
C | G | 12 | a0001c0001t0001g0150a0001c0001t0002g0145a0002c0002t0001g0152others(9): Show | 12 | HG00642.hp1 HG01255.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.105+624C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96392883 | ||||||
| chr14:96392918
|
G | T | 8 | a0001c0001t0001g0014a0001c0006t0001g0008a0001c0006t0002g0011others(5): Show | 8 | HG02451.hp2 HG02486.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.105+659G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96392918 | ||||||
| chr14:96392947
|
C | A | 256 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(253): Show | 256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.105+688C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96392947 | ||||||
| chr14:96393268
|
C | T | 84 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0239others(81): Show | 84 | HG00323.hp1 HG00609.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.105+1009C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96393268 | ||||||
| chr14:96393276
|
A | C | 3 | a0001c0001t0001g0230a0001c0001t0001g0232a0002c0002t0002g0231 | 3 | NA18959.hp2 NA18971.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.105+1017A>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96393276 | ||||||
| chr14:96393445
|
A | T | 1 | a0013c0017t0001g0316 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.105+1186A>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96393445 | ||||||
| chr14:96393598
|
G | A | 6 | a0001c0001t0001g0005a0001c0001t0001g0015a0002c0002t0002g0001others(3): Show | 6 | HG00621.hp2 HG02083.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.105+1339G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96393598 | ||||||
| chr14:96393599
|
G | A | 61 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0021others(58): Show | 61 | HG00099.hp2 HG00642.hp1 HG01099.hp2 others(58): Show |
intron_variant | MODIFIER | c.105+1340G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96393599 | ||||||
| chr14:96393828
|
CAG | C | 75 | a0001c0001t0001g0072a0001c0001t0001g0076a0001c0001t0001g0077others(72): Show | 75 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.105+1573_105+1574d others(4): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr14 | 96393828 | |||||
| chr14:96394038
|
G | T | 1 | a0001c0001t0001g0315 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.105+1779G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96394038 | ||||||
| chr14:96394108
|
C | CA | 11 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0017others(8): Show | 11 | HG02055.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.105+1863dupA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr14 | 96394108 | |||||
| chr14:96394473
|
G | A | 1 | a0003c0003t0002g0234 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.105+2214G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96394473 | ||||||
| chr14:96394510
|
G | T | 6 | a0002c0002t0001g0152a0004c0004t0001g0151a0004c0004t0001g0153others(3): Show | 6 | HG01255.hp1 HG02559.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.105+2251G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96394510 | ||||||
| chr14:96394585
|
A | G | 1 | a0006c0021t0003g0314 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.105+2326A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96394585 | ||||||
| chr14:96394702
|
A | G | 1 | a0001c0001t0001g0313 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.105+2443A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96394702 | ||||||
| chr14:96394750
|
C | T | 7 | a0001c0001t0001g0064a0002c0002t0001g0152a0004c0004t0001g0151others(4): Show | 7 | HG01099.hp2 HG01255.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.105+2491C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96394750 | ||||||
| chr14:96394777
|
A | G | 1 | a0001c0001t0001g0229 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.105+2518A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96394777 | ||||||
| chr14:96394814
|
A | G | 73 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(70): Show | 73 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.105+2555A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96394814 | ||||||
| chr14:96395006
|
C | T | 87 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0015others(84): Show | 87 | HG00099.hp1 HG00423.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.105+2747C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96395006 | ||||||
| chr14:96395034
|
TTATG | T | 3 | a0001c0001t0001g0160a0002c0002t0001g0161a0002c0002t0001g0162 | 3 | HG02818.hp2 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.105+2781_105+2784d others(6): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr14 | 96395034 | |||||
| chr14:96395070
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.105+2811G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96395070 | ||||||
| chr14:96395455
|
G | T | 45 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0061others(42): Show | 45 | HG00642.hp2 HG00733.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.106-2620G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96395455 | ||||||
| chr14:96395488
|
G | T | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.106-2587G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96395488 | ||||||
| chr14:96395554
|
A | G | 115 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0026others(112): Show | 115 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.106-2521A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96395554 | ||||||
| chr14:96395718
|
G | GA | 68 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(65): Show | 68 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.106-2331dupA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr14 | 96395718 | |||||
| chr14:96395718
|
G | GAA | 9 | a0001c0001t0001g0140a0001c0001t0001g0239a0001c0001t0001g0304others(6): Show | 9 | HG01891.hp2 HG02257.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.106-2332_106-2331d others(4): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr14 | 96395718 | |||||
| chr14:96395718
|
GAAAAAAA others(4): Show |
G | 31 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0022others(28): Show | 31 | HG00544.hp2 HG00642.hp1 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.106-2341_106-2331d others(13): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr14 | 96395718 | |||||
| chr14:96395755
|
A | G | 2 | a0001c0001t0002g0159a0002c0002t0005g0063 | 2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.106-2320A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96395755 | ||||||
| chr14:96395800
|
A | AT | 90 | a0001c0001t0001g0018a0001c0001t0001g0035a0001c0001t0001g0041others(87): Show | 90 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.106-2245dupT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr14 | 96395800 | |||||
| chr14:96395800
|
A | ATT | 35 | a0001c0001t0001g0029a0001c0001t0001g0062a0001c0001t0001g0132others(32): Show | 35 | HG00621.hp2 HG00738.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.106-2246_106-2245d others(4): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr14 | 96395800 | |||||
| chr14:96395800
|
A | ATTT | 6 | a0001c0001t0001g0131a0001c0001t0001g0140a0001c0001t0001g0278others(3): Show | 6 | HG00735.hp2 HG02257.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-2247_106-2245d others(5): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr14 | 96395800 | |||||
| chr14:96395800
|
AT | A | 69 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0025others(66): Show | 69 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.106-2245delT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr14 | 96395800 | |||||
| chr14:96395800
|
ATT | A | 8 | a0001c0001t0001g0239a0001c0001t0001g0304a0001c0001t0002g0067others(5): Show | 8 | HG01496.hp2 HG01891.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.106-2246_106-2245d others(4): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr14 | 96395800 | |||||
| chr14:96395800
|
ATTT | A | 12 | a0001c0001t0001g0084a0001c0001t0005g0065a0001c0001t0005g0258others(9): Show | 12 | HG00423.hp1 HG00639.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.106-2247_106-2245d others(5): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr14 | 96395800 | |||||
| chr14:96395837
|
G | C | 2 | a0002c0002t0001g0012a0002c0016t0002g0013 | 2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.106-2238G>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96395837 | ||||||
| chr14:96395865
|
A | G | 1 | a0002c0002t0002g0175 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.106-2210A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96395865 | ||||||
| chr14:96395913
|
G | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0022others(15): Show | 18 | HG00609.hp1 HG01099.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.106-2162G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96395913 | ||||||
| chr14:96395958
|
T | C | 2 | a0001c0001t0001g0201a0001c0001t0001g0204 | 2 | NA18945.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.106-2117T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96395958 | ||||||
| chr14:96395965
|
C | T | 7 | a0001c0001t0001g0304a0001c0001t0002g0068a0001c0001t0002g0163others(4): Show | 7 | HG02257.hp1 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.106-2110C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96395965 | ||||||
| chr14:96396270
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.106-1805G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96396270 | ||||||
| chr14:96396271
|
C | G | 1 | a0001c0001t0001g0121 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.106-1804C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96396271 | ||||||
| chr14:96396368
|
G | A | 4 | a0001c0001t0005g0065a0001c0001t0005g0258a0001c0001t0010g0260others(1): Show | 4 | HG02486.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-1707G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96396368 | ||||||
| chr14:96396426
|
T | A | 255 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(252): Show | 255 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.106-1649T>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96396426 | ||||||
| chr14:96396426
|
T | C | 1 | a0002c0002t0002g0288 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.106-1649T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96396426 | ||||||
| chr14:96396447
|
A | C | 1 | a0001c0001t0002g0171 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.106-1628A>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96396447 | ||||||
| chr14:96396472
|
T | C | 3 | a0001c0001t0001g0062a0001c0001t0001g0129a0001c0001t0001g0315 | 3 | HG02698.hp2 NA18970.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.106-1603T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96396472 | ||||||
| chr14:96396531
|
C | G | 27 | a0001c0001t0001g0037a0001c0001t0001g0072a0001c0001t0001g0130others(24): Show | 27 | HG00323.hp2 HG01167.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.106-1544C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96396531 | ||||||
| chr14:96396733
|
C | T | 27 | a0001c0001t0001g0037a0001c0001t0001g0072a0001c0001t0001g0130others(24): Show | 27 | HG00323.hp2 HG01167.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.106-1342C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96396733 | ||||||
| chr14:96396867
|
T | C | 1 | a0003c0005t0003g0030 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.106-1208T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96396867 | ||||||
| chr14:96396892
|
C | G | 1 | a0001c0001t0001g0217 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.106-1183C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96396892 | ||||||
| chr14:96396893
|
C | A | 1 | a0001c0001t0001g0217 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.106-1182C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96396893 | ||||||
| chr14:96396912
|
C | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0022others(16): Show | 19 | HG00738.hp1 HG01099.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.106-1163C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96396912 | ||||||
| chr14:96397003
|
C | T | 5 | a0001c0001t0001g0133a0001c0001t0001g0252a0001c0001t0002g0159others(2): Show | 5 | HG02280.hp1 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-1072C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96397003 | ||||||
| chr14:96397165
|
T | C | 3 | a0001c0001t0001g0062a0001c0001t0001g0129a0001c0001t0001g0315 | 3 | HG02698.hp2 NA18970.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.106-910T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96397165 | ||||||
| chr14:96397254
|
A | G | 27 | a0001c0001t0001g0037a0001c0001t0001g0072a0001c0001t0001g0130others(24): Show | 27 | HG00323.hp2 HG01167.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.106-821A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96397254 | ||||||
| chr14:96397381
|
G | A | 1 | a0003c0005t0003g0030 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.106-694G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96397381 | ||||||
| chr14:96397401
|
G | A | 227 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0025others(224): Show | 227 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(224): Show |
intron_variant | MODIFIER | c.106-674G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96397401 | ||||||
| chr14:96397439
|
A | G | 4 | a0001c0001t0005g0065a0001c0001t0005g0258a0001c0001t0010g0260others(1): Show | 4 | HG02486.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-636A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96397439 | ||||||
| chr14:96397650
|
G | A | 1 | a0001c0001t0001g0315 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.106-425G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96397650 | ||||||
| chr14:96397719
|
C | A | 253 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(250): Show | 253 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(250): Show |
intron_variant | MODIFIER | c.106-356C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96397719 | ||||||
| chr14:96397832
|
C | T | 27 | a0001c0001t0001g0037a0001c0001t0001g0072a0001c0001t0001g0130others(24): Show | 27 | HG00323.hp2 HG01167.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.106-243C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96397832 | ||||||
| chr14:96397972
|
A | G | 221 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0025others(218): Show | 221 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.106-103A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96397972 | ||||||
| chr14:96397990
|
A | G | 12 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0022others(9): Show | 12 | HG00738.hp1 HG01099.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.106-85A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96397990 | ||||||
| chr14:96398037
|
T | G | 6 | a0001c0001t0001g0084a0001c0001t0001g0150a0001c0001t0001g0160others(3): Show | 6 | HG01069.hp1 HG03130.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.106-38T>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96398037 | ||||||
| chr14:96398050
|
T | A | 1 | a0002c0002t0001g0167 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.106-25T>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 1/17 | chr14 | 96398050 | ||||||
| chr14:96398351
|
C | T | 6 | a0004c0004t0001g0070a0004c0004t0001g0151a0004c0004t0001g0153others(3): Show | 6 | HG00642.hp2 HG01255.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.294+88C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96398351 | ||||||
| chr14:96398558
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.294+295C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96398558 | ||||||
| chr14:96398562
|
T | A | 6 | a0001c0001t0001g0304a0001c0001t0002g0068a0001c0001t0002g0163others(3): Show | 6 | HG02630.hp1 HG02717.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.294+299T>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96398562 | ||||||
| chr14:96398578
|
T | C | 1 | a0001c0001t0002g0237 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.294+315T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96398578 | ||||||
| chr14:96398607
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.294+344C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96398607 | ||||||
| chr14:96398679
|
C | T | 1 | a0007c0012t0002g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.294+416C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96398679 | ||||||
| chr14:96398825
|
T | C | 1 | a0001c0001t0002g0237 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.294+562T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96398825 | ||||||
| chr14:96398976
|
C | CT | 60 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0025others(57): Show | 60 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.294+724dupT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr14 | 96398976 | |||||
| chr14:96398978
|
T | C | 1 | a0001c0001t0001g0313 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.294+715T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96398978 | ||||||
| chr14:96399027
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.294+764C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96399027 | ||||||
| chr14:96399089
|
C | CAT | 55 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0032others(52): Show | 55 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.294+829_294+830dup others(2): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr14 | 96399089 | |||||
| chr14:96399333
|
C | T | 1 | a0001c0001t0001g0309 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.294+1070C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96399333 | ||||||
| chr14:96399377
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.294+1114C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96399377 | ||||||
| chr14:96399495
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.294+1232C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96399495 | ||||||
| chr14:96399804
|
C | T | 4 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0002g0040others(1): Show | 4 | HG00741.hp1 HG01168.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+1541C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96399804 | ||||||
| chr14:96399815
|
G | T | 4 | a0001c0001t0005g0065a0001c0001t0005g0258a0001c0001t0010g0260others(1): Show | 4 | HG02486.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.294+1552G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96399815 | ||||||
| chr14:96399891
|
C | T | 3 | a0002c0002t0001g0152a0002c0002t0001g0167a0002c0002t0001g0308 | 3 | HG02630.hp2 HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.294+1628C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96399891 | ||||||
| chr14:96400030
|
C | CT | 17 | a0001c0001t0001g0025a0001c0001t0001g0106a0001c0001t0001g0131others(14): Show | 17 | HG00733.hp1 HG00733.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.294+1793dupT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr14 | 96400030 | |||||
| chr14:96400030
|
CT | C | 73 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0062others(70): Show | 73 | HG00323.hp2 HG00423.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.294+1793delT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr14 | 96400030 | |||||
| chr14:96400030
|
CTT | C | 44 | a0001c0001t0001g0069a0001c0001t0001g0158a0001c0001t0001g0186others(41): Show | 44 | HG00544.hp2 HG00741.hp2 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.294+1792_294+1793d others(4): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr14 | 96400030 | |||||
| chr14:96400030
|
CTTT | C | 6 | a0001c0001t0002g0171a0002c0002t0001g0052a0002c0002t0001g0053others(3): Show | 6 | HG03017.hp2 HG03098.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.294+1791_294+1793d others(5): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr14 | 96400030 | |||||
| chr14:96400072
|
T | A | 40 | a0001c0001t0001g0087a0001c0001t0001g0091a0001c0001t0001g0099others(37): Show | 40 | HG00423.hp1 HG00639.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.294+1809T>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96400072 | ||||||
| chr14:96400184
|
G | A | 27 | a0001c0001t0001g0037a0001c0001t0001g0072a0001c0001t0001g0130others(24): Show | 27 | HG00323.hp2 HG01167.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.294+1921G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96400184 | ||||||
| chr14:96400186
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.294+1923G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96400186 | ||||||
| chr14:96400189
|
C | T | 6 | a0001c0001t0001g0304a0001c0001t0002g0068a0001c0001t0002g0163others(3): Show | 6 | HG02630.hp1 HG02717.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.294+1926C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96400189 | ||||||
| chr14:96400332
|
G | A | 6 | a0001c0001t0001g0304a0001c0001t0002g0068a0001c0001t0002g0163others(3): Show | 6 | HG02630.hp1 HG02717.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.294+2069G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96400332 | ||||||
| chr14:96400648
|
C | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0022others(16): Show | 19 | HG00738.hp1 HG01099.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.294+2385C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96400648 | ||||||
| chr14:96400712
|
C | T | 34 | a0002c0002t0001g0012a0002c0002t0001g0016a0002c0002t0001g0019others(31): Show | 34 | HG00544.hp2 HG00741.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.294+2449C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96400712 | ||||||
| chr14:96400726
|
T | G | 1 | a0001c0001t0001g0182 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.294+2463T>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96400726 | ||||||
| chr14:96400871
|
T | A | 1 | a0001c0001t0001g0315 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.294+2608T>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96400871 | ||||||
| chr14:96400894
|
T | A | 11 | a0001c0001t0001g0014a0001c0001t0001g0304a0001c0001t0002g0068others(8): Show | 11 | HG02486.hp1 HG02630.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.294+2631T>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96400894 | ||||||
| chr14:96401160
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.294+2897C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96401160 | ||||||
| chr14:96401249
|
A | G | 1 | a0003c0005t0003g0120 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.294+2986A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96401249 | ||||||
| chr14:96401404
|
A | G | 58 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0032others(55): Show | 58 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.294+3141A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96401404 | ||||||
| chr14:96401447
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.294+3184G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96401447 | ||||||
| chr14:96401565
|
A | G | 55 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0032others(52): Show | 55 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.295-3192A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96401565 | ||||||
| chr14:96401646
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.295-3111C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96401646 | ||||||
| chr14:96401699
|
A | G | 254 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(251): Show | 254 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(251): Show |
intron_variant | MODIFIER | c.295-3058A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96401699 | ||||||
| chr14:96401736
|
T | C | 2 | a0001c0001t0001g0129a0001c0001t0001g0315 | 2 | HG02698.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.295-3021T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96401736 | ||||||
| chr14:96401842
|
T | C | 55 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0032others(52): Show | 55 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.295-2915T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96401842 | ||||||
| chr14:96401924
|
G | T | 1 | a0013c0017t0001g0316 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.295-2833G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96401924 | ||||||
| chr14:96402098
|
C | T | 3 | a0001c0001t0001g0069a0003c0009t0002g0165a0003c0009t0002g0166 | 3 | HG02970.hp2 HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.295-2659C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96402098 | ||||||
| chr14:96402185
|
G | GCA | 23 | a0001c0001t0001g0022a0001c0001t0001g0069a0001c0001t0001g0097others(20): Show | 23 | HG00280.hp1 HG00609.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.295-2539_295-2538d others(4): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr14 | 96402185 | |||||
| chr14:96402185
|
G | GCACA | 36 | a0001c0001t0001g0160a0002c0002t0001g0046a0002c0002t0001g0047others(33): Show | 36 | HG00544.hp2 HG00621.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.295-2541_295-2538d others(6): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr14 | 96402185 | |||||
| chr14:96402185
|
G | GCACACA | 31 | a0002c0002t0001g0012a0002c0002t0001g0016a0002c0002t0001g0019others(28): Show | 31 | HG00741.hp2 HG01978.hp2 HG02083.hp2 others(28): Show |
intron_variant | MODIFIER | c.295-2543_295-2538d others(8): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr14 | 96402185 | |||||
| chr14:96402185
|
G | GCACACAC others(1): Show |
5 | a0002c0002t0001g0162a0002c0002t0001g0202a0004c0004t0001g0170others(2): Show | 5 | HG02135.hp1 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.295-2545_295-2538d others(10): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr14 | 96402185 | |||||
| chr14:96402185
|
GCA | G | 53 | a0001c0001t0001g0006a0001c0001t0001g0027a0001c0001t0001g0029others(50): Show | 53 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.295-2539_295-2538d others(4): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr14 | 96402185 | |||||
| chr14:96402185
|
GCACA | G | 45 | a0001c0001t0001g0014a0001c0001t0001g0087a0001c0001t0001g0091others(42): Show | 45 | HG00423.hp1 HG00639.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.295-2541_295-2538d others(6): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr14 | 96402185 | |||||
| chr14:96402185
|
GCACACA | G | 5 | a0001c0001t0001g0277a0001c0001t0002g0310a0001c0001t0004g0268others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.295-2543_295-2538d others(8): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr14 | 96402185 | |||||
| chr14:96402189
|
A | C | 1 | a0001c0001t0001g0084 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.295-2568A>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96402189 | ||||||
| chr14:96402190
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.295-2567C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96402190 | ||||||
| chr14:96402265
|
A | G | 3 | a0001c0001t0001g0264a0001c0001t0001g0272a0001c0001t0001g0311 | 3 | HG02280.hp2 HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.295-2492A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96402265 | ||||||
| chr14:96402734
|
T | C | 1 | a0004c0004t0001g0293 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.295-2023T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96402734 | ||||||
| chr14:96402743
|
C | G | 1 | a0001c0001t0001g0069 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.295-2014C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96402743 | ||||||
| chr14:96402754
|
G | A | 11 | a0001c0001t0001g0014a0001c0001t0001g0304a0001c0001t0002g0068others(8): Show | 11 | HG02486.hp1 HG02630.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.295-2003G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96402754 | ||||||
| chr14:96402855
|
C | T | 39 | a0001c0001t0001g0087a0001c0001t0001g0091a0001c0001t0001g0099others(36): Show | 39 | HG00423.hp1 HG00639.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.295-1902C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96402855 | ||||||
| chr14:96402904
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0112 | 2 | HG02155.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.295-1853G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96402904 | ||||||
| chr14:96402921
|
GA | G | 27 | a0001c0001t0001g0037a0001c0001t0001g0072a0001c0001t0001g0130others(24): Show | 27 | HG00323.hp2 HG01167.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.295-1835delA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96402921 | ||||||
| chr14:96403007
|
C | T | 1 | a0001c0001t0009g0187 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.295-1750C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96403007 | ||||||
| chr14:96403040
|
T | G | 33 | a0001c0001t0001g0087a0001c0001t0001g0091a0001c0001t0001g0126others(30): Show | 33 | HG00423.hp1 HG00639.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.295-1717T>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96403040 | ||||||
| chr14:96403103
|
A | G | 254 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(251): Show | 254 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(251): Show |
intron_variant | MODIFIER | c.295-1654A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96403103 | ||||||
| chr14:96403114
|
T | TTAAA | 73 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0034others(70): Show | 73 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.295-1605_295-1602d others(6): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr14 | 96403114 | |||||
| chr14:96403114
|
T | TTAAATAA others(1): Show |
80 | a0001c0001t0001g0015a0001c0001t0001g0032a0001c0001t0001g0037others(77): Show | 80 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.295-1609_295-1602d others(10): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr14 | 96403114 | |||||
| chr14:96403114
|
T | TTAAATAA others(5): Show |
10 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0189others(7): Show | 10 | HG00323.hp2 HG02015.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.295-1613_295-1602d others(14): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr14 | 96403114 | |||||
| chr14:96403114
|
T | TTAAATAA others(9): Show |
1 | a0001c0001t0001g0098 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.295-1617_295-1602d others(18): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr14 | 96403114 | |||||
| chr14:96403114
|
TTAAA | T | 21 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0021others(18): Show | 21 | HG00738.hp1 HG00741.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.295-1605_295-1602d others(6): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr14 | 96403114 | |||||
| chr14:96403114
|
TTAAATAA others(1): Show |
T | 36 | a0001c0001t0001g0133a0001c0001t0001g0252a0001c0001t0002g0159others(33): Show | 36 | HG00544.hp2 HG01106.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.295-1609_295-1602d others(10): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr14 | 96403114 | |||||
| chr14:96403145
|
A | AATAAATA others(9): Show |
1 | a0001c0007t0003g0119 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.295-1602_295-1601i others(18): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr14 | 96403145 | |||||
| chr14:96403145
|
A | AATAAATA others(1): Show |
5 | a0001c0001t0001g0125a0001c0001t0001g0207a0001c0001t0001g0215others(2): Show | 5 | HG01346.hp2 NA18948.hp1 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.295-1605_295-1604i others(10): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr14 | 96403145 | |||||
| chr14:96403422
|
A | C | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.295-1335A>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96403422 | ||||||
| chr14:96403605
|
A | C | 1 | a0007c0012t0002g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.295-1152A>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96403605 | ||||||
| chr14:96403738
|
C | T | 1 | a0001c0001t0001g0315 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.295-1019C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96403738 | ||||||
| chr14:96404150
|
T | TA | 34 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0127others(31): Show | 34 | HG00323.hp2 HG01167.hp1 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.295-584dupA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr14 | 96404150 | |||||
| chr14:96404150
|
TA | T | 110 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0025others(107): Show | 110 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.295-584delA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr14 | 96404150 | |||||
| chr14:96404150
|
TAA | T | 13 | a0001c0001t0001g0084a0001c0001t0001g0150a0001c0001t0001g0160others(10): Show | 13 | HG01069.hp1 HG02451.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.295-585_295-584del others(2): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr14 | 96404150 | |||||
| chr14:96404162
|
A | C | 1 | a0001c0001t0001g0109 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.295-595A>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96404162 | ||||||
| chr14:96404171
|
A | AC | 6 | a0002c0002t0001g0012a0002c0002t0001g0039a0002c0002t0001g0194others(3): Show | 6 | HG01981.hp1 HG02145.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.295-586_295-585ins others(1): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96404171 | ||||||
| chr14:96404171
|
A | C | 74 | a0002c0002t0001g0016a0002c0002t0001g0019a0002c0002t0001g0023others(71): Show | 74 | HG00544.hp2 HG00621.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.295-586A>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96404171 | ||||||
| chr14:96404190
|
C | T | 27 | a0001c0001t0001g0037a0001c0001t0001g0072a0001c0001t0001g0130others(24): Show | 27 | HG00323.hp2 HG01167.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.295-567C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96404190 | ||||||
| chr14:96404273
|
G | A | 4 | a0001c0001t0001g0239a0003c0005t0003g0024a0003c0005t0003g0211others(1): Show | 4 | HG00423.hp1 HG02155.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.295-484G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96404273 | ||||||
| chr14:96404414
|
A | C | 7 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0055others(4): Show | 7 | HG01099.hp2 HG03688.hp1 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.295-343A>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 2/17 | chr14 | 96404414 | ||||||
| chr14:96405000
|
C | T | 80 | a0002c0002t0001g0012a0002c0002t0001g0016a0002c0002t0001g0019others(77): Show | 80 | HG00544.hp2 HG00621.hp2 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.403+135C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96405000 | ||||||
| chr14:96405001
|
C | T | 80 | a0002c0002t0001g0012a0002c0002t0001g0016a0002c0002t0001g0019others(77): Show | 80 | HG00544.hp2 HG00621.hp2 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.403+136C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96405001 | ||||||
| chr14:96405002
|
A | G | 5 | a0001c0001t0001g0133a0001c0001t0001g0252a0001c0001t0002g0159others(2): Show | 5 | HG02280.hp1 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.403+137A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96405002 | ||||||
| chr14:96405006
|
T | C | 1 | a0001c0001t0001g0281 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.403+141T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96405006 | ||||||
| chr14:96405011
|
A | G | 1 | a0007c0012t0002g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.403+146A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96405011 | ||||||
| chr14:96405037
|
G | C | 1 | a0001c0001t0002g0305 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.403+172G>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96405037 | ||||||
| chr14:96405111
|
C | T | 2 | a0003c0009t0002g0165a0003c0009t0002g0166 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.403+246C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96405111 | ||||||
| chr14:96405126
|
A | T | 1 | a0001c0001t0001g0284 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.403+261A>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96405126 | ||||||
| chr14:96405174
|
G | A | 4 | a0001c0001t0001g0069a0001c0001t0002g0286a0003c0009t0002g0165others(1): Show | 4 | HG02970.hp2 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.403+309G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96405174 | ||||||
| chr14:96405250
|
A | G | 40 | a0001c0001t0001g0087a0001c0001t0001g0091a0001c0001t0001g0099others(37): Show | 40 | HG00423.hp1 HG00639.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.403+385A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96405250 | ||||||
| chr14:96405267
|
C | T | 5 | a0002c0002t0001g0019a0002c0002t0001g0023a0002c0002t0001g0039others(2): Show | 5 | NA18956.hp2 NA18957.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.403+402C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96405267 | ||||||
| chr14:96405273
|
C | G | 1 | a0001c0001t0001g0022 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.403+408C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96405273 | ||||||
| chr14:96405351
|
T | C | 2 | a0001c0001t0001g0313a0001c0001t0002g0280 | 2 | HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.403+486T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96405351 | ||||||
| chr14:96405504
|
T | C | 2 | a0001c0001t0001g0076a0001c0001t0001g0257 | 2 | HG01516.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.403+639T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96405504 | ||||||
| chr14:96405527
|
C | T | 5 | a0001c0001t0001g0133a0001c0001t0001g0252a0001c0001t0002g0159others(2): Show | 5 | HG02280.hp1 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.403+662C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96405527 | ||||||
| chr14:96406005
|
G | A | 1 | a0008c0015t0002g0244 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.403+1140G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96406005 | ||||||
| chr14:96406057
|
AT | A | 200 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0017others(197): Show | 200 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.403+1206delT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr14 | 96406057 | |||||
| chr14:96406070
|
T | C | 4 | a0001c0001t0001g0158a0001c0001t0002g0171a0001c0001t0005g0265others(1): Show | 4 | HG01109.hp1 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.403+1205T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96406070 | ||||||
| chr14:96406146
|
C | T | 1 | a0002c0002t0001g0016 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.403+1281C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96406146 | ||||||
| chr14:96406221
|
A | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0022others(16): Show | 19 | HG00733.hp2 HG00738.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.403+1356A>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96406221 | ||||||
| chr14:96406440
|
G | A | 2 | a0001c0001t0001g0266a0001c0001t0002g0145 | 2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.403+1575G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96406440 | ||||||
| chr14:96406692
|
C | CT | 9 | a0001c0001t0001g0158a0001c0001t0005g0065a0001c0001t0005g0258others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.403+1837dupT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr14 | 96406692 | |||||
| chr14:96406738
|
T | C | 13 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0099others(10): Show | 13 | HG00099.hp2 HG00642.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.403+1873T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96406738 | ||||||
| chr14:96406962
|
A | G | 8 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0099others(5): Show | 8 | HG00099.hp2 HG00642.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.404-1885A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96406962 | ||||||
| chr14:96407149
|
A | G | 71 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0032others(68): Show | 71 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.404-1698A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96407149 | ||||||
| chr14:96407332
|
A | G | 1 | a0001c0001t0002g0303 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.404-1515A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96407332 | ||||||
| chr14:96407393
|
G | T | 1 | a0001c0001t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.404-1454G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96407393 | ||||||
| chr14:96407571
|
CTTTCT | C | 90 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(87): Show | 90 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.404-1267_404-1263d others(7): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr14 | 96407571 | |||||
| chr14:96407575
|
CTTTTCTT others(4): Show |
C | 1 | a0001c0001t0002g0286 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.404-1267_404-1257d others(13): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr14 | 96407575 | |||||
| chr14:96407579
|
TC | T | 99 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0032others(96): Show | 99 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.404-1267delC | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96407579 | ||||||
| chr14:96407580
|
C | CT | 17 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0294others(14): Show | 17 | HG00733.hp1 HG02630.hp1 HG02717.hp2 others(14): Show |
intron_variant | MODIFIER | c.404-1248dupT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr14 | 96407580 | |||||
| chr14:96407580
|
C | T | 9 | a0001c0001t0001g0131a0001c0001t0001g0215a0001c0001t0001g0247others(6): Show | 9 | HG00735.hp2 HG02602.hp2 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.404-1267C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96407580 | ||||||
| chr14:96407580
|
CT | C | 41 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0091others(38): Show | 41 | HG00280.hp1 HG00621.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.404-1248delT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr14 | 96407580 | |||||
| chr14:96407679
|
A | T | 3 | a0002c0002t0001g0052a0002c0002t0001g0056a0002c0002t0001g0205 | 3 | NA18941.hp2 NA18984.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.404-1168A>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96407679 | ||||||
| chr14:96407753
|
T | C | 3 | a0001c0001t0001g0277a0001c0001t0004g0268a0001c0006t0001g0008 | 3 | HG01167.hp2 HG01169.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.404-1094T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96407753 | ||||||
| chr14:96407771
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG00735.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.404-1076C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96407771 | ||||||
| chr14:96407805
|
T | A | 3 | a0001c0001t0001g0150a0001c0001t0001g0250a0001c0001t0008g0279 | 3 | HG03130.hp1 HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.404-1042T>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96407805 | ||||||
| chr14:96408025
|
T | C | 23 | a0001c0001t0001g0208a0001c0001t0001g0209a0002c0002t0001g0046others(20): Show | 23 | HG00642.hp2 HG01106.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.404-822T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96408025 | ||||||
| chr14:96408094
|
C | T | 7 | a0001c0001t0001g0158a0001c0001t0005g0065a0001c0001t0005g0258others(4): Show | 7 | HG01109.hp1 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.404-753C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96408094 | ||||||
| chr14:96408105
|
A | C | 13 | a0001c0001t0001g0133a0001c0001t0001g0252a0001c0001t0001g0266others(10): Show | 13 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.404-742A>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96408105 | ||||||
| chr14:96408208
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.404-639G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96408208 | ||||||
| chr14:96408209
|
A | G | 4 | a0001c0001t0001g0197a0001c0001t0001g0315a0001c0001t0002g0057others(1): Show | 4 | HG02698.hp2 HG03688.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.404-638A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96408209 | ||||||
| chr14:96408531
|
G | A | 2 | a0002c0002t0002g0169a0002c0002t0005g0063 | 2 | HG02257.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.404-316G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96408531 | ||||||
| chr14:96408621
|
A | C | 60 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0032others(57): Show | 60 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.404-226A>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96408621 | ||||||
| chr14:96408650
|
T | C | 285 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(282): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.404-197T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 3/17 | chr14 | 96408650 | ||||||
| chr14:96408980
|
G | A | 43 | a0001c0001t0001g0072a0001c0001t0001g0084a0001c0001t0001g0105others(40): Show | 43 | HG00323.hp2 HG00544.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.498+39G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96408980 | ||||||
| chr14:96408986
|
A | G | 1 | a0003c0003t0001g0101 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.498+45A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96408986 | ||||||
| chr14:96409195
|
T | C | 1 | a0001c0001t0001g0230 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.498+254T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96409195 | ||||||
| chr14:96409289
|
T | C | 2 | a0002c0002t0002g0169a0002c0002t0005g0063 | 2 | HG02257.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.498+348T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96409289 | ||||||
| chr14:96409433
|
G | A | 285 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(282): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.498+492G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96409433 | ||||||
| chr14:96409591
|
A | G | 2 | a0001c0001t0001g0261a0001c0001t0002g0031 | 2 | HG02165.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.498+650A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96409591 | ||||||
| chr14:96409729
|
G | A | 1 | a0001c0001t0001g0018 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.498+788G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96409729 | ||||||
| chr14:96409792
|
G | A | 1 | a0002c0002t0005g0059 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.498+851G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96409792 | ||||||
| chr14:96409876
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.498+935C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96409876 | ||||||
| chr14:96409922
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.498+981T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96409922 | ||||||
| chr14:96409927
|
A | G | 14 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0034others(11): Show | 14 | HG00099.hp2 HG00733.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.498+986A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96409927 | ||||||
| chr14:96410145
|
G | T | 2 | a0001c0001t0007g0243a0001c0001t0007g0287 | 2 | HG00639.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.498+1204G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96410145 | ||||||
| chr14:96410381
|
A | T | 49 | a0001c0001t0001g0072a0001c0001t0001g0084a0001c0001t0001g0105others(46): Show | 49 | HG00323.hp2 HG00544.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.498+1440A>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96410381 | ||||||
| chr14:96410473
|
A | G | 1 | a0001c0001t0002g0137 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.498+1532A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96410473 | ||||||
| chr14:96410476
|
C | T | 4 | a0001c0001t0005g0065a0001c0001t0005g0258a0001c0001t0010g0260others(1): Show | 4 | HG02486.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.498+1535C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96410476 | ||||||
| chr14:96410511
|
A | G | 1 | a0001c0001t0001g0014 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.498+1570A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96410511 | ||||||
| chr14:96410526
|
C | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0291 | 2 | NA18962.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.498+1585C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96410526 | ||||||
| chr14:96410660
|
G | A | 1 | a0001c0001t0002g0048 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.498+1719G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96410660 | ||||||
| chr14:96410824
|
G | A | 60 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0032others(57): Show | 60 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.498+1883G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96410824 | ||||||
| chr14:96410876
|
C | T | 3 | a0001c0001t0001g0264a0001c0001t0001g0272a0001c0001t0001g0311 | 3 | HG02280.hp2 HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.498+1935C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96410876 | ||||||
| chr14:96410885
|
T | C | 271 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(268): Show | 271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.498+1944T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96410885 | ||||||
| chr14:96411017
|
T | C | 1 | a0002c0002t0001g0039 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.498+2076T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96411017 | ||||||
| chr14:96411285
|
G | A | 2 | a0002c0002t0002g0169a0002c0002t0005g0063 | 2 | HG02257.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.498+2344G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96411285 | ||||||
| chr14:96411443
|
A | C | 34 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0091others(31): Show | 34 | HG00280.hp1 HG00621.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.498+2502A>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96411443 | ||||||
| chr14:96411484
|
C | G | 1 | a0002c0002t0001g0039 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.498+2543C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96411484 | ||||||
| chr14:96411485
|
T | G | 1 | a0002c0002t0001g0039 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.498+2544T>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96411485 | ||||||
| chr14:96411518
|
A | T | 2 | a0002c0002t0001g0012a0002c0016t0002g0013 | 2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.498+2577A>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96411518 | ||||||
| chr14:96411542
|
T | G | 6 | a0001c0001t0001g0304a0001c0001t0001g0313a0001c0001t0002g0163others(3): Show | 6 | HG02630.hp1 HG02717.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.498+2601T>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96411542 | ||||||
| chr14:96411837
|
A | G | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0144 | 3 | HG01070.hp1 HG01071.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.498+2896A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96411837 | ||||||
| chr14:96411995
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.498+3054G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96411995 | ||||||
| chr14:96412045
|
G | A | 1 | a0001c0001t0002g0237 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.498+3104G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96412045 | ||||||
| chr14:96412077
|
G | T | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0144 | 3 | HG01070.hp1 HG01071.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.498+3136G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96412077 | ||||||
| chr14:96412188
|
C | T | 1 | a0007c0012t0002g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.498+3247C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96412188 | ||||||
| chr14:96412193
|
A | G | 49 | a0001c0001t0001g0072a0001c0001t0001g0084a0001c0001t0001g0105others(46): Show | 49 | HG00323.hp2 HG00544.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.498+3252A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96412193 | ||||||
| chr14:96412213
|
C | T | 7 | a0001c0001t0001g0158a0001c0001t0005g0065a0001c0001t0005g0258others(4): Show | 7 | HG01109.hp1 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.498+3272C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96412213 | ||||||
| chr14:96412226
|
CT | C | 12 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0133others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.498+3304delT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96412226 | |||||
| chr14:96412226
|
CTT | C | 178 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.498+3303_498+3304d others(4): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96412226 | |||||
| chr14:96412226
|
CTTT | C | 89 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(86): Show | 89 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.498+3302_498+3304d others(5): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96412226 | |||||
| chr14:96412228
|
T | C | 1 | a0001c0001t0001g0214 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.498+3287T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96412228 | ||||||
| chr14:96412448
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.498+3507G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96412448 | ||||||
| chr14:96412515
|
A | G | 2 | a0001c0001t0001g0029a0001c0001t0001g0055 | 2 | HG03710.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.498+3574A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96412515 | ||||||
| chr14:96412525
|
G | A | 1 | a0001c0001t0001g0232 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.498+3584G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96412525 | ||||||
| chr14:96412527
|
C | T | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0144 | 3 | HG01070.hp1 HG01071.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.498+3586C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96412527 | ||||||
| chr14:96412528
|
G | A | 1 | a0001c0001t0002g0286 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.498+3587G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96412528 | ||||||
| chr14:96412571
|
CT | C | 11 | a0001c0001t0001g0035a0001c0001t0001g0144a0001c0001t0001g0158others(8): Show | 11 | HG01109.hp1 HG01256.hp2 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.498+3644delT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96412571 | |||||
| chr14:96412593
|
T | A | 1 | a0001c0001t0002g0286 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.498+3652T>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96412593 | ||||||
| chr14:96412657
|
C | A | 7 | a0001c0001t0001g0158a0001c0001t0005g0065a0001c0001t0005g0258others(4): Show | 7 | HG01109.hp1 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.498+3716C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96412657 | ||||||
| chr14:96412658
|
C | T | 1 | a0001c0001t0001g0014 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.498+3717C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96412658 | ||||||
| chr14:96412692
|
A | G | 34 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0091others(31): Show | 34 | HG00280.hp1 HG00621.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.498+3751A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96412692 | ||||||
| chr14:96412733
|
T | A | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(85): Show | 88 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.498+3792T>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96412733 | ||||||
| chr14:96412885
|
G | C | 1 | a0002c0002t0001g0167 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.498+3944G>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96412885 | ||||||
| chr14:96413118
|
C | A | 1 | a0001c0001t0001g0214 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.498+4177C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96413118 | ||||||
| chr14:96413229
|
C | A | 1 | a0001c0001t0001g0069 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.498+4288C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96413229 | ||||||
| chr14:96413270
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0022others(1): Show | 4 | NA18945.hp2 NA19000.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.498+4329G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96413270 | ||||||
| chr14:96413368
|
C | A | 1 | a0001c0001t0001g0214 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.498+4427C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96413368 | ||||||
| chr14:96413370
|
A | C | 1 | a0001c0001t0001g0214 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.498+4429A>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96413370 | ||||||
| chr14:96413483
|
G | A | 1 | a0002c0002t0001g0194 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.498+4542G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96413483 | ||||||
| chr14:96413504
|
C | T | 1 | a0001c0001t0002g0276 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.498+4563C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96413504 | ||||||
| chr14:96413640
|
T | C | 2 | a0002c0002t0002g0288a0002c0002t0002g0306 | 2 | HG02145.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.498+4699T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96413640 | ||||||
| chr14:96413839
|
C | G | 80 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(77): Show | 80 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.498+4898C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96413839 | ||||||
| chr14:96413878
|
T | C | 4 | a0001c0001t0001g0097a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG01258.hp1 HG01346.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.498+4937T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96413878 | ||||||
| chr14:96413982
|
C | T | 2 | a0001c0001t0001g0032a0002c0002t0002g0088 | 2 | NA18959.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.498+5041C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96413982 | ||||||
| chr14:96414123
|
C | A | 1 | a0001c0001t0001g0214 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.498+5182C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96414123 | ||||||
| chr14:96414295
|
C | T | 2 | a0001c0001t0001g0134a0001c0001t0001g0136 | 2 | HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.498+5354C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96414295 | ||||||
| chr14:96414362
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG00735.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.498+5421C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96414362 | ||||||
| chr14:96414486
|
C | T | 1 | a0003c0003t0002g0004 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.498+5545C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96414486 | ||||||
| chr14:96414634
|
G | T | 1 | a0002c0002t0011g0254 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.498+5693G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96414634 | ||||||
| chr14:96414635
|
G | T | 1 | a0002c0002t0011g0254 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.498+5694G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96414635 | ||||||
| chr14:96414744
|
A | C | 1 | a0005c0013t0002g0102 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.498+5803A>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96414744 | ||||||
| chr14:96414757
|
C | CT | 84 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(81): Show | 84 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.498+5839dupT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96414757 | |||||
| chr14:96414757
|
C | CTT | 74 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0025others(71): Show | 74 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.498+5838_498+5839d others(4): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96414757 | |||||
| chr14:96414757
|
C | CTTT | 8 | a0001c0001t0001g0060a0001c0001t0001g0125a0001c0001t0001g0247others(5): Show | 8 | HG01346.hp2 HG01891.hp1 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.498+5837_498+5839d others(5): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96414757 | |||||
| chr14:96414757
|
CT | C | 16 | a0001c0001t0001g0133a0001c0001t0001g0252a0001c0001t0001g0266others(13): Show | 16 | HG00642.hp1 HG01169.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.498+5839delT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96414757 | |||||
| chr14:96414757
|
CTT | C | 37 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0091others(34): Show | 37 | HG00280.hp1 HG00621.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.498+5838_498+5839d others(4): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96414757 | |||||
| chr14:96414904
|
C | T | 1 | a0012c0018t0001g0111 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.499-5918C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96414904 | ||||||
| chr14:96414953
|
C | T | 3 | a0006c0010t0001g0049a0006c0010t0002g0085a0006c0021t0003g0314 | 3 | HG00621.hp1 NA18960.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.499-5869C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96414953 | ||||||
| chr14:96415000
|
C | G | 2 | a0002c0002t0001g0152a0002c0002t0001g0308 | 2 | HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.499-5822C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96415000 | ||||||
| chr14:96415111
|
A | G | 1 | a0003c0003t0001g0110 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.499-5711A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96415111 | ||||||
| chr14:96415170
|
A | G | 1 | a0002c0002t0001g0039 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.499-5652A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96415170 | ||||||
| chr14:96415246
|
G | A | 5 | a0001c0001t0001g0061a0001c0001t0001g0098a0001c0001t0001g0104others(2): Show | 5 | NA18953.hp1 NA18979.hp2 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.499-5576G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96415246 | ||||||
| chr14:96415541
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.499-5281C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96415541 | ||||||
| chr14:96415607
|
G | A | 1 | a0003c0003t0001g0101 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.499-5215G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96415607 | ||||||
| chr14:96415669
|
C | T | 2 | a0002c0002t0002g0092a0002c0002t0002g0096 | 2 | NA18950.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.499-5153C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96415669 | ||||||
| chr14:96415744
|
A | AATTAAAT others(18): Show |
9 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0034others(6): Show | 9 | HG00099.hp2 HG00733.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.499-5077_499-5076i others(27): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96415744 | |||||
| chr14:96415744
|
A | AATTAAAT others(96): Show |
5 | a0001c0001t0001g0313a0001c0001t0002g0163a0001c0001t0002g0285others(2): Show | 5 | HG02717.hp2 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.499-5077_499-5076i others(105): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96415744 | |||||
| chr14:96415744
|
A | AATTAAAT others(122): Show |
1 | a0001c0001t0001g0304 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.499-5077_499-5076i others(131): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96415744 | |||||
| chr14:96415748
|
T | TA | 15 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0034others(12): Show | 15 | HG00099.hp2 HG00733.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.499-5072dupA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96415748 | |||||
| chr14:96415748
|
T | TAATCAAT others(19): Show |
1 | a0001c0001t0005g0265 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.499-5071_499-5070i others(28): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96415748 | |||||
| chr14:96415748
|
T | TAATTAAT others(19): Show |
69 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0029others(66): Show | 69 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.499-5024_499-4999d others(28): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96415748 | |||||
| chr14:96415748
|
T | TAATTAAT others(45): Show |
1 | a0001c0001t0001g0177 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.499-5050_499-4999d others(54): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96415748 | |||||
| chr14:96415748
|
TAATTAAT others(19): Show |
T | 4 | a0001c0001t0001g0035a0002c0002t0001g0066a0002c0002t0001g0161others(1): Show | 4 | HG01952.hp2 HG02818.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.499-5024_499-4999d others(28): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96415748 | |||||
| chr14:96415755
|
T | TTTAATAC others(19): Show |
1 | a0001c0001t0001g0230 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.499-5042_499-5041i others(28): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96415755 | |||||
| chr14:96415778
|
T | A | 44 | a0001c0001t0001g0072a0001c0001t0001g0084a0001c0001t0001g0105others(41): Show | 44 | HG00323.hp2 HG00544.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.499-5044T>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96415778 | ||||||
| chr14:96415785
|
A | G | 3 | a0001c0001t0001g0294a0001c0001t0002g0256a0001c0001t0002g0273 | 3 | HG03225.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.499-5037A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96415785 | ||||||
| chr14:96415788
|
C | T | 1 | a0002c0002t0001g0043 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.499-5034C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96415788 | ||||||
| chr14:96415807
|
T | A | 93 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0072others(90): Show | 93 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.499-5015T>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96415807 | ||||||
| chr14:96415918
|
T | C | 1 | a0002c0002t0001g0162 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.499-4904T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96415918 | ||||||
| chr14:96416095
|
G | T | 8 | a0001c0001t0001g0087a0001c0001t0001g0126a0001c0001t0001g0139others(5): Show | 8 | HG01099.hp1 HG01168.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.499-4727G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96416095 | ||||||
| chr14:96416105
|
C | T | 1 | a0001c0001t0002g0137 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.499-4717C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96416105 | ||||||
| chr14:96416275
|
T | C | 13 | a0001c0001t0002g0141a0002c0002t0001g0028a0002c0002t0002g0001others(10): Show | 13 | HG00621.hp2 HG02027.hp1 NA18950.hp2 others(10): Show |
intron_variant | MODIFIER | c.499-4547T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96416275 | ||||||
| chr14:96416385
|
C | CA | 60 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0032others(57): Show | 60 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.499-4424dupA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96416385 | |||||
| chr14:96416473
|
T | C | 1 | a0002c0002t0002g0002 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.499-4349T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96416473 | ||||||
| chr14:96416617
|
C | T | 1 | a0003c0005t0003g0212 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.499-4205C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96416617 | ||||||
| chr14:96416635
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.499-4187A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96416635 | ||||||
| chr14:96416706
|
A | T | 80 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(77): Show | 80 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.499-4116A>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96416706 | ||||||
| chr14:96416720
|
G | A | 1 | a0002c0002t0001g0184 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.499-4102G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96416720 | ||||||
| chr14:96416924
|
T | C | 3 | a0002c0002t0001g0066a0002c0002t0001g0161a0002c0002t0001g0162 | 3 | HG02818.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.499-3898T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96416924 | ||||||
| chr14:96416993
|
C | A | 1 | a0001c0001t0001g0185 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.499-3829C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96416993 | ||||||
| chr14:96417072
|
G | A | 1 | a0001c0001t0002g0159 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.499-3750G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96417072 | ||||||
| chr14:96417233
|
C | T | 1 | a0001c0006t0001g0008 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.499-3589C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96417233 | ||||||
| chr14:96417301
|
A | AT | 285 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(282): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.499-3520dupT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96417301 | |||||
| chr14:96417489
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.499-3333T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96417489 | ||||||
| chr14:96417632
|
C | T | 188 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.499-3190C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96417632 | ||||||
| chr14:96417747
|
T | C | 280 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(277): Show | 280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.499-3075T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96417747 | ||||||
| chr14:96418168
|
A | AT | 94 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(91): Show | 94 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.499-2645dupT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418168 | |||||
| chr14:96418172
|
T | C | 1 | a0005c0008t0003g0074 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.499-2650T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96418172 | ||||||
| chr14:96418273
|
G | A | 13 | a0001c0001t0001g0133a0001c0001t0001g0252a0001c0001t0001g0266others(10): Show | 13 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.499-2549G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96418273 | ||||||
| chr14:96418315
|
C | A | 1 | a0001c0001t0001g0014 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.499-2507C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96418315 | ||||||
| chr14:96418322
|
T | TAAAA | 24 | a0001c0001t0001g0208a0001c0001t0001g0209a0002c0002t0001g0046others(21): Show | 24 | HG00642.hp2 HG01106.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.499-2488_499-2485d others(6): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAA | 14 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0034others(11): Show | 14 | HG00099.hp2 HG00733.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.499-2489_499-2485d others(7): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAAAA others(3): Show |
1 | a0001c0001t0001g0076 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.499-2494_499-2485d others(12): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAAAA others(4): Show |
1 | a0001c0001t0001g0257 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.499-2495_499-2485d others(13): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAAAA others(5): Show |
2 | a0001c0001t0001g0233a0001c0001t0002g0145 | 2 | HG00738.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.499-2496_499-2485d others(14): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAAAA others(6): Show |
2 | a0001c0001t0001g0133a0001c0001t0002g0067 | 2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.499-2497_499-2485d others(15): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAAAA others(7): Show |
1 | a0001c0001t0001g0266 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.499-2498_499-2485d others(16): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAAAA others(8): Show |
3 | a0001c0001t0001g0060a0001c0001t0001g0230a0001c0001t0004g0271 | 3 | HG03041.hp1 NA18966.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.499-2499_499-2485d others(17): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAAAA others(9): Show |
15 | a0001c0001t0001g0062a0001c0001t0001g0122a0001c0001t0001g0124others(12): Show | 15 | HG01243.hp2 HG01258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.499-2485_499-2484i others(18): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAAAA others(10): Show |
28 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0091others(25): Show | 28 | HG00280.hp1 HG00621.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.499-2485_499-2484i others(19): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAAAA others(11): Show |
2 | a0001c0001t0001g0018a0001c0007t0003g0181 | 2 | NA18946.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.499-2485_499-2484i others(20): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAAAA others(12): Show |
14 | a0001c0001t0001g0100a0001c0001t0001g0105a0001c0001t0001g0158others(11): Show | 14 | HG00544.hp2 HG01070.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.499-2485_499-2484i others(21): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAAAA others(13): Show |
19 | a0001c0001t0001g0072a0001c0001t0001g0099a0001c0001t0001g0125others(16): Show | 19 | HG00738.hp1 HG01071.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.499-2485_499-2484i others(22): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAAAA others(14): Show |
12 | a0001c0001t0001g0144a0001c0001t0001g0189a0001c0001t0002g0045others(9): Show | 12 | HG00323.hp2 HG00642.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.499-2485_499-2484i others(23): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAAAA others(15): Show |
11 | a0001c0001t0001g0104a0001c0001t0002g0048a0001c0001t0002g0071others(8): Show | 11 | HG00621.hp2 HG02027.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.499-2485_499-2484i others(24): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAAAA others(16): Show |
3 | a0001c0001t0001g0084a0002c0002t0002g0245a0008c0015t0002g0244 | 3 | HG01069.hp1 HG01261.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.499-2485_499-2484i others(25): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAAAA others(17): Show |
2 | a0001c0001t0001g0069a0001c0001t0002g0256 | 2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.499-2485_499-2484i others(26): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAAAA others(18): Show |
3 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0185 | 3 | NA19000.hp1 NA19007.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.499-2485_499-2484i others(27): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAAAA others(19): Show |
7 | a0001c0001t0001g0022a0001c0001t0001g0126a0001c0001t0001g0239others(4): Show | 7 | HG00639.hp1 HG01516.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.499-2485_499-2484i others(28): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAAAA others(20): Show |
9 | a0001c0001t0001g0087a0001c0001t0001g0131a0001c0001t0001g0132others(6): Show | 9 | HG00735.hp2 HG01168.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.499-2485_499-2484i others(29): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAAAA others(21): Show |
2 | a0001c0001t0001g0292a0001c0001t0002g0040 | 2 | HG01099.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.499-2485_499-2484i others(30): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAAAA others(22): Show |
6 | a0001c0001t0001g0283a0001c0001t0002g0094a0001c0001t0002g0310others(3): Show | 6 | HG01069.hp2 HG01258.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.499-2485_499-2484i others(31): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAAAA others(23): Show |
23 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0055others(20): Show | 23 | HG00733.hp2 HG00741.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.499-2485_499-2484i others(32): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAAAA others(24): Show |
10 | a0001c0001t0001g0035a0001c0001t0001g0078a0001c0001t0001g0089others(7): Show | 10 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(7): Show |
intron_variant | MODIFIER | c.499-2485_499-2484i others(33): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAAAA others(25): Show |
8 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0081others(5): Show | 8 | HG00280.hp2 HG01255.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.499-2485_499-2484i others(34): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAAAA others(26): Show |
11 | a0001c0001t0001g0077a0001c0001t0001g0079a0001c0001t0001g0197others(8): Show | 11 | HG00735.hp1 HG01167.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.499-2485_499-2484i others(35): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAAAA others(27): Show |
2 | a0001c0001t0001g0289a0001c0001t0002g0137 | 2 | HG00099.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.499-2485_499-2484i others(36): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAAAA others(28): Show |
7 | a0001c0001t0001g0108a0001c0001t0001g0252a0001c0001t0001g0277others(4): Show | 7 | HG00639.hp2 HG01169.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.499-2485_499-2484i others(37): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAAAA others(29): Show |
16 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0038others(13): Show | 16 | HG00609.hp1 HG02015.hp1 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.499-2485_499-2484i others(38): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAAAA others(30): Show |
9 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0106others(6): Show | 9 | HG02074.hp2 NA18955.hp1 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.499-2485_499-2484i others(39): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAAAA others(31): Show |
5 | a0001c0001t0001g0032a0001c0001t0001g0098a0001c0001t0001g0103others(2): Show | 5 | HG02155.hp1 NA18948.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.499-2485_499-2484i others(40): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAAAA others(32): Show |
2 | a0001c0001t0001g0109a0001c0001t0001g0112 | 2 | NA18943.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.499-2485_499-2484i others(41): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAAAA others(37): Show |
1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.499-2485_499-2484i others(46): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418322
|
T | TAAAAAAA others(38): Show |
1 | a0001c0001t0001g0176 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.499-2485_499-2484i others(47): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418322 | |||||
| chr14:96418434
|
G | A | 1 | a0002c0002t0001g0225 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.499-2388G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96418434 | ||||||
| chr14:96418468
|
A | AT | 94 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(91): Show | 94 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.499-2350dupT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418468 | |||||
| chr14:96418506
|
C | CTTTTTG | 80 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(77): Show | 80 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.499-2292_499-2287d others(8): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418506 | |||||
| chr14:96418506
|
CTTTTTG | C | 43 | a0001c0001t0001g0072a0001c0001t0001g0084a0001c0001t0001g0105others(40): Show | 43 | HG00323.hp2 HG00544.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.499-2292_499-2287d others(8): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96418506 | |||||
| chr14:96418894
|
T | C | 80 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(77): Show | 80 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.499-1928T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96418894 | ||||||
| chr14:96418950
|
A | G | 1 | a0007c0012t0002g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.499-1872A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96418950 | ||||||
| chr14:96418986
|
A | G | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(85): Show | 88 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.499-1836A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96418986 | ||||||
| chr14:96419122
|
G | A | 188 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.499-1700G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96419122 | ||||||
| chr14:96419419
|
C | T | 14 | a0001c0001t0001g0133a0001c0001t0001g0252a0001c0001t0001g0266others(11): Show | 14 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.499-1403C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96419419 | ||||||
| chr14:96419579
|
A | G | 1 | a0001c0001t0001g0229 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.499-1243A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96419579 | ||||||
| chr14:96419694
|
AC | A | 3 | a0002c0002t0001g0066a0002c0002t0001g0161a0002c0002t0001g0162 | 3 | HG02818.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.499-1126delC | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96419694 | |||||
| chr14:96419741
|
T | C | 35 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0091others(32): Show | 35 | HG00280.hp1 HG00621.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.499-1081T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96419741 | ||||||
| chr14:96419770
|
AT | A | 18 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0032others(15): Show | 18 | HG00099.hp2 HG00733.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.499-1043delT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96419770 | |||||
| chr14:96419784
|
C | CT | 95 | a0001c0001t0001g0015a0001c0001t0001g0032a0001c0001t0001g0036others(92): Show | 95 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.499-1034dupT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96419784 | |||||
| chr14:96419784
|
C | CTT | 18 | a0001c0001t0001g0037a0001c0001t0001g0129a0001c0001t0001g0130others(15): Show | 18 | HG00741.hp2 HG01106.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.499-1035_499-1034d others(4): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96419784 | |||||
| chr14:96419785
|
T | TTTC | 15 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(12): Show | 15 | HG01891.hp2 HG02109.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.499-1035_499-1034i others(5): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96419785 | |||||
| chr14:96419788
|
T | C | 12 | a0001c0001t0001g0105a0001c0001t0001g0186a0001c0001t0001g0201others(9): Show | 12 | HG02027.hp2 HG02074.hp1 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.499-1034T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96419788 | ||||||
| chr14:96419788
|
TC | T | 12 | a0001c0001t0001g0014a0001c0001t0001g0089a0001c0001t0001g0188others(9): Show | 12 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(9): Show |
intron_variant | MODIFIER | c.499-1033delC | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96419788 | ||||||
| chr14:96419789
|
C | T | 267 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0015others(264): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.499-1033C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96419789 | ||||||
| chr14:96419850
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.499-972G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96419850 | ||||||
| chr14:96419852
|
G | A | 3 | a0002c0002t0001g0066a0002c0002t0001g0161a0002c0002t0001g0162 | 3 | HG02818.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.499-970G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96419852 | ||||||
| chr14:96419857
|
C | G | 1 | a0003c0009t0002g0165 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.499-965C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96419857 | ||||||
| chr14:96419969
|
A | G | 2 | a0003c0009t0002g0165a0003c0009t0002g0166 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.499-853A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96419969 | ||||||
| chr14:96419978
|
G | A | 35 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0091others(32): Show | 35 | HG00280.hp1 HG00621.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.499-844G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96419978 | ||||||
| chr14:96420023
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.499-799G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96420023 | ||||||
| chr14:96420096
|
C | T | 1 | a0001c0001t0001g0304 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.499-726C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96420096 | ||||||
| chr14:96420216
|
G | T | 1 | a0001c0001t0002g0159 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.499-606G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96420216 | ||||||
| chr14:96420310
|
A | G | 79 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(76): Show | 79 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.499-512A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96420310 | ||||||
| chr14:96420387
|
T | C | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.499-435T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96420387 | ||||||
| chr14:96420523
|
A | AAAATG | 4 | a0001c0001t0005g0065a0001c0001t0005g0258a0001c0001t0010g0260others(1): Show | 4 | HG02486.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.499-284_499-280dup others(5): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96420523 | |||||
| chr14:96420544
|
T | TAATAA | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.499-257_499-253dup others(5): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr14 | 96420544 | |||||
| chr14:96420598
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.499-224C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96420598 | ||||||
| chr14:96420814
|
T | C | 1 | a0009c0011t0002g0007 | 1 | HG02451.hp2 | splice_region_variant&intron_variant | LOW | c.499-8T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 4/17 | chr14 | 96420814 | ||||||
| chr14:96420945
|
T | G | 4 | a0001c0001t0005g0065a0001c0001t0005g0258a0001c0001t0010g0260others(1): Show | 4 | HG02486.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.609+13T>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96420945 | ||||||
| chr14:96420978
|
A | G | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.609+46A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96420978 | ||||||
| chr14:96421046
|
C | T | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.609+114C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96421046 | ||||||
| chr14:96421140
|
A | G | 2 | a0002c0002t0002g0169a0002c0002t0005g0063 | 2 | HG02257.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.609+208A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96421140 | ||||||
| chr14:96421228
|
C | A | 23 | a0001c0001t0001g0208a0001c0001t0001g0209a0002c0002t0001g0046others(20): Show | 23 | HG00642.hp2 HG01106.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.609+296C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96421228 | ||||||
| chr14:96421282
|
A | G | 4 | a0001c0001t0001g0197a0001c0001t0001g0315a0001c0001t0002g0057others(1): Show | 4 | HG02698.hp2 HG03688.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.609+350A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96421282 | ||||||
| chr14:96421424
|
T | C | 1 | a0001c0001t0001g0005 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.609+492T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96421424 | ||||||
| chr14:96421512
|
C | T | 1 | a0001c0001t0002g0171 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.609+580C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96421512 | ||||||
| chr14:96421513
|
G | A | 1 | a0002c0002t0005g0059 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.609+581G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96421513 | ||||||
| chr14:96421607
|
C | CT | 7 | a0001c0001t0001g0037a0001c0001t0001g0078a0001c0001t0001g0104others(4): Show | 7 | HG02004.hp1 HG03130.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.609+691dupT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr14 | 96421607 | |||||
| chr14:96421669
|
G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0182 | 2 | NA20805.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.609+737G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96421669 | ||||||
| chr14:96421799
|
G | T | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.609+867G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96421799 | ||||||
| chr14:96421856
|
G | T | 284 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(281): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.609+924G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96421856 | ||||||
| chr14:96421978
|
G | A | 22 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(19): Show | 22 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.609+1046G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96421978 | ||||||
| chr14:96421987
|
G | C | 2 | a0001c0001t0002g0093a0001c0001t0002g0094 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.609+1055G>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96421987 | ||||||
| chr14:96422015
|
T | C | 35 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0091others(32): Show | 35 | HG00280.hp1 HG00621.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.609+1083T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96422015 | ||||||
| chr14:96422373
|
G | C | 284 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(281): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.609+1441G>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96422373 | ||||||
| chr14:96422626
|
A | T | 2 | a0003c0009t0002g0165a0003c0009t0002g0166 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.609+1694A>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96422626 | ||||||
| chr14:96422661
|
C | T | 78 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(75): Show | 78 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.609+1729C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96422661 | ||||||
| chr14:96422690
|
TGGCATTG others(9): Show |
T | 2 | a0001c0001t0001g0122a0001c0001t0001g0290 | 2 | HG03704.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.609+1759_609+1774d others(18): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96422690 | ||||||
| chr14:96422718
|
C | A | 1 | a0001c0001t0001g0130 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.609+1786C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96422718 | ||||||
| chr14:96422722
|
T | A | 1 | a0001c0001t0001g0104 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.609+1790T>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96422722 | ||||||
| chr14:96422725
|
G | A | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0144 | 3 | HG01070.hp1 HG01071.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.609+1793G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96422725 | ||||||
| chr14:96422743
|
A | C | 78 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(75): Show | 78 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.609+1811A>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96422743 | ||||||
| chr14:96422784
|
C | T | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(85): Show | 88 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.609+1852C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96422784 | ||||||
| chr14:96423004
|
G | A | 44 | a0001c0001t0001g0072a0001c0001t0001g0084a0001c0001t0001g0105others(41): Show | 44 | HG00323.hp2 HG00544.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.609+2072G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96423004 | ||||||
| chr14:96423278
|
G | A | 2 | a0002c0002t0001g0220a0002c0002t0001g0221 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.609+2346G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96423278 | ||||||
| chr14:96423496
|
CA | C | 19 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0034others(16): Show | 19 | HG00099.hp2 HG00733.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.609+2568delA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr14 | 96423496 | |||||
| chr14:96423557
|
C | A | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.609+2625C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96423557 | ||||||
| chr14:96423563
|
C | T | 78 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(75): Show | 78 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.609+2631C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96423563 | ||||||
| chr14:96423568
|
T | C | 1 | a0001c0001t0002g0171 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.609+2636T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96423568 | ||||||
| chr14:96423622
|
T | C | 4 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0022others(1): Show | 4 | NA18945.hp2 NA19000.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.609+2690T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96423622 | ||||||
| chr14:96423715
|
C | T | 2 | a0002c0002t0002g0288a0002c0002t0002g0306 | 2 | HG02145.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.609+2783C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96423715 | ||||||
| chr14:96424095
|
G | A | 1 | a0001c0001t0002g0276 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.609+3163G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96424095 | ||||||
| chr14:96424160
|
T | C | 267 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(264): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.609+3228T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96424160 | ||||||
| chr14:96424602
|
G | A | 2 | a0002c0002t0001g0046a0002c0002t0001g0047 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.609+3670G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96424602 | ||||||
| chr14:96424717
|
G | A | 1 | a0001c0001t0002g0305 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.609+3785G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96424717 | ||||||
| chr14:96424753
|
T | C | 1 | a0001c0001t0001g0104 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.609+3821T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96424753 | ||||||
| chr14:96424776
|
G | C | 1 | a0001c0001t0001g0104 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.609+3844G>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96424776 | ||||||
| chr14:96424781
|
A | T | 1 | a0001c0001t0001g0104 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.609+3849A>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96424781 | ||||||
| chr14:96424874
|
A | T | 1 | a0001c0001t0001g0104 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.609+3942A>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96424874 | ||||||
| chr14:96424898
|
C | A | 3 | a0001c0001t0001g0014a0002c0002t0001g0012a0002c0016t0002g0013 | 3 | HG03139.hp2 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.609+3966C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96424898 | ||||||
| chr14:96424899
|
A | T | 1 | a0001c0001t0001g0104 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.609+3967A>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96424899 | ||||||
| chr14:96425044
|
T | A | 1 | a0001c0001t0001g0104 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.609+4112T>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96425044 | ||||||
| chr14:96425064
|
A | G | 2 | a0001c0001t0001g0150a0001c0001t0008g0279 | 2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.609+4132A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96425064 | ||||||
| chr14:96425128
|
A | G | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(85): Show | 88 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.609+4196A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96425128 | ||||||
| chr14:96425212
|
C | A | 186 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.609+4280C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96425212 | ||||||
| chr14:96425453
|
G | A | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(85): Show | 88 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.609+4521G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96425453 | ||||||
| chr14:96425480
|
A | AT | 10 | a0001c0001t0001g0108a0001c0001t0001g0264a0001c0001t0001g0272others(7): Show | 10 | HG00639.hp2 HG01169.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.609+4568dupT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr14 | 96425480 | |||||
| chr14:96425480
|
A | ATT | 171 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0032others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.609+4567_609+4568d others(4): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr14 | 96425480 | |||||
| chr14:96425480
|
A | ATTT | 47 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0087others(44): Show | 47 | HG00733.hp1 HG01070.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.609+4566_609+4568d others(5): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr14 | 96425480 | |||||
| chr14:96425480
|
A | ATTTT | 50 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0018others(47): Show | 50 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.609+4565_609+4568d others(6): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr14 | 96425480 | |||||
| chr14:96425480
|
A | ATTTTT | 8 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0081others(5): Show | 8 | HG00738.hp2 HG01952.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.609+4564_609+4568d others(7): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr14 | 96425480 | |||||
| chr14:96425523
|
C | T | 2 | a0001c0001t0001g0177a0001c0001t0002g0305 | 2 | HG02723.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.609+4591C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96425523 | ||||||
| chr14:96425551
|
C | G | 1 | a0001c0001t0001g0104 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.609+4619C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96425551 | ||||||
| chr14:96425588
|
C | T | 35 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0091others(32): Show | 35 | HG00280.hp1 HG00621.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.609+4656C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96425588 | ||||||
| chr14:96425783
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.609+4851C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96425783 | ||||||
| chr14:96425993
|
T | G | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.609+5061T>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96425993 | ||||||
| chr14:96426051
|
G | T | 35 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0091others(32): Show | 35 | HG00280.hp1 HG00621.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.609+5119G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96426051 | ||||||
| chr14:96426125
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.609+5193G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96426125 | ||||||
| chr14:96426398
|
A | AT | 35 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0091others(32): Show | 35 | HG00280.hp1 HG00621.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.609+5474dupT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr14 | 96426398 | |||||
| chr14:96426536
|
A | G | 1 | a0002c0002t0001g0167 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.609+5604A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96426536 | ||||||
| chr14:96426544
|
C | A | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(85): Show | 88 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.609+5612C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96426544 | ||||||
| chr14:96426651
|
T | C | 2 | a0003c0009t0002g0165a0003c0009t0002g0166 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.609+5719T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96426651 | ||||||
| chr14:96426968
|
G | A | 4 | a0001c0001t0001g0197a0001c0001t0001g0315a0001c0001t0002g0057others(1): Show | 4 | HG02698.hp2 HG03688.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.609+6036G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96426968 | ||||||
| chr14:96427056
|
G | C | 4 | a0004c0004t0001g0151a0004c0004t0001g0153a0004c0004t0001g0154others(1): Show | 4 | HG02559.hp2 HG02723.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.609+6124G>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96427056 | ||||||
| chr14:96427063
|
T | A | 1 | a0001c0001t0001g0026 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.609+6131T>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96427063 | ||||||
| chr14:96427096
|
T | G | 1 | a0003c0003t0001g0110 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.609+6164T>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96427096 | ||||||
| chr14:96427167
|
C | T | 1 | a0002c0002t0001g0116 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.609+6235C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96427167 | ||||||
| chr14:96427233
|
G | A | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.609+6301G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96427233 | ||||||
| chr14:96427335
|
C | G | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.609+6403C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96427335 | ||||||
| chr14:96427410
|
G | A | 35 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0091others(32): Show | 35 | HG00280.hp1 HG00621.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.609+6478G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96427410 | ||||||
| chr14:96427503
|
G | A | 1 | a0001c0001t0002g0305 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.609+6571G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96427503 | ||||||
| chr14:96427552
|
C | T | 1 | a0001c0001t0002g0045 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.609+6620C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96427552 | ||||||
| chr14:96427653
|
A | G | 1 | a0001c0001t0001g0204 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.609+6721A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96427653 | ||||||
| chr14:96427680
|
C | T | 1 | a0002c0002t0002g0200 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.609+6748C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96427680 | ||||||
| chr14:96428032
|
T | C | 43 | a0001c0001t0001g0072a0001c0001t0001g0084a0001c0001t0001g0105others(40): Show | 43 | HG00323.hp2 HG00544.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.609+7100T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96428032 | ||||||
| chr14:96428127
|
C | T | 2 | a0001c0001t0002g0159a0001c0001t0006g0235 | 2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.609+7195C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96428127 | ||||||
| chr14:96428221
|
T | C | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.609+7289T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96428221 | ||||||
| chr14:96428227
|
C | T | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.609+7295C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96428227 | ||||||
| chr14:96428232
|
C | T | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.609+7300C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96428232 | ||||||
| chr14:96428233
|
A | G | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.609+7301A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96428233 | ||||||
| chr14:96428234
|
A | T | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.609+7302A>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96428234 | ||||||
| chr14:96428244
|
C | G | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.609+7312C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96428244 | ||||||
| chr14:96428252
|
T | C | 17 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0032others(14): Show | 17 | HG00609.hp1 HG00639.hp2 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.609+7320T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96428252 | ||||||
| chr14:96428533
|
C | T | 1 | a0002c0002t0005g0059 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.609+7601C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96428533 | ||||||
| chr14:96428621
|
A | C | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0144 | 3 | HG01070.hp1 HG01071.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.609+7689A>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96428621 | ||||||
| chr14:96428648
|
T | C | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.609+7716T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96428648 | ||||||
| chr14:96428689
|
T | G | 1 | a0002c0002t0001g0066 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.609+7757T>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96428689 | ||||||
| chr14:96428747
|
T | C | 1 | a0001c0001t0001g0299 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.609+7815T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96428747 | ||||||
| chr14:96428785
|
C | A | 1 | a0001c0001t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.609+7853C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96428785 | ||||||
| chr14:96428789
|
C | G | 1 | a0001c0001t0001g0239 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.609+7857C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96428789 | ||||||
| chr14:96428789
|
C | T | 2 | a0001c0001t0002g0114a0001c0001t0002g0267 | 2 | HG00738.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.609+7857C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96428789 | ||||||
| chr14:96428795
|
C | T | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.609+7863C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96428795 | ||||||
| chr14:96428809
|
T | TGTTTGAT others(32): Show |
2 | a0001c0001t0001g0069a0001c0001t0001g0160 | 2 | HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.609+7879_609+7917d others(41): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr14 | 96428809 | |||||
| chr14:96428893
|
T | C | 4 | a0001c0001t0001g0097a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG01258.hp1 HG01346.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.609+7961T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96428893 | ||||||
| chr14:96429025
|
G | T | 284 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(281): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.609+8093G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96429025 | ||||||
| chr14:96429172
|
T | TC | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.609+8240_609+8241i others(3): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96429172 | ||||||
| chr14:96429442
|
C | A | 89 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(86): Show | 89 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.610-8393C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96429442 | ||||||
| chr14:96429443
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.610-8392G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96429443 | ||||||
| chr14:96429460
|
C | T | 1 | a0005c0008t0003g0274 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.610-8375C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96429460 | ||||||
| chr14:96429834
|
G | A | 1 | a0001c0001t0001g0215 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.610-8001G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96429834 | ||||||
| chr14:96429988
|
T | C | 59 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0032others(56): Show | 59 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.610-7847T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96429988 | ||||||
| chr14:96430183
|
AT | A | 77 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0022others(74): Show | 77 | HG00323.hp2 HG00544.hp2 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.610-7632delT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr14 | 96430183 | |||||
| chr14:96430183
|
ATT | A | 196 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.610-7633_610-7632d others(4): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr14 | 96430183 | |||||
| chr14:96430209
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.610-7626G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96430209 | ||||||
| chr14:96430277
|
C | T | 4 | a0001c0001t0001g0097a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG01258.hp1 HG01346.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.610-7558C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96430277 | ||||||
| chr14:96430426
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.610-7409G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96430426 | ||||||
| chr14:96430586
|
G | A | 2 | a0001c0001t0001g0261a0001c0001t0002g0031 | 2 | HG02165.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.610-7249G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96430586 | ||||||
| chr14:96430611
|
G | T | 1 | a0001c0001t0001g0014 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.610-7224G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96430611 | ||||||
| chr14:96430796
|
T | A | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.610-7039T>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96430796 | ||||||
| chr14:96430820
|
A | G | 4 | a0002c0002t0002g0146a0002c0002t0002g0297a0002c0002t0007g0298others(1): Show | 4 | HG02109.hp1 HG02647.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.610-7015A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96430820 | ||||||
| chr14:96430894
|
G | A | 6 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0144others(3): Show | 6 | HG01070.hp1 HG01071.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.610-6941G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96430894 | ||||||
| chr14:96430923
|
G | A | 1 | a0002c0002t0001g0225 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.610-6912G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96430923 | ||||||
| chr14:96431011
|
T | G | 35 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0091others(32): Show | 35 | HG00280.hp1 HG00621.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.610-6824T>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96431011 | ||||||
| chr14:96431183
|
C | G | 1 | a0001c0001t0001g0252 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.610-6652C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96431183 | ||||||
| chr14:96431293
|
T | C | 1 | a0004c0004t0001g0164 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.610-6542T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96431293 | ||||||
| chr14:96431392
|
T | C | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.610-6443T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96431392 | ||||||
| chr14:96431483
|
G | A | 1 | a0002c0002t0001g0116 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.610-6352G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96431483 | ||||||
| chr14:96431505
|
G | A | 2 | a0004c0004t0001g0170a0004c0004t0002g0147 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.610-6330G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96431505 | ||||||
| chr14:96431560
|
T | C | 2 | a0001c0001t0001g0278a0001c0001t0002g0303 | 2 | HG03834.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.610-6275T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96431560 | ||||||
| chr14:96431562
|
C | T | 1 | a0006c0010t0001g0049 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.610-6273C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96431562 | ||||||
| chr14:96431590
|
G | A | 1 | a0002c0002t0002g0275 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.610-6245G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96431590 | ||||||
| chr14:96431603
|
T | C | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.610-6232T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96431603 | ||||||
| chr14:96431834
|
A | G | 2 | a0004c0004t0006g0148a0004c0004t0006g0168 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.610-6001A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96431834 | ||||||
| chr14:96432202
|
C | CT | 76 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(73): Show | 76 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.610-5613dupT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr14 | 96432202 | |||||
| chr14:96432202
|
C | CTT | 11 | a0001c0001t0001g0055a0001c0001t0001g0064a0001c0001t0001g0087others(8): Show | 11 | HG00280.hp2 HG00735.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.610-5614_610-5613d others(4): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr14 | 96432202 | |||||
| chr14:96432202
|
CT | C | 47 | a0001c0001t0001g0072a0001c0001t0001g0084a0001c0001t0001g0105others(44): Show | 47 | HG00323.hp2 HG00544.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.610-5613delT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr14 | 96432202 | |||||
| chr14:96432202
|
CTT | C | 73 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(70): Show | 73 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.610-5614_610-5613d others(4): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr14 | 96432202 | |||||
| chr14:96432202
|
CTTT | C | 19 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(16): Show | 19 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.610-5615_610-5613d others(5): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr14 | 96432202 | |||||
| chr14:96432266
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.610-5569G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96432266 | ||||||
| chr14:96432640
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.610-5195C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96432640 | ||||||
| chr14:96432645
|
C | T | 1 | a0001c0001t0002g0305 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.610-5190C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96432645 | ||||||
| chr14:96432745
|
G | A | 1 | a0002c0002t0001g0019 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.610-5090G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96432745 | ||||||
| chr14:96432765
|
A | G | 1 | a0001c0001t0001g0017 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.610-5070A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96432765 | ||||||
| chr14:96432766
|
C | G | 1 | a0001c0001t0002g0068 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.610-5069C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96432766 | ||||||
| chr14:96432787
|
A | G | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(85): Show | 88 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.610-5048A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96432787 | ||||||
| chr14:96432828
|
C | CA | 46 | a0001c0001t0001g0014a0001c0001t0001g0037a0001c0001t0001g0091others(43): Show | 46 | HG00280.hp1 HG00423.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.610-4990dupA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr14 | 96432828 | |||||
| chr14:96432828
|
C | CAA | 15 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0062others(12): Show | 15 | HG00099.hp2 HG00733.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.610-4991_610-4990d others(4): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr14 | 96432828 | |||||
| chr14:96432828
|
CA | C | 134 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(131): Show | 134 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.610-4990delA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr14 | 96432828 | |||||
| chr14:96432851
|
G | A | 7 | a0001c0001t0001g0158a0001c0001t0005g0065a0001c0001t0005g0258others(4): Show | 7 | HG01109.hp1 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.610-4984G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96432851 | ||||||
| chr14:96432851
|
G | C | 3 | a0001c0001t0001g0025a0001c0001t0001g0108a0001c0001t0001g0246 | 3 | HG00639.hp2 HG02293.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.610-4984G>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96432851 | ||||||
| chr14:96432950
|
C | T | 1 | a0002c0002t0002g0175 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.610-4885C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96432950 | ||||||
| chr14:96433121
|
T | C | 284 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(281): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.610-4714T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96433121 | ||||||
| chr14:96433304
|
C | T | 2 | a0002c0002t0001g0046a0002c0002t0001g0047 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.610-4531C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96433304 | ||||||
| chr14:96433305
|
G | A | 35 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0091others(32): Show | 35 | HG00280.hp1 HG00621.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.610-4530G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96433305 | ||||||
| chr14:96433530
|
T | A | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(85): Show | 88 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.610-4305T>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96433530 | ||||||
| chr14:96433540
|
T | TCTACACT others(1): Show |
35 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0091others(32): Show | 35 | HG00280.hp1 HG00621.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.610-4294_610-4287d others(10): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr14 | 96433540 | |||||
| chr14:96433709
|
C | T | 78 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(75): Show | 78 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.610-4126C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96433709 | ||||||
| chr14:96433881
|
C | T | 1 | a0001c0001t0002g0137 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.610-3954C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96433881 | ||||||
| chr14:96433918
|
T | C | 1 | a0001c0001t0001g0014 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.610-3917T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96433918 | ||||||
| chr14:96433935
|
C | T | 1 | a0002c0002t0001g0242 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.610-3900C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96433935 | ||||||
| chr14:96434171
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0022others(1): Show | 4 | NA18945.hp2 NA19000.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.610-3664G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96434171 | ||||||
| chr14:96434363
|
G | A | 3 | a0002c0002t0001g0046a0002c0002t0001g0047a0002c0002t0001g0253 | 3 | HG01168.hp1 HG01169.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.610-3472G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96434363 | ||||||
| chr14:96434422
|
G | GTC | 11 | a0001c0001t0001g0069a0001c0001t0001g0084a0001c0001t0001g0160others(8): Show | 11 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.610-3379_610-3378d others(4): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr14 | 96434422 | |||||
| chr14:96434422
|
G | GTCTCTCT others(5): Show |
3 | a0001c0001t0001g0249a0001c0001t0001g0251a0001c0001t0001g0300 | 3 | HG01167.hp1 HG02615.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.610-3389_610-3378d others(14): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr14 | 96434422 | |||||
| chr14:96434422
|
G | GTCTCTCT others(7): Show |
2 | a0001c0001t0001g0301a0002c0002t0001g0167 | 2 | HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.610-3391_610-3378d others(16): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr14 | 96434422 | |||||
| chr14:96434422
|
GTC | G | 41 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0115others(38): Show | 41 | HG00280.hp1 HG00621.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.610-3379_610-3378d others(4): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr14 | 96434422 | |||||
| chr14:96434422
|
GTCTCTC | G | 9 | a0001c0001t0001g0295a0001c0001t0001g0304a0001c0001t0001g0313others(6): Show | 9 | HG00733.hp1 HG02630.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.610-3383_610-3378d others(8): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr14 | 96434422 | |||||
| chr14:96434422
|
GTCTCTCT others(1): Show |
G | 165 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.610-3385_610-3378d others(10): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr14 | 96434422 | |||||
| chr14:96434422
|
GTCTCTCT others(5): Show |
G | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.610-3389_610-3378d others(14): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr14 | 96434422 | |||||
| chr14:96434422
|
GTCTCTCT others(9): Show |
G | 1 | a0001c0001t0001g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.610-3393_610-3378d others(18): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr14 | 96434422 | |||||
| chr14:96434426
|
C | G | 13 | a0001c0001t0001g0105a0001c0001t0001g0186a0001c0001t0001g0201others(10): Show | 13 | HG02027.hp2 HG02074.hp1 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.610-3409C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96434426 | ||||||
| chr14:96434609
|
AC | A | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.610-3225delC | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96434609 | ||||||
| chr14:96434767
|
G | A | 3 | a0001c0001t0001g0294a0001c0001t0002g0256a0001c0001t0002g0273 | 3 | HG03225.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.610-3068G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96434767 | ||||||
| chr14:96434775
|
G | A | 5 | a0001c0001t0001g0097a0001c0001t0001g0281a0001c0001t0001g0282others(2): Show | 5 | HG01258.hp1 HG01346.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.610-3060G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96434775 | ||||||
| chr14:96434859
|
T | C | 194 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.610-2976T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96434859 | ||||||
| chr14:96435076
|
C | G | 4 | a0001c0001t0001g0197a0001c0001t0001g0315a0001c0001t0002g0057others(1): Show | 4 | HG02698.hp2 HG03688.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.610-2759C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96435076 | ||||||
| chr14:96435261
|
G | C | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.610-2574G>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96435261 | ||||||
| chr14:96435353
|
G | A | 59 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0032others(56): Show | 59 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.610-2482G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96435353 | ||||||
| chr14:96435479
|
C | T | 79 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(76): Show | 79 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.610-2356C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96435479 | ||||||
| chr14:96435672
|
G | A | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.610-2163G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96435672 | ||||||
| chr14:96435680
|
C | T | 1 | a0002c0002t0001g0073 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.610-2155C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96435680 | ||||||
| chr14:96435893
|
TGGTGAG | T | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0144 | 3 | HG01070.hp1 HG01071.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.610-1937_610-1932d others(8): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr14 | 96435893 | |||||
| chr14:96436089
|
T | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0291 | 2 | NA18962.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.610-1746T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96436089 | ||||||
| chr14:96436141
|
C | T | 6 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0144others(3): Show | 6 | HG01070.hp1 HG01071.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.610-1694C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96436141 | ||||||
| chr14:96436142
|
T | G | 6 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0144others(3): Show | 6 | HG01070.hp1 HG01071.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.610-1693T>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96436142 | ||||||
| chr14:96436258
|
A | G | 1 | a0001c0001t0001g0032 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.610-1577A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96436258 | ||||||
| chr14:96436357
|
C | G | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.610-1478C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96436357 | ||||||
| chr14:96436421
|
A | G | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.610-1414A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96436421 | ||||||
| chr14:96436584
|
G | A | 1 | a0001c0001t0001g0201 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.610-1251G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96436584 | ||||||
| chr14:96436715
|
T | C | 292 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(289): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.610-1120T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96436715 | ||||||
| chr14:96436908
|
T | C | 1 | a0013c0017t0001g0316 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.610-927T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96436908 | ||||||
| chr14:96437075
|
TG | T | 35 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0091others(32): Show | 35 | HG00280.hp1 HG00621.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.610-754delG | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr14 | 96437075 | |||||
| chr14:96437326
|
A | C | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0144 | 3 | HG01070.hp1 HG01071.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.610-509A>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96437326 | ||||||
| chr14:96437377
|
G | A | 194 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.610-458G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96437377 | ||||||
| chr14:96437483
|
G | A | 1 | a0001c0001t0002g0045 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.610-352G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96437483 | ||||||
| chr14:96437671
|
G | A | 59 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0032others(56): Show | 59 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.610-164G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 5/17 | chr14 | 96437671 | ||||||
| chr14:96437951
|
G | C | 1 | a0001c0001t0001g0121 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.690+36G>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96437951 | ||||||
| chr14:96437959
|
C | A | 1 | a0001c0001t0002g0310 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.690+44C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96437959 | ||||||
| chr14:96438098
|
C | A | 24 | a0001c0001t0001g0069a0001c0001t0001g0133a0001c0001t0001g0150others(21): Show | 24 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.690+183C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96438098 | ||||||
| chr14:96438209
|
T | C | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.690+294T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96438209 | ||||||
| chr14:96438230
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.690+315G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96438230 | ||||||
| chr14:96438430
|
A | T | 1 | a0001c0001t0001g0084 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.690+515A>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96438430 | ||||||
| chr14:96438464
|
G | T | 1 | a0003c0005t0003g0120 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.690+549G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96438464 | ||||||
| chr14:96438661
|
T | C | 2 | a0001c0001t0007g0243a0001c0001t0007g0287 | 2 | HG00639.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.690+746T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96438661 | ||||||
| chr14:96438820
|
G | A | 1 | a0001c0001t0008g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.690+905G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96438820 | ||||||
| chr14:96438828
|
T | C | 1 | a0001c0001t0001g0296 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.690+913T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96438828 | ||||||
| chr14:96438879
|
C | T | 24 | a0001c0001t0001g0069a0001c0001t0001g0133a0001c0001t0001g0150others(21): Show | 24 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.690+964C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96438879 | ||||||
| chr14:96439007
|
A | G | 290 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.690+1092A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96439007 | ||||||
| chr14:96439122
|
T | C | 8 | a0001c0001t0001g0026a0001c0001t0001g0035a0001c0001t0001g0077others(5): Show | 8 | HG00735.hp1 HG01070.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.690+1207T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96439122 | ||||||
| chr14:96439328
|
G | A | 2 | a0001c0001t0002g0114a0001c0001t0002g0267 | 2 | HG00738.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.690+1413G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96439328 | ||||||
| chr14:96439478
|
CA | C | 15 | a0001c0001t0001g0134a0001c0001t0001g0136a0001c0001t0001g0158others(12): Show | 15 | HG01109.hp1 HG01167.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.690+1564delA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96439478 | ||||||
| chr14:96439506
|
T | C | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(85): Show | 88 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.690+1591T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96439506 | ||||||
| chr14:96439525
|
A | G | 43 | a0001c0001t0001g0072a0001c0001t0001g0084a0001c0001t0001g0105others(40): Show | 43 | HG00323.hp2 HG00544.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.690+1610A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96439525 | ||||||
| chr14:96439663
|
CA | C | 223 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(220): Show | 223 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.690+1766delA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr14 | 96439663 | |||||
| chr14:96439663
|
CAA | C | 62 | a0001c0001t0001g0015a0001c0001t0001g0032a0001c0001t0001g0041others(59): Show | 62 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.690+1765_690+1766d others(4): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr14 | 96439663 | |||||
| chr14:96439851
|
A | G | 1 | a0001c0001t0001g0218 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.690+1936A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96439851 | ||||||
| chr14:96439904
|
G | A | 1 | a0002c0002t0001g0073 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.690+1989G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96439904 | ||||||
| chr14:96440080
|
G | A | 292 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(289): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.690+2165G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96440080 | ||||||
| chr14:96440205
|
A | T | 3 | a0002c0002t0001g0066a0002c0002t0001g0161a0002c0002t0001g0162 | 3 | HG02818.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.690+2290A>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96440205 | ||||||
| chr14:96440217
|
G | A | 16 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0197others(13): Show | 16 | HG00099.hp2 HG00733.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.690+2302G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96440217 | ||||||
| chr14:96440220
|
C | T | 1 | a0002c0002t0002g0149 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.690+2305C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96440220 | ||||||
| chr14:96440260
|
A | G | 3 | a0002c0002t0001g0066a0002c0002t0001g0161a0002c0002t0001g0162 | 3 | HG02818.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.690+2345A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96440260 | ||||||
| chr14:96440403
|
G | T | 79 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(76): Show | 79 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.691-2327G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96440403 | ||||||
| chr14:96440725
|
A | G | 2 | a0001c0001t0001g0189a0001c0001t0002g0222 | 2 | HG00323.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.691-2005A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96440725 | ||||||
| chr14:96440867
|
A | T | 24 | a0001c0001t0001g0069a0001c0001t0001g0133a0001c0001t0001g0150others(21): Show | 24 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.691-1863A>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96440867 | ||||||
| chr14:96440921
|
C | T | 100 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0072others(97): Show | 100 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.691-1809C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96440921 | ||||||
| chr14:96441183
|
G | A | 1 | a0002c0002t0002g0001 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.691-1547G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96441183 | ||||||
| chr14:96441213
|
T | C | 4 | a0001c0001t0001g0197a0001c0001t0001g0315a0001c0001t0002g0057others(1): Show | 4 | HG02698.hp2 HG03688.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.691-1517T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96441213 | ||||||
| chr14:96441235
|
T | C | 3 | a0001c0001t0001g0133a0001c0001t0001g0266a0001c0001t0002g0145 | 3 | HG02109.hp2 HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.691-1495T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96441235 | ||||||
| chr14:96441531
|
C | T | 8 | a0001c0001t0001g0158a0001c0001t0001g0270a0001c0001t0005g0065others(5): Show | 8 | HG01109.hp1 HG02055.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.691-1199C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96441531 | ||||||
| chr14:96441571
|
A | G | 8 | a0001c0001t0001g0158a0001c0001t0001g0270a0001c0001t0005g0065others(5): Show | 8 | HG01109.hp1 HG02055.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.691-1159A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96441571 | ||||||
| chr14:96441642
|
C | CA | 255 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(252): Show | 255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.691-1068dupA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr14 | 96441642 | |||||
| chr14:96441642
|
C | CAA | 9 | a0001c0001t0001g0029a0001c0001t0001g0160a0001c0001t0001g0208others(6): Show | 9 | HG02135.hp2 HG02738.hp1 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.691-1069_691-1068d others(4): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr14 | 96441642 | |||||
| chr14:96441664
|
A | T | 59 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0032others(56): Show | 59 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.691-1066A>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96441664 | ||||||
| chr14:96441971
|
G | T | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(85): Show | 88 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.691-759G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96441971 | ||||||
| chr14:96442133
|
T | C | 19 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0034others(16): Show | 19 | HG00099.hp2 HG00733.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.691-597T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96442133 | ||||||
| chr14:96442188
|
C | T | 2 | a0002c0002t0002g0169a0002c0002t0005g0063 | 2 | HG02257.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.691-542C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96442188 | ||||||
| chr14:96442280
|
C | T | 59 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0032others(56): Show | 59 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.691-450C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96442280 | ||||||
| chr14:96442553
|
C | T | 1 | a0001c0006t0001g0008 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.691-177C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96442553 | ||||||
| chr14:96442688
|
A | G | 59 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0032others(56): Show | 59 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.691-42A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 6/17 | chr14 | 96442688 | ||||||
| chr14:96443055
|
A | G | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.779+237A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | chr14 | 96443055 | ||||||
| chr14:96443062
|
A | G | 24 | a0001c0001t0001g0069a0001c0001t0001g0133a0001c0001t0001g0150others(21): Show | 24 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.779+244A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | chr14 | 96443062 | ||||||
| chr14:96443622
|
T | G | 2 | a0002c0002t0002g0169a0002c0002t0005g0063 | 2 | HG02257.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.779+804T>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | chr14 | 96443622 | ||||||
| chr14:96443692
|
T | G | 1 | a0002c0002t0002g0092 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.779+874T>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | chr14 | 96443692 | ||||||
| chr14:96443717
|
T | A | 24 | a0001c0001t0001g0069a0001c0001t0001g0133a0001c0001t0001g0150others(21): Show | 24 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.779+899T>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | chr14 | 96443717 | ||||||
| chr14:96443736
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.779+918C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | chr14 | 96443736 | ||||||
| chr14:96443780
|
A | ATTTTTT | 91 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(88): Show | 91 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.779+968_779+973dup others(6): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr14 | 96443780 | |||||
| chr14:96443780
|
A | ATTTTTTT | 192 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.779+967_779+973dup others(7): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr14 | 96443780 | |||||
| chr14:96443780
|
A | ATTTTTTT others(1): Show |
6 | a0001c0001t0001g0186a0002c0002t0001g0202a0002c0002t0001g0205others(3): Show | 6 | HG00642.hp1 HG02135.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.779+966_779+973dup others(8): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr14 | 96443780 | |||||
| chr14:96443877
|
C | A | 2 | a0002c0002t0001g0053a0002c0002t0001g0054 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.779+1059C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | chr14 | 96443877 | ||||||
| chr14:96443896
|
C | T | 11 | a0004c0004t0001g0070a0004c0004t0001g0151a0004c0004t0001g0153others(8): Show | 11 | HG00642.hp2 HG01255.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.779+1078C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | chr14 | 96443896 | ||||||
| chr14:96443924
|
C | G | 2 | a0002c0002t0002g0169a0002c0002t0005g0063 | 2 | HG02257.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.779+1106C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | chr14 | 96443924 | ||||||
| chr14:96444055
|
G | A | 10 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0098others(7): Show | 10 | HG02155.hp1 NA18943.hp2 NA18953.hp1 others(7): Show |
intron_variant | MODIFIER | c.779+1237G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | chr14 | 96444055 | ||||||
| chr14:96444068
|
C | T | 2 | a0001c0001t0002g0228a0001c0001t0002g0248 | 2 | HG02735.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.779+1250C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | chr14 | 96444068 | ||||||
| chr14:96444273
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.779+1455G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | chr14 | 96444273 | ||||||
| chr14:96444567
|
G | T | 1 | a0007c0012t0002g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.779+1749G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | chr14 | 96444567 | ||||||
| chr14:96444626
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.779+1808A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | chr14 | 96444626 | ||||||
| chr14:96444759
|
C | G | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.780-1758C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | chr14 | 96444759 | ||||||
| chr14:96444903
|
A | C | 6 | a0001c0001t0001g0304a0001c0001t0001g0313a0001c0001t0002g0163others(3): Show | 6 | HG02630.hp1 HG02717.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.780-1614A>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | chr14 | 96444903 | ||||||
| chr14:96444952
|
A | G | 5 | a0001c0001t0001g0264a0001c0001t0001g0272a0001c0001t0001g0309others(2): Show | 5 | HG01106.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.780-1565A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | chr14 | 96444952 | ||||||
| chr14:96445009
|
C | T | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(85): Show | 88 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.780-1508C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | chr14 | 96445009 | ||||||
| chr14:96445094
|
T | C | 2 | a0003c0009t0002g0165a0003c0009t0002g0166 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.780-1423T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | chr14 | 96445094 | ||||||
| chr14:96445336
|
A | G | 1 | a0003c0003t0002g0234 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.780-1181A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | chr14 | 96445336 | ||||||
| chr14:96445368
|
G | A | 189 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0015others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.780-1149G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | chr14 | 96445368 | ||||||
| chr14:96445439
|
C | T | 1 | a0001c0001t0002g0203 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.780-1078C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | chr14 | 96445439 | ||||||
| chr14:96445514
|
G | T | 1 | a0001c0001t0001g0115 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.780-1003G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | chr14 | 96445514 | ||||||
| chr14:96445590
|
T | G | 290 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.780-927T>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | chr14 | 96445590 | ||||||
| chr14:96445730
|
C | T | 1 | a0001c0007t0003g0044 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.780-787C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | chr14 | 96445730 | ||||||
| chr14:96446049
|
G | A | 3 | a0001c0001t0001g0133a0001c0001t0001g0266a0001c0001t0002g0145 | 3 | HG02109.hp2 HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.780-468G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | chr14 | 96446049 | ||||||
| chr14:96446086
|
T | C | 2 | a0002c0002t0001g0152a0002c0002t0001g0308 | 2 | HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.780-431T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | chr14 | 96446086 | ||||||
| chr14:96446168
|
G | GGGTCCTG others(9): Show |
18 | a0001c0001t0001g0208a0001c0001t0001g0209a0002c0002t0001g0152others(15): Show | 18 | HG00642.hp2 HG01255.hp1 HG02135.hp2 others(15): Show |
intron_variant | MODIFIER | c.780-333_780-318dup others(16): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr14 | 96446168 | |||||
| chr14:96446219
|
CAG | C | 4 | a0001c0001t0001g0197a0001c0001t0001g0315a0001c0001t0002g0057others(1): Show | 4 | HG02698.hp2 HG03688.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.780-297_780-296del others(2): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | chr14 | 96446219 | ||||||
| chr14:96446229
|
T | C | 4 | a0001c0001t0001g0069a0001c0001t0001g0160a0001c0001t0007g0243others(1): Show | 4 | HG00639.hp1 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.780-288T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | chr14 | 96446229 | ||||||
| chr14:96446344
|
T | G | 1 | a0001c0001t0001g0021 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.780-173T>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | chr14 | 96446344 | ||||||
| chr14:96446382
|
G | C | 19 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0034others(16): Show | 19 | HG00099.hp2 HG00733.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.780-135G>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | chr14 | 96446382 | ||||||
| chr14:96446463
|
C | T | 1 | a0001c0001t0002g0137 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.780-54C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 7/17 | chr14 | 96446463 | ||||||
| chr14:96446809
|
G | A | 3 | a0002c0002t0001g0066a0002c0002t0001g0161a0002c0002t0001g0162 | 3 | HG02818.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.870+202G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96446809 | ||||||
| chr14:96446947
|
T | TA | 19 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0034others(16): Show | 19 | HG00099.hp2 HG00733.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.870+346dupA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr14 | 96446947 | |||||
| chr14:96446955
|
A | T | 290 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.870+348A>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96446955 | ||||||
| chr14:96447038
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.870+431C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96447038 | ||||||
| chr14:96447046
|
C | G | 8 | a0001c0001t0001g0134a0001c0001t0001g0136a0001c0001t0001g0249others(5): Show | 8 | HG01167.hp1 HG02615.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.870+439C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96447046 | ||||||
| chr14:96447081
|
G | A | 290 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.870+474G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96447081 | ||||||
| chr14:96447100
|
C | A | 35 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0091others(32): Show | 35 | HG00280.hp1 HG00621.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.870+493C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96447100 | ||||||
| chr14:96447222
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.870+615C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96447222 | ||||||
| chr14:96447225
|
A | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0034 | 2 | HG00099.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.870+618A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96447225 | ||||||
| chr14:96447252
|
T | C | 3 | a0002c0002t0001g0066a0002c0002t0001g0161a0002c0002t0001g0162 | 3 | HG02818.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.870+645T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96447252 | ||||||
| chr14:96447366
|
G | T | 9 | a0001c0001t0001g0014a0001c0001t0001g0087a0001c0001t0001g0126others(6): Show | 9 | HG01099.hp1 HG01168.hp2 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.870+759G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96447366 | ||||||
| chr14:96447476
|
G | A | 61 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0032others(58): Show | 61 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.870+869G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96447476 | ||||||
| chr14:96447704
|
A | C | 25 | a0001c0001t0001g0069a0001c0001t0001g0133a0001c0001t0001g0150others(22): Show | 25 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.870+1097A>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96447704 | ||||||
| chr14:96447722
|
TC | T | 37 | a0001c0001t0001g0072a0001c0001t0001g0084a0001c0001t0001g0105others(34): Show | 37 | HG00323.hp2 HG00544.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.870+1116delC | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96447722 | ||||||
| chr14:96447863
|
C | T | 1 | a0001c0001t0008g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.870+1256C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96447863 | ||||||
| chr14:96447973
|
A | G | 1 | a0003c0003t0001g0226 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.870+1366A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96447973 | ||||||
| chr14:96447990
|
G | T | 3 | a0002c0002t0001g0066a0002c0002t0001g0161a0002c0002t0001g0162 | 3 | HG02818.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.870+1383G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96447990 | ||||||
| chr14:96448126
|
CA | C | 6 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0002g0171others(3): Show | 6 | HG01099.hp2 HG02257.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.870+1535delA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr14 | 96448126 | |||||
| chr14:96448292
|
A | C | 292 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(289): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.871-1510A>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96448292 | ||||||
| chr14:96448334
|
C | A | 1 | a0001c0001t0004g0198 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.871-1468C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96448334 | ||||||
| chr14:96448489
|
G | C | 7 | a0001c0001t0001g0158a0001c0001t0005g0065a0001c0001t0005g0258others(4): Show | 7 | HG01109.hp1 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.871-1313G>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96448489 | ||||||
| chr14:96448499
|
G | A | 1 | a0002c0002t0001g0128 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.871-1303G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96448499 | ||||||
| chr14:96448579
|
A | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0269 | 2 | HG00609.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.871-1223A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96448579 | ||||||
| chr14:96448612
|
A | C | 7 | a0001c0001t0001g0158a0001c0001t0005g0065a0001c0001t0005g0258others(4): Show | 7 | HG01109.hp1 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.871-1190A>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96448612 | ||||||
| chr14:96448630
|
T | TA | 61 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0001t0001g0025others(58): Show | 61 | HG00423.hp2 HG00558.hp2 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.871-1138dupA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr14 | 96448630 | |||||
| chr14:96448630
|
T | TAA | 18 | a0001c0001t0001g0005a0001c0001t0001g0036a0001c0001t0001g0041others(15): Show | 18 | HG00423.hp1 HG00544.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.871-1139_871-1138d others(4): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr14 | 96448630 | |||||
| chr14:96448630
|
TA | T | 7 | a0001c0001t0001g0127a0001c0001t0001g0281a0001c0001t0001g0292others(4): Show | 7 | HG00323.hp1 HG01099.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.871-1138delA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr14 | 96448630 | |||||
| chr14:96448630
|
TAAAAA | T | 11 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0034others(8): Show | 11 | HG00099.hp2 HG02630.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.871-1142_871-1138d others(7): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr14 | 96448630 | |||||
| chr14:96448630
|
TAAAAAAA others(5): Show |
T | 2 | a0003c0009t0002g0165a0003c0009t0002g0166 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.871-1149_871-1138d others(14): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr14 | 96448630 | |||||
| chr14:96448630
|
TAAAAAAA others(7): Show |
T | 4 | a0001c0001t0001g0186a0001c0001t0002g0031a0001c0001t0002g0171others(1): Show | 4 | HG03098.hp1 NA19000.hp2 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.871-1151_871-1138d others(16): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr14 | 96448630 | |||||
| chr14:96448630
|
TAAAAAAA others(8): Show |
T | 116 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0069others(113): Show | 116 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.871-1152_871-1138d others(17): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr14 | 96448630 | |||||
| chr14:96448630
|
TAAAAAAA others(9): Show |
T | 1 | a0001c0001t0001g0300 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.871-1153_871-1138d others(18): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr14 | 96448630 | |||||
| chr14:96448892
|
G | A | 44 | a0001c0001t0001g0072a0001c0001t0001g0084a0001c0001t0001g0105others(41): Show | 44 | HG00323.hp2 HG00544.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.871-910G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96448892 | ||||||
| chr14:96448968
|
AC | A | 42 | a0001c0001t0001g0072a0001c0001t0001g0084a0001c0001t0001g0105others(39): Show | 42 | HG00323.hp2 HG00544.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.871-833delC | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96448968 | ||||||
| chr14:96448984
|
GA | G | 100 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0072others(97): Show | 100 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.871-808delA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr14 | 96448984 | |||||
| chr14:96449125
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.871-677A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96449125 | ||||||
| chr14:96449324
|
C | G | 1 | a0003c0003t0001g0226 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.871-478C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96449324 | ||||||
| chr14:96449378
|
T | G | 2 | a0002c0002t0002g0169a0002c0002t0005g0063 | 2 | HG02257.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.871-424T>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96449378 | ||||||
| chr14:96449380
|
C | T | 1 | a0001c0001t0001g0239 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.871-422C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96449380 | ||||||
| chr14:96449386
|
A | T | 1 | a0001c0006t0002g0011 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.871-416A>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96449386 | ||||||
| chr14:96449419
|
G | GATGT | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.871-383_871-382ins others(4): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96449419 | ||||||
| chr14:96449420
|
G | GTGTT | 47 | a0001c0001t0001g0072a0001c0001t0001g0084a0001c0001t0001g0105others(44): Show | 47 | HG00323.hp2 HG00544.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.871-359_871-356dup others(4): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr14 | 96449420 | |||||
| chr14:96449420
|
G | T | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.871-382G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96449420 | ||||||
| chr14:96449543
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.871-259C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96449543 | ||||||
| chr14:96449668
|
G | A | 24 | a0001c0001t0001g0069a0001c0001t0001g0133a0001c0001t0001g0150others(21): Show | 24 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.871-134G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96449668 | ||||||
| chr14:96449785
|
C | T | 3 | a0002c0002t0001g0066a0002c0002t0001g0161a0002c0002t0001g0162 | 3 | HG02818.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.871-17C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 8/17 | chr14 | 96449785 | ||||||
| chr14:96449891
|
C | T | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(85): Show | 88 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.948+12C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 9/17 | chr14 | 96449891 | ||||||
| chr14:96449895
|
G | GT | 282 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(279): Show | 282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.948+29dupT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr14 | 96449895 | |||||
| chr14:96449895
|
G | GTT | 6 | a0001c0001t0001g0133a0001c0001t0001g0266a0001c0001t0002g0145others(3): Show | 6 | HG01978.hp2 HG02109.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.948+28_948+29dupTT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr14 | 96449895 | |||||
| chr14:96450138
|
C | T | 47 | a0001c0001t0001g0072a0001c0001t0001g0084a0001c0001t0001g0099others(44): Show | 47 | HG00323.hp2 HG00544.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.948+259C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 9/17 | chr14 | 96450138 | ||||||
| chr14:96450139
|
G | A | 42 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0026others(39): Show | 42 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.948+260G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 9/17 | chr14 | 96450139 | ||||||
| chr14:96450233
|
C | A | 292 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(289): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.948+354C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 9/17 | chr14 | 96450233 | ||||||
| chr14:96450431
|
TA | T | 83 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0025others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.948+566delA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr14 | 96450431 | |||||
| chr14:96450550
|
G | A | 2 | a0003c0009t0002g0165a0003c0009t0002g0166 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.948+671G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 9/17 | chr14 | 96450550 | ||||||
| chr14:96450569
|
C | CA | 24 | a0001c0001t0001g0069a0001c0001t0001g0133a0001c0001t0001g0150others(21): Show | 24 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.948+703dupA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr14 | 96450569 | |||||
| chr14:96450569
|
CA | C | 67 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0032others(64): Show | 67 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.948+703delA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr14 | 96450569 | |||||
| chr14:96450569
|
CAA | C | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(85): Show | 88 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.948+702_948+703del others(2): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr14 | 96450569 | |||||
| chr14:96450572
|
A | C | 43 | a0001c0001t0001g0072a0001c0001t0001g0084a0001c0001t0001g0105others(40): Show | 43 | HG00323.hp2 HG00544.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.948+693A>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 9/17 | chr14 | 96450572 | ||||||
| chr14:96450575
|
A | C | 1 | a0001c0001t0001g0186 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.948+696A>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 9/17 | chr14 | 96450575 | ||||||
| chr14:96450768
|
C | CT | 36 | a0001c0001t0001g0014a0001c0001t0001g0037a0001c0001t0001g0064others(33): Show | 36 | HG00639.hp2 HG01099.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.949-629dupT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr14 | 96450768 | |||||
| chr14:96450768
|
CT | C | 27 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0069others(24): Show | 27 | HG00099.hp2 HG00639.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.949-629delT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr14 | 96450768 | |||||
| chr14:96450768
|
CTTTTTTT others(7): Show |
C | 2 | a0003c0009t0002g0165a0003c0009t0002g0166 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.949-642_949-629del others(14): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr14 | 96450768 | |||||
| chr14:96450797
|
C | T | 1 | a0001c0001t0005g0065 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.949-624C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 9/17 | chr14 | 96450797 | ||||||
| chr14:96450806
|
A | G | 9 | a0001c0001t0001g0014a0001c0001t0001g0134a0001c0001t0001g0136others(6): Show | 9 | HG01167.hp1 HG02615.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.949-615A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 9/17 | chr14 | 96450806 | ||||||
| chr14:96450837
|
C | T | 26 | a0001c0001t0001g0069a0001c0001t0001g0133a0001c0001t0001g0150others(23): Show | 26 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.949-584C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 9/17 | chr14 | 96450837 | ||||||
| chr14:96450876
|
G | A | 1 | a0002c0002t0002g0169 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.949-545G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 9/17 | chr14 | 96450876 | ||||||
| chr14:96450923
|
T | C | 24 | a0001c0001t0001g0069a0001c0001t0001g0133a0001c0001t0001g0150others(21): Show | 24 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.949-498T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 9/17 | chr14 | 96450923 | ||||||
| chr14:96450932
|
G | A | 1 | a0001c0001t0001g0313 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.949-489G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 9/17 | chr14 | 96450932 | ||||||
| chr14:96451021
|
G | A | 1 | a0001c0001t0002g0286 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.949-400G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 9/17 | chr14 | 96451021 | ||||||
| chr14:96451039
|
GC | G | 24 | a0001c0001t0001g0069a0001c0001t0001g0133a0001c0001t0001g0150others(21): Show | 24 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.949-381delC | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 9/17 | chr14 | 96451039 | ||||||
| chr14:96451169
|
A | T | 1 | a0001c0001t0001g0195 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.949-252A>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 9/17 | chr14 | 96451169 | ||||||
| chr14:96451309
|
C | T | 1 | a0001c0001t0002g0171 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.949-112C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 9/17 | chr14 | 96451309 | ||||||
| chr14:96451327
|
T | G | 1 | a0001c0001t0001g0250 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.949-94T>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 9/17 | chr14 | 96451327 | ||||||
| chr14:96451878
|
C | T | 290 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1098+308C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96451878 | ||||||
| chr14:96451960
|
T | G | 1 | a0001c0001t0001g0296 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1098+390T>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96451960 | ||||||
| chr14:96451967
|
C | T | 59 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0032others(56): Show | 59 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.1098+397C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96451967 | ||||||
| chr14:96452022
|
C | G | 59 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0032others(56): Show | 59 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.1098+452C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96452022 | ||||||
| chr14:96452096
|
G | T | 2 | a0001c0001t0002g0159a0001c0001t0006g0235 | 2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1098+526G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96452096 | ||||||
| chr14:96452266
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1098+696G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96452266 | ||||||
| chr14:96452267
|
G | T | 2 | a0003c0009t0002g0165a0003c0009t0002g0166 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1098+697G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96452267 | ||||||
| chr14:96452282
|
A | G | 1 | a0007c0012t0002g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1098+712A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96452282 | ||||||
| chr14:96452291
|
A | G | 24 | a0001c0001t0001g0069a0001c0001t0001g0133a0001c0001t0001g0150others(21): Show | 24 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1098+721A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96452291 | ||||||
| chr14:96452325
|
C | CT | 19 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0034others(16): Show | 19 | HG00099.hp2 HG00733.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1098+767dupT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr14 | 96452325 | |||||
| chr14:96452454
|
TACCTGAG others(13): Show |
T | 5 | a0001c0001t0001g0249a0001c0001t0001g0251a0001c0001t0001g0300others(2): Show | 5 | HG01167.hp1 HG02615.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1098+888_1098+907d others(22): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr14 | 96452454 | |||||
| chr14:96452455
|
A | G | 1 | a0001c0001t0001g0018 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1098+885A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96452455 | ||||||
| chr14:96452456
|
C | T | 59 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0032others(56): Show | 59 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.1098+886C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96452456 | ||||||
| chr14:96452484
|
T | C | 292 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(289): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.1098+914T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96452484 | ||||||
| chr14:96452527
|
T | C | 3 | a0002c0002t0001g0066a0002c0002t0001g0161a0002c0002t0001g0162 | 3 | HG02818.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1098+957T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96452527 | ||||||
| chr14:96452562
|
G | A | 1 | a0003c0003t0001g0042 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1098+992G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96452562 | ||||||
| chr14:96452563
|
C | T | 1 | a0002c0002t0004g0020 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1098+993C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96452563 | ||||||
| chr14:96452667
|
C | CT | 13 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0034others(10): Show | 13 | HG00099.hp2 HG00733.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1098+1106dupT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr14 | 96452667 | |||||
| chr14:96452668
|
T | C | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(85): Show | 88 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.1098+1098T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96452668 | ||||||
| chr14:96452699
|
C | G | 10 | a0001c0001t0001g0158a0001c0001t0005g0065a0001c0001t0005g0258others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1098+1129C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96452699 | ||||||
| chr14:96452736
|
G | T | 1 | a0001c0001t0001g0006 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1098+1166G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96452736 | ||||||
| chr14:96452822
|
G | A | 290 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1098+1252G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96452822 | ||||||
| chr14:96453003
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1098+1433G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96453003 | ||||||
| chr14:96453202
|
G | C | 2 | a0003c0009t0002g0165a0003c0009t0002g0166 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1098+1632G>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96453202 | ||||||
| chr14:96453283
|
G | A | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(85): Show | 88 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.1098+1713G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96453283 | ||||||
| chr14:96453354
|
A | G | 5 | a0001c0001t0001g0264a0001c0001t0001g0272a0001c0001t0001g0309others(2): Show | 5 | HG01106.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1098+1784A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96453354 | ||||||
| chr14:96453454
|
G | T | 1 | a0001c0001t0001g0118 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1098+1884G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96453454 | ||||||
| chr14:96453483
|
A | G | 1 | a0001c0001t0001g0251 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1098+1913A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96453483 | ||||||
| chr14:96453524
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1098+1954C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96453524 | ||||||
| chr14:96453650
|
T | C | 1 | a0005c0013t0002g0102 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1098+2080T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96453650 | ||||||
| chr14:96454003
|
G | A | 3 | a0002c0002t0001g0016a0002c0002t0001g0184a0002c0002t0004g0020 | 3 | NA18943.hp1 NA19011.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1099-2344G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96454003 | ||||||
| chr14:96454057
|
G | A | 2 | a0001c0001t0001g0124a0001c0007t0003g0044 | 2 | HG01243.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1099-2290G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96454057 | ||||||
| chr14:96454065
|
G | T | 3 | a0001c0001t0001g0294a0001c0001t0002g0256a0001c0001t0002g0273 | 3 | HG03225.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1099-2282G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96454065 | ||||||
| chr14:96454193
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1099-2154G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96454193 | ||||||
| chr14:96454236
|
G | A | 18 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0197others(15): Show | 18 | HG00099.hp2 HG00733.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1099-2111G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96454236 | ||||||
| chr14:96454261
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1099-2086C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96454261 | ||||||
| chr14:96454414
|
A | G | 2 | a0001c0001t0001g0236a0011c0019t0001g0262 | 2 | HG02015.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.1099-1933A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96454414 | ||||||
| chr14:96454482
|
C | A | 169 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0015others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.1099-1865C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96454482 | ||||||
| chr14:96454566
|
C | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0055others(2): Show | 5 | HG03688.hp1 HG03710.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.1099-1781C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96454566 | ||||||
| chr14:96454662
|
A | T | 1 | a0001c0001t0002g0045 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1099-1685A>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96454662 | ||||||
| chr14:96454663
|
A | AT | 8 | a0001c0001t0001g0294a0001c0001t0002g0040a0001c0001t0002g0256others(5): Show | 8 | HG01433.hp2 HG02257.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.1099-1669dupT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr14 | 96454663 | |||||
| chr14:96454663
|
A | T | 41 | a0001c0001t0001g0072a0001c0001t0001g0084a0001c0001t0001g0105others(38): Show | 41 | HG00323.hp2 HG00544.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1099-1684A>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96454663 | ||||||
| chr14:96454663
|
AT | A | 91 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0037others(88): Show | 91 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.1099-1669delT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr14 | 96454663 | |||||
| chr14:96454892
|
C | T | 1 | a0002c0002t0005g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1099-1455C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96454892 | ||||||
| chr14:96455035
|
C | T | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0144 | 3 | HG01070.hp1 HG01071.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.1099-1312C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96455035 | ||||||
| chr14:96455426
|
A | G | 2 | a0002c0002t0002g0169a0002c0002t0005g0063 | 2 | HG02257.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1099-921A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96455426 | ||||||
| chr14:96455626
|
C | T | 2 | a0002c0002t0002g0169a0002c0002t0005g0063 | 2 | HG02257.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1099-721C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96455626 | ||||||
| chr14:96455753
|
T | C | 2 | a0004c0004t0006g0148a0004c0004t0006g0168 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1099-594T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96455753 | ||||||
| chr14:96456020
|
C | T | 2 | a0002c0002t0002g0288a0002c0002t0002g0306 | 2 | HG02145.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1099-327C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96456020 | ||||||
| chr14:96456164
|
G | C | 1 | a0003c0003t0002g0004 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1099-183G>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96456164 | ||||||
| chr14:96456207
|
A | G | 3 | a0001c0001t0002g0048a0001c0001t0002g0213a0002c0002t0002g0178 | 3 | NA18948.hp2 NA18960.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.1099-140A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96456207 | ||||||
| chr14:96456238
|
CA | C | 21 | a0001c0001t0001g0032a0001c0001t0001g0041a0001c0001t0001g0072others(18): Show | 21 | HG00423.hp2 HG01261.hp2 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1099-86delA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr14 | 96456238 | |||||
| chr14:96456238
|
CAA | C | 177 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0017others(174): Show | 177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.1099-87_1099-86del others(2): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr14 | 96456238 | |||||
| chr14:96456238
|
CAAA | C | 88 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0021others(85): Show | 88 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.1099-88_1099-86del others(3): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr14 | 96456238 | |||||
| chr14:96456239
|
A | T | 1 | a0001c0001t0001g0015 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1099-108A>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 10/17 | chr14 | 96456239 | ||||||
| chr14:96456535
|
A | G | 4 | a0001c0001t0001g0069a0001c0001t0001g0160a0001c0001t0007g0243others(1): Show | 4 | HG00639.hp1 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1227+60A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 11/17 | chr14 | 96456535 | ||||||
| chr14:96456611
|
T | C | 24 | a0001c0001t0001g0069a0001c0001t0001g0133a0001c0001t0001g0150others(21): Show | 24 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1227+136T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 11/17 | chr14 | 96456611 | ||||||
| chr14:96456692
|
C | T | 8 | a0001c0001t0001g0134a0001c0001t0001g0136a0001c0001t0001g0249others(5): Show | 8 | HG01167.hp1 HG02615.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1227+217C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 11/17 | chr14 | 96456692 | ||||||
| chr14:96456776
|
G | A | 9 | a0001c0001t0001g0014a0001c0001t0001g0134a0001c0001t0001g0136others(6): Show | 9 | HG01167.hp1 HG02615.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1227+301G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 11/17 | chr14 | 96456776 | ||||||
| chr14:96456797
|
G | A | 3 | a0001c0001t0001g0277a0001c0001t0004g0268a0001c0006t0001g0008 | 3 | HG01167.hp2 HG01169.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1227+322G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 11/17 | chr14 | 96456797 | ||||||
| chr14:96456809
|
T | A | 4 | a0001c0001t0001g0069a0001c0001t0001g0160a0001c0001t0007g0243others(1): Show | 4 | HG00639.hp1 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1227+334T>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 11/17 | chr14 | 96456809 | ||||||
| chr14:96456880
|
C | A | 2 | a0001c0001t0001g0238a0002c0002t0001g0117 | 2 | NA18951.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1227+405C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 11/17 | chr14 | 96456880 | ||||||
| chr14:96456884
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1227+409C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 11/17 | chr14 | 96456884 | ||||||
| chr14:96457054
|
C | CT | 76 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0032others(73): Show | 76 | HG00280.hp1 HG00609.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1227+603dupT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr14 | 96457054 | |||||
| chr14:96457054
|
C | CTT | 6 | a0001c0001t0001g0272a0001c0001t0001g0309a0001c0001t0001g0311others(3): Show | 6 | HG01106.hp2 HG02970.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1227+602_1227+603d others(4): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr14 | 96457054 | |||||
| chr14:96457054
|
CT | C | 10 | a0001c0001t0001g0060a0001c0001t0001g0099a0001c0001t0001g0100others(7): Show | 10 | HG00323.hp1 HG00639.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.1227+603delT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr14 | 96457054 | |||||
| chr14:96457054
|
CTTTTTTT others(5): Show |
C | 18 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0197others(15): Show | 18 | HG00099.hp2 HG00733.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1227+592_1227+603d others(14): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr14 | 96457054 | |||||
| chr14:96457183
|
C | T | 1 | a0002c0002t0001g0116 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1227+708C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 11/17 | chr14 | 96457183 | ||||||
| chr14:96457221
|
C | A | 5 | a0001c0001t0001g0249a0001c0001t0001g0251a0001c0001t0001g0300others(2): Show | 5 | HG01167.hp1 HG02615.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1227+746C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 11/17 | chr14 | 96457221 | ||||||
| chr14:96457540
|
G | A | 4 | a0003c0005t0003g0024a0003c0005t0003g0030a0003c0005t0003g0211others(1): Show | 4 | HG00423.hp1 HG02155.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1228-543G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 11/17 | chr14 | 96457540 | ||||||
| chr14:96457542
|
C | A | 1 | a0001c0001t0001g0062 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1228-541C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 11/17 | chr14 | 96457542 | ||||||
| chr14:96457830
|
A | G | 1 | a0001c0001t0001g0240 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1228-253A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 11/17 | chr14 | 96457830 | ||||||
| chr14:96457847
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1228-236A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 11/17 | chr14 | 96457847 | ||||||
| chr14:96457952
|
G | A | 44 | a0001c0001t0001g0072a0001c0001t0001g0084a0001c0001t0001g0105others(41): Show | 44 | HG00323.hp2 HG00544.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1228-131G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 11/17 | chr14 | 96457952 | ||||||
| chr14:96458030
|
A | G | 4 | a0001c0001t0001g0069a0001c0001t0001g0160a0001c0001t0007g0243others(1): Show | 4 | HG00639.hp1 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1228-53A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 11/17 | chr14 | 96458030 | ||||||
| chr14:96458033
|
G | A | 1 | a0004c0004t0001g0293 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1228-50G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 11/17 | chr14 | 96458033 | ||||||
| chr14:96458288
|
T | A | 4 | a0001c0001t0001g0197a0001c0001t0001g0315a0001c0001t0002g0057others(1): Show | 4 | HG02698.hp2 HG03688.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1357+76T>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96458288 | ||||||
| chr14:96458317
|
C | T | 2 | a0003c0009t0002g0165a0003c0009t0002g0166 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1357+105C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96458317 | ||||||
| chr14:96458321
|
C | T | 7 | a0001c0001t0001g0158a0001c0001t0005g0065a0001c0001t0005g0258others(4): Show | 7 | HG01109.hp1 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1357+109C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96458321 | ||||||
| chr14:96458512
|
C | T | 2 | a0001c0001t0007g0243a0001c0001t0007g0287 | 2 | HG00639.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1357+300C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96458512 | ||||||
| chr14:96458560
|
G | A | 6 | a0001c0001t0001g0086a0001c0001t0001g0125a0001c0001t0001g0176others(3): Show | 6 | HG00423.hp2 HG00544.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.1357+348G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96458560 | ||||||
| chr14:96458587
|
A | C | 6 | a0001c0001t0001g0304a0001c0001t0001g0313a0001c0001t0002g0163others(3): Show | 6 | HG02630.hp1 HG02717.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1357+375A>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96458587 | ||||||
| chr14:96458742
|
C | CA | 46 | a0001c0001t0001g0041a0001c0001t0001g0072a0001c0001t0001g0084others(43): Show | 46 | HG00323.hp2 HG00544.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.1357+549dupA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96458742 | |||||
| chr14:96458742
|
CA | C | 10 | a0001c0001t0001g0061a0001c0001t0001g0086a0001c0001t0001g0133others(7): Show | 10 | HG00323.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1357+549delA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96458742 | |||||
| chr14:96458760
|
A | AC | 3 | a0002c0002t0001g0066a0002c0002t0001g0161a0002c0002t0001g0162 | 3 | HG02818.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1357+548_1357+549i others(3): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96458760 | ||||||
| chr14:96458840
|
G | A | 292 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(289): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.1357+628G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96458840 | ||||||
| chr14:96458912
|
C | CA | 32 | a0001c0001t0001g0025a0001c0001t0001g0041a0001c0001t0001g0124others(29): Show | 32 | HG00423.hp1 HG00621.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.1357+726dupA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96458912 | |||||
| chr14:96458912
|
CA | C | 18 | a0001c0001t0001g0201a0001c0001t0001g0250a0001c0001t0001g0251others(15): Show | 18 | HG01167.hp2 HG01169.hp2 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.1357+726delA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96458912 | |||||
| chr14:96458912
|
CAA | C | 18 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0197others(15): Show | 18 | HG00099.hp2 HG00733.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1357+725_1357+726d others(4): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96458912 | |||||
| chr14:96458934
|
A | AG | 3 | a0001c0001t0002g0159a0002c0002t0001g0116a0002c0002t0007g0298 | 3 | HG01106.hp1 HG02109.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1357+722_1357+723i others(3): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96458934 | ||||||
| chr14:96458934
|
A | G | 84 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(81): Show | 84 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.1357+722A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96458934 | ||||||
| chr14:96458960
|
C | CA | 121 | a0001c0001t0001g0014a0001c0001t0001g0037a0001c0001t0001g0062others(118): Show | 121 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.1357+758dupA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96458960 | |||||
| chr14:96458960
|
CA | C | 89 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(86): Show | 89 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.1357+758delA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96458960 | |||||
| chr14:96459034
|
C | G | 1 | a0001c0001t0002g0203 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1357+822C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96459034 | ||||||
| chr14:96459124
|
G | A | 1 | a0002c0002t0001g0167 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1357+912G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96459124 | ||||||
| chr14:96459231
|
G | C | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1357+1019G>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96459231 | ||||||
| chr14:96459286
|
C | T | 1 | a0002c0014t0003g0058 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1357+1074C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96459286 | ||||||
| chr14:96459402
|
G | T | 1 | a0007c0012t0002g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1357+1190G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96459402 | ||||||
| chr14:96459539
|
A | G | 1 | a0001c0001t0002g0057 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1357+1327A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96459539 | ||||||
| chr14:96459561
|
T | C | 1 | a0001c0001t0001g0018 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1357+1349T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96459561 | ||||||
| chr14:96459587
|
C | T | 10 | a0001c0001t0001g0158a0001c0001t0005g0065a0001c0001t0005g0258others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1357+1375C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96459587 | ||||||
| chr14:96459600
|
CTGTAATC others(4): Show |
C | 4 | a0001c0001t0001g0061a0001c0001t0001g0104a0002c0002t0001g0180others(1): Show | 4 | HG01256.hp1 HG01258.hp2 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.1357+1409_1357+141 others(15): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96459600 | |||||
| chr14:96459646
|
T | C | 292 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(289): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.1357+1434T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96459646 | ||||||
| chr14:96459740
|
G | A | 9 | a0001c0001t0001g0014a0001c0001t0001g0134a0001c0001t0001g0136others(6): Show | 9 | HG01167.hp1 HG02615.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1357+1528G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96459740 | ||||||
| chr14:96459769
|
C | T | 1 | a0002c0002t0001g0253 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1357+1557C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96459769 | ||||||
| chr14:96459876
|
C | CA | 6 | a0001c0001t0001g0158a0001c0001t0005g0065a0001c0001t0005g0258others(3): Show | 6 | HG01109.hp1 HG02055.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1357+1673dupA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96459876 | |||||
| chr14:96459910
|
A | T | 1 | a0002c0002t0001g0116 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1357+1698A>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96459910 | ||||||
| chr14:96460023
|
G | T | 1 | a0001c0006t0002g0011 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1357+1811G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96460023 | ||||||
| chr14:96460242
|
T | G | 10 | a0001c0001t0001g0158a0001c0001t0005g0065a0001c0001t0005g0258others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1357+2030T>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96460242 | ||||||
| chr14:96460299
|
T | C | 35 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0091others(32): Show | 35 | HG00280.hp1 HG00621.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1357+2087T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96460299 | ||||||
| chr14:96460376
|
C | T | 4 | a0001c0001t0001g0197a0001c0001t0001g0315a0001c0001t0002g0057others(1): Show | 4 | HG02698.hp2 HG03688.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1357+2164C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96460376 | ||||||
| chr14:96460469
|
T | A | 1 | a0001c0001t0001g0299 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1357+2257T>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96460469 | ||||||
| chr14:96460545
|
A | G | 118 | a0001c0001t0001g0014a0001c0001t0001g0037a0001c0001t0001g0062others(115): Show | 118 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.1357+2333A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96460545 | ||||||
| chr14:96460632
|
G | A | 1 | a0001c0001t0002g0256 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1357+2420G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96460632 | ||||||
| chr14:96460662
|
C | T | 1 | a0001c0001t0005g0265 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1357+2450C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96460662 | ||||||
| chr14:96460690
|
C | T | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(85): Show | 88 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.1357+2478C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96460690 | ||||||
| chr14:96460773
|
A | G | 1 | a0002c0002t0001g0073 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1357+2561A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96460773 | ||||||
| chr14:96460963
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1357+2751C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96460963 | ||||||
| chr14:96461036
|
A | G | 9 | a0001c0001t0001g0014a0001c0001t0001g0134a0001c0001t0001g0136others(6): Show | 9 | HG01167.hp1 HG02615.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1357+2824A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96461036 | ||||||
| chr14:96461076
|
G | T | 2 | a0001c0001t0001g0252a0001c0001t0002g0237 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1357+2864G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96461076 | ||||||
| chr14:96461226
|
A | G | 4 | a0001c0001t0001g0069a0001c0001t0001g0160a0001c0001t0007g0243others(1): Show | 4 | HG00639.hp1 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1357+3014A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96461226 | ||||||
| chr14:96461320
|
C | T | 1 | a0001c0001t0001g0309 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1357+3108C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96461320 | ||||||
| chr14:96461660
|
C | T | 1 | a0001c0001t0001g0195 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1357+3448C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96461660 | ||||||
| chr14:96461725
|
C | T | 11 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0022others(8): Show | 11 | HG00733.hp2 HG01258.hp1 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.1357+3513C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96461725 | ||||||
| chr14:96461736
|
C | G | 20 | a0001c0001t0001g0133a0001c0001t0001g0150a0001c0001t0001g0250others(17): Show | 20 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1357+3524C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96461736 | ||||||
| chr14:96461808
|
A | G | 2 | a0003c0009t0002g0165a0003c0009t0002g0166 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1357+3596A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96461808 | ||||||
| chr14:96461866
|
G | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0055a0001c0001t0001g0278others(1): Show | 4 | HG03710.hp1 HG03834.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1357+3654G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96461866 | ||||||
| chr14:96462144
|
G | A | 4 | a0001c0001t0001g0069a0001c0001t0001g0160a0001c0001t0007g0243others(1): Show | 4 | HG00639.hp1 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1357+3932G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96462144 | ||||||
| chr14:96462161
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1357+3949G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96462161 | ||||||
| chr14:96462290
|
G | A | 4 | a0001c0001t0001g0069a0001c0001t0001g0160a0001c0001t0007g0243others(1): Show | 4 | HG00639.hp1 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1357+4078G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96462290 | ||||||
| chr14:96462421
|
C | G | 1 | a0001c0001t0001g0176 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1357+4209C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96462421 | ||||||
| chr14:96462529
|
C | T | 7 | a0001c0001t0001g0158a0001c0001t0005g0065a0001c0001t0005g0258others(4): Show | 7 | HG01109.hp1 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1357+4317C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96462529 | ||||||
| chr14:96462744
|
A | T | 2 | a0002c0002t0002g0169a0002c0002t0005g0063 | 2 | HG02257.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1357+4532A>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96462744 | ||||||
| chr14:96462779
|
GCTAT | G | 4 | a0001c0001t0001g0069a0001c0001t0001g0160a0001c0001t0007g0243others(1): Show | 4 | HG00639.hp1 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1357+4571_1357+457 others(8): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96462779 | |||||
| chr14:96462800
|
A | G | 6 | a0001c0001t0001g0304a0001c0001t0001g0313a0001c0001t0002g0163others(3): Show | 6 | HG02630.hp1 HG02717.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1357+4588A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96462800 | ||||||
| chr14:96462888
|
A | G | 35 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0091others(32): Show | 35 | HG00280.hp1 HG00621.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1357+4676A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96462888 | ||||||
| chr14:96462912
|
C | T | 103 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0032others(100): Show | 103 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1357+4700C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96462912 | ||||||
| chr14:96462928
|
A | G | 292 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(289): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.1357+4716A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96462928 | ||||||
| chr14:96463116
|
A | G | 4 | a0001c0001t0001g0069a0001c0001t0001g0160a0001c0001t0007g0243others(1): Show | 4 | HG00639.hp1 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1357+4904A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96463116 | ||||||
| chr14:96463139
|
A | AAAAC | 38 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0091others(35): Show | 38 | HG00280.hp1 HG00621.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.1357+4955_1357+495 others(8): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96463139 | |||||
| chr14:96463139
|
AAAAC | A | 93 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(90): Show | 93 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.1357+4955_1357+495 others(8): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96463139 | |||||
| chr14:96463139
|
AAAACAAA others(5): Show |
A | 1 | a0001c0001t0001g0072 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1357+4947_1357+495 others(16): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96463139 | |||||
| chr14:96463166
|
A | G | 2 | a0003c0009t0002g0165a0003c0009t0002g0166 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1357+4954A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96463166 | ||||||
| chr14:96463207
|
A | T | 1 | a0002c0002t0001g0162 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1357+4995A>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96463207 | ||||||
| chr14:96463250
|
T | C | 19 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0034others(16): Show | 19 | HG00099.hp2 HG00733.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1357+5038T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96463250 | ||||||
| chr14:96463282
|
C | T | 2 | a0003c0009t0002g0165a0003c0009t0002g0166 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1357+5070C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96463282 | ||||||
| chr14:96463314
|
T | C | 3 | a0001c0001t0001g0277a0001c0001t0004g0268a0001c0006t0001g0008 | 3 | HG01167.hp2 HG01169.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1357+5102T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96463314 | ||||||
| chr14:96463409
|
T | TA | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(85): Show | 88 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.1357+5205dupA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96463409 | |||||
| chr14:96463415
|
A | T | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0144 | 3 | HG01070.hp1 HG01071.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.1357+5203A>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96463415 | ||||||
| chr14:96463458
|
T | G | 5 | a0001c0001t0001g0249a0001c0001t0001g0251a0001c0001t0001g0300others(2): Show | 5 | HG01167.hp1 HG02615.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1357+5246T>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96463458 | ||||||
| chr14:96463612
|
C | T | 2 | a0002c0002t0001g0012a0002c0016t0002g0013 | 2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1357+5400C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96463612 | ||||||
| chr14:96463696
|
G | GGC | 3 | a0003c0005t0003g0024a0003c0005t0003g0030a0003c0005t0003g0211 | 3 | HG00423.hp1 NA18983.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.1357+5486_1357+548 others(6): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96463696 | |||||
| chr14:96463698
|
C | T | 1 | a0003c0003t0001g0110 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1357+5486C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96463698 | ||||||
| chr14:96463699
|
G | A | 14 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0295others(11): Show | 14 | HG00099.hp2 HG00733.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1357+5487G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96463699 | ||||||
| chr14:96463719
|
C | CA | 34 | a0001c0001t0001g0062a0001c0001t0001g0091a0001c0001t0001g0115others(31): Show | 34 | HG00280.hp1 HG00621.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.1357+5526dupA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96463719 | |||||
| chr14:96463719
|
CA | C | 183 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0015others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1357+5526delA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96463719 | |||||
| chr14:96463806
|
C | T | 292 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(289): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.1357+5594C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96463806 | ||||||
| chr14:96463902
|
C | T | 1 | a0002c0002t0002g0175 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1357+5690C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96463902 | ||||||
| chr14:96464036
|
G | A | 2 | a0003c0009t0002g0165a0003c0009t0002g0166 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1357+5824G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96464036 | ||||||
| chr14:96464090
|
T | C | 2 | a0001c0001t0001g0189a0001c0001t0002g0222 | 2 | HG00323.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1357+5878T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96464090 | ||||||
| chr14:96464198
|
G | A | 1 | a0002c0002t0002g0002 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1357+5986G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96464198 | ||||||
| chr14:96464282
|
C | T | 35 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0091others(32): Show | 35 | HG00280.hp1 HG00621.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1357+6070C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96464282 | ||||||
| chr14:96464299
|
G | A | 1 | a0001c0001t0009g0187 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1357+6087G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96464299 | ||||||
| chr14:96464339
|
G | T | 18 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0197others(15): Show | 18 | HG00099.hp2 HG00733.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1357+6127G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96464339 | ||||||
| chr14:96464382
|
T | C | 1 | a0001c0001t0002g0075 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1357+6170T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96464382 | ||||||
| chr14:96464411
|
G | A | 59 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0032others(56): Show | 59 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.1357+6199G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96464411 | ||||||
| chr14:96464411
|
G | C | 24 | a0001c0001t0001g0069a0001c0001t0001g0133a0001c0001t0001g0150others(21): Show | 24 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1357+6199G>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96464411 | ||||||
| chr14:96464423
|
G | T | 8 | a0001c0001t0001g0026a0001c0001t0001g0035a0001c0001t0001g0077others(5): Show | 8 | HG00735.hp1 HG01070.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.1357+6211G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96464423 | ||||||
| chr14:96464544
|
C | CA | 102 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0018others(99): Show | 102 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.1357+6356dupA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96464544 | |||||
| chr14:96464544
|
C | CAA | 129 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0021others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1357+6355_1357+635 others(6): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96464544 | |||||
| chr14:96464544
|
C | CAAA | 38 | a0001c0001t0001g0015a0001c0001t0001g0072a0001c0001t0001g0091others(35): Show | 38 | HG00423.hp2 HG00621.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.1357+6354_1357+635 others(7): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96464544 | |||||
| chr14:96464544
|
CAAAAAAA others(6): Show |
C | 3 | a0003c0005t0003g0024a0003c0005t0003g0030a0003c0005t0003g0211 | 3 | HG00423.hp1 NA18983.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.1357+6344_1357+635 others(17): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96464544 | |||||
| chr14:96464630
|
A | G | 3 | a0001c0001t0001g0133a0001c0001t0001g0266a0001c0001t0002g0145 | 3 | HG02109.hp2 HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1357+6418A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96464630 | ||||||
| chr14:96464709
|
C | CTAT | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0144 | 3 | HG01070.hp1 HG01071.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.1357+6501_1357+650 others(7): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96464709 | |||||
| chr14:96464765
|
A | C | 97 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(94): Show | 97 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.1357+6553A>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96464765 | ||||||
| chr14:96464903
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1358-6575T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96464903 | ||||||
| chr14:96464999
|
G | A | 4 | a0001c0001t0001g0069a0001c0001t0001g0160a0001c0001t0007g0243others(1): Show | 4 | HG00639.hp1 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1358-6479G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96464999 | ||||||
| chr14:96465312
|
T | A | 23 | a0001c0001t0001g0069a0001c0001t0001g0133a0001c0001t0001g0150others(20): Show | 23 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.1358-6166T>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96465312 | ||||||
| chr14:96465337
|
C | T | 3 | a0002c0002t0001g0066a0002c0002t0001g0161a0002c0002t0001g0162 | 3 | HG02818.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1358-6141C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96465337 | ||||||
| chr14:96465383
|
A | G | 3 | a0002c0002t0001g0066a0002c0002t0001g0161a0002c0002t0001g0162 | 3 | HG02818.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1358-6095A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96465383 | ||||||
| chr14:96465462
|
T | TA | 25 | a0001c0001t0001g0069a0001c0001t0001g0133a0001c0001t0001g0150others(22): Show | 25 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.1358-6004dupA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96465462 | |||||
| chr14:96465470
|
A | T | 3 | a0002c0002t0001g0066a0002c0002t0001g0161a0002c0002t0001g0162 | 3 | HG02818.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1358-6008A>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96465470 | ||||||
| chr14:96465559
|
C | G | 292 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(289): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.1358-5919C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96465559 | ||||||
| chr14:96465738
|
G | A | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(85): Show | 88 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.1358-5740G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96465738 | ||||||
| chr14:96465749
|
C | T | 1 | a0004c0004t0001g0155 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1358-5729C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96465749 | ||||||
| chr14:96465754
|
A | G | 290 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1358-5724A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96465754 | ||||||
| chr14:96465763
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1358-5715G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96465763 | ||||||
| chr14:96465781
|
G | C | 2 | a0002c0002t0002g0169a0002c0002t0005g0063 | 2 | HG02257.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1358-5697G>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96465781 | ||||||
| chr14:96465873
|
G | A | 59 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0032others(56): Show | 59 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.1358-5605G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96465873 | ||||||
| chr14:96466009
|
C | CA | 132 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(129): Show | 132 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.1358-5452dupA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96466009 | |||||
| chr14:96466009
|
C | CAA | 21 | a0001c0001t0001g0133a0001c0001t0001g0250a0001c0001t0001g0252others(18): Show | 21 | HG00642.hp1 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.1358-5453_1358-545 others(6): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96466009 | |||||
| chr14:96466009
|
CA | C | 24 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0099others(21): Show | 24 | HG00099.hp2 HG00733.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.1358-5452delA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96466009 | |||||
| chr14:96466071
|
T | C | 7 | a0001c0001t0001g0158a0001c0001t0005g0065a0001c0001t0005g0258others(4): Show | 7 | HG01109.hp1 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1358-5407T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96466071 | ||||||
| chr14:96466133
|
A | G | 1 | a0001c0001t0001g0014 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1358-5345A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96466133 | ||||||
| chr14:96466267
|
C | T | 2 | a0002c0002t0002g0288a0002c0002t0002g0306 | 2 | HG02145.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1358-5211C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96466267 | ||||||
| chr14:96466268
|
G | A | 1 | a0002c0002t0002g0088 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1358-5210G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96466268 | ||||||
| chr14:96466290
|
G | A | 10 | a0001c0001t0001g0014a0001c0001t0001g0134a0001c0001t0001g0136others(7): Show | 10 | HG01167.hp1 HG02615.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1358-5188G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96466290 | ||||||
| chr14:96466299
|
T | A | 1 | a0001c0001t0001g0017 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1358-5179T>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96466299 | ||||||
| chr14:96466441
|
C | T | 23 | a0001c0001t0001g0069a0001c0001t0001g0133a0001c0001t0001g0150others(20): Show | 23 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.1358-5037C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96466441 | ||||||
| chr14:96466565
|
A | C | 10 | a0001c0001t0001g0014a0001c0001t0001g0134a0001c0001t0001g0136others(7): Show | 10 | HG01167.hp1 HG02615.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1358-4913A>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96466565 | ||||||
| chr14:96466792
|
A | G | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(85): Show | 88 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.1358-4686A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96466792 | ||||||
| chr14:96466879
|
T | C | 59 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0032others(56): Show | 59 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.1358-4599T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96466879 | ||||||
| chr14:96466998
|
A | G | 1 | a0001c0001t0004g0198 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1358-4480A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96466998 | ||||||
| chr14:96467032
|
T | C | 4 | a0001c0001t0001g0097a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG01258.hp1 HG01346.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1358-4446T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96467032 | ||||||
| chr14:96467046
|
T | TA | 193 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(190): Show | 193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1358-4416dupA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96467046 | |||||
| chr14:96467046
|
T | TAA | 6 | a0001c0001t0001g0186a0001c0001t0001g0315a0001c0001t0002g0075others(3): Show | 6 | HG00642.hp1 HG00741.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1358-4417_1358-441 others(6): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96467046 | |||||
| chr14:96467046
|
TA | T | 62 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0032others(59): Show | 62 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1358-4416delA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96467046 | |||||
| chr14:96467077
|
T | C | 42 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0026others(39): Show | 42 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.1358-4401T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96467077 | ||||||
| chr14:96467331
|
C | CT | 91 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(88): Show | 91 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1358-4134dupT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96467331 | |||||
| chr14:96467331
|
CT | C | 10 | a0001c0001t0001g0134a0001c0001t0001g0136a0001c0001t0001g0160others(7): Show | 10 | HG01167.hp1 HG02615.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1358-4134delT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96467331 | |||||
| chr14:96467347
|
C | T | 9 | a0001c0001t0001g0134a0001c0001t0001g0136a0001c0001t0001g0160others(6): Show | 9 | HG01167.hp1 HG02615.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1358-4131C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96467347 | ||||||
| chr14:96467401
|
T | C | 19 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0034others(16): Show | 19 | HG00099.hp2 HG00733.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1358-4077T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96467401 | ||||||
| chr14:96467466
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0077 | 2 | HG01255.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.1358-4012G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96467466 | ||||||
| chr14:96467484
|
C | T | 1 | a0002c0002t0001g0225 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1358-3994C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96467484 | ||||||
| chr14:96467528
|
C | T | 1 | a0001c0001t0002g0068 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1358-3950C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96467528 | ||||||
| chr14:96467565
|
C | G | 1 | a0001c0001t0001g0304 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1358-3913C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96467565 | ||||||
| chr14:96467657
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1358-3821T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96467657 | ||||||
| chr14:96467713
|
C | T | 1 | a0003c0003t0001g0110 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1358-3765C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96467713 | ||||||
| chr14:96467776
|
A | C | 1 | a0001c0001t0001g0144 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1358-3702A>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96467776 | ||||||
| chr14:96467985
|
C | G | 1 | a0001c0001t0001g0144 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1358-3493C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96467985 | ||||||
| chr14:96467995
|
G | C | 2 | a0003c0009t0002g0165a0003c0009t0002g0166 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1358-3483G>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96467995 | ||||||
| chr14:96468073
|
C | CA | 96 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0032others(93): Show | 96 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.1358-3382dupA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96468073 | |||||
| chr14:96468073
|
C | CAA | 22 | a0001c0001t0001g0072a0001c0001t0001g0118a0001c0001t0001g0125others(19): Show | 22 | HG00642.hp1 HG00738.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1358-3383_1358-338 others(6): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96468073 | |||||
| chr14:96468073
|
CA | C | 79 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0018others(76): Show | 79 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.1358-3382delA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96468073 | |||||
| chr14:96468105
|
G | A | 38 | a0001c0001t0001g0072a0001c0001t0001g0084a0001c0001t0001g0105others(35): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.1358-3373G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96468105 | ||||||
| chr14:96468119
|
G | A | 1 | a0003c0003t0002g0004 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1358-3359G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96468119 | ||||||
| chr14:96468214
|
C | CA | 79 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(76): Show | 79 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.1358-3249dupA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96468214 | |||||
| chr14:96468214
|
C | CAA | 33 | a0001c0001t0001g0032a0001c0001t0001g0069a0001c0001t0001g0133others(30): Show | 33 | HG00639.hp1 HG00733.hp1 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.1358-3250_1358-324 others(6): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96468214 | |||||
| chr14:96468214
|
CA | C | 39 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0091others(36): Show | 39 | HG00280.hp1 HG00621.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.1358-3249delA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96468214 | |||||
| chr14:96468296
|
C | CT | 32 | a0001c0001t0001g0027a0001c0001t0001g0150a0001c0001t0001g0158others(29): Show | 32 | HG00621.hp2 HG00733.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.1358-3159dupT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96468296 | |||||
| chr14:96468296
|
C | CTT | 7 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0034others(4): Show | 7 | HG00099.hp2 HG00733.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1358-3160_1358-315 others(6): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96468296 | |||||
| chr14:96468296
|
C | CTTT | 9 | a0001c0001t0001g0197a0001c0001t0001g0304a0001c0001t0001g0313others(6): Show | 9 | HG02630.hp1 HG02698.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1358-3161_1358-315 others(7): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96468296 | |||||
| chr14:96468296
|
CT | C | 58 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0032others(55): Show | 58 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.1358-3159delT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96468296 | |||||
| chr14:96468296
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0246 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1358-3169_1358-315 others(15): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96468296 | |||||
| chr14:96468297
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1358-3181T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96468297 | ||||||
| chr14:96468359
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1358-3119G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96468359 | ||||||
| chr14:96468452
|
C | T | 12 | a0001c0001t0001g0134a0001c0001t0001g0136a0001c0001t0001g0150others(9): Show | 12 | HG01167.hp1 HG02615.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1358-3026C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96468452 | ||||||
| chr14:96468563
|
C | T | 2 | a0002c0002t0002g0169a0002c0002t0005g0063 | 2 | HG02257.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1358-2915C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96468563 | ||||||
| chr14:96468588
|
C | A | 35 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0091others(32): Show | 35 | HG00280.hp1 HG00621.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1358-2890C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96468588 | ||||||
| chr14:96468830
|
A | AT | 6 | a0001c0001t0001g0158a0001c0001t0005g0258a0001c0001t0005g0265others(3): Show | 6 | HG01109.hp1 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1358-2634dupT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96468830 | |||||
| chr14:96468830
|
AT | A | 6 | a0001c0001t0001g0177a0001c0001t0001g0189a0001c0001t0002g0094others(3): Show | 6 | HG00323.hp2 HG01069.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1358-2634delT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96468830 | |||||
| chr14:96469307
|
G | T | 1 | a0004c0004t0001g0151 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1358-2171G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96469307 | ||||||
| chr14:96469327
|
C | T | 1 | a0002c0002t0001g0167 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1358-2151C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96469327 | ||||||
| chr14:96469332
|
C | T | 10 | a0001c0001t0001g0087a0001c0001t0001g0126a0001c0001t0001g0139others(7): Show | 10 | HG01099.hp1 HG01168.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.1358-2146C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96469332 | ||||||
| chr14:96469386
|
G | C | 21 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0197others(18): Show | 21 | HG00099.hp2 HG00733.hp1 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.1358-2092G>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96469386 | ||||||
| chr14:96469387
|
T | C | 35 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0091others(32): Show | 35 | HG00280.hp1 HG00621.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1358-2091T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96469387 | ||||||
| chr14:96469417
|
C | T | 1 | a0002c0002t0001g0242 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1358-2061C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96469417 | ||||||
| chr14:96469457
|
A | G | 57 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0032others(54): Show | 57 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.1358-2021A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96469457 | ||||||
| chr14:96469509
|
A | AG | 293 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(290): Show | 293 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.1358-1969_1358-196 others(5): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96469509 | ||||||
| chr14:96469536
|
A | G | 12 | a0001c0001t0001g0252a0001c0001t0001g0277a0001c0001t0002g0068others(9): Show | 12 | HG01167.hp2 HG01169.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1358-1942A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96469536 | ||||||
| chr14:96469711
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1358-1767A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96469711 | ||||||
| chr14:96469745
|
G | A | 2 | a0001c0001t0008g0279a0002c0002t0002g0306 | 2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1358-1733G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96469745 | ||||||
| chr14:96469749
|
C | A | 1 | a0001c0001t0001g0182 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1358-1729C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96469749 | ||||||
| chr14:96469823
|
T | C | 1 | a0001c0001t0001g0109 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1358-1655T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96469823 | ||||||
| chr14:96469859
|
C | A | 1 | a0001c0001t0001g0144 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1358-1619C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96469859 | ||||||
| chr14:96469945
|
G | C | 56 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0084others(53): Show | 56 | HG00323.hp2 HG00544.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.1358-1533G>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96469945 | ||||||
| chr14:96470107
|
C | T | 5 | a0001c0001t0002g0135a0001c0001t0006g0235a0001c0006t0006g0009others(2): Show | 5 | HG02602.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1358-1371C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96470107 | ||||||
| chr14:96470109
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1358-1369C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96470109 | ||||||
| chr14:96470117
|
C | T | 2 | a0001c0001t0001g0109a0002c0002t0001g0162 | 2 | HG02818.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1358-1361C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96470117 | ||||||
| chr14:96470486
|
G | T | 1 | a0002c0014t0003g0058 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1358-992G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96470486 | ||||||
| chr14:96471008
|
G | A | 28 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0091others(25): Show | 28 | HG00280.hp1 HG00423.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.1358-470G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96471008 | ||||||
| chr14:96471187
|
T | C | 290 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1358-291T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96471187 | ||||||
| chr14:96471333
|
T | TA | 45 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0069others(42): Show | 45 | HG00639.hp1 HG00642.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.1358-124dupA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96471333 | |||||
| chr14:96471333
|
TA | T | 6 | a0001c0001t0001g0291a0001c0001t0004g0271a0001c0001t0010g0260others(3): Show | 6 | HG02818.hp2 HG02896.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1358-124delA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96471333 | |||||
| chr14:96471396
|
A | ATTTTTGA others(6): Show |
4 | a0001c0001t0006g0235a0001c0006t0006g0009a0004c0004t0006g0148others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1358-78_1358-66dup others(13): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr14 | 96471396 | |||||
| chr14:96471471
|
T | C | 1 | a0001c0001t0001g0173 | 1 | NA18950.hp1 | splice_region_variant&intron_variant | LOW | c.1358-7T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 12/17 | chr14 | 96471471 | ||||||
| chr14:96471754
|
T | C | 3 | a0001c0001t0001g0217a0002c0002t0001g0023a0002c0002t0001g0043 | 3 | NA18957.hp1 NA18979.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1486+148T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 13/17 | chr14 | 96471754 | ||||||
| chr14:96471762
|
C | T | 1 | a0001c0001t0002g0157 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1486+156C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 13/17 | chr14 | 96471762 | ||||||
| chr14:96471763
|
T | C | 1 | a0001c0001t0002g0157 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1486+157T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 13/17 | chr14 | 96471763 | ||||||
| chr14:96471771
|
T | C | 4 | a0001c0001t0001g0084a0001c0001t0002g0137a0002c0002t0002g0245others(1): Show | 4 | HG00099.hp1 HG01069.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1486+165T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 13/17 | chr14 | 96471771 | ||||||
| chr14:96471773
|
C | T | 27 | a0001c0001t0001g0014a0001c0001t0001g0069a0001c0001t0001g0099others(24): Show | 27 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1486+167C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 13/17 | chr14 | 96471773 | ||||||
| chr14:96471837
|
T | C | 5 | a0001c0001t0001g0130a0001c0001t0001g0252a0001c0001t0001g0277others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1486+231T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 13/17 | chr14 | 96471837 | ||||||
| chr14:96471892
|
C | T | 1 | a0001c0001t0002g0286 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1486+286C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 13/17 | chr14 | 96471892 | ||||||
| chr14:96471893
|
G | A | 1 | a0001c0001t0004g0271 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1486+287G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 13/17 | chr14 | 96471893 | ||||||
| chr14:96471945
|
T | G | 1 | a0001c0001t0001g0229 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1486+339T>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 13/17 | chr14 | 96471945 | ||||||
| chr14:96471948
|
T | C | 16 | a0001c0001t0001g0014a0001c0001t0001g0099a0001c0001t0001g0100others(13): Show | 16 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.1486+342T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 13/17 | chr14 | 96471948 | ||||||
| chr14:96472118
|
T | C | 14 | a0001c0001t0001g0087a0001c0001t0001g0126a0001c0001t0001g0139others(11): Show | 14 | HG01099.hp1 HG01168.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.1486+512T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 13/17 | chr14 | 96472118 | ||||||
| chr14:96472202
|
G | A | 2 | a0003c0009t0002g0165a0003c0009t0002g0166 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1487-485G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 13/17 | chr14 | 96472202 | ||||||
| chr14:96472323
|
G | A | 132 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0017others(129): Show | 132 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1487-364G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 13/17 | chr14 | 96472323 | ||||||
| chr14:96472420
|
G | T | 1 | a0001c0001t0001g0125 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1487-267G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 13/17 | chr14 | 96472420 | ||||||
| chr14:96472511
|
C | G | 1 | a0003c0003t0002g0004 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1487-176C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 13/17 | chr14 | 96472511 | ||||||
| chr14:96472533
|
G | A | 1 | a0003c0003t0001g0226 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1487-154G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 13/17 | chr14 | 96472533 | ||||||
| chr14:96472771
|
T | C | 108 | a0001c0001t0001g0014a0001c0001t0001g0069a0001c0001t0001g0099others(105): Show | 108 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.1555+16T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96472771 | ||||||
| chr14:96472807
|
C | T | 6 | a0001c0001t0005g0065a0001c0001t0005g0258a0001c0001t0005g0265others(3): Show | 6 | HG01109.hp1 HG02257.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1555+52C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96472807 | ||||||
| chr14:96473031
|
G | A | 1 | a0001c0006t0001g0008 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1555+276G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96473031 | ||||||
| chr14:96473039
|
G | A | 1 | a0001c0001t0001g0201 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1555+284G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96473039 | ||||||
| chr14:96473096
|
T | C | 4 | a0001c0001t0001g0197a0001c0001t0001g0299a0001c0001t0001g0315others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1555+341T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96473096 | ||||||
| chr14:96473172
|
A | AT | 19 | a0001c0001t0001g0069a0001c0001t0001g0087a0001c0001t0001g0126others(16): Show | 19 | HG01099.hp1 HG01168.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.1555+433dupT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr14 | 96473172 | |||||
| chr14:96473172
|
AT | A | 138 | a0001c0001t0001g0014a0001c0001t0001g0062a0001c0001t0001g0072others(135): Show | 138 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1555+433delT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr14 | 96473172 | |||||
| chr14:96473232
|
G | A | 39 | a0001c0001t0001g0062a0001c0001t0001g0072a0001c0001t0001g0097others(36): Show | 39 | HG00280.hp1 HG00280.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.1555+477G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96473232 | ||||||
| chr14:96473264
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1555+509G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96473264 | ||||||
| chr14:96473300
|
A | C | 1 | a0001c0001t0001g0261 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1555+545A>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96473300 | ||||||
| chr14:96473362
|
G | C | 2 | a0001c0001t0002g0171a0009c0011t0002g0007 | 2 | HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1555+607G>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96473362 | ||||||
| chr14:96473382
|
A | G | 1 | a0001c0001t0001g0229 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1555+627A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96473382 | ||||||
| chr14:96473455
|
G | T | 3 | a0001c0001t0007g0243a0001c0001t0007g0287a0002c0002t0007g0298 | 3 | HG00639.hp1 HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1555+700G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96473455 | ||||||
| chr14:96473464
|
C | CT | 9 | a0001c0001t0002g0312a0001c0001t0005g0065a0001c0001t0005g0258others(6): Show | 9 | HG01109.hp1 HG01978.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1555+724dupT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr14 | 96473464 | |||||
| chr14:96473464
|
CT | C | 18 | a0001c0001t0001g0232a0001c0001t0001g0294a0001c0001t0002g0067others(15): Show | 18 | HG01891.hp2 HG02572.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.1555+724delT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr14 | 96473464 | |||||
| chr14:96473718
|
A | G | 14 | a0001c0007t0003g0044a0001c0007t0003g0119a0001c0007t0003g0181others(11): Show | 14 | HG00423.hp1 HG02074.hp1 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.1555+963A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96473718 | ||||||
| chr14:96473842
|
C | T | 4 | a0001c0001t0006g0235a0001c0006t0006g0009a0004c0004t0006g0148others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1555+1087C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96473842 | ||||||
| chr14:96473916
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1555+1161C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96473916 | ||||||
| chr14:96474146
|
A | T | 1 | a0002c0002t0002g0149 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1555+1391A>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96474146 | ||||||
| chr14:96474239
|
A | G | 10 | a0001c0001t0001g0294a0001c0001t0002g0067a0001c0001t0002g0068others(7): Show | 10 | HG01891.hp2 HG02572.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1555+1484A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96474239 | ||||||
| chr14:96474446
|
T | TA | 38 | a0001c0001t0001g0037a0001c0001t0001g0091a0001c0001t0001g0207others(35): Show | 38 | HG00423.hp1 HG01243.hp1 HG01261.hp1 others(35): Show |
intron_variant | MODIFIER | c.1555+1712dupA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr14 | 96474446 | |||||
| chr14:96474446
|
TA | T | 6 | a0001c0001t0001g0072a0001c0001t0001g0122a0001c0001t0001g0232others(3): Show | 6 | HG02738.hp2 HG03704.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.1555+1712delA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr14 | 96474446 | |||||
| chr14:96474593
|
C | T | 5 | a0001c0001t0002g0286a0002c0016t0002g0013a0003c0009t0002g0165others(2): Show | 5 | HG02970.hp2 HG02976.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1555+1838C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96474593 | ||||||
| chr14:96474747
|
C | T | 1 | a0001c0001t0002g0248 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1555+1992C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96474747 | ||||||
| chr14:96475002
|
G | C | 1 | a0001c0001t0002g0280 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1555+2247G>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96475002 | ||||||
| chr14:96475153
|
C | A | 1 | a0002c0002t0005g0059 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1555+2398C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96475153 | ||||||
| chr14:96475404
|
G | T | 2 | a0001c0001t0002g0114a0001c0001t0002g0267 | 2 | HG00738.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1555+2649G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96475404 | ||||||
| chr14:96475535
|
T | G | 13 | a0001c0001t0001g0313a0001c0001t0002g0145a0001c0001t0002g0159others(10): Show | 13 | HG02109.hp2 HG02451.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.1555+2780T>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96475535 | ||||||
| chr14:96475990
|
G | A | 5 | a0001c0001t0001g0105a0001c0001t0006g0235a0001c0006t0006g0009others(2): Show | 5 | HG02895.hp1 HG02896.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1556-2475G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96475990 | ||||||
| chr14:96475990
|
GA | G | 302 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(299): Show | 302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.1556-2464delA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr14 | 96475990 | |||||
| chr14:96475991
|
A | G | 6 | a0001c0001t0001g0105a0001c0001t0006g0235a0001c0006t0006g0009others(3): Show | 6 | HG02895.hp1 HG02896.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1556-2474A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96475991 | ||||||
| chr14:96476139
|
T | C | 13 | a0001c0001t0001g0313a0001c0001t0002g0145a0001c0001t0002g0159others(10): Show | 13 | HG02109.hp2 HG02451.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.1556-2326T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96476139 | ||||||
| chr14:96476341
|
A | G | 2 | a0001c0001t0008g0279a0002c0002t0001g0162 | 2 | HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1556-2124A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96476341 | ||||||
| chr14:96476462
|
G | A | 2 | a0001c0001t0001g0232a0001c0001t0001g0289 | 2 | NA18959.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.1556-2003G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96476462 | ||||||
| chr14:96476505
|
C | CA | 14 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0097others(11): Show | 14 | HG01109.hp2 HG01255.hp2 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.1556-1941dupA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr14 | 96476505 | |||||
| chr14:96476505
|
CA | C | 91 | a0001c0001t0001g0014a0001c0001t0001g0099a0001c0001t0001g0100others(88): Show | 91 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.1556-1941delA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr14 | 96476505 | |||||
| chr14:96476523
|
A | C | 11 | a0001c0001t0001g0313a0001c0001t0002g0145a0001c0001t0002g0163others(8): Show | 11 | HG02109.hp2 HG02451.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.1556-1942A>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96476523 | ||||||
| chr14:96476859
|
G | A | 1 | a0001c0001t0001g0018 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1556-1606G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96476859 | ||||||
| chr14:96477086
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1556-1379A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96477086 | ||||||
| chr14:96477153
|
T | G | 1 | a0003c0005t0003g0212 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1556-1312T>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96477153 | ||||||
| chr14:96477187
|
G | T | 1 | a0001c0001t0001g0236 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1556-1278G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96477187 | ||||||
| chr14:96477283
|
G | A | 3 | a0001c0001t0002g0219a0002c0002t0002g0175a0005c0013t0002g0102 | 3 | HG00544.hp2 NA18941.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1556-1182G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96477283 | ||||||
| chr14:96477322
|
T | G | 1 | a0003c0005t0003g0212 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1556-1143T>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96477322 | ||||||
| chr14:96477640
|
T | A | 11 | a0001c0001t0001g0313a0001c0001t0002g0145a0001c0001t0002g0163others(8): Show | 11 | HG02109.hp2 HG02451.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.1556-825T>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96477640 | ||||||
| chr14:96477706
|
A | G | 1 | a0001c0001t0002g0237 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1556-759A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96477706 | ||||||
| chr14:96478030
|
A | G | 1 | a0001c0001t0001g0129 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1556-435A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96478030 | ||||||
| chr14:96478192
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1556-273G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96478192 | ||||||
| chr14:96478246
|
A | T | 1 | a0001c0001t0001g0130 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1556-219A>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96478246 | ||||||
| chr14:96478254
|
C | G | 5 | a0001c0001t0001g0160a0001c0006t0004g0010a0004c0004t0001g0070others(2): Show | 5 | HG00642.hp2 HG01255.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1556-211C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96478254 | ||||||
| chr14:96478341
|
T | C | 1 | a0002c0002t0004g0020 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1556-124T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96478341 | ||||||
| chr14:96478396
|
C | A | 1 | a0001c0001t0002g0305 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1556-69C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 14/17 | chr14 | 96478396 | ||||||
| chr14:96478728
|
G | C | 1 | a0001c0001t0001g0089 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1753+66G>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96478728 | ||||||
| chr14:96478745
|
G | C | 13 | a0001c0001t0001g0313a0001c0001t0002g0145a0001c0001t0002g0159others(10): Show | 13 | HG02109.hp2 HG02451.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.1753+83G>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96478745 | ||||||
| chr14:96478831
|
G | A | 2 | a0002c0002t0001g0184a0002c0002t0004g0020 | 2 | NA18943.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1753+169G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96478831 | ||||||
| chr14:96478907
|
C | CT | 29 | a0001c0001t0001g0313a0001c0001t0002g0145a0001c0001t0002g0159others(26): Show | 29 | HG00423.hp1 HG02074.hp1 HG02109.hp2 others(26): Show |
intron_variant | MODIFIER | c.1753+259dupT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr14 | 96478907 | |||||
| chr14:96478940
|
G | C | 4 | a0001c0001t0006g0235a0001c0006t0006g0009a0004c0004t0006g0148others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1753+278G>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96478940 | ||||||
| chr14:96479001
|
C | T | 2 | a0003c0003t0001g0101a0012c0018t0001g0111 | 2 | HG01358.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1753+339C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96479001 | ||||||
| chr14:96479046
|
C | T | 1 | a0003c0003t0002g0234 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1753+384C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96479046 | ||||||
| chr14:96479075
|
A | T | 3 | a0001c0001t0001g0018a0002c0002t0001g0116a0002c0002t0001g0253 | 3 | HG01106.hp1 HG03831.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1753+413A>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96479075 | ||||||
| chr14:96479111
|
C | T | 4 | a0001c0001t0006g0235a0001c0006t0006g0009a0004c0004t0006g0148others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1753+449C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96479111 | ||||||
| chr14:96479163
|
G | A | 66 | a0001c0001t0001g0014a0001c0001t0001g0099a0001c0001t0001g0100others(63): Show | 66 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.1753+501G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96479163 | ||||||
| chr14:96479233
|
T | C | 195 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0034others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.1753+571T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96479233 | ||||||
| chr14:96479296
|
C | T | 2 | a0001c0001t0008g0279a0002c0002t0001g0162 | 2 | HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1753+634C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96479296 | ||||||
| chr14:96479323
|
C | T | 1 | a0001c0001t0001g0014 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1753+661C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96479323 | ||||||
| chr14:96479347
|
G | A | 2 | a0001c0001t0001g0069a0004c0004t0001g0164 | 2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1753+685G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96479347 | ||||||
| chr14:96479372
|
T | G | 4 | a0001c0001t0001g0017a0001c0001t0001g0034a0002c0002t0001g0046others(1): Show | 4 | HG00099.hp2 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1753+710T>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96479372 | ||||||
| chr14:96479385
|
C | CT | 88 | a0001c0001t0001g0014a0001c0001t0001g0099a0001c0001t0001g0100others(85): Show | 88 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.1753+739dupT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr14 | 96479385 | |||||
| chr14:96479385
|
C | CTT | 16 | a0001c0001t0001g0150a0001c0001t0002g0145a0001c0001t0002g0159others(13): Show | 16 | HG02109.hp2 HG02451.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.1753+738_1753+739d others(4): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr14 | 96479385 | |||||
| chr14:96479400
|
T | C | 1 | a0001c0001t0001g0017 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1753+738T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96479400 | ||||||
| chr14:96479483
|
T | C | 6 | a0001c0001t0001g0133a0001c0001t0001g0249a0001c0001t0001g0251others(3): Show | 6 | HG01167.hp1 HG02280.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1753+821T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96479483 | ||||||
| chr14:96479496
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1753+834C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96479496 | ||||||
| chr14:96479782
|
G | A | 14 | a0001c0007t0003g0044a0001c0007t0003g0119a0001c0007t0003g0181others(11): Show | 14 | HG00423.hp1 HG02074.hp1 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.1753+1120G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96479782 | ||||||
| chr14:96479805
|
C | T | 2 | a0001c0001t0002g0114a0001c0001t0002g0267 | 2 | HG00738.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1753+1143C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96479805 | ||||||
| chr14:96479868
|
C | T | 17 | a0001c0001t0001g0014a0001c0001t0001g0099a0001c0001t0001g0100others(14): Show | 17 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1753+1206C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96479868 | ||||||
| chr14:96479879
|
A | G | 1 | a0002c0014t0003g0058 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1753+1217A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96479879 | ||||||
| chr14:96479909
|
G | GGA | 74 | a0001c0001t0001g0014a0001c0001t0001g0099a0001c0001t0001g0100others(71): Show | 74 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.1753+1249_1753+125 others(6): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr14 | 96479909 | |||||
| chr14:96479997
|
T | C | 1 | a0005c0008t0003g0274 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1753+1335T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96479997 | ||||||
| chr14:96480115
|
G | A | 17 | a0001c0001t0001g0014a0001c0001t0001g0099a0001c0001t0001g0100others(14): Show | 17 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1753+1453G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96480115 | ||||||
| chr14:96480126
|
C | T | 16 | a0001c0001t0001g0294a0001c0001t0002g0067a0001c0001t0002g0068others(13): Show | 16 | HG01109.hp1 HG01891.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1753+1464C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96480126 | ||||||
| chr14:96480142
|
A | T | 1 | a0001c0001t0001g0290 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1753+1480A>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96480142 | ||||||
| chr14:96480173
|
T | C | 2 | a0001c0001t0001g0069a0004c0004t0001g0164 | 2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1753+1511T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96480173 | ||||||
| chr14:96480187
|
A | G | 11 | a0001c0001t0001g0313a0001c0001t0002g0145a0001c0001t0002g0163others(8): Show | 11 | HG02109.hp2 HG02451.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.1753+1525A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96480187 | ||||||
| chr14:96480437
|
A | G | 2 | a0001c0001t0008g0279a0002c0002t0001g0162 | 2 | HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1753+1775A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96480437 | ||||||
| chr14:96480493
|
C | T | 27 | a0001c0001t0002g0031a0001c0001t0002g0040a0001c0001t0002g0045others(24): Show | 27 | HG00099.hp1 HG00544.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.1753+1831C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96480493 | ||||||
| chr14:96480603
|
A | G | 3 | a0002c0002t0001g0053a0002c0002t0001g0054a0002c0002t0001g0242 | 3 | HG03017.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1753+1941A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96480603 | ||||||
| chr14:96480880
|
G | A | 1 | a0001c0001t0002g0307 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1754-2119G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96480880 | ||||||
| chr14:96480905
|
C | G | 4 | a0001c0001t0001g0197a0001c0001t0001g0299a0001c0001t0001g0315others(1): Show | 4 | HG02698.hp2 HG03017.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1754-2094C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96480905 | ||||||
| chr14:96481177
|
A | C | 1 | a0001c0001t0001g0250 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1754-1822A>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96481177 | ||||||
| chr14:96481520
|
G | A | 109 | a0001c0001t0001g0014a0001c0001t0001g0099a0001c0001t0001g0100others(106): Show | 109 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.1754-1479G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96481520 | ||||||
| chr14:96481597
|
C | T | 42 | a0001c0001t0001g0189a0001c0001t0002g0031a0001c0001t0002g0040others(39): Show | 42 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.1754-1402C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96481597 | ||||||
| chr14:96481626
|
G | A | 42 | a0001c0001t0001g0189a0001c0001t0002g0031a0001c0001t0002g0040others(39): Show | 42 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.1754-1373G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96481626 | ||||||
| chr14:96481664
|
C | A | 1 | a0002c0002t0002g0002 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1754-1335C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96481664 | ||||||
| chr14:96481695
|
G | A | 3 | a0001c0001t0001g0122a0001c0001t0001g0290a0001c0001t0002g0113 | 3 | HG02486.hp2 HG03704.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1754-1304G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96481695 | ||||||
| chr14:96481697
|
C | T | 1 | a0002c0002t0005g0059 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1754-1302C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96481697 | ||||||
| chr14:96481704
|
C | CT | 38 | a0001c0001t0001g0014a0001c0001t0001g0099a0001c0001t0001g0100others(35): Show | 38 | HG00323.hp2 HG00639.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.1754-1277dupT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr14 | 96481704 | |||||
| chr14:96481704
|
C | CTT | 7 | a0001c0001t0001g0313a0001c0001t0002g0163a0001c0001t0002g0285others(4): Show | 7 | HG02717.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1754-1278_1754-127 others(6): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr14 | 96481704 | |||||
| chr14:96481704
|
CT | C | 8 | a0001c0001t0002g0123a0001c0001t0002g0286a0002c0002t0002g0149others(5): Show | 8 | HG00642.hp1 HG01517.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1754-1277delT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr14 | 96481704 | |||||
| chr14:96481760
|
A | G | 16 | a0001c0001t0001g0294a0001c0001t0002g0067a0001c0001t0002g0068others(13): Show | 16 | HG01109.hp1 HG01891.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1754-1239A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96481760 | ||||||
| chr14:96481798
|
G | C | 17 | a0001c0001t0001g0014a0001c0001t0001g0099a0001c0001t0001g0100others(14): Show | 17 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1754-1201G>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96481798 | ||||||
| chr14:96481928
|
C | A | 42 | a0001c0001t0001g0189a0001c0001t0002g0031a0001c0001t0002g0040others(39): Show | 42 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.1754-1071C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96481928 | ||||||
| chr14:96481986
|
A | G | 118 | a0001c0001t0001g0014a0001c0001t0001g0099a0001c0001t0001g0100others(115): Show | 118 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1754-1013A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96481986 | ||||||
| chr14:96482193
|
T | G | 1 | a0001c0001t0002g0219 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1754-806T>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96482193 | ||||||
| chr14:96482267
|
G | A | 62 | a0001c0001t0001g0014a0001c0001t0001g0099a0001c0001t0001g0100others(59): Show | 62 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.1754-732G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96482267 | ||||||
| chr14:96482301
|
C | T | 13 | a0001c0001t0001g0313a0001c0001t0002g0145a0001c0001t0002g0159others(10): Show | 13 | HG02109.hp2 HG02451.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.1754-698C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96482301 | ||||||
| chr14:96482912
|
C | T | 9 | a0001c0001t0001g0294a0001c0001t0002g0067a0001c0001t0002g0068others(6): Show | 9 | HG01891.hp2 HG02572.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1754-87C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 15/17 | chr14 | 96482912 | ||||||
| chr14:96483410
|
GT | G | 18 | a0001c0001t0006g0235a0001c0006t0006g0009a0001c0007t0003g0044others(15): Show | 18 | HG00423.hp1 HG02074.hp1 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.1974+204delT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr14 | 96483410 | |||||
| chr14:96483438
|
T | C | 3 | a0001c0001t0002g0171a0002c0002t0002g0169a0009c0011t0002g0007 | 3 | HG02451.hp2 HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1974+219T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | chr14 | 96483438 | ||||||
| chr14:96483514
|
C | T | 2 | a0001c0001t0001g0132a0001c0001t0002g0145 | 2 | HG01358.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1974+295C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | chr14 | 96483514 | ||||||
| chr14:96483515
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1974+296G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | chr14 | 96483515 | ||||||
| chr14:96483582
|
C | T | 3 | a0002c0002t0001g0012a0002c0002t0001g0152a0002c0002t0001g0308 | 3 | HG02630.hp2 HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1974+363C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | chr14 | 96483582 | ||||||
| chr14:96483691
|
G | T | 1 | a0001c0001t0001g0091 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1974+472G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | chr14 | 96483691 | ||||||
| chr14:96483720
|
C | T | 6 | a0001c0001t0001g0133a0001c0001t0001g0249a0001c0001t0001g0251others(3): Show | 6 | HG01167.hp1 HG02280.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1974+501C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | chr14 | 96483720 | ||||||
| chr14:96483785
|
G | A | 9 | a0001c0001t0001g0294a0001c0001t0002g0067a0001c0001t0002g0068others(6): Show | 9 | HG01891.hp2 HG02572.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1974+566G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | chr14 | 96483785 | ||||||
| chr14:96483990
|
G | C | 3 | a0001c0001t0002g0171a0002c0002t0002g0169a0009c0011t0002g0007 | 3 | HG02451.hp2 HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1974+771G>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | chr14 | 96483990 | ||||||
| chr14:96483994
|
G | C | 70 | a0001c0001t0001g0014a0001c0001t0001g0099a0001c0001t0001g0100others(67): Show | 70 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1974+775G>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | chr14 | 96483994 | ||||||
| chr14:96484149
|
G | A | 17 | a0001c0001t0001g0014a0001c0001t0001g0099a0001c0001t0001g0100others(14): Show | 17 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1974+930G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | chr14 | 96484149 | ||||||
| chr14:96484302
|
C | G | 2 | a0001c0001t0001g0133a0002c0002t0001g0167 | 2 | HG02280.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1974+1083C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | chr14 | 96484302 | ||||||
| chr14:96484394
|
C | T | 3 | a0001c0001t0005g0065a0001c0001t0005g0258a0001c0001t0010g0260 | 3 | HG02896.hp2 HG02897.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1974+1175C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | chr14 | 96484394 | ||||||
| chr14:96484710
|
T | G | 1 | a0002c0002t0002g0178 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1974+1491T>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | chr14 | 96484710 | ||||||
| chr14:96485154
|
T | C | 2 | a0001c0001t0001g0069a0004c0004t0001g0164 | 2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1975-1744T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | chr14 | 96485154 | ||||||
| chr14:96485424
|
G | C | 1 | a0001c0001t0001g0034 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1975-1474G>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | chr14 | 96485424 | ||||||
| chr14:96485442
|
G | T | 1 | a0001c0001t0001g0247 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1975-1456G>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | chr14 | 96485442 | ||||||
| chr14:96485754
|
T | C | 2 | a0001c0001t0001g0236a0001c0001t0001g0241 | 2 | HG02015.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.1975-1144T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | chr14 | 96485754 | ||||||
| chr14:96485776
|
A | G | 9 | a0001c0001t0001g0294a0001c0001t0002g0067a0001c0001t0002g0068others(6): Show | 9 | HG01891.hp2 HG02572.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1975-1122A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | chr14 | 96485776 | ||||||
| chr14:96485794
|
C | CT | 22 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0032others(19): Show | 22 | HG00558.hp2 HG01243.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.1975-1085dupT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr14 | 96485794 | |||||
| chr14:96485794
|
CT | C | 94 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0037others(91): Show | 94 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.1975-1085delT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr14 | 96485794 | |||||
| chr14:96485794
|
CTT | C | 6 | a0001c0001t0001g0313a0001c0001t0002g0286a0002c0016t0002g0013others(3): Show | 6 | HG02970.hp2 HG02976.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1975-1086_1975-108 others(6): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr14 | 96485794 | |||||
| chr14:96485886
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1975-1012C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | chr14 | 96485886 | ||||||
| chr14:96486073
|
C | T | 1 | a0001c0001t0008g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1975-825C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | chr14 | 96486073 | ||||||
| chr14:96486076
|
G | A | 1 | a0006c0021t0003g0314 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1975-822G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | chr14 | 96486076 | ||||||
| chr14:96486165
|
G | C | 4 | a0001c0001t0002g0040a0001c0001t0002g0075a0001c0001t0002g0093others(1): Show | 4 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1975-733G>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | chr14 | 96486165 | ||||||
| chr14:96486204
|
C | G | 5 | a0001c0001t0002g0286a0002c0016t0002g0013a0003c0009t0002g0165others(2): Show | 5 | HG02970.hp2 HG02976.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1975-694C>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | chr14 | 96486204 | ||||||
| chr14:96486261
|
C | T | 2 | a0001c0007t0003g0181a0001c0007t0003g0191 | 2 | HG02074.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.1975-637C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | chr14 | 96486261 | ||||||
| chr14:96486382
|
C | T | 9 | a0001c0001t0001g0294a0001c0001t0002g0067a0001c0001t0002g0068others(6): Show | 9 | HG01891.hp2 HG02572.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1975-516C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | chr14 | 96486382 | ||||||
| chr14:96486610
|
T | G | 2 | a0001c0001t0002g0093a0001c0001t0002g0094 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1975-288T>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | chr14 | 96486610 | ||||||
| chr14:96486627
|
A | G | 1 | a0001c0001t0001g0301 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1975-271A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | chr14 | 96486627 | ||||||
| chr14:96486637
|
C | CTT | 10 | a0001c0001t0001g0072a0001c0001t0001g0294a0001c0001t0002g0067others(7): Show | 10 | HG01891.hp2 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1975-247_1975-246d others(4): Show |
AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr14 | 96486637 | |||||
| chr14:96486637
|
CT | C | 17 | a0001c0001t0001g0014a0001c0001t0001g0099a0001c0001t0001g0100others(14): Show | 17 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1975-246delT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr14 | 96486637 | |||||
| chr14:96486739
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1975-159A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 16/17 | chr14 | 96486739 | ||||||
| chr14:96487075
|
A | T | 16 | a0001c0001t0001g0069a0001c0007t0003g0044a0001c0007t0003g0119others(13): Show | 16 | HG00423.hp1 HG02074.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.2133+19A>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 17/17 | chr14 | 96487075 | ||||||
| chr14:96487111
|
A | G | 1 | a0001c0001t0008g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2133+55A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 17/17 | chr14 | 96487111 | ||||||
| chr14:96487147
|
A | G | 113 | a0001c0001t0001g0014a0001c0001t0001g0069a0001c0001t0001g0099others(110): Show | 113 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.2133+91A>G | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 17/17 | chr14 | 96487147 | ||||||
| chr14:96487219
|
C | CA | 22 | a0001c0001t0001g0041a0001c0001t0001g0108a0001c0001t0001g0160others(19): Show | 22 | HG00639.hp2 HG00741.hp2 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.2133+179dupA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr14 | 96487219 | |||||
| chr14:96487236
|
T | A | 1 | a0002c0002t0001g0167 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2133+180T>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 17/17 | chr14 | 96487236 | ||||||
| chr14:96487255
|
C | T | 1 | a0001c0001t0001g0304 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2133+199C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 17/17 | chr14 | 96487255 | ||||||
| chr14:96487258
|
G | A | 1 | a0003c0003t0002g0234 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2133+202G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 17/17 | chr14 | 96487258 | ||||||
| chr14:96487299
|
G | A | 1 | a0003c0003t0002g0033 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2133+243G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 17/17 | chr14 | 96487299 | ||||||
| chr14:96487383
|
C | CA | 26 | a0001c0001t0001g0029a0001c0001t0001g0087a0001c0001t0001g0100others(23): Show | 26 | HG01070.hp1 HG01099.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.2133+344dupA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr14 | 96487383 | |||||
| chr14:96487383
|
CA | C | 92 | a0001c0001t0001g0015a0001c0001t0001g0032a0001c0001t0001g0041others(89): Show | 92 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.2133+344delA | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr14 | 96487383 | |||||
| chr14:96487388
|
A | C | 1 | a0013c0017t0001g0316 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2133+332A>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 17/17 | chr14 | 96487388 | ||||||
| chr14:96487411
|
G | A | 2 | a0001c0001t0001g0115a0001c0001t0001g0223 | 2 | HG00280.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.2133+355G>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 17/17 | chr14 | 96487411 | ||||||
| chr14:96487424
|
G | C | 1 | a0001c0001t0001g0086 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2133+368G>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 17/17 | chr14 | 96487424 | ||||||
| chr14:96487432
|
C | CT | 16 | a0001c0001t0001g0032a0001c0001t0001g0313a0001c0001t0002g0145others(13): Show | 16 | HG02109.hp2 HG02451.hp2 HG02683.hp1 others(13): Show |
intron_variant | MODIFIER | c.2133+391dupT | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr14 | 96487432 | |||||
| chr14:96487439
|
T | C | 1 | a0001c0001t0001g0281 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2133+383T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 17/17 | chr14 | 96487439 | ||||||
| chr14:96487836
|
C | T | 1 | a0001c0001t0001g0207 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2134-469C>T | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 17/17 | chr14 | 96487836 | ||||||
| chr14:96488037
|
C | A | 2 | a0001c0001t0001g0189a0001c0001t0002g0222 | 2 | HG00323.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.2134-268C>A | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 17/17 | chr14 | 96488037 | ||||||
| chr14:96488262
|
T | C | 4 | a0001c0001t0006g0235a0001c0006t0006g0009a0004c0004t0006g0148others(1): Show | 4 | HG02895.hp1 HG02896.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2134-43T>C | AK7 | ENSG00000140057.9 | transcript | ENST00000267584.9 | protein_coding | 17/17 | chr14 | 96488262 |