| geneid | 161436 |
|---|---|
| ensemblid | ENSG00000165521.16 |
| hgncid | 18197 |
| symbol | EML5 |
| name | EMAP like 5 |
| refseq_nuc | NM_183387.3 |
| refseq_prot | NP_899243.1 |
| ensembl_nuc | ENST00000554922.6 |
| ensembl_prot | ENSP00000451998.1 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 88612431 |
| end | 88792953 |
| strand | - |
| ver | v1.2 |
| region | chr14:88612431-88792953 |
| region5000 | chr14:88607431-88797953 |
| regionname0 | EML5_chr14_88612431_88792953 |
| regionname5000 | EML5_chr14_88607431_88797953 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1977 | 235 | 73 | 43 | 77 | 11 | 29 | 61 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0002 | 0/0 | 1977 | 85 | 8 | 22 | 44 | 4 | 7 | 32 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0003 | 0/0 | 1977 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0004 | 0/0 | 1977 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0005 | 0/0 | 1977 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0006 | 0/0 | 1977 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0007 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0008 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0009 | 0/0 | 1977 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0010 | 0/0 | 1977 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0011 | 0/0 | 1977 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 5934 | 200 | 53 | 41 | 70 | 11 | 23 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| c0002 | 0/0 | 5934 | 80 | 8 | 19 | 44 | 3 | 6 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| c0003 | 0/0 | 5934 | 32 | 19 | 0 | 7 | 0 | 6 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| c0004 | 0/0 | 5934 | 5 | 0 | 3 | 0 | 1 | 1 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| c0005 | 0/0 | 5934 | 3 | 3 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| c0006 | 0/0 | 5934 | 2 | 0 | 2 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| c0007 | 0/0 | 5934 | 2 | 0 | 0 | 2 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| c0008 | 0/0 | 5934 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| c0009 | 0/0 | 5934 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| c0010 | 0/0 | 5934 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| c0011 | 0/0 | 5934 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| c0012 | 0/0 | 5934 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| c0013 | 0/0 | 5934 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| c0014 | 0/0 | 5934 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| c0015 | 0/0 | 5934 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 3838 | 71 | 6 | 18 | 37 | 4 | 6 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0002 | 0/0 | 3837 | 69 | 9 | 16 | 35 | 3 | 6 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0003 | 0/0 | 3838 | 55 | 13 | 11 | 17 | 1 | 13 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0004 | 0/0 | 3848 | 24 | 14 | 0 | 5 | 0 | 5 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0005 | 0/0 | 3837 | 17 | 0 | 2 | 14 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0006 | 0/0 | 3837 | 14 | 6 | 4 | 2 | 2 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0007 | 0/1 | 3839 | 13 | 1 | 5 | 0 | 4 | 2 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0008 | 0/0 | 3837 | 7 | 7 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0009 | 0/0 | 3839 | 5 | 0 | 4 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0010 | 0/0 | 3837 | 4 | 0 | 0 | 4 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0011 | 0/0 | 3837 | 4 | 4 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0012 | 0/0 | 3847 | 4 | 0 | 0 | 4 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0013 | 0/0 | 3848 | 4 | 4 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0014 | 0/0 | 3838 | 3 | 3 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0015 | 0/0 | 3837 | 3 | 3 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0016 | 0/0 | 3837 | 2 | 0 | 0 | 2 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0017 | 0/0 | 3836 | 2 | 2 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0018 | 1/0 | 3838 | 2 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0019 | 0/0 | 3837 | 2 | 2 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0020 | 0/0 | 3838 | 2 | 0 | 0 | 2 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0021 | 0/0 | 3838 | 2 | 0 | 2 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0022 | 0/0 | 3834 | 2 | 2 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0023 | 0/0 | 3835 | 2 | 2 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0024 | 0/0 | 3834 | 2 | 2 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0025 | 0/0 | 3837 | 2 | 0 | 0 | 2 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0026 | 0/0 | 3837 | 2 | 2 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0027 | 0/0 | 3837 | 2 | 1 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0028 | 0/0 | 3838 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0029 | 0/0 | 3837 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0030 | 0/0 | 3837 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0031 | 0/0 | 3839 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0032 | 0/0 | 3838 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0033 | 0/0 | 3878 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0034 | 0/0 | 3838 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0035 | 0/0 | 3835 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0036 | 0/0 | 3834 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0037 | 0/0 | 3838 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| t0038 | 0/0 | 3838 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| 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 | 2 | 0 | 2 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0075 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0078 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 5934 | 200 | 53 | 41 | 70 | 11 | 23 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0003 | 0/0 | 5934 | 32 | 19 | 0 | 7 | 0 | 6 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0006 | 0/0 | 5934 | 2 | 0 | 2 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0009 | 0/0 | 5934 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0002c0002 | 0/0 | 5934 | 80 | 8 | 19 | 44 | 3 | 6 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0002c0004 | 0/0 | 5934 | 5 | 0 | 3 | 0 | 1 | 1 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0003c0005 | 0/0 | 5934 | 3 | 3 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0004c0007 | 0/0 | 5934 | 2 | 0 | 0 | 2 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0005c0014 | 0/0 | 5934 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0006c0008 | 0/0 | 5934 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0007c0010 | 0/0 | 5934 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0008c0011 | 0/0 | 5934 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0009c0012 | 0/0 | 5934 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0010c0013 | 0/0 | 5934 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0011c0015 | 0/0 | 5934 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 9771 | 7 | 4 | 1 | 0 | 0 | 2 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0001t0002 | 0/0 | 9770 | 68 | 8 | 16 | 35 | 3 | 6 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0001t0003 | 0/0 | 9771 | 35 | 6 | 6 | 11 | 1 | 11 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0001t0005 | 0/0 | 9770 | 17 | 0 | 2 | 14 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0001t0006 | 0/0 | 9770 | 12 | 5 | 4 | 1 | 2 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0001t0007 | 0/1 | 9772 | 11 | 1 | 4 | 0 | 4 | 1 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0001t0008 | 0/0 | 9770 | 6 | 6 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0001t0009 | 0/0 | 9772 | 5 | 0 | 4 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0001t0010 | 0/0 | 9770 | 4 | 0 | 0 | 4 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0001t0011 | 0/0 | 9770 | 4 | 4 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0001t0012 | 0/0 | 9780 | 4 | 0 | 0 | 4 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0001t0014 | 0/0 | 9771 | 3 | 3 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0001t0017 | 0/0 | 9769 | 2 | 2 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0001t0018 | 1/0 | 9771 | 1 | 0 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0001t0019 | 0/0 | 9770 | 2 | 2 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0001t0022 | 0/0 | 9767 | 2 | 2 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0001t0023 | 0/0 | 9768 | 2 | 2 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0001t0024 | 0/0 | 9767 | 2 | 2 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0001t0025 | 0/0 | 9770 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0001t0026 | 0/0 | 9770 | 2 | 2 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0001t0027 | 0/0 | 9770 | 2 | 1 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0001t0028 | 0/0 | 9771 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0001t0029 | 0/0 | 9770 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0001t0030 | 0/0 | 9770 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0001t0031 | 0/0 | 9772 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0001t0032 | 0/0 | 9771 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0001t0034 | 0/0 | 9771 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0001t0035 | 0/0 | 9768 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0001t0036 | 0/0 | 9767 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0003t0002 | 0/0 | 9770 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0003t0004 | 0/0 | 9781 | 24 | 14 | 0 | 5 | 0 | 5 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0003t0006 | 0/0 | 9770 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0003t0013 | 0/0 | 9781 | 3 | 3 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0003t0018 | 0/0 | 9771 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0003t0020 | 0/0 | 9771 | 2 | 0 | 0 | 2 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0006t0003 | 0/0 | 9771 | 2 | 0 | 2 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0001c0009t0013 | 0/0 | 9781 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0002c0002t0001 | 0/0 | 9771 | 57 | 2 | 14 | 36 | 2 | 3 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0002c0002t0003 | 0/0 | 9771 | 16 | 6 | 3 | 5 | 0 | 2 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0002c0002t0006 | 0/0 | 9770 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0002c0002t0007 | 0/0 | 9772 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0002c0002t0021 | 0/0 | 9771 | 2 | 0 | 2 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0002c0002t0033 | 0/0 | 9811 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0002c0002t0037 | 0/0 | 9771 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0002c0002t0038 | 0/0 | 9771 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0002c0004t0001 | 0/0 | 9771 | 5 | 0 | 3 | 0 | 1 | 1 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0003c0005t0015 | 0/0 | 9770 | 3 | 3 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0004c0007t0016 | 0/0 | 9770 | 2 | 0 | 0 | 2 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0005c0014t0001 | 0/0 | 9771 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0006c0008t0025 | 0/0 | 9770 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0007c0010t0003 | 0/0 | 9771 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0008c0011t0008 | 0/0 | 9770 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0009c0012t0001 | 0/0 | 9771 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0010c0013t0003 | 0/0 | 9771 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| a0011c0015t0007 | 0/0 | 9772 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | copy fasta | chr14 | 88607431 | 88797953 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0005g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0005g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0005g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0005g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0005g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0005g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0005g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0005g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0005g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0005g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0005g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0005g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0005g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0006g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0006g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0006g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0006g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0006g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0006g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0006g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0006g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0007g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0007g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0007g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0007g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0007g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0007g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0007g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0007g0078 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0007g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0007g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0007g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0008g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0008g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0008g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0008g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0008g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0008g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0009g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0009g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0009g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0009g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0009g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0010g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0010g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0010g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0010g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0011g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0011g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0011g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0011g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0012g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0012g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0012g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0012g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0014g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0014g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0014g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0017g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0017g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0018g0075 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0019g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0019g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0022g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0022g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0023g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0023g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0024g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0024g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0025g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0026g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0026g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0027g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0027g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0028g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0029g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0030g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0031g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0032g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0034g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0035g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0001t0036g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0003t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0003t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0003t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0003t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0003t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0003t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0003t0004g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0003t0004g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0003t0004g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0003t0004g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0003t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0003t0004g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0003t0004g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0003t0004g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0003t0004g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0003t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0003t0004g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0003t0004g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0003t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0003t0004g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0003t0004g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0003t0004g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0003t0004g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0003t0004g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0003t0004g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0003t0006g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0003t0013g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0003t0013g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0003t0013g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0003t0018g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0003t0020g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0003t0020g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0006t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0006t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0001c0009t0013g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0006g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0007g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0021g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0021g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0033g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0037g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0002t0038g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0004t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0004t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0004t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0004t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0002c0004t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0003c0005t0015g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0003c0005t0015g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0003c0005t0015g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0004c0007t0016g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0004c0007t0016g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0005c0014t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0006c0008t0025g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0007c0010t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0008c0011t0008g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0009c0012t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0010c0013t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| a0011c0015t0007g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0007 | g0065 | EUR | GBR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG00099 | hp2 | a0002 | c0004 | t0001 | g0241 | EUR | GBR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0156 | EUR | FIN | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0276 | EUR | FIN | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG00323 | hp1 | a0002 | c0002 | t0038 | g0297 | EUR | FIN | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG00323 | hp2 | a0001 | c0001 | t0007 | g0085 | EUR | FIN | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG00408 | hp1 | a0001 | c0003 | t0004 | g0319 | EAS | CHS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | CHS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG00423 | hp1 | a0001 | c0001 | t0005 | g0175 | EAS | CHS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | CHS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0249 | EAS | CHS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | CHS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG00544 | hp1 | a0001 | c0001 | t0010 | g0034 | EAS | CHS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0277 | EAS | CHS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG00609 | hp1 | a0001 | c0001 | t0012 | g0326 | EAS | CHS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0279 | EAS | CHS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0275 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG00639 | hp2 | a0001 | c0001 | t0007 | g0038 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG00642 | hp2 | a0001 | c0001 | t0027 | g0296 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG00673 | hp1 | a0001 | c0001 | t0005 | g0181 | EAS | CHS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0200 | EAS | CHS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG00733 | hp1 | a0002 | c0002 | t0021 | g0292 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0063 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG00738 | hp1 | a0001 | c0001 | t0009 | g0058 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG00738 | hp2 | a0002 | c0002 | t0021 | g0273 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0166 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG00741 | hp2 | a0001 | c0001 | t0006 | g0284 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0163 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0258 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0259 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01071 | hp2 | a0001 | c0001 | t0007 | g0072 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01074 | hp1 | a0001 | c0006 | t0003 | g0162 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0246 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0274 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0243 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01109 | hp2 | a0001 | c0001 | t0030 | g0135 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0260 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01167 | hp2 | a0001 | c0001 | t0029 | g0157 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01168 | hp2 | a0002 | c0004 | t0001 | g0228 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01175 | hp2 | a0001 | c0006 | t0003 | g0161 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01243 | hp1 | a0001 | c0001 | t0036 | g0205 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0062 | AMR | PUR | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0209 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0056 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01256 | hp1 | a0001 | c0001 | t0007 | g0071 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01256 | hp2 | a0001 | c0001 | t0006 | g0286 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01257 | hp1 | a0001 | c0001 | t0006 | g0287 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0064 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0091 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0239 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01358 | hp2 | a0001 | c0001 | t0009 | g0076 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01361 | hp1 | a0002 | c0002 | t0003 | g0024 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0095 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0255 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0186 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0068 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0145 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01515 | hp1 | a0005 | c0014 | t0001 | g0272 | EUR | IBS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01515 | hp2 | a0001 | c0001 | t0006 | g0003 | EUR | IBS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01516 | hp1 | a0001 | c0001 | t0007 | g0069 | EUR | IBS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0113 | EUR | IBS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01517 | hp1 | a0001 | c0001 | t0006 | g0003 | EUR | IBS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0112 | EUR | IBS | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01884 | hp1 | a0001 | c0001 | t0017 | g0010 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01884 | hp2 | a0001 | c0001 | t0024 | g0206 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01891 | hp1 | a0002 | c0002 | t0003 | g0018 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01928 | hp2 | a0002 | c0002 | t0003 | g0026 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0238 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0256 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01943 | hp2 | a0001 | c0001 | t0009 | g0059 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01952 | hp2 | a0002 | c0002 | t0003 | g0027 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0257 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01975 | hp2 | a0001 | c0001 | t0005 | g0185 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01978 | hp1 | a0002 | c0004 | t0001 | g0240 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01993 | hp1 | a0001 | c0001 | t0009 | g0042 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02004 | hp1 | a0001 | c0001 | t0006 | g0285 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02015 | hp1 | a0001 | c0001 | t0005 | g0182 | EAS | KHV | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0271 | EAS | KHV | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02027 | hp1 | a0001 | c0001 | t0010 | g0032 | EAS | KHV | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | KHV | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02040 | hp1 | a0004 | c0007 | t0016 | g0008 | EAS | KHV | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0289 | EAS | KHV | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02055 | hp2 | a0001 | c0003 | t0004 | g0302 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0269 | EAS | KHV | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | KHV | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0278 | EAS | KHV | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02135 | hp2 | a0001 | c0003 | t0004 | g0320 | EAS | KHV | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02145 | hp1 | a0001 | c0001 | t0026 | g0294 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0208 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02165 | hp1 | a0010 | c0013 | t0003 | g0022 | EAS | CDX | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | CDX | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02257 | hp1 | a0001 | c0003 | t0004 | g0307 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0230 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0100 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0083 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02280 | hp1 | a0001 | c0001 | t0011 | g0214 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02280 | hp2 | a0001 | c0003 | t0004 | g0312 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02293 | hp1 | a0011 | c0015 | t0007 | g0079 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0245 | AMR | PEL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02451 | hp1 | a0003 | c0005 | t0015 | g0013 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02523 | hp1 | a0001 | c0001 | t0010 | g0033 | EAS | KHV | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02523 | hp2 | a0002 | c0002 | t0006 | g0237 | EAS | KHV | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02572 | hp1 | a0001 | c0003 | t0006 | g0221 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0165 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02602 | hp1 | a0001 | c0001 | t0005 | g0183 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0128 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02615 | hp1 | a0002 | c0002 | t0003 | g0029 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02615 | hp2 | a0001 | c0001 | t0011 | g0215 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0048 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02622 | hp2 | a0001 | c0003 | t0004 | g0306 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02630 | hp2 | a0001 | c0001 | t0011 | g0216 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02647 | hp2 | a0001 | c0001 | t0032 | g0077 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02683 | hp2 | a0001 | c0003 | t0004 | g0315 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02717 | hp1 | a0001 | c0003 | t0004 | g0314 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02717 | hp2 | a0001 | c0001 | t0014 | g0004 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02723 | hp1 | a0003 | c0005 | t0015 | g0015 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02723 | hp2 | a0001 | c0001 | t0011 | g0213 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0127 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02735 | hp2 | a0001 | c0003 | t0018 | g0016 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0051 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0036 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02809 | hp1 | a0001 | c0003 | t0004 | g0305 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02809 | hp2 | a0001 | c0003 | t0002 | g0012 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02818 | hp1 | a0002 | c0002 | t0003 | g0092 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02886 | hp1 | a0001 | c0001 | t0035 | g0196 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02886 | hp2 | a0001 | c0003 | t0013 | g0299 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02895 | hp1 | a0001 | c0003 | t0004 | g0303 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02895 | hp2 | a0001 | c0001 | t0008 | g0102 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02897 | hp1 | a0001 | c0003 | t0004 | g0304 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02897 | hp2 | a0001 | c0001 | t0008 | g0103 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02922 | hp1 | a0001 | c0003 | t0004 | g0309 | AFR | ESN | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02922 | hp2 | a0001 | c0001 | t0034 | g0198 | AFR | ESN | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02976 | hp1 | a0001 | c0001 | t0022 | g0203 | AFR | ESN | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | ESN | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03017 | hp1 | a0001 | c0003 | t0004 | g0317 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0164 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03041 | hp1 | a0001 | c0001 | t0022 | g0204 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03098 | hp1 | a0001 | c0003 | t0013 | g0300 | AFR | MSL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03098 | hp2 | a0001 | c0001 | t0017 | g0011 | AFR | MSL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03130 | hp1 | a0001 | c0003 | t0004 | g0313 | AFR | ESN | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03130 | hp2 | a0001 | c0001 | t0008 | g0131 | AFR | ESN | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03139 | hp1 | a0001 | c0001 | t0008 | g0104 | AFR | ESN | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03139 | hp2 | a0002 | c0002 | t0003 | g0031 | AFR | ESN | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0084 | AFR | ESN | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0219 | AFR | ESN | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03209 | hp1 | a0001 | c0003 | t0013 | g0298 | AFR | MSL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03209 | hp2 | a0001 | c0001 | t0019 | g0212 | AFR | MSL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | MSL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03225 | hp2 | a0002 | c0002 | t0003 | g0017 | AFR | MSL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03453 | hp1 | a0001 | c0003 | t0004 | g0311 | AFR | MSL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03453 | hp2 | a0003 | c0005 | t0015 | g0014 | AFR | MSL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03486 | hp2 | a0001 | c0001 | t0008 | g0099 | AFR | MSL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0046 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0254 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0244 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0045 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0188 | AFR | ESN | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03516 | hp2 | a0001 | c0001 | t0019 | g0217 | AFR | ESN | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03540 | hp1 | a0001 | c0003 | t0004 | g0329 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03540 | hp2 | a0001 | c0009 | t0013 | g0301 | AFR | GWD | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03579 | hp1 | a0001 | c0001 | t0024 | g0207 | AFR | MSL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0050 | AFR | MSL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03654 | hp1 | a0001 | c0001 | t0007 | g0134 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0044 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03669 | hp1 | a0001 | c0003 | t0004 | g0322 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0055 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03704 | hp1 | a0002 | c0002 | t0003 | g0025 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0070 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0155 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03710 | hp2 | a0001 | c0001 | t0009 | g0060 | SAS | PJL | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | BEB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0106 | SAS | BEB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03927 | hp1 | a0002 | c0004 | t0001 | g0234 | SAS | BEB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03927 | hp2 | a0001 | c0003 | t0004 | g0321 | SAS | BEB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03942 | hp1 | a0001 | c0001 | t0028 | g0009 | SAS | BEB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0073 | SAS | BEB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0167 | SAS | STU | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | STU | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0037 | SAS | BEB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0263 | SAS | BEB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG04204 | hp1 | a0002 | c0002 | t0007 | g0030 | SAS | STU | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG04204 | hp2 | a0001 | c0003 | t0004 | g0323 | SAS | STU | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG04228 | hp1 | a0002 | c0002 | t0003 | g0094 | SAS | STU | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0047 | SAS | STU | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18522 | hp1 | a0001 | c0001 | t0014 | g0006 | AFR | YRI | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0220 | AFR | YRI | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18612 | hp1 | a0001 | c0001 | t0005 | g0178 | EAS | CHB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | CHB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0281 | EAS | CHB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18747 | hp2 | a0001 | c0003 | t0004 | g0328 | EAS | CHB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18906 | hp1 | a0001 | c0003 | t0004 | g0310 | AFR | YRI | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18906 | hp2 | a0001 | c0001 | t0027 | g0295 | AFR | YRI | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18939 | hp2 | a0001 | c0003 | t0020 | g0174 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18948 | hp1 | a0001 | c0001 | t0005 | g0179 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18948 | hp2 | a0002 | c0002 | t0003 | g0023 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18951 | hp1 | a0002 | c0002 | t0003 | g0093 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18952 | hp1 | a0001 | c0001 | t0005 | g0184 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18953 | hp1 | a0001 | c0001 | t0012 | g0325 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18956 | hp1 | a0001 | c0001 | t0005 | g0177 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0288 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18959 | hp1 | a0002 | c0002 | t0003 | g0020 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0232 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18963 | hp2 | a0001 | c0001 | t0005 | g0189 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18964 | hp2 | a0001 | c0001 | t0012 | g0324 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18971 | hp1 | a0001 | c0001 | t0006 | g0202 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18971 | hp2 | a0001 | c0001 | t0010 | g0035 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18978 | hp1 | a0001 | c0001 | t0012 | g0327 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0291 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18980 | hp2 | a0004 | c0007 | t0016 | g0007 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18982 | hp2 | a0002 | c0002 | t0003 | g0019 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0172 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18986 | hp1 | a0001 | c0003 | t0004 | g0316 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18987 | hp1 | a0002 | c0002 | t0033 | g0170 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18990 | hp1 | a0001 | c0003 | t0020 | g0173 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA18995 | hp2 | a0006 | c0008 | t0025 | g0190 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0226 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19002 | hp2 | a0001 | c0001 | t0025 | g0191 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19030 | hp1 | a0001 | c0003 | t0004 | g0308 | AFR | LWK | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19030 | hp2 | a0001 | c0001 | t0023 | g0195 | AFR | LWK | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19043 | hp1 | a0001 | c0001 | t0014 | g0005 | AFR | LWK | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19043 | hp2 | a0002 | c0002 | t0003 | g0028 | AFR | LWK | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19054 | hp2 | a0001 | c0001 | t0005 | g0180 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19056 | hp1 | a0001 | c0003 | t0004 | g0318 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0250 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19058 | hp1 | a0009 | c0012 | t0001 | g0247 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19060 | hp2 | a0001 | c0001 | t0005 | g0192 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0282 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19065 | hp1 | a0001 | c0001 | t0005 | g0187 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19081 | hp2 | a0002 | c0002 | t0003 | g0021 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19084 | hp2 | a0001 | c0001 | t0005 | g0176 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19086 | hp1 | a0002 | c0002 | t0037 | g0262 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19090 | hp1 | a0001 | c0001 | t0005 | g0171 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0251 | EAS | JPT | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19240 | hp1 | a0007 | c0010 | t0003 | g0080 | AFR | YRI | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | YRI | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0193 | AFR | ASW | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | ASW | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0054 | EUR | TSI | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA20752 | hp2 | a0001 | c0001 | t0007 | g0067 | EUR | TSI | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0194 | EUR | TSI | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA20805 | hp2 | a0001 | c0001 | t0031 | g0066 | EUR | TSI | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01123 | hp1 | a0002 | c0004 | t0001 | g0242 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0149 | AMR | CLM | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0218 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG02559 | hp2 | a0001 | c0001 | t0023 | g0197 | AFR | ACB | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG06807 | hp1 | a0008 | c0011 | t0008 | g0101 | AFR | USA | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| HG06807 | hp2 | a0001 | c0001 | t0026 | g0293 | AFR | USA | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | USA | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | USA | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0007 | g0078 | REF | REF | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0018 | g0075 | REF | REF | EML5_chr14_88607431_88797953 | EML5 | chr14 | 88607431 | 88797953 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:88612433
|
C | T | 1 | a0001 | 1 | NA20805.hp2 | splice_region_variant | LOW | c.*3385G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | chr14 | 88612433 | ||||||
| chr14:88620769
|
G | T | 1 | a0003 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
missense_variant | MODERATE | c.5360C>A | p.Ala1787Glu | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/44 | 5810/9771 | 5360/5934 | 1787/1977 | chr14 | 88620769 | ||
| chr14:88664517
|
T | C | 1 | a0006 | 1 | NA18995.hp2 | missense_variant | MODERATE | c.3385A>G | p.Thr1129Ala | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 23/44 | 3835/9771 | 3385/5934 | 1129/1977 | chr14 | 88664517 | ||
| chr14:88664528
|
G | A | 1 | a0009 | 1 | NA19058.hp1 | missense_variant | MODERATE | c.3374C>T | p.Thr1125Ile | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 23/44 | 3824/9771 | 3374/5934 | 1125/1977 | chr14 | 88664528 | ||
| chr14:88665408
|
G | A | 1 | a0010 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.3206C>T | p.Ala1069Val | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 22/44 | 3656/9771 | 3206/5934 | 1069/1977 | chr14 | 88665408 | ||
| chr14:88695454
|
G | A | 1 | a0007 | 1 | NA19240.hp1 | missense_variant&splice_region_variant | MODERATE | c.2345C>T | p.Ala782Val | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 16/44 | 2795/9771 | 2345/5934 | 782/1977 | chr14 | 88695454 | ||
| chr14:88705517
|
T | C | 1 | a0004 | 2 | HG02040.hp1 NA18980.hp2 |
missense_variant | MODERATE | c.1897A>G | p.Ile633Val | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 12/44 | 2347/9771 | 1897/5934 | 633/1977 | chr14 | 88705517 | ||
| chr14:88712367
|
T | C | 1 | a0008 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.1561A>G | p.Ile521Val | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/44 | 2011/9771 | 1561/5934 | 521/1977 | chr14 | 88712367 | ||
| chr14:88738921
|
T | C | 4 | a0002a0005a0009others(1): Show | 88 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(85): Show |
missense_variant | MODERATE | c.805A>G | p.Ile269Val | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/44 | 1255/9771 | 805/5934 | 269/1977 | chr14 | 88738921 | ||
| chr14:88740517
|
G | A | 1 | a0005 | 1 | HG01515.hp1 | missense_variant | MODERATE | c.581C>T | p.Thr194Met | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 5/44 | 1031/9771 | 581/5934 | 194/1977 | chr14 | 88740517 | ||
| chr14:88746208
|
T | C | 1 | a0011 | 1 | HG02293.hp1 | missense_variant | MODERATE | c.433A>G | p.Met145Val | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/44 | 883/9771 | 433/5934 | 145/1977 | chr14 | 88746208 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:88626910
|
A | G | 1 | a0001c0009 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.4668T>C | p.Leu1556Leu | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/44 | 5118/9771 | 4668/5934 | 1556/1977 | chr14 | 88626910 | ||
| chr14:88685048
|
C | A | 1 | a0002c0004 | 5 | HG00099.hp2 HG01123.hp1 HG01168.hp2 others(2): Show |
synonymous_variant | LOW | c.2949G>T | p.Val983Val | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/44 | 3399/9771 | 2949/5934 | 983/1977 | chr14 | 88685048 | ||
| chr14:88688280
|
T | C | 2 | a0001c0003a0001c0009 | 33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
synonymous_variant | LOW | c.2733A>G | p.Ala911Ala | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 18/44 | 3183/9771 | 2733/5934 | 911/1977 | chr14 | 88688280 | ||
| chr14:88688310
|
C | T | 1 | a0001c0006 | 2 | HG01074.hp1 HG01175.hp2 |
synonymous_variant | LOW | c.2703G>A | p.Ala901Ala | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 18/44 | 3153/9771 | 2703/5934 | 901/1977 | chr14 | 88688310 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:88612583
|
A | G | 51 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(48): Show | 304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
3_prime_UTR_variant | MODIFIER | c.*3235T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 3235 | chr14 | 88612583 | |||||
| chr14:88612690
|
T | C | 2 | a0002c0002t0021a0002c0002t0038 | 3 | HG00323.hp1 HG00733.hp1 HG00738.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3128A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 3128 | chr14 | 88612690 | |||||
| chr14:88612752
|
G | T | 1 | a0004c0007t0016 | 2 | HG02040.hp1 NA18980.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3066C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 3066 | chr14 | 88612752 | |||||
| chr14:88612780
|
TAC | T | 3 | a0001c0001t0017a0001c0001t0023a0001c0001t0035 | 5 | HG01884.hp1 HG02559.hp2 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3036_*3037delGT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 3036 | chr14 | 88612780 | |||||
| chr14:88612832
|
A | T | 1 | a0001c0001t0030 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2986T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 2986 | chr14 | 88612832 | |||||
| chr14:88612979
|
T | TA | 5 | a0001c0001t0007a0001c0001t0009a0001c0001t0031others(2): Show | 19 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2838dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 2838 | chr14 | 88612979 | |||||
| chr14:88612979
|
TA | T | 23 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(20): Show | 138 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*2838delT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 2838 | chr14 | 88612979 | |||||
| chr14:88613216
|
C | T | 2 | a0001c0001t0008a0008c0011t0008 | 7 | HG02258.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2602G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 2602 | chr14 | 88613216 | |||||
| chr14:88613347
|
G | C | 2 | a0001c0001t0025a0006c0008t0025 | 2 | NA18995.hp2 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2471C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 2471 | chr14 | 88613347 | |||||
| chr14:88613405
|
ATAGT | A | 3 | a0001c0001t0022a0001c0001t0024a0001c0001t0036 | 5 | HG01243.hp1 HG01884.hp2 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2409_*2412delACTA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 2409 | chr14 | 88613405 | |||||
| chr14:88613524
|
T | G | 1 | a0001c0001t0027 | 2 | HG00642.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2294A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 2294 | chr14 | 88613524 | |||||
| chr14:88613550
|
T | A | 1 | a0003c0005t0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2268A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 2268 | chr14 | 88613550 | |||||
| chr14:88613620
|
T | C | 1 | a0001c0001t0036 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2198A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 2198 | chr14 | 88613620 | |||||
| chr14:88613623
|
C | T | 1 | a0001c0001t0029 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2195G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 2195 | chr14 | 88613623 | |||||
| chr14:88613907
|
G | A | 1 | a0001c0001t0009 | 5 | HG00738.hp1 HG01358.hp2 HG01943.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1911C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 1911 | chr14 | 88613907 | |||||
| chr14:88613933
|
T | C | 1 | a0004c0007t0016 | 2 | HG02040.hp1 NA18980.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1885A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 1885 | chr14 | 88613933 | |||||
| chr14:88614167
|
A | G | 1 | a0001c0001t0011 | 4 | HG02280.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1651T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 1651 | chr14 | 88614167 | |||||
| chr14:88614574
|
T | C | 1 | a0001c0001t0023 | 2 | HG02559.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1244A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 1244 | chr14 | 88614574 | |||||
| chr14:88614697
|
T | A | 1 | a0001c0001t0032 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1121A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 1121 | chr14 | 88614697 | |||||
| chr14:88614799
|
G | A | 1 | a0001c0001t0034 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1019C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 1019 | chr14 | 88614799 | |||||
| chr14:88615073
|
T | C | 1 | a0002c0002t0037 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*745A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 745 | chr14 | 88615073 | |||||
| chr14:88615112
|
G | A | 1 | a0004c0007t0016 | 2 | HG02040.hp1 NA18980.hp2 |
3_prime_UTR_variant | MODIFIER | c.*706C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 706 | chr14 | 88615112 | |||||
| chr14:88615254
|
T | C | 1 | a0001c0001t0024 | 2 | HG01884.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*564A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 564 | chr14 | 88615254 | |||||
| chr14:88615379
|
C | T | 2 | a0001c0001t0011a0001c0001t0019 | 6 | HG02280.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*439G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 439 | chr14 | 88615379 | |||||
| chr14:88615385
|
T | C | 4 | a0001c0001t0005a0001c0001t0010a0001c0001t0025others(1): Show | 23 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*433A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 433 | chr14 | 88615385 | |||||
| chr14:88615399
|
A | G | 1 | a0001c0001t0034 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*419T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 44/44 | 419 | chr14 | 88615399 | |||||
| chr14:88792525
|
T | TCCCGCTC others(34): Show |
1 | a0002c0002t0033 | 1 | NA18987.hp1 | 5_prime_UTR_variant | MODIFIER | c.-63_-23dupGGCCGCCG others(33): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/44 | 23 | chr14 | 88792525 | |||||
| chr14:88792533
|
G | A | 30 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(27): Show | 164 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(161): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-30C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/44 | chr14 | 88792533 | ||||||
| chr14:88792533
|
G | T | 1 | a0001c0001t0028 | 1 | HG03942.hp1 | 5_prime_UTR_variant | MODIFIER | c.-30C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/44 | 30 | chr14 | 88792533 | |||||
| chr14:88792747
|
G | C | 2 | a0001c0001t0026a0001c0001t0027 | 4 | HG00642.hp2 HG02145.hp1 HG06807.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-244C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/44 | 244 | chr14 | 88792747 | |||||
| chr14:88792880
|
G | A | 1 | a0002c0002t0038 | 1 | HG00323.hp1 | 5_prime_UTR_variant | MODIFIER | c.-377C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/44 | 377 | chr14 | 88792880 | |||||
| chr14:88792887
|
C | G | 1 | a0004c0007t0016 | 2 | HG02040.hp1 NA18980.hp2 |
5_prime_UTR_variant | MODIFIER | c.-384G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/44 | 384 | chr14 | 88792887 | |||||
| chr14:88792920
|
A | C | 1 | a0001c0001t0014 | 3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
5_prime_UTR_variant | MODIFIER | c.-417T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/44 | 417 | chr14 | 88792920 | |||||
| chr14:88792946
|
G | GCGAGCCG others(3): Show |
4 | a0001c0001t0012a0001c0003t0004a0001c0003t0013others(1): Show | 32 | HG00408.hp1 HG00609.hp1 HG02055.hp2 others(29): Show |
5_prime_UTR_variant | MODIFIER | c.-444_-443insGCTCGG others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/44 | 444 | chr14 | 88792946 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:88615905
|
C | A | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.5898-51G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 43/43 | chr14 | 88615905 | ||||||
| chr14:88615945
|
A | G | 105 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0002g0001others(102): Show | 107 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.5898-91T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 43/43 | chr14 | 88615945 | ||||||
| chr14:88615997
|
T | G | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.5898-143A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 43/43 | chr14 | 88615997 | ||||||
| chr14:88616052
|
A | AT | 90 | a0001c0001t0017g0010a0001c0001t0017g0011a0002c0002t0001g0193others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.5897+89dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 43/43 | chr14 | 88616052 | ||||||
| chr14:88616313
|
A | C | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5797-71T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 42/43 | chr14 | 88616313 | ||||||
| chr14:88617091
|
T | C | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.5643-212A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 41/43 | chr14 | 88617091 | ||||||
| chr14:88617150
|
C | CT | 7 | a0001c0001t0002g0168a0001c0003t0002g0012a0001c0003t0006g0221others(4): Show | 7 | HG01891.hp2 HG02572.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.5643-272dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 41/43 | chr14 | 88617150 | ||||||
| chr14:88617188
|
C | T | 2 | a0001c0001t0002g0112a0001c0001t0002g0113 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.5643-309G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 41/43 | chr14 | 88617188 | ||||||
| chr14:88617296
|
C | T | 2 | a0001c0001t0017g0010a0001c0001t0017g0011 | 2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5643-417G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 41/43 | chr14 | 88617296 | ||||||
| chr14:88617394
|
C | T | 6 | a0002c0002t0001g0255a0002c0002t0001g0256a0002c0002t0001g0257others(3): Show | 6 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.5643-515G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 41/43 | chr14 | 88617394 | ||||||
| chr14:88617399
|
G | A | 63 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0280others(60): Show | 63 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.5643-520C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 41/43 | chr14 | 88617399 | ||||||
| chr14:88617436
|
G | A | 3 | a0002c0002t0001g0224a0002c0002t0001g0225a0002c0002t0001g0226 | 3 | NA18968.hp1 NA18994.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.5643-557C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 41/43 | chr14 | 88617436 | ||||||
| chr14:88617493
|
G | C | 3 | a0002c0002t0001g0263a0002c0002t0003g0094a0002c0002t0007g0030 | 3 | HG04184.hp2 HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.5643-614C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 41/43 | chr14 | 88617493 | ||||||
| chr14:88617604
|
T | C | 6 | a0001c0001t0011g0213a0001c0001t0011g0214a0001c0001t0011g0215others(3): Show | 6 | HG02280.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.5642+624A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 41/43 | chr14 | 88617604 | ||||||
| chr14:88617633
|
G | C | 1 | a0002c0002t0001g0277 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.5642+595C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 41/43 | chr14 | 88617633 | ||||||
| chr14:88617902
|
G | A | 1 | a0001c0001t0007g0134 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.5642+326C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 41/43 | chr14 | 88617902 | ||||||
| chr14:88617903
|
A | G | 1 | a0001c0001t0002g0088 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.5642+325T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 41/43 | chr14 | 88617903 | ||||||
| chr14:88618011
|
T | TA | 327 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(324): Show | 330 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.5642+216dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 41/43 | chr14 | 88618011 | ||||||
| chr14:88618185
|
C | T | 1 | a0001c0001t0002g0142 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.5642+43G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 41/43 | chr14 | 88618185 | ||||||
| chr14:88618497
|
T | G | 5 | a0001c0001t0003g0043a0001c0001t0003g0052a0001c0001t0003g0053others(2): Show | 5 | NA18951.hp2 NA18954.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.5538+153A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 40/43 | chr14 | 88618497 | ||||||
| chr14:88618510
|
G | A | 103 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(100): Show | 105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.5538+140C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 40/43 | chr14 | 88618510 | ||||||
| chr14:88618907
|
C | T | 6 | a0001c0001t0011g0213a0001c0001t0011g0214a0001c0001t0011g0215others(3): Show | 6 | HG02280.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.5376-95G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/43 | chr14 | 88618907 | ||||||
| chr14:88618922
|
C | T | 1 | a0001c0001t0011g0216 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5376-110G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/43 | chr14 | 88618922 | ||||||
| chr14:88618980
|
A | G | 1 | a0001c0001t0002g0108 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.5376-168T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/43 | chr14 | 88618980 | ||||||
| chr14:88619029
|
A | G | 1 | a0001c0001t0003g0040 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.5376-217T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/43 | chr14 | 88619029 | ||||||
| chr14:88619239
|
C | T | 1 | a0001c0001t0002g0130 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.5376-427G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/43 | chr14 | 88619239 | ||||||
| chr14:88619258
|
G | A | 9 | a0001c0001t0014g0004a0001c0001t0014g0005a0001c0001t0014g0006others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.5376-446C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/43 | chr14 | 88619258 | ||||||
| chr14:88619376
|
A | G | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.5376-564T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/43 | chr14 | 88619376 | ||||||
| chr14:88619487
|
G | A | 1 | a0001c0001t0003g0073 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.5376-675C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/43 | chr14 | 88619487 | ||||||
| chr14:88619494
|
A | C | 275 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0280others(272): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.5376-682T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/43 | chr14 | 88619494 | ||||||
| chr14:88619685
|
A | AT | 124 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(121): Show | 126 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.5376-874dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/43 | chr14 | 88619685 | ||||||
| chr14:88619735
|
C | T | 7 | a0001c0001t0001g0283a0001c0001t0002g0158a0001c0001t0006g0003others(4): Show | 8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.5376-923G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/43 | chr14 | 88619735 | ||||||
| chr14:88620076
|
T | C | 1 | a0001c0001t0001g0280 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.5375+678A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/43 | chr14 | 88620076 | ||||||
| chr14:88620123
|
T | C | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.5375+631A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/43 | chr14 | 88620123 | ||||||
| chr14:88620427
|
A | T | 122 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(119): Show | 124 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.5375+327T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/43 | chr14 | 88620427 | ||||||
| chr14:88620571
|
G | T | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.5375+183C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/43 | chr14 | 88620571 | ||||||
| chr14:88620616
|
A | T | 1 | a0001c0001t0006g0208 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.5375+138T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 39/43 | chr14 | 88620616 | ||||||
| chr14:88620934
|
T | TA | 169 | a0001c0001t0001g0280a0001c0001t0001g0290a0001c0001t0002g0001others(166): Show | 171 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.5203-9dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 38/43 | chr14 | 88620934 | ||||||
| chr14:88620934
|
T | TAA | 7 | a0001c0001t0003g0068a0001c0001t0006g0218a0001c0001t0006g0219others(4): Show | 7 | HG01496.hp1 HG02559.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.5203-10_5203-9dupT others(1): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 38/43 | chr14 | 88620934 | ||||||
| chr14:88620984
|
A | G | 1 | a0002c0002t0001g0230 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.5203-58T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 38/43 | chr14 | 88620984 | ||||||
| chr14:88621457
|
A | G | 61 | a0001c0001t0001g0280a0001c0001t0001g0290a0001c0001t0003g0036others(58): Show | 61 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.5014-156T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 37/43 | chr14 | 88621457 | ||||||
| chr14:88621747
|
C | A | 1 | a0001c0001t0003g0043 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.5014-446G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 37/43 | chr14 | 88621747 | ||||||
| chr14:88621833
|
C | T | 6 | a0001c0001t0011g0213a0001c0001t0011g0214a0001c0001t0011g0215others(3): Show | 6 | HG02280.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.5014-532G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 37/43 | chr14 | 88621833 | ||||||
| chr14:88621834
|
G | A | 1 | a0001c0001t0003g0047 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.5014-533C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 37/43 | chr14 | 88621834 | ||||||
| chr14:88621922
|
C | T | 90 | a0001c0001t0017g0010a0001c0001t0017g0011a0002c0002t0001g0193others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.5014-621G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 37/43 | chr14 | 88621922 | ||||||
| chr14:88622013
|
G | A | 92 | a0001c0001t0002g0120a0001c0001t0002g0133a0001c0001t0017g0010others(89): Show | 92 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.5013+591C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 37/43 | chr14 | 88622013 | ||||||
| chr14:88622044
|
G | C | 328 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(325): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.5013+560C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 37/43 | chr14 | 88622044 | ||||||
| chr14:88622144
|
G | A | 3 | a0002c0002t0001g0224a0002c0002t0001g0225a0002c0002t0001g0226 | 3 | NA18968.hp1 NA18994.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.5013+460C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 37/43 | chr14 | 88622144 | ||||||
| chr14:88622256
|
C | T | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.5013+348G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 37/43 | chr14 | 88622256 | ||||||
| chr14:88622379
|
T | C | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.5013+225A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 37/43 | chr14 | 88622379 | ||||||
| chr14:88622391
|
A | G | 1 | a0001c0001t0010g0035 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.5013+213T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 37/43 | chr14 | 88622391 | ||||||
| chr14:88622418
|
T | C | 4 | a0001c0001t0002g0168a0001c0001t0006g0218a0001c0001t0006g0219others(1): Show | 4 | HG01891.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.5013+186A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 37/43 | chr14 | 88622418 | ||||||
| chr14:88622582
|
A | G | 1 | a0001c0001t0002g0147 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.5013+22T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 37/43 | chr14 | 88622582 | ||||||
| chr14:88622745
|
G | A | 1 | a0001c0003t0004g0323 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.4899-27C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88622745 | ||||||
| chr14:88622794
|
A | T | 2 | a0001c0003t0004g0302a0001c0003t0004g0329 | 2 | HG02055.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.4899-76T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88622794 | ||||||
| chr14:88622805
|
C | CT | 295 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(292): Show | 298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.4899-88dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88622805 | ||||||
| chr14:88622816
|
A | T | 1 | a0003c0005t0015g0013 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4899-98T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88622816 | ||||||
| chr14:88622895
|
A | G | 63 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0280others(60): Show | 63 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.4899-177T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88622895 | ||||||
| chr14:88623017
|
C | CT | 208 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0087others(205): Show | 210 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.4899-300dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88623017 | ||||||
| chr14:88623017
|
C | CTT | 16 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(13): Show | 17 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.4899-301_4899-300d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88623017 | ||||||
| chr14:88623141
|
G | A | 104 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0002g0001others(101): Show | 106 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.4899-423C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88623141 | ||||||
| chr14:88623222
|
G | A | 1 | a0001c0009t0013g0301 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4899-504C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88623222 | ||||||
| chr14:88623466
|
C | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4899-748G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88623466 | ||||||
| chr14:88623648
|
G | A | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.4899-930C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88623648 | ||||||
| chr14:88623655
|
G | A | 1 | a0002c0002t0003g0020 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.4899-937C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88623655 | ||||||
| chr14:88623663
|
C | T | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.4899-945G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88623663 | ||||||
| chr14:88623717
|
C | T | 1 | a0001c0003t0004g0322 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.4899-999G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88623717 | ||||||
| chr14:88623773
|
T | C | 1 | a0009c0012t0001g0247 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.4899-1055A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88623773 | ||||||
| chr14:88623790
|
A | G | 4 | a0001c0001t0002g0168a0001c0001t0006g0218a0001c0001t0006g0219others(1): Show | 4 | HG01891.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.4899-1072T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88623790 | ||||||
| chr14:88623991
|
G | A | 3 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0035g0196 | 3 | HG02559.hp2 HG02886.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4898+979C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88623991 | ||||||
| chr14:88624067
|
T | A | 1 | a0001c0001t0002g0091 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.4898+903A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88624067 | ||||||
| chr14:88624075
|
T | G | 1 | a0001c0001t0002g0091 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.4898+895A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88624075 | ||||||
| chr14:88624127
|
G | A | 1 | a0001c0001t0019g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4898+843C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88624127 | ||||||
| chr14:88624139
|
C | T | 7 | a0001c0001t0001g0283a0001c0001t0002g0158a0001c0001t0006g0003others(4): Show | 8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.4898+831G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88624139 | ||||||
| chr14:88624209
|
A | T | 295 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(292): Show | 298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.4898+761T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88624209 | ||||||
| chr14:88624312
|
C | T | 7 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(4): Show | 7 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.4898+658G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88624312 | ||||||
| chr14:88624417
|
A | T | 90 | a0001c0001t0017g0010a0001c0001t0017g0011a0002c0002t0001g0193others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.4898+553T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88624417 | ||||||
| chr14:88624479
|
T | C | 153 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0280others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.4898+491A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88624479 | ||||||
| chr14:88624584
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0201 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4898+386C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88624584 | ||||||
| chr14:88624858
|
G | GGAA | 105 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0002g0001others(102): Show | 107 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.4898+109_4898+111d others(5): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88624858 | ||||||
| chr14:88624874
|
C | G | 1 | a0001c0001t0002g0087 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.4898+96G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88624874 | ||||||
| chr14:88624877
|
T | A | 1 | a0001c0001t0002g0087 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.4898+93A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 36/43 | chr14 | 88624877 | ||||||
| chr14:88625317
|
T | C | 2 | a0001c0001t0001g0199a0001c0001t0001g0201 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4741-190A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88625317 | ||||||
| chr14:88625389
|
T | C | 1 | a0001c0003t0004g0328 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.4741-262A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88625389 | ||||||
| chr14:88625480
|
C | T | 11 | a0001c0001t0003g0039a0001c0001t0003g0040a0001c0001t0003g0041others(8): Show | 11 | HG02738.hp1 HG03490.hp1 HG03492.hp2 others(8): Show |
intron_variant | MODIFIER | c.4741-353G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88625480 | ||||||
| chr14:88625489
|
C | T | 2 | a0001c0001t0002g0114a0001c0001t0002g0115 | 2 | NA18973.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.4741-362G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88625489 | ||||||
| chr14:88625558
|
C | T | 1 | a0001c0001t0003g0081 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.4741-431G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88625558 | ||||||
| chr14:88625559
|
G | A | 1 | a0001c0001t0003g0081 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.4741-432C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88625559 | ||||||
| chr14:88625670
|
GGGATTAT others(6): Show |
G | 1 | a0002c0002t0001g0226 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.4741-556_4741-544d others(15): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88625670 | ||||||
| chr14:88625687
|
C | T | 6 | a0001c0001t0011g0213a0001c0001t0011g0214a0001c0001t0011g0215others(3): Show | 6 | HG02280.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.4741-560G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88625687 | ||||||
| chr14:88625698
|
G | A | 4 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0035g0196others(1): Show | 4 | HG02559.hp2 HG02818.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.4741-571C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88625698 | ||||||
| chr14:88625707
|
C | T | 1 | a0005c0014t0001g0272 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.4741-580G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88625707 | ||||||
| chr14:88625807
|
G | A | 6 | a0001c0003t0002g0012a0001c0003t0006g0221a0001c0003t0013g0298others(3): Show | 6 | HG02572.hp1 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.4741-680C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88625807 | ||||||
| chr14:88625912
|
C | T | 1 | a0002c0002t0003g0027 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.4741-785G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88625912 | ||||||
| chr14:88625956
|
C | T | 1 | a0001c0003t0004g0302 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4741-829G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88625956 | ||||||
| chr14:88626063
|
T | C | 104 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0002g0001others(101): Show | 106 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.4740+775A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88626063 | ||||||
| chr14:88626101
|
C | T | 1 | a0002c0002t0001g0230 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4740+737G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88626101 | ||||||
| chr14:88626354
|
G | T | 14 | a0002c0002t0001g0235a0002c0002t0001g0236a0002c0002t0001g0250others(11): Show | 14 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.4740+484C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88626354 | ||||||
| chr14:88626359
|
T | C | 79 | a0002c0002t0001g0193a0002c0002t0001g0194a0002c0002t0001g0200others(76): Show | 79 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.4740+479A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88626359 | ||||||
| chr14:88626576
|
C | T | 2 | a0001c0001t0003g0044a0001c0001t0003g0047 | 2 | HG03654.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.4740+262G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88626576 | ||||||
| chr14:88626616
|
C | CA | 7 | a0001c0001t0001g0283a0001c0001t0002g0138a0001c0001t0009g0042others(4): Show | 7 | HG00609.hp1 HG01993.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.4740+221dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88626616 | ||||||
| chr14:88626616
|
CA | C | 94 | a0001c0001t0002g0116a0001c0001t0002g0122a0001c0001t0007g0071others(91): Show | 94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.4740+221delT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88626616 | ||||||
| chr14:88626634
|
C | A | 3 | a0001c0001t0006g0218a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02559.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4740+204G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88626634 | ||||||
| chr14:88626721
|
G | A | 10 | a0001c0001t0003g0039a0001c0001t0003g0040a0001c0001t0003g0041others(7): Show | 10 | HG02738.hp1 HG03490.hp1 HG03492.hp2 others(7): Show |
intron_variant | MODIFIER | c.4740+117C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88626721 | ||||||
| chr14:88626723
|
A | G | 1 | a0001c0001t0032g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4740+115T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 35/43 | chr14 | 88626723 | ||||||
| chr14:88627137
|
A | G | 1 | a0002c0002t0001g0281 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.4532-91T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 34/43 | chr14 | 88627137 | ||||||
| chr14:88627287
|
G | C | 1 | a0001c0001t0014g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4532-241C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 34/43 | chr14 | 88627287 | ||||||
| chr14:88627372
|
T | C | 4 | a0001c0001t0011g0213a0001c0001t0011g0214a0001c0001t0011g0215others(1): Show | 4 | HG02280.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.4531+274A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 34/43 | chr14 | 88627372 | ||||||
| chr14:88627899
|
G | C | 282 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(279): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.4358-80C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88627899 | ||||||
| chr14:88628555
|
A | G | 1 | a0002c0002t0007g0030 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.4358-736T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88628555 | ||||||
| chr14:88628653
|
A | G | 1 | a0001c0001t0002g0106 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4358-834T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88628653 | ||||||
| chr14:88628681
|
A | G | 1 | a0001c0001t0003g0163 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.4358-862T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88628681 | ||||||
| chr14:88628871
|
T | A | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.4358-1052A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88628871 | ||||||
| chr14:88628908
|
C | T | 282 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(279): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.4358-1089G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88628908 | ||||||
| chr14:88629115
|
T | C | 2 | a0001c0001t0017g0010a0001c0001t0017g0011 | 2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4358-1296A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88629115 | ||||||
| chr14:88629143
|
A | C | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4358-1324T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88629143 | ||||||
| chr14:88629206
|
A | G | 1 | a0002c0004t0001g0228 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.4358-1387T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88629206 | ||||||
| chr14:88629449
|
T | C | 1 | a0001c0001t0003g0068 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.4358-1630A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88629449 | ||||||
| chr14:88629506
|
C | G | 104 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0002g0001others(101): Show | 106 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.4358-1687G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88629506 | ||||||
| chr14:88629546
|
T | C | 3 | a0001c0001t0003g0048a0001c0001t0003g0049a0001c0001t0003g0050 | 3 | HG02622.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.4358-1727A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88629546 | ||||||
| chr14:88629872
|
A | C | 1 | a0002c0002t0001g0231 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.4358-2053T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88629872 | ||||||
| chr14:88630008
|
T | C | 104 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0002g0001others(101): Show | 106 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.4358-2189A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88630008 | ||||||
| chr14:88630023
|
A | AT | 10 | a0001c0001t0003g0054a0001c0001t0014g0004a0001c0001t0014g0005others(7): Show | 10 | HG01243.hp1 HG02135.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.4358-2205dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88630023 | ||||||
| chr14:88630023
|
AT | A | 103 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0002g0156others(100): Show | 103 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.4358-2205delA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88630023 | ||||||
| chr14:88630023
|
ATT | A | 90 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(87): Show | 91 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.4358-2206_4358-220 others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88630023 | ||||||
| chr14:88630023
|
ATTT | A | 24 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(21): Show | 26 | HG01106.hp1 HG01109.hp2 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.4358-2207_4358-220 others(7): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88630023 | ||||||
| chr14:88630341
|
T | G | 282 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(279): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.4358-2522A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88630341 | ||||||
| chr14:88630395
|
T | C | 295 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(292): Show | 298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.4358-2576A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88630395 | ||||||
| chr14:88630644
|
C | T | 1 | a0002c0002t0037g0262 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.4358-2825G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88630644 | ||||||
| chr14:88630904
|
G | A | 7 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(4): Show | 7 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.4358-3085C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88630904 | ||||||
| chr14:88631056
|
A | C | 1 | a0001c0001t0006g0284 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.4358-3237T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88631056 | ||||||
| chr14:88631066
|
A | G | 1 | a0001c0001t0011g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4358-3247T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88631066 | ||||||
| chr14:88631164
|
GAT | G | 13 | a0001c0001t0001g0283a0001c0001t0002g0158a0001c0001t0006g0003others(10): Show | 14 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.4357+3303_4357+330 others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88631164 | ||||||
| chr14:88631290
|
C | T | 90 | a0001c0001t0017g0010a0001c0001t0017g0011a0002c0002t0001g0193others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.4357+3179G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88631290 | ||||||
| chr14:88631299
|
G | A | 13 | a0001c0001t0001g0283a0001c0001t0002g0158a0001c0001t0006g0003others(10): Show | 14 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.4357+3170C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88631299 | ||||||
| chr14:88631338
|
C | A | 2 | a0001c0001t0017g0010a0001c0001t0017g0011 | 2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4357+3131G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88631338 | ||||||
| chr14:88631694
|
C | T | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.4357+2775G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88631694 | ||||||
| chr14:88632060
|
C | G | 88 | a0002c0002t0001g0193a0002c0002t0001g0194a0002c0002t0001g0200others(85): Show | 88 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.4357+2409G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88632060 | ||||||
| chr14:88632277
|
T | A | 1 | a0001c0001t0002g0155 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4357+2192A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88632277 | ||||||
| chr14:88632287
|
T | G | 7 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(4): Show | 7 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.4357+2182A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88632287 | ||||||
| chr14:88632306
|
G | A | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.4357+2163C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88632306 | ||||||
| chr14:88632389
|
C | T | 4 | a0001c0001t0026g0293a0001c0001t0026g0294a0001c0001t0027g0295others(1): Show | 4 | HG00642.hp2 HG02145.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.4357+2080G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88632389 | ||||||
| chr14:88632746
|
G | A | 1 | a0001c0001t0002g0140 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4357+1723C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88632746 | ||||||
| chr14:88632775
|
G | A | 2 | a0001c0001t0002g0121a0001c0001t0002g0122 | 2 | HG03041.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4357+1694C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88632775 | ||||||
| chr14:88632981
|
C | T | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4357+1488G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88632981 | ||||||
| chr14:88633027
|
A | G | 1 | a0001c0001t0001g0201 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4357+1442T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88633027 | ||||||
| chr14:88633030
|
T | C | 1 | a0001c0001t0019g0212 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4357+1439A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88633030 | ||||||
| chr14:88633207
|
T | C | 1 | a0001c0001t0003g0039 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.4357+1262A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88633207 | ||||||
| chr14:88633635
|
AGAT | A | 63 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0280others(60): Show | 63 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.4357+831_4357+833d others(5): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88633635 | ||||||
| chr14:88633674
|
C | T | 13 | a0001c0001t0001g0283a0001c0001t0002g0158a0001c0001t0006g0003others(10): Show | 14 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.4357+795G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88633674 | ||||||
| chr14:88633874
|
G | A | 104 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0002g0001others(101): Show | 106 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.4357+595C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88633874 | ||||||
| chr14:88633938
|
T | C | 7 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(4): Show | 7 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.4357+531A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88633938 | ||||||
| chr14:88634109
|
T | C | 151 | a0001c0001t0001g0280a0001c0001t0001g0290a0001c0001t0003g0036others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.4357+360A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88634109 | ||||||
| chr14:88634174
|
C | T | 3 | a0001c0001t0006g0218a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02559.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4357+295G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88634174 | ||||||
| chr14:88634307
|
C | A | 3 | a0001c0001t0014g0004a0001c0001t0014g0005a0001c0001t0014g0006 | 3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4357+162G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 33/43 | chr14 | 88634307 | ||||||
| chr14:88634601
|
C | T | 1 | a0001c0001t0002g0123 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4337-112G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88634601 | ||||||
| chr14:88634632
|
C | T | 1 | a0001c0001t0002g0097 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.4337-143G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88634632 | ||||||
| chr14:88634730
|
A | C | 1 | a0001c0001t0003g0043 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.4337-241T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88634730 | ||||||
| chr14:88634742
|
A | G | 1 | a0001c0001t0003g0048 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4337-253T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88634742 | ||||||
| chr14:88634910
|
G | A | 11 | a0002c0002t0001g0193a0002c0002t0001g0194a0002c0002t0001g0209others(8): Show | 11 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.4337-421C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88634910 | ||||||
| chr14:88635022
|
C | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4337-533G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88635022 | ||||||
| chr14:88635266
|
G | C | 105 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0002g0001others(102): Show | 107 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.4337-777C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88635266 | ||||||
| chr14:88635304
|
A | G | 1 | a0001c0003t0006g0221 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4337-815T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88635304 | ||||||
| chr14:88635500
|
AT | A | 3 | a0002c0002t0001g0232a0002c0002t0001g0233a0002c0002t0001g0261 | 3 | NA18947.hp2 NA18962.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.4337-1012delA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88635500 | ||||||
| chr14:88635522
|
C | T | 1 | a0001c0001t0005g0172 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.4337-1033G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88635522 | ||||||
| chr14:88635623
|
A | T | 1 | a0002c0002t0001g0281 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.4337-1134T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88635623 | ||||||
| chr14:88635826
|
C | T | 90 | a0001c0001t0017g0010a0001c0001t0017g0011a0002c0002t0001g0193others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.4337-1337G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88635826 | ||||||
| chr14:88636214
|
T | C | 60 | a0001c0001t0001g0280a0001c0001t0001g0290a0001c0001t0003g0036others(57): Show | 60 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.4337-1725A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88636214 | ||||||
| chr14:88636340
|
T | C | 105 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0002g0001others(102): Show | 107 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.4337-1851A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88636340 | ||||||
| chr14:88636370
|
G | A | 7 | a0002c0002t0001g0278a0002c0002t0003g0019a0002c0002t0003g0020others(4): Show | 7 | HG02135.hp1 HG02165.hp1 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.4337-1881C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88636370 | ||||||
| chr14:88636391
|
G | A | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4337-1902C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88636391 | ||||||
| chr14:88636703
|
G | T | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.4336+2106C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88636703 | ||||||
| chr14:88637028
|
C | A | 90 | a0001c0001t0017g0010a0001c0001t0017g0011a0002c0002t0001g0193others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.4336+1781G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88637028 | ||||||
| chr14:88637079
|
G | A | 19 | a0001c0001t0006g0208a0001c0001t0006g0218a0001c0001t0006g0219others(16): Show | 19 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.4336+1730C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88637079 | ||||||
| chr14:88637119
|
A | T | 23 | a0001c0001t0005g0171a0001c0001t0005g0172a0001c0001t0005g0175others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.4336+1690T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88637119 | ||||||
| chr14:88637162
|
T | C | 1 | a0008c0011t0008g0101 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4336+1647A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88637162 | ||||||
| chr14:88637670
|
T | C | 1 | a0001c0001t0002g0107 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.4336+1139A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88637670 | ||||||
| chr14:88637786
|
G | A | 1 | a0001c0001t0010g0034 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.4336+1023C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88637786 | ||||||
| chr14:88637839
|
G | A | 1 | a0001c0001t0032g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4336+970C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88637839 | ||||||
| chr14:88637883
|
T | C | 7 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(4): Show | 7 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.4336+926A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88637883 | ||||||
| chr14:88637916
|
C | T | 1 | a0002c0002t0001g0249 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4336+893G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88637916 | ||||||
| chr14:88637985
|
G | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4336+824C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88637985 | ||||||
| chr14:88638287
|
A | G | 1 | a0002c0002t0001g0223 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.4336+522T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88638287 | ||||||
| chr14:88638391
|
CT | C | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4336+417delA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88638391 | ||||||
| chr14:88638411
|
C | T | 301 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(298): Show | 304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.4336+398G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88638411 | ||||||
| chr14:88638617
|
C | T | 1 | a0002c0002t0001g0278 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.4336+192G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 32/43 | chr14 | 88638617 | ||||||
| chr14:88638943
|
T | A | 152 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0280others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.4238-36A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88638943 | ||||||
| chr14:88639142
|
C | A | 1 | a0001c0001t0006g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4238-235G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88639142 | ||||||
| chr14:88639192
|
A | G | 44 | a0001c0001t0001g0280a0001c0001t0001g0290a0001c0001t0003g0036others(41): Show | 44 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.4238-285T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88639192 | ||||||
| chr14:88639317
|
T | C | 7 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(4): Show | 7 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.4238-410A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88639317 | ||||||
| chr14:88639461
|
C | T | 282 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(279): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.4238-554G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88639461 | ||||||
| chr14:88639544
|
A | G | 105 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0002g0001others(102): Show | 107 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.4238-637T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88639544 | ||||||
| chr14:88639572
|
A | G | 1 | a0004c0007t0016g0007 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.4238-665T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88639572 | ||||||
| chr14:88639870
|
C | T | 1 | a0001c0001t0011g0213 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4238-963G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88639870 | ||||||
| chr14:88639877
|
A | G | 3 | a0001c0001t0014g0004a0001c0001t0014g0005a0001c0001t0014g0006 | 3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4238-970T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88639877 | ||||||
| chr14:88639961
|
G | A | 1 | a0001c0001t0002g0128 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.4238-1054C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88639961 | ||||||
| chr14:88640142
|
G | T | 4 | a0001c0001t0002g0168a0003c0005t0015g0013a0003c0005t0015g0014others(1): Show | 4 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.4238-1235C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640142 | ||||||
| chr14:88640145
|
A | C | 4 | a0001c0001t0002g0168a0003c0005t0015g0013a0003c0005t0015g0014others(1): Show | 4 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.4238-1238T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640145 | ||||||
| chr14:88640146
|
G | T | 4 | a0001c0001t0002g0168a0003c0005t0015g0013a0003c0005t0015g0014others(1): Show | 4 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.4238-1239C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640146 | ||||||
| chr14:88640148
|
T | C | 4 | a0001c0001t0002g0168a0003c0005t0015g0013a0003c0005t0015g0014others(1): Show | 4 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.4238-1241A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640148 | ||||||
| chr14:88640150
|
A | T | 4 | a0001c0001t0002g0168a0003c0005t0015g0013a0003c0005t0015g0014others(1): Show | 4 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.4238-1243T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640150 | ||||||
| chr14:88640152
|
C | G | 4 | a0001c0001t0002g0168a0003c0005t0015g0013a0003c0005t0015g0014others(1): Show | 4 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.4238-1245G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640152 | ||||||
| chr14:88640154
|
A | T | 4 | a0001c0001t0002g0168a0003c0005t0015g0013a0003c0005t0015g0014others(1): Show | 4 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.4238-1247T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640154 | ||||||
| chr14:88640156
|
G | A | 4 | a0001c0001t0002g0168a0003c0005t0015g0013a0003c0005t0015g0014others(1): Show | 4 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.4238-1249C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640156 | ||||||
| chr14:88640158
|
A | C | 4 | a0001c0001t0002g0168a0003c0005t0015g0013a0003c0005t0015g0014others(1): Show | 4 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.4238-1251T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640158 | ||||||
| chr14:88640159
|
G | T | 4 | a0001c0001t0002g0168a0003c0005t0015g0013a0003c0005t0015g0014others(1): Show | 4 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.4238-1252C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640159 | ||||||
| chr14:88640162
|
A | C | 4 | a0001c0001t0002g0168a0003c0005t0015g0013a0003c0005t0015g0014others(1): Show | 4 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.4238-1255T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640162 | ||||||
| chr14:88640397
|
G | T | 315 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(312): Show | 318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.4238-1490C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640397 | ||||||
| chr14:88640398
|
C | T | 19 | a0001c0001t0006g0208a0001c0001t0006g0218a0001c0001t0006g0219others(16): Show | 19 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.4238-1491G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640398 | ||||||
| chr14:88640513
|
G | A | 1 | a0001c0001t0002g0133 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.4238-1606C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640513 | ||||||
| chr14:88640551
|
G | A | 2 | a0001c0001t0006g0003a0001c0001t0006g0286 | 3 | HG01256.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.4238-1644C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640551 | ||||||
| chr14:88640613
|
A | G | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4238-1706T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640613 | ||||||
| chr14:88640939
|
C | A | 2 | a0002c0002t0003g0017a0002c0002t0003g0018 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4237+1954G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640939 | ||||||
| chr14:88640988
|
A | G | 2 | a0001c0001t0011g0214a0001c0001t0011g0215 | 2 | HG02280.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.4237+1905T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88640988 | ||||||
| chr14:88641147
|
C | G | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.4237+1746G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88641147 | ||||||
| chr14:88641162
|
G | A | 4 | a0001c0001t0002g0136a0001c0001t0002g0137a0001c0001t0002g0138others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.4237+1731C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88641162 | ||||||
| chr14:88641226
|
T | C | 1 | a0002c0002t0003g0031 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4237+1667A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88641226 | ||||||
| chr14:88641501
|
T | C | 1 | a0001c0001t0006g0003 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.4237+1392A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88641501 | ||||||
| chr14:88641808
|
C | T | 1 | a0001c0001t0006g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4237+1085G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88641808 | ||||||
| chr14:88641851
|
T | G | 1 | a0002c0002t0001g0263 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.4237+1042A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88641851 | ||||||
| chr14:88642002
|
T | C | 4 | a0001c0001t0002g0168a0001c0001t0006g0218a0001c0001t0006g0219others(1): Show | 4 | HG01891.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.4237+891A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88642002 | ||||||
| chr14:88642088
|
A | G | 4 | a0001c0001t0002g0168a0001c0001t0006g0218a0001c0001t0006g0219others(1): Show | 4 | HG01891.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.4237+805T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88642088 | ||||||
| chr14:88642290
|
T | C | 1 | a0001c0001t0009g0059 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.4237+603A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88642290 | ||||||
| chr14:88642374
|
A | G | 4 | a0001c0001t0002g0168a0001c0001t0006g0218a0001c0001t0006g0219others(1): Show | 4 | HG01891.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.4237+519T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88642374 | ||||||
| chr14:88642434
|
G | A | 107 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0002g0001others(104): Show | 109 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.4237+459C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88642434 | ||||||
| chr14:88642527
|
C | T | 4 | a0001c0001t0003g0039a0001c0001t0003g0040a0001c0001t0003g0041others(1): Show | 4 | NA18953.hp2 NA18960.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.4237+366G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88642527 | ||||||
| chr14:88642588
|
A | G | 1 | a0001c0001t0003g0082 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.4237+305T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 31/43 | chr14 | 88642588 | ||||||
| chr14:88643138
|
G | C | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.4108-116C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 30/43 | chr14 | 88643138 | ||||||
| chr14:88643423
|
A | C | 1 | a0001c0001t0014g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4108-401T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 30/43 | chr14 | 88643423 | ||||||
| chr14:88643523
|
A | G | 88 | a0002c0002t0001g0193a0002c0002t0001g0194a0002c0002t0001g0200others(85): Show | 88 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.4108-501T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 30/43 | chr14 | 88643523 | ||||||
| chr14:88643836
|
G | A | 1 | a0001c0001t0005g0175 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.4107+597C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 30/43 | chr14 | 88643836 | ||||||
| chr14:88643872
|
G | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4107+561C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 30/43 | chr14 | 88643872 | ||||||
| chr14:88643884
|
G | A | 6 | a0001c0001t0006g0208a0001c0001t0022g0203a0001c0001t0022g0204others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.4107+549C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 30/43 | chr14 | 88643884 | ||||||
| chr14:88643951
|
A | G | 282 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(279): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.4107+482T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 30/43 | chr14 | 88643951 | ||||||
| chr14:88644047
|
A | G | 1 | a0001c0001t0007g0062 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4107+386T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 30/43 | chr14 | 88644047 | ||||||
| chr14:88644200
|
A | G | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.4107+233T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 30/43 | chr14 | 88644200 | ||||||
| chr14:88644382
|
A | G | 1 | a0001c0003t0006g0221 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4107+51T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 30/43 | chr14 | 88644382 | ||||||
| chr14:88644629
|
C | A | 1 | a0001c0001t0003g0056 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.4029-118G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88644629 | ||||||
| chr14:88644750
|
G | A | 1 | a0001c0001t0002g0140 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4029-239C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88644750 | ||||||
| chr14:88644959
|
G | A | 6 | a0001c0001t0007g0038a0001c0001t0007g0069a0001c0001t0007g0071others(3): Show | 6 | HG00323.hp2 HG00639.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.4029-448C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88644959 | ||||||
| chr14:88645012
|
C | T | 2 | a0001c0003t0004g0318a0001c0003t0004g0319 | 2 | HG00408.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.4029-501G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88645012 | ||||||
| chr14:88645027
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4029-516G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88645027 | ||||||
| chr14:88645033
|
T | C | 1 | a0002c0004t0001g0234 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.4029-522A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88645033 | ||||||
| chr14:88645045
|
T | A | 6 | a0001c0001t0006g0208a0001c0001t0022g0203a0001c0001t0022g0204others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.4029-534A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88645045 | ||||||
| chr14:88645053
|
GTTTCAC | G | 62 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0280others(59): Show | 62 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.4029-548_4029-543d others(8): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88645053 | ||||||
| chr14:88645083
|
G | A | 2 | a0001c0001t0006g0003a0001c0001t0006g0286 | 3 | HG01256.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.4029-572C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88645083 | ||||||
| chr14:88645210
|
G | A | 1 | a0002c0002t0001g0263 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.4029-699C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88645210 | ||||||
| chr14:88645334
|
A | C | 62 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0280others(59): Show | 62 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.4029-823T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88645334 | ||||||
| chr14:88645350
|
G | A | 4 | a0002c0002t0001g0209a0002c0002t0001g0245a0002c0002t0003g0024others(1): Show | 4 | HG01255.hp1 HG01361.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.4029-839C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88645350 | ||||||
| chr14:88645351
|
T | G | 1 | a0001c0001t0003g0081 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.4029-840A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88645351 | ||||||
| chr14:88645449
|
C | T | 90 | a0001c0001t0017g0010a0001c0001t0017g0011a0002c0002t0001g0193others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.4029-938G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88645449 | ||||||
| chr14:88645555
|
C | T | 1 | a0001c0001t0034g0198 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4029-1044G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88645555 | ||||||
| chr14:88645666
|
G | A | 7 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(4): Show | 7 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.4029-1155C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88645666 | ||||||
| chr14:88645848
|
T | C | 1 | a0001c0001t0007g0038 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.4028+1099A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88645848 | ||||||
| chr14:88645942
|
C | T | 1 | a0001c0003t0004g0306 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4028+1005G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88645942 | ||||||
| chr14:88645968
|
T | A | 1 | a0002c0002t0001g0256 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.4028+979A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88645968 | ||||||
| chr14:88646016
|
T | C | 1 | a0001c0001t0003g0043 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.4028+931A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88646016 | ||||||
| chr14:88646230
|
A | C | 1 | a0002c0002t0001g0245 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.4028+717T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88646230 | ||||||
| chr14:88646244
|
A | G | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4028+703T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88646244 | ||||||
| chr14:88646254
|
C | T | 3 | a0002c0002t0001g0224a0002c0002t0001g0225a0002c0002t0001g0226 | 3 | NA18968.hp1 NA18994.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.4028+693G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88646254 | ||||||
| chr14:88646328
|
T | A | 2 | a0001c0001t0002g0089a0001c0001t0002g0090 | 2 | NA19006.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.4028+619A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88646328 | ||||||
| chr14:88646364
|
A | G | 60 | a0001c0001t0001g0280a0001c0001t0001g0290a0001c0001t0003g0036others(57): Show | 60 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.4028+583T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88646364 | ||||||
| chr14:88646833
|
A | C | 7 | a0001c0001t0001g0283a0001c0001t0002g0158a0001c0001t0006g0003others(4): Show | 8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.4028+114T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88646833 | ||||||
| chr14:88646880
|
A | G | 1 | a0001c0001t0006g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4028+67T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 29/43 | chr14 | 88646880 | ||||||
| chr14:88646983
|
A | G | 1 | a0001c0001t0011g0213 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4020-28T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88646983 | ||||||
| chr14:88647231
|
G | T | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.4020-276C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647231 | ||||||
| chr14:88647235
|
G | A | 1 | a0001c0001t0008g0100 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4020-280C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647235 | ||||||
| chr14:88647296
|
G | A | 1 | a0001c0001t0019g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4020-341C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647296 | ||||||
| chr14:88647322
|
T | A | 1 | a0002c0002t0003g0020 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.4020-367A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647322 | ||||||
| chr14:88647325
|
G | A | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4020-370C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647325 | ||||||
| chr14:88647421
|
G | A | 19 | a0001c0001t0006g0208a0001c0001t0006g0218a0001c0001t0006g0219others(16): Show | 19 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.4020-466C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647421 | ||||||
| chr14:88647687
|
C | CA | 83 | a0001c0001t0003g0036a0001c0001t0003g0041a0001c0001t0003g0044others(80): Show | 83 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.4020-733dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647687 | ||||||
| chr14:88647687
|
C | CAA | 21 | a0001c0001t0002g0141a0001c0001t0008g0103a0001c0001t0012g0324others(18): Show | 21 | HG00438.hp1 HG00639.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.4020-734_4020-733d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647687 | ||||||
| chr14:88647687
|
C | CAAA | 89 | a0001c0001t0001g0211a0001c0001t0002g0001a0001c0001t0002g0002others(86): Show | 91 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.4020-735_4020-733d others(5): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647687 | ||||||
| chr14:88647687
|
C | CAAAA | 15 | a0001c0001t0001g0210a0001c0001t0002g0090a0001c0001t0002g0105others(12): Show | 15 | HG01074.hp2 HG01099.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.4020-736_4020-733d others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647687 | ||||||
| chr14:88647687
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0014g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4020-747_4020-733d others(17): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647687 | ||||||
| chr14:88647687
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0014g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4020-748_4020-733d others(18): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647687 | ||||||
| chr14:88647687
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0014g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4020-749_4020-733d others(19): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647687 | ||||||
| chr14:88647687
|
C | CAAAAAAA others(11): Show |
3 | a0001c0001t0022g0204a0001c0001t0024g0206a0001c0001t0036g0205 | 3 | HG01243.hp1 HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.4020-750_4020-733d others(20): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647687 | ||||||
| chr14:88647687
|
C | CAAAAAAA others(12): Show |
2 | a0001c0001t0022g0203a0001c0001t0024g0207 | 2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4020-751_4020-733d others(21): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647687 | ||||||
| chr14:88647687
|
C | CAAAAAAA others(13): Show |
1 | a0001c0001t0006g0208 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4020-752_4020-733d others(22): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647687 | ||||||
| chr14:88647687
|
CA | C | 35 | a0001c0001t0003g0040a0001c0001t0009g0058a0001c0001t0034g0198others(32): Show | 35 | HG00408.hp1 HG00738.hp1 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.4020-733delT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647687 | ||||||
| chr14:88647687
|
CAAA | C | 7 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(4): Show | 7 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.4020-735_4020-733d others(5): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647687 | ||||||
| chr14:88647777
|
G | A | 5 | a0002c0004t0001g0228a0002c0004t0001g0234a0002c0004t0001g0240others(2): Show | 5 | HG00099.hp2 HG01123.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.4020-822C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88647777 | ||||||
| chr14:88648094
|
T | G | 46 | a0001c0001t0001g0283a0001c0001t0002g0158a0001c0001t0006g0003others(43): Show | 47 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(44): Show |
intron_variant | MODIFIER | c.4020-1139A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88648094 | ||||||
| chr14:88648293
|
C | A | 4 | a0001c0001t0011g0213a0001c0001t0011g0214a0001c0001t0011g0215others(1): Show | 4 | HG02280.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.4020-1338G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88648293 | ||||||
| chr14:88648660
|
T | C | 16 | a0001c0001t0005g0171a0001c0001t0005g0172a0001c0001t0005g0175others(13): Show | 16 | HG00423.hp1 HG00673.hp1 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.4019+1252A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88648660 | ||||||
| chr14:88648690
|
A | T | 3 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0007g0134 | 3 | HG01516.hp2 HG01517.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.4019+1222T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88648690 | ||||||
| chr14:88648816
|
T | C | 7 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(4): Show | 7 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.4019+1096A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88648816 | ||||||
| chr14:88648872
|
A | AT | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4019+1039dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88648872 | ||||||
| chr14:88649139
|
C | T | 1 | a0001c0001t0002g0133 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.4019+773G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88649139 | ||||||
| chr14:88649256
|
G | C | 2 | a0001c0001t0002g0109a0001c0001t0002g0110 | 2 | HG02165.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.4019+656C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88649256 | ||||||
| chr14:88649336
|
T | C | 33 | a0001c0003t0002g0012a0001c0003t0004g0302a0001c0003t0004g0303others(30): Show | 33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.4019+576A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88649336 | ||||||
| chr14:88649619
|
T | G | 1 | a0001c0001t0003g0055 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.4019+293A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88649619 | ||||||
| chr14:88649830
|
G | GA | 4 | a0001c0001t0012g0324a0001c0001t0012g0325a0001c0001t0012g0326others(1): Show | 4 | HG00609.hp1 NA18953.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.4019+81dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 28/43 | chr14 | 88649830 | ||||||
| chr14:88649978
|
A | G | 1 | a0002c0002t0003g0028 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4005-52T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88649978 | ||||||
| chr14:88650145
|
T | C | 1 | a0001c0001t0006g0208 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4005-219A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88650145 | ||||||
| chr14:88650174
|
T | C | 289 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(286): Show | 292 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.4005-248A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88650174 | ||||||
| chr14:88650190
|
T | C | 7 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(4): Show | 7 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.4005-264A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88650190 | ||||||
| chr14:88650282
|
G | A | 8 | a0001c0001t0001g0283a0001c0001t0002g0158a0001c0001t0006g0003others(5): Show | 9 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.4005-356C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88650282 | ||||||
| chr14:88650381
|
G | A | 1 | a0001c0001t0006g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4005-455C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88650381 | ||||||
| chr14:88650849
|
C | G | 1 | a0001c0001t0006g0218 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4005-923G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88650849 | ||||||
| chr14:88650870
|
A | G | 269 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(266): Show | 272 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.4005-944T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88650870 | ||||||
| chr14:88650915
|
T | C | 1 | a0001c0001t0003g0057 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.4005-989A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88650915 | ||||||
| chr14:88650957
|
G | T | 2 | a0001c0001t0011g0214a0001c0001t0011g0215 | 2 | HG02280.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.4005-1031C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88650957 | ||||||
| chr14:88651023
|
A | T | 1 | a0002c0002t0001g0278 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.4005-1097T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88651023 | ||||||
| chr14:88651131
|
G | A | 326 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(323): Show | 329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.4005-1205C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88651131 | ||||||
| chr14:88651154
|
CT | C | 230 | a0001c0001t0001g0283a0001c0001t0002g0001a0001c0001t0002g0002others(227): Show | 232 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.4005-1229delA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88651154 | ||||||
| chr14:88651154
|
CTT | C | 40 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0002g0096others(37): Show | 41 | HG00673.hp2 HG00738.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.4005-1230_4005-122 others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88651154 | ||||||
| chr14:88651160
|
T | C | 2 | a0001c0001t0017g0010a0001c0001t0017g0011 | 2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4005-1234A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88651160 | ||||||
| chr14:88651163
|
T | C | 6 | a0001c0001t0006g0208a0001c0001t0022g0203a0001c0001t0022g0204others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.4005-1237A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88651163 | ||||||
| chr14:88651208
|
C | T | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4005-1282G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88651208 | ||||||
| chr14:88651246
|
T | TGTC | 4 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0034g0198others(1): Show | 4 | HG02559.hp2 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.4005-1323_4005-132 others(7): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88651246 | ||||||
| chr14:88651398
|
A | G | 1 | a0001c0001t0002g0114 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.4005-1472T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88651398 | ||||||
| chr14:88651554
|
T | A | 1 | a0001c0003t0018g0016 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4005-1628A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88651554 | ||||||
| chr14:88651807
|
G | A | 5 | a0002c0004t0001g0228a0002c0004t0001g0234a0002c0004t0001g0240others(2): Show | 5 | HG00099.hp2 HG01123.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.4005-1881C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88651807 | ||||||
| chr14:88652043
|
T | C | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4005-2117A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88652043 | ||||||
| chr14:88652347
|
C | T | 103 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(100): Show | 105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.4005-2421G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88652347 | ||||||
| chr14:88652433
|
C | A | 2 | a0001c0001t0005g0171a0001c0001t0005g0172 | 2 | NA18983.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.4005-2507G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88652433 | ||||||
| chr14:88652535
|
T | C | 2 | a0002c0002t0001g0229a0002c0002t0001g0279 | 2 | HG00609.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.4005-2609A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88652535 | ||||||
| chr14:88652720
|
T | C | 2 | a0001c0001t0002g0112a0001c0001t0002g0113 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.4005-2794A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88652720 | ||||||
| chr14:88652734
|
C | T | 1 | a0001c0001t0008g0100 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4005-2808G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88652734 | ||||||
| chr14:88652843
|
T | C | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.4005-2917A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88652843 | ||||||
| chr14:88652873
|
C | T | 2 | a0001c0001t0002g0091a0001c0001t0002g0155 | 2 | HG01261.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.4005-2947G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88652873 | ||||||
| chr14:88653121
|
C | T | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4005-3195G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88653121 | ||||||
| chr14:88653157
|
C | T | 33 | a0001c0003t0002g0012a0001c0003t0004g0302a0001c0003t0004g0303others(30): Show | 33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.4005-3231G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88653157 | ||||||
| chr14:88653340
|
A | G | 6 | a0002c0002t0003g0019a0002c0002t0003g0020a0002c0002t0003g0021others(3): Show | 6 | HG02165.hp1 NA18948.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.4005-3414T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88653340 | ||||||
| chr14:88653408
|
T | C | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4005-3482A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88653408 | ||||||
| chr14:88653472
|
C | T | 1 | a0001c0001t0006g0208 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4005-3546G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88653472 | ||||||
| chr14:88653512
|
C | T | 3 | a0001c0001t0006g0218a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02559.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4005-3586G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88653512 | ||||||
| chr14:88653524
|
G | A | 1 | a0001c0001t0003g0169 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.4005-3598C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88653524 | ||||||
| chr14:88653551
|
A | G | 1 | a0001c0001t0003g0039 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.4005-3625T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88653551 | ||||||
| chr14:88653724
|
C | T | 10 | a0001c0003t0004g0303a0001c0003t0004g0304a0001c0003t0004g0305others(7): Show | 10 | HG02257.hp1 HG02280.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.4004+3652G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88653724 | ||||||
| chr14:88653988
|
G | C | 6 | a0001c0001t0006g0208a0001c0001t0022g0203a0001c0001t0022g0204others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.4004+3388C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88653988 | ||||||
| chr14:88654097
|
A | G | 103 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(100): Show | 105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.4004+3279T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88654097 | ||||||
| chr14:88654298
|
C | A | 27 | a0001c0003t0004g0302a0001c0003t0004g0303a0001c0003t0004g0304others(24): Show | 27 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(24): Show |
intron_variant | MODIFIER | c.4004+3078G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88654298 | ||||||
| chr14:88654528
|
C | T | 267 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(264): Show | 270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.4004+2848G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88654528 | ||||||
| chr14:88655153
|
A | G | 1 | a0002c0002t0003g0021 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.4004+2223T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88655153 | ||||||
| chr14:88655279
|
T | G | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.4004+2097A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88655279 | ||||||
| chr14:88656471
|
G | A | 1 | a0001c0001t0017g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4004+905C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88656471 | ||||||
| chr14:88656615
|
A | AT | 4 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0034g0198others(1): Show | 4 | HG02559.hp2 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.4004+760dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88656615 | ||||||
| chr14:88656746
|
GGACT | G | 175 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(172): Show | 178 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.4004+626_4004+629d others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88656746 | ||||||
| chr14:88656907
|
A | G | 1 | a0009c0012t0001g0247 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.4004+469T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88656907 | ||||||
| chr14:88656968
|
T | A | 18 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(15): Show | 19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.4004+408A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88656968 | ||||||
| chr14:88657019
|
G | A | 1 | a0001c0001t0007g0084 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4004+357C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88657019 | ||||||
| chr14:88657145
|
C | G | 103 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(100): Show | 105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.4004+231G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88657145 | ||||||
| chr14:88657286
|
T | C | 1 | a0001c0001t0005g0175 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.4004+90A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88657286 | ||||||
| chr14:88657337
|
A | G | 1 | a0001c0001t0005g0186 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.4004+39T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 27/43 | chr14 | 88657337 | ||||||
| chr14:88657570
|
A | G | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3878-68T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 26/43 | chr14 | 88657570 | ||||||
| chr14:88657647
|
C | T | 2 | a0001c0001t0024g0206a0001c0001t0024g0207 | 2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3878-145G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 26/43 | chr14 | 88657647 | ||||||
| chr14:88657830
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0201 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3878-328C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 26/43 | chr14 | 88657830 | ||||||
| chr14:88657870
|
C | T | 1 | a0001c0001t0002g0128 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3877+317G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 26/43 | chr14 | 88657870 | ||||||
| chr14:88657881
|
T | C | 23 | a0001c0001t0005g0171a0001c0001t0005g0172a0001c0001t0005g0175others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.3877+306A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 26/43 | chr14 | 88657881 | ||||||
| chr14:88657937
|
A | G | 1 | a0001c0001t0007g0062 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3877+250T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 26/43 | chr14 | 88657937 | ||||||
| chr14:88658076
|
TACC | T | 175 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(172): Show | 178 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.3877+108_3877+110d others(5): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 26/43 | chr14 | 88658076 | ||||||
| chr14:88658799
|
ATAGT | A | 17 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(14): Show | 17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.3676-415_3676-412d others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88658799 | ||||||
| chr14:88658918
|
G | A | 1 | a0001c0001t0007g0072 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.3676-530C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88658918 | ||||||
| chr14:88658940
|
T | A | 1 | a0001c0001t0017g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3676-552A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88658940 | ||||||
| chr14:88658944
|
G | A | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.3676-556C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88658944 | ||||||
| chr14:88659236
|
ACT | A | 3 | a0002c0002t0021g0273a0002c0002t0021g0292a0002c0002t0038g0297 | 3 | HG00323.hp1 HG00733.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.3676-850_3676-849d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88659236 | ||||||
| chr14:88659241
|
C | CT | 34 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(31): Show | 36 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.3676-854dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88659241 | ||||||
| chr14:88659330
|
C | T | 33 | a0001c0003t0002g0012a0001c0003t0004g0302a0001c0003t0004g0303others(30): Show | 33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.3676-942G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88659330 | ||||||
| chr14:88659540
|
G | C | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.3676-1152C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88659540 | ||||||
| chr14:88659679
|
C | T | 2 | a0001c0001t0024g0206a0001c0001t0024g0207 | 2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3676-1291G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88659679 | ||||||
| chr14:88659717
|
C | G | 1 | a0001c0001t0002g0091 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3676-1329G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88659717 | ||||||
| chr14:88659808
|
A | G | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.3676-1420T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88659808 | ||||||
| chr14:88660011
|
C | T | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3676-1623G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88660011 | ||||||
| chr14:88660144
|
A | G | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.3675+1510T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88660144 | ||||||
| chr14:88660184
|
G | A | 51 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(48): Show | 52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.3675+1470C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88660184 | ||||||
| chr14:88660187
|
G | A | 2 | a0001c0001t0003g0044a0001c0001t0003g0047 | 2 | HG03654.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.3675+1467C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88660187 | ||||||
| chr14:88660202
|
G | A | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.3675+1452C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88660202 | ||||||
| chr14:88660282
|
T | TA | 57 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(54): Show | 58 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(55): Show |
intron_variant | MODIFIER | c.3675+1371dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88660282 | ||||||
| chr14:88660282
|
TA | T | 7 | a0001c0001t0002g0109a0001c0001t0002g0112a0001c0001t0003g0046others(4): Show | 7 | HG01069.hp2 HG01168.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.3675+1371delT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88660282 | ||||||
| chr14:88660341
|
T | A | 1 | a0001c0001t0032g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3675+1313A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88660341 | ||||||
| chr14:88660517
|
C | T | 1 | a0001c0001t0002g0122 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3675+1137G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88660517 | ||||||
| chr14:88660700
|
G | A | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.3675+954C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88660700 | ||||||
| chr14:88660748
|
A | AAAAAAAG | 170 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(167): Show | 173 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.3675+899_3675+905d others(9): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88660748 | ||||||
| chr14:88660806
|
T | C | 8 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(5): Show | 8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.3675+848A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88660806 | ||||||
| chr14:88661021
|
T | C | 102 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(99): Show | 104 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.3675+633A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88661021 | ||||||
| chr14:88661095
|
G | C | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3675+559C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88661095 | ||||||
| chr14:88661112
|
A | G | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.3675+542T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88661112 | ||||||
| chr14:88661261
|
T | G | 11 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0006g0218others(8): Show | 11 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.3675+393A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88661261 | ||||||
| chr14:88661449
|
T | C | 1 | a0001c0001t0003g0040 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3675+205A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 25/43 | chr14 | 88661449 | ||||||
| chr14:88661954
|
A | C | 8 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(5): Show | 8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.3499-124T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88661954 | ||||||
| chr14:88662286
|
T | TA | 157 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(154): Show | 160 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.3499-457dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662286 | ||||||
| chr14:88662286
|
T | TAA | 20 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(17): Show | 20 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.3499-458_3499-457d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662286 | ||||||
| chr14:88662339
|
G | GT | 148 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(145): Show | 150 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.3499-510dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662339 | ||||||
| chr14:88662339
|
G | GTT | 69 | a0001c0001t0002g0090a0001c0001t0002g0091a0001c0001t0002g0098others(66): Show | 70 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.3499-511_3499-510d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662339 | ||||||
| chr14:88662339
|
G | GTTT | 14 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(11): Show | 14 | HG01106.hp2 HG01433.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.3499-512_3499-510d others(5): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662339 | ||||||
| chr14:88662339
|
G | GTTTTTTT others(3): Show |
2 | a0001c0001t0014g0004a0001c0001t0014g0006 | 2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3499-519_3499-510d others(12): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662339 | ||||||
| chr14:88662339
|
GTTTTTTT others(11): Show |
G | 4 | a0001c0003t0004g0310a0001c0003t0004g0311a0001c0003t0004g0312others(1): Show | 4 | HG02280.hp2 HG02717.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.3499-527_3499-510d others(20): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662339 | ||||||
| chr14:88662396
|
A | G | 1 | a0001c0001t0006g0208 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3499-566T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662396 | ||||||
| chr14:88662407
|
C | T | 106 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(103): Show | 108 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.3499-577G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662407 | ||||||
| chr14:88662542
|
C | CT | 62 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0280others(59): Show | 62 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.3498+488dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662542 | ||||||
| chr14:88662560
|
T | A | 24 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(21): Show | 25 | HG00642.hp2 HG00741.hp2 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.3498+471A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662560 | ||||||
| chr14:88662560
|
T | TA | 121 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(118): Show | 123 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.3498+470dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662560 | ||||||
| chr14:88662560
|
T | TAA | 29 | a0001c0003t0002g0012a0001c0003t0004g0302a0001c0003t0004g0303others(26): Show | 29 | HG00408.hp1 HG02055.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.3498+469_3498+470d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662560 | ||||||
| chr14:88662628
|
C | T | 1 | a0001c0001t0036g0205 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3498+403G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662628 | ||||||
| chr14:88662629
|
G | A | 1 | a0001c0001t0011g0213 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3498+402C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662629 | ||||||
| chr14:88662763
|
T | C | 2 | a0001c0001t0002g0126a0001c0001t0002g0127 | 2 | HG01175.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.3498+268A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662763 | ||||||
| chr14:88662958
|
T | C | 1 | a0002c0002t0001g0209 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3498+73A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662958 | ||||||
| chr14:88662960
|
G | C | 103 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(100): Show | 105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.3498+71C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 24/43 | chr14 | 88662960 | ||||||
| chr14:88663235
|
T | G | 8 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(5): Show | 8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.3410-116A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 23/43 | chr14 | 88663235 | ||||||
| chr14:88663262
|
CATTTT | C | 3 | a0001c0001t0014g0004a0001c0001t0014g0005a0001c0001t0014g0006 | 3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3410-148_3410-144d others(7): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 23/43 | chr14 | 88663262 | ||||||
| chr14:88663452
|
TATATAGT others(8): Show |
T | 18 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(15): Show | 19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.3410-348_3410-334d others(17): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 23/43 | chr14 | 88663452 | ||||||
| chr14:88663467
|
A | G | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3410-348T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 23/43 | chr14 | 88663467 | ||||||
| chr14:88663490
|
A | G | 5 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0006g0218others(2): Show | 5 | HG02559.hp1 HG02647.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.3410-371T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 23/43 | chr14 | 88663490 | ||||||
| chr14:88663731
|
C | T | 8 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(5): Show | 8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.3410-612G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 23/43 | chr14 | 88663731 | ||||||
| chr14:88663834
|
C | T | 1 | a0001c0001t0014g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3409+659G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 23/43 | chr14 | 88663834 | ||||||
| chr14:88663908
|
C | A | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.3409+585G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 23/43 | chr14 | 88663908 | ||||||
| chr14:88663908
|
C | T | 265 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(262): Show | 268 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.3409+585G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 23/43 | chr14 | 88663908 | ||||||
| chr14:88664044
|
A | C | 1 | a0001c0001t0002g0090 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.3409+449T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 23/43 | chr14 | 88664044 | ||||||
| chr14:88664275
|
C | CA | 72 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(69): Show | 73 | HG00408.hp1 HG00642.hp2 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.3409+217dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 23/43 | chr14 | 88664275 | ||||||
| chr14:88664275
|
C | CAAA | 100 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(97): Show | 102 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.3409+215_3409+217d others(5): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 23/43 | chr14 | 88664275 | ||||||
| chr14:88664275
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0003g0163 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.3409+208_3409+217d others(12): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 23/43 | chr14 | 88664275 | ||||||
| chr14:88664296
|
G | GAAAAAGG others(2): Show |
3 | a0002c0002t0001g0232a0002c0002t0001g0233a0002c0002t0001g0261 | 3 | NA18947.hp2 NA18962.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.3409+188_3409+196d others(11): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 23/43 | chr14 | 88664296 | ||||||
| chr14:88664881
|
T | C | 18 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(15): Show | 19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.3278-257A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 22/43 | chr14 | 88664881 | ||||||
| chr14:88665089
|
A | T | 7 | a0001c0001t0001g0283a0001c0001t0002g0158a0001c0001t0006g0003others(4): Show | 8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.3277+248T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 22/43 | chr14 | 88665089 | ||||||
| chr14:88665103
|
G | C | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.3277+234C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 22/43 | chr14 | 88665103 | ||||||
| chr14:88665644
|
T | C | 1 | a0001c0001t0002g0120 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3125-155A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88665644 | ||||||
| chr14:88665648
|
A | G | 9 | a0001c0001t0002g0168a0001c0001t0023g0195a0001c0001t0023g0197others(6): Show | 9 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.3125-159T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88665648 | ||||||
| chr14:88665739
|
A | G | 1 | a0001c0001t0006g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3125-250T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88665739 | ||||||
| chr14:88665822
|
T | C | 90 | a0001c0001t0017g0010a0001c0001t0017g0011a0002c0002t0001g0193others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.3125-333A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88665822 | ||||||
| chr14:88665826
|
T | G | 1 | a0001c0001t0003g0165 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3125-337A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88665826 | ||||||
| chr14:88665836
|
A | T | 1 | a0005c0014t0001g0272 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3125-347T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88665836 | ||||||
| chr14:88665907
|
C | CA | 9 | a0001c0001t0002g0124a0001c0001t0014g0004a0001c0003t0006g0221others(6): Show | 9 | HG00544.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.3125-419dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88665907 | ||||||
| chr14:88665907
|
CA | C | 6 | a0001c0001t0003g0056a0002c0002t0001g0268a0002c0002t0003g0028others(3): Show | 6 | HG01255.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.3125-419delT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88665907 | ||||||
| chr14:88665920
|
A | T | 7 | a0001c0001t0001g0283a0001c0001t0002g0158a0001c0001t0006g0003others(4): Show | 8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.3125-431T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88665920 | ||||||
| chr14:88666072
|
A | G | 2 | a0001c0001t0005g0176a0001c0001t0005g0177 | 2 | NA18956.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.3125-583T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88666072 | ||||||
| chr14:88666257
|
T | C | 267 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(264): Show | 270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.3125-768A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88666257 | ||||||
| chr14:88666378
|
C | T | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3125-889G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88666378 | ||||||
| chr14:88666501
|
C | T | 1 | a0001c0001t0002g0147 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3125-1012G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88666501 | ||||||
| chr14:88666511
|
C | T | 2 | a0003c0005t0015g0014a0003c0005t0015g0015 | 2 | HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3125-1022G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88666511 | ||||||
| chr14:88666588
|
G | A | 267 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(264): Show | 270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.3125-1099C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88666588 | ||||||
| chr14:88666620
|
G | T | 103 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(100): Show | 105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.3125-1131C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88666620 | ||||||
| chr14:88666626
|
TTTA | T | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3125-1140_3125-113 others(7): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88666626 | ||||||
| chr14:88666629
|
A | C | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.3125-1140T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88666629 | ||||||
| chr14:88666948
|
T | A | 1 | a0001c0003t0004g0322 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3125-1459A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88666948 | ||||||
| chr14:88666975
|
A | G | 1 | a0001c0001t0002g0141 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3125-1486T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88666975 | ||||||
| chr14:88667056
|
G | A | 1 | a0001c0001t0002g0111 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3125-1567C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88667056 | ||||||
| chr14:88667096
|
T | C | 1 | a0001c0001t0003g0040 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3125-1607A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88667096 | ||||||
| chr14:88667104
|
A | G | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(16): Show | 20 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.3125-1615T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88667104 | ||||||
| chr14:88667117
|
C | T | 1 | a0001c0001t0027g0295 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3125-1628G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88667117 | ||||||
| chr14:88667337
|
T | C | 3 | a0001c0001t0014g0004a0001c0001t0014g0005a0001c0001t0014g0006 | 3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3125-1848A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88667337 | ||||||
| chr14:88667597
|
G | C | 2 | a0001c0001t0017g0010a0001c0001t0017g0011 | 2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.3125-2108C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88667597 | ||||||
| chr14:88667801
|
C | T | 1 | a0002c0002t0001g0245 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3125-2312G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88667801 | ||||||
| chr14:88668016
|
C | T | 269 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(266): Show | 272 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.3125-2527G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88668016 | ||||||
| chr14:88668018
|
C | A | 1 | a0002c0002t0003g0031 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3125-2529G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88668018 | ||||||
| chr14:88668136
|
C | T | 88 | a0002c0002t0001g0193a0002c0002t0001g0194a0002c0002t0001g0200others(85): Show | 88 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.3125-2647G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88668136 | ||||||
| chr14:88668270
|
C | T | 3 | a0001c0001t0006g0218a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02559.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3125-2781G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88668270 | ||||||
| chr14:88668299
|
G | A | 72 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(69): Show | 74 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.3125-2810C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88668299 | ||||||
| chr14:88668338
|
T | G | 2 | a0001c0001t0002g0137a0001c0001t0002g0138 | 2 | HG02055.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.3125-2849A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88668338 | ||||||
| chr14:88668342
|
A | G | 176 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(173): Show | 179 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.3125-2853T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88668342 | ||||||
| chr14:88668371
|
A | G | 8 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(5): Show | 8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.3125-2882T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88668371 | ||||||
| chr14:88668434
|
G | A | 2 | a0001c0001t0001g0280a0001c0001t0003g0083 | 2 | HG00642.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.3125-2945C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88668434 | ||||||
| chr14:88668445
|
G | C | 1 | a0001c0001t0010g0033 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3125-2956C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88668445 | ||||||
| chr14:88668937
|
C | T | 1 | a0001c0001t0003g0051 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3125-3448G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88668937 | ||||||
| chr14:88668943
|
C | T | 1 | a0002c0002t0003g0025 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3125-3454G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88668943 | ||||||
| chr14:88668945
|
G | A | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3125-3456C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88668945 | ||||||
| chr14:88669190
|
C | T | 33 | a0001c0003t0002g0012a0001c0003t0004g0302a0001c0003t0004g0303others(30): Show | 33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.3125-3701G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88669190 | ||||||
| chr14:88669391
|
T | G | 1 | a0002c0002t0001g0231 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.3125-3902A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88669391 | ||||||
| chr14:88669528
|
G | A | 1 | a0001c0003t0004g0323 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3125-4039C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88669528 | ||||||
| chr14:88669790
|
T | G | 14 | a0002c0002t0001g0235a0002c0002t0001g0236a0002c0002t0001g0250others(11): Show | 14 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.3125-4301A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88669790 | ||||||
| chr14:88669815
|
A | G | 103 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(100): Show | 105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.3125-4326T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88669815 | ||||||
| chr14:88669930
|
T | C | 1 | a0001c0001t0006g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3125-4441A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88669930 | ||||||
| chr14:88670012
|
T | C | 300 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(297): Show | 303 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.3125-4523A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88670012 | ||||||
| chr14:88670083
|
G | A | 2 | a0001c0001t0002g0124a0001c0001t0002g0125 | 2 | NA18943.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.3125-4594C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88670083 | ||||||
| chr14:88670108
|
G | A | 177 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(174): Show | 180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.3125-4619C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88670108 | ||||||
| chr14:88670162
|
A | C | 50 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(47): Show | 51 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(48): Show |
intron_variant | MODIFIER | c.3125-4673T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88670162 | ||||||
| chr14:88670319
|
C | CA | 152 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0280others(149): Show | 155 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.3125-4831dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88670319 | ||||||
| chr14:88670319
|
C | CAA | 30 | a0001c0001t0002g0111a0001c0001t0002g0149a0001c0001t0002g0155others(27): Show | 30 | HG00642.hp2 HG00673.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.3125-4832_3125-483 others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88670319 | ||||||
| chr14:88670347
|
G | T | 1 | a0001c0003t0004g0323 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3125-4858C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88670347 | ||||||
| chr14:88670579
|
G | A | 3 | a0001c0001t0014g0004a0001c0001t0014g0005a0001c0001t0014g0006 | 3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3125-5090C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88670579 | ||||||
| chr14:88670892
|
G | A | 4 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0034g0198others(1): Show | 4 | HG02559.hp2 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.3125-5403C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88670892 | ||||||
| chr14:88670980
|
G | A | 1 | a0001c0001t0028g0009 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3125-5491C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88670980 | ||||||
| chr14:88671259
|
A | G | 1 | a0001c0001t0005g0172 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3125-5770T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88671259 | ||||||
| chr14:88671397
|
G | A | 8 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(5): Show | 8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.3125-5908C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88671397 | ||||||
| chr14:88671479
|
C | T | 1 | a0002c0002t0001g0263 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3125-5990G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88671479 | ||||||
| chr14:88671516
|
G | C | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.3125-6027C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88671516 | ||||||
| chr14:88671581
|
G | T | 1 | a0001c0003t0013g0298 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3125-6092C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88671581 | ||||||
| chr14:88671582
|
C | T | 8 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(5): Show | 8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.3125-6093G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88671582 | ||||||
| chr14:88671679
|
C | G | 1 | a0001c0001t0003g0063 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3125-6190G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88671679 | ||||||
| chr14:88671992
|
A | C | 328 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(325): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.3125-6503T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88671992 | ||||||
| chr14:88672011
|
A | G | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.3125-6522T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88672011 | ||||||
| chr14:88672135
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0201 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3125-6646C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88672135 | ||||||
| chr14:88672286
|
C | T | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.3125-6797G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88672286 | ||||||
| chr14:88672287
|
C | T | 1 | a0001c0001t0005g0171 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.3125-6798G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88672287 | ||||||
| chr14:88672373
|
G | C | 8 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(5): Show | 8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.3125-6884C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88672373 | ||||||
| chr14:88672515
|
G | A | 2 | a0001c0001t0024g0206a0001c0001t0024g0207 | 2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3125-7026C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88672515 | ||||||
| chr14:88672631
|
A | G | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3125-7142T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88672631 | ||||||
| chr14:88672636
|
A | G | 102 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(99): Show | 104 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.3125-7147T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88672636 | ||||||
| chr14:88672701
|
G | A | 103 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(100): Show | 105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.3125-7212C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88672701 | ||||||
| chr14:88672778
|
G | A | 4 | a0001c0003t0013g0298a0001c0003t0013g0299a0001c0003t0013g0300others(1): Show | 4 | HG02886.hp2 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.3125-7289C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88672778 | ||||||
| chr14:88672829
|
C | T | 1 | a0001c0001t0003g0043 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.3125-7340G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88672829 | ||||||
| chr14:88672860
|
G | A | 1 | a0001c0003t0004g0317 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3125-7371C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88672860 | ||||||
| chr14:88672865
|
A | G | 85 | a0002c0002t0001g0193a0002c0002t0001g0194a0002c0002t0001g0200others(82): Show | 85 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.3125-7376T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88672865 | ||||||
| chr14:88672888
|
G | A | 1 | a0001c0001t0003g0041 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.3125-7399C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88672888 | ||||||
| chr14:88672963
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0201 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3125-7474C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88672963 | ||||||
| chr14:88673344
|
C | T | 1 | a0002c0002t0001g0275 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3125-7855G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88673344 | ||||||
| chr14:88673611
|
T | C | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3125-8122A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88673611 | ||||||
| chr14:88673813
|
T | C | 177 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(174): Show | 180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.3124+8077A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88673813 | ||||||
| chr14:88673848
|
C | T | 1 | a0002c0002t0001g0253 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3124+8042G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88673848 | ||||||
| chr14:88674272
|
AAACAAC | A | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3124+7612_3124+761 others(10): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88674272 | ||||||
| chr14:88674412
|
C | G | 3 | a0001c0001t0008g0102a0001c0001t0008g0103a0001c0001t0008g0104 | 3 | HG02895.hp2 HG02897.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3124+7478G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88674412 | ||||||
| chr14:88674582
|
G | A | 1 | a0001c0001t0032g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3124+7308C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88674582 | ||||||
| chr14:88674591
|
T | C | 2 | a0002c0002t0003g0023a0002c0002t0033g0170 | 2 | NA18948.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.3124+7299A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88674591 | ||||||
| chr14:88674678
|
T | C | 1 | a0001c0003t0004g0315 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3124+7212A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88674678 | ||||||
| chr14:88674728
|
T | C | 33 | a0001c0003t0002g0012a0001c0003t0004g0302a0001c0003t0004g0303others(30): Show | 33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.3124+7162A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88674728 | ||||||
| chr14:88674821
|
TG | T | 103 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(100): Show | 105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.3124+7068delC | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88674821 | ||||||
| chr14:88674904
|
C | T | 7 | a0001c0001t0001g0283a0001c0001t0002g0158a0001c0001t0006g0003others(4): Show | 8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.3124+6986G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88674904 | ||||||
| chr14:88675052
|
C | T | 1 | a0001c0001t0002g0095 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3124+6838G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88675052 | ||||||
| chr14:88675178
|
C | T | 8 | a0001c0001t0002g0095a0001c0001t0002g0111a0001c0001t0002g0112others(5): Show | 8 | HG00438.hp2 HG01099.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.3124+6712G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88675178 | ||||||
| chr14:88675298
|
G | A | 1 | a0002c0002t0033g0170 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.3124+6592C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88675298 | ||||||
| chr14:88675506
|
G | A | 1 | a0001c0001t0003g0047 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3124+6384C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88675506 | ||||||
| chr14:88675518
|
G | A | 103 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(100): Show | 105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.3124+6372C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88675518 | ||||||
| chr14:88675727
|
T | A | 3 | a0002c0002t0021g0273a0002c0002t0021g0292a0002c0002t0038g0297 | 3 | HG00323.hp1 HG00733.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.3124+6163A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88675727 | ||||||
| chr14:88676077
|
A | G | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.3124+5813T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88676077 | ||||||
| chr14:88676146
|
T | C | 1 | a0001c0001t0003g0040 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3124+5744A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88676146 | ||||||
| chr14:88676500
|
C | T | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.3124+5390G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88676500 | ||||||
| chr14:88676505
|
A | G | 267 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(264): Show | 270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.3124+5385T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88676505 | ||||||
| chr14:88676532
|
G | A | 1 | a0001c0003t0004g0315 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3124+5358C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88676532 | ||||||
| chr14:88676755
|
A | G | 1 | a0001c0003t0004g0311 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3124+5135T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88676755 | ||||||
| chr14:88676790
|
T | C | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3124+5100A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88676790 | ||||||
| chr14:88677169
|
T | C | 1 | a0001c0001t0011g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3124+4721A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88677169 | ||||||
| chr14:88677268
|
G | A | 4 | a0001c0003t0004g0310a0001c0003t0004g0311a0001c0003t0004g0312others(1): Show | 4 | HG02280.hp2 HG02717.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.3124+4622C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88677268 | ||||||
| chr14:88677327
|
T | C | 18 | a0001c0001t0002g0168a0001c0001t0006g0208a0001c0001t0014g0004others(15): Show | 18 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.3124+4563A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88677327 | ||||||
| chr14:88677390
|
C | T | 1 | a0001c0001t0003g0081 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.3124+4500G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88677390 | ||||||
| chr14:88677415
|
G | T | 1 | a0001c0001t0002g0121 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3124+4475C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88677415 | ||||||
| chr14:88677473
|
G | A | 1 | a0001c0001t0005g0183 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3124+4417C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88677473 | ||||||
| chr14:88677507
|
G | T | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.3124+4383C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88677507 | ||||||
| chr14:88678047
|
C | T | 1 | a0001c0001t0002g0107 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3124+3843G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88678047 | ||||||
| chr14:88678313
|
G | C | 1 | a0001c0001t0002g0106 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3124+3577C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88678313 | ||||||
| chr14:88678534
|
T | C | 1 | a0001c0001t0007g0084 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3124+3356A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88678534 | ||||||
| chr14:88678549
|
A | G | 1 | a0001c0001t0002g0106 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3124+3341T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88678549 | ||||||
| chr14:88678645
|
T | A | 33 | a0001c0003t0002g0012a0001c0003t0004g0302a0001c0003t0004g0303others(30): Show | 33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.3124+3245A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88678645 | ||||||
| chr14:88678656
|
G | T | 18 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(15): Show | 19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.3124+3234C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88678656 | ||||||
| chr14:88678738
|
T | C | 18 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(15): Show | 19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.3124+3152A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88678738 | ||||||
| chr14:88678811
|
T | C | 18 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(15): Show | 19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.3124+3079A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88678811 | ||||||
| chr14:88678818
|
T | C | 1 | a0002c0002t0001g0226 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3124+3072A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88678818 | ||||||
| chr14:88678946
|
T | G | 63 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(60): Show | 65 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.3124+2944A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88678946 | ||||||
| chr14:88678952
|
G | A | 2 | a0002c0002t0001g0243a0002c0002t0001g0246 | 2 | HG01099.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.3124+2938C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88678952 | ||||||
| chr14:88679069
|
T | C | 2 | a0001c0001t0001g0199a0001c0001t0001g0201 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3124+2821A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88679069 | ||||||
| chr14:88679509
|
T | C | 1 | a0001c0003t0004g0315 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3124+2381A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88679509 | ||||||
| chr14:88679529
|
T | C | 1 | a0002c0002t0001g0281 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3124+2361A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88679529 | ||||||
| chr14:88679553
|
G | A | 3 | a0001c0001t0006g0218a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02559.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3124+2337C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88679553 | ||||||
| chr14:88679560
|
C | T | 1 | a0001c0001t0002g0138 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3124+2330G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88679560 | ||||||
| chr14:88679561
|
G | A | 52 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(49): Show | 53 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(50): Show |
intron_variant | MODIFIER | c.3124+2329C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88679561 | ||||||
| chr14:88679566
|
C | T | 1 | a0001c0001t0006g0220 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3124+2324G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88679566 | ||||||
| chr14:88679624
|
G | A | 90 | a0001c0001t0017g0010a0001c0001t0017g0011a0002c0002t0001g0193others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.3124+2266C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88679624 | ||||||
| chr14:88680053
|
T | C | 1 | a0002c0002t0003g0094 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3124+1837A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88680053 | ||||||
| chr14:88680628
|
A | G | 1 | a0001c0001t0002g0118 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.3124+1262T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88680628 | ||||||
| chr14:88680801
|
A | G | 267 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(264): Show | 270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.3124+1089T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88680801 | ||||||
| chr14:88680833
|
G | C | 1 | a0001c0001t0008g0100 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3124+1057C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88680833 | ||||||
| chr14:88680922
|
C | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0201 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3124+968G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88680922 | ||||||
| chr14:88681122
|
T | C | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3124+768A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88681122 | ||||||
| chr14:88681365
|
C | T | 103 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(100): Show | 105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.3124+525G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88681365 | ||||||
| chr14:88681454
|
A | G | 2 | a0001c0003t0004g0309a0001c0003t0004g0313 | 2 | HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3124+436T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88681454 | ||||||
| chr14:88681669
|
G | A | 10 | a0002c0002t0001g0250a0002c0002t0001g0251a0002c0002t0001g0252others(7): Show | 10 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.3124+221C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88681669 | ||||||
| chr14:88681742
|
A | G | 1 | a0001c0003t0004g0328 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3124+148T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88681742 | ||||||
| chr14:88681877
|
G | T | 1 | a0001c0001t0003g0169 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3124+13C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 21/43 | chr14 | 88681877 | ||||||
| chr14:88682142
|
C | T | 90 | a0001c0001t0017g0010a0001c0001t0017g0011a0002c0002t0001g0193others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.2983-111G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88682142 | ||||||
| chr14:88682204
|
T | C | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.2983-173A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88682204 | ||||||
| chr14:88682208
|
T | C | 1 | a0001c0003t0004g0321 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2983-177A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88682208 | ||||||
| chr14:88682408
|
T | TA | 36 | a0001c0003t0002g0012a0001c0003t0004g0302a0001c0003t0004g0303others(33): Show | 36 | HG00408.hp1 HG01433.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.2983-378dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88682408 | ||||||
| chr14:88682408
|
TA | T | 20 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0006g0208others(17): Show | 20 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.2983-378delT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88682408 | ||||||
| chr14:88682622
|
C | G | 1 | a0001c0001t0003g0055 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2983-591G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88682622 | ||||||
| chr14:88682683
|
G | A | 1 | a0001c0003t0006g0221 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2983-652C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88682683 | ||||||
| chr14:88682858
|
C | T | 1 | a0001c0003t0013g0299 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2983-827G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88682858 | ||||||
| chr14:88682866
|
G | A | 102 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(99): Show | 104 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.2983-835C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88682866 | ||||||
| chr14:88682927
|
C | T | 1 | a0001c0001t0005g0171 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2983-896G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88682927 | ||||||
| chr14:88683130
|
T | A | 1 | a0002c0002t0001g0282 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2983-1099A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88683130 | ||||||
| chr14:88683176
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2983-1145C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88683176 | ||||||
| chr14:88683179
|
G | A | 2 | a0001c0001t0005g0171a0001c0001t0005g0172 | 2 | NA18983.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2983-1148C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88683179 | ||||||
| chr14:88683231
|
G | C | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2983-1200C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88683231 | ||||||
| chr14:88683513
|
A | G | 7 | a0001c0001t0002g0002a0001c0001t0002g0086a0001c0001t0002g0141others(4): Show | 8 | NA18960.hp2 NA18968.hp2 NA18974.hp2 others(5): Show |
intron_variant | MODIFIER | c.2983-1482T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88683513 | ||||||
| chr14:88683773
|
A | G | 52 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(49): Show | 53 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(50): Show |
intron_variant | MODIFIER | c.2982+1242T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88683773 | ||||||
| chr14:88683860
|
G | C | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2982+1155C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88683860 | ||||||
| chr14:88683876
|
C | T | 1 | a0002c0002t0001g0235 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2982+1139G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88683876 | ||||||
| chr14:88683938
|
T | C | 1 | a0001c0001t0019g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2982+1077A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88683938 | ||||||
| chr14:88683964
|
T | C | 3 | a0001c0001t0014g0004a0001c0001t0014g0005a0001c0001t0014g0006 | 3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2982+1051A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88683964 | ||||||
| chr14:88683997
|
T | C | 18 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(15): Show | 19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.2982+1018A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88683997 | ||||||
| chr14:88684103
|
C | T | 4 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0034g0198others(1): Show | 4 | HG02559.hp2 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2982+912G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684103 | ||||||
| chr14:88684225
|
G | T | 8 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(5): Show | 8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2982+790C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684225 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2720): Show |
3 | a0001c0001t0003g0043a0001c0001t0003g0052a0001c0001t0003g0082 | 3 | NA18954.hp2 NA18995.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2729): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2720): Show |
1 | a0001c0001t0003g0053 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2729): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2708): Show |
1 | a0001c0001t0032g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2717): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2715): Show |
1 | a0002c0002t0003g0028 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2724): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2717): Show |
1 | a0002c0002t0003g0025 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2726): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2719): Show |
2 | a0001c0001t0003g0039a0001c0001t0003g0040 | 2 | NA18953.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2728): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2717): Show |
3 | a0002c0004t0001g0234a0002c0004t0001g0241a0002c0004t0001g0242 | 3 | HG00099.hp2 HG01123.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2726): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2717): Show |
11 | a0002c0002t0001g0222a0002c0002t0001g0229a0002c0002t0001g0254others(8): Show | 11 | HG00609.hp2 HG01891.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2726): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2717): Show |
52 | a0002c0002t0001g0193a0002c0002t0001g0194a0002c0002t0001g0200others(49): Show | 52 | HG00280.hp2 HG00323.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2726): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2717): Show |
8 | a0002c0002t0001g0231a0002c0002t0001g0249a0002c0002t0001g0263others(5): Show | 8 | HG00438.hp1 HG01978.hp1 HG04184.hp2 others(5): Show |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2726): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2711): Show |
1 | a0002c0002t0001g0227 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2720): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2718): Show |
3 | a0002c0002t0001g0232a0002c0002t0001g0233a0002c0002t0001g0261 | 3 | NA18947.hp2 NA18962.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2727): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2720): Show |
2 | a0001c0001t0002g0122a0008c0011t0008g0101 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2729): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2718): Show |
1 | a0002c0002t0001g0239 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2727): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2718): Show |
1 | a0002c0002t0001g0288 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2727): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2718): Show |
5 | a0002c0002t0001g0243a0002c0002t0001g0244a0002c0002t0001g0246others(2): Show | 5 | HG01099.hp2 HG01109.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2727): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2719): Show |
4 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0034g0198others(1): Show | 4 | HG02559.hp2 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2728): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2719): Show |
2 | a0001c0001t0026g0293a0001c0001t0026g0294 | 2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2728): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2719): Show |
2 | a0001c0001t0027g0295a0001c0001t0027g0296 | 2 | HG00642.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2728): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2720): Show |
1 | a0001c0001t0003g0055 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2729): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2716): Show |
1 | a0001c0001t0022g0204 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2725): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2720): Show |
1 | a0001c0001t0003g0041 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2729): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2720): Show |
4 | a0001c0001t0003g0163a0001c0001t0003g0164a0001c0001t0003g0166others(1): Show | 4 | HG00741.hp1 HG01069.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2729): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2719): Show |
1 | a0001c0003t0013g0298 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2728): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2720): Show |
29 | a0001c0001t0001g0280a0001c0001t0001g0290a0001c0001t0003g0045others(26): Show | 29 | HG00323.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2729): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2721): Show |
1 | a0001c0001t0003g0051 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2719): Show |
3 | a0001c0003t0013g0299a0001c0003t0013g0300a0001c0009t0013g0301 | 3 | HG02886.hp2 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2728): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2720): Show |
18 | a0001c0001t0003g0044a0001c0001t0003g0048a0001c0001t0003g0049others(15): Show | 18 | HG00099.hp1 HG01074.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2729): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2721): Show |
1 | a0001c0003t0004g0323 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2720): Show |
17 | a0001c0003t0004g0305a0001c0003t0004g0306a0001c0003t0004g0307others(14): Show | 17 | HG02257.hp1 HG02280.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2729): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2721): Show |
1 | a0001c0003t0004g0315 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2721): Show |
2 | a0001c0003t0004g0316a0001c0003t0004g0317 | 2 | HG03017.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2714): Show |
2 | a0001c0003t0004g0318a0001c0003t0004g0319 | 2 | HG00408.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2723): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2719): Show |
1 | a0001c0001t0017g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2728): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2718): Show |
1 | a0001c0001t0017g0011 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2727): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2721): Show |
1 | a0001c0003t0004g0320 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2721): Show |
1 | a0001c0001t0005g0187 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2721): Show |
6 | a0001c0001t0002g0089a0001c0001t0008g0102a0001c0001t0008g0103others(3): Show | 6 | HG02895.hp2 HG02897.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2721): Show |
19 | a0001c0001t0005g0171a0001c0001t0005g0172a0001c0001t0005g0175others(16): Show | 19 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2721): Show |
62 | a0001c0001t0002g0001a0001c0001t0002g0087a0001c0001t0002g0088others(59): Show | 63 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2722): Show |
1 | a0001c0001t0006g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2731): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2721): Show |
1 | a0001c0001t0005g0184 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2720): Show |
1 | a0001c0001t0002g0148 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2729): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2721): Show |
1 | a0001c0001t0002g0116 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2722): Show |
7 | a0001c0001t0002g0002a0001c0001t0002g0086a0001c0001t0002g0098others(4): Show | 8 | NA18960.hp2 NA18968.hp2 NA18974.hp2 others(5): Show |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2731): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2721): Show |
1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2722): Show |
1 | a0001c0001t0012g0326 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2731): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2716): Show |
7 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(4): Show | 7 | HG01243.hp1 HG02145.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2725): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2720): Show |
1 | a0001c0003t0004g0302 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2729): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2717): Show |
1 | a0001c0001t0024g0206 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2726): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2719): Show |
2 | a0001c0001t0001g0199a0001c0001t0001g0201 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2728): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2710): Show |
1 | a0001c0001t0019g0212 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2719): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2721): Show |
2 | a0001c0001t0003g0036a0001c0001t0003g0037 | 2 | HG02738.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2721): Show |
1 | a0001c0001t0019g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2718): Show |
1 | a0001c0001t0006g0220 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2727): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2721): Show |
3 | a0001c0001t0011g0214a0001c0001t0011g0215a0001c0001t0011g0216 | 3 | HG02280.hp1 HG02615.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2718): Show |
4 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0006g0218others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2727): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2715): Show |
1 | a0001c0001t0011g0213 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2724): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2721): Show |
7 | a0001c0001t0001g0283a0001c0001t0002g0158a0001c0001t0006g0003others(4): Show | 8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2721): Show |
1 | a0001c0001t0008g0100 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2730): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2716): Show |
3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2982+778_2982+779i others(2725): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684236
|
A | ATAAATTT others(2717): Show |
1 | a0002c0004t0001g0228 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2982+778_2982+779i others(2726): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684236 | ||||||
| chr14:88684272
|
G | A | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2982+743C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684272 | ||||||
| chr14:88684306
|
G | A | 4 | a0001c0001t0002g0158a0001c0001t0006g0284a0001c0001t0006g0285others(1): Show | 4 | HG00741.hp2 HG01257.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.2982+709C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684306 | ||||||
| chr14:88684317
|
C | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2982+698G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684317 | ||||||
| chr14:88684349
|
C | T | 177 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(174): Show | 180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.2982+666G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684349 | ||||||
| chr14:88684359
|
A | G | 1 | a0001c0001t0003g0056 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2982+656T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684359 | ||||||
| chr14:88684391
|
C | T | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2982+624G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684391 | ||||||
| chr14:88684421
|
C | G | 51 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(48): Show | 52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.2982+594G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684421 | ||||||
| chr14:88684459
|
C | T | 4 | a0001c0001t0003g0048a0001c0001t0003g0049a0001c0001t0003g0050others(1): Show | 4 | HG02622.hp1 HG02818.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2982+556G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684459 | ||||||
| chr14:88684460
|
G | A | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2982+555C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684460 | ||||||
| chr14:88684529
|
A | ACATT | 267 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(264): Show | 270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.2982+482_2982+485d others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684529 | ||||||
| chr14:88684678
|
G | T | 267 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(264): Show | 270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.2982+337C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684678 | ||||||
| chr14:88684818
|
A | T | 1 | a0001c0001t0002g0148 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2982+197T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684818 | ||||||
| chr14:88684852
|
G | A | 269 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(266): Show | 272 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.2982+163C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684852 | ||||||
| chr14:88684879
|
AT | A | 102 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(99): Show | 104 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.2982+135delA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684879 | ||||||
| chr14:88684978
|
T | C | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2982+37A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684978 | ||||||
| chr14:88684999
|
T | C | 51 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(48): Show | 52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.2982+16A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 20/43 | chr14 | 88684999 | ||||||
| chr14:88685303
|
T | G | 1 | a0001c0001t0010g0035 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2855-161A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 19/43 | chr14 | 88685303 | ||||||
| chr14:88685409
|
A | G | 6 | a0002c0002t0003g0019a0002c0002t0003g0020a0002c0002t0003g0021others(3): Show | 6 | HG02165.hp1 NA18948.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.2855-267T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 19/43 | chr14 | 88685409 | ||||||
| chr14:88685453
|
T | C | 11 | a0001c0001t0003g0039a0001c0001t0003g0040a0001c0001t0003g0041others(8): Show | 11 | HG02738.hp1 HG03490.hp1 HG03492.hp2 others(8): Show |
intron_variant | MODIFIER | c.2855-311A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 19/43 | chr14 | 88685453 | ||||||
| chr14:88685488
|
T | C | 1 | a0001c0001t0007g0078 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2855-346A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 19/43 | chr14 | 88685488 | ||||||
| chr14:88685772
|
T | C | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2855-630A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 19/43 | chr14 | 88685772 | ||||||
| chr14:88685978
|
G | T | 1 | a0002c0002t0037g0262 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2855-836C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 19/43 | chr14 | 88685978 | ||||||
| chr14:88686051
|
C | T | 4 | a0001c0001t0011g0213a0001c0001t0011g0214a0001c0001t0011g0215others(1): Show | 4 | HG02280.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.2855-909G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 19/43 | chr14 | 88686051 | ||||||
| chr14:88686308
|
C | T | 27 | a0001c0003t0004g0302a0001c0003t0004g0303a0001c0003t0004g0304others(24): Show | 27 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(24): Show |
intron_variant | MODIFIER | c.2854+908G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 19/43 | chr14 | 88686308 | ||||||
| chr14:88686559
|
C | T | 1 | a0001c0001t0008g0104 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2854+657G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 19/43 | chr14 | 88686559 | ||||||
| chr14:88686634
|
G | A | 5 | a0001c0001t0003g0074a0001c0001t0003g0163a0001c0001t0003g0164others(2): Show | 5 | HG00741.hp1 HG01069.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2854+582C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 19/43 | chr14 | 88686634 | ||||||
| chr14:88686683
|
C | T | 1 | a0001c0003t0004g0309 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2854+533G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 19/43 | chr14 | 88686683 | ||||||
| chr14:88686706
|
G | A | 1 | a0001c0001t0003g0054 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2854+510C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 19/43 | chr14 | 88686706 | ||||||
| chr14:88686765
|
T | C | 2 | a0002c0002t0001g0258a0002c0002t0001g0259 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2854+451A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 19/43 | chr14 | 88686765 | ||||||
| chr14:88687401
|
G | T | 2 | a0001c0001t0017g0010a0001c0001t0017g0011 | 2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2743-74C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 18/43 | chr14 | 88687401 | ||||||
| chr14:88687682
|
T | TA | 269 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(266): Show | 272 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.2743-356_2743-355i others(3): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 18/43 | chr14 | 88687682 | ||||||
| chr14:88687765
|
C | CA | 52 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(49): Show | 53 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(50): Show |
intron_variant | MODIFIER | c.2743-439dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 18/43 | chr14 | 88687765 | ||||||
| chr14:88687803
|
C | T | 8 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(5): Show | 8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2742+468G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 18/43 | chr14 | 88687803 | ||||||
| chr14:88687910
|
A | T | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2742+361T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 18/43 | chr14 | 88687910 | ||||||
| chr14:88687948
|
G | A | 6 | a0001c0003t0004g0303a0001c0003t0004g0304a0001c0003t0004g0305others(3): Show | 6 | HG02257.hp1 HG02622.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2742+323C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 18/43 | chr14 | 88687948 | ||||||
| chr14:88687996
|
A | G | 33 | a0001c0003t0002g0012a0001c0003t0004g0302a0001c0003t0004g0303others(30): Show | 33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.2742+275T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 18/43 | chr14 | 88687996 | ||||||
| chr14:88688572
|
AG | A | 6 | a0001c0003t0004g0303a0001c0003t0004g0304a0001c0003t0004g0305others(3): Show | 6 | HG02257.hp1 HG02622.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2540-100delC | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88688572 | ||||||
| chr14:88688811
|
C | T | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2540-338G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88688811 | ||||||
| chr14:88688845
|
A | G | 1 | a0001c0001t0005g0175 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2540-372T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88688845 | ||||||
| chr14:88688864
|
T | C | 8 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(5): Show | 8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2540-391A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88688864 | ||||||
| chr14:88688875
|
C | T | 1 | a0002c0002t0001g0278 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2540-402G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88688875 | ||||||
| chr14:88688897
|
T | C | 3 | a0001c0001t0014g0004a0001c0001t0014g0005a0001c0001t0014g0006 | 3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2540-424A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88688897 | ||||||
| chr14:88689068
|
T | C | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2540-595A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88689068 | ||||||
| chr14:88689138
|
T | A | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.2540-665A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88689138 | ||||||
| chr14:88689237
|
T | A | 4 | a0001c0003t0013g0298a0001c0003t0013g0299a0001c0003t0013g0300others(1): Show | 4 | HG02886.hp2 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2540-764A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88689237 | ||||||
| chr14:88689321
|
TTA | T | 77 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(74): Show | 79 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.2540-850_2540-849d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88689321 | ||||||
| chr14:88689515
|
C | A | 1 | a0001c0001t0005g0180 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2540-1042G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88689515 | ||||||
| chr14:88689618
|
C | T | 11 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0006g0218others(8): Show | 11 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.2540-1145G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88689618 | ||||||
| chr14:88689756
|
A | G | 5 | a0001c0001t0008g0102a0001c0001t0008g0103a0001c0001t0008g0104others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2540-1283T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88689756 | ||||||
| chr14:88689862
|
G | A | 90 | a0001c0001t0017g0010a0001c0001t0017g0011a0002c0002t0001g0193others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.2540-1389C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88689862 | ||||||
| chr14:88690067
|
A | T | 6 | a0001c0003t0004g0303a0001c0003t0004g0304a0001c0003t0004g0305others(3): Show | 6 | HG02257.hp1 HG02622.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2540-1594T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88690067 | ||||||
| chr14:88690129
|
A | G | 14 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(11): Show | 15 | HG01256.hp2 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.2540-1656T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88690129 | ||||||
| chr14:88690360
|
G | T | 27 | a0001c0003t0004g0302a0001c0003t0004g0303a0001c0003t0004g0304others(24): Show | 27 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(24): Show |
intron_variant | MODIFIER | c.2540-1887C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88690360 | ||||||
| chr14:88690434
|
C | T | 1 | a0001c0003t0004g0322 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2540-1961G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88690434 | ||||||
| chr14:88690598
|
G | C | 1 | a0001c0001t0001g0210 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2540-2125C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88690598 | ||||||
| chr14:88690599
|
T | C | 3 | a0002c0002t0001g0239a0002c0002t0001g0243a0002c0002t0001g0246 | 3 | HG01099.hp2 HG01109.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.2540-2126A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88690599 | ||||||
| chr14:88690631
|
G | A | 1 | a0001c0001t0002g0143 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2540-2158C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88690631 | ||||||
| chr14:88691185
|
G | C | 1 | a0001c0001t0036g0205 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2540-2712C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88691185 | ||||||
| chr14:88691632
|
C | T | 2 | a0001c0001t0002g0129a0001c0001t0002g0130 | 2 | NA18986.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.2539+2675G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88691632 | ||||||
| chr14:88691652
|
T | G | 2 | a0001c0001t0001g0199a0001c0001t0001g0201 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2539+2655A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88691652 | ||||||
| chr14:88691674
|
T | C | 2 | a0001c0001t0019g0212a0001c0001t0019g0217 | 2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2539+2633A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88691674 | ||||||
| chr14:88691739
|
A | T | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.2539+2568T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88691739 | ||||||
| chr14:88691823
|
T | C | 1 | a0001c0001t0003g0052 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2539+2484A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88691823 | ||||||
| chr14:88692015
|
C | T | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.2539+2292G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88692015 | ||||||
| chr14:88692146
|
G | A | 1 | a0002c0002t0001g0222 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2539+2161C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88692146 | ||||||
| chr14:88692245
|
C | T | 51 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(48): Show | 52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.2539+2062G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88692245 | ||||||
| chr14:88692308
|
T | C | 269 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(266): Show | 272 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.2539+1999A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88692308 | ||||||
| chr14:88692342
|
A | C | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2539+1965T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88692342 | ||||||
| chr14:88692379
|
A | G | 103 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(100): Show | 105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.2539+1928T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88692379 | ||||||
| chr14:88692668
|
A | T | 269 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(266): Show | 272 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.2539+1639T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88692668 | ||||||
| chr14:88692703
|
C | T | 106 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(103): Show | 108 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.2539+1604G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88692703 | ||||||
| chr14:88692710
|
G | A | 3 | a0001c0001t0003g0048a0001c0001t0003g0049a0001c0001t0003g0050 | 3 | HG02622.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2539+1597C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88692710 | ||||||
| chr14:88692783
|
C | T | 1 | a0002c0002t0007g0030 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2539+1524G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88692783 | ||||||
| chr14:88692861
|
G | C | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.2539+1446C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88692861 | ||||||
| chr14:88693371
|
G | A | 103 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(100): Show | 105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.2539+936C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88693371 | ||||||
| chr14:88693379
|
T | C | 1 | a0001c0001t0010g0033 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2539+928A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88693379 | ||||||
| chr14:88693432
|
G | C | 1 | a0001c0001t0019g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2539+875C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88693432 | ||||||
| chr14:88693614
|
C | A | 1 | a0001c0001t0005g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2539+693G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88693614 | ||||||
| chr14:88693763
|
C | CT | 14 | a0001c0001t0001g0210a0001c0001t0003g0036a0001c0001t0003g0051others(11): Show | 14 | HG00733.hp2 HG01175.hp2 HG02293.hp1 others(11): Show |
intron_variant | MODIFIER | c.2539+543dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88693763 | ||||||
| chr14:88693763
|
CT | C | 202 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0002g0001others(199): Show | 204 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.2539+543delA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88693763 | ||||||
| chr14:88693763
|
CTT | C | 14 | a0001c0001t0002g0107a0001c0001t0002g0125a0001c0001t0002g0129others(11): Show | 14 | HG00642.hp2 HG01167.hp1 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.2539+542_2539+543d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88693763 | ||||||
| chr14:88693763
|
CTTTT | C | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2539+540_2539+543d others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88693763 | ||||||
| chr14:88693819
|
T | G | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2539+488A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88693819 | ||||||
| chr14:88693848
|
G | A | 1 | a0001c0001t0007g0084 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2539+459C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88693848 | ||||||
| chr14:88693937
|
A | AT | 17 | a0001c0001t0002g0151a0001c0001t0003g0040a0001c0001t0007g0062others(14): Show | 17 | HG00642.hp2 HG01109.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.2539+369dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88693937 | ||||||
| chr14:88694015
|
C | G | 3 | a0002c0002t0001g0224a0002c0002t0001g0225a0002c0002t0001g0226 | 3 | NA18968.hp1 NA18994.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.2539+292G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88694015 | ||||||
| chr14:88694074
|
A | G | 1 | a0002c0002t0001g0264 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2539+233T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88694074 | ||||||
| chr14:88694280
|
T | C | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2539+27A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 17/43 | chr14 | 88694280 | ||||||
| chr14:88694737
|
A | G | 1 | a0001c0001t0005g0183 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2439-330T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 16/43 | chr14 | 88694737 | ||||||
| chr14:88694796
|
T | C | 1 | a0002c0002t0001g0279 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2439-389A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 16/43 | chr14 | 88694796 | ||||||
| chr14:88694951
|
A | C | 2 | a0001c0001t0022g0203a0001c0001t0022g0204 | 2 | HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2438+410T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 16/43 | chr14 | 88694951 | ||||||
| chr14:88695063
|
C | T | 1 | a0002c0002t0001g0279 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2438+298G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 16/43 | chr14 | 88695063 | ||||||
| chr14:88695171
|
C | T | 2 | a0001c0001t0002g0120a0001c0001t0002g0133 | 2 | NA18962.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.2438+190G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 16/43 | chr14 | 88695171 | ||||||
| chr14:88695175
|
G | A | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.2438+186C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 16/43 | chr14 | 88695175 | ||||||
| chr14:88695209
|
CTATGAT | C | 90 | a0001c0001t0017g0010a0001c0001t0017g0011a0002c0002t0001g0193others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.2438+146_2438+151d others(8): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 16/43 | chr14 | 88695209 | ||||||
| chr14:88695299
|
A | T | 1 | a0001c0003t0004g0323 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2438+62T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 16/43 | chr14 | 88695299 | ||||||
| chr14:88695626
|
A | C | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(16): Show | 20 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.2345-172T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 15/43 | chr14 | 88695626 | ||||||
| chr14:88695665
|
G | A | 2 | a0001c0001t0003g0044a0001c0001t0003g0047 | 2 | HG03654.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.2345-211C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 15/43 | chr14 | 88695665 | ||||||
| chr14:88695808
|
A | G | 1 | a0002c0002t0003g0031 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2345-354T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 15/43 | chr14 | 88695808 | ||||||
| chr14:88695844
|
T | C | 2 | a0001c0001t0002g0109a0001c0001t0002g0110 | 2 | HG02165.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.2345-390A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 15/43 | chr14 | 88695844 | ||||||
| chr14:88695847
|
T | A | 1 | a0001c0001t0009g0076 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2345-393A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 15/43 | chr14 | 88695847 | ||||||
| chr14:88695894
|
C | T | 2 | a0001c0001t0024g0206a0001c0001t0024g0207 | 2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2345-440G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 15/43 | chr14 | 88695894 | ||||||
| chr14:88696015
|
G | A | 4 | a0001c0001t0002g0136a0001c0001t0002g0137a0001c0001t0002g0138others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2345-561C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 15/43 | chr14 | 88696015 | ||||||
| chr14:88696164
|
A | AAT | 20 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(17): Show | 21 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.2344+681_2344+682d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 15/43 | chr14 | 88696164 | ||||||
| chr14:88696164
|
AAT | A | 204 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(201): Show | 206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2344+681_2344+682d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 15/43 | chr14 | 88696164 | ||||||
| chr14:88696199
|
T | C | 103 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(100): Show | 105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.2344+648A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 15/43 | chr14 | 88696199 | ||||||
| chr14:88696238
|
A | G | 11 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0006g0218others(8): Show | 11 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.2344+609T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 15/43 | chr14 | 88696238 | ||||||
| chr14:88696452
|
A | T | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.2344+395T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 15/43 | chr14 | 88696452 | ||||||
| chr14:88696565
|
A | G | 4 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0116others(1): Show | 4 | HG01168.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.2344+282T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 15/43 | chr14 | 88696565 | ||||||
| chr14:88696584
|
G | A | 52 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(49): Show | 53 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(50): Show |
intron_variant | MODIFIER | c.2344+263C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 15/43 | chr14 | 88696584 | ||||||
| chr14:88696634
|
A | G | 267 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(264): Show | 270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.2344+213T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 15/43 | chr14 | 88696634 | ||||||
| chr14:88696774
|
C | G | 33 | a0001c0003t0002g0012a0001c0003t0004g0302a0001c0003t0004g0303others(30): Show | 33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.2344+73G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 15/43 | chr14 | 88696774 | ||||||
| chr14:88697167
|
T | C | 6 | a0001c0003t0002g0012a0001c0003t0006g0221a0001c0003t0013g0298others(3): Show | 6 | HG02572.hp1 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2239-215A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88697167 | ||||||
| chr14:88697217
|
T | C | 4 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0034g0198others(1): Show | 4 | HG02559.hp2 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2239-265A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88697217 | ||||||
| chr14:88697231
|
A | G | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2239-279T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88697231 | ||||||
| chr14:88697496
|
C | T | 4 | a0001c0001t0002g0091a0001c0001t0002g0155a0001c0001t0002g0156others(1): Show | 4 | HG00280.hp1 HG01167.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.2239-544G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88697496 | ||||||
| chr14:88697536
|
C | T | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.2239-584G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88697536 | ||||||
| chr14:88697607
|
C | T | 3 | a0002c0002t0001g0200a0002c0002t0001g0248a0002c0002t0001g0249 | 3 | HG00438.hp1 HG00673.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.2239-655G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88697607 | ||||||
| chr14:88697693
|
TAATA | T | 7 | a0002c0002t0001g0227a0002c0002t0001g0264a0002c0002t0001g0265others(4): Show | 7 | HG02132.hp1 NA18943.hp1 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.2239-745_2239-742d others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88697693 | ||||||
| chr14:88697712
|
A | G | 103 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(100): Show | 105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.2239-760T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88697712 | ||||||
| chr14:88697806
|
G | C | 1 | a0001c0001t0006g0208 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2239-854C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88697806 | ||||||
| chr14:88697896
|
C | T | 17 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(14): Show | 17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2239-944G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88697896 | ||||||
| chr14:88697897
|
A | G | 177 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(174): Show | 180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.2239-945T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88697897 | ||||||
| chr14:88697963
|
C | G | 5 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(2): Show | 5 | HG01099.hp1 HG01168.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2239-1011G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88697963 | ||||||
| chr14:88698083
|
C | T | 5 | a0001c0001t0008g0102a0001c0001t0008g0103a0001c0001t0008g0104others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2239-1131G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88698083 | ||||||
| chr14:88698172
|
A | T | 90 | a0001c0001t0017g0010a0001c0001t0017g0011a0002c0002t0001g0193others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.2239-1220T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88698172 | ||||||
| chr14:88698203
|
T | C | 18 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(15): Show | 19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.2239-1251A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88698203 | ||||||
| chr14:88698265
|
C | CT | 189 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(186): Show | 191 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.2239-1314dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88698265 | ||||||
| chr14:88698265
|
C | CTT | 56 | a0001c0001t0001g0211a0001c0001t0001g0283a0001c0001t0006g0003others(53): Show | 57 | HG00408.hp1 HG00609.hp1 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.2239-1315_2239-131 others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88698265 | ||||||
| chr14:88698265
|
C | CTTT | 13 | a0001c0001t0001g0210a0001c0001t0002g0168a0001c0001t0006g0208others(10): Show | 13 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.2239-1316_2239-131 others(7): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88698265 | ||||||
| chr14:88698307
|
C | T | 1 | a0001c0001t0006g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2239-1355G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88698307 | ||||||
| chr14:88698391
|
C | G | 11 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0006g0218others(8): Show | 11 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.2239-1439G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88698391 | ||||||
| chr14:88698813
|
T | G | 2 | a0002c0002t0001g0288a0002c0002t0001g0289 | 2 | HG02040.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.2239-1861A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88698813 | ||||||
| chr14:88698878
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2239-1926C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88698878 | ||||||
| chr14:88698895
|
C | T | 1 | a0001c0001t0003g0169 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2239-1943G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88698895 | ||||||
| chr14:88698989
|
T | A | 1 | a0002c0002t0003g0094 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2239-2037A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88698989 | ||||||
| chr14:88699166
|
C | G | 1 | a0001c0003t0004g0306 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2239-2214G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88699166 | ||||||
| chr14:88699320
|
T | G | 1 | a0002c0002t0003g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2239-2368A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88699320 | ||||||
| chr14:88699451
|
C | T | 1 | a0001c0001t0002g0141 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2239-2499G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88699451 | ||||||
| chr14:88699453
|
C | A | 1 | a0001c0001t0003g0074 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2239-2501G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88699453 | ||||||
| chr14:88699472
|
A | G | 2 | a0001c0003t0020g0173a0001c0003t0020g0174 | 2 | NA18939.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.2239-2520T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88699472 | ||||||
| chr14:88699579
|
G | C | 90 | a0001c0001t0017g0010a0001c0001t0017g0011a0002c0002t0001g0193others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.2239-2627C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88699579 | ||||||
| chr14:88699680
|
A | G | 1 | a0001c0001t0002g0148 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2239-2728T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88699680 | ||||||
| chr14:88699839
|
C | T | 6 | a0001c0001t0006g0208a0001c0001t0022g0203a0001c0001t0022g0204others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.2238+2607G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88699839 | ||||||
| chr14:88700224
|
G | A | 3 | a0001c0001t0014g0004a0001c0001t0014g0005a0001c0001t0014g0006 | 3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2238+2222C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88700224 | ||||||
| chr14:88700308
|
A | T | 22 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(19): Show | 23 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.2238+2138T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88700308 | ||||||
| chr14:88700495
|
A | G | 5 | a0001c0003t0004g0318a0001c0003t0004g0319a0001c0003t0004g0322others(2): Show | 5 | HG00408.hp1 HG03669.hp1 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.2238+1951T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88700495 | ||||||
| chr14:88700614
|
C | T | 11 | a0001c0001t0003g0039a0001c0001t0003g0040a0001c0001t0003g0041others(8): Show | 11 | HG02738.hp1 HG03490.hp1 HG03492.hp2 others(8): Show |
intron_variant | MODIFIER | c.2238+1832G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88700614 | ||||||
| chr14:88701075
|
G | A | 1 | a0002c0002t0001g0274 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2238+1371C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88701075 | ||||||
| chr14:88701083
|
T | C | 33 | a0001c0003t0002g0012a0001c0003t0004g0302a0001c0003t0004g0303others(30): Show | 33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.2238+1363A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88701083 | ||||||
| chr14:88701186
|
T | C | 177 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(174): Show | 180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.2238+1260A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88701186 | ||||||
| chr14:88701499
|
A | G | 1 | a0001c0001t0002g0120 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2238+947T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88701499 | ||||||
| chr14:88701603
|
G | A | 2 | a0001c0001t0002g0126a0001c0001t0002g0127 | 2 | HG01175.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.2238+843C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88701603 | ||||||
| chr14:88701771
|
A | T | 1 | a0002c0002t0001g0275 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2238+675T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88701771 | ||||||
| chr14:88701962
|
G | A | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2238+484C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88701962 | ||||||
| chr14:88702024
|
C | A | 1 | a0001c0001t0003g0047 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2238+422G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88702024 | ||||||
| chr14:88702088
|
A | T | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2238+358T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88702088 | ||||||
| chr14:88702278
|
T | C | 1 | a0002c0002t0001g0249 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2238+168A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 14/43 | chr14 | 88702278 | ||||||
| chr14:88702752
|
T | C | 1 | a0002c0002t0001g0230 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2052-120A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 13/43 | chr14 | 88702752 | ||||||
| chr14:88702958
|
T | C | 2 | a0001c0001t0017g0010a0001c0001t0017g0011 | 2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2052-326A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 13/43 | chr14 | 88702958 | ||||||
| chr14:88703005
|
C | T | 5 | a0001c0001t0002g0097a0001c0001t0002g0118a0001c0001t0002g0132others(2): Show | 5 | HG00408.hp2 NA18954.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.2052-373G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 13/43 | chr14 | 88703005 | ||||||
| chr14:88703184
|
T | C | 3 | a0001c0001t0002g0089a0001c0001t0002g0090a0001c0001t0006g0202 | 3 | NA18971.hp1 NA19006.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.2052-552A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 13/43 | chr14 | 88703184 | ||||||
| chr14:88703419
|
C | T | 10 | a0002c0002t0001g0250a0002c0002t0001g0251a0002c0002t0001g0252others(7): Show | 10 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.2052-787G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 13/43 | chr14 | 88703419 | ||||||
| chr14:88703721
|
T | C | 1 | a0001c0001t0002g0115 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2052-1089A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 13/43 | chr14 | 88703721 | ||||||
| chr14:88703957
|
T | C | 101 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(98): Show | 103 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.2051+903A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 13/43 | chr14 | 88703957 | ||||||
| chr14:88704197
|
T | C | 1 | a0001c0001t0002g0142 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2051+663A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 13/43 | chr14 | 88704197 | ||||||
| chr14:88704200
|
T | G | 1 | a0009c0012t0001g0247 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2051+660A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 13/43 | chr14 | 88704200 | ||||||
| chr14:88704253
|
T | C | 1 | a0001c0001t0014g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2051+607A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 13/43 | chr14 | 88704253 | ||||||
| chr14:88704298
|
C | G | 3 | a0001c0001t0009g0042a0001c0001t0009g0059a0001c0001t0009g0060 | 3 | HG01943.hp2 HG01993.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.2051+562G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 13/43 | chr14 | 88704298 | ||||||
| chr14:88704357
|
A | C | 4 | a0001c0001t0002g0158a0001c0001t0006g0284a0001c0001t0006g0285others(1): Show | 4 | HG00741.hp2 HG01257.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.2051+503T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 13/43 | chr14 | 88704357 | ||||||
| chr14:88704662
|
A | T | 5 | a0001c0001t0014g0004a0001c0001t0014g0005a0001c0001t0014g0006others(2): Show | 5 | HG02040.hp1 HG02717.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.2051+198T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 13/43 | chr14 | 88704662 | ||||||
| chr14:88704993
|
A | G | 6 | a0001c0001t0006g0208a0001c0001t0022g0203a0001c0001t0022g0204others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1933-15T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 12/43 | chr14 | 88704993 | ||||||
| chr14:88705031
|
T | G | 1 | a0001c0001t0028g0009 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1933-53A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 12/43 | chr14 | 88705031 | ||||||
| chr14:88705182
|
C | T | 78 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(75): Show | 80 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.1933-204G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 12/43 | chr14 | 88705182 | ||||||
| chr14:88705251
|
T | C | 1 | a0001c0001t0014g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1932+231A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 12/43 | chr14 | 88705251 | ||||||
| chr14:88705367
|
C | T | 51 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(48): Show | 52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.1932+115G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 12/43 | chr14 | 88705367 | ||||||
| chr14:88705615
|
C | T | 1 | a0002c0002t0007g0030 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1826-27G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 11/43 | chr14 | 88705615 | ||||||
| chr14:88705645
|
G | T | 1 | a0001c0001t0002g0123 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1826-57C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 11/43 | chr14 | 88705645 | ||||||
| chr14:88705762
|
A | G | 1 | a0001c0001t0002g0117 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1826-174T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 11/43 | chr14 | 88705762 | ||||||
| chr14:88705873
|
C | T | 1 | a0001c0001t0007g0084 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1826-285G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 11/43 | chr14 | 88705873 | ||||||
| chr14:88705948
|
A | T | 1 | a0001c0001t0002g0121 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1825+311T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 11/43 | chr14 | 88705948 | ||||||
| chr14:88706563
|
T | C | 106 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(103): Show | 108 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.1658-137A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88706563 | ||||||
| chr14:88706573
|
G | A | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1658-147C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88706573 | ||||||
| chr14:88706796
|
G | T | 1 | a0001c0003t0004g0317 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1658-370C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88706796 | ||||||
| chr14:88706984
|
T | C | 1 | a0001c0003t0004g0310 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1658-558A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88706984 | ||||||
| chr14:88707200
|
T | C | 7 | a0001c0001t0002g0106a0001c0001t0002g0123a0001c0001t0002g0136others(4): Show | 7 | HG01109.hp2 HG02055.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1658-774A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88707200 | ||||||
| chr14:88707270
|
T | TTTTA | 139 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0280others(136): Show | 142 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.1658-848_1658-845d others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88707270 | ||||||
| chr14:88707270
|
T | TTTTATTT others(1): Show |
31 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(28): Show | 31 | HG00438.hp2 HG00642.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.1658-852_1658-845d others(10): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88707270 | ||||||
| chr14:88707270
|
T | TTTTATTT others(5): Show |
3 | a0001c0001t0005g0187a0001c0001t0014g0005a0001c0001t0023g0195 | 3 | NA19030.hp2 NA19043.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1658-856_1658-845d others(14): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88707270 | ||||||
| chr14:88707270
|
TTTTA | T | 3 | a0001c0001t0007g0062a0001c0001t0017g0010a0002c0004t0001g0240 | 3 | HG01243.hp2 HG01884.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1658-848_1658-845d others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88707270 | ||||||
| chr14:88707270
|
TTTTATTT others(5): Show |
T | 5 | a0002c0002t0001g0200a0002c0002t0001g0238a0002c0002t0001g0248others(2): Show | 5 | HG00438.hp1 HG00673.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.1658-856_1658-845d others(14): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88707270 | ||||||
| chr14:88707276
|
T | G | 1 | a0001c0001t0003g0053 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1658-850A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88707276 | ||||||
| chr14:88707343
|
G | A | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1658-917C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88707343 | ||||||
| chr14:88707496
|
T | C | 1 | a0002c0002t0003g0029 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1658-1070A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88707496 | ||||||
| chr14:88707549
|
C | T | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1658-1123G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88707549 | ||||||
| chr14:88707948
|
A | G | 18 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(15): Show | 19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1658-1522T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88707948 | ||||||
| chr14:88707951
|
A | G | 1 | a0002c0002t0001g0232 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1658-1525T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88707951 | ||||||
| chr14:88708242
|
A | C | 1 | a0001c0001t0008g0131 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1658-1816T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88708242 | ||||||
| chr14:88708323
|
T | C | 1 | a0001c0001t0002g0143 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1658-1897A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88708323 | ||||||
| chr14:88708616
|
C | T | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1658-2190G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88708616 | ||||||
| chr14:88708871
|
T | C | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1658-2445A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88708871 | ||||||
| chr14:88709008
|
G | A | 1 | a0002c0002t0003g0094 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1658-2582C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88709008 | ||||||
| chr14:88709024
|
T | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1658-2598A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88709024 | ||||||
| chr14:88709083
|
A | C | 1 | a0001c0001t0003g0052 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1658-2657T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88709083 | ||||||
| chr14:88709158
|
A | AT | 177 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(174): Show | 180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.1658-2733_1658-273 others(5): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88709158 | ||||||
| chr14:88709381
|
A | ATATAAAG others(191): Show |
3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1657+2889_1657+289 others(202): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88709381 | ||||||
| chr14:88709479
|
C | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1657+2792G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88709479 | ||||||
| chr14:88709809
|
T | A | 1 | a0002c0002t0001g0253 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1657+2462A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88709809 | ||||||
| chr14:88709819
|
A | G | 1 | a0001c0001t0006g0208 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1657+2452T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88709819 | ||||||
| chr14:88709911
|
T | C | 1 | a0001c0001t0028g0009 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1657+2360A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88709911 | ||||||
| chr14:88710057
|
C | T | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1657+2214G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88710057 | ||||||
| chr14:88710159
|
C | T | 1 | a0002c0002t0007g0030 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1657+2112G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88710159 | ||||||
| chr14:88710208
|
T | A | 107 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(104): Show | 109 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.1657+2063A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88710208 | ||||||
| chr14:88710216
|
G | T | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1657+2055C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88710216 | ||||||
| chr14:88710268
|
G | A | 51 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(48): Show | 52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.1657+2003C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88710268 | ||||||
| chr14:88710409
|
T | C | 1 | a0001c0001t0002g0142 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1657+1862A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88710409 | ||||||
| chr14:88710739
|
C | CA | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1657+1531dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88710739 | ||||||
| chr14:88710910
|
A | C | 5 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(2): Show | 5 | HG00423.hp2 NA18944.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.1657+1361T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88710910 | ||||||
| chr14:88710974
|
A | G | 1 | a0002c0002t0001g0223 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1657+1297T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88710974 | ||||||
| chr14:88711085
|
A | T | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1657+1186T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711085 | ||||||
| chr14:88711090
|
A | C | 2 | a0001c0001t0002g0121a0001c0001t0002g0122 | 2 | HG03041.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1657+1181T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711090 | ||||||
| chr14:88711251
|
G | A | 90 | a0001c0001t0017g0010a0001c0001t0017g0011a0002c0002t0001g0193others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1657+1020C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711251 | ||||||
| chr14:88711328
|
G | A | 1 | a0001c0001t0002g0145 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1657+943C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711328 | ||||||
| chr14:88711354
|
T | C | 90 | a0001c0001t0017g0010a0001c0001t0017g0011a0002c0002t0001g0193others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1657+917A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711354 | ||||||
| chr14:88711376
|
G | GCAGTTCC others(1381): Show |
1 | a0001c0003t0018g0016 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1657+894_1657+895i others(1390): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | ||||||
| chr14:88711376
|
G | GCAGTTCC others(1382): Show |
25 | a0001c0003t0004g0303a0001c0003t0004g0304a0001c0003t0004g0305others(22): Show | 25 | HG00408.hp1 HG02135.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.1657+894_1657+895i others(1391): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | ||||||
| chr14:88711376
|
G | GCAGTTCC others(1383): Show |
1 | a0001c0001t0024g0206 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1657+894_1657+895i others(1392): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | ||||||
| chr14:88711376
|
G | GCAGTTCC others(1383): Show |
1 | a0001c0001t0006g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1657+894_1657+895i others(1392): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | ||||||
| chr14:88711376
|
G | GCAGTTCC others(1383): Show |
9 | a0001c0001t0002g0127a0001c0001t0002g0152a0001c0003t0002g0012others(6): Show | 9 | HG02055.hp2 HG02572.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.1657+894_1657+895i others(1392): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | ||||||
| chr14:88711376
|
G | GCAGTTCC others(1384): Show |
1 | a0001c0001t0027g0296 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1657+894_1657+895i others(1393): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | ||||||
| chr14:88711376
|
G | GCAGTTCC others(1384): Show |
10 | a0001c0001t0014g0004a0001c0001t0014g0005a0001c0001t0014g0006others(7): Show | 10 | HG02145.hp1 HG02559.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1657+894_1657+895i others(1393): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | ||||||
| chr14:88711376
|
G | GCAGTTCC others(1384): Show |
5 | a0001c0001t0002g0168a0001c0001t0022g0203a0001c0001t0022g0204others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1657+894_1657+895i others(1393): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | ||||||
| chr14:88711376
|
G | GCAGTTCC others(1384): Show |
2 | a0001c0001t0019g0212a0001c0001t0019g0217 | 2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1657+894_1657+895i others(1393): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | ||||||
| chr14:88711376
|
G | GCAGTTCC others(1384): Show |
6 | a0001c0001t0002g0158a0001c0001t0006g0003a0001c0001t0006g0284others(3): Show | 7 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1657+894_1657+895i others(1393): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | ||||||
| chr14:88711376
|
G | GCAGTTCC others(1384): Show |
9 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0006g0218others(6): Show | 9 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1657+894_1657+895i others(1393): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | ||||||
| chr14:88711376
|
G | GCAGTTCC others(1384): Show |
1 | a0001c0001t0002g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1657+894_1657+895i others(1393): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | ||||||
| chr14:88711376
|
G | GCAGTTCC others(1384): Show |
1 | a0001c0001t0005g0184 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1657+894_1657+895i others(1393): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | ||||||
| chr14:88711376
|
G | GCAGTTCC others(1384): Show |
1 | a0001c0001t0002g0141 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1657+894_1657+895i others(1393): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | ||||||
| chr14:88711376
|
G | GCAGTTCC others(1383): Show |
1 | a0001c0001t0002g0095 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1657+894_1657+895i others(1392): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | ||||||
| chr14:88711376
|
G | GCAGTTCC others(1385): Show |
1 | a0001c0001t0005g0179 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1657+894_1657+895i others(1394): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | ||||||
| chr14:88711376
|
G | GCAGTTCC others(1384): Show |
86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(83): Show | 88 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.1657+894_1657+895i others(1393): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | ||||||
| chr14:88711376
|
G | GCAGTTCC others(1376): Show |
1 | a0001c0001t0002g0126 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1657+894_1657+895i others(1385): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | ||||||
| chr14:88711376
|
G | GCAGTTCC others(1385): Show |
3 | a0001c0001t0006g0208a0004c0007t0016g0007a0004c0007t0016g0008 | 3 | HG02040.hp1 HG02145.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1657+894_1657+895i others(1394): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | ||||||
| chr14:88711376
|
G | GCAGTTCC others(1385): Show |
1 | a0001c0001t0001g0283 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1657+894_1657+895i others(1394): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | ||||||
| chr14:88711376
|
G | GCAGTTCC others(1385): Show |
10 | a0001c0001t0002g0091a0001c0001t0002g0106a0001c0001t0002g0114others(7): Show | 10 | HG00423.hp1 HG01261.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1657+894_1657+895i others(1394): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | ||||||
| chr14:88711376
|
G | GCAGTTCC others(1386): Show |
1 | a0003c0005t0015g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1657+894_1657+895i others(1395): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711376 | ||||||
| chr14:88711488
|
A | G | 3 | a0001c0001t0014g0004a0001c0001t0014g0005a0001c0001t0014g0006 | 3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1657+783T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711488 | ||||||
| chr14:88711857
|
G | A | 1 | a0001c0001t0032g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1657+414C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711857 | ||||||
| chr14:88711942
|
C | CA | 26 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(23): Show | 28 | HG00673.hp2 HG01074.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1657+328dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711942 | ||||||
| chr14:88711942
|
C | T | 4 | a0001c0001t0010g0032a0001c0001t0010g0033a0001c0001t0010g0034others(1): Show | 4 | HG00544.hp1 HG02027.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.1657+329G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711942 | ||||||
| chr14:88711942
|
CA | C | 43 | a0001c0001t0008g0102a0001c0001t0023g0195a0001c0001t0023g0197others(40): Show | 43 | HG00408.hp1 HG00642.hp2 HG02055.hp2 others(40): Show |
intron_variant | MODIFIER | c.1657+328delT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88711942 | ||||||
| chr14:88712001
|
G | A | 1 | a0001c0003t0004g0320 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1657+270C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88712001 | ||||||
| chr14:88712058
|
C | A | 1 | a0001c0001t0002g0146 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1657+213G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88712058 | ||||||
| chr14:88712095
|
T | C | 1 | a0001c0001t0036g0205 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1657+176A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88712095 | ||||||
| chr14:88712120
|
C | G | 27 | a0001c0003t0004g0302a0001c0003t0004g0303a0001c0003t0004g0304others(24): Show | 27 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(24): Show |
intron_variant | MODIFIER | c.1657+151G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 10/43 | chr14 | 88712120 | ||||||
| chr14:88712574
|
T | C | 1 | a0002c0002t0001g0263 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1445-91A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88712574 | ||||||
| chr14:88712799
|
G | A | 3 | a0001c0001t0014g0004a0001c0001t0014g0005a0001c0001t0014g0006 | 3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1445-316C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88712799 | ||||||
| chr14:88712964
|
G | A | 177 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(174): Show | 180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.1445-481C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88712964 | ||||||
| chr14:88713082
|
C | T | 33 | a0001c0003t0002g0012a0001c0003t0004g0302a0001c0003t0004g0303others(30): Show | 33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.1445-599G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713082 | ||||||
| chr14:88713326
|
A | G | 11 | a0001c0001t0003g0039a0001c0001t0003g0040a0001c0001t0003g0041others(8): Show | 11 | HG02738.hp1 HG03490.hp1 HG03492.hp2 others(8): Show |
intron_variant | MODIFIER | c.1445-843T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713326 | ||||||
| chr14:88713329
|
C | A | 1 | a0002c0002t0003g0026 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1445-846G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713329 | ||||||
| chr14:88713334
|
G | C | 2 | a0001c0001t0001g0199a0001c0001t0001g0201 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1445-851C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713334 | ||||||
| chr14:88713382
|
A | T | 1 | a0002c0002t0003g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1445-899T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713382 | ||||||
| chr14:88713391
|
CA | C | 265 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(262): Show | 268 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.1445-909delT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713391 | ||||||
| chr14:88713468
|
T | C | 269 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(266): Show | 272 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.1445-985A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713468 | ||||||
| chr14:88713499
|
C | T | 1 | a0001c0001t0002g0116 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1445-1016G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713499 | ||||||
| chr14:88713572
|
G | T | 2 | a0001c0003t0020g0173a0001c0003t0020g0174 | 2 | NA18939.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1445-1089C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713572 | ||||||
| chr14:88713619
|
A | AT | 9 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0140others(6): Show | 9 | HG00738.hp1 HG01943.hp2 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.1445-1137dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713619 | ||||||
| chr14:88713619
|
AT | A | 17 | a0001c0001t0001g0283a0001c0001t0002g0136a0001c0001t0002g0158others(14): Show | 18 | HG00741.hp2 HG01109.hp2 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.1445-1137delA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713619 | ||||||
| chr14:88713698
|
C | T | 1 | a0001c0001t0002g0116 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1445-1215G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713698 | ||||||
| chr14:88713785
|
A | C | 8 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(5): Show | 8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1444+1154T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713785 | ||||||
| chr14:88713840
|
G | GT | 23 | a0001c0001t0002g0109a0001c0001t0002g0111a0001c0001t0002g0117others(20): Show | 23 | HG00099.hp2 HG00438.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.1444+1098dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713840 | ||||||
| chr14:88713840
|
GT | G | 85 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0280others(82): Show | 86 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.1444+1098delA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713840 | ||||||
| chr14:88713929
|
C | T | 3 | a0001c0001t0014g0004a0001c0001t0014g0005a0001c0001t0014g0006 | 3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1444+1010G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713929 | ||||||
| chr14:88713971
|
G | A | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1444+968C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713971 | ||||||
| chr14:88713996
|
C | T | 103 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(100): Show | 105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.1444+943G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88713996 | ||||||
| chr14:88714096
|
C | T | 4 | a0001c0003t0004g0315a0001c0003t0004g0316a0001c0003t0004g0317others(1): Show | 4 | HG02683.hp2 HG03017.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1444+843G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88714096 | ||||||
| chr14:88714249
|
C | T | 90 | a0001c0001t0017g0010a0001c0001t0017g0011a0002c0002t0001g0193others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1444+690G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88714249 | ||||||
| chr14:88714250
|
A | C | 90 | a0001c0001t0017g0010a0001c0001t0017g0011a0002c0002t0001g0193others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1444+689T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88714250 | ||||||
| chr14:88714318
|
T | C | 2 | a0001c0001t0017g0010a0001c0001t0017g0011 | 2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1444+621A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88714318 | ||||||
| chr14:88714332
|
T | C | 90 | a0001c0001t0017g0010a0001c0001t0017g0011a0002c0002t0001g0193others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1444+607A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88714332 | ||||||
| chr14:88714388
|
G | A | 4 | a0001c0001t0002g0136a0001c0001t0002g0137a0001c0001t0002g0138others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1444+551C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88714388 | ||||||
| chr14:88714553
|
C | CCA | 3 | a0002c0002t0001g0263a0002c0002t0003g0094a0002c0002t0007g0030 | 3 | HG04184.hp2 HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1444+384_1444+385d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88714553 | ||||||
| chr14:88714575
|
A | T | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1444+364T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 9/43 | chr14 | 88714575 | ||||||
| chr14:88715349
|
A | G | 1 | a0001c0001t0022g0204 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1188-154T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88715349 | ||||||
| chr14:88715464
|
A | G | 88 | a0002c0002t0001g0193a0002c0002t0001g0194a0002c0002t0001g0200others(85): Show | 88 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.1188-269T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88715464 | ||||||
| chr14:88716310
|
A | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0201 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1188-1115T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88716310 | ||||||
| chr14:88716511
|
G | A | 1 | a0001c0001t0002g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1188-1316C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88716511 | ||||||
| chr14:88716732
|
A | AAC | 81 | a0001c0001t0017g0010a0001c0001t0017g0011a0002c0002t0001g0193others(78): Show | 81 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.1188-1539_1188-153 others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88716732 | ||||||
| chr14:88716732
|
A | AACAC | 11 | a0001c0001t0003g0048a0002c0002t0001g0230a0002c0002t0001g0255others(8): Show | 11 | HG01433.hp1 HG01978.hp1 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.1188-1541_1188-153 others(8): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88716732 | ||||||
| chr14:88716732
|
AAC | A | 164 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0280others(161): Show | 166 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1188-1539_1188-153 others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88716732 | ||||||
| chr14:88716732
|
AACAC | A | 55 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(52): Show | 56 | HG00408.hp1 HG00741.hp2 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.1188-1541_1188-153 others(8): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88716732 | ||||||
| chr14:88716797
|
C | CTGAT | 3 | a0001c0003t0004g0320a0001c0003t0004g0321a0001c0003t0004g0328 | 3 | HG02135.hp2 HG03927.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1188-1606_1188-160 others(8): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88716797 | ||||||
| chr14:88716835
|
T | C | 3 | a0001c0001t0014g0004a0001c0001t0014g0005a0001c0001t0014g0006 | 3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1188-1640A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88716835 | ||||||
| chr14:88716861
|
A | G | 90 | a0001c0001t0017g0010a0001c0001t0017g0011a0002c0002t0001g0193others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1188-1666T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88716861 | ||||||
| chr14:88716890
|
A | G | 11 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0006g0218others(8): Show | 11 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1188-1695T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88716890 | ||||||
| chr14:88716995
|
A | G | 107 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(104): Show | 109 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.1188-1800T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88716995 | ||||||
| chr14:88717056
|
G | C | 2 | a0001c0001t0024g0206a0001c0001t0024g0207 | 2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1188-1861C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717056 | ||||||
| chr14:88717083
|
C | T | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1188-1888G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717083 | ||||||
| chr14:88717165
|
TC | T | 3 | a0001c0001t0003g0039a0001c0001t0003g0040a0001c0001t0003g0041 | 3 | NA18953.hp2 NA18960.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1188-1971delG | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717165 | ||||||
| chr14:88717291
|
C | A | 7 | a0001c0001t0001g0283a0001c0001t0002g0158a0001c0001t0006g0003others(4): Show | 8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1188-2096G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717291 | ||||||
| chr14:88717297
|
C | T | 6 | a0001c0003t0004g0303a0001c0003t0004g0304a0001c0003t0004g0305others(3): Show | 6 | HG02257.hp1 HG02622.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1188-2102G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717297 | ||||||
| chr14:88717326
|
C | A | 24 | a0001c0001t0002g0141a0001c0001t0005g0171a0001c0001t0005g0172others(21): Show | 24 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1188-2131G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717326 | ||||||
| chr14:88717454
|
G | C | 1 | a0001c0001t0005g0187 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1188-2259C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717454 | ||||||
| chr14:88717482
|
G | T | 33 | a0001c0003t0002g0012a0001c0003t0004g0302a0001c0003t0004g0303others(30): Show | 33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.1188-2287C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717482 | ||||||
| chr14:88717505
|
T | A | 92 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0017g0010others(89): Show | 92 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1188-2310A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717505 | ||||||
| chr14:88717679
|
C | T | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1188-2484G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717679 | ||||||
| chr14:88717700
|
A | C | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1188-2505T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717700 | ||||||
| chr14:88717756
|
A | AAAC | 76 | a0002c0002t0001g0193a0002c0002t0001g0194a0002c0002t0001g0200others(73): Show | 76 | HG00323.hp1 HG00544.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.1188-2564_1188-256 others(7): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717756 | ||||||
| chr14:88717756
|
A | AAACAAC | 9 | a0002c0002t0001g0224a0002c0002t0001g0239a0002c0002t0001g0250others(6): Show | 9 | HG00099.hp2 HG01123.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.1188-2567_1188-256 others(10): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717756 | ||||||
| chr14:88717756
|
AAAC | A | 3 | a0002c0002t0001g0248a0002c0002t0001g0249a0002c0002t0001g0276 | 3 | HG00280.hp2 HG00438.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.1188-2564_1188-256 others(7): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717756 | ||||||
| chr14:88717756
|
AAACAAC | A | 174 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(171): Show | 177 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.1188-2567_1188-256 others(10): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717756 | ||||||
| chr14:88717756
|
AAACAACA others(5): Show |
A | 3 | a0001c0001t0006g0208a0001c0001t0024g0206a0001c0001t0024g0207 | 3 | HG01884.hp2 HG02145.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1188-2573_1188-256 others(16): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717756 | ||||||
| chr14:88717806
|
T | C | 88 | a0002c0002t0001g0193a0002c0002t0001g0194a0002c0002t0001g0200others(85): Show | 88 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.1188-2611A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717806 | ||||||
| chr14:88717861
|
T | A | 2 | a0001c0001t0002g0158a0001c0001t0006g0287 | 2 | HG01257.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1188-2666A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717861 | ||||||
| chr14:88717931
|
G | A | 51 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(48): Show | 52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.1188-2736C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88717931 | ||||||
| chr14:88718174
|
T | G | 1 | a0001c0003t0013g0300 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1188-2979A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88718174 | ||||||
| chr14:88718654
|
T | C | 1 | a0001c0003t0004g0329 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1188-3459A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88718654 | ||||||
| chr14:88718740
|
G | C | 18 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(15): Show | 19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1188-3545C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88718740 | ||||||
| chr14:88718902
|
C | T | 1 | a0001c0001t0032g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1188-3707G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88718902 | ||||||
| chr14:88718986
|
T | C | 14 | a0001c0001t0002g0141a0001c0001t0005g0171a0001c0001t0005g0172others(11): Show | 14 | HG00423.hp1 HG00673.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.1188-3791A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88718986 | ||||||
| chr14:88719121
|
C | G | 3 | a0001c0003t0004g0320a0001c0003t0004g0321a0001c0003t0004g0328 | 3 | HG02135.hp2 HG03927.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1188-3926G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88719121 | ||||||
| chr14:88719182
|
T | C | 1 | a0002c0002t0003g0025 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1188-3987A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88719182 | ||||||
| chr14:88719214
|
A | G | 3 | a0001c0001t0022g0203a0001c0001t0022g0204a0001c0001t0036g0205 | 3 | HG01243.hp1 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1188-4019T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88719214 | ||||||
| chr14:88719318
|
C | G | 269 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(266): Show | 272 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.1188-4123G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88719318 | ||||||
| chr14:88719327
|
AGTGAGCT | A | 102 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(99): Show | 104 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.1188-4139_1188-413 others(11): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88719327 | ||||||
| chr14:88719563
|
T | C | 11 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0006g0218others(8): Show | 11 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1188-4368A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88719563 | ||||||
| chr14:88719673
|
C | CT | 13 | a0001c0001t0003g0043a0001c0001t0003g0052a0001c0001t0003g0053others(10): Show | 13 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1188-4479dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88719673 | ||||||
| chr14:88719724
|
G | A | 267 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(264): Show | 270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.1188-4529C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88719724 | ||||||
| chr14:88720147
|
T | C | 1 | a0002c0002t0001g0254 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1188-4952A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88720147 | ||||||
| chr14:88720271
|
C | T | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1188-5076G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88720271 | ||||||
| chr14:88720292
|
C | T | 1 | a0001c0001t0005g0187 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1188-5097G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88720292 | ||||||
| chr14:88720546
|
G | A | 1 | a0008c0011t0008g0101 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1188-5351C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88720546 | ||||||
| chr14:88720613
|
T | C | 79 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(76): Show | 81 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.1188-5418A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88720613 | ||||||
| chr14:88720673
|
T | C | 2 | a0001c0001t0002g0112a0001c0001t0002g0113 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1188-5478A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88720673 | ||||||
| chr14:88720882
|
G | A | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1187+5659C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88720882 | ||||||
| chr14:88721249
|
G | T | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1187+5292C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88721249 | ||||||
| chr14:88721348
|
G | A | 6 | a0001c0003t0002g0012a0001c0003t0006g0221a0001c0003t0013g0298others(3): Show | 6 | HG02572.hp1 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1187+5193C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88721348 | ||||||
| chr14:88721361
|
A | G | 5 | a0001c0001t0008g0102a0001c0001t0008g0103a0001c0001t0008g0104others(2): Show | 5 | HG02895.hp2 HG02897.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1187+5180T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88721361 | ||||||
| chr14:88721538
|
T | C | 33 | a0001c0003t0002g0012a0001c0003t0004g0302a0001c0003t0004g0303others(30): Show | 33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.1187+5003A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88721538 | ||||||
| chr14:88721568
|
G | A | 177 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(174): Show | 180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.1187+4973C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88721568 | ||||||
| chr14:88721724
|
G | T | 2 | a0001c0001t0026g0293a0001c0001t0026g0294 | 2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1187+4817C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88721724 | ||||||
| chr14:88721730
|
G | A | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1187+4811C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88721730 | ||||||
| chr14:88721990
|
G | A | 3 | a0001c0001t0006g0218a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02559.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1187+4551C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88721990 | ||||||
| chr14:88722076
|
G | A | 11 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(8): Show | 11 | HG00642.hp2 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1187+4465C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88722076 | ||||||
| chr14:88722329
|
G | C | 1 | a0001c0001t0032g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1187+4212C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88722329 | ||||||
| chr14:88722331
|
A | G | 1 | a0007c0010t0003g0080 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1187+4210T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88722331 | ||||||
| chr14:88722371
|
C | G | 2 | a0001c0001t0010g0032a0001c0001t0010g0033 | 2 | HG02027.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.1187+4170G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88722371 | ||||||
| chr14:88722553
|
G | A | 177 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(174): Show | 180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.1187+3988C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88722553 | ||||||
| chr14:88722565
|
G | T | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1187+3976C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88722565 | ||||||
| chr14:88722688
|
C | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0201 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1187+3853G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88722688 | ||||||
| chr14:88722783
|
A | G | 1 | a0001c0001t0002g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1187+3758T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88722783 | ||||||
| chr14:88722825
|
A | G | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1187+3716T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88722825 | ||||||
| chr14:88722944
|
A | T | 1 | a0001c0001t0003g0051 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1187+3597T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88722944 | ||||||
| chr14:88723168
|
T | C | 51 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(48): Show | 52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.1187+3373A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88723168 | ||||||
| chr14:88723242
|
G | A | 8 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(5): Show | 8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1187+3299C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88723242 | ||||||
| chr14:88723385
|
T | C | 3 | a0001c0001t0014g0004a0001c0001t0014g0005a0001c0001t0014g0006 | 3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1187+3156A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88723385 | ||||||
| chr14:88723533
|
G | A | 1 | a0001c0001t0002g0129 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1187+3008C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88723533 | ||||||
| chr14:88723534
|
C | T | 7 | a0001c0001t0001g0283a0001c0001t0002g0158a0001c0001t0006g0003others(4): Show | 8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1187+3007G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88723534 | ||||||
| chr14:88723992
|
C | T | 267 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(264): Show | 270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.1187+2549G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88723992 | ||||||
| chr14:88724114
|
C | CA | 164 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(161): Show | 167 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.1187+2426dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88724114 | ||||||
| chr14:88724114
|
C | CAA | 102 | a0001c0001t0002g0120a0001c0001t0002g0133a0001c0001t0006g0285others(99): Show | 102 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1187+2425_1187+242 others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88724114 | ||||||
| chr14:88724157
|
C | T | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1187+2384G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88724157 | ||||||
| chr14:88724224
|
G | A | 4 | a0001c0001t0011g0213a0001c0001t0011g0214a0001c0001t0011g0215others(1): Show | 4 | HG02280.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1187+2317C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88724224 | ||||||
| chr14:88724273
|
C | CA | 8 | a0001c0001t0002g0095a0001c0001t0002g0098a0001c0001t0002g0106others(5): Show | 8 | HG01361.hp2 HG01884.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1187+2267dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88724273 | ||||||
| chr14:88724273
|
CA | C | 71 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(68): Show | 72 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(69): Show |
intron_variant | MODIFIER | c.1187+2267delT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88724273 | ||||||
| chr14:88724338
|
A | C | 5 | a0001c0001t0003g0043a0001c0001t0003g0052a0001c0001t0003g0053others(2): Show | 5 | NA18951.hp2 NA18954.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.1187+2203T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88724338 | ||||||
| chr14:88724382
|
T | TAAGAAGA others(309): Show |
3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1187+2158_1187+215 others(320): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88724382 | ||||||
| chr14:88724569
|
T | TA | 98 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(95): Show | 100 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1187+1971dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88724569 | ||||||
| chr14:88724595
|
T | C | 284 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(281): Show | 287 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.1187+1946A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88724595 | ||||||
| chr14:88724659
|
A | G | 267 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(264): Show | 270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.1187+1882T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88724659 | ||||||
| chr14:88724740
|
A | C | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1187+1801T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88724740 | ||||||
| chr14:88725059
|
T | C | 1 | a0002c0002t0001g0270 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1187+1482A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88725059 | ||||||
| chr14:88725213
|
G | C | 107 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(104): Show | 109 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.1187+1328C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88725213 | ||||||
| chr14:88725502
|
T | C | 2 | a0001c0001t0019g0212a0001c0001t0019g0217 | 2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1187+1039A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88725502 | ||||||
| chr14:88725652
|
G | A | 3 | a0002c0002t0003g0017a0002c0002t0003g0018a0002c0002t0003g0092 | 3 | HG01891.hp1 HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1187+889C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88725652 | ||||||
| chr14:88725799
|
C | A | 1 | a0001c0001t0003g0040 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1187+742G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88725799 | ||||||
| chr14:88725908
|
A | C | 1 | a0001c0001t0006g0208 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1187+633T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88725908 | ||||||
| chr14:88725945
|
A | C | 2 | a0001c0001t0026g0293a0001c0001t0026g0294 | 2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1187+596T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88725945 | ||||||
| chr14:88725985
|
T | C | 1 | a0001c0003t0002g0012 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1187+556A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88725985 | ||||||
| chr14:88726038
|
T | C | 51 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(48): Show | 52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.1187+503A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88726038 | ||||||
| chr14:88726102
|
TTACTC | T | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1187+434_1187+438d others(7): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88726102 | ||||||
| chr14:88726228
|
T | C | 1 | a0001c0003t0004g0319 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1187+313A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88726228 | ||||||
| chr14:88726472
|
A | T | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1187+69T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 8/43 | chr14 | 88726472 | ||||||
| chr14:88726735
|
A | C | 8 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(5): Show | 8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1050-57T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88726735 | ||||||
| chr14:88726876
|
G | C | 18 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(15): Show | 19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1050-198C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88726876 | ||||||
| chr14:88726888
|
C | T | 2 | a0001c0001t0008g0099a0001c0001t0008g0100 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1050-210G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88726888 | ||||||
| chr14:88726903
|
C | T | 3 | a0001c0001t0006g0218a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02559.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1050-225G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88726903 | ||||||
| chr14:88727038
|
T | TTTG | 90 | a0001c0001t0005g0176a0001c0001t0005g0177a0001c0001t0017g0010others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1050-363_1050-361d others(5): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88727038 | ||||||
| chr14:88727121
|
C | A | 87 | a0002c0002t0001g0193a0002c0002t0001g0194a0002c0002t0001g0200others(84): Show | 87 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.1050-443G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88727121 | ||||||
| chr14:88727367
|
T | A | 177 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(174): Show | 180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.1050-689A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88727367 | ||||||
| chr14:88727396
|
A | G | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1050-718T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88727396 | ||||||
| chr14:88727401
|
A | AT | 24 | a0001c0001t0003g0056a0001c0001t0023g0195a0001c0001t0023g0197others(21): Show | 24 | HG00642.hp2 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.1050-724dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88727401 | ||||||
| chr14:88727401
|
A | ATT | 156 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0002g0001others(153): Show | 159 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1050-725_1050-724d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88727401 | ||||||
| chr14:88727401
|
A | ATTT | 10 | a0001c0001t0001g0283a0001c0001t0002g0106a0001c0001t0002g0118others(7): Show | 10 | HG01109.hp2 HG02040.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.1050-726_1050-724d others(5): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88727401 | ||||||
| chr14:88727447
|
G | A | 1 | a0005c0014t0001g0272 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1050-769C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88727447 | ||||||
| chr14:88727598
|
A | G | 59 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(56): Show | 60 | HG00408.hp1 HG00642.hp2 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.1050-920T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88727598 | ||||||
| chr14:88727796
|
C | T | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1050-1118G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88727796 | ||||||
| chr14:88727849
|
A | C | 1 | a0002c0002t0003g0025 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1050-1171T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88727849 | ||||||
| chr14:88727918
|
G | A | 4 | a0001c0003t0004g0315a0001c0003t0004g0316a0001c0003t0004g0317others(1): Show | 4 | HG02683.hp2 HG03017.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1050-1240C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88727918 | ||||||
| chr14:88727928
|
T | TAAGAATT others(358): Show |
1 | a0001c0001t0002g0147 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1050-1251_1050-125 others(369): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88727928 | ||||||
| chr14:88728093
|
A | C | 1 | a0002c0002t0001g0271 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1050-1415T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88728093 | ||||||
| chr14:88728200
|
C | CT | 259 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0002g0001others(256): Show | 261 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.1050-1523dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88728200 | ||||||
| chr14:88728211
|
T | TG | 7 | a0001c0001t0001g0283a0001c0001t0002g0158a0001c0001t0006g0003others(4): Show | 8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1050-1534dupC | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88728211 | ||||||
| chr14:88728289
|
A | G | 1 | a0001c0001t0017g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1050-1611T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88728289 | ||||||
| chr14:88728321
|
TGCACCAG others(6): Show |
T | 99 | a0001c0001t0002g0168a0001c0001t0017g0010a0001c0001t0017g0011others(96): Show | 99 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1050-1656_1050-164 others(17): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88728321 | ||||||
| chr14:88728334
|
A | G | 103 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(100): Show | 105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.1050-1656T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88728334 | ||||||
| chr14:88728608
|
T | A | 1 | a0002c0002t0003g0031 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1050-1930A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88728608 | ||||||
| chr14:88728788
|
C | A | 103 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(100): Show | 105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.1050-2110G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88728788 | ||||||
| chr14:88728834
|
A | C | 1 | a0001c0001t0007g0062 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1050-2156T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88728834 | ||||||
| chr14:88729084
|
A | G | 5 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0006g0218others(2): Show | 5 | HG02559.hp1 HG02647.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1050-2406T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729084 | ||||||
| chr14:88729088
|
C | CAT | 91 | a0002c0002t0001g0193a0002c0002t0001g0194a0002c0002t0001g0200others(88): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.1050-2412_1050-241 others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729088 | ||||||
| chr14:88729474
|
T | C | 111 | a0001c0001t0002g0168a0001c0001t0006g0208a0001c0001t0014g0004others(108): Show | 111 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1050-2796A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729474 | ||||||
| chr14:88729558
|
G | GT | 20 | a0001c0003t0004g0302a0001c0003t0004g0309a0001c0003t0004g0311others(17): Show | 20 | HG00280.hp2 HG02055.hp2 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.1050-2881dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729558 | ||||||
| chr14:88729561
|
TTTTG | T | 6 | a0001c0003t0002g0012a0001c0003t0006g0221a0001c0003t0013g0298others(3): Show | 6 | HG02572.hp1 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1050-2887_1050-288 others(8): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729561 | ||||||
| chr14:88729565
|
G | T | 282 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(279): Show | 285 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.1050-2887C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729565 | ||||||
| chr14:88729568
|
T | G | 103 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(100): Show | 105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.1050-2890A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729568 | ||||||
| chr14:88729569
|
T | G | 4 | a0002c0002t0001g0263a0002c0002t0001g0278a0002c0002t0003g0094others(1): Show | 4 | HG02135.hp1 HG04184.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.1050-2891A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729569 | ||||||
| chr14:88729569
|
T | TG | 6 | a0001c0003t0004g0303a0001c0003t0004g0304a0001c0003t0004g0305others(3): Show | 6 | HG02257.hp1 HG02622.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1050-2892_1050-289 others(5): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729569 | ||||||
| chr14:88729572
|
G | T | 6 | a0001c0003t0002g0012a0001c0003t0006g0221a0001c0003t0013g0298others(3): Show | 6 | HG02572.hp1 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1050-2894C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729572 | ||||||
| chr14:88729577
|
T | G | 6 | a0001c0003t0002g0012a0001c0003t0006g0221a0001c0003t0013g0298others(3): Show | 6 | HG02572.hp1 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1050-2899A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729577 | ||||||
| chr14:88729685
|
G | T | 1 | a0001c0001t0022g0203 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1050-3007C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729685 | ||||||
| chr14:88729742
|
G | A | 33 | a0001c0003t0002g0012a0001c0003t0004g0302a0001c0003t0004g0303others(30): Show | 33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.1050-3064C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729742 | ||||||
| chr14:88729857
|
G | A | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1050-3179C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729857 | ||||||
| chr14:88729866
|
T | TTTTC | 182 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(179): Show | 184 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.1050-3189_1050-318 others(8): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729866 | ||||||
| chr14:88729869
|
T | TCTTTG | 12 | a0001c0001t0001g0283a0001c0001t0002g0087a0001c0001t0002g0143others(9): Show | 13 | HG00423.hp2 HG00741.hp2 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.1050-3192_1050-319 others(9): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729869 | ||||||
| chr14:88729870
|
G | C | 74 | a0001c0001t0002g0106a0001c0001t0002g0121a0001c0001t0002g0122others(71): Show | 74 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.1050-3192C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729870 | ||||||
| chr14:88729870
|
G | T | 16 | a0001c0001t0001g0283a0001c0001t0002g0087a0001c0001t0002g0143others(13): Show | 17 | HG00423.hp2 HG00741.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.1050-3192C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729870 | ||||||
| chr14:88729871
|
T | TTTG | 74 | a0001c0001t0002g0106a0001c0001t0002g0121a0001c0001t0002g0122others(71): Show | 74 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.1050-3194_1050-319 others(7): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729871 | ||||||
| chr14:88729883
|
G | T | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1050-3205C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729883 | ||||||
| chr14:88729976
|
C | T | 6 | a0001c0001t0002g0095a0001c0001t0002g0111a0001c0001t0002g0112others(3): Show | 6 | HG01099.hp1 HG01168.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.1050-3298G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88729976 | ||||||
| chr14:88730022
|
A | C | 1 | a0001c0001t0011g0216 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1050-3344T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88730022 | ||||||
| chr14:88730045
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1050-3367T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88730045 | ||||||
| chr14:88730112
|
A | G | 1 | a0001c0001t0003g0061 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1050-3434T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88730112 | ||||||
| chr14:88730120
|
T | C | 2 | a0002c0002t0001g0248a0002c0002t0001g0249 | 2 | HG00438.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.1050-3442A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88730120 | ||||||
| chr14:88730178
|
T | C | 1 | a0001c0001t0002g0108 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1050-3500A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88730178 | ||||||
| chr14:88730473
|
T | C | 1 | a0001c0001t0006g0003 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1050-3795A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88730473 | ||||||
| chr14:88730684
|
C | G | 3 | a0001c0001t0014g0004a0001c0001t0014g0005a0001c0001t0014g0006 | 3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1050-4006G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88730684 | ||||||
| chr14:88730746
|
C | A | 1 | a0001c0001t0003g0037 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1050-4068G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88730746 | ||||||
| chr14:88730875
|
G | A | 91 | a0001c0001t0002g0168a0001c0001t0017g0010a0001c0001t0017g0011others(88): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.1050-4197C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88730875 | ||||||
| chr14:88730904
|
T | C | 1 | a0002c0002t0003g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1050-4226A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88730904 | ||||||
| chr14:88730949
|
T | A | 4 | a0001c0003t0004g0315a0001c0003t0004g0316a0001c0003t0004g0317others(1): Show | 4 | HG02683.hp2 HG03017.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1050-4271A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88730949 | ||||||
| chr14:88731146
|
C | T | 1 | a0001c0001t0002g0087 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1050-4468G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88731146 | ||||||
| chr14:88731208
|
A | G | 267 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(264): Show | 270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.1050-4530T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88731208 | ||||||
| chr14:88731218
|
C | G | 103 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(100): Show | 105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.1050-4540G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88731218 | ||||||
| chr14:88731226
|
C | T | 1 | a0002c0002t0003g0029 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1050-4548G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88731226 | ||||||
| chr14:88731269
|
T | A | 1 | a0001c0001t0011g0213 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1050-4591A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88731269 | ||||||
| chr14:88731315
|
C | T | 2 | a0001c0003t0013g0300a0001c0009t0013g0301 | 2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1050-4637G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88731315 | ||||||
| chr14:88731316
|
A | G | 2 | a0001c0003t0013g0300a0001c0009t0013g0301 | 2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1050-4638T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88731316 | ||||||
| chr14:88731324
|
G | GT | 267 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(264): Show | 270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.1050-4647dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88731324 | ||||||
| chr14:88731755
|
A | G | 1 | a0002c0002t0003g0031 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1049+4609T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88731755 | ||||||
| chr14:88731809
|
C | T | 1 | a0001c0001t0014g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1049+4555G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88731809 | ||||||
| chr14:88732052
|
A | G | 1 | a0001c0001t0009g0058 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1049+4312T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88732052 | ||||||
| chr14:88732087
|
A | G | 24 | a0001c0001t0002g0141a0001c0001t0005g0171a0001c0001t0005g0172others(21): Show | 24 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1049+4277T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88732087 | ||||||
| chr14:88732126
|
G | A | 1 | a0004c0007t0016g0007 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1049+4238C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88732126 | ||||||
| chr14:88732219
|
A | C | 1 | a0001c0001t0001g0280 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1049+4145T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88732219 | ||||||
| chr14:88732325
|
C | T | 4 | a0001c0001t0011g0213a0001c0001t0011g0214a0001c0001t0011g0215others(1): Show | 4 | HG02280.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1049+4039G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88732325 | ||||||
| chr14:88732326
|
G | A | 14 | a0002c0002t0001g0235a0002c0002t0001g0236a0002c0002t0001g0250others(11): Show | 14 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1049+4038C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88732326 | ||||||
| chr14:88732380
|
G | A | 1 | a0001c0001t0002g0126 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1049+3984C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88732380 | ||||||
| chr14:88732385
|
G | A | 177 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(174): Show | 180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.1049+3979C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88732385 | ||||||
| chr14:88732466
|
T | C | 2 | a0001c0001t0005g0175a0001c0001t0005g0182 | 2 | HG00423.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.1049+3898A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88732466 | ||||||
| chr14:88732540
|
G | T | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1049+3824C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88732540 | ||||||
| chr14:88732593
|
T | C | 1 | a0002c0002t0033g0170 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1049+3771A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88732593 | ||||||
| chr14:88732888
|
G | T | 3 | a0001c0001t0014g0004a0001c0001t0014g0005a0001c0001t0014g0006 | 3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1049+3476C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88732888 | ||||||
| chr14:88732917
|
A | G | 90 | a0001c0001t0017g0010a0001c0001t0017g0011a0002c0002t0001g0193others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1049+3447T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88732917 | ||||||
| chr14:88733085
|
A | C | 1 | a0001c0001t0003g0074 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1049+3279T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88733085 | ||||||
| chr14:88733143
|
G | C | 267 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(264): Show | 270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.1049+3221C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88733143 | ||||||
| chr14:88733147
|
C | T | 1 | a0001c0001t0002g0128 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1049+3217G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88733147 | ||||||
| chr14:88733203
|
T | C | 5 | a0001c0003t0004g0318a0001c0003t0004g0319a0001c0003t0004g0322others(2): Show | 5 | HG00408.hp1 HG03669.hp1 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.1049+3161A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88733203 | ||||||
| chr14:88733668
|
C | T | 8 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(5): Show | 8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1049+2696G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88733668 | ||||||
| chr14:88733681
|
A | G | 1 | a0001c0003t0013g0300 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1049+2683T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88733681 | ||||||
| chr14:88733713
|
T | A | 7 | a0001c0001t0001g0283a0001c0001t0002g0158a0001c0001t0006g0003others(4): Show | 8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1049+2651A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88733713 | ||||||
| chr14:88733731
|
T | C | 1 | a0001c0001t0006g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1049+2633A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88733731 | ||||||
| chr14:88733741
|
C | G | 4 | a0001c0001t0003g0043a0001c0001t0003g0052a0001c0001t0003g0053others(1): Show | 4 | NA18954.hp2 NA18959.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.1049+2623G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88733741 | ||||||
| chr14:88733922
|
T | C | 1 | a0002c0002t0001g0268 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1049+2442A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88733922 | ||||||
| chr14:88733959
|
TAACAAC | T | 17 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(14): Show | 17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1049+2399_1049+240 others(10): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88733959 | ||||||
| chr14:88734117
|
A | G | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1049+2247T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88734117 | ||||||
| chr14:88734160
|
A | G | 27 | a0001c0003t0004g0302a0001c0003t0004g0303a0001c0003t0004g0304others(24): Show | 27 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(24): Show |
intron_variant | MODIFIER | c.1049+2204T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88734160 | ||||||
| chr14:88734413
|
T | C | 267 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(264): Show | 270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.1049+1951A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88734413 | ||||||
| chr14:88734423
|
T | G | 177 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(174): Show | 180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.1049+1941A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88734423 | ||||||
| chr14:88734910
|
A | G | 3 | a0002c0002t0001g0263a0002c0002t0003g0094a0002c0002t0007g0030 | 3 | HG04184.hp2 HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1049+1454T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88734910 | ||||||
| chr14:88735003
|
C | T | 2 | a0001c0001t0019g0212a0001c0001t0019g0217 | 2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1049+1361G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88735003 | ||||||
| chr14:88735004
|
T | C | 18 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(15): Show | 19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1049+1360A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88735004 | ||||||
| chr14:88735016
|
G | T | 1 | a0001c0001t0035g0196 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1049+1348C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88735016 | ||||||
| chr14:88735158
|
C | T | 1 | a0001c0001t0003g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1049+1206G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88735158 | ||||||
| chr14:88735292
|
T | G | 1 | a0001c0001t0003g0074 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1049+1072A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88735292 | ||||||
| chr14:88735321
|
A | G | 2 | a0001c0001t0001g0199a0001c0001t0001g0201 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1049+1043T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88735321 | ||||||
| chr14:88735430
|
A | G | 1 | a0001c0001t0009g0042 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1049+934T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88735430 | ||||||
| chr14:88735510
|
C | T | 1 | a0001c0001t0005g0184 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1049+854G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88735510 | ||||||
| chr14:88735689
|
C | T | 1 | a0011c0015t0007g0079 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1049+675G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88735689 | ||||||
| chr14:88735734
|
G | T | 1 | a0002c0002t0006g0237 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1049+630C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88735734 | ||||||
| chr14:88736003
|
CT | C | 246 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(243): Show | 249 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.1049+360delA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88736003 | ||||||
| chr14:88736028
|
G | C | 1 | a0001c0003t0013g0298 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1049+336C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88736028 | ||||||
| chr14:88736073
|
G | A | 8 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(5): Show | 8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1049+291C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88736073 | ||||||
| chr14:88736087
|
G | A | 4 | a0001c0001t0011g0213a0001c0001t0011g0214a0001c0001t0011g0215others(1): Show | 4 | HG02280.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1049+277C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88736087 | ||||||
| chr14:88736187
|
G | T | 177 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(174): Show | 180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.1049+177C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88736187 | ||||||
| chr14:88736225
|
C | T | 267 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(264): Show | 270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.1049+139G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88736225 | ||||||
| chr14:88736282
|
A | G | 1 | a0001c0001t0025g0191 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1049+82T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 7/43 | chr14 | 88736282 | ||||||
| chr14:88736695
|
G | C | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.848-130C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88736695 | ||||||
| chr14:88736798
|
A | G | 18 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(15): Show | 19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.848-233T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88736798 | ||||||
| chr14:88736921
|
C | T | 1 | a0002c0002t0006g0237 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.848-356G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88736921 | ||||||
| chr14:88736950
|
G | C | 1 | a0001c0001t0025g0191 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.848-385C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88736950 | ||||||
| chr14:88736976
|
G | A | 8 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(5): Show | 8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.848-411C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88736976 | ||||||
| chr14:88737165
|
T | G | 2 | a0001c0003t0004g0302a0001c0003t0004g0329 | 2 | HG02055.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.848-600A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88737165 | ||||||
| chr14:88737437
|
A | G | 284 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(281): Show | 287 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.848-872T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88737437 | ||||||
| chr14:88737569
|
T | C | 1 | a0001c0001t0003g0057 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.848-1004A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88737569 | ||||||
| chr14:88737650
|
T | C | 4 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0034g0198others(1): Show | 4 | HG02559.hp2 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.848-1085A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88737650 | ||||||
| chr14:88737775
|
C | T | 1 | a0002c0002t0001g0281 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.847+1104G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88737775 | ||||||
| chr14:88737901
|
T | A | 1 | a0002c0002t0003g0027 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.847+978A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88737901 | ||||||
| chr14:88738010
|
C | T | 177 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(174): Show | 180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.847+869G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88738010 | ||||||
| chr14:88738397
|
A | AT | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.847+481dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88738397 | ||||||
| chr14:88738417
|
G | GA | 89 | a0001c0001t0017g0010a0001c0001t0017g0011a0002c0002t0001g0193others(86): Show | 89 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.847+461dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88738417 | ||||||
| chr14:88738417
|
GA | G | 9 | a0001c0001t0011g0213a0001c0001t0011g0214a0001c0001t0011g0215others(6): Show | 9 | HG02040.hp1 HG02280.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.847+461delT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88738417 | ||||||
| chr14:88738469
|
A | T | 20 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(17): Show | 22 | HG01074.hp2 HG01106.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.847+410T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88738469 | ||||||
| chr14:88738864
|
T | A | 1 | a0001c0001t0002g0090 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.847+15A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88738864 | ||||||
| chr14:88738866
|
G | A | 1 | a0001c0001t0002g0090 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.847+13C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 6/43 | chr14 | 88738866 | ||||||
| chr14:88739328
|
T | C | 1 | a0001c0001t0003g0037 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.712-314A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 5/43 | chr14 | 88739328 | ||||||
| chr14:88739899
|
A | G | 18 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(15): Show | 19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.711+488T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 5/43 | chr14 | 88739899 | ||||||
| chr14:88739942
|
G | A | 5 | a0001c0003t0004g0318a0001c0003t0004g0319a0001c0003t0004g0322others(2): Show | 5 | HG00408.hp1 HG03669.hp1 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.711+445C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 5/43 | chr14 | 88739942 | ||||||
| chr14:88740084
|
T | C | 1 | a0001c0001t0003g0169 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.711+303A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 5/43 | chr14 | 88740084 | ||||||
| chr14:88740196
|
T | C | 6 | a0001c0003t0002g0012a0001c0003t0006g0221a0001c0003t0013g0298others(3): Show | 6 | HG02572.hp1 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.711+191A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 5/43 | chr14 | 88740196 | ||||||
| chr14:88740249
|
A | G | 8 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(5): Show | 8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.711+138T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 5/43 | chr14 | 88740249 | ||||||
| chr14:88740803
|
G | T | 5 | a0001c0001t0009g0042a0001c0001t0009g0058a0001c0001t0009g0059others(2): Show | 5 | HG00738.hp1 HG01358.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.526-231C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88740803 | ||||||
| chr14:88740829
|
T | C | 2 | a0001c0003t0004g0318a0001c0003t0004g0319 | 2 | HG00408.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.526-257A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88740829 | ||||||
| chr14:88740862
|
C | G | 2 | a0001c0001t0024g0206a0001c0001t0024g0207 | 2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.526-290G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88740862 | ||||||
| chr14:88740977
|
A | G | 1 | a0001c0001t0002g0137 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.526-405T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88740977 | ||||||
| chr14:88741122
|
C | T | 91 | a0001c0001t0002g0168a0001c0001t0017g0010a0001c0001t0017g0011others(88): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.526-550G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88741122 | ||||||
| chr14:88741142
|
G | A | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.526-570C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88741142 | ||||||
| chr14:88741176
|
T | A | 91 | a0001c0001t0002g0168a0001c0001t0017g0010a0001c0001t0017g0011others(88): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.526-604A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88741176 | ||||||
| chr14:88741231
|
T | C | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.526-659A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88741231 | ||||||
| chr14:88741404
|
A | G | 6 | a0001c0001t0006g0208a0001c0001t0022g0203a0001c0001t0022g0204others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.526-832T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88741404 | ||||||
| chr14:88741580
|
C | T | 17 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(14): Show | 17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.526-1008G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88741580 | ||||||
| chr14:88741826
|
A | T | 1 | a0001c0001t0002g0116 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.526-1254T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88741826 | ||||||
| chr14:88742169
|
T | G | 1 | a0002c0002t0001g0236 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.526-1597A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88742169 | ||||||
| chr14:88742210
|
A | C | 1 | a0001c0001t0003g0083 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.526-1638T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88742210 | ||||||
| chr14:88742365
|
T | G | 1 | a0001c0003t0004g0319 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.525+1658A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88742365 | ||||||
| chr14:88742535
|
A | G | 267 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(264): Show | 270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.525+1488T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88742535 | ||||||
| chr14:88742563
|
G | A | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.525+1460C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88742563 | ||||||
| chr14:88742564
|
C | T | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.525+1459G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88742564 | ||||||
| chr14:88742623
|
A | G | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.525+1400T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88742623 | ||||||
| chr14:88743034
|
T | C | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.525+989A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88743034 | ||||||
| chr14:88743053
|
C | T | 8 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(5): Show | 8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.525+970G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88743053 | ||||||
| chr14:88743170
|
G | A | 177 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(174): Show | 180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.525+853C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88743170 | ||||||
| chr14:88743521
|
C | T | 1 | a0001c0001t0003g0057 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.525+502G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88743521 | ||||||
| chr14:88743613
|
G | A | 1 | a0001c0001t0007g0078 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.525+410C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88743613 | ||||||
| chr14:88743613
|
G | C | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.525+410C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 4/43 | chr14 | 88743613 | ||||||
| chr14:88744220
|
C | G | 1 | a0001c0001t0003g0055 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.457-129G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88744220 | ||||||
| chr14:88744245
|
A | G | 11 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0006g0218others(8): Show | 11 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.457-154T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88744245 | ||||||
| chr14:88744402
|
C | T | 1 | a0002c0002t0003g0031 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.457-311G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88744402 | ||||||
| chr14:88744463
|
C | T | 177 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(174): Show | 180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.457-372G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88744463 | ||||||
| chr14:88744540
|
T | A | 51 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(48): Show | 52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.457-449A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88744540 | ||||||
| chr14:88744679
|
C | T | 1 | a0001c0003t0004g0310 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.457-588G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88744679 | ||||||
| chr14:88744697
|
C | T | 3 | a0001c0001t0001g0199a0001c0001t0001g0201a0002c0002t0006g0237 | 3 | HG02451.hp2 HG02523.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.457-606G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88744697 | ||||||
| chr14:88744951
|
T | C | 18 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(15): Show | 19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.457-860A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88744951 | ||||||
| chr14:88744976
|
A | G | 1 | a0002c0002t0001g0274 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.457-885T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88744976 | ||||||
| chr14:88745045
|
C | T | 1 | a0001c0001t0002g0141 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.457-954G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745045 | ||||||
| chr14:88745046
|
G | A | 1 | a0002c0002t0001g0223 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.457-955C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745046 | ||||||
| chr14:88745047
|
G | C | 1 | a0001c0001t0022g0204 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.457-956C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745047 | ||||||
| chr14:88745163
|
G | GTGTTTGT others(1): Show |
8 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(5): Show | 8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.456+1021_456+1022i others(10): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745163 | ||||||
| chr14:88745167
|
T | TTG | 66 | a0001c0001t0003g0047a0001c0001t0003g0166a0001c0001t0003g0169others(63): Show | 66 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.456+1016_456+1017d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | ||||||
| chr14:88745167
|
T | TTGTG | 9 | a0001c0001t0001g0199a0001c0001t0001g0201a0002c0002t0001g0254others(6): Show | 9 | HG01515.hp1 HG01952.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.456+1014_456+1017d others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | ||||||
| chr14:88745167
|
T | TTGTGTG | 4 | a0001c0001t0017g0010a0001c0001t0017g0011a0002c0002t0003g0017others(1): Show | 4 | HG01884.hp1 HG01891.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.456+1012_456+1017d others(8): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | ||||||
| chr14:88745167
|
T | TTGTTTGT others(3): Show |
15 | a0001c0001t0002g0002a0001c0001t0002g0086a0001c0001t0002g0096others(12): Show | 16 | HG00408.hp2 HG02165.hp2 HG03654.hp1 others(13): Show |
intron_variant | MODIFIER | c.456+1017_456+1018i others(12): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | ||||||
| chr14:88745167
|
T | TTGTTTGT others(5): Show |
33 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(30): Show | 33 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.456+1017_456+1018i others(14): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | ||||||
| chr14:88745167
|
T | TTGTTTGT others(7): Show |
11 | a0001c0001t0002g0001a0001c0001t0002g0116a0001c0001t0002g0139others(8): Show | 12 | HG01074.hp2 HG01106.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.456+1017_456+1018i others(16): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | ||||||
| chr14:88745167
|
T | TTGTTTGT others(9): Show |
2 | a0001c0001t0002g0095a0001c0001t0002g0147 | 2 | HG01361.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.456+1017_456+1018i others(18): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | ||||||
| chr14:88745167
|
T | TTGTTTGT others(18): Show |
1 | a0001c0001t0006g0208 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.456+1017_456+1018i others(27): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | ||||||
| chr14:88745167
|
T | TTGTTTGT others(3): Show |
3 | a0001c0001t0008g0099a0001c0001t0010g0033a0001c0003t0004g0310 | 3 | HG02523.hp1 HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.456+1017_456+1018i others(12): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | ||||||
| chr14:88745167
|
T | TTGTTTGT others(5): Show |
40 | a0001c0001t0006g0188a0001c0001t0008g0102a0001c0001t0008g0103others(37): Show | 40 | HG00544.hp1 HG02055.hp2 HG02135.hp2 others(37): Show |
intron_variant | MODIFIER | c.456+1017_456+1018i others(14): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | ||||||
| chr14:88745167
|
T | TTGTTTGT others(7): Show |
29 | a0001c0001t0002g0106a0001c0001t0002g0121a0001c0001t0002g0123others(26): Show | 29 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.456+1017_456+1018i others(16): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | ||||||
| chr14:88745167
|
T | TTGTTTGT others(9): Show |
2 | a0001c0001t0002g0122a0001c0001t0002g0167 | 2 | HG04115.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.456+1017_456+1018i others(18): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | ||||||
| chr14:88745167
|
T | TTGTTTGT others(11): Show |
9 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0002g0168others(6): Show | 10 | HG01515.hp2 HG01517.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.456+1017_456+1018i others(20): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | ||||||
| chr14:88745167
|
T | TTGTTTGT others(13): Show |
10 | a0001c0001t0001g0283a0001c0001t0006g0284a0001c0001t0006g0285others(7): Show | 10 | HG00741.hp2 HG02004.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.456+1017_456+1018i others(22): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | ||||||
| chr14:88745167
|
T | TTGTTTGT others(15): Show |
4 | a0001c0001t0006g0286a0001c0001t0011g0214a0001c0001t0022g0203others(1): Show | 4 | HG01256.hp2 HG01884.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.456+1017_456+1018i others(24): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | ||||||
| chr14:88745167
|
T | TTGTTTGT others(17): Show |
5 | a0001c0001t0002g0158a0001c0001t0006g0287a0001c0001t0011g0215others(2): Show | 5 | HG01243.hp1 HG01257.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.456+1017_456+1018i others(26): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | ||||||
| chr14:88745167
|
T | TTGTTTGT others(21): Show |
1 | a0001c0001t0011g0216 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.456+1017_456+1018i others(30): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | ||||||
| chr14:88745167
|
TTG | T | 9 | a0001c0001t0003g0048a0001c0001t0003g0049a0001c0001t0003g0050others(6): Show | 9 | HG01074.hp1 HG01175.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.456+1016_456+1017d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745167 | ||||||
| chr14:88745171
|
G | T | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.456+1014C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745171 | ||||||
| chr14:88745201
|
T | C | 1 | a0001c0001t0003g0169 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.456+984A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745201 | ||||||
| chr14:88745255
|
T | C | 1 | a0002c0002t0003g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.456+930A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745255 | ||||||
| chr14:88745456
|
T | C | 51 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(48): Show | 52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.456+729A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745456 | ||||||
| chr14:88745501
|
A | G | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.456+684T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745501 | ||||||
| chr14:88745530
|
A | T | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.456+655T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745530 | ||||||
| chr14:88745601
|
T | C | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.456+584A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745601 | ||||||
| chr14:88745611
|
G | T | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.456+574C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745611 | ||||||
| chr14:88745629
|
C | G | 90 | a0001c0001t0017g0010a0001c0001t0017g0011a0002c0002t0001g0193others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.456+556G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745629 | ||||||
| chr14:88745834
|
T | C | 2 | a0001c0001t0019g0212a0001c0001t0019g0217 | 2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.456+351A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745834 | ||||||
| chr14:88745890
|
A | C | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.456+295T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745890 | ||||||
| chr14:88745903
|
G | A | 1 | a0001c0001t0007g0134 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.456+282C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745903 | ||||||
| chr14:88745931
|
A | G | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.456+254T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 3/43 | chr14 | 88745931 | ||||||
| chr14:88746933
|
T | G | 33 | a0001c0003t0002g0012a0001c0003t0004g0302a0001c0003t0004g0303others(30): Show | 33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.358-650A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88746933 | ||||||
| chr14:88746980
|
G | A | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.358-697C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88746980 | ||||||
| chr14:88747057
|
G | C | 2 | a0001c0001t0019g0212a0001c0001t0019g0217 | 2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.358-774C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747057 | ||||||
| chr14:88747061
|
T | C | 267 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(264): Show | 270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.358-778A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747061 | ||||||
| chr14:88747111
|
C | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.358-828G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747111 | ||||||
| chr14:88747140
|
C | T | 3 | a0002c0002t0001g0232a0002c0002t0001g0233a0002c0002t0001g0261 | 3 | NA18947.hp2 NA18962.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.358-857G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747140 | ||||||
| chr14:88747213
|
A | G | 7 | a0001c0001t0001g0283a0001c0001t0002g0158a0001c0001t0006g0003others(4): Show | 8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.358-930T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747213 | ||||||
| chr14:88747281
|
T | C | 2 | a0001c0001t0003g0036a0001c0001t0003g0037 | 2 | HG02738.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.358-998A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747281 | ||||||
| chr14:88747305
|
G | A | 1 | a0002c0002t0003g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.358-1022C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747305 | ||||||
| chr14:88747366
|
C | T | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.358-1083G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747366 | ||||||
| chr14:88747397
|
G | A | 1 | a0001c0001t0002g0137 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.358-1114C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747397 | ||||||
| chr14:88747420
|
G | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.358-1137C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747420 | ||||||
| chr14:88747558
|
A | G | 1 | a0001c0001t0025g0191 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.358-1275T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747558 | ||||||
| chr14:88747661
|
A | T | 1 | a0001c0001t0010g0034 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.358-1378T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747661 | ||||||
| chr14:88747850
|
C | A | 7 | a0001c0001t0001g0283a0001c0001t0002g0158a0001c0001t0006g0003others(4): Show | 8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.358-1567G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747850 | ||||||
| chr14:88747854
|
G | A | 2 | a0001c0001t0002g0109a0001c0001t0002g0110 | 2 | HG02165.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.358-1571C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747854 | ||||||
| chr14:88747887
|
G | A | 2 | a0001c0001t0003g0052a0001c0001t0003g0053 | 2 | NA18959.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.358-1604C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747887 | ||||||
| chr14:88747974
|
G | T | 11 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0006g0218others(8): Show | 11 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.358-1691C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747974 | ||||||
| chr14:88747976
|
G | C | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.358-1693C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88747976 | ||||||
| chr14:88748024
|
G | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.358-1741C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88748024 | ||||||
| chr14:88748054
|
C | T | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.358-1771G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88748054 | ||||||
| chr14:88748243
|
T | G | 1 | a0001c0003t0020g0174 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.358-1960A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88748243 | ||||||
| chr14:88748406
|
A | G | 2 | a0001c0001t0017g0010a0001c0001t0017g0011 | 2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.358-2123T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88748406 | ||||||
| chr14:88748567
|
G | A | 90 | a0001c0001t0017g0010a0001c0001t0017g0011a0002c0002t0001g0193others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.358-2284C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88748567 | ||||||
| chr14:88748978
|
GGA | G | 4 | a0001c0001t0003g0039a0001c0001t0003g0040a0001c0001t0003g0041others(1): Show | 4 | NA18953.hp2 NA18960.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.358-2697_358-2696d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88748978 | ||||||
| chr14:88749075
|
G | A | 1 | a0002c0002t0001g0231 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.358-2792C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88749075 | ||||||
| chr14:88749412
|
A | G | 1 | a0002c0002t0003g0031 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.358-3129T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88749412 | ||||||
| chr14:88749666
|
T | C | 77 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(74): Show | 79 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.358-3383A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88749666 | ||||||
| chr14:88749711
|
T | C | 91 | a0001c0001t0002g0168a0001c0001t0017g0010a0001c0001t0017g0011others(88): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.358-3428A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88749711 | ||||||
| chr14:88749850
|
T | G | 8 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(5): Show | 8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.358-3567A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88749850 | ||||||
| chr14:88749868
|
A | G | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.358-3585T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88749868 | ||||||
| chr14:88750160
|
G | T | 1 | a0001c0001t0003g0055 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.358-3877C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88750160 | ||||||
| chr14:88750403
|
T | C | 1 | a0001c0001t0006g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.357+4109A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88750403 | ||||||
| chr14:88750459
|
C | T | 2 | a0001c0001t0008g0099a0001c0001t0008g0100 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.357+4053G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88750459 | ||||||
| chr14:88750511
|
G | A | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.357+4001C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88750511 | ||||||
| chr14:88750729
|
G | T | 1 | a0004c0007t0016g0007 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.357+3783C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88750729 | ||||||
| chr14:88750911
|
T | C | 4 | a0001c0001t0003g0048a0001c0001t0003g0049a0001c0001t0003g0050others(1): Show | 4 | HG02622.hp1 HG02818.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.357+3601A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88750911 | ||||||
| chr14:88750971
|
G | C | 1 | a0002c0002t0001g0229 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.357+3541C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88750971 | ||||||
| chr14:88751314
|
T | C | 1 | a0001c0003t0006g0221 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.357+3198A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88751314 | ||||||
| chr14:88751448
|
C | T | 63 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(60): Show | 65 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.357+3064G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88751448 | ||||||
| chr14:88751507
|
G | GT | 7 | a0001c0001t0001g0283a0001c0001t0002g0158a0001c0001t0006g0003others(4): Show | 8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.357+3004dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88751507 | ||||||
| chr14:88751581
|
G | A | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.357+2931C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88751581 | ||||||
| chr14:88751614
|
AGAGTT | A | 103 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(100): Show | 105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.357+2893_357+2897d others(7): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88751614 | ||||||
| chr14:88751721
|
C | T | 3 | a0001c0001t0014g0004a0001c0001t0014g0005a0001c0001t0014g0006 | 3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.357+2791G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88751721 | ||||||
| chr14:88751918
|
T | C | 267 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(264): Show | 270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.357+2594A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88751918 | ||||||
| chr14:88752194
|
C | A | 1 | a0001c0001t0019g0212 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.357+2318G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88752194 | ||||||
| chr14:88752194
|
C | G | 266 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(263): Show | 269 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.357+2318G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88752194 | ||||||
| chr14:88752240
|
T | C | 2 | a0001c0001t0017g0010a0001c0001t0017g0011 | 2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.357+2272A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88752240 | ||||||
| chr14:88752298
|
T | C | 1 | a0001c0001t0002g0148 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.357+2214A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88752298 | ||||||
| chr14:88752471
|
T | C | 267 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(264): Show | 270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.357+2041A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88752471 | ||||||
| chr14:88752756
|
A | G | 9 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(6): Show | 9 | HG00423.hp2 HG00609.hp1 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.357+1756T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88752756 | ||||||
| chr14:88752758
|
C | A | 1 | a0001c0001t0002g0127 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.357+1754G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88752758 | ||||||
| chr14:88753006
|
C | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0201 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.357+1506G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88753006 | ||||||
| chr14:88753100
|
C | T | 328 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(325): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.357+1412G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88753100 | ||||||
| chr14:88753229
|
C | T | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.357+1283G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88753229 | ||||||
| chr14:88753302
|
G | A | 1 | a0001c0001t0003g0041 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.357+1210C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88753302 | ||||||
| chr14:88753788
|
C | A | 6 | a0002c0002t0001g0255a0002c0002t0001g0256a0002c0002t0001g0257others(3): Show | 6 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.357+724G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88753788 | ||||||
| chr14:88753996
|
G | A | 8 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(5): Show | 8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.357+516C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88753996 | ||||||
| chr14:88754005
|
T | C | 1 | a0001c0001t0006g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.357+507A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88754005 | ||||||
| chr14:88754044
|
G | A | 267 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(264): Show | 270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.357+468C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88754044 | ||||||
| chr14:88754047
|
A | G | 91 | a0001c0001t0002g0168a0001c0001t0017g0010a0001c0001t0017g0011others(88): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.357+465T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88754047 | ||||||
| chr14:88754151
|
T | C | 1 | a0001c0001t0003g0051 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.357+361A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 2/43 | chr14 | 88754151 | ||||||
| chr14:88754817
|
T | C | 91 | a0001c0001t0002g0168a0001c0001t0017g0010a0001c0001t0017g0011others(88): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.198-146A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88754817 | ||||||
| chr14:88754828
|
G | C | 18 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(15): Show | 19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.198-157C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88754828 | ||||||
| chr14:88754963
|
C | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0201 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.198-292G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88754963 | ||||||
| chr14:88755104
|
G | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.198-433C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88755104 | ||||||
| chr14:88755147
|
C | T | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.198-476G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88755147 | ||||||
| chr14:88755289
|
T | C | 17 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(14): Show | 17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.198-618A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88755289 | ||||||
| chr14:88755478
|
C | T | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.198-807G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88755478 | ||||||
| chr14:88755616
|
T | G | 267 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(264): Show | 270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.198-945A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88755616 | ||||||
| chr14:88755719
|
G | A | 1 | a0002c0002t0001g0200 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.198-1048C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88755719 | ||||||
| chr14:88755724
|
G | A | 1 | a0001c0001t0028g0009 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.198-1053C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88755724 | ||||||
| chr14:88755840
|
T | A | 6 | a0001c0001t0006g0208a0001c0001t0022g0203a0001c0001t0022g0204others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.198-1169A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88755840 | ||||||
| chr14:88755984
|
C | T | 11 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0006g0218others(8): Show | 11 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.198-1313G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88755984 | ||||||
| chr14:88756090
|
C | G | 4 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0109others(1): Show | 4 | HG02165.hp2 NA18939.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.198-1419G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88756090 | ||||||
| chr14:88756217
|
A | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0201 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.198-1546T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88756217 | ||||||
| chr14:88756238
|
G | T | 33 | a0001c0003t0002g0012a0001c0003t0004g0302a0001c0003t0004g0303others(30): Show | 33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.198-1567C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88756238 | ||||||
| chr14:88756245
|
C | A | 1 | a0002c0002t0003g0024 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.198-1574G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88756245 | ||||||
| chr14:88756312
|
T | A | 33 | a0001c0003t0002g0012a0001c0003t0004g0302a0001c0003t0004g0303others(30): Show | 33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.198-1641A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88756312 | ||||||
| chr14:88756372
|
T | C | 6 | a0001c0003t0002g0012a0001c0003t0006g0221a0001c0003t0013g0298others(3): Show | 6 | HG02572.hp1 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.198-1701A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88756372 | ||||||
| chr14:88756416
|
T | C | 1 | a0001c0001t0012g0327 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.198-1745A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88756416 | ||||||
| chr14:88756449
|
A | G | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.198-1778T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88756449 | ||||||
| chr14:88756537
|
A | G | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.198-1866T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88756537 | ||||||
| chr14:88756693
|
C | T | 51 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(48): Show | 52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.198-2022G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88756693 | ||||||
| chr14:88756752
|
A | C | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.198-2081T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88756752 | ||||||
| chr14:88756848
|
GAC | G | 11 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0006g0218others(8): Show | 11 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.198-2179_198-2178d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88756848 | ||||||
| chr14:88756870
|
A | G | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.198-2199T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88756870 | ||||||
| chr14:88756908
|
T | C | 18 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(15): Show | 19 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.198-2237A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88756908 | ||||||
| chr14:88756987
|
C | T | 284 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(281): Show | 287 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.198-2316G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88756987 | ||||||
| chr14:88757197
|
G | T | 1 | a0001c0001t0014g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.198-2526C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88757197 | ||||||
| chr14:88757446
|
CA | C | 19 | a0001c0001t0002g0106a0001c0001t0002g0167a0001c0001t0006g0208others(16): Show | 19 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.198-2776delT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88757446 | ||||||
| chr14:88757714
|
C | T | 1 | a0001c0001t0002g0133 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.198-3043G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88757714 | ||||||
| chr14:88758019
|
A | AT | 92 | a0001c0001t0003g0036a0001c0001t0003g0037a0001c0001t0003g0054others(89): Show | 92 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.198-3349dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88758019 | ||||||
| chr14:88758019
|
A | ATT | 9 | a0001c0001t0002g0105a0002c0002t0001g0209a0002c0002t0001g0229others(6): Show | 9 | HG01255.hp1 HG01934.hp2 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.198-3350_198-3349d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88758019 | ||||||
| chr14:88758019
|
AT | A | 36 | a0001c0001t0005g0189a0001c0001t0024g0207a0001c0001t0036g0205others(33): Show | 36 | HG00408.hp1 HG01243.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.198-3349delA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88758019 | ||||||
| chr14:88758057
|
A | G | 8 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(5): Show | 8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.198-3386T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88758057 | ||||||
| chr14:88758093
|
G | C | 176 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(173): Show | 179 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.198-3422C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88758093 | ||||||
| chr14:88758200
|
A | T | 2 | a0002c0002t0001g0229a0002c0002t0001g0279 | 2 | HG00609.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.198-3529T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88758200 | ||||||
| chr14:88758319
|
A | G | 2 | a0001c0001t0010g0032a0001c0001t0010g0033 | 2 | HG02027.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.198-3648T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88758319 | ||||||
| chr14:88758487
|
G | A | 4 | a0001c0001t0011g0213a0001c0001t0011g0214a0001c0001t0011g0215others(1): Show | 4 | HG02280.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.198-3816C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88758487 | ||||||
| chr14:88758744
|
C | T | 1 | a0001c0001t0022g0203 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.198-4073G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88758744 | ||||||
| chr14:88758918
|
A | G | 2 | a0001c0001t0002g0091a0001c0001t0002g0155 | 2 | HG01261.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.198-4247T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88758918 | ||||||
| chr14:88758959
|
C | T | 2 | a0001c0003t0020g0173a0001c0003t0020g0174 | 2 | NA18939.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.198-4288G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88758959 | ||||||
| chr14:88759026
|
G | A | 4 | a0001c0001t0026g0293a0001c0001t0026g0294a0001c0001t0027g0295others(1): Show | 4 | HG00642.hp2 HG02145.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.198-4355C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759026 | ||||||
| chr14:88759032
|
G | A | 11 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0006g0218others(8): Show | 11 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.198-4361C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759032 | ||||||
| chr14:88759117
|
T | C | 1 | a0001c0001t0005g0183 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.198-4446A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759117 | ||||||
| chr14:88759147
|
G | A | 2 | a0001c0001t0006g0003a0001c0001t0006g0286 | 3 | HG01256.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.198-4476C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759147 | ||||||
| chr14:88759175
|
GA | G | 51 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(48): Show | 52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.198-4505delT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759175 | ||||||
| chr14:88759188
|
G | T | 1 | a0002c0004t0001g0228 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.198-4517C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759188 | ||||||
| chr14:88759313
|
C | T | 7 | a0001c0001t0008g0099a0001c0001t0008g0100a0001c0001t0008g0102others(4): Show | 7 | HG02258.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.198-4642G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759313 | ||||||
| chr14:88759453
|
G | T | 1 | a0002c0002t0003g0024 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.198-4782C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759453 | ||||||
| chr14:88759685
|
T | TAAAA | 77 | a0001c0001t0002g0168a0001c0001t0017g0010a0001c0001t0017g0011others(74): Show | 77 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.198-5018_198-5015d others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759685 | ||||||
| chr14:88759685
|
T | TAAAAA | 10 | a0002c0002t0001g0223a0002c0002t0001g0261a0002c0002t0001g0270others(7): Show | 10 | HG02165.hp1 NA18948.hp2 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.198-5019_198-5015d others(7): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759685 | ||||||
| chr14:88759685
|
T | TAAAAAAA | 60 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(57): Show | 62 | HG00280.hp1 HG00408.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.198-5021_198-5015d others(9): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759685 | ||||||
| chr14:88759685
|
T | TAAAAAAA others(1): Show |
37 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0095others(34): Show | 37 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.198-5022_198-5015d others(10): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759685 | ||||||
| chr14:88759685
|
T | TAAAAAAA others(7): Show |
1 | a0001c0001t0019g0212 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.198-5028_198-5015d others(16): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759685 | ||||||
| chr14:88759685
|
T | TAAAAAAA others(8): Show |
6 | a0001c0001t0006g0287a0001c0001t0019g0217a0001c0003t0004g0309others(3): Show | 6 | HG01257.hp1 HG02922.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.198-5029_198-5015d others(17): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759685 | ||||||
| chr14:88759685
|
T | TAAAAAAA others(9): Show |
6 | a0001c0003t0004g0302a0001c0003t0004g0317a0001c0003t0004g0320others(3): Show | 6 | HG02055.hp2 HG02135.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.198-5030_198-5015d others(18): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759685 | ||||||
| chr14:88759685
|
T | TAAAAAAA others(10): Show |
7 | a0001c0001t0014g0006a0001c0003t0002g0012a0001c0003t0004g0310others(4): Show | 7 | HG02280.hp2 HG02572.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.198-5031_198-5015d others(19): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759685 | ||||||
| chr14:88759685
|
T | TAAAAAAA others(11): Show |
6 | a0001c0001t0014g0004a0001c0001t0014g0005a0001c0001t0024g0207others(3): Show | 6 | HG02717.hp2 HG03130.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.198-5032_198-5015d others(20): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759685 | ||||||
| chr14:88759685
|
T | TAAAAAAA others(12): Show |
9 | a0001c0001t0024g0206a0001c0003t0004g0303a0001c0003t0004g0304others(6): Show | 9 | HG01884.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.198-5033_198-5015d others(21): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759685 | ||||||
| chr14:88759685
|
T | TAAAAAAA others(13): Show |
3 | a0001c0003t0004g0306a0001c0003t0004g0307a0001c0003t0004g0315 | 3 | HG02257.hp1 HG02622.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.198-5015_198-5014i others(22): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759685 | ||||||
| chr14:88759685
|
T | TAAAAAAA others(14): Show |
1 | a0001c0003t0004g0308 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.198-5015_198-5014i others(23): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759685 | ||||||
| chr14:88759698
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001g0283 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.198-5028_198-5027i others(18): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759698 | ||||||
| chr14:88759698
|
A | AAAAAAAA others(8): Show |
6 | a0001c0001t0002g0158a0001c0001t0006g0003a0001c0001t0006g0284others(3): Show | 7 | HG00741.hp2 HG01256.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.198-5028_198-5027i others(17): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759698 | ||||||
| chr14:88759698
|
A | AAAAAAAA others(7): Show |
3 | a0001c0001t0011g0213a0001c0001t0011g0214a0001c0001t0011g0215 | 3 | HG02280.hp1 HG02615.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.198-5028_198-5027i others(16): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759698 | ||||||
| chr14:88759698
|
A | AAAAAAAA others(4): Show |
2 | a0003c0005t0015g0014a0003c0005t0015g0015 | 2 | HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.198-5028_198-5027i others(13): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759698 | ||||||
| chr14:88759698
|
A | AAAAAAAA others(3): Show |
1 | a0003c0005t0015g0013 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.198-5028_198-5027i others(12): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759698 | ||||||
| chr14:88759698
|
A | AAAAACAA others(7): Show |
5 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0006g0218others(2): Show | 5 | HG02559.hp1 HG02647.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.198-5028_198-5027i others(16): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759698 | ||||||
| chr14:88759698
|
A | AAAACAAA others(6): Show |
3 | a0001c0001t0022g0203a0001c0001t0022g0204a0001c0001t0036g0205 | 3 | HG01243.hp1 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.198-5028_198-5027i others(15): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759698 | ||||||
| chr14:88759698
|
A | AAAACAAA others(5): Show |
2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.198-5028_198-5027i others(14): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759698 | ||||||
| chr14:88759698
|
A | AC | 8 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(5): Show | 8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.198-5028_198-5027i others(3): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759698 | ||||||
| chr14:88759728
|
C | T | 3 | a0001c0001t0014g0004a0001c0001t0014g0005a0001c0001t0014g0006 | 3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.198-5057G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759728 | ||||||
| chr14:88759846
|
A | C | 1 | a0001c0001t0032g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.198-5175T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759846 | ||||||
| chr14:88759870
|
C | T | 1 | a0001c0001t0002g0129 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.198-5199G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88759870 | ||||||
| chr14:88760343
|
G | GTTGT | 239 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(236): Show | 242 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.198-5676_198-5673d others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88760343 | ||||||
| chr14:88760349
|
T | TGTTC | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.198-5679_198-5678i others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88760349 | ||||||
| chr14:88760479
|
AC | A | 91 | a0001c0001t0002g0168a0001c0001t0017g0010a0001c0001t0017g0011others(88): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.198-5809delG | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88760479 | ||||||
| chr14:88760528
|
T | C | 90 | a0001c0001t0017g0010a0001c0001t0017g0011a0002c0002t0001g0193others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.198-5857A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88760528 | ||||||
| chr14:88760800
|
G | A | 1 | a0002c0002t0001g0270 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.198-6129C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88760800 | ||||||
| chr14:88761205
|
T | A | 2 | a0001c0001t0002g0124a0001c0001t0002g0125 | 2 | NA18943.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.198-6534A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88761205 | ||||||
| chr14:88761250
|
G | A | 176 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(173): Show | 179 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.198-6579C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88761250 | ||||||
| chr14:88761813
|
A | G | 177 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(174): Show | 180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.198-7142T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88761813 | ||||||
| chr14:88761893
|
G | A | 1 | a0001c0001t0006g0202 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.198-7222C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88761893 | ||||||
| chr14:88762022
|
A | G | 90 | a0001c0001t0017g0010a0001c0001t0017g0011a0002c0002t0001g0193others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.198-7351T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88762022 | ||||||
| chr14:88762139
|
C | T | 27 | a0001c0003t0004g0302a0001c0003t0004g0303a0001c0003t0004g0304others(24): Show | 27 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(24): Show |
intron_variant | MODIFIER | c.198-7468G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88762139 | ||||||
| chr14:88762141
|
CTCTGATG others(16): Show |
C | 1 | a0001c0001t0035g0196 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.198-7493_198-7471d others(25): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88762141 | ||||||
| chr14:88762167
|
T | C | 1 | a0001c0001t0002g0097 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.198-7496A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88762167 | ||||||
| chr14:88762171
|
C | T | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.198-7500G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88762171 | ||||||
| chr14:88762225
|
C | G | 267 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(264): Show | 270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.198-7554G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88762225 | ||||||
| chr14:88762328
|
C | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.198-7657G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88762328 | ||||||
| chr14:88762366
|
G | C | 269 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(266): Show | 272 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.198-7695C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88762366 | ||||||
| chr14:88762672
|
T | C | 91 | a0001c0001t0002g0168a0001c0001t0017g0010a0001c0001t0017g0011others(88): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.198-8001A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88762672 | ||||||
| chr14:88762899
|
C | T | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.198-8228G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88762899 | ||||||
| chr14:88763005
|
A | G | 1 | a0001c0001t0001g0283 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.198-8334T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88763005 | ||||||
| chr14:88763018
|
G | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.198-8347C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88763018 | ||||||
| chr14:88763247
|
T | C | 5 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0006g0218others(2): Show | 5 | HG02559.hp1 HG02647.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.198-8576A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88763247 | ||||||
| chr14:88763600
|
C | T | 1 | a0002c0002t0001g0282 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.198-8929G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88763600 | ||||||
| chr14:88763622
|
T | C | 1 | a0001c0001t0019g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.198-8951A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88763622 | ||||||
| chr14:88763628
|
A | C | 8 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(5): Show | 8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.198-8957T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88763628 | ||||||
| chr14:88763662
|
C | T | 1 | a0002c0002t0003g0028 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.198-8991G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88763662 | ||||||
| chr14:88763894
|
C | T | 3 | a0002c0002t0001g0224a0002c0002t0001g0225a0002c0002t0001g0226 | 3 | NA18968.hp1 NA18994.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.198-9223G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88763894 | ||||||
| chr14:88763895
|
G | T | 8 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(5): Show | 8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.198-9224C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88763895 | ||||||
| chr14:88764020
|
A | G | 267 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(264): Show | 270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.198-9349T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88764020 | ||||||
| chr14:88764277
|
T | C | 4 | a0001c0001t0002g0091a0001c0001t0002g0155a0001c0001t0002g0156others(1): Show | 4 | HG00280.hp1 HG01167.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.198-9606A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88764277 | ||||||
| chr14:88764459
|
T | C | 91 | a0001c0001t0002g0168a0001c0001t0017g0010a0001c0001t0017g0011others(88): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.198-9788A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88764459 | ||||||
| chr14:88764510
|
G | C | 2 | a0001c0003t0020g0173a0001c0003t0020g0174 | 2 | NA18939.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.198-9839C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88764510 | ||||||
| chr14:88764907
|
G | A | 2 | a0001c0001t0002g0089a0001c0001t0002g0090 | 2 | NA19006.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.198-10236C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88764907 | ||||||
| chr14:88765102
|
T | C | 1 | a0002c0002t0003g0018 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.198-10431A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88765102 | ||||||
| chr14:88765121
|
TCACAAAT others(3): Show |
T | 91 | a0001c0001t0002g0168a0001c0001t0017g0010a0001c0001t0017g0011others(88): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.198-10460_198-1045 others(14): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88765121 | ||||||
| chr14:88765141
|
A | G | 1 | a0001c0001t0007g0084 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.198-10470T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88765141 | ||||||
| chr14:88765145
|
C | T | 267 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(264): Show | 270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.198-10474G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88765145 | ||||||
| chr14:88765361
|
T | C | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.198-10690A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88765361 | ||||||
| chr14:88765473
|
T | C | 1 | a0001c0001t0005g0185 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.198-10802A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88765473 | ||||||
| chr14:88765501
|
T | C | 91 | a0001c0001t0002g0168a0001c0001t0017g0010a0001c0001t0017g0011others(88): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.198-10830A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88765501 | ||||||
| chr14:88765940
|
G | C | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.198-11269C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88765940 | ||||||
| chr14:88766072
|
C | T | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.198-11401G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766072 | ||||||
| chr14:88766185
|
A | G | 17 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(14): Show | 17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.198-11514T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766185 | ||||||
| chr14:88766199
|
C | T | 2 | a0001c0001t0017g0010a0001c0001t0017g0011 | 2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.198-11528G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766199 | ||||||
| chr14:88766201
|
G | A | 1 | a0005c0014t0001g0272 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.198-11530C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766201 | ||||||
| chr14:88766225
|
T | C | 23 | a0001c0001t0005g0171a0001c0001t0005g0172a0001c0001t0005g0175others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.198-11554A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766225 | ||||||
| chr14:88766286
|
C | T | 103 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(100): Show | 105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.198-11615G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766286 | ||||||
| chr14:88766337
|
C | A | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.198-11666G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766337 | ||||||
| chr14:88766476
|
G | A | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.198-11805C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766476 | ||||||
| chr14:88766478
|
G | A | 2 | a0001c0001t0019g0212a0001c0001t0019g0217 | 2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.198-11807C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766478 | ||||||
| chr14:88766498
|
G | A | 104 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(101): Show | 106 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.198-11827C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766498 | ||||||
| chr14:88766509
|
T | C | 267 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(264): Show | 270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.198-11838A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766509 | ||||||
| chr14:88766533
|
G | A | 9 | a0001c0001t0012g0326a0001c0001t0023g0195a0001c0001t0023g0197others(6): Show | 9 | HG00609.hp1 HG00642.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.198-11862C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766533 | ||||||
| chr14:88766553
|
G | T | 269 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(266): Show | 272 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.198-11882C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766553 | ||||||
| chr14:88766559
|
C | T | 1 | a0001c0001t0005g0181 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.198-11888G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766559 | ||||||
| chr14:88766560
|
T | A | 2 | a0001c0001t0017g0010a0001c0001t0017g0011 | 2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.198-11889A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766560 | ||||||
| chr14:88766758
|
G | A | 103 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(100): Show | 105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.198-12087C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766758 | ||||||
| chr14:88766774
|
G | A | 4 | a0001c0001t0002g0136a0001c0001t0002g0137a0001c0001t0002g0138others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.198-12103C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766774 | ||||||
| chr14:88766956
|
T | G | 176 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(173): Show | 179 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.198-12285A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88766956 | ||||||
| chr14:88767149
|
C | A | 1 | a0001c0003t0004g0323 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.198-12478G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88767149 | ||||||
| chr14:88767631
|
T | C | 1 | a0005c0014t0001g0272 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.198-12960A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88767631 | ||||||
| chr14:88767822
|
C | T | 11 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0006g0218others(8): Show | 11 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.198-13151G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88767822 | ||||||
| chr14:88767882
|
CA | C | 289 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(286): Show | 292 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.198-13212delT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88767882 | ||||||
| chr14:88767908
|
T | C | 1 | a0001c0001t0014g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.198-13237A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88767908 | ||||||
| chr14:88768417
|
C | CT | 87 | a0002c0002t0001g0193a0002c0002t0001g0194a0002c0002t0001g0200others(84): Show | 87 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.198-13747dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88768417 | ||||||
| chr14:88768485
|
G | A | 11 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0006g0218others(8): Show | 11 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.198-13814C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88768485 | ||||||
| chr14:88768596
|
C | G | 267 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(264): Show | 270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.198-13925G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88768596 | ||||||
| chr14:88768748
|
C | T | 91 | a0001c0001t0002g0168a0001c0001t0017g0010a0001c0001t0017g0011others(88): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.198-14077G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88768748 | ||||||
| chr14:88768875
|
G | A | 33 | a0001c0003t0002g0012a0001c0003t0004g0302a0001c0003t0004g0303others(30): Show | 33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.198-14204C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88768875 | ||||||
| chr14:88769290
|
G | A | 1 | a0001c0001t0005g0180 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.198-14619C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88769290 | ||||||
| chr14:88769343
|
C | T | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.198-14672G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88769343 | ||||||
| chr14:88769357
|
T | G | 91 | a0001c0001t0002g0168a0001c0001t0017g0010a0001c0001t0017g0011others(88): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.198-14686A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88769357 | ||||||
| chr14:88769538
|
A | G | 1 | a0001c0001t0010g0033 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.198-14867T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88769538 | ||||||
| chr14:88769649
|
G | C | 8 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(5): Show | 8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.198-14978C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88769649 | ||||||
| chr14:88769830
|
T | C | 1 | a0001c0001t0019g0212 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.198-15159A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88769830 | ||||||
| chr14:88769913
|
T | C | 1 | a0001c0001t0009g0076 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.198-15242A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88769913 | ||||||
| chr14:88769966
|
G | GT | 97 | a0001c0001t0002g0140a0001c0001t0002g0168a0001c0001t0003g0043others(94): Show | 97 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.198-15296dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88769966 | ||||||
| chr14:88769983
|
G | C | 1 | a0001c0001t0005g0186 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.198-15312C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88769983 | ||||||
| chr14:88770042
|
T | C | 1 | a0001c0001t0005g0187 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.198-15371A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88770042 | ||||||
| chr14:88770314
|
A | G | 33 | a0001c0003t0002g0012a0001c0003t0004g0302a0001c0003t0004g0303others(30): Show | 33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.198-15643T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88770314 | ||||||
| chr14:88770464
|
A | G | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.198-15793T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88770464 | ||||||
| chr14:88770477
|
G | C | 2 | a0001c0001t0017g0010a0001c0001t0017g0011 | 2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.198-15806C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88770477 | ||||||
| chr14:88770570
|
T | A | 1 | a0001c0001t0019g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.198-15899A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88770570 | ||||||
| chr14:88770745
|
A | C | 1 | a0001c0001t0019g0212 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.198-16074T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88770745 | ||||||
| chr14:88770750
|
T | C | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.198-16079A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88770750 | ||||||
| chr14:88770766
|
T | G | 2 | a0001c0001t0024g0206a0001c0001t0024g0207 | 2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.198-16095A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88770766 | ||||||
| chr14:88770820
|
C | T | 90 | a0001c0001t0017g0010a0001c0001t0017g0011a0002c0002t0001g0193others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.198-16149G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88770820 | ||||||
| chr14:88770984
|
A | G | 1 | a0001c0001t0002g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.198-16313T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88770984 | ||||||
| chr14:88771066
|
T | C | 1 | a0002c0002t0001g0282 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.198-16395A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88771066 | ||||||
| chr14:88771352
|
C | G | 1 | a0001c0001t0002g0095 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.198-16681G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88771352 | ||||||
| chr14:88771398
|
C | T | 8 | a0001c0001t0001g0283a0001c0001t0002g0158a0001c0001t0006g0003others(5): Show | 9 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.198-16727G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88771398 | ||||||
| chr14:88771493
|
C | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.198-16822G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88771493 | ||||||
| chr14:88771635
|
C | T | 1 | a0002c0002t0001g0223 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.198-16964G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88771635 | ||||||
| chr14:88771729
|
T | C | 51 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(48): Show | 52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.198-17058A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88771729 | ||||||
| chr14:88771891
|
G | A | 1 | a0002c0002t0001g0274 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.198-17220C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88771891 | ||||||
| chr14:88771956
|
T | G | 1 | a0001c0001t0003g0041 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.198-17285A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88771956 | ||||||
| chr14:88772146
|
T | A | 1 | a0002c0002t0001g0291 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.198-17475A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88772146 | ||||||
| chr14:88772147
|
C | T | 1 | a0002c0002t0001g0291 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.198-17476G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88772147 | ||||||
| chr14:88772149
|
T | C | 1 | a0002c0002t0001g0291 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.198-17478A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88772149 | ||||||
| chr14:88772445
|
G | A | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.198-17774C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88772445 | ||||||
| chr14:88772448
|
C | T | 13 | a0001c0003t0004g0303a0001c0003t0004g0304a0001c0003t0004g0305others(10): Show | 13 | HG02257.hp1 HG02280.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.198-17777G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88772448 | ||||||
| chr14:88772484
|
G | A | 1 | a0001c0001t0034g0198 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.198-17813C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88772484 | ||||||
| chr14:88772614
|
G | T | 17 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(14): Show | 17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.198-17943C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88772614 | ||||||
| chr14:88772686
|
G | A | 1 | a0001c0001t0032g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.198-18015C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88772686 | ||||||
| chr14:88772835
|
C | T | 1 | a0001c0001t0028g0009 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.198-18164G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88772835 | ||||||
| chr14:88772848
|
A | G | 267 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(264): Show | 270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.198-18177T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88772848 | ||||||
| chr14:88772917
|
C | T | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.198-18246G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88772917 | ||||||
| chr14:88772969
|
C | T | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.198-18298G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88772969 | ||||||
| chr14:88773101
|
T | C | 1 | a0002c0002t0001g0275 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.198-18430A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88773101 | ||||||
| chr14:88773200
|
A | C | 1 | a0002c0002t0001g0291 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.198-18529T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88773200 | ||||||
| chr14:88773206
|
C | T | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.198-18535G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88773206 | ||||||
| chr14:88773255
|
G | A | 23 | a0001c0001t0005g0171a0001c0001t0005g0172a0001c0001t0005g0175others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.198-18584C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88773255 | ||||||
| chr14:88773300
|
G | C | 2 | a0001c0001t0002g0126a0001c0001t0002g0127 | 2 | HG01175.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.198-18629C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88773300 | ||||||
| chr14:88773318
|
T | C | 1 | a0001c0001t0017g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.198-18647A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88773318 | ||||||
| chr14:88773379
|
A | T | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.198-18708T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88773379 | ||||||
| chr14:88773639
|
C | T | 6 | a0002c0002t0003g0019a0002c0002t0003g0020a0002c0002t0003g0021others(3): Show | 6 | HG02165.hp1 NA18948.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.197+18668G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88773639 | ||||||
| chr14:88773776
|
G | C | 1 | a0001c0001t0002g0128 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.197+18531C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88773776 | ||||||
| chr14:88773819
|
TA | T | 268 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(265): Show | 271 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.197+18487delT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88773819 | ||||||
| chr14:88774093
|
G | A | 103 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(100): Show | 105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.197+18214C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88774093 | ||||||
| chr14:88774128
|
A | G | 5 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(2): Show | 5 | HG00423.hp2 NA18944.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.197+18179T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88774128 | ||||||
| chr14:88774135
|
G | A | 5 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(2): Show | 5 | HG00423.hp2 NA18944.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.197+18172C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88774135 | ||||||
| chr14:88774187
|
T | C | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.197+18120A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88774187 | ||||||
| chr14:88774216
|
T | G | 8 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(5): Show | 8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.197+18091A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88774216 | ||||||
| chr14:88774242
|
G | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.197+18065C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88774242 | ||||||
| chr14:88774297
|
C | T | 1 | a0001c0001t0005g0180 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.197+18010G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88774297 | ||||||
| chr14:88774305
|
G | A | 103 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(100): Show | 105 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.197+18002C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88774305 | ||||||
| chr14:88774412
|
C | T | 80 | a0002c0002t0001g0193a0002c0002t0001g0194a0002c0002t0001g0200others(77): Show | 80 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.197+17895G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88774412 | ||||||
| chr14:88774445
|
T | A | 1 | a0002c0002t0001g0291 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.197+17862A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88774445 | ||||||
| chr14:88774807
|
A | G | 4 | a0001c0001t0005g0176a0001c0001t0005g0177a0001c0001t0005g0178others(1): Show | 4 | NA18612.hp1 NA18948.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.197+17500T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88774807 | ||||||
| chr14:88774991
|
C | T | 1 | a0001c0001t0023g0195 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.197+17316G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88774991 | ||||||
| chr14:88775235
|
G | C | 1 | a0002c0002t0001g0276 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.197+17072C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88775235 | ||||||
| chr14:88775243
|
T | C | 92 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0017g0010others(89): Show | 92 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.197+17064A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88775243 | ||||||
| chr14:88775355
|
G | C | 8 | a0001c0001t0023g0195a0001c0001t0023g0197a0001c0001t0026g0293others(5): Show | 8 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.197+16952C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88775355 | ||||||
| chr14:88775610
|
G | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.197+16697C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88775610 | ||||||
| chr14:88775679
|
G | A | 1 | a0001c0001t0029g0157 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.197+16628C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88775679 | ||||||
| chr14:88775905
|
A | AAG | 7 | a0001c0001t0001g0283a0001c0001t0002g0158a0001c0001t0006g0003others(4): Show | 8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.197+16400_197+1640 others(6): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88775905 | ||||||
| chr14:88775905
|
AAGAG | A | 17 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(14): Show | 17 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.197+16398_197+1640 others(8): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88775905 | ||||||
| chr14:88775996
|
G | T | 177 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(174): Show | 180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.197+16311C>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88775996 | ||||||
| chr14:88776244
|
C | T | 90 | a0001c0001t0017g0010a0001c0001t0017g0011a0002c0002t0001g0193others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.197+16063G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88776244 | ||||||
| chr14:88776620
|
C | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.197+15687G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88776620 | ||||||
| chr14:88776691
|
C | T | 174 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(171): Show | 177 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.197+15616G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88776691 | ||||||
| chr14:88776718
|
C | CA | 174 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(171): Show | 177 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.197+15588dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88776718 | ||||||
| chr14:88776942
|
T | C | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.197+15365A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88776942 | ||||||
| chr14:88777247
|
C | CA | 176 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(173): Show | 179 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.197+15059dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88777247 | ||||||
| chr14:88777437
|
C | T | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.197+14870G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88777437 | ||||||
| chr14:88777487
|
T | C | 2 | a0001c0001t0024g0206a0001c0001t0024g0207 | 2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.197+14820A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88777487 | ||||||
| chr14:88777699
|
G | A | 90 | a0001c0001t0017g0010a0001c0001t0017g0011a0002c0002t0001g0193others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.197+14608C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88777699 | ||||||
| chr14:88777703
|
A | T | 1 | a0001c0001t0005g0175 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.197+14604T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88777703 | ||||||
| chr14:88777897
|
C | G | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.197+14410G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88777897 | ||||||
| chr14:88778042
|
G | A | 3 | a0001c0001t0006g0218a0001c0001t0006g0219a0001c0001t0006g0220 | 3 | HG02559.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.197+14265C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88778042 | ||||||
| chr14:88778247
|
A | G | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.197+14060T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88778247 | ||||||
| chr14:88778387
|
G | A | 1 | a0001c0001t0002g0130 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.197+13920C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88778387 | ||||||
| chr14:88778519
|
G | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.197+13788C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88778519 | ||||||
| chr14:88778759
|
C | T | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.197+13548G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88778759 | ||||||
| chr14:88778778
|
A | AAAAAC | 6 | a0001c0001t0006g0208a0001c0001t0022g0203a0001c0001t0022g0204others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.197+13524_197+1352 others(9): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88778778 | ||||||
| chr14:88778913
|
T | G | 1 | a0011c0015t0007g0079 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.197+13394A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88778913 | ||||||
| chr14:88779463
|
C | T | 5 | a0001c0001t0001g0199a0001c0001t0001g0201a0002c0002t0003g0017others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.197+12844G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88779463 | ||||||
| chr14:88779686
|
G | A | 1 | a0001c0001t0014g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.197+12621C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88779686 | ||||||
| chr14:88780030
|
T | C | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.197+12277A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88780030 | ||||||
| chr14:88780043
|
C | T | 51 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(48): Show | 52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.197+12264G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88780043 | ||||||
| chr14:88780254
|
G | A | 267 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(264): Show | 270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.197+12053C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88780254 | ||||||
| chr14:88780381
|
TTTG | T | 176 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(173): Show | 179 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.197+11923_197+1192 others(7): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88780381 | ||||||
| chr14:88780513
|
G | A | 2 | a0001c0001t0002g0129a0001c0001t0002g0130 | 2 | NA18986.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.197+11794C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88780513 | ||||||
| chr14:88780573
|
C | CT | 8 | a0001c0001t0001g0283a0001c0001t0002g0158a0001c0001t0006g0003others(5): Show | 9 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.197+11733dupA | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88780573 | ||||||
| chr14:88780628
|
T | C | 33 | a0001c0003t0002g0012a0001c0003t0004g0302a0001c0003t0004g0303others(30): Show | 33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.197+11679A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88780628 | ||||||
| chr14:88780678
|
C | T | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.197+11629G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88780678 | ||||||
| chr14:88780968
|
G | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.197+11339C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88780968 | ||||||
| chr14:88780975
|
T | G | 51 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(48): Show | 52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.197+11332A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88780975 | ||||||
| chr14:88781188
|
T | C | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.197+11119A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88781188 | ||||||
| chr14:88781518
|
C | T | 6 | a0001c0001t0006g0208a0001c0001t0022g0203a0001c0001t0022g0204others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.197+10789G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88781518 | ||||||
| chr14:88781682
|
C | T | 50 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0002g0158others(47): Show | 51 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(48): Show |
intron_variant | MODIFIER | c.197+10625G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88781682 | ||||||
| chr14:88781760
|
A | G | 1 | a0001c0001t0009g0042 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.197+10547T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88781760 | ||||||
| chr14:88781791
|
T | C | 1 | a0001c0001t0006g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.197+10516A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88781791 | ||||||
| chr14:88781900
|
C | G | 91 | a0001c0001t0002g0098a0001c0001t0017g0010a0001c0001t0017g0011others(88): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.197+10407G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88781900 | ||||||
| chr14:88781941
|
G | C | 1 | a0007c0010t0003g0080 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.197+10366C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88781941 | ||||||
| chr14:88782099
|
T | C | 1 | a0001c0001t0003g0081 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.197+10208A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88782099 | ||||||
| chr14:88782163
|
A | G | 102 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(99): Show | 104 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.197+10144T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88782163 | ||||||
| chr14:88782176
|
A | G | 267 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(264): Show | 270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.197+10131T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88782176 | ||||||
| chr14:88782193
|
G | C | 1 | a0001c0003t0004g0314 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.197+10114C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88782193 | ||||||
| chr14:88782241
|
C | T | 4 | a0001c0001t0003g0039a0001c0001t0003g0040a0001c0001t0003g0041others(1): Show | 4 | NA18953.hp2 NA18960.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.197+10066G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88782241 | ||||||
| chr14:88782246
|
C | A | 1 | a0001c0001t0003g0082 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.197+10061G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88782246 | ||||||
| chr14:88782302
|
G | C | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.197+10005C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88782302 | ||||||
| chr14:88782746
|
C | G | 1 | a0001c0001t0003g0036 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.197+9561G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88782746 | ||||||
| chr14:88782794
|
C | T | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.197+9513G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88782794 | ||||||
| chr14:88782807
|
C | T | 1 | a0001c0001t0002g0097 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.197+9500G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88782807 | ||||||
| chr14:88782842
|
G | A | 1 | a0002c0002t0001g0222 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.197+9465C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88782842 | ||||||
| chr14:88782855
|
G | A | 1 | a0001c0001t0003g0083 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.197+9452C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88782855 | ||||||
| chr14:88782859
|
C | A | 2 | a0004c0007t0016g0007a0004c0007t0016g0008 | 2 | HG02040.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.197+9448G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88782859 | ||||||
| chr14:88782887
|
C | T | 1 | a0001c0001t0002g0095 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.197+9420G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88782887 | ||||||
| chr14:88782888
|
G | A | 1 | a0001c0001t0012g0327 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.197+9419C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88782888 | ||||||
| chr14:88783123
|
C | T | 17 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0002g0158others(14): Show | 18 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.197+9184G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88783123 | ||||||
| chr14:88783129
|
C | T | 1 | a0002c0002t0001g0222 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.197+9178G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88783129 | ||||||
| chr14:88783130
|
G | A | 1 | a0001c0001t0014g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.197+9177C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88783130 | ||||||
| chr14:88783157
|
G | A | 1 | a0001c0001t0008g0131 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.197+9150C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88783157 | ||||||
| chr14:88783168
|
G | A | 1 | a0001c0001t0002g0132 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.197+9139C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88783168 | ||||||
| chr14:88783411
|
C | T | 1 | a0001c0001t0002g0096 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.197+8896G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88783411 | ||||||
| chr14:88783442
|
A | G | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.197+8865T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88783442 | ||||||
| chr14:88783813
|
C | T | 1 | a0001c0001t0007g0038 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.197+8494G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88783813 | ||||||
| chr14:88783858
|
A | T | 1 | a0001c0001t0001g0210 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.197+8449T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88783858 | ||||||
| chr14:88783903
|
G | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.197+8404C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88783903 | ||||||
| chr14:88784021
|
G | A | 14 | a0001c0003t0004g0302a0001c0003t0004g0315a0001c0003t0004g0316others(11): Show | 14 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.197+8286C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88784021 | ||||||
| chr14:88784099
|
C | G | 1 | a0001c0001t0012g0324 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.197+8208G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88784099 | ||||||
| chr14:88784198
|
G | C | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.197+8109C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88784198 | ||||||
| chr14:88784367
|
T | A | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0002g0158others(16): Show | 20 | HG00544.hp2 HG00741.hp2 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.197+7940A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88784367 | ||||||
| chr14:88784424
|
T | C | 1 | a0001c0001t0002g0133 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.197+7883A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88784424 | ||||||
| chr14:88784492
|
G | A | 1 | a0001c0001t0007g0134 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.197+7815C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88784492 | ||||||
| chr14:88784725
|
A | T | 2 | a0001c0006t0003g0161a0001c0006t0003g0162 | 2 | HG01074.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.197+7582T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88784725 | ||||||
| chr14:88784887
|
C | T | 27 | a0001c0003t0004g0302a0001c0003t0004g0303a0001c0003t0004g0304others(24): Show | 27 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(24): Show |
intron_variant | MODIFIER | c.197+7420G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88784887 | ||||||
| chr14:88785131
|
A | T | 1 | a0001c0001t0002g0095 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.197+7176T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88785131 | ||||||
| chr14:88785157
|
T | C | 4 | a0001c0001t0002g0136a0001c0001t0002g0137a0001c0001t0002g0138others(1): Show | 4 | HG01109.hp2 HG02055.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.197+7150A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88785157 | ||||||
| chr14:88785230
|
G | A | 1 | a0001c0001t0007g0084 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.197+7077C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88785230 | ||||||
| chr14:88785369
|
T | A | 1 | a0002c0002t0001g0278 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.197+6938A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88785369 | ||||||
| chr14:88785738
|
AC | A | 33 | a0001c0003t0002g0012a0001c0003t0004g0302a0001c0003t0004g0303others(30): Show | 33 | HG00408.hp1 HG02055.hp2 HG02135.hp2 others(30): Show |
intron_variant | MODIFIER | c.197+6568delG | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88785738 | ||||||
| chr14:88785760
|
C | A | 1 | a0001c0001t0007g0085 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.197+6547G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88785760 | ||||||
| chr14:88785794
|
T | C | 6 | a0001c0001t0002g0002a0001c0001t0002g0086a0001c0001t0002g0151others(3): Show | 7 | NA18960.hp2 NA18968.hp2 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.197+6513A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88785794 | ||||||
| chr14:88785821
|
G | C | 177 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(174): Show | 180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.197+6486C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88785821 | ||||||
| chr14:88786077
|
C | T | 51 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(48): Show | 52 | HG00408.hp1 HG00741.hp2 HG01256.hp2 others(49): Show |
intron_variant | MODIFIER | c.197+6230G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88786077 | ||||||
| chr14:88786289
|
T | C | 1 | a0001c0003t0002g0012 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.197+6018A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88786289 | ||||||
| chr14:88786756
|
G | A | 1 | a0001c0001t0006g0188 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.197+5551C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88786756 | ||||||
| chr14:88786848
|
C | T | 6 | a0001c0003t0004g0303a0001c0003t0004g0304a0001c0003t0004g0305others(3): Show | 6 | HG02257.hp1 HG02622.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.197+5459G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88786848 | ||||||
| chr14:88786903
|
T | C | 1 | a0001c0001t0017g0011 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.197+5404A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88786903 | ||||||
| chr14:88787141
|
C | A | 1 | a0002c0002t0001g0279 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.197+5166G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88787141 | ||||||
| chr14:88787291
|
T | C | 19 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0086others(16): Show | 21 | HG01074.hp2 HG01106.hp1 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.197+5016A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88787291 | ||||||
| chr14:88787294
|
G | C | 1 | a0001c0001t0006g0208 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.197+5013C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88787294 | ||||||
| chr14:88787527
|
T | A | 7 | a0001c0001t0001g0283a0001c0001t0002g0158a0001c0001t0006g0003others(4): Show | 8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.197+4780A>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88787527 | ||||||
| chr14:88787577
|
C | T | 267 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(264): Show | 270 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.197+4730G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88787577 | ||||||
| chr14:88787687
|
C | A | 1 | a0001c0001t0014g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.197+4620G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88787687 | ||||||
| chr14:88787783
|
T | C | 4 | a0001c0001t0002g0091a0001c0001t0002g0155a0001c0001t0002g0156others(1): Show | 4 | HG00280.hp1 HG01167.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.197+4524A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88787783 | ||||||
| chr14:88787821
|
T | C | 7 | a0001c0001t0001g0283a0001c0001t0002g0158a0001c0001t0006g0003others(4): Show | 8 | HG00741.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.197+4486A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88787821 | ||||||
| chr14:88788183
|
C | CA | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.197+4123dupT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88788183 | ||||||
| chr14:88788185
|
A | C | 2 | a0001c0003t0004g0302a0001c0003t0004g0329 | 2 | HG02055.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.197+4122T>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88788185 | ||||||
| chr14:88788222
|
C | T | 1 | a0001c0001t0002g0091 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.197+4085G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88788222 | ||||||
| chr14:88788245
|
C | G | 3 | a0003c0005t0015g0013a0003c0005t0015g0014a0003c0005t0015g0015 | 3 | HG02451.hp1 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.197+4062G>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88788245 | ||||||
| chr14:88788245
|
C | T | 9 | a0001c0001t0006g0208a0001c0001t0014g0004a0001c0001t0014g0005others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.197+4062G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88788245 | ||||||
| chr14:88788250
|
G | A | 2 | a0002c0002t0001g0288a0002c0002t0001g0289 | 2 | HG02040.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.197+4057C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88788250 | ||||||
| chr14:88788422
|
A | T | 5 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(2): Show | 5 | HG00423.hp2 NA18944.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.197+3885T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88788422 | ||||||
| chr14:88788536
|
TA | T | 19 | a0001c0001t0002g0086a0001c0001t0006g0208a0001c0001t0014g0004others(16): Show | 19 | HG01243.hp1 HG01255.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.197+3770delT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88788536 | ||||||
| chr14:88788786
|
G | A | 1 | a0001c0001t0005g0189 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.197+3521C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88788786 | ||||||
| chr14:88788829
|
G | A | 2 | a0001c0001t0002g0159a0001c0001t0002g0160 | 2 | NA18954.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.197+3478C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88788829 | ||||||
| chr14:88788898
|
GA | G | 259 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0283others(256): Show | 262 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.197+3408delT | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88788898 | ||||||
| chr14:88788898
|
GAA | G | 9 | a0001c0001t0014g0004a0001c0001t0014g0005a0001c0001t0014g0006others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.197+3407_197+3408d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88788898 | ||||||
| chr14:88788980
|
C | T | 269 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0210others(266): Show | 272 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.197+3327G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88788980 | ||||||
| chr14:88789070
|
A | G | 2 | a0001c0001t0005g0171a0001c0001t0005g0172 | 2 | NA18983.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.197+3237T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88789070 | ||||||
| chr14:88789447
|
C | CACTGAGA others(104): Show |
13 | a0001c0001t0014g0004a0001c0001t0014g0005a0001c0001t0014g0006others(10): Show | 13 | HG00642.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.197+2749_197+2859d others(113): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88789447 | ||||||
| chr14:88789447
|
C | CACTGAGA others(326): Show |
1 | a0001c0001t0001g0199 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.197+2527_197+2859d others(335): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88789447 | ||||||
| chr14:88789447
|
CACTGAGA others(104): Show |
C | 101 | a0001c0001t0001g0283a0001c0001t0001g0290a0001c0001t0002g0001others(98): Show | 104 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.197+2749_197+2859d others(2): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88789447 | ||||||
| chr14:88789447
|
CACTGAGA others(215): Show |
C | 1 | a0001c0001t0002g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.197+2638_197+2859d others(2): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88789447 | ||||||
| chr14:88790536
|
T | G | 1 | a0001c0003t0004g0329 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.197+1771A>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88790536 | ||||||
| chr14:88790782
|
A | T | 3 | a0001c0001t0014g0004a0001c0001t0014g0005a0001c0001t0014g0006 | 3 | HG02717.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.197+1525T>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88790782 | ||||||
| chr14:88790843
|
T | C | 94 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0280others(91): Show | 95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.197+1464A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88790843 | ||||||
| chr14:88790928
|
T | C | 1 | a0002c0002t0001g0291 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.197+1379A>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88790928 | ||||||
| chr14:88791033
|
C | A | 1 | a0001c0001t0002g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.197+1274G>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88791033 | ||||||
| chr14:88791086
|
CTT | C | 28 | a0001c0001t0012g0324a0001c0001t0012g0325a0001c0001t0012g0326others(25): Show | 28 | HG00408.hp1 HG00609.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.197+1219_197+1220d others(4): Show |
EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88791086 | ||||||
| chr14:88791249
|
G | A | 11 | a0001c0001t0014g0004a0001c0001t0014g0005a0001c0001t0014g0006others(8): Show | 11 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.197+1058C>T | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88791249 | ||||||
| chr14:88791356
|
C | T | 11 | a0001c0001t0014g0004a0001c0001t0014g0005a0001c0001t0014g0006others(8): Show | 11 | HG00642.hp2 HG02145.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.197+951G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88791356 | ||||||
| chr14:88791917
|
G | C | 1 | a0001c0001t0003g0169 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.197+390C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88791917 | ||||||
| chr14:88791986
|
A | G | 2 | a0002c0002t0001g0193a0002c0002t0001g0194 | 2 | NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.197+321T>C | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88791986 | ||||||
| chr14:88792139
|
G | C | 1 | a0002c0002t0021g0292 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.197+168C>G | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88792139 | ||||||
| chr14:88792269
|
C | T | 54 | a0001c0001t0005g0171a0001c0001t0005g0172a0001c0001t0005g0175others(51): Show | 54 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.197+38G>A | EML5 | ENSG00000165521.16 | transcript | ENST00000554922.6 | protein_coding | 1/43 | chr14 | 88792269 |