| geneid | 2043 |
|---|---|
| ensemblid | ENSG00000116106.12 |
| hgncid | 3388 |
| symbol | EPHA4 |
| name | EPH receptor A4 |
| refseq_nuc | NM_004438.5 |
| refseq_prot | NP_004429.1 |
| ensembl_nuc | ENST00000281821.7 |
| ensembl_prot | ENSP00000281821.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 221418027 |
| end | 221572304 |
| strand | - |
| ver | v1.2 |
| region | chr2:221418027-221572304 |
| region5000 | chr2:221413027-221577304 |
| regionname0 | EPHA4_chr2_221418027_221572304 |
| regionname5000 | EPHA4_chr2_221413027_221577304 |
| 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 | 986 | 293 | 77 | 54 | 118 | 6 | 36 | 90 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0002 | 0/0 | 986 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| 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 | 2961 | 231 | 56 | 40 | 105 | 2 | 26 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| c0002 | 0/0 | 2961 | 28 | 7 | 7 | 11 | 0 | 3 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| c0003 | 0/0 | 2961 | 22 | 8 | 6 | 0 | 4 | 4 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| c0004 | 0/0 | 2961 | 3 | 2 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| c0005 | 0/0 | 2961 | 3 | 0 | 0 | 0 | 0 | 3 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| c0006 | 0/0 | 2961 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| c0007 | 0/0 | 2961 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| c0008 | 0/0 | 2961 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| c0009 | 0/0 | 2961 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| c0010 | 0/0 | 2961 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| c0011 | 0/0 | 2961 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| c0012 | 0/0 | 2961 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| 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 | 1/1 | 3402 | 121 | 10 | 29 | 61 | 4 | 15 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0002 | 0/0 | 3402 | 53 | 7 | 13 | 25 | 0 | 8 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0003 | 0/0 | 3406 | 19 | 10 | 5 | 0 | 0 | 4 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0004 | 0/0 | 3402 | 14 | 3 | 4 | 5 | 1 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0005 | 0/0 | 3402 | 13 | 1 | 1 | 9 | 0 | 2 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0006 | 0/0 | 3406 | 6 | 2 | 0 | 4 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0007 | 0/0 | 3402 | 4 | 0 | 0 | 4 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0008 | 0/0 | 3402 | 4 | 4 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0009 | 0/0 | 3402 | 3 | 3 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0010 | 0/0 | 3401 | 3 | 3 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0011 | 0/0 | 3402 | 3 | 3 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0012 | 0/0 | 3406 | 3 | 3 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0013 | 0/0 | 3402 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0014 | 0/0 | 3402 | 2 | 0 | 0 | 0 | 0 | 2 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0015 | 0/0 | 3402 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0016 | 0/0 | 3402 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0017 | 0/0 | 3402 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0018 | 0/0 | 3406 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0019 | 0/0 | 3406 | 2 | 1 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0020 | 0/0 | 3402 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0021 | 0/0 | 3406 | 2 | 0 | 0 | 0 | 0 | 2 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0022 | 0/0 | 3402 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0023 | 0/0 | 3402 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0024 | 0/0 | 3406 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0025 | 0/0 | 3401 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0026 | 0/0 | 3402 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0027 | 0/0 | 3402 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0028 | 0/0 | 3406 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0029 | 0/0 | 3406 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0030 | 0/0 | 3402 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0031 | 0/0 | 3402 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0032 | 0/0 | 3402 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0033 | 0/0 | 3402 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0034 | 0/0 | 3402 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0035 | 0/0 | 3402 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0036 | 0/0 | 3402 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0037 | 0/0 | 3402 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0038 | 0/0 | 3402 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0039 | 0/0 | 3402 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0040 | 0/0 | 3402 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0041 | 0/0 | 3402 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0042 | 0/0 | 3402 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0043 | 0/0 | 3406 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0044 | 0/0 | 3406 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0045 | 0/0 | 3406 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0046 | 0/0 | 3406 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0047 | 0/0 | 3402 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0048 | 0/0 | 3402 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| t0049 | 0/0 | 3406 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0217 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0261 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| 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 | 2961 | 231 | 56 | 40 | 105 | 2 | 26 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0002 | 0/0 | 2961 | 28 | 7 | 7 | 11 | 0 | 3 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0003 | 0/0 | 2961 | 22 | 8 | 6 | 0 | 4 | 4 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0004 | 0/0 | 2961 | 3 | 2 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0005 | 0/0 | 2961 | 3 | 0 | 0 | 0 | 0 | 3 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0006 | 0/0 | 2961 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0007 | 0/0 | 2961 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0008 | 0/0 | 2961 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0009 | 0/0 | 2961 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0010 | 0/0 | 2961 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0012 | 0/0 | 2961 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0002c0011 | 0/0 | 2961 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 6362 | 98 | 10 | 21 | 54 | 2 | 9 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0002 | 0/0 | 6362 | 50 | 6 | 12 | 24 | 0 | 8 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0003 | 0/0 | 6366 | 4 | 0 | 3 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0004 | 0/0 | 6362 | 10 | 2 | 2 | 5 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0005 | 0/0 | 6362 | 12 | 1 | 1 | 8 | 0 | 2 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0006 | 0/0 | 6366 | 6 | 2 | 0 | 4 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0007 | 0/0 | 6362 | 3 | 0 | 0 | 3 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0008 | 0/0 | 6362 | 4 | 4 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0009 | 0/0 | 6362 | 3 | 3 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0010 | 0/0 | 6361 | 3 | 3 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0011 | 0/0 | 6362 | 3 | 3 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0012 | 0/0 | 6366 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0013 | 0/0 | 6362 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0014 | 0/0 | 6362 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0015 | 0/0 | 6362 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0016 | 0/0 | 6362 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0017 | 0/0 | 6362 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0018 | 0/0 | 6366 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0020 | 0/0 | 6362 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0021 | 0/0 | 6366 | 2 | 0 | 0 | 0 | 0 | 2 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0024 | 0/0 | 6366 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0025 | 0/0 | 6361 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0027 | 0/0 | 6362 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0030 | 0/0 | 6362 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0031 | 0/0 | 6362 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0032 | 0/0 | 6362 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0033 | 0/0 | 6362 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0034 | 0/0 | 6362 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0036 | 0/0 | 6362 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0037 | 0/0 | 6362 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0038 | 0/0 | 6362 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0039 | 0/0 | 6362 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0040 | 0/0 | 6362 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0041 | 0/0 | 6362 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0042 | 0/0 | 6362 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0043 | 0/0 | 6366 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0044 | 0/0 | 6366 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0045 | 0/0 | 6366 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0048 | 0/0 | 6362 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0001t0049 | 0/0 | 6366 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0002t0001 | 0/0 | 6362 | 14 | 0 | 5 | 6 | 0 | 3 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0002t0002 | 0/0 | 6362 | 2 | 0 | 1 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0002t0004 | 0/0 | 6362 | 2 | 1 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0002t0007 | 0/0 | 6362 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0002t0012 | 0/0 | 6366 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0002t0022 | 0/0 | 6362 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0002t0023 | 0/0 | 6362 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0002t0028 | 0/0 | 6366 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0002t0029 | 0/0 | 6366 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0002t0047 | 0/0 | 6362 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0003t0001 | 0/0 | 6362 | 6 | 0 | 3 | 0 | 2 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0003t0003 | 0/0 | 6366 | 13 | 8 | 2 | 0 | 0 | 3 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0003t0004 | 0/0 | 6362 | 2 | 0 | 1 | 0 | 1 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0003t0046 | 0/0 | 6366 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0004t0019 | 0/0 | 6366 | 2 | 1 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0004t0035 | 0/0 | 6362 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0005t0001 | 0/0 | 6362 | 2 | 0 | 0 | 0 | 0 | 2 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0005t0014 | 0/0 | 6362 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0006t0003 | 0/0 | 6366 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0007t0005 | 0/0 | 6362 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0008t0003 | 0/0 | 6366 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0009t0002 | 0/0 | 6362 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0010t0001 | 0/0 | 6362 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0001c0012t0018 | 0/0 | 6366 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| a0002c0011t0026 | 0/0 | 6362 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | copy fasta | chr2 | 221413027 | 221577304 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0217 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0261 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0004g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0005g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0005g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0005g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0005g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0005g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0005g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0005g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0005g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0006g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0006g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0006g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0006g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0006g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0006g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0007g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0007g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0007g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0008g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0008g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0008g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0008g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0009g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0009g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0009g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0010g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0010g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0010g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0011g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0011g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0011g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0012g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0013g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0013g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0014g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0015g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0015g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0016g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0016g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0017g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0017g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0018g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0020g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0020g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0021g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0021g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0024g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0025g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0027g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0030g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0031g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0032g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0033g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0034g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0036g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0037g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0038g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0039g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0040g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0041g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0042g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0043g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0044g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0045g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0048g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0001t0049g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0002t0004g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0002t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0002t0007g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0002t0012g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0002t0012g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0002t0022g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0002t0022g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0002t0023g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0002t0023g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0002t0028g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0002t0029g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0002t0047g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0003t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0003t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0003t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0003t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0003t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0003t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0003t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0003t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0003t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0003t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0003t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0003t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0003t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0003t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0003t0003g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0003t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0003t0004g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0003t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0003t0046g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0004t0019g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0004t0019g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0004t0035g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0005t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0005t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0005t0014g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0006t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0007t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0008t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0009t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0010t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0001c0012t0018g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| a0002c0011t0026g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0220 | EUR | FIN | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG00280 | hp2 | a0001 | c0003 | t0001 | g0031 | EUR | FIN | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG00323 | hp1 | a0001 | c0003 | t0001 | g0030 | EUR | FIN | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG00323 | hp2 | a0001 | c0003 | t0004 | g0084 | EUR | FIN | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | CHS | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG00423 | hp1 | a0001 | c0001 | t0005 | g0015 | EAS | CHS | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG00544 | hp2 | a0001 | c0001 | t0005 | g0049 | EAS | CHS | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG00558 | hp1 | a0001 | c0001 | t0005 | g0009 | EAS | CHS | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0195 | EAS | CHS | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0185 | AMR | PUR | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | PUR | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG00673 | hp1 | a0001 | c0002 | t0023 | g0219 | EAS | CHS | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0186 | AMR | PUR | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG00733 | hp2 | a0001 | c0003 | t0001 | g0087 | AMR | PUR | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG00735 | hp2 | a0001 | c0003 | t0003 | g0056 | AMR | PUR | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0054 | AMR | PUR | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0276 | AMR | PUR | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0267 | AMR | PUR | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0216 | AMR | PUR | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0203 | AMR | PUR | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0280 | AMR | PUR | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0277 | AMR | PUR | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0194 | AMR | PUR | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | PUR | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0289 | AMR | PUR | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0047 | AMR | PUR | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0266 | AMR | PUR | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01169 | hp1 | a0001 | c0003 | t0004 | g0088 | AMR | PUR | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0048 | AMR | PUR | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01243 | hp2 | a0001 | c0004 | t0019 | g0236 | AMR | PUR | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | CLM | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | CLM | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01261 | hp1 | a0001 | c0003 | t0001 | g0085 | AMR | CLM | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01361 | hp2 | a0001 | c0003 | t0003 | g0265 | AMR | CLM | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0043 | AMR | CLM | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01884 | hp1 | a0001 | c0001 | t0008 | g0132 | AFR | ACB | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01884 | hp2 | a0001 | c0002 | t0029 | g0269 | AFR | ACB | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01891 | hp1 | a0001 | c0001 | t0015 | g0286 | AFR | ACB | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01975 | hp2 | a0001 | c0002 | t0004 | g0104 | AMR | PEL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0052 | AMR | PEL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | PEL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0271 | AMR | PEL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0055 | AMR | PEL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02015 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | KHV | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | KHV | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | KHV | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02055 | hp1 | a0001 | c0004 | t0035 | g0108 | AFR | ACB | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0057 | EAS | KHV | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | KHV | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | KHV | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02129 | hp2 | a0001 | c0001 | t0006 | g0238 | EAS | KHV | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0235 | AFR | ACB | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02145 | hp2 | a0001 | c0001 | t0011 | g0138 | AFR | ACB | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | CDX | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CDX | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02257 | hp1 | a0001 | c0003 | t0003 | g0133 | AFR | ACB | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02258 | hp1 | a0001 | c0001 | t0034 | g0243 | AFR | ACB | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02258 | hp2 | a0001 | c0003 | t0003 | g0292 | AFR | ACB | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02280 | hp1 | a0001 | c0002 | t0012 | g0099 | AFR | ACB | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02280 | hp2 | a0001 | c0001 | t0044 | g0232 | AFR | ACB | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | GWD | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02572 | hp2 | a0001 | c0001 | t0012 | g0275 | AFR | GWD | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0136 | SAS | PJL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0279 | SAS | PJL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02615 | hp1 | a0001 | c0001 | t0017 | g0103 | AFR | GWD | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02615 | hp2 | a0001 | c0009 | t0002 | g0094 | AFR | GWD | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02630 | hp1 | a0001 | c0001 | t0009 | g0214 | AFR | GWD | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02630 | hp2 | a0001 | c0001 | t0024 | g0129 | AFR | GWD | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02717 | hp1 | a0001 | c0001 | t0017 | g0098 | AFR | GWD | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02717 | hp2 | a0001 | c0001 | t0040 | g0128 | AFR | GWD | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02723 | hp1 | a0001 | c0003 | t0003 | g0093 | AFR | GWD | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02723 | hp2 | a0001 | c0001 | t0010 | g0288 | AFR | GWD | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0089 | SAS | PJL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02735 | hp2 | a0001 | c0003 | t0003 | g0281 | SAS | PJL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | GWD | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02895 | hp1 | a0001 | c0001 | t0039 | g0131 | AFR | GWD | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0223 | AFR | GWD | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02896 | hp1 | a0001 | c0001 | t0008 | g0117 | AFR | GWD | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02896 | hp2 | a0001 | c0001 | t0011 | g0241 | AFR | GWD | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02897 | hp1 | a0001 | c0001 | t0011 | g0240 | AFR | GWD | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | GWD | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02922 | hp1 | a0001 | c0001 | t0015 | g0244 | AFR | ESN | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02970 | hp1 | a0001 | c0003 | t0003 | g0079 | AFR | ESN | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02970 | hp2 | a0001 | c0001 | t0010 | g0110 | AFR | ESN | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ESN | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | PJL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03041 | hp1 | a0001 | c0002 | t0028 | g0242 | AFR | GWD | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03041 | hp2 | a0001 | c0003 | t0003 | g0091 | AFR | GWD | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0246 | AFR | MSL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03098 | hp2 | a0001 | c0001 | t0013 | g0290 | AFR | MSL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03139 | hp1 | a0001 | c0002 | t0012 | g0101 | AFR | ESN | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03139 | hp2 | a0001 | c0008 | t0003 | g0157 | AFR | ESN | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03195 | hp1 | a0001 | c0001 | t0049 | g0227 | AFR | ESN | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03195 | hp2 | a0001 | c0001 | t0018 | g0113 | AFR | ESN | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03209 | hp1 | a0002 | c0011 | t0026 | g0109 | AFR | MSL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0228 | AFR | MSL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03225 | hp1 | a0001 | c0003 | t0003 | g0082 | AFR | MSL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03225 | hp2 | a0001 | c0001 | t0009 | g0212 | AFR | MSL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0179 | SAS | PJL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0020 | SAS | PJL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03453 | hp1 | a0001 | c0001 | t0045 | g0096 | AFR | MSL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0134 | AFR | MSL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03486 | hp1 | a0001 | c0001 | t0008 | g0135 | AFR | MSL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03486 | hp2 | a0001 | c0001 | t0033 | g0170 | AFR | MSL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03491 | hp1 | a0001 | c0003 | t0003 | g0126 | SAS | PJL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0125 | SAS | PJL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0149 | SAS | PJL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03516 | hp1 | a0001 | c0002 | t0022 | g0090 | AFR | ESN | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03516 | hp2 | a0001 | c0001 | t0009 | g0274 | AFR | ESN | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03540 | hp1 | a0001 | c0002 | t0004 | g0234 | AFR | GWD | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03540 | hp2 | a0001 | c0001 | t0013 | g0293 | AFR | GWD | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | MSL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03579 | hp2 | a0001 | c0001 | t0036 | g0115 | AFR | MSL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03654 | hp1 | a0001 | c0001 | t0021 | g0083 | SAS | PJL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03704 | hp1 | a0001 | c0003 | t0003 | g0161 | SAS | PJL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0285 | SAS | PJL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0158 | SAS | BEB | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | BEB | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0206 | SAS | BEB | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03834 | hp2 | a0001 | c0005 | t0014 | g0040 | SAS | BEB | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03927 | hp2 | a0001 | c0001 | t0005 | g0165 | SAS | BEB | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03942 | hp1 | a0001 | c0001 | t0031 | g0046 | SAS | BEB | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03942 | hp2 | a0001 | c0001 | t0032 | g0251 | SAS | BEB | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG04115 | hp1 | a0001 | c0005 | t0001 | g0029 | SAS | STU | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | STU | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG04184 | hp1 | a0001 | c0001 | t0014 | g0213 | SAS | BEB | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG04184 | hp2 | a0001 | c0003 | t0001 | g0086 | SAS | BEB | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG04199 | hp1 | a0001 | c0005 | t0001 | g0034 | SAS | STU | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG04199 | hp2 | a0001 | c0001 | t0021 | g0156 | SAS | STU | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0284 | SAS | STU | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | STU | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | CHB | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0174 | EAS | CHB | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18747 | hp1 | a0001 | c0002 | t0023 | g0218 | EAS | CHB | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | CHB | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18906 | hp1 | a0001 | c0006 | t0003 | g0118 | AFR | YRI | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18906 | hp2 | a0001 | c0001 | t0010 | g0107 | AFR | YRI | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18941 | hp1 | a0001 | c0001 | t0048 | g0162 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18944 | hp2 | a0001 | c0001 | t0016 | g0058 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18948 | hp2 | a0001 | c0007 | t0005 | g0061 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18953 | hp1 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18965 | hp1 | a0001 | c0001 | t0007 | g0201 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18973 | hp2 | a0001 | c0002 | t0047 | g0229 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18986 | hp2 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18989 | hp1 | a0001 | c0001 | t0007 | g0078 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18989 | hp2 | a0001 | c0001 | t0005 | g0072 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18991 | hp1 | a0001 | c0001 | t0020 | g0077 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18998 | hp2 | a0001 | c0001 | t0007 | g0076 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA18999 | hp2 | a0001 | c0002 | t0007 | g0239 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19002 | hp2 | a0001 | c0001 | t0020 | g0173 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19004 | hp2 | a0001 | c0001 | t0016 | g0191 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19009 | hp1 | a0001 | c0001 | t0005 | g0023 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19010 | hp1 | a0001 | c0001 | t0042 | g0153 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0074 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19030 | hp1 | a0001 | c0012 | t0018 | g0272 | AFR | LWK | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19030 | hp2 | a0001 | c0003 | t0003 | g0226 | AFR | LWK | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0258 | AFR | LWK | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19043 | hp2 | a0001 | c0001 | t0037 | g0100 | AFR | LWK | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19057 | hp1 | a0001 | c0001 | t0006 | g0250 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19062 | hp1 | a0001 | c0001 | t0005 | g0143 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19066 | hp2 | a0001 | c0001 | t0041 | g0122 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19068 | hp2 | a0001 | c0010 | t0001 | g0176 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19081 | hp2 | a0001 | c0001 | t0006 | g0028 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19087 | hp1 | a0001 | c0001 | t0005 | g0145 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19240 | hp1 | a0001 | c0003 | t0003 | g0114 | AFR | YRI | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA19240 | hp2 | a0001 | c0002 | t0022 | g0273 | AFR | YRI | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA20129 | hp1 | a0001 | c0001 | t0027 | g0137 | AFR | ASW | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA20129 | hp2 | a0001 | c0004 | t0019 | g0237 | AFR | ASW | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA20752 | hp1 | a0001 | c0003 | t0046 | g0278 | EUR | TSI | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0268 | EUR | TSI | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01123 | hp1 | a0001 | c0001 | t0043 | g0124 | AMR | CLM | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0127 | AMR | CLM | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0291 | AFR | ACB | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG02559 | hp2 | a0001 | c0001 | t0038 | g0102 | AFR | ACB | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03471 | hp1 | a0001 | c0001 | t0030 | g0130 | AFR | MSL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | MSL | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA20300 | hp1 | a0001 | c0001 | t0025 | g0233 | AFR | USA | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0116 | AFR | USA | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | LWK | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | LWK | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0217 | REF | REF | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0261 | REF | REF | EPHA4_chr2_221413027_221577304 | EPHA4 | chr2 | 221413027 | 221577304 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:221426613
|
G | C | 1 | a0002 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.2697C>G | p.Asn899Lys | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 16/18 | 2753/6362 | 2697/2961 | 899/986 | chr2 | 221426613 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:221426109
|
C | T | 3 | a0001c0003a0001c0006a0001c0008 | 24 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(21): Show |
synonymous_variant | LOW | c.2880G>A | p.Thr960Thr | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/18 | 2936/6362 | 2880/2961 | 960/986 | chr2 | 221426109 | ||
| chr2:221434262
|
C | T | 1 | a0001c0010 | 1 | NA19068.hp2 | synonymous_variant | LOW | c.2376G>A | p.Ala792Ala | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/18 | 2432/6362 | 2376/2961 | 792/986 | chr2 | 221434262 | ||
| chr2:221443506
|
T | C | 4 | a0001c0002a0001c0004a0001c0012others(1): Show | 33 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(30): Show |
synonymous_variant | LOW | c.1875A>G | p.Lys625Lys | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 10/18 | 1931/6362 | 1875/2961 | 625/986 | chr2 | 221443506 | ||
| chr2:221446175
|
A | G | 1 | a0001c0009 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.1722T>C | p.Ser574Ser | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/18 | 1778/6362 | 1722/2961 | 574/986 | chr2 | 221446175 | ||
| chr2:221456620
|
G | A | 1 | a0001c0004 | 3 | HG01243.hp2 HG02055.hp1 NA20129.hp2 |
synonymous_variant | LOW | c.1596C>T | p.Thr532Thr | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 7/18 | 1652/6362 | 1596/2961 | 532/986 | chr2 | 221456620 | ||
| chr2:221456760
|
G | T | 1 | a0001c0008 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.1456C>A | p.Arg486Arg | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 7/18 | 1512/6362 | 1456/2961 | 486/986 | chr2 | 221456760 | ||
| chr2:221457965
|
C | T | 1 | a0001c0007 | 1 | NA18948.hp2 | synonymous_variant | LOW | c.1344G>A | p.Gln448Gln | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 6/18 | 1400/6362 | 1344/2961 | 448/986 | chr2 | 221457965 | ||
| chr2:221501042
|
G | A | 1 | a0001c0012 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.954C>T | p.Asn318Asn | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/18 | 1010/6362 | 954/2961 | 318/986 | chr2 | 221501042 | ||
| chr2:221563966
|
T | C | 1 | a0001c0005 | 3 | HG03834.hp2 HG04115.hp1 HG04199.hp1 |
synonymous_variant | LOW | c.588A>G | p.Ser196Ser | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/18 | 644/6362 | 588/2961 | 196/986 | chr2 | 221563966 | ||
| chr2:221564215
|
G | T | 1 | a0001c0006 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.339C>A | p.Gly113Gly | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/18 | 395/6362 | 339/2961 | 113/986 | chr2 | 221564215 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:221418045
|
C | T | 36 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(33): Show | 124 | HG00323.hp2 HG00408.hp1 HG00639.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*3327G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 7983 | chr2 | 221418045 | |||||
| chr2:221418203
|
T | C | 2 | a0001c0001t0013a0001c0001t0034 | 3 | HG02258.hp1 HG03098.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3169A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 7825 | chr2 | 221418203 | |||||
| chr2:221418239
|
G | T | 37 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(34): Show | 127 | HG00323.hp2 HG00408.hp1 HG00639.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*3133C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 7789 | chr2 | 221418239 | |||||
| chr2:221418248
|
G | A | 2 | a0001c0001t0018a0001c0012t0018 | 2 | HG03195.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3124C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 7780 | chr2 | 221418248 | |||||
| chr2:221418280
|
A | T | 44 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(41): Show | 139 | HG00323.hp2 HG00408.hp1 HG00639.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*3092T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 7748 | chr2 | 221418280 | |||||
| chr2:221418307
|
C | A | 1 | a0001c0001t0045 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3065G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 7721 | chr2 | 221418307 | |||||
| chr2:221418308
|
C | G | 1 | a0001c0001t0039 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3064G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 7720 | chr2 | 221418308 | |||||
| chr2:221418505
|
G | A | 1 | a0001c0001t0042 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2867C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 7523 | chr2 | 221418505 | |||||
| chr2:221418512
|
C | T | 1 | a0001c0001t0038 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2860G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 7516 | chr2 | 221418512 | |||||
| chr2:221418561
|
T | C | 37 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(34): Show | 127 | HG00323.hp2 HG00408.hp1 HG00639.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*2811A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 7467 | chr2 | 221418561 | |||||
| chr2:221418567
|
C | T | 1 | a0001c0002t0047 | 1 | NA18973.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2805G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 7461 | chr2 | 221418567 | |||||
| chr2:221418761
|
C | T | 1 | a0001c0001t0020 | 2 | NA18991.hp1 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2611G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 7267 | chr2 | 221418761 | |||||
| chr2:221418784
|
C | T | 37 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(34): Show | 127 | HG00323.hp2 HG00408.hp1 HG00639.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*2588G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 7244 | chr2 | 221418784 | |||||
| chr2:221418794
|
C | T | 37 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(34): Show | 127 | HG00323.hp2 HG00408.hp1 HG00639.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*2578G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 7234 | chr2 | 221418794 | |||||
| chr2:221418802
|
T | G | 4 | a0001c0001t0013a0001c0001t0015a0001c0001t0030others(1): Show | 6 | HG01891.hp1 HG02258.hp1 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2570A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 7226 | chr2 | 221418802 | |||||
| chr2:221419052
|
T | C | 3 | a0001c0001t0017a0001c0001t0027a0001c0001t0040 | 4 | HG02615.hp1 HG02717.hp1 HG02717.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2320A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 6976 | chr2 | 221419052 | |||||
| chr2:221419057
|
T | C | 1 | a0001c0001t0043 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2315A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 6971 | chr2 | 221419057 | |||||
| chr2:221419110
|
T | C | 1 | a0001c0001t0008 | 4 | HG01884.hp1 HG02896.hp1 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2262A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 6918 | chr2 | 221419110 | |||||
| chr2:221419314
|
G | C | 19 | a0001c0001t0003a0001c0001t0006a0001c0001t0012others(16): Show | 42 | HG00735.hp2 HG01071.hp1 HG01109.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*2058C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 6714 | chr2 | 221419314 | |||||
| chr2:221419385
|
A | C | 1 | a0001c0001t0037 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1987T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 6643 | chr2 | 221419385 | |||||
| chr2:221419445
|
C | T | 1 | a0001c0001t0036 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1927G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 6583 | chr2 | 221419445 | |||||
| chr2:221419450
|
A | G | 1 | a0001c0004t0035 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1922T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 6578 | chr2 | 221419450 | |||||
| chr2:221419485
|
G | A | 1 | a0001c0001t0016 | 2 | NA18944.hp2 NA19004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1887C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 6543 | chr2 | 221419485 | |||||
| chr2:221419557
|
C | T | 9 | a0001c0001t0003a0001c0001t0021a0001c0001t0024others(6): Show | 25 | HG00735.hp2 HG01071.hp1 HG01109.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1815G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 6471 | chr2 | 221419557 | |||||
| chr2:221419626
|
G | C | 1 | a0001c0004t0019 | 2 | HG01243.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1746C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 6402 | chr2 | 221419626 | |||||
| chr2:221419755
|
A | G | 1 | a0001c0001t0048 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1617T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 6273 | chr2 | 221419755 | |||||
| chr2:221419764
|
G | A | 1 | a0001c0003t0046 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1608C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 6264 | chr2 | 221419764 | |||||
| chr2:221419809
|
G | A | 2 | a0001c0001t0012a0001c0002t0012 | 3 | HG02280.hp1 HG02572.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1563C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 6219 | chr2 | 221419809 | |||||
| chr2:221419847
|
T | C | 2 | a0001c0001t0007a0001c0002t0007 | 4 | NA18965.hp1 NA18989.hp1 NA18998.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1525A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 6181 | chr2 | 221419847 | |||||
| chr2:221419926
|
C | T | 38 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(35): Show | 131 | HG00323.hp2 HG00408.hp1 HG00639.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*1446G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 6102 | chr2 | 221419926 | |||||
| chr2:221419959
|
G | T | 1 | a0001c0001t0032 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1413C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 6069 | chr2 | 221419959 | |||||
| chr2:221419966
|
G | C | 38 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(35): Show | 131 | HG00323.hp2 HG00408.hp1 HG00639.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*1406C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 6062 | chr2 | 221419966 | |||||
| chr2:221420001
|
A | T | 4 | a0001c0001t0013a0001c0001t0015a0001c0001t0030others(1): Show | 6 | HG01891.hp1 HG02258.hp1 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1371T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 6027 | chr2 | 221420001 | |||||
| chr2:221420105
|
T | C | 1 | a0001c0001t0017 | 2 | HG02615.hp1 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1267A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 5923 | chr2 | 221420105 | |||||
| chr2:221420160
|
T | G | 1 | a0001c0001t0041 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1212A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 5868 | chr2 | 221420160 | |||||
| chr2:221420206
|
C | T | 2 | a0001c0001t0049a0001c0002t0029 | 2 | HG01884.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1166G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 5822 | chr2 | 221420206 | |||||
| chr2:221420248
|
A | AGTCT | 19 | a0001c0001t0003a0001c0001t0006a0001c0001t0012others(16): Show | 42 | HG00735.hp2 HG01071.hp1 HG01109.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1120_*1123dupAGAC | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 5779 | chr2 | 221420248 | |||||
| chr2:221420253
|
G | A | 1 | a0001c0001t0042 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1119C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 5775 | chr2 | 221420253 | |||||
| chr2:221420272
|
G | C | 19 | a0001c0001t0003a0001c0001t0006a0001c0001t0012others(16): Show | 42 | HG00735.hp2 HG01071.hp1 HG01109.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1100C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 5756 | chr2 | 221420272 | |||||
| chr2:221420280
|
T | C | 1 | a0001c0001t0025 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1092A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 5748 | chr2 | 221420280 | |||||
| chr2:221420354
|
C | T | 1 | a0001c0001t0033 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1018G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 5674 | chr2 | 221420354 | |||||
| chr2:221420548
|
A | G | 3 | a0001c0001t0014a0001c0001t0032a0001c0005t0014 | 3 | HG03834.hp2 HG03942.hp2 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*824T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 18/18 | 5480 | chr2 | 221420548 | |||||
| chr2:221425307
|
T | G | 9 | a0001c0001t0002a0001c0001t0005a0001c0001t0020others(6): Show | 72 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*721A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/18 | 721 | chr2 | 221425307 | |||||
| chr2:221425406
|
T | C | 1 | a0001c0002t0022 | 2 | HG03516.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*622A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/18 | 622 | chr2 | 221425406 | |||||
| chr2:221425446
|
C | T | 1 | a0001c0001t0031 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*582G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/18 | 582 | chr2 | 221425446 | |||||
| chr2:221425473
|
G | T | 1 | a0001c0001t0030 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*555C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/18 | 555 | chr2 | 221425473 | |||||
| chr2:221425507
|
C | T | 1 | a0001c0002t0029 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*521G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/18 | 521 | chr2 | 221425507 | |||||
| chr2:221425541
|
G | C | 1 | a0001c0002t0023 | 2 | HG00673.hp1 NA18747.hp1 |
3_prime_UTR_variant | MODIFIER | c.*487C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/18 | 487 | chr2 | 221425541 | |||||
| chr2:221425544
|
A | G | 3 | a0001c0001t0027a0001c0002t0028a0002c0011t0026 | 3 | HG03041.hp1 HG03209.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*484T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/18 | 484 | chr2 | 221425544 | |||||
| chr2:221425550
|
CA | C | 2 | a0001c0001t0010a0001c0001t0025 | 4 | HG02723.hp2 HG02970.hp2 NA18906.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*477delT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/18 | 477 | chr2 | 221425550 | |||||
| chr2:221425790
|
G | C | 1 | a0001c0001t0049 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*238C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/18 | 238 | chr2 | 221425790 | |||||
| chr2:221425862
|
C | G | 1 | a0001c0001t0013 | 2 | HG03098.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*166G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/18 | 166 | chr2 | 221425862 | |||||
| chr2:221425885
|
A | G | 2 | a0001c0001t0009a0001c0001t0024 | 4 | HG02630.hp1 HG02630.hp2 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*143T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/18 | 143 | chr2 | 221425885 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:221420645
|
G | C | 42 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0279others(39): Show | 42 | HG00735.hp2 HG01071.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.*820-93C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221420645 | ||||||
| chr2:221420730
|
G | A | 42 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0279others(39): Show | 42 | HG00735.hp2 HG01071.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.*820-178C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221420730 | ||||||
| chr2:221420733
|
C | CAA | 42 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0279others(39): Show | 42 | HG00735.hp2 HG01071.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.*820-183_*820-182d others(4): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221420733 | ||||||
| chr2:221420742
|
C | A | 42 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0279others(39): Show | 42 | HG00735.hp2 HG01071.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.*820-190G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221420742 | ||||||
| chr2:221420857
|
C | T | 2 | a0001c0001t0018g0113a0001c0012t0018g0272 | 2 | HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.*820-305G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221420857 | ||||||
| chr2:221420979
|
C | T | 40 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0279others(37): Show | 40 | HG00735.hp2 HG01071.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.*820-427G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221420979 | ||||||
| chr2:221421052
|
G | A | 20 | a0001c0001t0004g0203a0001c0001t0008g0117a0001c0001t0008g0132others(17): Show | 20 | HG01074.hp1 HG01884.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.*820-500C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221421052 | ||||||
| chr2:221421068
|
T | C | 2 | a0001c0001t0001g0070a0001c0002t0023g0218 | 2 | HG00423.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.*820-516A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221421068 | ||||||
| chr2:221421080
|
G | A | 1 | a0002c0011t0026g0109 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.*820-528C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221421080 | ||||||
| chr2:221421112
|
G | A | 130 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0010others(127): Show | 130 | HG00323.hp2 HG00408.hp1 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.*820-560C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221421112 | ||||||
| chr2:221421113
|
T | C | 4 | a0001c0001t0011g0138a0001c0001t0011g0240a0001c0001t0011g0241others(1): Show | 4 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.*820-561A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221421113 | ||||||
| chr2:221421166
|
G | A | 42 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0279others(39): Show | 42 | HG00735.hp2 HG01071.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.*820-614C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221421166 | ||||||
| chr2:221421169
|
C | T | 1 | a0002c0011t0026g0109 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.*820-617G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221421169 | ||||||
| chr2:221421172
|
C | T | 1 | a0001c0001t0002g0179 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.*820-620G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221421172 | ||||||
| chr2:221421175
|
T | C | 133 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0010others(130): Show | 133 | HG00323.hp2 HG00408.hp1 HG00639.hp2 others(130): Show |
intron_variant | MODIFIER | c.*820-623A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221421175 | ||||||
| chr2:221421224
|
T | C | 135 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0010others(132): Show | 135 | HG00323.hp2 HG00408.hp1 HG00639.hp2 others(132): Show |
intron_variant | MODIFIER | c.*820-672A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221421224 | ||||||
| chr2:221421265
|
T | A | 137 | a0001c0001t0001g0171a0001c0001t0002g0005a0001c0001t0002g0008others(134): Show | 137 | HG00323.hp2 HG00408.hp1 HG00639.hp2 others(134): Show |
intron_variant | MODIFIER | c.*820-713A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221421265 | ||||||
| chr2:221421271
|
G | A | 136 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0010others(133): Show | 136 | HG00323.hp2 HG00408.hp1 HG00639.hp2 others(133): Show |
intron_variant | MODIFIER | c.*820-719C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221421271 | ||||||
| chr2:221421278
|
T | C | 1 | a0001c0001t0001g0171 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.*820-726A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221421278 | ||||||
| chr2:221421294
|
T | G | 2 | a0001c0001t0002g0160a0001c0001t0002g0277 | 2 | HG00738.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.*820-742A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221421294 | ||||||
| chr2:221421340
|
G | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0105 | 2 | HG01361.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.*820-788C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221421340 | ||||||
| chr2:221421358
|
G | T | 134 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0010others(131): Show | 134 | HG00323.hp2 HG00408.hp1 HG00639.hp2 others(131): Show |
intron_variant | MODIFIER | c.*820-806C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221421358 | ||||||
| chr2:221421375
|
G | C | 1 | a0001c0001t0001g0141 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.*820-823C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221421375 | ||||||
| chr2:221421413
|
G | A | 71 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0010others(68): Show | 71 | HG00323.hp2 HG00408.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.*820-861C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221421413 | ||||||
| chr2:221421425
|
A | G | 2 | a0001c0001t0049g0227a0001c0002t0029g0269 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.*820-873T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221421425 | ||||||
| chr2:221421474
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.*820-922C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221421474 | ||||||
| chr2:221421489
|
T | C | 6 | a0001c0001t0013g0290a0001c0001t0013g0293a0001c0001t0015g0244others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.*820-937A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221421489 | ||||||
| chr2:221421580
|
C | T | 1 | a0001c0001t0002g0147 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.*820-1028G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221421580 | ||||||
| chr2:221422074
|
T | TA | 36 | a0001c0001t0001g0033a0001c0001t0003g0266a0001c0001t0003g0267others(33): Show | 36 | HG00735.hp2 HG01071.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.*820-1523dupT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221422074 | ||||||
| chr2:221422074
|
TA | T | 11 | a0001c0001t0001g0282a0001c0001t0002g0005a0001c0001t0004g0291others(8): Show | 11 | HG01257.hp1 HG02559.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.*820-1523delT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221422074 | ||||||
| chr2:221422128
|
G | T | 46 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0279others(43): Show | 46 | HG00735.hp2 HG01071.hp1 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.*820-1576C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221422128 | ||||||
| chr2:221422402
|
A | G | 1 | a0001c0001t0006g0004 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.*820-1850T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221422402 | ||||||
| chr2:221422403
|
G | A | 1 | a0001c0001t0006g0004 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.*820-1851C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221422403 | ||||||
| chr2:221422408
|
A | G | 1 | a0001c0001t0006g0004 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.*820-1856T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221422408 | ||||||
| chr2:221422541
|
C | T | 2 | a0001c0002t0022g0090a0001c0002t0022g0273 | 2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.*820-1989G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221422541 | ||||||
| chr2:221422613
|
G | A | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.*820-2061C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221422613 | ||||||
| chr2:221422644
|
T | C | 1 | a0001c0001t0011g0138 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.*820-2092A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221422644 | ||||||
| chr2:221422707
|
G | A | 4 | a0001c0001t0001g0080a0001c0001t0001g0182a0001c0001t0001g0184others(1): Show | 4 | HG01081.hp1 HG01257.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.*820-2155C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221422707 | ||||||
| chr2:221422894
|
A | C | 1 | a0001c0001t0006g0004 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.*819+2315T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221422894 | ||||||
| chr2:221422949
|
A | C | 1 | a0001c0001t0006g0004 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.*819+2260T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221422949 | ||||||
| chr2:221422981
|
C | A | 1 | a0001c0004t0035g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.*819+2228G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221422981 | ||||||
| chr2:221423013
|
C | A | 3 | a0001c0001t0011g0138a0001c0001t0011g0240a0001c0001t0011g0241 | 3 | HG02145.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.*819+2196G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221423013 | ||||||
| chr2:221423123
|
G | A | 2 | a0001c0001t0017g0098a0001c0001t0017g0103 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.*819+2086C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221423123 | ||||||
| chr2:221423124
|
T | C | 136 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0010others(133): Show | 136 | HG00323.hp2 HG00408.hp1 HG00639.hp2 others(133): Show |
intron_variant | MODIFIER | c.*819+2085A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221423124 | ||||||
| chr2:221423127
|
C | T | 1 | a0001c0002t0001g0019 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.*819+2082G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221423127 | ||||||
| chr2:221423149
|
T | C | 39 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0279others(36): Show | 39 | HG00735.hp2 HG01071.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.*819+2060A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221423149 | ||||||
| chr2:221423653
|
T | C | 1 | a0001c0001t0039g0131 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.*819+1556A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221423653 | ||||||
| chr2:221423660
|
T | C | 36 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0279others(33): Show | 36 | HG00735.hp2 HG01071.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.*819+1549A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221423660 | ||||||
| chr2:221423716
|
T | C | 36 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0279others(33): Show | 36 | HG00735.hp2 HG01071.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.*819+1493A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221423716 | ||||||
| chr2:221423736
|
C | A | 36 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0279others(33): Show | 36 | HG00735.hp2 HG01071.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.*819+1473G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221423736 | ||||||
| chr2:221423761
|
GA | G | 49 | a0001c0001t0001g0006a0001c0001t0002g0223a0001c0001t0003g0266others(46): Show | 49 | HG00735.hp2 HG01071.hp1 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.*819+1447delT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221423761 | ||||||
| chr2:221423761
|
GAA | G | 6 | a0001c0001t0006g0028a0001c0001t0006g0228a0001c0001t0006g0238others(3): Show | 6 | HG02129.hp2 HG03098.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.*819+1446_*819+144 others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221423761 | ||||||
| chr2:221423762
|
A | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0164 | 2 | HG01975.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.*819+1447T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221423762 | ||||||
| chr2:221423775
|
A | C | 8 | a0001c0001t0001g0092a0001c0001t0001g0192a0001c0001t0001g0200others(5): Show | 8 | HG00741.hp1 HG01074.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.*819+1434T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221423775 | ||||||
| chr2:221423850
|
C | T | 26 | a0001c0001t0004g0203a0001c0001t0004g0235a0001c0001t0004g0291others(23): Show | 26 | HG01074.hp1 HG01884.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.*819+1359G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221423850 | ||||||
| chr2:221424050
|
G | A | 1 | a0001c0001t0037g0100 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.*819+1159C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221424050 | ||||||
| chr2:221424057
|
T | C | 3 | a0001c0001t0011g0138a0001c0001t0011g0240a0001c0001t0011g0241 | 3 | HG02145.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.*819+1152A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221424057 | ||||||
| chr2:221424071
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.*819+1138T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221424071 | ||||||
| chr2:221424140
|
A | AT | 15 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(12): Show | 15 | HG01981.hp1 HG02004.hp1 HG02004.hp2 others(12): Show |
intron_variant | MODIFIER | c.*819+1068dupA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221424140 | ||||||
| chr2:221424140
|
A | T | 1 | a0001c0001t0037g0100 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.*819+1069T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221424140 | ||||||
| chr2:221424140
|
AT | A | 73 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0010others(70): Show | 73 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.*819+1068delA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221424140 | ||||||
| chr2:221424141
|
T | TAA | 36 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0279others(33): Show | 36 | HG00735.hp2 HG01071.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.*819+1067_*819+106 others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221424141 | ||||||
| chr2:221424142
|
T | A | 1 | a0001c0001t0006g0004 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.*819+1067A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221424142 | ||||||
| chr2:221424202
|
C | T | 36 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0279others(33): Show | 36 | HG00735.hp2 HG01071.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.*819+1007G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221424202 | ||||||
| chr2:221424266
|
T | C | 5 | a0001c0001t0008g0117a0001c0001t0008g0132a0001c0001t0008g0134others(2): Show | 5 | HG01884.hp1 HG01975.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.*819+943A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221424266 | ||||||
| chr2:221424267
|
T | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0168 | 2 | NA18959.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.*819+942A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221424267 | ||||||
| chr2:221424476
|
C | CA | 70 | a0001c0001t0002g0005a0001c0001t0002g0008a0001c0001t0002g0010others(67): Show | 70 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.*819+732dupT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221424476 | ||||||
| chr2:221424476
|
CA | C | 7 | a0001c0001t0001g0042a0001c0001t0004g0203a0001c0001t0004g0235others(4): Show | 7 | HG01074.hp1 HG02145.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.*819+732delT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221424476 | ||||||
| chr2:221424476
|
CAA | C | 35 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0279others(32): Show | 35 | HG00735.hp2 HG01071.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.*819+731_*819+732d others(4): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221424476 | ||||||
| chr2:221424633
|
T | A | 1 | a0001c0001t0001g0183 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.*819+576A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221424633 | ||||||
| chr2:221424778
|
T | C | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.*819+431A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221424778 | ||||||
| chr2:221424888
|
G | T | 2 | a0001c0001t0018g0113a0001c0002t0028g0242 | 2 | HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.*819+321C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221424888 | ||||||
| chr2:221424919
|
G | A | 4 | a0001c0001t0010g0107a0001c0001t0010g0110a0001c0001t0010g0288others(1): Show | 4 | HG02723.hp2 HG02970.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.*819+290C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221424919 | ||||||
| chr2:221424954
|
TCTAGGAC others(198): Show |
T | 2 | a0001c0002t0022g0090a0001c0002t0022g0273 | 2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.*819+50_*819+254de others(1): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221424954 | ||||||
| chr2:221425111
|
G | C | 2 | a0001c0002t0004g0104a0001c0002t0029g0269 | 2 | HG01884.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.*819+98C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 17/17 | chr2 | 221425111 | ||||||
| chr2:221426182
|
A | G | 137 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0026others(134): Show | 137 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.2847-40T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 16/17 | chr2 | 221426182 | ||||||
| chr2:221426218
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2847-76T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 16/17 | chr2 | 221426218 | ||||||
| chr2:221426224
|
G | A | 1 | a0001c0001t0001g0017 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2847-82C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 16/17 | chr2 | 221426224 | ||||||
| chr2:221426243
|
A | C | 5 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0196others(2): Show | 5 | HG00639.hp2 HG00733.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.2847-101T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 16/17 | chr2 | 221426243 | ||||||
| chr2:221426381
|
G | A | 1 | a0001c0001t0004g0194 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2846+83C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 16/17 | chr2 | 221426381 | ||||||
| chr2:221426938
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2691-319G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 15/17 | chr2 | 221426938 | ||||||
| chr2:221427085
|
G | C | 1 | a0001c0001t0010g0288 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2691-466C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 15/17 | chr2 | 221427085 | ||||||
| chr2:221427426
|
C | T | 3 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0221 | 3 | HG01361.hp1 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2691-807G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 15/17 | chr2 | 221427426 | ||||||
| chr2:221427525
|
C | T | 54 | a0001c0001t0001g0225a0001c0001t0001g0287a0001c0001t0003g0279others(51): Show | 54 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.2691-906G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 15/17 | chr2 | 221427525 | ||||||
| chr2:221427540
|
T | G | 54 | a0001c0001t0001g0225a0001c0001t0001g0287a0001c0001t0003g0279others(51): Show | 54 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.2691-921A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 15/17 | chr2 | 221427540 | ||||||
| chr2:221427598
|
T | C | 4 | a0001c0001t0049g0227a0001c0002t0022g0090a0001c0002t0022g0273others(1): Show | 4 | HG01884.hp2 HG03195.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2691-979A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 15/17 | chr2 | 221427598 | ||||||
| chr2:221427675
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2691-1056C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 15/17 | chr2 | 221427675 | ||||||
| chr2:221427724
|
T | C | 1 | a0001c0001t0002g0123 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2691-1105A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 15/17 | chr2 | 221427724 | ||||||
| chr2:221427852
|
C | T | 2 | a0001c0002t0022g0090a0001c0002t0022g0273 | 2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2691-1233G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 15/17 | chr2 | 221427852 | ||||||
| chr2:221427949
|
G | T | 237 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(234): Show | 237 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(234): Show |
intron_variant | MODIFIER | c.2691-1330C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 15/17 | chr2 | 221427949 | ||||||
| chr2:221428104
|
A | G | 5 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0221others(2): Show | 5 | HG01361.hp1 HG02976.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.2691-1485T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 15/17 | chr2 | 221428104 | ||||||
| chr2:221428237
|
A | G | 41 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(38): Show | 41 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.2691-1618T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 15/17 | chr2 | 221428237 | ||||||
| chr2:221428471
|
T | C | 5 | a0001c0001t0006g0228a0001c0001t0010g0107a0001c0001t0010g0110others(2): Show | 5 | HG02723.hp2 HG02970.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2690+1487A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 15/17 | chr2 | 221428471 | ||||||
| chr2:221428646
|
C | G | 26 | a0001c0001t0003g0279a0001c0001t0004g0235a0001c0003t0001g0030others(23): Show | 26 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.2690+1312G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 15/17 | chr2 | 221428646 | ||||||
| chr2:221428697
|
C | T | 1 | a0001c0002t0029g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2690+1261G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 15/17 | chr2 | 221428697 | ||||||
| chr2:221429044
|
C | A | 1 | a0001c0001t0049g0227 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2690+914G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 15/17 | chr2 | 221429044 | ||||||
| chr2:221429067
|
G | A | 2 | a0001c0001t0002g0010a0001c0001t0002g0011 | 2 | NA18972.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.2690+891C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 15/17 | chr2 | 221429067 | ||||||
| chr2:221429208
|
G | A | 1 | a0001c0002t0001g0019 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2690+750C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 15/17 | chr2 | 221429208 | ||||||
| chr2:221429283
|
A | G | 3 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0221 | 3 | HG01361.hp1 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2690+675T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 15/17 | chr2 | 221429283 | ||||||
| chr2:221429548
|
G | A | 237 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(234): Show | 237 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(234): Show |
intron_variant | MODIFIER | c.2690+410C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 15/17 | chr2 | 221429548 | ||||||
| chr2:221429858
|
G | A | 1 | a0001c0001t0044g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2690+100C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 15/17 | chr2 | 221429858 | ||||||
| chr2:221430408
|
C | A | 4 | a0001c0001t0011g0138a0001c0001t0011g0240a0001c0001t0011g0241others(1): Show | 4 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2497-257G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221430408 | ||||||
| chr2:221430491
|
C | T | 3 | a0001c0001t0033g0170a0001c0001t0040g0128a0001c0004t0035g0108 | 3 | HG02055.hp1 HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2497-340G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221430491 | ||||||
| chr2:221430675
|
C | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0150 | 2 | HG00544.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.2497-524G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221430675 | ||||||
| chr2:221430794
|
T | A | 180 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(177): Show | 180 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.2497-643A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221430794 | ||||||
| chr2:221430861
|
G | A | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2497-710C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221430861 | ||||||
| chr2:221431040
|
C | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(132): Show | 135 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.2497-889G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221431040 | ||||||
| chr2:221431432
|
C | T | 6 | a0001c0001t0006g0228a0001c0001t0010g0107a0001c0001t0010g0110others(3): Show | 6 | HG02723.hp2 HG02970.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.2497-1281G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221431432 | ||||||
| chr2:221431472
|
T | C | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2497-1321A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221431472 | ||||||
| chr2:221431542
|
A | G | 1 | a0001c0001t0004g0057 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2497-1391T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221431542 | ||||||
| chr2:221431578
|
T | C | 3 | a0001c0001t0002g0075a0001c0001t0002g0175a0001c0001t0002g0210 | 3 | NA18956.hp1 NA18998.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.2497-1427A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221431578 | ||||||
| chr2:221431600
|
C | T | 123 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(120): Show | 123 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.2497-1449G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221431600 | ||||||
| chr2:221431644
|
C | T | 1 | a0001c0001t0002g0073 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2497-1493G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221431644 | ||||||
| chr2:221431678
|
A | T | 41 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(38): Show | 41 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.2497-1527T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221431678 | ||||||
| chr2:221431680
|
T | C | 1 | a0001c0001t0001g0283 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2497-1529A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221431680 | ||||||
| chr2:221431855
|
C | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(132): Show | 135 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.2497-1704G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221431855 | ||||||
| chr2:221431933
|
C | A | 8 | a0001c0001t0001g0287a0001c0001t0004g0291a0001c0001t0013g0290others(5): Show | 8 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2497-1782G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221431933 | ||||||
| chr2:221431978
|
A | G | 58 | a0001c0001t0001g0112a0001c0001t0001g0190a0001c0001t0001g0225others(55): Show | 58 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.2497-1827T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221431978 | ||||||
| chr2:221432034
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2497-1883A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221432034 | ||||||
| chr2:221432127
|
G | T | 3 | a0001c0001t0001g0112a0001c0001t0001g0190a0001c0001t0036g0115 | 3 | HG00642.hp2 HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2497-1976C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221432127 | ||||||
| chr2:221432127
|
GT | G | 12 | a0001c0001t0001g0287a0001c0001t0004g0203a0001c0001t0004g0291others(9): Show | 12 | HG01074.hp1 HG01891.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2497-1977delA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221432127 | ||||||
| chr2:221432133
|
T | A | 3 | a0001c0001t0001g0112a0001c0001t0001g0190a0001c0001t0036g0115 | 3 | HG00642.hp2 HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2497-1982A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221432133 | ||||||
| chr2:221432133
|
T | TA | 42 | a0001c0001t0001g0225a0001c0001t0003g0279a0001c0001t0004g0235others(39): Show | 42 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.2497-1983_2497-198 others(5): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221432133 | ||||||
| chr2:221432139
|
A | G | 1 | a0001c0001t0033g0170 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2497-1988T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221432139 | ||||||
| chr2:221432141
|
A | G | 45 | a0001c0001t0001g0112a0001c0001t0001g0190a0001c0001t0001g0225others(42): Show | 45 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.2497-1990T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221432141 | ||||||
| chr2:221432147
|
G | A | 43 | a0001c0001t0001g0112a0001c0001t0001g0190a0001c0001t0001g0225others(40): Show | 43 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.2496+1995C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221432147 | ||||||
| chr2:221432166
|
A | G | 2 | a0001c0001t0017g0098a0001c0001t0017g0103 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2496+1976T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221432166 | ||||||
| chr2:221432293
|
C | G | 1 | a0001c0001t0001g0182 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2496+1849G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221432293 | ||||||
| chr2:221432303
|
C | T | 12 | a0001c0001t0001g0287a0001c0001t0004g0203a0001c0001t0004g0291others(9): Show | 12 | HG01074.hp1 HG01891.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2496+1839G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221432303 | ||||||
| chr2:221432304
|
A | G | 57 | a0001c0001t0001g0112a0001c0001t0001g0190a0001c0001t0001g0225others(54): Show | 57 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.2496+1838T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221432304 | ||||||
| chr2:221432387
|
C | T | 31 | a0001c0001t0001g0112a0001c0001t0001g0190a0001c0001t0003g0279others(28): Show | 31 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.2496+1755G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221432387 | ||||||
| chr2:221432550
|
G | A | 57 | a0001c0001t0001g0112a0001c0001t0001g0190a0001c0001t0001g0225others(54): Show | 57 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.2496+1592C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221432550 | ||||||
| chr2:221432646
|
A | AC | 11 | a0001c0001t0001g0121a0001c0001t0001g0193a0001c0003t0003g0082others(8): Show | 11 | HG00741.hp2 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2496+1495_2496+149 others(5): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221432646 | ||||||
| chr2:221432646
|
A | AT | 48 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0036others(45): Show | 48 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.2496+1495dupA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221432646 | ||||||
| chr2:221432647
|
T | C | 22 | a0001c0001t0001g0112a0001c0001t0001g0190a0001c0001t0003g0279others(19): Show | 22 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.2496+1495A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221432647 | ||||||
| chr2:221432654
|
T | A | 5 | a0001c0001t0006g0228a0001c0001t0010g0107a0001c0001t0010g0110others(2): Show | 5 | HG02723.hp2 HG02970.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2496+1488A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221432654 | ||||||
| chr2:221432789
|
G | C | 57 | a0001c0001t0001g0112a0001c0001t0001g0190a0001c0001t0001g0225others(54): Show | 57 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.2496+1353C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221432789 | ||||||
| chr2:221432794
|
C | T | 2 | a0001c0001t0017g0098a0001c0001t0017g0103 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2496+1348G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221432794 | ||||||
| chr2:221432818
|
A | AT | 65 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0022others(62): Show | 65 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.2496+1323dupA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221432818 | ||||||
| chr2:221432818
|
A | ATT | 6 | a0001c0001t0001g0192a0001c0001t0004g0003a0001c0001t0005g0145others(3): Show | 6 | HG02080.hp1 HG02615.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.2496+1322_2496+132 others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221432818 | ||||||
| chr2:221432818
|
AT | A | 9 | a0001c0001t0001g0050a0001c0001t0001g0249a0001c0001t0002g0035others(6): Show | 9 | HG01243.hp2 HG02273.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.2496+1323delA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221432818 | ||||||
| chr2:221432818
|
ATTT | A | 14 | a0001c0001t0001g0287a0001c0001t0003g0279a0001c0001t0004g0203others(11): Show | 14 | HG01074.hp1 HG01891.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.2496+1321_2496+132 others(7): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221432818 | ||||||
| chr2:221432818
|
ATTTT | A | 36 | a0001c0001t0001g0225a0001c0001t0006g0246a0001c0001t0011g0138others(33): Show | 36 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.2496+1320_2496+132 others(8): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221432818 | ||||||
| chr2:221432818
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0008t0003g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2496+1312_2496+132 others(16): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221432818 | ||||||
| chr2:221432845
|
G | A | 1 | a0001c0001t0037g0100 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2496+1297C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221432845 | ||||||
| chr2:221432885
|
C | G | 12 | a0001c0001t0001g0287a0001c0001t0004g0203a0001c0001t0004g0291others(9): Show | 12 | HG01074.hp1 HG01891.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2496+1257G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221432885 | ||||||
| chr2:221432915
|
C | G | 57 | a0001c0001t0001g0112a0001c0001t0001g0190a0001c0001t0001g0225others(54): Show | 57 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.2496+1227G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221432915 | ||||||
| chr2:221432978
|
C | T | 3 | a0001c0001t0033g0170a0001c0001t0040g0128a0001c0004t0035g0108 | 3 | HG02055.hp1 HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2496+1164G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221432978 | ||||||
| chr2:221433011
|
A | C | 3 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0221 | 3 | HG01361.hp1 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2496+1131T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221433011 | ||||||
| chr2:221433071
|
G | A | 57 | a0001c0001t0001g0112a0001c0001t0001g0190a0001c0001t0001g0225others(54): Show | 57 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.2496+1071C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221433071 | ||||||
| chr2:221433119
|
C | T | 4 | a0001c0001t0001g0120a0001c0001t0001g0205a0001c0001t0001g0211others(1): Show | 4 | HG01243.hp1 HG01261.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.2496+1023G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221433119 | ||||||
| chr2:221433426
|
C | T | 1 | a0001c0001t0005g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2496+716G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221433426 | ||||||
| chr2:221433441
|
C | T | 1 | a0001c0001t0049g0227 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2496+701G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221433441 | ||||||
| chr2:221433615
|
C | T | 111 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0017others(108): Show | 111 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.2496+527G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221433615 | ||||||
| chr2:221433706
|
G | A | 2 | a0001c0003t0001g0087a0001c0003t0001g0276 | 2 | HG00733.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.2496+436C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221433706 | ||||||
| chr2:221433781
|
T | C | 111 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0017others(108): Show | 111 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.2496+361A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221433781 | ||||||
| chr2:221433816
|
G | A | 10 | a0001c0001t0001g0225a0001c0001t0006g0246a0001c0001t0011g0138others(7): Show | 10 | HG02055.hp2 HG02145.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.2496+326C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221433816 | ||||||
| chr2:221433924
|
A | G | 4 | a0001c0001t0001g0112a0001c0001t0001g0190a0001c0001t0004g0235others(1): Show | 4 | HG00642.hp2 HG02145.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2496+218T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221433924 | ||||||
| chr2:221434061
|
C | T | 3 | a0001c0001t0003g0289a0001c0001t0008g0117a0001c0001t0008g0132 | 3 | HG01109.hp2 HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.2496+81G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221434061 | ||||||
| chr2:221434062
|
G | A | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2496+80C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 14/17 | chr2 | 221434062 | ||||||
| chr2:221434420
|
C | T | 3 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0002t0001g0163 | 3 | NA18968.hp1 NA18991.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.2347-129G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 13/17 | chr2 | 221434420 | ||||||
| chr2:221434450
|
G | C | 3 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0221 | 3 | HG01361.hp1 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2347-159C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 13/17 | chr2 | 221434450 | ||||||
| chr2:221434494
|
CTAAG | C | 12 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0221others(9): Show | 12 | HG01361.hp1 HG01884.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2347-207_2347-204d others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 13/17 | chr2 | 221434494 | ||||||
| chr2:221434526
|
C | T | 1 | a0001c0001t0036g0115 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2347-235G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 13/17 | chr2 | 221434526 | ||||||
| chr2:221434899
|
TA | T | 243 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(240): Show | 243 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(240): Show |
intron_variant | MODIFIER | c.2347-609delT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 13/17 | chr2 | 221434899 | ||||||
| chr2:221435069
|
G | A | 3 | a0001c0001t0004g0203a0001c0001t0008g0134a0001c0001t0008g0135 | 3 | HG01074.hp1 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2347-778C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 13/17 | chr2 | 221435069 | ||||||
| chr2:221435086
|
G | C | 127 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(124): Show | 127 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.2347-795C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 13/17 | chr2 | 221435086 | ||||||
| chr2:221435162
|
T | C | 220 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(217): Show | 220 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.2347-871A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 13/17 | chr2 | 221435162 | ||||||
| chr2:221435207
|
G | A | 228 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(225): Show | 228 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.2347-916C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 13/17 | chr2 | 221435207 | ||||||
| chr2:221435236
|
G | A | 223 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(220): Show | 223 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.2347-945C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 13/17 | chr2 | 221435236 | ||||||
| chr2:221435248
|
T | C | 3 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0221 | 3 | HG01361.hp1 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2347-957A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 13/17 | chr2 | 221435248 | ||||||
| chr2:221435257
|
C | A | 1 | a0001c0001t0002g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2347-966G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 13/17 | chr2 | 221435257 | ||||||
| chr2:221435279
|
T | C | 235 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(232): Show | 235 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(232): Show |
intron_variant | MODIFIER | c.2347-988A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 13/17 | chr2 | 221435279 | ||||||
| chr2:221435337
|
C | T | 192 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(189): Show | 192 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.2347-1046G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 13/17 | chr2 | 221435337 | ||||||
| chr2:221435396
|
C | T | 82 | a0001c0001t0001g0063a0001c0001t0001g0141a0001c0001t0001g0154others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.2346+1003G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 13/17 | chr2 | 221435396 | ||||||
| chr2:221435413
|
CAA | C | 123 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(120): Show | 123 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.2346+984_2346+985d others(4): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 13/17 | chr2 | 221435413 | ||||||
| chr2:221435541
|
G | C | 1 | a0001c0001t0004g0285 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2346+858C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 13/17 | chr2 | 221435541 | ||||||
| chr2:221435558
|
G | A | 1 | a0001c0001t0040g0128 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2346+841C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 13/17 | chr2 | 221435558 | ||||||
| chr2:221435566
|
G | C | 2 | a0001c0001t0045g0096a0001c0012t0018g0272 | 2 | HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2346+833C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 13/17 | chr2 | 221435566 | ||||||
| chr2:221435683
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2346+716C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 13/17 | chr2 | 221435683 | ||||||
| chr2:221435714
|
CT | C | 3 | a0001c0001t0044g0232a0001c0001t0045g0096a0001c0012t0018g0272 | 3 | HG02280.hp2 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2346+684delA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 13/17 | chr2 | 221435714 | ||||||
| chr2:221435809
|
T | C | 34 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0022others(31): Show | 34 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.2346+590A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 13/17 | chr2 | 221435809 | ||||||
| chr2:221435937
|
C | CA | 184 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(181): Show | 184 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.2346+461dupT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 13/17 | chr2 | 221435937 | ||||||
| chr2:221436373
|
G | C | 2 | a0001c0001t0001g0164a0001c0001t0002g0271 | 2 | HG01975.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.2346+26C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 13/17 | chr2 | 221436373 | ||||||
| chr2:221436386
|
C | G | 1 | a0001c0003t0003g0161 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2346+13G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 13/17 | chr2 | 221436386 | ||||||
| chr2:221436637
|
T | C | 161 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(158): Show | 161 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.2137-29A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 12/17 | chr2 | 221436637 | ||||||
| chr2:221436729
|
T | C | 3 | a0001c0001t0009g0212a0001c0001t0017g0098a0001c0001t0017g0103 | 3 | HG02615.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2137-121A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 12/17 | chr2 | 221436729 | ||||||
| chr2:221436756
|
G | A | 3 | a0001c0001t0009g0212a0001c0001t0017g0098a0001c0001t0017g0103 | 3 | HG02615.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2137-148C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 12/17 | chr2 | 221436756 | ||||||
| chr2:221436824
|
C | G | 1 | a0001c0004t0035g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2137-216G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 12/17 | chr2 | 221436824 | ||||||
| chr2:221436834
|
T | A | 3 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0221 | 3 | HG01361.hp1 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2137-226A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 12/17 | chr2 | 221436834 | ||||||
| chr2:221436993
|
C | T | 53 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(50): Show | 53 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.2136+68G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 12/17 | chr2 | 221436993 | ||||||
| chr2:221437162
|
C | T | 1 | a0001c0006t0003g0118 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2075-40G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221437162 | ||||||
| chr2:221437192
|
C | T | 53 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(50): Show | 53 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.2075-70G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221437192 | ||||||
| chr2:221437280
|
G | A | 50 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(47): Show | 50 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.2075-158C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221437280 | ||||||
| chr2:221437300
|
G | A | 2 | a0001c0001t0001g0255a0001c0001t0038g0102 | 2 | HG02559.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.2075-178C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221437300 | ||||||
| chr2:221437316
|
C | T | 1 | a0001c0007t0005g0061 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2075-194G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221437316 | ||||||
| chr2:221437331
|
A | C | 53 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(50): Show | 53 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.2075-209T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221437331 | ||||||
| chr2:221437548
|
T | C | 1 | a0001c0001t0045g0096 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2075-426A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221437548 | ||||||
| chr2:221437612
|
C | T | 53 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(50): Show | 53 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.2075-490G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221437612 | ||||||
| chr2:221437669
|
T | C | 53 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(50): Show | 53 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.2075-547A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221437669 | ||||||
| chr2:221437670
|
G | A | 5 | a0001c0001t0006g0228a0001c0001t0010g0107a0001c0001t0010g0110others(2): Show | 5 | HG02723.hp2 HG02970.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2075-548C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221437670 | ||||||
| chr2:221437685
|
T | G | 53 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(50): Show | 53 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.2075-563A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221437685 | ||||||
| chr2:221437691
|
T | C | 53 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(50): Show | 53 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.2075-569A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221437691 | ||||||
| chr2:221437715
|
A | C | 53 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(50): Show | 53 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.2075-593T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221437715 | ||||||
| chr2:221437740
|
C | T | 33 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0022others(30): Show | 33 | HG00408.hp2 HG00673.hp2 HG01978.hp1 others(30): Show |
intron_variant | MODIFIER | c.2075-618G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221437740 | ||||||
| chr2:221437757
|
C | CA | 6 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0208others(3): Show | 6 | HG02055.hp2 NA18939.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2075-636dupT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221437757 | ||||||
| chr2:221437757
|
C | CAAAAA | 38 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(35): Show | 38 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.2075-640_2075-636d others(7): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221437757 | ||||||
| chr2:221437757
|
C | CAAAAAA | 12 | a0001c0001t0001g0062a0001c0001t0001g0080a0001c0001t0001g0184others(9): Show | 12 | HG01081.hp1 HG01257.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.2075-641_2075-636d others(8): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221437757 | ||||||
| chr2:221437757
|
CA | C | 26 | a0001c0002t0001g0019a0001c0002t0001g0020a0001c0002t0001g0039others(23): Show | 26 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.2075-636delT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221437757 | ||||||
| chr2:221437784
|
A | G | 62 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(59): Show | 62 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.2075-662T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221437784 | ||||||
| chr2:221437785
|
T | C | 62 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(59): Show | 62 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.2075-663A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221437785 | ||||||
| chr2:221437796
|
G | T | 1 | a0001c0003t0003g0161 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2075-674C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221437796 | ||||||
| chr2:221437862
|
G | A | 6 | a0001c0001t0001g0245a0001c0001t0002g0095a0001c0001t0002g0097others(3): Show | 6 | HG02615.hp2 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2075-740C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221437862 | ||||||
| chr2:221437872
|
G | A | 1 | a0001c0001t0049g0227 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2075-750C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221437872 | ||||||
| chr2:221437897
|
TGGG | T | 267 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 267 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.2075-778_2075-776d others(5): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221437897 | ||||||
| chr2:221437922
|
G | C | 62 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(59): Show | 62 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.2075-800C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221437922 | ||||||
| chr2:221437927
|
A | G | 3 | a0001c0001t0001g0200a0001c0001t0001g0202a0001c0001t0004g0285 | 3 | HG01074.hp2 HG01433.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.2075-805T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221437927 | ||||||
| chr2:221437941
|
A | C | 3 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0221 | 3 | HG01361.hp1 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2075-819T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221437941 | ||||||
| chr2:221437944
|
AC | A | 62 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(59): Show | 62 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.2075-823delG | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221437944 | ||||||
| chr2:221438010
|
C | A | 105 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(102): Show | 105 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.2075-888G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221438010 | ||||||
| chr2:221438080
|
C | A | 94 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(91): Show | 94 | HG00280.hp1 HG00423.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.2075-958G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221438080 | ||||||
| chr2:221438181
|
A | AT | 32 | a0001c0002t0001g0019a0001c0002t0001g0020a0001c0002t0001g0039others(29): Show | 32 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.2075-1060dupA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221438181 | ||||||
| chr2:221438191
|
T | C | 2 | a0001c0001t0017g0098a0001c0001t0017g0103 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2075-1069A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221438191 | ||||||
| chr2:221438405
|
C | T | 52 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(49): Show | 52 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.2075-1283G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221438405 | ||||||
| chr2:221438478
|
A | T | 3 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0221 | 3 | HG01361.hp1 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2075-1356T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221438478 | ||||||
| chr2:221438647
|
G | A | 1 | a0001c0004t0035g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2075-1525C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221438647 | ||||||
| chr2:221438678
|
G | T | 5 | a0001c0001t0006g0228a0001c0001t0010g0107a0001c0001t0010g0110others(2): Show | 5 | HG02723.hp2 HG02970.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2075-1556C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221438678 | ||||||
| chr2:221438692
|
A | G | 61 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(58): Show | 61 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.2075-1570T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221438692 | ||||||
| chr2:221438693
|
G | A | 1 | a0001c0002t0028g0242 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2075-1571C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221438693 | ||||||
| chr2:221438726
|
A | G | 1 | a0001c0001t0001g0255 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2075-1604T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221438726 | ||||||
| chr2:221438783
|
T | TA | 61 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(58): Show | 61 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.2075-1662dupT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221438783 | ||||||
| chr2:221438797
|
TA | T | 142 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0022others(139): Show | 142 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.2075-1676delT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221438797 | ||||||
| chr2:221438842
|
A | G | 1 | a0001c0001t0001g0245 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2075-1720T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221438842 | ||||||
| chr2:221438889
|
C | T | 2 | a0001c0002t0004g0234a0001c0002t0029g0269 | 2 | HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2075-1767G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221438889 | ||||||
| chr2:221438961
|
C | G | 61 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(58): Show | 61 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.2075-1839G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221438961 | ||||||
| chr2:221439028
|
A | G | 3 | a0001c0001t0009g0212a0001c0001t0017g0098a0001c0001t0017g0103 | 3 | HG02615.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2075-1906T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221439028 | ||||||
| chr2:221439228
|
C | T | 61 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(58): Show | 61 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.2075-2106G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221439228 | ||||||
| chr2:221439309
|
A | G | 61 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(58): Show | 61 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.2075-2187T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221439309 | ||||||
| chr2:221439316
|
C | T | 1 | a0001c0001t0002g0271 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2075-2194G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221439316 | ||||||
| chr2:221439330
|
C | CA | 17 | a0001c0001t0001g0016a0001c0001t0001g0120a0001c0001t0001g0144others(14): Show | 17 | HG01109.hp2 HG01243.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.2075-2209dupT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221439330 | ||||||
| chr2:221439330
|
C | CAA | 43 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(40): Show | 43 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.2075-2210_2075-220 others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221439330 | ||||||
| chr2:221439330
|
C | CAAA | 8 | a0001c0001t0001g0062a0001c0001t0001g0245a0001c0001t0002g0095others(5): Show | 8 | HG02615.hp2 HG02809.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.2075-2211_2075-220 others(7): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221439330 | ||||||
| chr2:221439330
|
CA | C | 76 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0022others(73): Show | 76 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.2075-2209delT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221439330 | ||||||
| chr2:221439353
|
G | A | 3 | a0001c0001t0002g0075a0001c0001t0002g0175a0001c0001t0002g0210 | 3 | NA18956.hp1 NA18998.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.2075-2231C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221439353 | ||||||
| chr2:221439427
|
C | T | 10 | a0001c0001t0001g0225a0001c0001t0001g0287a0001c0001t0004g0235others(7): Show | 10 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.2075-2305G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221439427 | ||||||
| chr2:221439496
|
T | C | 3 | a0001c0001t0011g0138a0001c0001t0018g0113a0001c0001t0027g0137 | 3 | HG02145.hp2 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2075-2374A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221439496 | ||||||
| chr2:221439541
|
A | G | 61 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(58): Show | 61 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.2075-2419T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221439541 | ||||||
| chr2:221439558
|
A | G | 61 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(58): Show | 61 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.2075-2436T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221439558 | ||||||
| chr2:221439714
|
A | G | 17 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0060others(14): Show | 17 | HG00408.hp2 HG01978.hp1 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.2075-2592T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221439714 | ||||||
| chr2:221439868
|
C | T | 3 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0221 | 3 | HG01361.hp1 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2075-2746G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221439868 | ||||||
| chr2:221439913
|
C | A | 49 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0041others(46): Show | 49 | HG00544.hp1 HG00733.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.2075-2791G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221439913 | ||||||
| chr2:221439947
|
C | T | 3 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0259 | 3 | HG01167.hp1 HG01169.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.2075-2825G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221439947 | ||||||
| chr2:221439952
|
C | T | 49 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(46): Show | 49 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.2075-2830G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221439952 | ||||||
| chr2:221440189
|
A | G | 6 | a0001c0001t0001g0245a0001c0001t0002g0095a0001c0001t0002g0097others(3): Show | 6 | HG02615.hp2 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2074+2640T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221440189 | ||||||
| chr2:221440241
|
T | C | 49 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(46): Show | 49 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.2074+2588A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221440241 | ||||||
| chr2:221440401
|
T | C | 5 | a0001c0001t0006g0228a0001c0001t0010g0107a0001c0001t0010g0110others(2): Show | 5 | HG02723.hp2 HG02970.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2074+2428A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221440401 | ||||||
| chr2:221440410
|
A | T | 1 | a0001c0001t0044g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2074+2419T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221440410 | ||||||
| chr2:221440425
|
T | C | 33 | a0001c0002t0001g0019a0001c0002t0001g0020a0001c0002t0001g0039others(30): Show | 33 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.2074+2404A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221440425 | ||||||
| chr2:221440434
|
G | T | 2 | a0001c0001t0044g0232a0001c0001t0049g0227 | 2 | HG02280.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2074+2395C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221440434 | ||||||
| chr2:221440440
|
T | G | 35 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0022others(32): Show | 35 | HG00408.hp2 HG00673.hp2 HG01978.hp1 others(32): Show |
intron_variant | MODIFIER | c.2074+2389A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221440440 | ||||||
| chr2:221440574
|
T | C | 61 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(58): Show | 61 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.2074+2255A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221440574 | ||||||
| chr2:221440605
|
T | A | 1 | a0001c0001t0032g0251 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2074+2224A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221440605 | ||||||
| chr2:221440608
|
C | CT | 66 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0022others(63): Show | 66 | HG00408.hp1 HG00408.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.2074+2220dupA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221440608 | ||||||
| chr2:221440608
|
CT | C | 13 | a0001c0001t0001g0164a0001c0001t0002g0089a0001c0001t0003g0289others(10): Show | 13 | HG01109.hp2 HG01884.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.2074+2220delA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221440608 | ||||||
| chr2:221440879
|
G | A | 34 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0022others(31): Show | 34 | HG00408.hp2 HG00673.hp2 HG01978.hp1 others(31): Show |
intron_variant | MODIFIER | c.2074+1950C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221440879 | ||||||
| chr2:221440908
|
C | T | 5 | a0001c0002t0028g0242a0001c0004t0019g0236a0001c0004t0019g0237others(2): Show | 5 | HG01243.hp2 HG02055.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2074+1921G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221440908 | ||||||
| chr2:221441120
|
T | C | 1 | a0001c0001t0005g0049 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2074+1709A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221441120 | ||||||
| chr2:221441153
|
A | T | 3 | a0001c0001t0011g0138a0001c0001t0018g0113a0001c0001t0027g0137 | 3 | HG02145.hp2 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2074+1676T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221441153 | ||||||
| chr2:221441197
|
C | CT | 20 | a0001c0001t0001g0225a0001c0001t0001g0287a0001c0001t0002g0010others(17): Show | 20 | HG00738.hp1 HG01433.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.2074+1631dupA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221441197 | ||||||
| chr2:221441197
|
CT | C | 61 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(58): Show | 61 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.2074+1631delA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221441197 | ||||||
| chr2:221441202
|
T | C | 3 | a0001c0002t0023g0218a0001c0002t0023g0219a0001c0002t0028g0242 | 3 | HG00673.hp1 HG03041.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.2074+1627A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221441202 | ||||||
| chr2:221441203
|
T | C | 3 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0221 | 3 | HG01361.hp1 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2074+1626A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221441203 | ||||||
| chr2:221441552
|
C | A | 34 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0022others(31): Show | 34 | HG00408.hp2 HG00673.hp2 HG01978.hp1 others(31): Show |
intron_variant | MODIFIER | c.2074+1277G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221441552 | ||||||
| chr2:221441573
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2074+1256C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221441573 | ||||||
| chr2:221441640
|
G | T | 11 | a0001c0001t0003g0289a0001c0001t0006g0246a0001c0001t0008g0117others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.2074+1189C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221441640 | ||||||
| chr2:221441697
|
G | A | 2 | a0001c0001t0001g0225a0001c0001t0012g0275 | 2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.2074+1132C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221441697 | ||||||
| chr2:221441788
|
C | T | 6 | a0001c0001t0001g0245a0001c0001t0002g0095a0001c0001t0002g0097others(3): Show | 6 | HG02615.hp2 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2074+1041G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221441788 | ||||||
| chr2:221441791
|
C | T | 2 | a0001c0001t0001g0231a0001c0001t0002g0206 | 2 | HG03834.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.2074+1038G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221441791 | ||||||
| chr2:221442328
|
C | A | 1 | a0001c0001t0001g0141 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2074+501G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221442328 | ||||||
| chr2:221442395
|
C | T | 1 | a0001c0001t0049g0227 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2074+434G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221442395 | ||||||
| chr2:221442398
|
G | A | 6 | a0001c0001t0001g0245a0001c0001t0002g0095a0001c0001t0002g0097others(3): Show | 6 | HG02615.hp2 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2074+431C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221442398 | ||||||
| chr2:221442440
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2074+389T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221442440 | ||||||
| chr2:221442481
|
GC | G | 34 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0022others(31): Show | 34 | HG00408.hp2 HG00673.hp2 HG01978.hp1 others(31): Show |
intron_variant | MODIFIER | c.2074+347delG | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221442481 | ||||||
| chr2:221442512
|
T | G | 1 | a0001c0001t0045g0096 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2074+317A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221442512 | ||||||
| chr2:221442575
|
T | A | 61 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(58): Show | 61 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.2074+254A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221442575 | ||||||
| chr2:221442590
|
C | A | 247 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(244): Show | 247 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.2074+239G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221442590 | ||||||
| chr2:221442814
|
G | T | 61 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(58): Show | 61 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.2074+15C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 11/17 | chr2 | 221442814 | ||||||
| chr2:221443058
|
CAAGATGA | C | 46 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(43): Show | 46 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1889-51_1889-45del others(7): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 10/17 | chr2 | 221443058 | ||||||
| chr2:221443079
|
AACATT | A | 12 | a0001c0001t0003g0289a0001c0001t0006g0246a0001c0001t0008g0117others(9): Show | 12 | HG01109.hp2 HG01884.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1889-70_1889-66del others(5): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 10/17 | chr2 | 221443079 | ||||||
| chr2:221443111
|
T | C | 61 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(58): Show | 61 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.1889-97A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 10/17 | chr2 | 221443111 | ||||||
| chr2:221443114
|
T | G | 61 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(58): Show | 61 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.1889-100A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 10/17 | chr2 | 221443114 | ||||||
| chr2:221443185
|
C | T | 1 | a0001c0001t0002g0010 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1889-171G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 10/17 | chr2 | 221443185 | ||||||
| chr2:221443251
|
CAG | C | 34 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0022others(31): Show | 34 | HG00408.hp2 HG00673.hp2 HG01978.hp1 others(31): Show |
intron_variant | MODIFIER | c.1889-239_1889-238d others(4): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 10/17 | chr2 | 221443251 | ||||||
| chr2:221443290
|
T | C | 1 | a0001c0005t0014g0040 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1888+203A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 10/17 | chr2 | 221443290 | ||||||
| chr2:221443336
|
G | A | 61 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(58): Show | 61 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.1888+157C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 10/17 | chr2 | 221443336 | ||||||
| chr2:221443399
|
A | AAT | 16 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0060others(13): Show | 16 | HG00408.hp2 HG01978.hp1 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.1888+92_1888+93dup others(2): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 10/17 | chr2 | 221443399 | ||||||
| chr2:221443780
|
T | C | 9 | a0001c0001t0003g0289a0001c0001t0006g0246a0001c0001t0008g0117others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1775-174A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221443780 | ||||||
| chr2:221443940
|
C | T | 1 | a0001c0005t0001g0029 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1775-334G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221443940 | ||||||
| chr2:221443961
|
T | G | 3 | a0001c0001t0011g0138a0001c0001t0018g0113a0001c0001t0027g0137 | 3 | HG02145.hp2 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1775-355A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221443961 | ||||||
| chr2:221444106
|
T | C | 1 | a0001c0001t0049g0227 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1775-500A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221444106 | ||||||
| chr2:221444124
|
T | G | 95 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(92): Show | 95 | HG00280.hp1 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.1775-518A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221444124 | ||||||
| chr2:221444164
|
T | TC | 104 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(101): Show | 104 | HG00280.hp1 HG00423.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.1775-559dupG | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221444164 | ||||||
| chr2:221444264
|
G | C | 3 | a0001c0001t0011g0138a0001c0001t0018g0113a0001c0001t0027g0137 | 3 | HG02145.hp2 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1775-658C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221444264 | ||||||
| chr2:221444309
|
A | G | 3 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0221 | 3 | HG01361.hp1 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1775-703T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221444309 | ||||||
| chr2:221444312
|
T | C | 1 | a0001c0001t0049g0227 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1775-706A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221444312 | ||||||
| chr2:221444363
|
A | G | 1 | a0001c0003t0003g0056 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1775-757T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221444363 | ||||||
| chr2:221444387
|
C | T | 131 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0022others(128): Show | 131 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.1775-781G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221444387 | ||||||
| chr2:221444459
|
T | TGGTG | 46 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(43): Show | 46 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1775-854_1775-853i others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221444459 | ||||||
| chr2:221444460
|
C | T | 46 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(43): Show | 46 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1775-854G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221444460 | ||||||
| chr2:221444465
|
C | T | 67 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(64): Show | 67 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.1775-859G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221444465 | ||||||
| chr2:221444648
|
G | C | 104 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(101): Show | 104 | HG00280.hp1 HG00423.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.1775-1042C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221444648 | ||||||
| chr2:221444723
|
A | G | 3 | a0001c0001t0011g0138a0001c0001t0018g0113a0001c0001t0027g0137 | 3 | HG02145.hp2 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1775-1117T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221444723 | ||||||
| chr2:221444744
|
C | CT | 100 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0017others(97): Show | 100 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1775-1139dupA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221444744 | ||||||
| chr2:221444744
|
C | CTT | 25 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0033others(22): Show | 25 | HG00735.hp1 HG01106.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.1775-1140_1775-113 others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221444744 | ||||||
| chr2:221444744
|
CTT | C | 8 | a0001c0001t0001g0155a0001c0001t0001g0167a0001c0001t0001g0183others(5): Show | 8 | HG02145.hp2 HG04199.hp2 NA18972.hp2 others(5): Show |
intron_variant | MODIFIER | c.1775-1140_1775-113 others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221444744 | ||||||
| chr2:221444744
|
CTTT | C | 26 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0042others(23): Show | 26 | HG00408.hp2 HG00673.hp2 HG01978.hp1 others(23): Show |
intron_variant | MODIFIER | c.1775-1141_1775-113 others(7): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221444744 | ||||||
| chr2:221444744
|
CTTTTT | C | 15 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0221others(12): Show | 15 | HG01109.hp2 HG01361.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1775-1143_1775-113 others(9): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221444744 | ||||||
| chr2:221444744
|
CTTTTTT | C | 31 | a0001c0001t0009g0212a0001c0002t0001g0019a0001c0002t0001g0020others(28): Show | 31 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1775-1144_1775-113 others(10): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221444744 | ||||||
| chr2:221444744
|
CTTTTTTT | C | 19 | a0001c0001t0001g0193a0001c0001t0001g0225a0001c0001t0001g0245others(16): Show | 19 | HG00741.hp2 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1775-1145_1775-113 others(11): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221444744 | ||||||
| chr2:221444744
|
CTTTTTTT others(1): Show |
C | 38 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(35): Show | 38 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1775-1146_1775-113 others(12): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221444744 | ||||||
| chr2:221444744
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1775-1148_1775-113 others(14): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221444744 | ||||||
| chr2:221444772
|
T | C | 33 | a0001c0002t0001g0019a0001c0002t0001g0020a0001c0002t0001g0039others(30): Show | 33 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.1775-1166A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221444772 | ||||||
| chr2:221444834
|
T | C | 2 | a0001c0001t0001g0231a0001c0001t0002g0206 | 2 | HG03834.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1775-1228A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221444834 | ||||||
| chr2:221444900
|
G | A | 1 | a0001c0001t0001g0283 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1774+1223C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221444900 | ||||||
| chr2:221444932
|
ATT | A | 9 | a0001c0001t0003g0289a0001c0001t0006g0246a0001c0001t0008g0117others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1774+1189_1774+119 others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221444932 | ||||||
| chr2:221444977
|
C | T | 1 | a0001c0001t0005g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1774+1146G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221444977 | ||||||
| chr2:221444990
|
T | C | 56 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(53): Show | 56 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.1774+1133A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221444990 | ||||||
| chr2:221444998
|
T | C | 1 | a0001c0001t0009g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1774+1125A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221444998 | ||||||
| chr2:221445053
|
C | T | 1 | a0001c0001t0049g0227 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1774+1070G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221445053 | ||||||
| chr2:221445190
|
G | A | 2 | a0001c0001t0004g0285a0001c0001t0005g0284 | 2 | HG03704.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1774+933C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221445190 | ||||||
| chr2:221445317
|
C | T | 3 | a0001c0004t0019g0236a0001c0004t0019g0237a0001c0004t0035g0108 | 3 | HG01243.hp2 HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1774+806G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221445317 | ||||||
| chr2:221445361
|
G | A | 104 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(101): Show | 104 | HG00280.hp1 HG00423.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.1774+762C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221445361 | ||||||
| chr2:221445458
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1774+665G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221445458 | ||||||
| chr2:221445465
|
C | T | 2 | a0001c0001t0001g0164a0001c0001t0002g0271 | 2 | HG01975.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1774+658G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221445465 | ||||||
| chr2:221445521
|
C | T | 104 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(101): Show | 104 | HG00280.hp1 HG00423.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.1774+602G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221445521 | ||||||
| chr2:221445538
|
C | T | 3 | a0001c0001t0009g0212a0001c0001t0017g0098a0001c0001t0017g0103 | 3 | HG02615.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1774+585G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221445538 | ||||||
| chr2:221445539
|
A | G | 104 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(101): Show | 104 | HG00280.hp1 HG00423.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.1774+584T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221445539 | ||||||
| chr2:221445569
|
G | A | 33 | a0001c0002t0001g0019a0001c0002t0001g0020a0001c0002t0001g0039others(30): Show | 33 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.1774+554C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221445569 | ||||||
| chr2:221445589
|
G | GA | 11 | a0001c0001t0001g0225a0001c0001t0004g0235a0001c0001t0004g0291others(8): Show | 11 | HG01261.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1774+533dupT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221445589 | ||||||
| chr2:221445589
|
GA | G | 133 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(130): Show | 133 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.1774+533delT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221445589 | ||||||
| chr2:221445607
|
A | G | 2 | a0001c0001t0017g0098a0001c0001t0017g0103 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1774+516T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221445607 | ||||||
| chr2:221445738
|
C | T | 34 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0022others(31): Show | 34 | HG00408.hp2 HG00673.hp2 HG01978.hp1 others(31): Show |
intron_variant | MODIFIER | c.1774+385G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221445738 | ||||||
| chr2:221445783
|
C | G | 104 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(101): Show | 104 | HG00280.hp1 HG00423.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.1774+340G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221445783 | ||||||
| chr2:221445926
|
C | G | 9 | a0001c0001t0003g0289a0001c0001t0006g0246a0001c0001t0008g0117others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1774+197G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221445926 | ||||||
| chr2:221446004
|
G | T | 3 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0221 | 3 | HG01361.hp1 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1774+119C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221446004 | ||||||
| chr2:221446069
|
A | G | 5 | a0001c0001t0006g0228a0001c0001t0010g0107a0001c0001t0010g0110others(2): Show | 5 | HG02723.hp2 HG02970.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1774+54T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221446069 | ||||||
| chr2:221446075
|
C | T | 1 | a0001c0002t0001g0259 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1774+48G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221446075 | ||||||
| chr2:221446095
|
T | C | 1 | a0001c0001t0003g0289 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1774+28A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 9/17 | chr2 | 221446095 | ||||||
| chr2:221446236
|
A | G | 1 | a0001c0003t0001g0087 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1716-55T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221446236 | ||||||
| chr2:221446307
|
A | G | 6 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0221others(3): Show | 6 | HG01361.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1716-126T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221446307 | ||||||
| chr2:221446346
|
G | A | 34 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0022others(31): Show | 34 | HG00408.hp2 HG00673.hp2 HG01978.hp1 others(31): Show |
intron_variant | MODIFIER | c.1716-165C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221446346 | ||||||
| chr2:221446589
|
C | T | 1 | a0001c0001t0016g0058 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1716-408G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221446589 | ||||||
| chr2:221446875
|
T | C | 104 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(101): Show | 104 | HG00280.hp1 HG00423.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.1716-694A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221446875 | ||||||
| chr2:221446905
|
C | T | 1 | a0001c0002t0001g0039 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1716-724G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221446905 | ||||||
| chr2:221446922
|
G | C | 1 | a0001c0002t0001g0039 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1716-741C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221446922 | ||||||
| chr2:221447021
|
T | C | 104 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(101): Show | 104 | HG00280.hp1 HG00423.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.1716-840A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221447021 | ||||||
| chr2:221447087
|
T | G | 3 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0221 | 3 | HG01361.hp1 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1716-906A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221447087 | ||||||
| chr2:221447309
|
G | A | 3 | a0001c0001t0011g0138a0001c0001t0018g0113a0001c0001t0027g0137 | 3 | HG02145.hp2 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1716-1128C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221447309 | ||||||
| chr2:221447317
|
A | G | 1 | a0001c0001t0009g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1716-1136T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221447317 | ||||||
| chr2:221447619
|
A | T | 104 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(101): Show | 104 | HG00280.hp1 HG00423.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.1716-1438T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221447619 | ||||||
| chr2:221447682
|
T | C | 247 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(244): Show | 247 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.1716-1501A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221447682 | ||||||
| chr2:221447695
|
G | T | 1 | a0001c0002t0028g0242 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1716-1514C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221447695 | ||||||
| chr2:221447821
|
T | TTTTA | 188 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(185): Show | 188 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.1716-1644_1716-164 others(8): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221447821 | ||||||
| chr2:221447821
|
T | TTTTATTT others(9): Show |
39 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(36): Show | 39 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1716-1656_1716-164 others(20): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221447821 | ||||||
| chr2:221447821
|
T | TTTTATTT others(13): Show |
15 | a0001c0001t0001g0121a0001c0001t0001g0177a0001c0001t0001g0193others(12): Show | 15 | HG00741.hp2 HG01123.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1716-1660_1716-164 others(24): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221447821 | ||||||
| chr2:221447821
|
T | TTTTATTT others(17): Show |
2 | a0001c0001t0001g0245a0001c0001t0004g0235 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1716-1664_1716-164 others(28): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221447821 | ||||||
| chr2:221447870
|
G | A | 5 | a0001c0001t0001g0200a0001c0001t0001g0202a0001c0001t0001g0268others(2): Show | 5 | HG01071.hp1 HG01074.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.1716-1689C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221447870 | ||||||
| chr2:221447890
|
G | A | 7 | a0001c0002t0001g0052a0001c0002t0001g0054a0001c0002t0001g0055others(4): Show | 7 | HG00738.hp1 HG01433.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.1716-1709C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221447890 | ||||||
| chr2:221447938
|
C | T | 106 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(103): Show | 106 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.1716-1757G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221447938 | ||||||
| chr2:221448004
|
G | A | 3 | a0001c0001t0011g0138a0001c0001t0018g0113a0001c0001t0027g0137 | 3 | HG02145.hp2 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1716-1823C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221448004 | ||||||
| chr2:221448033
|
G | C | 106 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(103): Show | 106 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.1716-1852C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221448033 | ||||||
| chr2:221448041
|
C | T | 104 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(101): Show | 104 | HG00280.hp1 HG00423.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.1716-1860G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221448041 | ||||||
| chr2:221448099
|
C | T | 1 | a0001c0003t0003g0161 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1716-1918G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221448099 | ||||||
| chr2:221448131
|
C | T | 104 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(101): Show | 104 | HG00280.hp1 HG00423.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.1716-1950G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221448131 | ||||||
| chr2:221448164
|
C | A | 3 | a0001c0001t0011g0138a0001c0001t0018g0113a0001c0001t0027g0137 | 3 | HG02145.hp2 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1716-1983G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221448164 | ||||||
| chr2:221448250
|
G | T | 3 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0221 | 3 | HG01361.hp1 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1716-2069C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221448250 | ||||||
| chr2:221448319
|
A | C | 104 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(101): Show | 104 | HG00280.hp1 HG00423.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.1716-2138T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221448319 | ||||||
| chr2:221448437
|
A | G | 1 | a0001c0001t0045g0096 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1716-2256T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221448437 | ||||||
| chr2:221448452
|
C | G | 104 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(101): Show | 104 | HG00280.hp1 HG00423.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.1716-2271G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221448452 | ||||||
| chr2:221448462
|
T | C | 1 | a0001c0001t0001g0247 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1716-2281A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221448462 | ||||||
| chr2:221448511
|
T | C | 9 | a0001c0001t0003g0289a0001c0001t0006g0246a0001c0001t0008g0117others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1716-2330A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221448511 | ||||||
| chr2:221448639
|
C | T | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1716-2458G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221448639 | ||||||
| chr2:221448712
|
T | C | 20 | a0001c0001t0001g0026a0001c0001t0001g0092a0001c0001t0001g0106others(17): Show | 20 | HG00642.hp2 HG01074.hp1 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.1716-2531A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221448712 | ||||||
| chr2:221448725
|
A | T | 150 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(147): Show | 150 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.1716-2544T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221448725 | ||||||
| chr2:221448893
|
G | A | 2 | a0001c0001t0017g0098a0001c0001t0017g0103 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1716-2712C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221448893 | ||||||
| chr2:221449004
|
T | C | 1 | a0001c0001t0038g0102 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1716-2823A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221449004 | ||||||
| chr2:221449064
|
T | C | 1 | a0001c0001t0001g0062 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1716-2883A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221449064 | ||||||
| chr2:221449136
|
C | A | 136 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0022others(133): Show | 136 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1716-2955G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221449136 | ||||||
| chr2:221449279
|
T | C | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1716-3098A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221449279 | ||||||
| chr2:221449346
|
T | C | 1 | a0001c0005t0001g0034 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1716-3165A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221449346 | ||||||
| chr2:221449622
|
G | A | 93 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0022others(90): Show | 93 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.1716-3441C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221449622 | ||||||
| chr2:221449644
|
G | A | 3 | a0001c0001t0011g0138a0001c0001t0018g0113a0001c0001t0027g0137 | 3 | HG02145.hp2 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1716-3463C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221449644 | ||||||
| chr2:221449680
|
T | G | 2 | a0001c0004t0019g0236a0001c0004t0019g0237 | 2 | HG01243.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1716-3499A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221449680 | ||||||
| chr2:221449694
|
TAACA | T | 7 | a0001c0001t0001g0287a0001c0001t0004g0291a0001c0001t0013g0290others(4): Show | 7 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1716-3517_1716-351 others(8): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221449694 | ||||||
| chr2:221449695
|
A | G | 117 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0022others(114): Show | 117 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.1716-3514T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221449695 | ||||||
| chr2:221449699
|
A | G | 7 | a0001c0001t0001g0287a0001c0001t0004g0291a0001c0001t0013g0290others(4): Show | 7 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1716-3518T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221449699 | ||||||
| chr2:221449712
|
C | G | 163 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(160): Show | 163 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1716-3531G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221449712 | ||||||
| chr2:221449762
|
A | G | 210 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(207): Show | 210 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.1716-3581T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221449762 | ||||||
| chr2:221449940
|
C | A | 10 | a0001c0001t0001g0225a0001c0001t0001g0287a0001c0001t0004g0235others(7): Show | 10 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1716-3759G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221449940 | ||||||
| chr2:221449996
|
T | C | 36 | a0001c0001t0011g0138a0001c0001t0018g0113a0001c0001t0027g0137others(33): Show | 36 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.1716-3815A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221449996 | ||||||
| chr2:221450021
|
T | C | 33 | a0001c0002t0001g0019a0001c0002t0001g0020a0001c0002t0001g0039others(30): Show | 33 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.1716-3840A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221450021 | ||||||
| chr2:221450086
|
A | G | 53 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0022others(50): Show | 53 | HG00408.hp2 HG00673.hp2 HG01361.hp1 others(50): Show |
intron_variant | MODIFIER | c.1716-3905T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221450086 | ||||||
| chr2:221450457
|
C | G | 12 | a0001c0001t0001g0062a0001c0001t0001g0065a0001c0001t0001g0070others(9): Show | 12 | HG00423.hp2 HG02015.hp1 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.1716-4276G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221450457 | ||||||
| chr2:221450588
|
A | G | 37 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0022others(34): Show | 37 | HG00408.hp2 HG00673.hp2 HG01978.hp1 others(34): Show |
intron_variant | MODIFIER | c.1716-4407T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221450588 | ||||||
| chr2:221450625
|
C | T | 10 | a0001c0001t0001g0225a0001c0001t0001g0287a0001c0001t0004g0235others(7): Show | 10 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1716-4444G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221450625 | ||||||
| chr2:221450785
|
A | T | 2 | a0001c0001t0001g0106a0001c0006t0003g0118 | 2 | HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1716-4604T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221450785 | ||||||
| chr2:221450935
|
C | G | 1 | a0001c0002t0023g0219 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1715+4612G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221450935 | ||||||
| chr2:221450935
|
C | T | 1 | a0001c0001t0009g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1715+4612G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221450935 | ||||||
| chr2:221451238
|
C | T | 24 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0152others(21): Show | 24 | HG00544.hp1 HG01071.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.1715+4309G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221451238 | ||||||
| chr2:221451360
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1715+4187T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221451360 | ||||||
| chr2:221451441
|
T | C | 246 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 246 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.1715+4106A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221451441 | ||||||
| chr2:221451470
|
A | T | 1 | a0001c0002t0047g0229 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1715+4077T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221451470 | ||||||
| chr2:221451504
|
A | T | 33 | a0001c0002t0001g0019a0001c0002t0001g0020a0001c0002t0001g0039others(30): Show | 33 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.1715+4043T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221451504 | ||||||
| chr2:221451583
|
C | T | 1 | a0001c0001t0049g0227 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1715+3964G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221451583 | ||||||
| chr2:221451588
|
T | C | 56 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0022others(53): Show | 56 | HG00408.hp2 HG00673.hp2 HG01361.hp1 others(53): Show |
intron_variant | MODIFIER | c.1715+3959A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221451588 | ||||||
| chr2:221451617
|
C | G | 6 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0221others(3): Show | 6 | HG01361.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1715+3930G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221451617 | ||||||
| chr2:221451772
|
A | T | 176 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(173): Show | 176 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.1715+3775T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221451772 | ||||||
| chr2:221451855
|
T | G | 176 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(173): Show | 176 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.1715+3692A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221451855 | ||||||
| chr2:221452237
|
T | C | 267 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 267 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.1715+3310A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221452237 | ||||||
| chr2:221452369
|
T | C | 1 | a0001c0001t0001g0283 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1715+3178A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221452369 | ||||||
| chr2:221452383
|
T | C | 7 | a0001c0001t0003g0289a0001c0001t0008g0117a0001c0001t0008g0132others(4): Show | 7 | HG01109.hp2 HG01884.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1715+3164A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221452383 | ||||||
| chr2:221452395
|
C | T | 33 | a0001c0002t0001g0019a0001c0002t0001g0020a0001c0002t0001g0039others(30): Show | 33 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.1715+3152G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221452395 | ||||||
| chr2:221452560
|
A | G | 4 | a0001c0001t0001g0106a0001c0001t0011g0240a0001c0001t0011g0241others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1715+2987T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221452560 | ||||||
| chr2:221452597
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1715+2950C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221452597 | ||||||
| chr2:221452653
|
A | C | 33 | a0001c0002t0001g0019a0001c0002t0001g0020a0001c0002t0001g0039others(30): Show | 33 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.1715+2894T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221452653 | ||||||
| chr2:221452711
|
A | AT | 207 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(204): Show | 207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1715+2835dupA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221452711 | ||||||
| chr2:221452771
|
A | G | 36 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0221others(33): Show | 36 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.1715+2776T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221452771 | ||||||
| chr2:221452825
|
C | T | 31 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(28): Show | 31 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.1715+2722G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221452825 | ||||||
| chr2:221452904
|
C | A | 1 | a0001c0001t0032g0251 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1715+2643G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221452904 | ||||||
| chr2:221452908
|
G | T | 1 | a0001c0010t0001g0176 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1715+2639C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221452908 | ||||||
| chr2:221453089
|
A | C | 33 | a0001c0002t0001g0019a0001c0002t0001g0020a0001c0002t0001g0039others(30): Show | 33 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.1715+2458T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221453089 | ||||||
| chr2:221453432
|
C | T | 33 | a0001c0002t0001g0019a0001c0002t0001g0020a0001c0002t0001g0039others(30): Show | 33 | HG00558.hp2 HG00673.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.1715+2115G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221453432 | ||||||
| chr2:221453452
|
T | G | 1 | a0001c0002t0028g0242 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1715+2095A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221453452 | ||||||
| chr2:221453456
|
T | C | 3 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0221 | 3 | HG01361.hp1 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1715+2091A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221453456 | ||||||
| chr2:221453491
|
G | C | 1 | a0001c0001t0004g0203 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1715+2056C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221453491 | ||||||
| chr2:221453643
|
G | C | 3 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0221 | 3 | HG01361.hp1 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1715+1904C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221453643 | ||||||
| chr2:221453645
|
A | G | 105 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(102): Show | 105 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1715+1902T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221453645 | ||||||
| chr2:221453649
|
G | C | 47 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0041others(44): Show | 47 | HG00544.hp1 HG00733.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.1715+1898C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221453649 | ||||||
| chr2:221453754
|
A | G | 3 | a0001c0001t0011g0138a0001c0001t0018g0113a0001c0001t0027g0137 | 3 | HG02145.hp2 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1715+1793T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221453754 | ||||||
| chr2:221453793
|
G | A | 105 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(102): Show | 105 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1715+1754C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221453793 | ||||||
| chr2:221453857
|
A | G | 40 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0022others(37): Show | 40 | HG00408.hp2 HG00673.hp2 HG01361.hp1 others(37): Show |
intron_variant | MODIFIER | c.1715+1690T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221453857 | ||||||
| chr2:221453898
|
C | T | 6 | a0001c0001t0008g0117a0001c0001t0008g0132a0001c0001t0008g0134others(3): Show | 6 | HG01884.hp1 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1715+1649G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221453898 | ||||||
| chr2:221454008
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1715+1539G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221454008 | ||||||
| chr2:221454115
|
C | A | 37 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0022others(34): Show | 37 | HG00408.hp2 HG00673.hp2 HG01978.hp1 others(34): Show |
intron_variant | MODIFIER | c.1715+1432G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221454115 | ||||||
| chr2:221454272
|
A | T | 10 | a0001c0001t0001g0225a0001c0001t0001g0287a0001c0001t0004g0235others(7): Show | 10 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1715+1275T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221454272 | ||||||
| chr2:221454470
|
G | T | 1 | a0001c0001t0004g0203 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1715+1077C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221454470 | ||||||
| chr2:221454606
|
A | G | 1 | a0001c0005t0001g0029 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1715+941T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221454606 | ||||||
| chr2:221454624
|
G | C | 2 | a0001c0002t0004g0234a0001c0002t0029g0269 | 2 | HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1715+923C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221454624 | ||||||
| chr2:221454898
|
A | C | 40 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0022others(37): Show | 40 | HG00408.hp2 HG00673.hp2 HG01978.hp1 others(37): Show |
intron_variant | MODIFIER | c.1715+649T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221454898 | ||||||
| chr2:221455029
|
T | C | 37 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0022others(34): Show | 37 | HG00408.hp2 HG00673.hp2 HG01978.hp1 others(34): Show |
intron_variant | MODIFIER | c.1715+518A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221455029 | ||||||
| chr2:221455067
|
T | C | 246 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 246 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.1715+480A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221455067 | ||||||
| chr2:221455260
|
C | T | 3 | a0001c0001t0009g0212a0001c0001t0017g0098a0001c0001t0017g0103 | 3 | HG02615.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1715+287G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221455260 | ||||||
| chr2:221455346
|
G | A | 105 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(102): Show | 105 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1715+201C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221455346 | ||||||
| chr2:221455368
|
GGTA | G | 13 | a0001c0001t0001g0225a0001c0001t0001g0287a0001c0001t0004g0235others(10): Show | 13 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1715+176_1715+178d others(5): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 8/17 | chr2 | 221455368 | ||||||
| chr2:221455707
|
G | A | 205 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(202): Show | 205 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.1604-49C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 7/17 | chr2 | 221455707 | ||||||
| chr2:221455869
|
C | T | 3 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0221 | 3 | HG01361.hp1 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1604-211G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 7/17 | chr2 | 221455869 | ||||||
| chr2:221455876
|
C | G | 1 | a0001c0001t0001g0141 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1604-218G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 7/17 | chr2 | 221455876 | ||||||
| chr2:221455954
|
T | G | 1 | a0001c0001t0001g0140 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1604-296A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 7/17 | chr2 | 221455954 | ||||||
| chr2:221456002
|
T | A | 8 | a0001c0001t0001g0287a0001c0001t0004g0235a0001c0001t0004g0291others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1604-344A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 7/17 | chr2 | 221456002 | ||||||
| chr2:221456132
|
G | A | 41 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0022others(38): Show | 41 | HG00408.hp2 HG00673.hp2 HG01978.hp1 others(38): Show |
intron_variant | MODIFIER | c.1604-474C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 7/17 | chr2 | 221456132 | ||||||
| chr2:221456172
|
T | TA | 12 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0155others(9): Show | 12 | HG00323.hp2 HG01169.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.1603+440dupT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 7/17 | chr2 | 221456172 | ||||||
| chr2:221456172
|
T | TAA | 39 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0022others(36): Show | 39 | HG00408.hp2 HG00673.hp2 HG01978.hp1 others(36): Show |
intron_variant | MODIFIER | c.1603+439_1603+440d others(4): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 7/17 | chr2 | 221456172 | ||||||
| chr2:221456172
|
TA | T | 6 | a0001c0001t0003g0266a0001c0001t0006g0246a0001c0001t0038g0102others(3): Show | 6 | HG01167.hp2 HG02258.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1603+440delT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 7/17 | chr2 | 221456172 | ||||||
| chr2:221456205
|
AAAT | A | 14 | a0001c0001t0001g0018a0001c0001t0001g0060a0001c0001t0001g0140others(11): Show | 14 | HG00408.hp2 HG01978.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.1603+405_1603+407d others(5): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 7/17 | chr2 | 221456205 | ||||||
| chr2:221456505
|
C | T | 207 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(204): Show | 207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1603+108G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 7/17 | chr2 | 221456505 | ||||||
| chr2:221456878
|
A | C | 1 | a0001c0001t0008g0117 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1444-106T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 6/17 | chr2 | 221456878 | ||||||
| chr2:221456992
|
C | T | 3 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0221 | 3 | HG01361.hp1 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1444-220G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 6/17 | chr2 | 221456992 | ||||||
| chr2:221457075
|
C | T | 239 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(236): Show | 239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1444-303G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 6/17 | chr2 | 221457075 | ||||||
| chr2:221457123
|
T | C | 1 | a0001c0001t0003g0279 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1444-351A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 6/17 | chr2 | 221457123 | ||||||
| chr2:221457228
|
T | C | 1 | a0001c0001t0045g0096 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1444-456A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 6/17 | chr2 | 221457228 | ||||||
| chr2:221457833
|
A | G | 1 | a0001c0001t0037g0100 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1443+33T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 6/17 | chr2 | 221457833 | ||||||
| chr2:221458380
|
C | G | 6 | a0001c0001t0001g0245a0001c0001t0002g0095a0001c0001t0002g0097others(3): Show | 6 | HG02615.hp2 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1319-390G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221458380 | ||||||
| chr2:221458388
|
A | G | 1 | a0001c0003t0003g0226 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1319-398T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221458388 | ||||||
| chr2:221458424
|
C | T | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1319-434G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221458424 | ||||||
| chr2:221458474
|
A | T | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1319-484T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221458474 | ||||||
| chr2:221458600
|
C | T | 16 | a0001c0001t0001g0140a0001c0001t0001g0166a0001c0001t0001g0167others(13): Show | 16 | HG00408.hp2 HG00735.hp1 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.1319-610G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221458600 | ||||||
| chr2:221458942
|
C | A | 2 | a0001c0001t0001g0092a0001c0001t0040g0128 | 2 | HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1319-952G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221458942 | ||||||
| chr2:221459145
|
C | G | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1319-1155G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221459145 | ||||||
| chr2:221459184
|
T | C | 1 | a0001c0001t0001g0262 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1319-1194A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221459184 | ||||||
| chr2:221459200
|
T | C | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1319-1210A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221459200 | ||||||
| chr2:221459221
|
G | A | 236 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(233): Show | 236 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.1319-1231C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221459221 | ||||||
| chr2:221459288
|
G | A | 1 | a0001c0002t0007g0239 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1319-1298C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221459288 | ||||||
| chr2:221459288
|
G | GCA | 6 | a0001c0001t0001g0231a0001c0001t0001g0287a0001c0001t0010g0107others(3): Show | 6 | HG02257.hp2 HG03516.hp1 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.1319-1300_1319-129 others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221459288 | ||||||
| chr2:221459290
|
A | G | 210 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(207): Show | 210 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.1319-1300T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221459290 | ||||||
| chr2:221459292
|
A | G | 7 | a0001c0001t0001g0121a0001c0001t0001g0177a0001c0001t0001g0184others(4): Show | 7 | HG00639.hp1 HG00741.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1319-1302T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221459292 | ||||||
| chr2:221459308
|
A | C | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1319-1318T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221459308 | ||||||
| chr2:221459316
|
A | AT | 191 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(188): Show | 191 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.1319-1327dupA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221459316 | ||||||
| chr2:221459348
|
A | G | 3 | a0001c0001t0001g0092a0001c0001t0040g0128a0001c0012t0018g0272 | 3 | HG02717.hp2 NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1319-1358T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221459348 | ||||||
| chr2:221459565
|
A | G | 17 | a0001c0001t0001g0106a0001c0001t0001g0225a0001c0001t0003g0289others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.1319-1575T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221459565 | ||||||
| chr2:221459713
|
A | C | 1 | a0001c0001t0001g0062 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1319-1723T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221459713 | ||||||
| chr2:221460137
|
G | A | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1319-2147C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221460137 | ||||||
| chr2:221460178
|
G | A | 3 | a0001c0001t0002g0064a0001c0001t0002g0066a0001c0001t0007g0078 | 3 | NA18975.hp1 NA18989.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1319-2188C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221460178 | ||||||
| chr2:221460419
|
T | C | 44 | a0001c0001t0001g0036a0001c0001t0001g0062a0001c0001t0001g0063others(41): Show | 44 | HG00280.hp1 HG00423.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.1319-2429A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221460419 | ||||||
| chr2:221460611
|
C | T | 184 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(181): Show | 184 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.1319-2621G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221460611 | ||||||
| chr2:221460618
|
A | G | 1 | a0001c0002t0028g0242 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1319-2628T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221460618 | ||||||
| chr2:221460820
|
T | C | 6 | a0001c0001t0001g0200a0001c0001t0001g0202a0001c0001t0001g0268others(3): Show | 6 | HG01071.hp1 HG01074.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.1319-2830A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221460820 | ||||||
| chr2:221460854
|
C | T | 26 | a0001c0001t0001g0038a0001c0001t0001g0092a0001c0001t0001g0260others(23): Show | 26 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1319-2864G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221460854 | ||||||
| chr2:221460878
|
C | T | 184 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(181): Show | 184 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.1319-2888G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221460878 | ||||||
| chr2:221461076
|
G | A | 18 | a0001c0001t0001g0106a0001c0001t0001g0225a0001c0001t0003g0289others(15): Show | 18 | HG01109.hp2 HG01243.hp2 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.1319-3086C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221461076 | ||||||
| chr2:221461129
|
G | A | 249 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(246): Show | 249 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.1319-3139C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221461129 | ||||||
| chr2:221461220
|
T | C | 284 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(281): Show | 284 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.1319-3230A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221461220 | ||||||
| chr2:221461386
|
A | C | 1 | a0001c0001t0001g0063 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1319-3396T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221461386 | ||||||
| chr2:221461455
|
CAA | C | 184 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(181): Show | 184 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.1319-3467_1319-346 others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221461455 | ||||||
| chr2:221461506
|
A | G | 26 | a0001c0001t0001g0038a0001c0001t0001g0092a0001c0001t0001g0260others(23): Show | 26 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1319-3516T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221461506 | ||||||
| chr2:221461510
|
G | A | 184 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(181): Show | 184 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.1319-3520C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221461510 | ||||||
| chr2:221461637
|
G | A | 1 | a0001c0001t0037g0100 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1319-3647C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221461637 | ||||||
| chr2:221461924
|
A | G | 7 | a0001c0001t0001g0245a0001c0001t0002g0095a0001c0001t0002g0097others(4): Show | 7 | HG02055.hp1 HG02615.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1319-3934T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221461924 | ||||||
| chr2:221461953
|
C | T | 132 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0033others(129): Show | 132 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1319-3963G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221461953 | ||||||
| chr2:221461985
|
C | CTT | 133 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0033others(130): Show | 133 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1319-3997_1319-399 others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221461985 | ||||||
| chr2:221461985
|
C | CTTT | 27 | a0001c0001t0001g0038a0001c0001t0001g0092a0001c0001t0010g0107others(24): Show | 27 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.1319-3998_1319-399 others(7): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221461985 | ||||||
| chr2:221461985
|
C | CTTTTTT | 48 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(45): Show | 48 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.1319-4001_1319-399 others(10): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221461985 | ||||||
| chr2:221462135
|
T | C | 1 | a0001c0001t0001g0007 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1319-4145A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221462135 | ||||||
| chr2:221462216
|
T | C | 1 | a0001c0001t0038g0102 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1319-4226A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221462216 | ||||||
| chr2:221462291
|
T | G | 1 | a0001c0004t0035g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1319-4301A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221462291 | ||||||
| chr2:221462330
|
A | G | 231 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(228): Show | 231 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.1319-4340T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221462330 | ||||||
| chr2:221462363
|
T | C | 185 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(182): Show | 185 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.1319-4373A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221462363 | ||||||
| chr2:221462450
|
A | G | 1 | a0001c0002t0004g0234 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1319-4460T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221462450 | ||||||
| chr2:221462465
|
T | C | 1 | a0001c0001t0002g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1319-4475A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221462465 | ||||||
| chr2:221462922
|
G | A | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1319-4932C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221462922 | ||||||
| chr2:221463108
|
G | C | 1 | a0001c0001t0032g0251 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1319-5118C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221463108 | ||||||
| chr2:221463150
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1319-5160G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221463150 | ||||||
| chr2:221463237
|
C | T | 26 | a0001c0001t0001g0038a0001c0001t0001g0092a0001c0001t0001g0260others(23): Show | 26 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1319-5247G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221463237 | ||||||
| chr2:221463315
|
T | C | 26 | a0001c0001t0001g0038a0001c0001t0001g0092a0001c0001t0001g0260others(23): Show | 26 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1319-5325A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221463315 | ||||||
| chr2:221463452
|
C | A | 1 | a0001c0001t0009g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1319-5462G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221463452 | ||||||
| chr2:221463474
|
T | C | 1 | a0001c0001t0017g0098 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1319-5484A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221463474 | ||||||
| chr2:221463584
|
A | G | 1 | a0001c0003t0001g0087 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1319-5594T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221463584 | ||||||
| chr2:221463779
|
A | C | 2 | a0001c0001t0011g0138a0001c0001t0027g0137 | 2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1319-5789T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221463779 | ||||||
| chr2:221463809
|
G | A | 1 | a0001c0004t0035g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1319-5819C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221463809 | ||||||
| chr2:221463821
|
G | A | 2 | a0001c0001t0003g0266a0001c0001t0003g0267 | 2 | HG01071.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.1319-5831C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221463821 | ||||||
| chr2:221464215
|
T | C | 1 | a0001c0001t0002g0206 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1319-6225A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221464215 | ||||||
| chr2:221464224
|
A | T | 1 | a0001c0001t0006g0238 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1319-6234T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221464224 | ||||||
| chr2:221464305
|
T | A | 131 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0033others(128): Show | 131 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.1319-6315A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221464305 | ||||||
| chr2:221464330
|
T | C | 26 | a0001c0001t0001g0038a0001c0001t0001g0092a0001c0001t0001g0260others(23): Show | 26 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1319-6340A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221464330 | ||||||
| chr2:221464412
|
A | T | 1 | a0001c0001t0009g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1319-6422T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221464412 | ||||||
| chr2:221464423
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1319-6433G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221464423 | ||||||
| chr2:221464443
|
C | T | 1 | a0001c0001t0003g0289 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1319-6453G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221464443 | ||||||
| chr2:221464445
|
T | C | 1 | a0001c0001t0012g0275 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1319-6455A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221464445 | ||||||
| chr2:221464450
|
G | A | 1 | a0001c0004t0035g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1319-6460C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221464450 | ||||||
| chr2:221464477
|
T | G | 1 | a0001c0004t0035g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1319-6487A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221464477 | ||||||
| chr2:221464478
|
T | A | 1 | a0001c0001t0001g0059 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1319-6488A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221464478 | ||||||
| chr2:221464658
|
C | T | 1 | a0001c0002t0001g0019 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1319-6668G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221464658 | ||||||
| chr2:221464875
|
CTTGA | C | 3 | a0001c0001t0001g0037a0001c0001t0001g0059a0001c0001t0002g0005 | 3 | NA18977.hp2 NA19063.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1319-6889_1319-688 others(8): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221464875 | ||||||
| chr2:221464886
|
T | C | 26 | a0001c0001t0001g0038a0001c0001t0001g0092a0001c0001t0001g0260others(23): Show | 26 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1319-6896A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221464886 | ||||||
| chr2:221464906
|
C | T | 26 | a0001c0001t0001g0038a0001c0001t0001g0092a0001c0001t0001g0260others(23): Show | 26 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1319-6916G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221464906 | ||||||
| chr2:221465047
|
AT | A | 27 | a0001c0001t0001g0038a0001c0001t0001g0065a0001c0001t0001g0092others(24): Show | 27 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.1319-7058delA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221465047 | ||||||
| chr2:221465130
|
C | T | 3 | a0001c0001t0011g0138a0001c0001t0018g0113a0001c0001t0027g0137 | 3 | HG02145.hp2 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1319-7140G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221465130 | ||||||
| chr2:221465218
|
T | C | 26 | a0001c0001t0001g0038a0001c0001t0001g0092a0001c0001t0001g0260others(23): Show | 26 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1319-7228A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221465218 | ||||||
| chr2:221465281
|
G | A | 12 | a0001c0001t0001g0287a0001c0001t0004g0235a0001c0001t0004g0291others(9): Show | 12 | HG01891.hp1 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1319-7291C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221465281 | ||||||
| chr2:221465294
|
C | T | 1 | a0001c0001t0037g0100 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1319-7304G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221465294 | ||||||
| chr2:221465402
|
G | A | 53 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(50): Show | 53 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.1319-7412C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221465402 | ||||||
| chr2:221465449
|
C | T | 137 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0033others(134): Show | 137 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.1319-7459G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221465449 | ||||||
| chr2:221465455
|
C | T | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1319-7465G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221465455 | ||||||
| chr2:221465522
|
G | A | 1 | a0001c0001t0009g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1319-7532C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221465522 | ||||||
| chr2:221465833
|
A | T | 16 | a0001c0001t0001g0140a0001c0001t0001g0164a0001c0001t0001g0166others(13): Show | 16 | HG00408.hp2 HG01975.hp1 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.1319-7843T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221465833 | ||||||
| chr2:221465934
|
T | C | 2 | a0001c0002t0012g0099a0001c0002t0012g0101 | 2 | HG02280.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1319-7944A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221465934 | ||||||
| chr2:221465973
|
C | G | 1 | a0001c0001t0002g0035 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1319-7983G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221465973 | ||||||
| chr2:221465988
|
G | T | 1 | a0001c0001t0001g0164 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1319-7998C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221465988 | ||||||
| chr2:221466020
|
C | T | 2 | a0001c0001t0036g0115a0001c0003t0003g0114 | 2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1319-8030G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221466020 | ||||||
| chr2:221466134
|
C | T | 26 | a0001c0001t0001g0038a0001c0001t0001g0092a0001c0001t0001g0260others(23): Show | 26 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1319-8144G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221466134 | ||||||
| chr2:221466216
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1319-8226A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221466216 | ||||||
| chr2:221466218
|
C | T | 1 | a0001c0003t0003g0056 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1319-8228G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221466218 | ||||||
| chr2:221466236
|
T | G | 7 | a0001c0001t0001g0106a0001c0001t0001g0225a0001c0001t0017g0098others(4): Show | 7 | HG01975.hp2 HG02055.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1319-8246A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221466236 | ||||||
| chr2:221466250
|
T | C | 26 | a0001c0001t0001g0038a0001c0001t0001g0092a0001c0001t0001g0260others(23): Show | 26 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1319-8260A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221466250 | ||||||
| chr2:221466435
|
T | C | 3 | a0001c0001t0011g0138a0001c0001t0018g0113a0001c0001t0027g0137 | 3 | HG02145.hp2 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1319-8445A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221466435 | ||||||
| chr2:221466503
|
T | C | 26 | a0001c0001t0001g0038a0001c0001t0001g0092a0001c0001t0001g0260others(23): Show | 26 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1319-8513A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221466503 | ||||||
| chr2:221466748
|
A | G | 26 | a0001c0001t0001g0038a0001c0001t0001g0092a0001c0001t0001g0260others(23): Show | 26 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1319-8758T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221466748 | ||||||
| chr2:221466886
|
C | CT | 18 | a0001c0001t0001g0106a0001c0001t0001g0225a0001c0001t0003g0289others(15): Show | 18 | HG01109.hp2 HG01243.hp2 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.1319-8897dupA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221466886 | ||||||
| chr2:221466961
|
A | G | 284 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(281): Show | 284 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.1319-8971T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221466961 | ||||||
| chr2:221467093
|
G | T | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1319-9103C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221467093 | ||||||
| chr2:221467585
|
A | T | 1 | a0001c0001t0038g0102 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1319-9595T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221467585 | ||||||
| chr2:221467768
|
C | G | 1 | a0001c0001t0040g0128 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1319-9778G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221467768 | ||||||
| chr2:221467929
|
G | A | 7 | a0001c0001t0001g0106a0001c0001t0001g0225a0001c0001t0017g0098others(4): Show | 7 | HG01975.hp2 HG02055.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1319-9939C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221467929 | ||||||
| chr2:221467944
|
G | A | 22 | a0001c0001t0001g0038a0001c0001t0001g0092a0001c0001t0001g0260others(19): Show | 22 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.1319-9954C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221467944 | ||||||
| chr2:221467948
|
G | A | 77 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(74): Show | 77 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.1319-9958C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221467948 | ||||||
| chr2:221468222
|
G | C | 54 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(51): Show | 54 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.1319-10232C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221468222 | ||||||
| chr2:221468233
|
GA | G | 26 | a0001c0001t0001g0038a0001c0001t0001g0092a0001c0001t0001g0260others(23): Show | 26 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1319-10244delT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221468233 | ||||||
| chr2:221468239
|
A | C | 1 | a0001c0001t0049g0227 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1319-10249T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221468239 | ||||||
| chr2:221468367
|
G | T | 1 | a0001c0001t0001g0172 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1319-10377C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221468367 | ||||||
| chr2:221468398
|
G | T | 1 | a0001c0001t0002g0248 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1319-10408C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221468398 | ||||||
| chr2:221468713
|
C | T | 1 | a0001c0001t0002g0008 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1319-10723G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221468713 | ||||||
| chr2:221468776
|
C | T | 2 | a0001c0001t0002g0160a0001c0001t0004g0194 | 2 | HG00738.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.1319-10786G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221468776 | ||||||
| chr2:221468823
|
A | G | 1 | a0001c0001t0004g0291 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1319-10833T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221468823 | ||||||
| chr2:221468883
|
T | C | 5 | a0001c0001t0010g0107a0001c0001t0025g0233a0001c0002t0001g0020others(2): Show | 5 | HG03239.hp2 HG03516.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.1319-10893A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221468883 | ||||||
| chr2:221469037
|
C | G | 1 | a0001c0001t0001g0231 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1319-11047G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221469037 | ||||||
| chr2:221469123
|
A | G | 5 | a0001c0001t0006g0246a0001c0001t0036g0115a0001c0001t0044g0232others(2): Show | 5 | HG02280.hp2 HG03098.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1319-11133T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221469123 | ||||||
| chr2:221469234
|
G | C | 1 | a0001c0002t0029g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1319-11244C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221469234 | ||||||
| chr2:221469488
|
T | A | 2 | a0001c0001t0003g0289a0001c0006t0003g0118 | 2 | HG01109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1319-11498A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221469488 | ||||||
| chr2:221469498
|
A | G | 236 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(233): Show | 236 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.1319-11508T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221469498 | ||||||
| chr2:221469638
|
C | T | 131 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0033others(128): Show | 131 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.1319-11648G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221469638 | ||||||
| chr2:221469765
|
C | G | 1 | a0001c0003t0003g0226 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1319-11775G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221469765 | ||||||
| chr2:221470022
|
C | T | 1 | a0001c0001t0045g0096 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1319-12032G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221470022 | ||||||
| chr2:221470128
|
A | G | 7 | a0001c0001t0001g0106a0001c0001t0001g0225a0001c0001t0017g0098others(4): Show | 7 | HG01975.hp2 HG02055.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1319-12138T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221470128 | ||||||
| chr2:221470301
|
A | G | 1 | a0001c0001t0002g0206 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1318+12051T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221470301 | ||||||
| chr2:221470332
|
G | C | 1 | a0001c0001t0049g0227 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1318+12020C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221470332 | ||||||
| chr2:221470334
|
C | CG | 19 | a0001c0001t0001g0045a0001c0001t0001g0148a0001c0001t0001g0171others(16): Show | 19 | HG00738.hp2 HG01978.hp1 HG02071.hp2 others(16): Show |
intron_variant | MODIFIER | c.1318+12017dupC | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221470334 | ||||||
| chr2:221470340
|
G | GGA | 23 | a0001c0001t0001g0038a0001c0001t0001g0260a0001c0001t0002g0178others(20): Show | 23 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.1318+12010_1318+12 others(8): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221470340 | ||||||
| chr2:221470370
|
A | G | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1318+11982T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221470370 | ||||||
| chr2:221470515
|
G | A | 12 | a0001c0001t0001g0287a0001c0001t0004g0235a0001c0001t0004g0291others(9): Show | 12 | HG01891.hp1 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1318+11837C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221470515 | ||||||
| chr2:221470524
|
T | TAGTATCA others(27): Show |
2 | a0001c0001t0001g0260a0001c0002t0001g0259 | 2 | HG02523.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.1318+11794_1318+11 others(40): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221470524 | ||||||
| chr2:221470544
|
TCTGCTTT others(59): Show |
T | 3 | a0001c0001t0011g0138a0001c0001t0018g0113a0001c0001t0027g0137 | 3 | HG02145.hp2 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1318+11742_1318+11 others(72): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221470544 | ||||||
| chr2:221470578
|
TCTGCTTT others(25): Show |
T | 77 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(74): Show | 77 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.1318+11742_1318+11 others(38): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221470578 | ||||||
| chr2:221470609
|
ACCTGCTT others(26): Show |
A | 1 | a0001c0001t0001g0016 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1318+11710_1318+11 others(39): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221470609 | ||||||
| chr2:221470610
|
C | CCT | 118 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0033others(115): Show | 118 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1318+11740_1318+11 others(8): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221470610 | ||||||
| chr2:221470610
|
C | CCTCTGCT others(29): Show |
9 | a0001c0001t0002g0179a0001c0001t0003g0266a0001c0001t0003g0267others(6): Show | 9 | HG01071.hp1 HG01167.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.1318+11741_1318+11 others(42): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221470610 | ||||||
| chr2:221470642
|
C | G | 26 | a0001c0001t0001g0038a0001c0001t0001g0092a0001c0001t0001g0260others(23): Show | 26 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1318+11710G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221470642 | ||||||
| chr2:221470809
|
C | T | 244 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(241): Show | 244 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.1318+11543G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221470809 | ||||||
| chr2:221470832
|
C | A | 26 | a0001c0001t0001g0038a0001c0001t0001g0092a0001c0001t0001g0260others(23): Show | 26 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1318+11520G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221470832 | ||||||
| chr2:221471017
|
T | C | 1 | a0001c0004t0035g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1318+11335A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221471017 | ||||||
| chr2:221471058
|
G | C | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1318+11294C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221471058 | ||||||
| chr2:221471196
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | NA19057.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1318+11156C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221471196 | ||||||
| chr2:221471248
|
A | T | 148 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0033others(145): Show | 148 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.1318+11104T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221471248 | ||||||
| chr2:221471296
|
G | A | 2 | a0001c0001t0008g0134a0001c0001t0008g0135 | 2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1318+11056C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221471296 | ||||||
| chr2:221471330
|
T | A | 148 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0033others(145): Show | 148 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.1318+11022A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221471330 | ||||||
| chr2:221471527
|
G | A | 1 | a0001c0004t0035g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1318+10825C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221471527 | ||||||
| chr2:221471573
|
C | G | 1 | a0001c0004t0035g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1318+10779G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221471573 | ||||||
| chr2:221471629
|
A | T | 6 | a0001c0001t0001g0245a0001c0001t0002g0095a0001c0001t0002g0097others(3): Show | 6 | HG02615.hp2 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1318+10723T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221471629 | ||||||
| chr2:221471677
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1318+10675A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221471677 | ||||||
| chr2:221471862
|
G | C | 5 | a0001c0001t0010g0107a0001c0001t0025g0233a0001c0002t0001g0020others(2): Show | 5 | HG03239.hp2 HG03516.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.1318+10490C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221471862 | ||||||
| chr2:221472044
|
T | C | 26 | a0001c0001t0001g0038a0001c0001t0001g0092a0001c0001t0001g0260others(23): Show | 26 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1318+10308A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221472044 | ||||||
| chr2:221472300
|
C | CA | 120 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(117): Show | 120 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1318+10051dupT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221472300 | ||||||
| chr2:221472300
|
CA | C | 12 | a0001c0001t0001g0042a0001c0001t0001g0062a0001c0001t0001g0080others(9): Show | 12 | HG00558.hp2 HG01243.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1318+10051delT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221472300 | ||||||
| chr2:221472300
|
CAAA | C | 26 | a0001c0001t0001g0038a0001c0001t0001g0092a0001c0001t0001g0260others(23): Show | 26 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1318+10049_1318+10 others(9): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221472300 | ||||||
| chr2:221472629
|
TAAAC | T | 26 | a0001c0001t0001g0038a0001c0001t0001g0092a0001c0001t0001g0260others(23): Show | 26 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1318+9719_1318+972 others(8): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221472629 | ||||||
| chr2:221472720
|
C | G | 1 | a0001c0001t0049g0227 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1318+9632G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221472720 | ||||||
| chr2:221472828
|
T | C | 1 | a0001c0001t0002g0169 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1318+9524A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221472828 | ||||||
| chr2:221472906
|
G | A | 235 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(232): Show | 235 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.1318+9446C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221472906 | ||||||
| chr2:221473090
|
C | T | 166 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0033others(163): Show | 166 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.1318+9262G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221473090 | ||||||
| chr2:221473136
|
C | T | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1318+9216G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221473136 | ||||||
| chr2:221473195
|
G | T | 53 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(50): Show | 53 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.1318+9157C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221473195 | ||||||
| chr2:221473226
|
G | A | 1 | a0001c0003t0003g0091 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1318+9126C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221473226 | ||||||
| chr2:221473342
|
T | C | 129 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(126): Show | 129 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1318+9010A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221473342 | ||||||
| chr2:221473552
|
G | GA | 151 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(148): Show | 151 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.1318+8799dupT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221473552 | ||||||
| chr2:221473552
|
G | GAA | 75 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(72): Show | 75 | HG00280.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1318+8798_1318+879 others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221473552 | ||||||
| chr2:221473552
|
G | GAAA | 6 | a0001c0001t0001g0018a0001c0001t0002g0127a0001c0001t0002g0199others(3): Show | 6 | HG00423.hp1 HG01109.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.1318+8797_1318+879 others(7): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221473552 | ||||||
| chr2:221473552
|
GAA | G | 22 | a0001c0001t0001g0092a0001c0001t0001g0260a0001c0001t0025g0233others(19): Show | 22 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.1318+8798_1318+879 others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221473552 | ||||||
| chr2:221473717
|
G | T | 1 | a0001c0003t0003g0161 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1318+8635C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221473717 | ||||||
| chr2:221473768
|
C | T | 1 | a0001c0002t0023g0218 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1318+8584G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221473768 | ||||||
| chr2:221473858
|
T | C | 1 | a0001c0001t0003g0289 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1318+8494A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221473858 | ||||||
| chr2:221473869
|
C | T | 12 | a0001c0001t0001g0287a0001c0001t0004g0235a0001c0001t0004g0291others(9): Show | 12 | HG01891.hp1 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1318+8483G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221473869 | ||||||
| chr2:221473870
|
A | T | 54 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(51): Show | 54 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.1318+8482T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221473870 | ||||||
| chr2:221474068
|
A | T | 18 | a0001c0001t0001g0106a0001c0001t0001g0112a0001c0001t0001g0190others(15): Show | 18 | HG00642.hp2 HG01975.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1318+8284T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221474068 | ||||||
| chr2:221474114
|
C | T | 136 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(133): Show | 136 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1318+8238G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221474114 | ||||||
| chr2:221474115
|
G | A | 26 | a0001c0001t0001g0038a0001c0001t0001g0092a0001c0001t0001g0260others(23): Show | 26 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1318+8237C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221474115 | ||||||
| chr2:221474260
|
G | C | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1318+8092C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221474260 | ||||||
| chr2:221474274
|
G | A | 1 | a0001c0004t0035g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1318+8078C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221474274 | ||||||
| chr2:221474281
|
C | T | 12 | a0001c0001t0001g0245a0001c0001t0002g0095a0001c0001t0002g0097others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1318+8071G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221474281 | ||||||
| chr2:221474299
|
G | T | 1 | a0001c0004t0035g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1318+8053C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221474299 | ||||||
| chr2:221474320
|
C | T | 1 | a0001c0004t0035g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1318+8032G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221474320 | ||||||
| chr2:221474388
|
C | T | 12 | a0001c0001t0001g0245a0001c0001t0002g0095a0001c0001t0002g0097others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1318+7964G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221474388 | ||||||
| chr2:221474422
|
T | TA | 211 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(208): Show | 211 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.1318+7929dupT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221474422 | ||||||
| chr2:221474422
|
T | TAAAA | 10 | a0001c0001t0001g0245a0001c0001t0002g0095a0001c0001t0002g0097others(7): Show | 10 | HG01109.hp2 HG01243.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1318+7926_1318+792 others(8): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221474422 | ||||||
| chr2:221474422
|
TA | T | 15 | a0001c0001t0001g0287a0001c0001t0002g0142a0001c0001t0004g0235others(12): Show | 15 | HG00323.hp2 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1318+7929delT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221474422 | ||||||
| chr2:221474484
|
G | A | 2 | a0001c0002t0001g0125a0001c0002t0001g0149 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1318+7868C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221474484 | ||||||
| chr2:221474536
|
CTGGCTCC others(11): Show |
C | 1 | a0001c0001t0005g0145 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1318+7798_1318+781 others(22): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221474536 | ||||||
| chr2:221474562
|
C | T | 1 | a0001c0001t0004g0291 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1318+7790G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221474562 | ||||||
| chr2:221474640
|
C | A | 50 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(47): Show | 50 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.1318+7712G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221474640 | ||||||
| chr2:221474640
|
C | T | 45 | a0001c0001t0001g0036a0001c0001t0001g0062a0001c0001t0001g0063others(42): Show | 45 | HG00280.hp1 HG00423.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.1318+7712G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221474640 | ||||||
| chr2:221474649
|
C | T | 1 | a0001c0004t0035g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1318+7703G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221474649 | ||||||
| chr2:221474650
|
G | C | 26 | a0001c0001t0001g0038a0001c0001t0001g0092a0001c0001t0001g0260others(23): Show | 26 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1318+7702C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221474650 | ||||||
| chr2:221474691
|
T | C | 147 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(144): Show | 147 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.1318+7661A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221474691 | ||||||
| chr2:221474801
|
G | A | 1 | a0001c0001t0002g0123 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1318+7551C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221474801 | ||||||
| chr2:221474867
|
C | A | 1 | a0001c0001t0001g0141 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1318+7485G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221474867 | ||||||
| chr2:221474937
|
T | C | 235 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(232): Show | 235 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.1318+7415A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221474937 | ||||||
| chr2:221475013
|
G | A | 1 | a0001c0001t0049g0227 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1318+7339C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221475013 | ||||||
| chr2:221475078
|
G | T | 141 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(138): Show | 141 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.1318+7274C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221475078 | ||||||
| chr2:221475204
|
A | C | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1318+7148T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221475204 | ||||||
| chr2:221475317
|
A | G | 152 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(149): Show | 152 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.1318+7035T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221475317 | ||||||
| chr2:221475362
|
T | C | 82 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(79): Show | 82 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.1318+6990A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221475362 | ||||||
| chr2:221475519
|
T | C | 152 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(149): Show | 152 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.1318+6833A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221475519 | ||||||
| chr2:221475621
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1318+6731G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221475621 | ||||||
| chr2:221475810
|
A | AAAAAGCC others(11): Show |
1 | a0001c0001t0005g0145 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1318+6541_1318+654 others(22): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221475810 | ||||||
| chr2:221475824
|
G | A | 6 | a0001c0001t0004g0235a0001c0001t0006g0246a0001c0001t0036g0115others(3): Show | 6 | HG02145.hp1 HG02280.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1318+6528C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221475824 | ||||||
| chr2:221475995
|
G | A | 1 | a0001c0001t0001g0230 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1318+6357C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221475995 | ||||||
| chr2:221476040
|
A | C | 1 | a0001c0001t0001g0257 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1318+6312T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221476040 | ||||||
| chr2:221476086
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1318+6266C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221476086 | ||||||
| chr2:221476258
|
A | G | 1 | a0001c0001t0001g0007 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1318+6094T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221476258 | ||||||
| chr2:221476259
|
C | T | 136 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(133): Show | 136 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1318+6093G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221476259 | ||||||
| chr2:221476468
|
G | A | 1 | a0001c0001t0002g0277 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1318+5884C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221476468 | ||||||
| chr2:221476535
|
T | C | 1 | a0001c0001t0037g0100 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1318+5817A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221476535 | ||||||
| chr2:221476626
|
A | G | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1318+5726T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221476626 | ||||||
| chr2:221476984
|
G | T | 26 | a0001c0001t0001g0038a0001c0001t0001g0092a0001c0001t0001g0260others(23): Show | 26 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1318+5368C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221476984 | ||||||
| chr2:221477046
|
T | TTTA | 5 | a0001c0001t0004g0235a0001c0001t0036g0115a0001c0002t0004g0234others(2): Show | 5 | HG02145.hp1 HG03540.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1318+5303_1318+530 others(7): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221477046 | ||||||
| chr2:221477046
|
TTTA | T | 142 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(139): Show | 142 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.1318+5303_1318+530 others(7): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221477046 | ||||||
| chr2:221477049
|
A | T | 1 | a0001c0004t0035g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1318+5303T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221477049 | ||||||
| chr2:221477320
|
A | T | 140 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(137): Show | 140 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.1318+5032T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221477320 | ||||||
| chr2:221477382
|
A | G | 136 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(133): Show | 136 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1318+4970T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221477382 | ||||||
| chr2:221477442
|
G | A | 1 | a0001c0001t0005g0009 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1318+4910C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221477442 | ||||||
| chr2:221477620
|
G | A | 1 | a0001c0003t0004g0084 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1318+4732C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221477620 | ||||||
| chr2:221477660
|
G | A | 2 | a0001c0001t0002g0178a0001c0001t0002g0248 | 2 | NA18959.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.1318+4692C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221477660 | ||||||
| chr2:221477849
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1318+4503A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221477849 | ||||||
| chr2:221477852
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | NA19057.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1318+4500G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221477852 | ||||||
| chr2:221477928
|
A | C | 3 | a0001c0001t0001g0164a0001c0001t0001g0188a0001c0001t0001g0264 | 3 | HG01975.hp1 HG01978.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1318+4424T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221477928 | ||||||
| chr2:221478085
|
A | T | 138 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(135): Show | 138 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.1318+4267T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221478085 | ||||||
| chr2:221478097
|
T | A | 1 | a0001c0001t0001g0059 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1318+4255A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221478097 | ||||||
| chr2:221478101
|
A | C | 1 | a0001c0001t0001g0059 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1318+4251T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221478101 | ||||||
| chr2:221478161
|
C | T | 8 | a0001c0001t0004g0235a0001c0001t0006g0246a0001c0001t0036g0115others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1318+4191G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221478161 | ||||||
| chr2:221478172
|
C | T | 138 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(135): Show | 138 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.1318+4180G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221478172 | ||||||
| chr2:221478220
|
C | CA | 58 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(55): Show | 58 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.1318+4131dupT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221478220 | ||||||
| chr2:221478223
|
A | C | 7 | a0001c0001t0004g0235a0001c0001t0006g0246a0001c0001t0036g0115others(4): Show | 7 | HG02145.hp1 HG02280.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1318+4129T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221478223 | ||||||
| chr2:221478411
|
T | C | 2 | a0001c0002t0001g0047a0001c0002t0001g0048 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1318+3941A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221478411 | ||||||
| chr2:221478449
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0024g0129 | 2 | HG02630.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1318+3903C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221478449 | ||||||
| chr2:221478526
|
G | C | 1 | a0001c0001t0001g0247 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1318+3826C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221478526 | ||||||
| chr2:221478529
|
G | T | 2 | a0001c0001t0002g0111a0001c0001t0010g0110 | 2 | HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1318+3823C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221478529 | ||||||
| chr2:221478667
|
C | A | 50 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(47): Show | 50 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.1318+3685G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221478667 | ||||||
| chr2:221478710
|
A | C | 1 | a0001c0001t0001g0059 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1318+3642T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221478710 | ||||||
| chr2:221478710
|
A | G | 2 | a0001c0003t0003g0079a0001c0003t0003g0133 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1318+3642T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221478710 | ||||||
| chr2:221478711
|
C | A | 1 | a0001c0001t0001g0059 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1318+3641G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221478711 | ||||||
| chr2:221478712
|
T | C | 1 | a0001c0001t0001g0059 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1318+3640A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221478712 | ||||||
| chr2:221478765
|
CAG | C | 134 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(131): Show | 134 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1318+3585_1318+358 others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221478765 | ||||||
| chr2:221478790
|
C | T | 6 | a0001c0001t0004g0235a0001c0001t0006g0246a0001c0001t0036g0115others(3): Show | 6 | HG02145.hp1 HG02280.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1318+3562G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221478790 | ||||||
| chr2:221478818
|
CA | C | 134 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(131): Show | 134 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1318+3533delT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221478818 | ||||||
| chr2:221478848
|
C | A | 2 | a0001c0001t0001g0059a0001c0001t0002g0005 | 2 | NA19063.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1318+3504G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221478848 | ||||||
| chr2:221479029
|
T | A | 1 | a0001c0001t0001g0059 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1318+3323A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221479029 | ||||||
| chr2:221479103
|
G | C | 150 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(147): Show | 150 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.1318+3249C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221479103 | ||||||
| chr2:221479132
|
T | C | 1 | a0001c0001t0037g0100 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1318+3220A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221479132 | ||||||
| chr2:221479237
|
C | A | 2 | a0001c0001t0004g0285a0001c0001t0005g0284 | 2 | HG03704.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1318+3115G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221479237 | ||||||
| chr2:221479377
|
C | A | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1318+2975G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221479377 | ||||||
| chr2:221479476
|
G | A | 135 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(132): Show | 135 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1318+2876C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221479476 | ||||||
| chr2:221479513
|
C | A | 1 | a0001c0001t0049g0227 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1318+2839G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221479513 | ||||||
| chr2:221479601
|
T | C | 2 | a0001c0001t0003g0289a0001c0006t0003g0118 | 2 | HG01109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1318+2751A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221479601 | ||||||
| chr2:221479617
|
G | T | 5 | a0001c0003t0003g0082a0001c0003t0003g0091a0001c0003t0003g0226others(2): Show | 5 | HG02258.hp2 HG03041.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1318+2735C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221479617 | ||||||
| chr2:221479718
|
A | G | 1 | a0001c0004t0035g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1318+2634T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221479718 | ||||||
| chr2:221479754
|
T | A | 4 | a0001c0001t0010g0107a0001c0001t0025g0233a0001c0002t0022g0090others(1): Show | 4 | HG03516.hp1 NA18906.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1318+2598A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221479754 | ||||||
| chr2:221479898
|
G | A | 1 | a0001c0001t0002g0271 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1318+2454C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221479898 | ||||||
| chr2:221479916
|
G | A | 1 | a0001c0001t0002g0206 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1318+2436C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221479916 | ||||||
| chr2:221480327
|
G | A | 1 | a0001c0001t0014g0213 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1318+2025C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221480327 | ||||||
| chr2:221480427
|
T | C | 137 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(134): Show | 137 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.1318+1925A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221480427 | ||||||
| chr2:221480648
|
C | T | 1 | a0001c0001t0002g0123 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1318+1704G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221480648 | ||||||
| chr2:221480952
|
A | T | 1 | a0001c0001t0002g0147 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1318+1400T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221480952 | ||||||
| chr2:221481100
|
T | C | 137 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(134): Show | 137 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.1318+1252A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221481100 | ||||||
| chr2:221481314
|
GCCGCCCC others(5): Show |
G | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1318+1026_1318+103 others(16): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221481314 | ||||||
| chr2:221481316
|
C | T | 2 | a0001c0001t0011g0138a0001c0001t0027g0137 | 2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1318+1036G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221481316 | ||||||
| chr2:221481336
|
C | T | 2 | a0001c0001t0009g0214a0001c0001t0009g0274 | 2 | HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1318+1016G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221481336 | ||||||
| chr2:221481351
|
G | A | 1 | a0001c0001t0012g0275 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1318+1001C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221481351 | ||||||
| chr2:221481483
|
C | T | 11 | a0001c0001t0001g0287a0001c0001t0004g0291a0001c0001t0006g0228others(8): Show | 11 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1318+869G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221481483 | ||||||
| chr2:221481515
|
A | G | 1 | a0001c0001t0044g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1318+837T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221481515 | ||||||
| chr2:221481610
|
C | T | 1 | a0001c0001t0012g0275 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1318+742G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221481610 | ||||||
| chr2:221481622
|
C | G | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1318+730G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221481622 | ||||||
| chr2:221482320
|
A | G | 1 | a0001c0004t0035g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1318+32T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 5/17 | chr2 | 221482320 | ||||||
| chr2:221482726
|
C | T | 1 | a0001c0001t0012g0275 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.980-36G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221482726 | ||||||
| chr2:221482895
|
A | G | 141 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(138): Show | 141 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.980-205T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221482895 | ||||||
| chr2:221482896
|
C | T | 1 | a0001c0002t0001g0020 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.980-206G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221482896 | ||||||
| chr2:221482935
|
A | C | 141 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(138): Show | 141 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.980-245T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221482935 | ||||||
| chr2:221483006
|
A | T | 1 | a0001c0001t0001g0006 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.980-316T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221483006 | ||||||
| chr2:221483091
|
T | C | 2 | a0001c0002t0012g0099a0001c0002t0012g0101 | 2 | HG02280.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.980-401A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221483091 | ||||||
| chr2:221483286
|
G | C | 1 | a0001c0004t0035g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.980-596C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221483286 | ||||||
| chr2:221483411
|
C | T | 7 | a0001c0001t0001g0033a0001c0001t0001g0222a0001c0001t0002g0158others(4): Show | 7 | HG00408.hp1 HG03831.hp1 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.980-721G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221483411 | ||||||
| chr2:221483500
|
T | TGTGTGTG others(10): Show |
1 | a0001c0001t0004g0235 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.980-811_980-810ins others(17): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221483500 | ||||||
| chr2:221483500
|
T | TTG | 55 | a0001c0001t0001g0036a0001c0001t0001g0062a0001c0001t0001g0063others(52): Show | 55 | HG00423.hp2 HG00558.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.980-812_980-811dup others(2): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221483500 | ||||||
| chr2:221483500
|
T | TTGTG | 7 | a0001c0001t0001g0065a0001c0001t0001g0112a0001c0001t0001g0121others(4): Show | 7 | HG02300.hp2 HG02698.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.980-814_980-811dup others(4): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221483500 | ||||||
| chr2:221483500
|
T | TTGTGTGT others(3): Show |
2 | a0001c0001t0012g0275a0001c0002t0029g0269 | 2 | HG01884.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.980-820_980-811dup others(10): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221483500 | ||||||
| chr2:221483500
|
T | TTGTGTGT others(5): Show |
2 | a0001c0001t0001g0105a0001c0012t0018g0272 | 2 | HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.980-822_980-811dup others(12): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221483500 | ||||||
| chr2:221483500
|
T | TTGTGTGT others(7): Show |
8 | a0001c0001t0001g0081a0001c0001t0001g0221a0001c0001t0001g0245others(5): Show | 8 | HG01361.hp1 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.980-824_980-811dup others(14): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221483500 | ||||||
| chr2:221483500
|
T | TTGTGTGT others(9): Show |
1 | a0001c0001t0001g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.980-826_980-811dup others(16): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221483500 | ||||||
| chr2:221483500
|
T | TTGTGTGT others(11): Show |
1 | a0001c0001t0040g0128 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.980-828_980-811dup others(18): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221483500 | ||||||
| chr2:221483500
|
TTG | T | 45 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(42): Show | 45 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.980-812_980-811del others(2): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221483500 | ||||||
| chr2:221483500
|
TTGTG | T | 4 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0002g0199others(1): Show | 4 | HG01981.hp2 HG02735.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.980-814_980-811del others(4): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221483500 | ||||||
| chr2:221483535
|
T | A | 1 | a0001c0001t0004g0235 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.980-845A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221483535 | ||||||
| chr2:221483535
|
T | TGTGTGA | 7 | a0001c0002t0001g0052a0001c0002t0001g0054a0001c0002t0001g0055others(4): Show | 7 | HG00738.hp1 HG01433.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.980-846_980-845ins others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221483535 | ||||||
| chr2:221483535
|
T | TGTGTGTG others(1): Show |
10 | a0001c0001t0001g0038a0001c0001t0001g0260a0001c0001t0031g0046others(7): Show | 10 | HG01167.hp1 HG01169.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.980-846_980-845ins others(8): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221483535 | ||||||
| chr2:221483535
|
T | TGTGTGTG others(3): Show |
3 | a0001c0001t0037g0100a0001c0002t0004g0234a0001c0005t0014g0040 | 3 | HG03540.hp1 HG03834.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.980-846_980-845ins others(10): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221483535 | ||||||
| chr2:221483535
|
T | TGTGTGTG others(5): Show |
2 | a0001c0001t0044g0232a0001c0002t0001g0159 | 2 | HG02280.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.980-846_980-845ins others(12): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221483535 | ||||||
| chr2:221483535
|
T | TGTGTGTG others(7): Show |
2 | a0001c0001t0006g0246a0001c0005t0001g0029 | 2 | HG03098.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.980-846_980-845ins others(14): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221483535 | ||||||
| chr2:221483656
|
C | T | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.980-966G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221483656 | ||||||
| chr2:221483714
|
A | G | 141 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(138): Show | 141 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.980-1024T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221483714 | ||||||
| chr2:221483741
|
C | T | 3 | a0001c0001t0018g0113a0001c0001t0049g0227a0001c0012t0018g0272 | 3 | HG03195.hp1 HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.980-1051G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221483741 | ||||||
| chr2:221483753
|
G | C | 31 | a0001c0001t0001g0106a0001c0001t0001g0112a0001c0001t0001g0190others(28): Show | 31 | HG00642.hp2 HG01975.hp2 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.980-1063C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221483753 | ||||||
| chr2:221484185
|
C | T | 25 | a0001c0001t0001g0038a0001c0001t0001g0260a0001c0001t0004g0235others(22): Show | 25 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.980-1495G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221484185 | ||||||
| chr2:221484228
|
A | G | 1 | a0001c0001t0004g0203 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.980-1538T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221484228 | ||||||
| chr2:221484383
|
C | A | 1 | a0001c0001t0045g0096 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.980-1693G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221484383 | ||||||
| chr2:221484677
|
C | T | 25 | a0001c0001t0001g0038a0001c0001t0001g0260a0001c0001t0004g0235others(22): Show | 25 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.980-1987G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221484677 | ||||||
| chr2:221484691
|
A | G | 1 | a0001c0001t0005g0049 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.980-2001T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221484691 | ||||||
| chr2:221484923
|
C | T | 1 | a0001c0001t0049g0227 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.980-2233G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221484923 | ||||||
| chr2:221484989
|
G | C | 1 | a0001c0002t0002g0043 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.980-2299C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221484989 | ||||||
| chr2:221485601
|
C | T | 140 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(137): Show | 140 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.980-2911G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221485601 | ||||||
| chr2:221485795
|
C | T | 1 | a0001c0001t0049g0227 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.980-3105G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221485795 | ||||||
| chr2:221485858
|
TA | T | 140 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(137): Show | 140 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.980-3169delT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221485858 | ||||||
| chr2:221485880
|
G | A | 140 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(137): Show | 140 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.980-3190C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221485880 | ||||||
| chr2:221486068
|
C | T | 140 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(137): Show | 140 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.980-3378G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221486068 | ||||||
| chr2:221486076
|
A | G | 1 | a0001c0001t0036g0115 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.980-3386T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221486076 | ||||||
| chr2:221486096
|
C | T | 10 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0221others(7): Show | 10 | HG01361.hp1 HG02615.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.980-3406G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221486096 | ||||||
| chr2:221486278
|
A | C | 2 | a0001c0001t0001g0092a0001c0001t0040g0128 | 2 | HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.980-3588T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221486278 | ||||||
| chr2:221486391
|
C | T | 1 | a0001c0001t0012g0275 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.980-3701G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221486391 | ||||||
| chr2:221486469
|
G | A | 58 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(55): Show | 58 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.980-3779C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221486469 | ||||||
| chr2:221486541
|
A | G | 3 | a0001c0001t0001g0256a0001c0001t0002g0044a0001c0002t0001g0195 | 3 | HG00558.hp2 NA19009.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.980-3851T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221486541 | ||||||
| chr2:221486600
|
G | T | 1 | a0001c0001t0037g0100 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.980-3910C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221486600 | ||||||
| chr2:221486735
|
A | AAAT | 161 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(158): Show | 161 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.980-4048_980-4046d others(5): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221486735 | ||||||
| chr2:221486735
|
A | AAATAAT | 45 | a0001c0001t0001g0025a0001c0001t0001g0038a0001c0001t0001g0059others(42): Show | 45 | HG00408.hp2 HG00544.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.980-4051_980-4046d others(8): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221486735 | ||||||
| chr2:221486735
|
AAAT | A | 5 | a0001c0001t0001g0092a0001c0001t0002g0142a0001c0001t0005g0165others(2): Show | 5 | HG02698.hp1 HG03195.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.980-4048_980-4046d others(5): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221486735 | ||||||
| chr2:221486735
|
AAATAATA others(5): Show |
A | 1 | a0001c0004t0035g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.980-4057_980-4046d others(14): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221486735 | ||||||
| chr2:221486753
|
T | C | 11 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0221others(8): Show | 11 | HG01361.hp1 HG02615.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.980-4063A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221486753 | ||||||
| chr2:221486892
|
T | G | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.980-4202A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221486892 | ||||||
| chr2:221487060
|
T | C | 1 | a0001c0001t0032g0251 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.980-4370A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221487060 | ||||||
| chr2:221487083
|
A | C | 1 | a0001c0004t0035g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.980-4393T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221487083 | ||||||
| chr2:221487139
|
CA | C | 138 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(135): Show | 138 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.980-4450delT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221487139 | ||||||
| chr2:221487169
|
A | G | 10 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0221others(7): Show | 10 | HG01361.hp1 HG02615.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.980-4479T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221487169 | ||||||
| chr2:221487219
|
C | G | 4 | a0001c0002t0001g0052a0001c0002t0001g0054a0001c0002t0001g0055others(1): Show | 4 | HG00738.hp1 HG01433.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.980-4529G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221487219 | ||||||
| chr2:221487368
|
C | T | 1 | a0001c0003t0003g0082 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.980-4678G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221487368 | ||||||
| chr2:221487685
|
C | T | 138 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(135): Show | 138 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.980-4995G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221487685 | ||||||
| chr2:221487720
|
A | G | 3 | a0001c0001t0001g0092a0001c0001t0040g0128a0001c0003t0003g0093 | 3 | HG02717.hp2 HG02723.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.980-5030T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221487720 | ||||||
| chr2:221487894
|
A | G | 10 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0221others(7): Show | 10 | HG01361.hp1 HG02615.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.980-5204T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221487894 | ||||||
| chr2:221487909
|
C | T | 143 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(140): Show | 143 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.980-5219G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221487909 | ||||||
| chr2:221487910
|
T | A | 1 | a0001c0001t0049g0227 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.980-5220A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221487910 | ||||||
| chr2:221487931
|
G | A | 1 | a0001c0004t0035g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.980-5241C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221487931 | ||||||
| chr2:221487992
|
G | A | 138 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(135): Show | 138 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.980-5302C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221487992 | ||||||
| chr2:221487995
|
G | A | 138 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(135): Show | 138 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.980-5305C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221487995 | ||||||
| chr2:221488025
|
A | T | 1 | a0001c0002t0028g0242 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.980-5335T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221488025 | ||||||
| chr2:221488044
|
A | G | 1 | a0001c0003t0001g0276 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.980-5354T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221488044 | ||||||
| chr2:221488139
|
T | G | 139 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(136): Show | 139 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.980-5449A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221488139 | ||||||
| chr2:221488183
|
C | T | 4 | a0001c0001t0004g0203a0001c0001t0014g0213a0001c0002t0023g0218others(1): Show | 4 | HG00673.hp1 HG01074.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.980-5493G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221488183 | ||||||
| chr2:221488294
|
C | T | 140 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(137): Show | 140 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.980-5604G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221488294 | ||||||
| chr2:221488667
|
T | C | 2 | a0001c0001t0002g0014a0001c0001t0002g0127 | 2 | HG01123.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.980-5977A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221488667 | ||||||
| chr2:221488693
|
G | A | 140 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(137): Show | 140 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.980-6003C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221488693 | ||||||
| chr2:221488698
|
C | T | 1 | a0001c0001t0001g0268 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.980-6008G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221488698 | ||||||
| chr2:221488721
|
A | G | 140 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(137): Show | 140 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.980-6031T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221488721 | ||||||
| chr2:221488788
|
G | A | 140 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(137): Show | 140 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.980-6098C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221488788 | ||||||
| chr2:221488891
|
T | C | 1 | a0001c0001t0001g0270 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.980-6201A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221488891 | ||||||
| chr2:221489041
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.980-6351C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221489041 | ||||||
| chr2:221489270
|
A | G | 1 | a0001c0001t0001g0262 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.980-6580T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221489270 | ||||||
| chr2:221489303
|
G | T | 2 | a0001c0001t0001g0036a0001c0001t0020g0077 | 2 | NA18991.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.980-6613C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221489303 | ||||||
| chr2:221489332
|
T | C | 30 | a0001c0001t0001g0106a0001c0001t0001g0112a0001c0001t0001g0190others(27): Show | 30 | HG00642.hp2 HG01975.hp2 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.980-6642A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221489332 | ||||||
| chr2:221489349
|
G | A | 1 | a0001c0001t0049g0227 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.980-6659C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221489349 | ||||||
| chr2:221489367
|
G | A | 10 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0221others(7): Show | 10 | HG01361.hp1 HG02615.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.980-6677C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221489367 | ||||||
| chr2:221489393
|
A | C | 32 | a0001c0001t0001g0038a0001c0001t0001g0260a0001c0001t0003g0289others(29): Show | 32 | HG00738.hp1 HG01109.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.980-6703T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221489393 | ||||||
| chr2:221489489
|
C | G | 2 | a0001c0001t0002g0215a0001c0001t0005g0216 | 2 | HG01071.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.980-6799G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221489489 | ||||||
| chr2:221489493
|
C | T | 141 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(138): Show | 141 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.980-6803G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221489493 | ||||||
| chr2:221489862
|
G | A | 32 | a0001c0001t0001g0038a0001c0001t0001g0260a0001c0001t0003g0289others(29): Show | 32 | HG00738.hp1 HG01109.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.980-7172C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221489862 | ||||||
| chr2:221489912
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.980-7222C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221489912 | ||||||
| chr2:221490005
|
G | T | 140 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(137): Show | 140 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.980-7315C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221490005 | ||||||
| chr2:221490145
|
C | CA | 6 | a0001c0001t0001g0041a0001c0001t0001g0253a0001c0001t0002g0223others(3): Show | 6 | HG02027.hp1 HG02895.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.980-7456dupT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221490145 | ||||||
| chr2:221490145
|
CA | C | 212 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(209): Show | 212 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.980-7456delT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221490145 | ||||||
| chr2:221490160
|
A | C | 2 | a0001c0001t0001g0092a0001c0001t0040g0128 | 2 | HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.980-7470T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221490160 | ||||||
| chr2:221490258
|
T | TA | 10 | a0001c0001t0008g0117a0001c0001t0008g0132a0001c0001t0008g0134others(7): Show | 10 | HG01884.hp1 HG02630.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.980-7569dupT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221490258 | ||||||
| chr2:221490258
|
TA | T | 13 | a0001c0001t0001g0022a0001c0001t0001g0081a0001c0001t0001g0092others(10): Show | 13 | HG01361.hp1 HG02165.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.980-7569delT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221490258 | ||||||
| chr2:221490753
|
G | C | 64 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0050others(61): Show | 64 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.980-8063C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221490753 | ||||||
| chr2:221490915
|
A | G | 1 | a0001c0002t0001g0195 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.980-8225T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221490915 | ||||||
| chr2:221491399
|
G | A | 141 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(138): Show | 141 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.980-8709C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221491399 | ||||||
| chr2:221491520
|
A | T | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.980-8830T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221491520 | ||||||
| chr2:221491738
|
G | A | 1 | a0001c0004t0035g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.980-9048C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221491738 | ||||||
| chr2:221492085
|
A | G | 1 | a0001c0003t0003g0281 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.979+8932T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221492085 | ||||||
| chr2:221492153
|
T | C | 2 | a0001c0001t0003g0289a0001c0006t0003g0118 | 2 | HG01109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.979+8864A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221492153 | ||||||
| chr2:221492372
|
T | A | 1 | a0001c0001t0049g0227 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.979+8645A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221492372 | ||||||
| chr2:221492515
|
T | C | 244 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(241): Show | 244 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.979+8502A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221492515 | ||||||
| chr2:221492606
|
G | T | 140 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(137): Show | 140 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.979+8411C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221492606 | ||||||
| chr2:221492684
|
G | A | 1 | a0001c0002t0029g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.979+8333C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221492684 | ||||||
| chr2:221492690
|
G | T | 4 | a0001c0001t0001g0121a0001c0001t0001g0184a0001c0001t0001g0193others(1): Show | 4 | HG00741.hp2 HG01081.hp1 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.979+8327C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221492690 | ||||||
| chr2:221493241
|
T | A | 141 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(138): Show | 141 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.979+7776A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221493241 | ||||||
| chr2:221493305
|
C | G | 1 | a0001c0001t0001g0007 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.979+7712G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221493305 | ||||||
| chr2:221493411
|
A | C | 2 | a0001c0001t0001g0287a0001c0001t0034g0243 | 2 | HG02257.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.979+7606T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221493411 | ||||||
| chr2:221493432
|
T | C | 1 | a0001c0001t0012g0275 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.979+7585A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221493432 | ||||||
| chr2:221493493
|
C | T | 1 | a0001c0001t0012g0275 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.979+7524G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221493493 | ||||||
| chr2:221493572
|
C | G | 212 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(209): Show | 212 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.979+7445G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221493572 | ||||||
| chr2:221493693
|
T | G | 1 | a0001c0001t0001g0225 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.979+7324A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221493693 | ||||||
| chr2:221493946
|
C | T | 1 | a0001c0001t0012g0275 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.979+7071G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221493946 | ||||||
| chr2:221493949
|
G | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0016others(3): Show | 6 | HG00558.hp1 HG02080.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.979+7068C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221493949 | ||||||
| chr2:221494055
|
C | T | 1 | a0001c0002t0028g0242 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.979+6962G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221494055 | ||||||
| chr2:221494082
|
C | G | 1 | a0001c0003t0003g0093 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.979+6935G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221494082 | ||||||
| chr2:221494087
|
C | T | 1 | a0001c0004t0035g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.979+6930G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221494087 | ||||||
| chr2:221494189
|
A | G | 39 | a0001c0001t0001g0036a0001c0001t0001g0062a0001c0001t0001g0063others(36): Show | 39 | HG00423.hp2 HG00558.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.979+6828T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221494189 | ||||||
| chr2:221494322
|
T | C | 65 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0050others(62): Show | 65 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.979+6695A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221494322 | ||||||
| chr2:221494329
|
T | G | 1 | a0001c0001t0001g0141 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.979+6688A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221494329 | ||||||
| chr2:221494362
|
G | A | 1 | a0001c0001t0012g0275 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.979+6655C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221494362 | ||||||
| chr2:221494379
|
G | A | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.979+6638C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221494379 | ||||||
| chr2:221494404
|
G | A | 1 | a0001c0001t0010g0110 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.979+6613C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221494404 | ||||||
| chr2:221494412
|
T | C | 2 | a0001c0001t0004g0203a0001c0001t0014g0213 | 2 | HG01074.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.979+6605A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221494412 | ||||||
| chr2:221494421
|
T | C | 1 | a0001c0001t0012g0275 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.979+6596A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221494421 | ||||||
| chr2:221494435
|
C | T | 140 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(137): Show | 140 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.979+6582G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221494435 | ||||||
| chr2:221494477
|
A | T | 1 | a0001c0001t0002g0136 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.979+6540T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221494477 | ||||||
| chr2:221494519
|
A | G | 1 | a0001c0001t0002g0158 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.979+6498T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221494519 | ||||||
| chr2:221494555
|
T | C | 266 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(263): Show | 266 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.979+6462A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221494555 | ||||||
| chr2:221494614
|
G | A | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.979+6403C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221494614 | ||||||
| chr2:221494623
|
A | G | 29 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(26): Show | 29 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.979+6394T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221494623 | ||||||
| chr2:221494635
|
A | G | 2 | a0001c0001t0003g0289a0001c0006t0003g0118 | 2 | HG01109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.979+6382T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221494635 | ||||||
| chr2:221494655
|
T | C | 3 | a0001c0003t0001g0276a0001c0003t0003g0281a0001c0003t0046g0278 | 3 | HG00741.hp1 HG02735.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.979+6362A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221494655 | ||||||
| chr2:221494854
|
C | T | 2 | a0001c0001t0001g0220a0001c0001t0010g0288 | 2 | HG00280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.979+6163G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221494854 | ||||||
| chr2:221494918
|
T | C | 1 | a0001c0003t0003g0082 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.979+6099A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221494918 | ||||||
| chr2:221495001
|
C | CA | 17 | a0001c0001t0001g0025a0001c0001t0001g0060a0001c0001t0002g0027others(14): Show | 17 | HG00423.hp1 HG00738.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.979+6015dupT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221495001 | ||||||
| chr2:221495001
|
CA | C | 136 | a0001c0001t0001g0007a0001c0001t0001g0036a0001c0001t0001g0050others(133): Show | 136 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.979+6015delT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221495001 | ||||||
| chr2:221495046
|
T | C | 1 | a0001c0001t0006g0004 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.979+5971A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221495046 | ||||||
| chr2:221495321
|
A | C | 4 | a0001c0001t0001g0260a0001c0002t0001g0047a0001c0002t0001g0048others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.979+5696T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221495321 | ||||||
| chr2:221495347
|
C | T | 1 | a0001c0001t0015g0244 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.979+5670G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221495347 | ||||||
| chr2:221495572
|
G | A | 1 | a0001c0001t0012g0275 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.979+5445C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221495572 | ||||||
| chr2:221495831
|
C | T | 1 | a0001c0001t0031g0046 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.979+5186G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221495831 | ||||||
| chr2:221496197
|
G | A | 1 | a0001c0001t0032g0251 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.979+4820C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221496197 | ||||||
| chr2:221496305
|
GGCTATTG others(14): Show |
G | 1 | a0001c0001t0015g0286 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.979+4691_979+4711d others(23): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221496305 | ||||||
| chr2:221496487
|
T | C | 2 | a0001c0001t0002g0215a0001c0001t0005g0216 | 2 | HG01071.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.979+4530A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221496487 | ||||||
| chr2:221496629
|
C | T | 1 | a0001c0001t0001g0012 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.979+4388G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221496629 | ||||||
| chr2:221496699
|
G | A | 26 | a0001c0001t0001g0038a0001c0001t0001g0260a0001c0001t0004g0235others(23): Show | 26 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.979+4318C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221496699 | ||||||
| chr2:221496737
|
A | G | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.979+4280T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221496737 | ||||||
| chr2:221496779
|
T | G | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.979+4238A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221496779 | ||||||
| chr2:221496903
|
C | T | 8 | a0001c0001t0004g0291a0001c0001t0006g0228a0001c0001t0010g0288others(5): Show | 8 | HG01891.hp1 HG02258.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.979+4114G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221496903 | ||||||
| chr2:221496926
|
G | C | 1 | a0001c0006t0003g0118 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.979+4091C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221496926 | ||||||
| chr2:221497026
|
G | A | 2 | a0001c0002t0023g0218a0001c0002t0023g0219 | 2 | HG00673.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.979+3991C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221497026 | ||||||
| chr2:221497070
|
TA | T | 285 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(282): Show | 285 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.979+3946delT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221497070 | ||||||
| chr2:221497142
|
A | G | 1 | a0001c0001t0001g0012 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.979+3875T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221497142 | ||||||
| chr2:221497170
|
C | T | 1 | a0001c0001t0010g0110 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.979+3847G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221497170 | ||||||
| chr2:221497239
|
C | T | 1 | a0001c0001t0009g0214 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.979+3778G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221497239 | ||||||
| chr2:221497363
|
G | A | 3 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0221 | 3 | HG01361.hp1 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.979+3654C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221497363 | ||||||
| chr2:221497375
|
G | A | 1 | a0001c0001t0002g0178 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.979+3642C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221497375 | ||||||
| chr2:221497394
|
C | G | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.979+3623G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221497394 | ||||||
| chr2:221497477
|
G | A | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.979+3540C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221497477 | ||||||
| chr2:221497522
|
T | G | 1 | a0001c0001t0049g0227 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.979+3495A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221497522 | ||||||
| chr2:221497542
|
C | T | 2 | a0001c0001t0002g0258a0001c0003t0003g0292 | 2 | HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.979+3475G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221497542 | ||||||
| chr2:221497673
|
T | C | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.979+3344A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221497673 | ||||||
| chr2:221497835
|
C | T | 1 | a0001c0001t0004g0235 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.979+3182G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221497835 | ||||||
| chr2:221497865
|
C | T | 1 | a0001c0001t0002g0158 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.979+3152G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221497865 | ||||||
| chr2:221497974
|
C | T | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.979+3043G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221497974 | ||||||
| chr2:221498092
|
G | A | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.979+2925C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221498092 | ||||||
| chr2:221498192
|
T | C | 1 | a0001c0001t0004g0235 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.979+2825A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221498192 | ||||||
| chr2:221498239
|
A | G | 1 | a0001c0001t0012g0275 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.979+2778T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221498239 | ||||||
| chr2:221498279
|
C | A | 140 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(137): Show | 140 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.979+2738G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221498279 | ||||||
| chr2:221498329
|
C | T | 1 | a0001c0002t0023g0218 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.979+2688G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221498329 | ||||||
| chr2:221498351
|
A | T | 1 | a0002c0011t0026g0109 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.979+2666T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221498351 | ||||||
| chr2:221498391
|
T | C | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.979+2626A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221498391 | ||||||
| chr2:221498609
|
T | A | 6 | a0001c0001t0001g0245a0001c0001t0002g0095a0001c0001t0002g0097others(3): Show | 6 | HG02615.hp2 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.979+2408A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221498609 | ||||||
| chr2:221498617
|
C | T | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.979+2400G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221498617 | ||||||
| chr2:221498779
|
A | AT | 7 | a0001c0001t0001g0245a0001c0001t0002g0095a0001c0001t0002g0097others(4): Show | 7 | HG02615.hp2 HG02809.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.979+2237dupA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221498779 | ||||||
| chr2:221498790
|
C | CT | 22 | a0001c0001t0001g0038a0001c0001t0001g0197a0001c0001t0001g0260others(19): Show | 22 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.979+2226dupA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221498790 | ||||||
| chr2:221498790
|
CTTTTTTT others(10): Show |
C | 64 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0068others(61): Show | 64 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.979+2210_979+2226d others(19): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221498790 | ||||||
| chr2:221498813
|
G | A | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.979+2204C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221498813 | ||||||
| chr2:221498834
|
T | C | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.979+2183A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221498834 | ||||||
| chr2:221498861
|
G | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0171 | 2 | NA19003.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.979+2156C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221498861 | ||||||
| chr2:221499115
|
A | C | 1 | a0001c0001t0001g0182 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.979+1902T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499115 | ||||||
| chr2:221499196
|
AGAATAAT others(9): Show |
A | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.979+1805_979+1820d others(18): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499196 | ||||||
| chr2:221499228
|
T | G | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.979+1789A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499228 | ||||||
| chr2:221499353
|
T | G | 1 | a0001c0001t0002g0158 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.979+1664A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499353 | ||||||
| chr2:221499646
|
G | T | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.979+1371C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499646 | ||||||
| chr2:221499670
|
T | C | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.979+1347A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499670 | ||||||
| chr2:221499676
|
G | A | 5 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0196others(2): Show | 5 | HG00639.hp2 HG00733.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.979+1341C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499676 | ||||||
| chr2:221499679
|
A | G | 1 | a0001c0001t0020g0173 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.979+1338T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499679 | ||||||
| chr2:221499715
|
A | AAT | 11 | a0001c0001t0001g0155a0001c0001t0001g0180a0001c0001t0001g0181others(8): Show | 11 | HG01169.hp1 HG01433.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.979+1300_979+1301d others(4): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499715 | ||||||
| chr2:221499715
|
A | AATAT | 4 | a0001c0001t0001g0197a0001c0001t0002g0199a0001c0001t0003g0279others(1): Show | 4 | HG01981.hp2 HG02602.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.979+1298_979+1301d others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499715 | ||||||
| chr2:221499715
|
AAT | A | 12 | a0001c0001t0001g0177a0001c0001t0001g0190a0001c0001t0001g0205others(9): Show | 12 | HG00639.hp2 HG00642.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.979+1300_979+1301d others(4): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499715 | ||||||
| chr2:221499715
|
AATAT | A | 11 | a0001c0001t0001g0007a0001c0001t0001g0112a0001c0001t0001g0287others(8): Show | 11 | HG00673.hp2 HG01106.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.979+1298_979+1301d others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499715 | ||||||
| chr2:221499715
|
AATATAT | A | 29 | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0001g0140others(26): Show | 29 | HG00408.hp2 HG00544.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.979+1296_979+1301d others(8): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499715 | ||||||
| chr2:221499715
|
AATATATA others(1): Show |
A | 28 | a0001c0001t0001g0036a0001c0001t0001g0062a0001c0001t0001g0063others(25): Show | 28 | HG00423.hp2 HG00558.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.979+1294_979+1301d others(10): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499715 | ||||||
| chr2:221499715
|
AATATATA others(3): Show |
A | 1 | a0001c0002t0028g0242 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.979+1292_979+1301d others(12): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499715 | ||||||
| chr2:221499715
|
AATATATA others(7): Show |
A | 2 | a0001c0001t0006g0004a0001c0007t0005g0061 | 2 | NA18948.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.979+1288_979+1301d others(16): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499715 | ||||||
| chr2:221499715
|
AATATATA others(11): Show |
A | 1 | a0001c0001t0001g0260 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.979+1284_979+1301d others(20): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499715 | ||||||
| chr2:221499723
|
T | C | 1 | a0001c0001t0002g0067 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.979+1294A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499723 | ||||||
| chr2:221499738
|
ATATATAT others(13): Show |
A | 2 | a0001c0002t0001g0163a0001c0002t0047g0229 | 2 | NA18973.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.979+1259_979+1278d others(22): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499738 | ||||||
| chr2:221499739
|
TATATATA others(6): Show |
T | 1 | a0001c0001t0005g0145 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.979+1265_979+1277d others(15): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499739 | ||||||
| chr2:221499739
|
TATATATA others(8): Show |
T | 3 | a0001c0001t0004g0003a0001c0001t0005g0001a0001c0001t0005g0143 | 3 | HG02015.hp1 HG02080.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.979+1263_979+1277d others(17): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499739 | ||||||
| chr2:221499742
|
ATATATAT others(9): Show |
A | 2 | a0001c0001t0001g0022a0001c0001t0004g0057 | 2 | HG02071.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.979+1259_979+1274d others(18): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499742 | ||||||
| chr2:221499744
|
ATATATAT others(14): Show |
A | 2 | a0001c0001t0036g0115a0001c0003t0003g0114 | 2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.979+1252_979+1272d others(23): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499744 | ||||||
| chr2:221499745
|
TATATA | T | 8 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0222others(5): Show | 8 | HG00544.hp1 HG02273.hp2 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.979+1267_979+1271d others(7): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499745 | ||||||
| chr2:221499745
|
TATATATA | T | 8 | a0001c0001t0001g0121a0001c0001t0001g0183a0001c0001t0001g0193others(5): Show | 8 | HG00639.hp1 HG00741.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.979+1265_979+1271d others(9): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499745 | ||||||
| chr2:221499745
|
TATATATA others(2): Show |
T | 5 | a0001c0001t0001g0151a0001c0001t0001g0208a0001c0001t0006g0238others(2): Show | 5 | HG02129.hp1 HG02129.hp2 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.979+1263_979+1271d others(11): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499745 | ||||||
| chr2:221499746
|
ATATATAT others(4): Show |
A | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.979+1260_979+1270d others(13): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499746 | ||||||
| chr2:221499746
|
ATATATAT others(6): Show |
A | 1 | a0001c0001t0049g0227 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.979+1258_979+1270d others(15): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499746 | ||||||
| chr2:221499747
|
TATATA | T | 14 | a0001c0001t0001g0069a0001c0001t0001g0141a0001c0001t0001g0148others(11): Show | 14 | HG02027.hp2 HG02071.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.979+1265_979+1269d others(7): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499747 | ||||||
| chr2:221499747
|
TATATATA | T | 5 | a0001c0001t0001g0171a0001c0001t0001g0187a0001c0001t0001g0207others(2): Show | 5 | HG02145.hp2 HG03516.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.979+1263_979+1269d others(9): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499747 | ||||||
| chr2:221499748
|
A | T | 3 | a0001c0001t0001g0205a0001c0001t0001g0217a0001c0010t0001g0176 | 3 | HG01891.hp2 NA19068.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.979+1269T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499748 | ||||||
| chr2:221499750
|
A | T | 6 | a0001c0001t0001g0120a0001c0001t0001g0205a0001c0001t0001g0211others(3): Show | 6 | HG00408.hp1 HG01243.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.979+1267T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499750 | ||||||
| chr2:221499750
|
ATATATAT others(3): Show |
A | 4 | a0001c0001t0006g0228a0001c0001t0013g0290a0001c0001t0015g0244others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.979+1257_979+1266d others(12): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499750 | ||||||
| chr2:221499751
|
TATA | T | 3 | a0001c0001t0002g0178a0001c0001t0040g0128a0001c0003t0003g0093 | 3 | HG02717.hp2 HG02723.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.979+1263_979+1265d others(5): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499751 | ||||||
| chr2:221499752
|
A | AT | 4 | a0001c0001t0001g0172a0001c0001t0002g0136a0001c0001t0002g0179others(1): Show | 4 | HG00735.hp1 HG01071.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.979+1264dupA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499752 | ||||||
| chr2:221499752
|
A | T | 19 | a0001c0001t0001g0033a0001c0001t0001g0050a0001c0001t0001g0068others(16): Show | 19 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.979+1265T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499752 | ||||||
| chr2:221499752
|
ATATAT | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0060a0001c0001t0005g0009others(4): Show | 7 | HG00558.hp1 HG02895.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.979+1260_979+1264d others(7): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499752 | ||||||
| chr2:221499752
|
ATATATT | A | 24 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0017others(21): Show | 24 | HG00423.hp1 HG00735.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.979+1259_979+1264d others(8): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499752 | ||||||
| chr2:221499752
|
ATATATTT others(3): Show |
A | 3 | a0001c0001t0009g0212a0001c0001t0034g0243a0001c0002t0004g0234 | 3 | HG02258.hp1 HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.979+1255_979+1264d others(12): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499752 | ||||||
| chr2:221499754
|
A | T | 108 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0036others(105): Show | 108 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.979+1263T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499754 | ||||||
| chr2:221499754
|
ATATT | A | 9 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0002g0027others(6): Show | 9 | HG00642.hp1 HG00738.hp1 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.979+1259_979+1262d others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499754 | ||||||
| chr2:221499754
|
ATATTTTT others(3): Show |
A | 2 | a0001c0002t0012g0099a0001c0002t0012g0101 | 2 | HG02280.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.979+1253_979+1262d others(12): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499754 | ||||||
| chr2:221499756
|
A | ATT | 7 | a0001c0001t0001g0042a0001c0001t0001g0253a0001c0001t0002g0254others(4): Show | 7 | HG00741.hp1 HG02027.hp1 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.979+1259_979+1260d others(4): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499756 | ||||||
| chr2:221499756
|
A | T | 146 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0033others(143): Show | 146 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.979+1261T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499756 | ||||||
| chr2:221499758
|
T | A | 8 | a0001c0001t0001g0038a0001c0001t0001g0197a0001c0001t0004g0285others(5): Show | 8 | HG01433.hp1 HG01981.hp1 HG03704.hp2 others(5): Show |
intron_variant | MODIFIER | c.979+1259A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499758 | ||||||
| chr2:221499759
|
T | A | 5 | a0001c0001t0001g0245a0001c0001t0004g0235a0001c0002t0001g0159others(2): Show | 5 | HG01884.hp2 HG02145.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.979+1258A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499759 | ||||||
| chr2:221499760
|
T | A | 2 | a0001c0001t0001g0197a0001c0005t0014g0040 | 2 | HG03834.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.979+1257A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499760 | ||||||
| chr2:221499761
|
T | A | 2 | a0001c0001t0004g0235a0001c0009t0002g0094 | 2 | HG02145.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.979+1256A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499761 | ||||||
| chr2:221499798
|
C | T | 1 | a0001c0001t0002g0185 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.979+1219G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499798 | ||||||
| chr2:221499821
|
G | A | 3 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0221 | 3 | HG01361.hp1 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.979+1196C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499821 | ||||||
| chr2:221499946
|
G | A | 1 | a0001c0001t0041g0122 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.979+1071C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221499946 | ||||||
| chr2:221500018
|
A | G | 1 | a0001c0001t0005g0116 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.979+999T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221500018 | ||||||
| chr2:221500160
|
A | G | 2 | a0001c0001t0049g0227a0001c0002t0029g0269 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.979+857T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221500160 | ||||||
| chr2:221500368
|
G | C | 2 | a0001c0001t0049g0227a0001c0002t0029g0269 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.979+649C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221500368 | ||||||
| chr2:221500422
|
G | A | 6 | a0001c0001t0004g0235a0001c0001t0006g0246a0001c0001t0036g0115others(3): Show | 6 | HG02145.hp1 HG02280.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.979+595C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221500422 | ||||||
| chr2:221500663
|
G | A | 7 | a0001c0001t0001g0245a0001c0001t0002g0095a0001c0001t0002g0097others(4): Show | 7 | HG02615.hp2 HG02809.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.979+354C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221500663 | ||||||
| chr2:221500857
|
C | G | 1 | a0001c0002t0028g0242 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.979+160G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221500857 | ||||||
| chr2:221500902
|
T | G | 8 | a0001c0001t0001g0245a0001c0001t0002g0095a0001c0001t0002g0097others(5): Show | 8 | HG02615.hp2 HG02809.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.979+115A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 4/17 | chr2 | 221500902 | ||||||
| chr2:221501218
|
T | C | 18 | a0001c0001t0001g0038a0001c0001t0001g0260a0001c0001t0031g0046others(15): Show | 18 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.824-46A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221501218 | ||||||
| chr2:221501254
|
T | C | 29 | a0001c0001t0001g0038a0001c0001t0001g0260a0001c0001t0004g0235others(26): Show | 29 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.824-82A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221501254 | ||||||
| chr2:221501490
|
G | A | 1 | a0001c0003t0003g0281 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.824-318C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221501490 | ||||||
| chr2:221501667
|
T | C | 13 | a0001c0001t0001g0245a0001c0001t0002g0095a0001c0001t0002g0097others(10): Show | 13 | HG02145.hp1 HG02615.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.824-495A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221501667 | ||||||
| chr2:221501735
|
G | A | 46 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(43): Show | 46 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.824-563C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221501735 | ||||||
| chr2:221501745
|
T | C | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.824-573A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221501745 | ||||||
| chr2:221501750
|
C | T | 2 | a0001c0001t0003g0289a0001c0006t0003g0118 | 2 | HG01109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.824-578G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221501750 | ||||||
| chr2:221501771
|
C | T | 2 | a0001c0003t0001g0030a0001c0003t0001g0031 | 2 | HG00280.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.824-599G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221501771 | ||||||
| chr2:221501793
|
G | C | 2 | a0001c0001t0003g0289a0001c0006t0003g0118 | 2 | HG01109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.824-621C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221501793 | ||||||
| chr2:221501892
|
A | T | 7 | a0001c0001t0001g0245a0001c0001t0002g0095a0001c0001t0002g0097others(4): Show | 7 | HG02615.hp2 HG02809.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.824-720T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221501892 | ||||||
| chr2:221501911
|
C | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(85): Show | 88 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.824-739G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221501911 | ||||||
| chr2:221501980
|
C | A | 1 | a0001c0001t0001g0171 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.824-808G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221501980 | ||||||
| chr2:221502008
|
G | A | 45 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(42): Show | 45 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.824-836C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221502008 | ||||||
| chr2:221502198
|
A | G | 39 | a0001c0001t0001g0036a0001c0001t0001g0062a0001c0001t0001g0063others(36): Show | 39 | HG00423.hp2 HG00558.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.824-1026T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221502198 | ||||||
| chr2:221502278
|
T | C | 1 | a0001c0001t0002g0005 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.824-1106A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221502278 | ||||||
| chr2:221502367
|
A | G | 4 | a0001c0001t0001g0260a0001c0002t0001g0047a0001c0002t0001g0048others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.824-1195T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221502367 | ||||||
| chr2:221502419
|
A | G | 2 | a0001c0003t0001g0030a0001c0003t0001g0031 | 2 | HG00280.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.824-1247T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221502419 | ||||||
| chr2:221502484
|
G | A | 1 | a0001c0001t0012g0275 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.824-1312C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221502484 | ||||||
| chr2:221502518
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.824-1346G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221502518 | ||||||
| chr2:221502763
|
G | A | 130 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(127): Show | 130 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.824-1591C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221502763 | ||||||
| chr2:221502879
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.824-1707G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221502879 | ||||||
| chr2:221503266
|
C | T | 1 | a0001c0001t0038g0102 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.824-2094G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221503266 | ||||||
| chr2:221503396
|
GACT | G | 19 | a0001c0001t0001g0038a0001c0001t0001g0260a0001c0001t0031g0046others(16): Show | 19 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.824-2227_824-2225d others(5): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221503396 | ||||||
| chr2:221503553
|
A | G | 1 | a0001c0001t0001g0007 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.824-2381T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221503553 | ||||||
| chr2:221503563
|
G | A | 1 | a0001c0001t0002g0014 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.824-2391C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221503563 | ||||||
| chr2:221503644
|
T | C | 6 | a0001c0001t0001g0245a0001c0001t0002g0095a0001c0001t0002g0097others(3): Show | 6 | HG02615.hp2 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.824-2472A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221503644 | ||||||
| chr2:221503690
|
T | C | 1 | a0001c0001t0002g0206 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.824-2518A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221503690 | ||||||
| chr2:221503736
|
G | A | 5 | a0001c0001t0008g0117a0001c0001t0008g0132a0001c0001t0008g0134others(2): Show | 5 | HG01884.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.824-2564C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221503736 | ||||||
| chr2:221503741
|
C | G | 1 | a0001c0002t0007g0239 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.824-2569G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221503741 | ||||||
| chr2:221503836
|
T | C | 19 | a0001c0001t0001g0038a0001c0001t0001g0260a0001c0001t0031g0046others(16): Show | 19 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.824-2664A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221503836 | ||||||
| chr2:221503842
|
C | CT | 22 | a0001c0001t0001g0038a0001c0001t0001g0260a0001c0001t0018g0113others(19): Show | 22 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.824-2671dupA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221503842 | ||||||
| chr2:221504079
|
G | T | 9 | a0001c0001t0001g0287a0001c0001t0004g0291a0001c0001t0006g0228others(6): Show | 9 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.824-2907C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221504079 | ||||||
| chr2:221504118
|
C | A | 1 | a0001c0001t0001g0068 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.824-2946G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221504118 | ||||||
| chr2:221504190
|
A | T | 1 | a0001c0001t0009g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.824-3018T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221504190 | ||||||
| chr2:221504195
|
T | A | 1 | a0001c0010t0001g0176 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.824-3023A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221504195 | ||||||
| chr2:221504265
|
C | T | 265 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(262): Show | 265 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.824-3093G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221504265 | ||||||
| chr2:221504344
|
T | TGGAGGAG others(8): Show |
85 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(82): Show | 85 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.824-3187_824-3173d others(17): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221504344 | ||||||
| chr2:221504450
|
T | C | 2 | a0001c0001t0009g0212a0001c0012t0018g0272 | 2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.824-3278A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221504450 | ||||||
| chr2:221504537
|
TTTTATA | T | 7 | a0001c0001t0001g0287a0001c0001t0004g0291a0001c0001t0013g0290others(4): Show | 7 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-3371_824-3366d others(8): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221504537 | ||||||
| chr2:221504539
|
TTA | T | 29 | a0001c0001t0001g0080a0001c0001t0001g0092a0001c0001t0001g0192others(26): Show | 29 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.824-3369_824-3368d others(4): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221504539 | ||||||
| chr2:221504539
|
TTATA | T | 18 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0152others(15): Show | 18 | HG00639.hp1 HG01109.hp2 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.824-3371_824-3368d others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221504539 | ||||||
| chr2:221504539
|
TTATATA | T | 238 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(235): Show | 238 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.824-3373_824-3368d others(8): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221504539 | ||||||
| chr2:221504833
|
T | A | 9 | a0001c0001t0001g0287a0001c0001t0004g0291a0001c0001t0006g0228others(6): Show | 9 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.824-3661A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221504833 | ||||||
| chr2:221505056
|
T | C | 96 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0050others(93): Show | 96 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.824-3884A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221505056 | ||||||
| chr2:221505150
|
A | G | 253 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(250): Show | 253 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.824-3978T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221505150 | ||||||
| chr2:221505156
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.824-3984C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221505156 | ||||||
| chr2:221505190
|
C | T | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.824-4018G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221505190 | ||||||
| chr2:221505199
|
C | A | 9 | a0001c0001t0001g0092a0001c0001t0004g0235a0001c0001t0006g0246others(6): Show | 9 | HG02145.hp1 HG02280.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.824-4027G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221505199 | ||||||
| chr2:221505338
|
T | A | 188 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(185): Show | 188 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.824-4166A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221505338 | ||||||
| chr2:221505570
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.824-4398G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221505570 | ||||||
| chr2:221505576
|
G | A | 1 | a0001c0003t0003g0082 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.824-4404C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221505576 | ||||||
| chr2:221505670
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.824-4498T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221505670 | ||||||
| chr2:221506400
|
C | G | 119 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(116): Show | 119 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.824-5228G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221506400 | ||||||
| chr2:221506549
|
C | T | 1 | a0001c0001t0006g0228 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.824-5377G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221506549 | ||||||
| chr2:221506582
|
T | C | 1 | a0001c0001t0003g0266 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.824-5410A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221506582 | ||||||
| chr2:221506760
|
A | G | 2 | a0001c0001t0018g0113a0001c0004t0035g0108 | 2 | HG02055.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.824-5588T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221506760 | ||||||
| chr2:221506852
|
A | T | 7 | a0001c0001t0001g0092a0001c0001t0002g0178a0001c0001t0002g0248others(4): Show | 7 | HG02055.hp1 HG02572.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.824-5680T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221506852 | ||||||
| chr2:221506972
|
G | C | 2 | a0001c0001t0018g0113a0001c0004t0035g0108 | 2 | HG02055.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.824-5800C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221506972 | ||||||
| chr2:221507051
|
T | C | 1 | a0001c0001t0001g0062 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.824-5879A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221507051 | ||||||
| chr2:221507198
|
C | A | 7 | a0001c0001t0004g0291a0001c0001t0006g0228a0001c0001t0010g0288others(4): Show | 7 | HG01891.hp1 HG02258.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-6026G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221507198 | ||||||
| chr2:221507243
|
A | G | 3 | a0001c0001t0012g0275a0001c0001t0018g0113a0001c0004t0035g0108 | 3 | HG02055.hp1 HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.824-6071T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221507243 | ||||||
| chr2:221507268
|
C | T | 1 | a0001c0002t0001g0054 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.824-6096G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221507268 | ||||||
| chr2:221507405
|
C | G | 117 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(114): Show | 117 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.824-6233G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221507405 | ||||||
| chr2:221507434
|
A | G | 3 | a0001c0001t0012g0275a0001c0001t0018g0113a0001c0004t0035g0108 | 3 | HG02055.hp1 HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.824-6262T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221507434 | ||||||
| chr2:221507532
|
T | C | 3 | a0001c0001t0012g0275a0001c0001t0018g0113a0001c0004t0035g0108 | 3 | HG02055.hp1 HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.824-6360A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221507532 | ||||||
| chr2:221507570
|
T | A | 1 | a0001c0001t0001g0294 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.824-6398A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221507570 | ||||||
| chr2:221508305
|
G | A | 4 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0196others(1): Show | 4 | HG00639.hp2 HG00733.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-7133C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221508305 | ||||||
| chr2:221508443
|
A | T | 3 | a0001c0001t0037g0100a0001c0002t0012g0099a0001c0002t0012g0101 | 3 | HG02280.hp1 HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.824-7271T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221508443 | ||||||
| chr2:221508586
|
G | GA | 43 | a0001c0001t0001g0062a0001c0001t0001g0065a0001c0001t0001g0068others(40): Show | 43 | HG00423.hp2 HG00544.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.824-7415dupT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221508586 | ||||||
| chr2:221508586
|
GA | G | 114 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0041others(111): Show | 114 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.824-7415delT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221508586 | ||||||
| chr2:221508755
|
G | T | 1 | a0001c0001t0012g0275 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.824-7583C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221508755 | ||||||
| chr2:221508802
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.824-7630T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221508802 | ||||||
| chr2:221508902
|
A | G | 2 | a0001c0001t0002g0044a0001c0002t0001g0195 | 2 | HG00558.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.824-7730T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221508902 | ||||||
| chr2:221508905
|
C | CTG | 266 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(263): Show | 266 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.824-7735_824-7734d others(4): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221508905 | ||||||
| chr2:221509080
|
C | G | 265 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(262): Show | 265 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.824-7908G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221509080 | ||||||
| chr2:221509227
|
C | A | 6 | a0001c0001t0001g0245a0001c0001t0002g0095a0001c0001t0002g0097others(3): Show | 6 | HG02615.hp2 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.824-8055G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221509227 | ||||||
| chr2:221509231
|
G | C | 110 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0062others(107): Show | 110 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.824-8059C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221509231 | ||||||
| chr2:221509360
|
C | T | 2 | a0001c0001t0049g0227a0001c0002t0029g0269 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.824-8188G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221509360 | ||||||
| chr2:221509477
|
A | G | 2 | a0001c0001t0018g0113a0001c0004t0035g0108 | 2 | HG02055.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.824-8305T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221509477 | ||||||
| chr2:221509703
|
T | C | 147 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(144): Show | 147 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.824-8531A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221509703 | ||||||
| chr2:221509827
|
G | T | 4 | a0001c0001t0011g0240a0001c0001t0011g0241a0001c0001t0015g0244others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.824-8655C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221509827 | ||||||
| chr2:221509979
|
G | C | 110 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0062others(107): Show | 110 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.824-8807C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221509979 | ||||||
| chr2:221510159
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.824-8987C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221510159 | ||||||
| chr2:221510246
|
T | C | 7 | a0001c0001t0001g0245a0001c0001t0002g0095a0001c0001t0002g0097others(4): Show | 7 | HG02615.hp2 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-9074A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221510246 | ||||||
| chr2:221510550
|
G | C | 1 | a0001c0001t0010g0110 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.824-9378C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221510550 | ||||||
| chr2:221510902
|
A | G | 1 | a0001c0010t0001g0176 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.824-9730T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221510902 | ||||||
| chr2:221510927
|
T | G | 1 | a0001c0001t0001g0294 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.824-9755A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221510927 | ||||||
| chr2:221510959
|
A | G | 1 | a0001c0001t0040g0128 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.824-9787T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221510959 | ||||||
| chr2:221511052
|
G | A | 2 | a0001c0001t0018g0113a0001c0004t0035g0108 | 2 | HG02055.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.824-9880C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221511052 | ||||||
| chr2:221511271
|
T | C | 6 | a0001c0001t0008g0117a0001c0001t0008g0132a0001c0001t0008g0134others(3): Show | 6 | HG01884.hp1 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.824-10099A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221511271 | ||||||
| chr2:221511330
|
G | C | 1 | a0001c0001t0001g0200 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.824-10158C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221511330 | ||||||
| chr2:221511456
|
G | GTTTCTGT others(33): Show |
32 | a0001c0001t0001g0062a0001c0001t0001g0065a0001c0001t0001g0068others(29): Show | 32 | HG00423.hp2 HG00544.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.824-10324_824-1028 others(44): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221511456 | ||||||
| chr2:221511456
|
GTTTCTGT others(13): Show |
G | 2 | a0001c0004t0019g0236a0001c0004t0019g0237 | 2 | HG01243.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.824-10304_824-1028 others(24): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221511456 | ||||||
| chr2:221511514
|
C | T | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.824-10342G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221511514 | ||||||
| chr2:221511864
|
C | G | 1 | a0001c0001t0001g0294 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.824-10692G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221511864 | ||||||
| chr2:221511901
|
C | A | 2 | a0001c0001t0049g0227a0001c0002t0029g0269 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.824-10729G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221511901 | ||||||
| chr2:221512495
|
A | G | 2 | a0001c0001t0018g0113a0001c0004t0035g0108 | 2 | HG02055.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.824-11323T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221512495 | ||||||
| chr2:221512689
|
C | T | 32 | a0001c0001t0001g0062a0001c0001t0001g0065a0001c0001t0001g0068others(29): Show | 32 | HG00423.hp2 HG00544.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.824-11517G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221512689 | ||||||
| chr2:221513185
|
C | A | 115 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(112): Show | 115 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.824-12013G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221513185 | ||||||
| chr2:221513413
|
C | T | 2 | a0001c0001t0018g0113a0001c0004t0035g0108 | 2 | HG02055.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.824-12241G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221513413 | ||||||
| chr2:221513536
|
G | A | 264 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(261): Show | 264 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.824-12364C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221513536 | ||||||
| chr2:221513731
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.824-12559C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221513731 | ||||||
| chr2:221513919
|
A | C | 1 | a0001c0003t0001g0086 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.824-12747T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221513919 | ||||||
| chr2:221514006
|
C | A | 15 | a0001c0001t0001g0080a0001c0001t0001g0220a0001c0001t0001g0282others(12): Show | 15 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.824-12834G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221514006 | ||||||
| chr2:221514091
|
G | C | 2 | a0001c0001t0018g0113a0001c0004t0035g0108 | 2 | HG02055.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.824-12919C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221514091 | ||||||
| chr2:221514093
|
G | GA | 105 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0062others(102): Show | 105 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.824-12922_824-1292 others(5): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221514093 | ||||||
| chr2:221514093
|
GGA | G | 100 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(97): Show | 100 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.824-12923_824-1292 others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221514093 | ||||||
| chr2:221514094
|
GA | G | 42 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0025others(39): Show | 42 | HG00738.hp1 HG01123.hp2 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.824-12923delT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221514094 | ||||||
| chr2:221514095
|
A | G | 118 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0038others(115): Show | 118 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.824-12923T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221514095 | ||||||
| chr2:221514096
|
G | T | 2 | a0001c0001t0006g0246a0001c0001t0044g0232 | 2 | HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.824-12924C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221514096 | ||||||
| chr2:221514098
|
G | A | 2 | a0001c0001t0018g0113a0001c0004t0035g0108 | 2 | HG02055.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.824-12926C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221514098 | ||||||
| chr2:221514200
|
T | A | 2 | a0001c0004t0019g0236a0001c0004t0019g0237 | 2 | HG01243.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.824-13028A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221514200 | ||||||
| chr2:221514274
|
G | A | 119 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(116): Show | 119 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.824-13102C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221514274 | ||||||
| chr2:221514293
|
G | A | 1 | a0001c0001t0004g0291 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.824-13121C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221514293 | ||||||
| chr2:221514591
|
G | A | 2 | a0001c0004t0019g0236a0001c0004t0019g0237 | 2 | HG01243.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.824-13419C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221514591 | ||||||
| chr2:221514672
|
G | A | 33 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(30): Show | 33 | HG00423.hp2 HG00544.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.824-13500C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221514672 | ||||||
| chr2:221514769
|
A | C | 109 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0062others(106): Show | 109 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.824-13597T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221514769 | ||||||
| chr2:221515010
|
T | C | 1 | a0001c0001t0001g0155 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.824-13838A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221515010 | ||||||
| chr2:221515159
|
G | A | 6 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0037others(3): Show | 6 | NA18977.hp2 NA18993.hp1 NA19003.hp2 others(3): Show |
intron_variant | MODIFIER | c.824-13987C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221515159 | ||||||
| chr2:221515169
|
C | G | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.824-13997G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221515169 | ||||||
| chr2:221515198
|
C | T | 2 | a0001c0001t0049g0227a0001c0002t0029g0269 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.824-14026G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221515198 | ||||||
| chr2:221515269
|
A | G | 1 | a0001c0004t0035g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.824-14097T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221515269 | ||||||
| chr2:221515441
|
T | C | 1 | a0001c0001t0004g0291 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.824-14269A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221515441 | ||||||
| chr2:221515651
|
C | G | 4 | a0001c0001t0002g0075a0001c0001t0007g0076a0001c0001t0007g0078others(1): Show | 4 | NA18989.hp1 NA18991.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-14479G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221515651 | ||||||
| chr2:221515909
|
T | G | 2 | a0001c0003t0001g0030a0001c0003t0001g0031 | 2 | HG00280.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.824-14737A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221515909 | ||||||
| chr2:221515960
|
G | GA | 176 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(173): Show | 176 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.824-14789dupT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221515960 | ||||||
| chr2:221515960
|
G | GAA | 10 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0002g0008others(7): Show | 10 | HG00558.hp1 HG01884.hp1 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.824-14790_824-1478 others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221515960 | ||||||
| chr2:221515961
|
A | G | 36 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(33): Show | 36 | HG00423.hp2 HG00544.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.824-14789T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221515961 | ||||||
| chr2:221515962
|
A | G | 2 | a0001c0001t0002g0014a0001c0001t0007g0201 | 2 | HG02300.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.824-14790T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221515962 | ||||||
| chr2:221516080
|
G | A | 71 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0120others(68): Show | 71 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.824-14908C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221516080 | ||||||
| chr2:221516168
|
A | G | 195 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(192): Show | 195 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.824-14996T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221516168 | ||||||
| chr2:221516352
|
A | AT | 7 | a0001c0001t0002g0147a0001c0001t0002g0206a0001c0003t0001g0085others(4): Show | 7 | HG00741.hp1 HG01169.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-15181dupA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221516352 | ||||||
| chr2:221516352
|
AT | A | 155 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(152): Show | 155 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.824-15181delA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221516352 | ||||||
| chr2:221516421
|
C | G | 1 | a0001c0001t0012g0275 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.824-15249G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221516421 | ||||||
| chr2:221516508
|
C | T | 195 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(192): Show | 195 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.824-15336G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221516508 | ||||||
| chr2:221516601
|
C | T | 3 | a0001c0001t0001g0222a0001c0001t0002g0175a0001c0001t0002g0210 | 3 | NA18956.hp1 NA18998.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.824-15429G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221516601 | ||||||
| chr2:221516739
|
A | C | 1 | a0001c0001t0017g0098 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.824-15567T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221516739 | ||||||
| chr2:221517043
|
G | A | 25 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0037others(22): Show | 25 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.824-15871C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221517043 | ||||||
| chr2:221517123
|
G | A | 2 | a0001c0004t0019g0236a0001c0004t0019g0237 | 2 | HG01243.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.824-15951C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221517123 | ||||||
| chr2:221517213
|
A | G | 8 | a0001c0001t0001g0287a0001c0001t0004g0291a0001c0001t0006g0228others(5): Show | 8 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.824-16041T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221517213 | ||||||
| chr2:221517452
|
G | C | 1 | a0001c0001t0001g0062 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.824-16280C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221517452 | ||||||
| chr2:221517571
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.824-16399C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221517571 | ||||||
| chr2:221517646
|
T | A | 262 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(259): Show | 262 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.824-16474A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221517646 | ||||||
| chr2:221517787
|
C | T | 1 | a0001c0002t0001g0039 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.824-16615G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221517787 | ||||||
| chr2:221517868
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.824-16696C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221517868 | ||||||
| chr2:221518045
|
G | A | 1 | a0001c0001t0003g0279 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.824-16873C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221518045 | ||||||
| chr2:221518247
|
A | G | 2 | a0001c0001t0012g0275a0001c0003t0003g0093 | 2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.824-17075T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221518247 | ||||||
| chr2:221518511
|
C | T | 27 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0037others(24): Show | 27 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.824-17339G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221518511 | ||||||
| chr2:221518546
|
T | C | 1 | a0001c0001t0001g0294 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.824-17374A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221518546 | ||||||
| chr2:221518549
|
G | A | 1 | a0001c0001t0009g0214 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.824-17377C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221518549 | ||||||
| chr2:221518997
|
A | G | 1 | a0001c0001t0001g0025 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.824-17825T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221518997 | ||||||
| chr2:221519065
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.824-17893C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221519065 | ||||||
| chr2:221519263
|
C | A | 222 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(219): Show | 222 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.824-18091G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221519263 | ||||||
| chr2:221519296
|
T | C | 1 | a0001c0001t0001g0294 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.824-18124A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221519296 | ||||||
| chr2:221519378
|
G | A | 1 | a0001c0001t0003g0279 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.824-18206C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221519378 | ||||||
| chr2:221519592
|
C | T | 5 | a0001c0001t0004g0235a0001c0001t0036g0115a0001c0002t0004g0234others(2): Show | 5 | HG02145.hp1 HG03041.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.824-18420G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221519592 | ||||||
| chr2:221519760
|
A | C | 158 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(155): Show | 158 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.824-18588T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221519760 | ||||||
| chr2:221519821
|
T | C | 1 | a0001c0001t0002g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.824-18649A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221519821 | ||||||
| chr2:221519968
|
C | T | 1 | a0001c0001t0040g0128 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.824-18796G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221519968 | ||||||
| chr2:221519969
|
G | A | 1 | a0001c0001t0004g0285 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.824-18797C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221519969 | ||||||
| chr2:221520252
|
C | T | 26 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0037others(23): Show | 26 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.824-19080G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221520252 | ||||||
| chr2:221520397
|
C | A | 26 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0037others(23): Show | 26 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.824-19225G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221520397 | ||||||
| chr2:221520504
|
AACCACAC others(4): Show |
A | 1 | a0001c0001t0002g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.824-19343_824-1933 others(15): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221520504 | ||||||
| chr2:221520506
|
CCA | C | 74 | a0001c0001t0001g0033a0001c0001t0001g0092a0001c0001t0001g0120others(71): Show | 74 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.824-19336_824-1933 others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221520506 | ||||||
| chr2:221520506
|
CCACACAC others(1): Show |
C | 7 | a0001c0001t0001g0060a0001c0001t0001g0068a0001c0001t0001g0121others(4): Show | 7 | HG00544.hp1 HG00741.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-19342_824-1933 others(12): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221520506 | ||||||
| chr2:221520506
|
CCACACAC others(3): Show |
C | 31 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0062others(28): Show | 31 | HG00423.hp2 HG00733.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.824-19344_824-1933 others(14): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221520506 | ||||||
| chr2:221520506
|
CCACACAC others(5): Show |
C | 4 | a0001c0001t0001g0026a0001c0001t0002g0271a0001c0001t0005g0023others(1): Show | 4 | HG01993.hp2 HG02129.hp1 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-19346_824-1933 others(16): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221520506 | ||||||
| chr2:221520533
|
CACACACA others(5): Show |
C | 48 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(45): Show | 48 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.824-19373_824-1936 others(16): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221520533 | ||||||
| chr2:221520535
|
CACACACA others(3): Show |
C | 81 | a0001c0001t0001g0081a0001c0001t0001g0105a0001c0001t0001g0106others(78): Show | 81 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.824-19373_824-1936 others(14): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221520535 | ||||||
| chr2:221520535
|
CACACACA others(5): Show |
C | 7 | a0001c0001t0001g0245a0001c0001t0002g0095a0001c0001t0002g0097others(4): Show | 7 | HG02615.hp2 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-19375_824-1936 others(16): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221520535 | ||||||
| chr2:221520537
|
CACACACA others(1): Show |
C | 3 | a0001c0001t0002g0254a0001c0001t0009g0212a0001c0001t0034g0243 | 3 | HG02258.hp1 HG03225.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.824-19373_824-1936 others(12): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221520537 | ||||||
| chr2:221520537
|
CACACACA others(3): Show |
C | 1 | a0001c0001t0049g0227 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.824-19375_824-1936 others(14): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221520537 | ||||||
| chr2:221520543
|
C | G | 10 | a0001c0001t0001g0033a0001c0001t0001g0121a0001c0001t0001g0193others(7): Show | 10 | HG00741.hp2 HG02300.hp2 HG03831.hp1 others(7): Show |
intron_variant | MODIFIER | c.824-19371G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221520543 | ||||||
| chr2:221520543
|
CAGAG | C | 3 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0005t0001g0034 | 3 | HG01167.hp1 HG01169.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.824-19375_824-1937 others(8): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221520543 | ||||||
| chr2:221520543
|
CAGAGAG | C | 18 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0037others(15): Show | 18 | HG00738.hp1 HG01433.hp1 HG01981.hp1 others(15): Show |
intron_variant | MODIFIER | c.824-19377_824-1937 others(10): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221520543 | ||||||
| chr2:221520545
|
G | C | 3 | a0001c0001t0001g0231a0001c0001t0002g0198a0001c0001t0009g0274 | 3 | HG00642.hp1 HG03516.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.824-19373C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221520545 | ||||||
| chr2:221520547
|
G | C | 1 | a0001c0001t0002g0044 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.824-19375C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221520547 | ||||||
| chr2:221520549
|
G | C | 4 | a0001c0001t0002g0044a0001c0002t0001g0047a0001c0002t0001g0048others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.824-19377C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221520549 | ||||||
| chr2:221520734
|
A | G | 24 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0037others(21): Show | 24 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.824-19562T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221520734 | ||||||
| chr2:221520824
|
G | A | 292 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(289): Show | 292 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.824-19652C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221520824 | ||||||
| chr2:221521059
|
C | G | 1 | a0001c0001t0001g0255 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.824-19887G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221521059 | ||||||
| chr2:221521444
|
G | A | 1 | a0001c0001t0002g0248 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.824-20272C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221521444 | ||||||
| chr2:221521508
|
G | A | 6 | a0001c0001t0002g0178a0001c0002t0001g0020a0001c0002t0007g0239others(3): Show | 6 | HG01243.hp2 HG03239.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.824-20336C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221521508 | ||||||
| chr2:221521728
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.824-20556C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221521728 | ||||||
| chr2:221521912
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.824-20740G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221521912 | ||||||
| chr2:221521980
|
A | G | 1 | a0001c0001t0004g0194 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.824-20808T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221521980 | ||||||
| chr2:221522002
|
A | C | 4 | a0001c0001t0002g0178a0001c0002t0001g0020a0001c0002t0007g0239others(1): Show | 4 | HG03239.hp2 NA18965.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-20830T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221522002 | ||||||
| chr2:221522005
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.824-20833T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221522005 | ||||||
| chr2:221522154
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.824-20982A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221522154 | ||||||
| chr2:221522212
|
T | C | 142 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(139): Show | 142 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.824-21040A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221522212 | ||||||
| chr2:221522231
|
C | T | 2 | a0001c0001t0006g0228a0001c0001t0010g0288 | 2 | HG02723.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.824-21059G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221522231 | ||||||
| chr2:221522350
|
C | A | 1 | a0001c0001t0007g0201 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.824-21178G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221522350 | ||||||
| chr2:221522378
|
A | T | 1 | a0001c0001t0049g0227 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.824-21206T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221522378 | ||||||
| chr2:221522735
|
CTAT | C | 3 | a0001c0001t0001g0092a0001c0001t0001g0148a0001c0001t0001g0202 | 3 | HG01433.hp2 HG02071.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.824-21566_824-2156 others(7): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221522735 | ||||||
| chr2:221522735
|
CTATTAT | C | 20 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0068others(17): Show | 20 | HG00423.hp2 HG00544.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.824-21569_824-2156 others(10): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221522735 | ||||||
| chr2:221522735
|
CTATTATT others(2): Show |
C | 9 | a0001c0001t0001g0245a0001c0001t0002g0095a0001c0001t0002g0097others(6): Show | 9 | HG02615.hp2 HG02717.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.824-21572_824-2156 others(13): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221522735 | ||||||
| chr2:221522735
|
CTATTATT others(11): Show |
C | 142 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(139): Show | 142 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.824-21581_824-2156 others(22): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221522735 | ||||||
| chr2:221522747
|
TTATTATT others(4): Show |
T | 1 | a0001c0001t0001g0038 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.824-21586_824-2157 others(15): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221522747 | ||||||
| chr2:221522750
|
TTATTATT others(4): Show |
T | 1 | a0001c0001t0002g0035 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.824-21589_824-2157 others(15): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221522750 | ||||||
| chr2:221522751
|
TATTATTA others(3): Show |
T | 20 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0037others(17): Show | 20 | HG00639.hp1 HG00738.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.824-21589_824-2158 others(14): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221522751 | ||||||
| chr2:221522753
|
TTATTATT others(4): Show |
T | 1 | a0001c0001t0003g0289 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.824-21592_824-2158 others(15): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221522753 | ||||||
| chr2:221522754
|
TATTATTA others(3): Show |
T | 1 | a0001c0002t0001g0163 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.824-21592_824-2158 others(14): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221522754 | ||||||
| chr2:221522758
|
A | T | 1 | a0001c0002t0047g0229 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.824-21586T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221522758 | ||||||
| chr2:221522761
|
A | T | 3 | a0001c0001t0001g0038a0001c0002t0001g0039a0001c0002t0047g0229 | 3 | NA18956.hp2 NA18973.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.824-21589T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221522761 | ||||||
| chr2:221522764
|
A | T | 24 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0037others(21): Show | 24 | HG00639.hp1 HG00738.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.824-21592T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221522764 | ||||||
| chr2:221522765
|
T | C | 1 | a0001c0003t0003g0126 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.824-21593A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221522765 | ||||||
| chr2:221522767
|
A | T | 26 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0037others(23): Show | 26 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.824-21595T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221522767 | ||||||
| chr2:221522770
|
A | T | 28 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0037others(25): Show | 28 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.824-21598T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221522770 | ||||||
| chr2:221522773
|
A | T | 31 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0037others(28): Show | 31 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.824-21601T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221522773 | ||||||
| chr2:221522776
|
T | A | 2 | a0001c0001t0001g0231a0001c0001t0012g0275 | 2 | HG02572.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.824-21604A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221522776 | ||||||
| chr2:221522785
|
C | T | 2 | a0001c0001t0012g0275a0001c0003t0003g0093 | 2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.824-21613G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221522785 | ||||||
| chr2:221522832
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.824-21660C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221522832 | ||||||
| chr2:221522854
|
G | T | 2 | a0001c0001t0002g0111a0001c0001t0010g0110 | 2 | HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.824-21682C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221522854 | ||||||
| chr2:221522880
|
G | T | 1 | a0001c0002t0001g0159 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.824-21708C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221522880 | ||||||
| chr2:221522881
|
C | T | 1 | a0001c0002t0001g0159 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.824-21709G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221522881 | ||||||
| chr2:221522892
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.824-21720A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221522892 | ||||||
| chr2:221523005
|
C | T | 26 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0037others(23): Show | 26 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.824-21833G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221523005 | ||||||
| chr2:221523135
|
C | T | 4 | a0001c0001t0001g0120a0001c0001t0002g0160a0001c0001t0002g0179others(1): Show | 4 | HG00738.hp2 HG01261.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.824-21963G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221523135 | ||||||
| chr2:221523228
|
A | C | 175 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(172): Show | 175 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.824-22056T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221523228 | ||||||
| chr2:221523276
|
A | G | 6 | a0001c0001t0001g0245a0001c0001t0002g0095a0001c0001t0002g0097others(3): Show | 6 | HG02615.hp2 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.824-22104T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221523276 | ||||||
| chr2:221523309
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.824-22137G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221523309 | ||||||
| chr2:221523351
|
G | A | 5 | a0001c0001t0004g0235a0001c0001t0036g0115a0001c0002t0004g0234others(2): Show | 5 | HG02145.hp1 HG03041.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.824-22179C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221523351 | ||||||
| chr2:221523472
|
A | T | 2 | a0001c0002t0001g0125a0001c0002t0001g0149 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.824-22300T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221523472 | ||||||
| chr2:221523512
|
C | T | 1 | a0001c0003t0001g0276 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.824-22340G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221523512 | ||||||
| chr2:221523539
|
G | A | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.824-22367C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221523539 | ||||||
| chr2:221523564
|
AGCATGAG others(292): Show |
A | 26 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0037others(23): Show | 26 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.824-22691_824-2239 others(4): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221523564 | ||||||
| chr2:221523891
|
T | C | 2 | a0001c0001t0002g0123a0001c0001t0041g0122 | 2 | HG02027.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.824-22719A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221523891 | ||||||
| chr2:221523894
|
A | G | 35 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0060others(32): Show | 35 | HG00423.hp2 HG00544.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.824-22722T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221523894 | ||||||
| chr2:221524015
|
A | T | 1 | a0001c0001t0002g0089 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.824-22843T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221524015 | ||||||
| chr2:221524193
|
G | A | 5 | a0001c0001t0021g0083a0001c0003t0001g0085a0001c0003t0001g0086others(2): Show | 5 | HG00323.hp2 HG01169.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.824-23021C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221524193 | ||||||
| chr2:221524278
|
C | T | 1 | a0001c0003t0003g0133 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.824-23106G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221524278 | ||||||
| chr2:221524568
|
A | G | 1 | a0001c0003t0003g0281 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.824-23396T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221524568 | ||||||
| chr2:221524689
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.824-23517C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221524689 | ||||||
| chr2:221524696
|
C | A | 1 | a0001c0001t0002g0111 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.824-23524G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221524696 | ||||||
| chr2:221524943
|
C | T | 1 | a0001c0001t0040g0128 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.824-23771G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221524943 | ||||||
| chr2:221525046
|
GAA | G | 142 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(139): Show | 142 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.824-23876_824-2387 others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221525046 | ||||||
| chr2:221525067
|
T | G | 2 | a0001c0001t0001g0069a0001c0001t0002g0067 | 2 | NA18981.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.824-23895A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221525067 | ||||||
| chr2:221525087
|
C | G | 3 | a0001c0001t0001g0121a0001c0001t0001g0193a0001c0001t0043g0124 | 3 | HG00741.hp2 HG01123.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.824-23915G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221525087 | ||||||
| chr2:221525145
|
A | C | 2 | a0001c0001t0012g0275a0001c0003t0003g0093 | 2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.824-23973T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221525145 | ||||||
| chr2:221525246
|
G | A | 1 | a0001c0001t0040g0128 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.824-24074C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221525246 | ||||||
| chr2:221525251
|
G | A | 142 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(139): Show | 142 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.824-24079C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221525251 | ||||||
| chr2:221525324
|
T | C | 2 | a0001c0001t0001g0260a0001c0002t0001g0259 | 2 | HG02523.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.824-24152A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221525324 | ||||||
| chr2:221525364
|
G | A | 1 | a0001c0001t0002g0089 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.824-24192C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221525364 | ||||||
| chr2:221525387
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.824-24215G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221525387 | ||||||
| chr2:221525388
|
G | A | 3 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0002g0199 | 3 | HG01981.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.824-24216C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221525388 | ||||||
| chr2:221525402
|
G | A | 24 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0037others(21): Show | 24 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.824-24230C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221525402 | ||||||
| chr2:221525840
|
A | G | 216 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(213): Show | 216 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.824-24668T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221525840 | ||||||
| chr2:221525983
|
C | A | 1 | a0001c0002t0029g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.824-24811G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221525983 | ||||||
| chr2:221526231
|
C | T | 55 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0060others(52): Show | 55 | HG00423.hp2 HG00544.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.824-25059G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221526231 | ||||||
| chr2:221526304
|
A | C | 24 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0037others(21): Show | 24 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.824-25132T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221526304 | ||||||
| chr2:221526463
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.824-25291C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221526463 | ||||||
| chr2:221526534
|
A | G | 1 | a0001c0001t0012g0275 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.824-25362T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221526534 | ||||||
| chr2:221526542
|
TA | T | 31 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0037others(28): Show | 31 | HG00738.hp1 HG01109.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.824-25371delT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221526542 | ||||||
| chr2:221526542
|
TAA | T | 139 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0013others(136): Show | 139 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.824-25372_824-2537 others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221526542 | ||||||
| chr2:221526559
|
A | T | 1 | a0001c0001t0040g0128 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.824-25387T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221526559 | ||||||
| chr2:221526768
|
A | C | 1 | a0001c0001t0002g0142 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.824-25596T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221526768 | ||||||
| chr2:221526772
|
G | C | 4 | a0001c0001t0002g0178a0001c0002t0001g0020a0001c0002t0007g0239others(1): Show | 4 | HG03239.hp2 NA18965.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-25600C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221526772 | ||||||
| chr2:221526809
|
C | T | 24 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0037others(21): Show | 24 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.824-25637G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221526809 | ||||||
| chr2:221526852
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0002g0097 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.824-25690_824-2568 others(14): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221526852 | ||||||
| chr2:221526852
|
C | CAAAAAAA others(5): Show |
2 | a0001c0001t0002g0223a0001c0001t0002g0224 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.824-25692_824-2568 others(16): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221526852 | ||||||
| chr2:221526852
|
CAAAA | C | 8 | a0001c0001t0001g0202a0001c0001t0001g0264a0001c0001t0002g0123others(5): Show | 8 | HG00673.hp1 HG01106.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.824-25684_824-2568 others(8): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221526852 | ||||||
| chr2:221526852
|
CAAAAA | C | 37 | a0001c0001t0001g0063a0001c0001t0001g0120a0001c0001t0001g0140others(34): Show | 37 | HG00735.hp1 HG01071.hp1 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.824-25685_824-2568 others(9): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221526852 | ||||||
| chr2:221526852
|
CAAAAAA | C | 29 | a0001c0001t0001g0033a0001c0001t0001g0041a0001c0001t0001g0042others(26): Show | 29 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.824-25686_824-2568 others(10): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221526852 | ||||||
| chr2:221526852
|
CAAAAAAA | C | 8 | a0001c0001t0001g0062a0001c0001t0001g0070a0001c0001t0001g0164others(5): Show | 8 | HG00423.hp2 HG01074.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.824-25687_824-2568 others(11): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221526852 | ||||||
| chr2:221526852
|
CAAAAAAA others(1): Show |
C | 7 | a0001c0001t0001g0068a0001c0001t0001g0208a0001c0001t0001g0245others(4): Show | 7 | HG00544.hp1 HG01123.hp1 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-25688_824-2568 others(12): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221526852 | ||||||
| chr2:221526852
|
CAAAAAAA others(2): Show |
C | 13 | a0001c0001t0001g0065a0001c0001t0001g0069a0001c0001t0001g0121others(10): Show | 13 | HG00741.hp2 HG02080.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.824-25689_824-2568 others(13): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221526852 | ||||||
| chr2:221526852
|
CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0001g0060a0001c0001t0014g0213a0001c0001t0016g0058 | 3 | HG04184.hp1 NA18944.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.824-25690_824-2568 others(14): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221526852 | ||||||
| chr2:221526852
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.824-25692_824-2568 others(16): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221526852 | ||||||
| chr2:221526852
|
CAAAAAAA others(10): Show |
C | 5 | a0001c0001t0001g0059a0001c0001t0002g0035a0001c0001t0031g0046others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.824-25697_824-2568 others(21): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221526852 | ||||||
| chr2:221526852
|
CAAAAAAA others(11): Show |
C | 20 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0037others(17): Show | 20 | HG00738.hp1 HG01433.hp1 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.824-25698_824-2568 others(22): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221526852 | ||||||
| chr2:221526852
|
CAAAAAAA others(12): Show |
C | 2 | a0001c0001t0015g0286a0001c0010t0001g0176 | 2 | HG01891.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.824-25699_824-2568 others(23): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221526852 | ||||||
| chr2:221526852
|
CAAAAAAA others(13): Show |
C | 33 | a0001c0001t0001g0006a0001c0001t0001g0112a0001c0001t0001g0190others(30): Show | 33 | HG00423.hp1 HG00639.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.824-25700_824-2568 others(24): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221526852 | ||||||
| chr2:221526852
|
CAAAAAAA others(14): Show |
C | 100 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0012others(97): Show | 100 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.824-25701_824-2568 others(25): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221526852 | ||||||
| chr2:221526852
|
CAAAAAAA others(15): Show |
C | 12 | a0001c0001t0001g0106a0001c0001t0001g0180a0001c0001t0001g0181others(9): Show | 12 | HG00323.hp2 HG01975.hp2 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.824-25702_824-2568 others(26): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221526852 | ||||||
| chr2:221526852
|
CAAAAAAA others(16): Show |
C | 2 | a0001c0001t0003g0289a0001c0001t0006g0004 | 2 | HG01109.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.824-25703_824-2568 others(27): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221526852 | ||||||
| chr2:221526852
|
CAAAAAAA others(22): Show |
C | 1 | a0001c0003t0003g0093 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.824-25709_824-2568 others(33): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221526852 | ||||||
| chr2:221526852
|
CAAAAAAA others(23): Show |
C | 2 | a0001c0001t0012g0275a0001c0001t0049g0227 | 2 | HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.824-25710_824-2568 others(34): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221526852 | ||||||
| chr2:221526903
|
C | T | 1 | a0001c0001t0040g0128 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.824-25731G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221526903 | ||||||
| chr2:221526966
|
C | CA | 142 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(139): Show | 142 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.824-25795dupT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221526966 | ||||||
| chr2:221527080
|
C | T | 1 | a0001c0002t0001g0039 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.824-25908G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221527080 | ||||||
| chr2:221527123
|
A | C | 212 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(209): Show | 212 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.824-25951T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221527123 | ||||||
| chr2:221527187
|
C | T | 1 | a0001c0001t0031g0046 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.824-26015G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221527187 | ||||||
| chr2:221527576
|
G | A | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.824-26404C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221527576 | ||||||
| chr2:221527634
|
T | G | 40 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0037others(37): Show | 40 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(37): Show |
intron_variant | MODIFIER | c.824-26462A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221527634 | ||||||
| chr2:221527643
|
G | A | 2 | a0001c0001t0003g0289a0001c0001t0040g0128 | 2 | HG01109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.824-26471C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221527643 | ||||||
| chr2:221527664
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.824-26492G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221527664 | ||||||
| chr2:221527683
|
C | CAACATAA others(3): Show |
1 | a0001c0001t0001g0006 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.824-26521_824-2651 others(14): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221527683 | ||||||
| chr2:221527760
|
T | C | 1 | a0001c0001t0012g0275 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.824-26588A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221527760 | ||||||
| chr2:221527829
|
CATGGCTA others(12): Show |
C | 1 | a0001c0001t0048g0162 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.824-26676_824-2665 others(23): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221527829 | ||||||
| chr2:221527900
|
C | A | 1 | a0001c0001t0040g0128 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.824-26728G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221527900 | ||||||
| chr2:221527903
|
A | T | 3 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0002g0199 | 3 | HG01981.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.824-26731T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221527903 | ||||||
| chr2:221528022
|
C | A | 141 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(138): Show | 141 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.824-26850G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221528022 | ||||||
| chr2:221528028
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.824-26856G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221528028 | ||||||
| chr2:221528087
|
T | C | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.824-26915A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221528087 | ||||||
| chr2:221528208
|
T | C | 3 | a0001c0001t0001g0106a0001c0002t0004g0104a0002c0011t0026g0109 | 3 | HG01975.hp2 HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.824-27036A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221528208 | ||||||
| chr2:221528306
|
G | T | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.824-27134C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221528306 | ||||||
| chr2:221528319
|
T | C | 1 | a0001c0001t0001g0294 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.824-27147A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221528319 | ||||||
| chr2:221528334
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.824-27162C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221528334 | ||||||
| chr2:221528348
|
C | T | 1 | a0001c0001t0040g0128 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.824-27176G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221528348 | ||||||
| chr2:221528580
|
C | T | 1 | a0001c0001t0040g0128 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.824-27408G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221528580 | ||||||
| chr2:221528891
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.824-27719C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221528891 | ||||||
| chr2:221528915
|
T | C | 140 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(137): Show | 140 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.824-27743A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221528915 | ||||||
| chr2:221528926
|
G | A | 33 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0060others(30): Show | 33 | HG00423.hp2 HG00544.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.824-27754C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221528926 | ||||||
| chr2:221529008
|
C | T | 139 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(136): Show | 139 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.824-27836G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221529008 | ||||||
| chr2:221529142
|
A | C | 2 | a0001c0001t0001g0002a0001c0001t0006g0004 | 2 | NA18953.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.824-27970T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221529142 | ||||||
| chr2:221529172
|
G | A | 1 | a0001c0001t0049g0227 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.824-28000C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221529172 | ||||||
| chr2:221529317
|
G | A | 1 | a0001c0001t0003g0289 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.824-28145C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221529317 | ||||||
| chr2:221529482
|
G | C | 1 | a0001c0001t0003g0289 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.824-28310C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221529482 | ||||||
| chr2:221529585
|
A | G | 210 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(207): Show | 210 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.824-28413T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221529585 | ||||||
| chr2:221529763
|
C | T | 1 | a0001c0003t0003g0093 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.824-28591G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221529763 | ||||||
| chr2:221529999
|
T | C | 1 | a0001c0001t0002g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.824-28827A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221529999 | ||||||
| chr2:221530043
|
G | A | 2 | a0001c0003t0003g0079a0001c0003t0003g0133 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.824-28871C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221530043 | ||||||
| chr2:221530048
|
C | G | 1 | a0001c0001t0001g0294 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.824-28876G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221530048 | ||||||
| chr2:221530096
|
T | C | 292 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(289): Show | 292 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.824-28924A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221530096 | ||||||
| chr2:221530165
|
CT | C | 7 | a0001c0001t0001g0141a0001c0001t0001g0245a0001c0001t0002g0095others(4): Show | 7 | HG02615.hp2 HG02698.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-28994delA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221530165 | ||||||
| chr2:221530195
|
G | A | 1 | a0001c0001t0004g0285 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.824-29023C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221530195 | ||||||
| chr2:221530403
|
G | A | 1 | a0001c0003t0003g0093 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.824-29231C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221530403 | ||||||
| chr2:221530478
|
G | C | 2 | a0001c0002t0001g0020a0001c0002t0007g0239 | 2 | HG03239.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.824-29306C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221530478 | ||||||
| chr2:221530625
|
C | T | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.824-29453G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221530625 | ||||||
| chr2:221530626
|
G | A | 1 | a0001c0001t0045g0096 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.824-29454C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221530626 | ||||||
| chr2:221530638
|
A | C | 2 | a0001c0001t0002g0111a0001c0001t0010g0110 | 2 | HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.824-29466T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221530638 | ||||||
| chr2:221530666
|
G | C | 138 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(135): Show | 138 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.824-29494C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221530666 | ||||||
| chr2:221530900
|
C | G | 10 | a0001c0001t0001g0245a0001c0001t0001g0294a0001c0001t0002g0095others(7): Show | 10 | HG00639.hp1 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.824-29728G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221530900 | ||||||
| chr2:221530901
|
C | G | 35 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0060others(32): Show | 35 | HG00423.hp2 HG00544.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.824-29729G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221530901 | ||||||
| chr2:221530985
|
T | G | 5 | a0001c0001t0001g0264a0001c0001t0001g0268a0001c0001t0003g0266others(2): Show | 5 | HG01071.hp1 HG01167.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-29813A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221530985 | ||||||
| chr2:221531170
|
T | G | 138 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(135): Show | 138 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.824-29998A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221531170 | ||||||
| chr2:221531426
|
A | G | 1 | a0001c0003t0046g0278 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.824-30254T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221531426 | ||||||
| chr2:221531596
|
A | G | 10 | a0001c0001t0001g0245a0001c0001t0001g0294a0001c0001t0002g0095others(7): Show | 10 | HG00639.hp1 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.824-30424T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221531596 | ||||||
| chr2:221531636
|
G | T | 11 | a0001c0001t0001g0063a0001c0001t0001g0189a0001c0001t0001g0208others(8): Show | 11 | NA18939.hp2 NA18943.hp1 NA18965.hp1 others(8): Show |
intron_variant | MODIFIER | c.824-30464C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221531636 | ||||||
| chr2:221531639
|
T | C | 1 | a0001c0001t0045g0096 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.824-30467A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221531639 | ||||||
| chr2:221531643
|
A | T | 1 | a0001c0001t0045g0096 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.824-30471T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221531643 | ||||||
| chr2:221531731
|
G | A | 26 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0037others(23): Show | 26 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.824-30559C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221531731 | ||||||
| chr2:221531732
|
C | CCTAA | 213 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(210): Show | 213 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.824-30564_824-3056 others(8): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221531732 | ||||||
| chr2:221531787
|
T | C | 6 | a0001c0001t0001g0245a0001c0001t0002g0095a0001c0001t0002g0097others(3): Show | 6 | HG02615.hp2 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.824-30615A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221531787 | ||||||
| chr2:221531854
|
T | C | 148 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(145): Show | 148 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.824-30682A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221531854 | ||||||
| chr2:221532125
|
TC | T | 8 | a0001c0001t0001g0245a0001c0001t0001g0294a0001c0001t0002g0095others(5): Show | 8 | HG00639.hp1 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.824-30954delG | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221532125 | ||||||
| chr2:221532126
|
CT | C | 135 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0012others(132): Show | 135 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.824-30955delA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221532126 | ||||||
| chr2:221532180
|
T | C | 138 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(135): Show | 138 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.824-31008A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221532180 | ||||||
| chr2:221532191
|
T | C | 148 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(145): Show | 148 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.824-31019A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221532191 | ||||||
| chr2:221532231
|
T | C | 1 | a0001c0003t0003g0093 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.824-31059A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221532231 | ||||||
| chr2:221532375
|
A | G | 213 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(210): Show | 213 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.824-31203T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221532375 | ||||||
| chr2:221532656
|
A | T | 10 | a0001c0001t0001g0245a0001c0001t0001g0294a0001c0001t0002g0095others(7): Show | 10 | HG00639.hp1 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.823+31075T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221532656 | ||||||
| chr2:221532771
|
G | T | 1 | a0001c0001t0001g0283 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.823+30960C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221532771 | ||||||
| chr2:221532788
|
G | C | 10 | a0001c0001t0001g0245a0001c0001t0001g0294a0001c0001t0002g0095others(7): Show | 10 | HG00639.hp1 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.823+30943C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221532788 | ||||||
| chr2:221532939
|
G | A | 1 | a0001c0001t0020g0173 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.823+30792C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221532939 | ||||||
| chr2:221533014
|
C | T | 1 | a0001c0001t0002g0073 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.823+30717G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221533014 | ||||||
| chr2:221533155
|
T | C | 1 | a0001c0001t0045g0096 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.823+30576A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221533155 | ||||||
| chr2:221533172
|
T | C | 35 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0060others(32): Show | 35 | HG00423.hp2 HG00544.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.823+30559A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221533172 | ||||||
| chr2:221533251
|
T | C | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.823+30480A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221533251 | ||||||
| chr2:221533292
|
A | T | 10 | a0001c0001t0001g0245a0001c0001t0001g0294a0001c0001t0002g0095others(7): Show | 10 | HG00639.hp1 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.823+30439T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221533292 | ||||||
| chr2:221533458
|
G | A | 2 | a0001c0004t0019g0236a0001c0004t0019g0237 | 2 | HG01243.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.823+30273C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221533458 | ||||||
| chr2:221533476
|
A | G | 1 | a0001c0001t0001g0002 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.823+30255T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221533476 | ||||||
| chr2:221533539
|
C | T | 1 | a0001c0001t0001g0006 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.823+30192G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221533539 | ||||||
| chr2:221533588
|
T | A | 1 | a0001c0001t0049g0227 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.823+30143A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221533588 | ||||||
| chr2:221533611
|
A | C | 10 | a0001c0001t0001g0245a0001c0001t0001g0294a0001c0001t0002g0095others(7): Show | 10 | HG00639.hp1 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.823+30120T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221533611 | ||||||
| chr2:221533612
|
G | A | 1 | a0001c0001t0003g0289 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.823+30119C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221533612 | ||||||
| chr2:221533617
|
T | C | 5 | a0001c0001t0021g0083a0001c0003t0001g0085a0001c0003t0001g0086others(2): Show | 5 | HG00323.hp2 HG01169.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.823+30114A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221533617 | ||||||
| chr2:221533725
|
C | CA | 9 | a0001c0001t0001g0167a0001c0001t0001g0177a0001c0001t0001g0202others(6): Show | 9 | HG00673.hp1 HG01167.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.823+30005dupT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221533725 | ||||||
| chr2:221533725
|
CA | C | 28 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0080others(25): Show | 28 | HG00423.hp2 HG00735.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.823+30005delT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221533725 | ||||||
| chr2:221533725
|
CAA | C | 135 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(132): Show | 135 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.823+30004_823+3000 others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221533725 | ||||||
| chr2:221533725
|
CAAA | C | 26 | a0001c0001t0001g0050a0001c0001t0001g0200a0001c0001t0002g0027others(23): Show | 26 | HG00323.hp2 HG00738.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.823+30003_823+3000 others(7): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221533725 | ||||||
| chr2:221533725
|
CAAAA | C | 23 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0037others(20): Show | 23 | HG01167.hp1 HG01169.hp2 HG02897.hp2 others(20): Show |
intron_variant | MODIFIER | c.823+30002_823+3000 others(8): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221533725 | ||||||
| chr2:221533852
|
C | T | 35 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0060others(32): Show | 35 | HG00423.hp2 HG00544.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.823+29879G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221533852 | ||||||
| chr2:221533950
|
G | C | 1 | a0001c0001t0001g0294 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.823+29781C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221533950 | ||||||
| chr2:221534158
|
T | C | 10 | a0001c0001t0001g0245a0001c0001t0001g0294a0001c0001t0002g0095others(7): Show | 10 | HG00639.hp1 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.823+29573A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221534158 | ||||||
| chr2:221534189
|
G | T | 1 | a0001c0001t0002g0095 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.823+29542C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221534189 | ||||||
| chr2:221534322
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.823+29409G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221534322 | ||||||
| chr2:221534407
|
C | T | 2 | a0001c0003t0001g0030a0001c0003t0001g0031 | 2 | HG00280.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.823+29324G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221534407 | ||||||
| chr2:221534568
|
C | T | 138 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(135): Show | 138 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.823+29163G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221534568 | ||||||
| chr2:221534592
|
A | C | 2 | a0001c0004t0019g0236a0001c0004t0019g0237 | 2 | HG01243.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.823+29139T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221534592 | ||||||
| chr2:221534657
|
A | G | 1 | a0001c0001t0003g0279 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.823+29074T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221534657 | ||||||
| chr2:221534848
|
C | T | 1 | a0001c0001t0001g0283 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.823+28883G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221534848 | ||||||
| chr2:221534892
|
T | C | 1 | a0001c0001t0001g0294 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.823+28839A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221534892 | ||||||
| chr2:221535063
|
A | C | 6 | a0001c0001t0001g0245a0001c0001t0002g0095a0001c0001t0002g0097others(3): Show | 6 | HG02615.hp2 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+28668T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221535063 | ||||||
| chr2:221535130
|
C | G | 1 | a0001c0001t0045g0096 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.823+28601G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221535130 | ||||||
| chr2:221535207
|
C | T | 5 | a0001c0001t0021g0083a0001c0003t0001g0085a0001c0003t0001g0086others(2): Show | 5 | HG00323.hp2 HG01169.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.823+28524G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221535207 | ||||||
| chr2:221535270
|
C | G | 26 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0037others(23): Show | 26 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.823+28461G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221535270 | ||||||
| chr2:221535396
|
T | C | 149 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(146): Show | 149 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.823+28335A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221535396 | ||||||
| chr2:221535503
|
G | A | 211 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(208): Show | 211 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.823+28228C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221535503 | ||||||
| chr2:221535587
|
GT | G | 10 | a0001c0001t0001g0245a0001c0001t0001g0294a0001c0001t0002g0095others(7): Show | 10 | HG00639.hp1 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.823+28143delA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221535587 | ||||||
| chr2:221535627
|
CT | C | 36 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0060others(33): Show | 36 | HG00423.hp2 HG00544.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.823+28103delA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221535627 | ||||||
| chr2:221535788
|
G | T | 10 | a0001c0001t0001g0245a0001c0001t0001g0294a0001c0001t0002g0095others(7): Show | 10 | HG00639.hp1 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.823+27943C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221535788 | ||||||
| chr2:221535897
|
G | T | 5 | a0001c0001t0001g0287a0001c0001t0004g0291a0001c0001t0013g0290others(2): Show | 5 | HG01891.hp1 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.823+27834C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221535897 | ||||||
| chr2:221535906
|
C | T | 1 | a0001c0001t0002g0051 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.823+27825G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221535906 | ||||||
| chr2:221536176
|
C | T | 1 | a0001c0001t0040g0128 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.823+27555G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221536176 | ||||||
| chr2:221536243
|
C | A | 10 | a0001c0001t0001g0245a0001c0001t0001g0294a0001c0001t0002g0095others(7): Show | 10 | HG00639.hp1 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.823+27488G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221536243 | ||||||
| chr2:221536366
|
G | T | 35 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0060others(32): Show | 35 | HG00423.hp2 HG00544.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.823+27365C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221536366 | ||||||
| chr2:221536443
|
G | A | 3 | a0001c0001t0001g0197a0001c0001t0001g0209a0001c0001t0002g0198 | 3 | HG00642.hp1 HG03654.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.823+27288C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221536443 | ||||||
| chr2:221536545
|
C | T | 148 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(145): Show | 148 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.823+27186G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221536545 | ||||||
| chr2:221536751
|
G | A | 1 | a0001c0001t0003g0289 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.823+26980C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221536751 | ||||||
| chr2:221536883
|
C | T | 10 | a0001c0001t0001g0245a0001c0001t0001g0294a0001c0001t0002g0095others(7): Show | 10 | HG00639.hp1 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.823+26848G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221536883 | ||||||
| chr2:221536904
|
A | G | 148 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(145): Show | 148 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.823+26827T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221536904 | ||||||
| chr2:221536977
|
G | A | 1 | a0001c0001t0049g0227 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.823+26754C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221536977 | ||||||
| chr2:221537031
|
A | C | 1 | a0001c0001t0001g0017 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.823+26700T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221537031 | ||||||
| chr2:221537170
|
C | A | 1 | a0001c0001t0040g0128 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.823+26561G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221537170 | ||||||
| chr2:221537296
|
G | A | 1 | a0001c0001t0002g0178 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.823+26435C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221537296 | ||||||
| chr2:221537324
|
C | T | 1 | a0001c0001t0032g0251 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.823+26407G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221537324 | ||||||
| chr2:221537331
|
A | T | 138 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(135): Show | 138 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.823+26400T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221537331 | ||||||
| chr2:221537353
|
C | T | 1 | a0001c0001t0003g0289 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.823+26378G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221537353 | ||||||
| chr2:221537384
|
C | G | 138 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(135): Show | 138 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.823+26347G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221537384 | ||||||
| chr2:221537633
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.823+26098A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221537633 | ||||||
| chr2:221537696
|
C | T | 1 | a0001c0001t0002g0206 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.823+26035G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221537696 | ||||||
| chr2:221537836
|
A | G | 2 | a0001c0003t0001g0276a0001c0003t0003g0281 | 2 | HG00741.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.823+25895T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221537836 | ||||||
| chr2:221537966
|
C | A | 1 | a0001c0001t0004g0174 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.823+25765G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221537966 | ||||||
| chr2:221537981
|
C | G | 1 | a0001c0001t0001g0017 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.823+25750G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221537981 | ||||||
| chr2:221538004
|
A | C | 138 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(135): Show | 138 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.823+25727T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221538004 | ||||||
| chr2:221538029
|
A | C | 1 | a0001c0001t0001g0294 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.823+25702T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221538029 | ||||||
| chr2:221538058
|
C | A | 1 | a0001c0001t0001g0164 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.823+25673G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221538058 | ||||||
| chr2:221538071
|
C | CA | 138 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(135): Show | 138 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.823+25659dupT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221538071 | ||||||
| chr2:221538128
|
A | C | 1 | a0001c0001t0001g0264 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.823+25603T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221538128 | ||||||
| chr2:221538224
|
A | G | 1 | a0001c0003t0003g0056 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.823+25507T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221538224 | ||||||
| chr2:221538354
|
G | A | 2 | a0001c0001t0036g0115a0001c0003t0003g0114 | 2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.823+25377C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221538354 | ||||||
| chr2:221538485
|
G | T | 1 | a0001c0001t0001g0294 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.823+25246C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221538485 | ||||||
| chr2:221538618
|
A | T | 2 | a0001c0001t0001g0016a0001c0001t0005g0009 | 2 | HG00558.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.823+25113T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221538618 | ||||||
| chr2:221538620
|
G | A | 6 | a0001c0001t0001g0245a0001c0001t0002g0095a0001c0001t0002g0097others(3): Show | 6 | HG02615.hp2 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+25111C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221538620 | ||||||
| chr2:221538621
|
C | T | 6 | a0001c0001t0001g0245a0001c0001t0002g0095a0001c0001t0002g0097others(3): Show | 6 | HG02615.hp2 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+25110G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221538621 | ||||||
| chr2:221538764
|
G | C | 2 | a0001c0004t0019g0236a0001c0004t0019g0237 | 2 | HG01243.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.823+24967C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221538764 | ||||||
| chr2:221538879
|
C | T | 138 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(135): Show | 138 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.823+24852G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221538879 | ||||||
| chr2:221538884
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.823+24847G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221538884 | ||||||
| chr2:221538904
|
C | T | 1 | a0001c0001t0003g0289 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.823+24827G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221538904 | ||||||
| chr2:221539044
|
A | C | 1 | a0001c0001t0002g0179 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.823+24687T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221539044 | ||||||
| chr2:221539359
|
T | C | 1 | a0001c0001t0002g0035 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.823+24372A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221539359 | ||||||
| chr2:221539505
|
T | A | 10 | a0001c0001t0001g0245a0001c0001t0001g0294a0001c0001t0002g0095others(7): Show | 10 | HG00639.hp1 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.823+24226A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221539505 | ||||||
| chr2:221539566
|
G | C | 1 | a0001c0001t0001g0141 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.823+24165C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221539566 | ||||||
| chr2:221539583
|
A | C | 10 | a0001c0001t0001g0245a0001c0001t0001g0294a0001c0001t0002g0095others(7): Show | 10 | HG00639.hp1 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.823+24148T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221539583 | ||||||
| chr2:221539627
|
C | T | 1 | a0001c0001t0002g0206 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.823+24104G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221539627 | ||||||
| chr2:221539679
|
G | A | 1 | a0001c0003t0003g0093 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.823+24052C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221539679 | ||||||
| chr2:221539869
|
C | A | 3 | a0001c0002t0007g0239a0001c0004t0019g0236a0001c0004t0019g0237 | 3 | HG01243.hp2 NA18999.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.823+23862G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221539869 | ||||||
| chr2:221540121
|
T | C | 2 | a0001c0001t0040g0128a0001c0001t0045g0096 | 2 | HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.823+23610A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221540121 | ||||||
| chr2:221540161
|
C | T | 1 | a0001c0001t0003g0289 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.823+23570G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221540161 | ||||||
| chr2:221540172
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0003g0279 | 2 | HG02602.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.823+23559C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221540172 | ||||||
| chr2:221540380
|
A | G | 9 | a0001c0001t0001g0245a0001c0001t0002g0095a0001c0001t0002g0097others(6): Show | 9 | HG02615.hp2 HG02717.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.823+23351T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221540380 | ||||||
| chr2:221540381
|
A | C | 148 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(145): Show | 148 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.823+23350T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221540381 | ||||||
| chr2:221540389
|
C | T | 148 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(145): Show | 148 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.823+23342G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221540389 | ||||||
| chr2:221540599
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0004g0074 | 2 | NA18963.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.823+23132C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221540599 | ||||||
| chr2:221540740
|
T | C | 34 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0060others(31): Show | 34 | HG00423.hp2 HG00544.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.823+22991A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221540740 | ||||||
| chr2:221540777
|
A | G | 33 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0060others(30): Show | 33 | HG00423.hp2 HG00544.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.823+22954T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221540777 | ||||||
| chr2:221540902
|
T | G | 10 | a0001c0001t0001g0245a0001c0001t0002g0095a0001c0001t0002g0097others(7): Show | 10 | HG02615.hp2 HG02717.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.823+22829A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221540902 | ||||||
| chr2:221540932
|
C | CT | 57 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(54): Show | 57 | HG00408.hp2 HG00735.hp1 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.823+22798dupA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221540932 | ||||||
| chr2:221540932
|
CT | C | 40 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0060others(37): Show | 40 | HG00423.hp2 HG00544.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.823+22798delA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221540932 | ||||||
| chr2:221540954
|
A | T | 2 | a0001c0003t0003g0226a0001c0008t0003g0157 | 2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.823+22777T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221540954 | ||||||
| chr2:221541164
|
GGCCTTGA others(3): Show |
G | 1 | a0001c0001t0001g0294 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.823+22557_823+2256 others(14): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221541164 | ||||||
| chr2:221541174
|
T | G | 2 | a0001c0003t0001g0030a0001c0003t0001g0031 | 2 | HG00280.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.823+22557A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221541174 | ||||||
| chr2:221541228
|
G | A | 35 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0060others(32): Show | 35 | HG00423.hp2 HG00544.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.823+22503C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221541228 | ||||||
| chr2:221541482
|
T | G | 1 | a0001c0001t0003g0289 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.823+22249A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221541482 | ||||||
| chr2:221541764
|
G | A | 2 | a0001c0001t0002g0111a0001c0001t0010g0110 | 2 | HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.823+21967C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221541764 | ||||||
| chr2:221541768
|
T | A | 26 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0037others(23): Show | 26 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.823+21963A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221541768 | ||||||
| chr2:221541848
|
G | A | 137 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(134): Show | 137 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.823+21883C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221541848 | ||||||
| chr2:221542151
|
A | G | 1 | a0001c0001t0001g0256 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.823+21580T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221542151 | ||||||
| chr2:221542152
|
C | A | 1 | a0001c0001t0001g0256 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.823+21579G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221542152 | ||||||
| chr2:221542250
|
G | A | 9 | a0001c0001t0001g0245a0001c0001t0002g0095a0001c0001t0002g0097others(6): Show | 9 | HG02615.hp2 HG02717.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.823+21481C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221542250 | ||||||
| chr2:221542337
|
A | T | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.823+21394T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221542337 | ||||||
| chr2:221542349
|
C | A | 1 | a0001c0001t0001g0256 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.823+21382G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221542349 | ||||||
| chr2:221542376
|
T | G | 1 | a0001c0005t0001g0034 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.823+21355A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221542376 | ||||||
| chr2:221542525
|
C | G | 1 | a0001c0001t0001g0062 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.823+21206G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221542525 | ||||||
| chr2:221542678
|
G | A | 148 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(145): Show | 148 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.823+21053C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221542678 | ||||||
| chr2:221542722
|
T | C | 137 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(134): Show | 137 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.823+21009A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221542722 | ||||||
| chr2:221543008
|
C | T | 1 | a0001c0001t0006g0246 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.823+20723G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221543008 | ||||||
| chr2:221543202
|
A | C | 27 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0037others(24): Show | 27 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.823+20529T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221543202 | ||||||
| chr2:221543253
|
C | T | 148 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(145): Show | 148 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.823+20478G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221543253 | ||||||
| chr2:221543468
|
T | A | 1 | a0001c0001t0045g0096 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.823+20263A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221543468 | ||||||
| chr2:221543517
|
G | T | 1 | a0001c0001t0002g0097 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.823+20214C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221543517 | ||||||
| chr2:221543558
|
G | T | 31 | a0001c0001t0001g0112a0001c0001t0001g0139a0001c0001t0001g0249others(28): Show | 31 | HG00408.hp1 HG01891.hp1 HG02015.hp2 others(28): Show |
intron_variant | MODIFIER | c.823+20173C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221543558 | ||||||
| chr2:221543587
|
T | G | 148 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(145): Show | 148 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.823+20144A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221543587 | ||||||
| chr2:221543604
|
G | C | 10 | a0001c0001t0001g0245a0001c0001t0001g0294a0001c0001t0002g0095others(7): Show | 10 | HG00639.hp1 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.823+20127C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221543604 | ||||||
| chr2:221543611
|
A | G | 1 | a0001c0001t0004g0203 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.823+20120T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221543611 | ||||||
| chr2:221543617
|
T | A | 138 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(135): Show | 138 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.823+20114A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221543617 | ||||||
| chr2:221543882
|
A | G | 1 | a0001c0001t0001g0208 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.823+19849T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221543882 | ||||||
| chr2:221543885
|
A | G | 10 | a0001c0001t0001g0245a0001c0001t0001g0294a0001c0001t0002g0095others(7): Show | 10 | HG00639.hp1 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.823+19846T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221543885 | ||||||
| chr2:221543948
|
C | T | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.823+19783G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221543948 | ||||||
| chr2:221544091
|
G | A | 1 | a0001c0001t0012g0275 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.823+19640C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221544091 | ||||||
| chr2:221544108
|
C | A | 1 | a0001c0001t0001g0294 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.823+19623G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221544108 | ||||||
| chr2:221544260
|
C | A | 1 | a0001c0001t0001g0256 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.823+19471G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221544260 | ||||||
| chr2:221544287
|
T | A | 1 | a0001c0001t0001g0120 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.823+19444A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221544287 | ||||||
| chr2:221544308
|
T | C | 1 | a0001c0001t0001g0017 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.823+19423A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221544308 | ||||||
| chr2:221544579
|
G | T | 27 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0037others(24): Show | 27 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.823+19152C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221544579 | ||||||
| chr2:221545199
|
G | A | 1 | a0001c0001t0012g0275 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.823+18532C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221545199 | ||||||
| chr2:221545212
|
CCGAGGTG others(15): Show |
C | 151 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(148): Show | 151 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.823+18497_823+1851 others(26): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221545212 | ||||||
| chr2:221545215
|
A | T | 1 | a0001c0003t0003g0093 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.823+18516T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221545215 | ||||||
| chr2:221545258
|
G | A | 1 | a0001c0003t0046g0278 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.823+18473C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221545258 | ||||||
| chr2:221545265
|
C | T | 9 | a0001c0001t0001g0245a0001c0001t0001g0294a0001c0001t0002g0095others(6): Show | 9 | HG00639.hp1 HG02615.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.823+18466G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221545265 | ||||||
| chr2:221545464
|
A | G | 168 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(165): Show | 168 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.823+18267T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221545464 | ||||||
| chr2:221545468
|
T | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(174): Show | 177 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.823+18263A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221545468 | ||||||
| chr2:221545479
|
A | AAAAAC | 3 | a0001c0005t0001g0029a0001c0005t0001g0034a0001c0005t0014g0040 | 3 | HG03834.hp2 HG04115.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.823+18247_823+1825 others(9): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221545479 | ||||||
| chr2:221545611
|
A | C | 169 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(166): Show | 169 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.823+18120T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221545611 | ||||||
| chr2:221545613
|
A | G | 27 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0037others(24): Show | 27 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.823+18118T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221545613 | ||||||
| chr2:221545648
|
G | A | 168 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(165): Show | 168 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.823+18083C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221545648 | ||||||
| chr2:221545679
|
C | T | 39 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(36): Show | 39 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.823+18052G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221545679 | ||||||
| chr2:221545806
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.823+17925G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221545806 | ||||||
| chr2:221545817
|
GACCTGGA others(4): Show |
G | 1 | a0001c0002t0007g0239 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.823+17903_823+1791 others(15): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221545817 | ||||||
| chr2:221545850
|
C | G | 1 | a0001c0001t0001g0208 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.823+17881G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221545850 | ||||||
| chr2:221546006
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.823+17725G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221546006 | ||||||
| chr2:221546007
|
T | C | 1 | a0001c0001t0001g0168 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.823+17724A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221546007 | ||||||
| chr2:221546518
|
T | C | 33 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0037others(30): Show | 33 | HG00544.hp2 HG00738.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.823+17213A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221546518 | ||||||
| chr2:221546681
|
G | C | 1 | a0001c0001t0002g0051 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.823+17050C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221546681 | ||||||
| chr2:221546791
|
C | G | 2 | a0001c0001t0036g0115a0001c0003t0003g0114 | 2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.823+16940G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221546791 | ||||||
| chr2:221546875
|
G | T | 6 | a0001c0001t0004g0235a0001c0001t0006g0246a0001c0001t0044g0232others(3): Show | 6 | HG02145.hp1 HG02280.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+16856C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221546875 | ||||||
| chr2:221546928
|
A | T | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.823+16803T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221546928 | ||||||
| chr2:221547732
|
C | T | 27 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0062others(24): Show | 27 | HG00423.hp2 HG00544.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.823+15999G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221547732 | ||||||
| chr2:221547756
|
G | A | 6 | a0001c0001t0004g0235a0001c0001t0006g0246a0001c0001t0044g0232others(3): Show | 6 | HG02145.hp1 HG02280.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+15975C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221547756 | ||||||
| chr2:221547785
|
C | G | 1 | a0001c0001t0001g0022 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.823+15946G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221547785 | ||||||
| chr2:221547803
|
A | T | 1 | a0001c0003t0001g0087 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.823+15928T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221547803 | ||||||
| chr2:221547817
|
G | A | 69 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(66): Show | 69 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.823+15914C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221547817 | ||||||
| chr2:221547967
|
C | A | 6 | a0001c0001t0001g0294a0001c0001t0018g0113a0001c0001t0036g0115others(3): Show | 6 | HG00639.hp1 HG03195.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+15764G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221547967 | ||||||
| chr2:221548128
|
G | A | 1 | a0001c0001t0006g0238 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.823+15603C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221548128 | ||||||
| chr2:221548186
|
G | C | 4 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0052others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.823+15545C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221548186 | ||||||
| chr2:221548222
|
C | T | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.823+15509G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221548222 | ||||||
| chr2:221548319
|
G | A | 1 | a0001c0005t0001g0034 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.823+15412C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221548319 | ||||||
| chr2:221548320
|
C | T | 5 | a0001c0001t0018g0113a0001c0001t0036g0115a0001c0003t0003g0114others(2): Show | 5 | HG03195.hp2 HG03579.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.823+15411G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221548320 | ||||||
| chr2:221548331
|
T | C | 28 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0060others(25): Show | 28 | HG00423.hp2 HG00544.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.823+15400A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221548331 | ||||||
| chr2:221548349
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.823+15382G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221548349 | ||||||
| chr2:221548358
|
G | A | 2 | a0001c0002t0001g0125a0001c0002t0001g0149 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.823+15373C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221548358 | ||||||
| chr2:221548608
|
C | T | 1 | a0001c0001t0040g0128 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.823+15123G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221548608 | ||||||
| chr2:221548712
|
G | A | 2 | a0001c0001t0033g0170a0001c0008t0003g0157 | 2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.823+15019C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221548712 | ||||||
| chr2:221548729
|
T | C | 3 | a0001c0001t0018g0113a0001c0006t0003g0118a0001c0012t0018g0272 | 3 | HG03195.hp2 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.823+15002A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221548729 | ||||||
| chr2:221548906
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.823+14825C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221548906 | ||||||
| chr2:221548921
|
G | A | 1 | a0001c0006t0003g0118 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.823+14810C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221548921 | ||||||
| chr2:221548923
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.823+14808G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221548923 | ||||||
| chr2:221549238
|
T | C | 5 | a0001c0001t0018g0113a0001c0001t0036g0115a0001c0003t0003g0114others(2): Show | 5 | HG03195.hp2 HG03579.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.823+14493A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221549238 | ||||||
| chr2:221549440
|
T | C | 69 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(66): Show | 69 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.823+14291A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221549440 | ||||||
| chr2:221549699
|
C | T | 1 | a0001c0002t0001g0019 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.823+14032G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221549699 | ||||||
| chr2:221549706
|
A | G | 5 | a0001c0001t0018g0113a0001c0001t0036g0115a0001c0003t0003g0114others(2): Show | 5 | HG03195.hp2 HG03579.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.823+14025T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221549706 | ||||||
| chr2:221549743
|
T | C | 28 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0060others(25): Show | 28 | HG00423.hp2 HG00544.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.823+13988A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221549743 | ||||||
| chr2:221549802
|
C | G | 14 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0112others(11): Show | 14 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.823+13929G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221549802 | ||||||
| chr2:221550108
|
A | G | 1 | a0001c0001t0006g0250 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.823+13623T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221550108 | ||||||
| chr2:221550181
|
G | A | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.823+13550C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221550181 | ||||||
| chr2:221550349
|
T | G | 3 | a0001c0001t0018g0113a0001c0006t0003g0118a0001c0012t0018g0272 | 3 | HG03195.hp2 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.823+13382A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221550349 | ||||||
| chr2:221550396
|
A | G | 1 | a0001c0001t0005g0023 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.823+13335T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221550396 | ||||||
| chr2:221550416
|
G | GGA | 17 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0002g0095others(14): Show | 17 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.823+13314_823+1331 others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221550416 | ||||||
| chr2:221550416
|
G | GGAGA | 27 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(24): Show | 27 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.823+13314_823+1331 others(8): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221550416 | ||||||
| chr2:221550416
|
G | GGAGAGA | 30 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0022others(27): Show | 30 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.823+13314_823+1331 others(10): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221550416 | ||||||
| chr2:221550416
|
G | GGAGAGAG others(1): Show |
13 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0060others(10): Show | 13 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.823+13314_823+1331 others(12): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221550416 | ||||||
| chr2:221550416
|
G | GGAGAGAG others(3): Show |
4 | a0001c0001t0001g0200a0001c0003t0001g0087a0001c0005t0001g0029others(1): Show | 4 | HG00733.hp2 HG01074.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.823+13314_823+1331 others(14): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221550416 | ||||||
| chr2:221550416
|
G | GGAGAGAG others(5): Show |
10 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0121others(7): Show | 10 | HG00544.hp1 HG01123.hp1 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.823+13314_823+1331 others(16): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221550416 | ||||||
| chr2:221550416
|
G | GGAGAGAG others(7): Show |
2 | a0001c0001t0001g0063a0001c0007t0005g0061 | 2 | NA18943.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.823+13314_823+1331 others(18): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221550416 | ||||||
| chr2:221550416
|
G | GGAGAGAG others(9): Show |
2 | a0001c0001t0007g0076a0001c0001t0007g0078 | 2 | NA18989.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.823+13314_823+1331 others(20): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221550416 | ||||||
| chr2:221550416
|
G | GGAGAGAG others(11): Show |
4 | a0001c0001t0001g0042a0001c0001t0002g0123a0001c0001t0004g0003others(1): Show | 4 | HG02015.hp1 HG02027.hp2 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.823+13314_823+1331 others(22): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221550416 | ||||||
| chr2:221550416
|
G | GGAGAGAG others(13): Show |
1 | a0001c0003t0003g0093 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.823+13314_823+1331 others(24): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221550416 | ||||||
| chr2:221550416
|
G | GGAGAGAG others(15): Show |
1 | a0001c0001t0001g0062 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.823+13314_823+1331 others(26): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221550416 | ||||||
| chr2:221550416
|
G | GGAGAGAG others(19): Show |
1 | a0001c0001t0001g0041 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.823+13314_823+1331 others(30): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221550416 | ||||||
| chr2:221550416
|
GGGGAGAG others(3): Show |
G | 3 | a0001c0001t0036g0115a0001c0003t0003g0114a0001c0012t0018g0272 | 3 | HG03579.hp2 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.823+13305_823+1331 others(14): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221550416 | ||||||
| chr2:221550416
|
GGGGAGAG others(5): Show |
G | 2 | a0001c0001t0018g0113a0001c0006t0003g0118 | 2 | HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.823+13303_823+1331 others(16): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221550416 | ||||||
| chr2:221550418
|
G | A | 114 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(111): Show | 114 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.823+13313C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221550418 | ||||||
| chr2:221550418
|
G | GGA | 6 | a0001c0001t0001g0231a0001c0001t0001g0260a0001c0001t0021g0156others(3): Show | 6 | HG02523.hp1 HG03491.hp1 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+13311_823+1331 others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221550418 | ||||||
| chr2:221550418
|
GGA | G | 15 | a0001c0001t0001g0152a0001c0001t0001g0190a0001c0001t0002g0111others(12): Show | 15 | HG00642.hp2 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.823+13311_823+1331 others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221550418 | ||||||
| chr2:221550418
|
GGAGA | G | 7 | a0001c0001t0001g0287a0001c0001t0004g0291a0001c0001t0013g0290others(4): Show | 7 | HG00741.hp1 HG01891.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.823+13309_823+1331 others(8): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221550418 | ||||||
| chr2:221550418
|
GGAGAGA | G | 51 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0092others(48): Show | 51 | HG00280.hp1 HG00408.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.823+13307_823+1331 others(10): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221550418 | ||||||
| chr2:221550478
|
A | G | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0002g0067 | 3 | HG00544.hp1 NA18981.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.823+13253T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221550478 | ||||||
| chr2:221550886
|
C | T | 1 | a0001c0006t0003g0118 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.823+12845G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221550886 | ||||||
| chr2:221551457
|
C | T | 6 | a0001c0001t0001g0294a0001c0001t0018g0113a0001c0001t0036g0115others(3): Show | 6 | HG00639.hp1 HG03195.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+12274G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221551457 | ||||||
| chr2:221551705
|
C | T | 1 | a0001c0002t0002g0043 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.823+12026G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221551705 | ||||||
| chr2:221551845
|
T | C | 4 | a0001c0001t0001g0120a0001c0001t0002g0179a0001c0001t0004g0194others(1): Show | 4 | HG01106.hp2 HG01261.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.823+11886A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221551845 | ||||||
| chr2:221551892
|
T | A | 1 | a0001c0001t0002g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.823+11839A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221551892 | ||||||
| chr2:221551983
|
G | A | 5 | a0001c0001t0018g0113a0001c0001t0036g0115a0001c0003t0003g0114others(2): Show | 5 | HG03195.hp2 HG03579.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.823+11748C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221551983 | ||||||
| chr2:221551985
|
A | T | 5 | a0001c0001t0018g0113a0001c0001t0036g0115a0001c0003t0003g0114others(2): Show | 5 | HG03195.hp2 HG03579.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.823+11746T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221551985 | ||||||
| chr2:221552109
|
G | T | 3 | a0001c0001t0018g0113a0001c0006t0003g0118a0001c0012t0018g0272 | 3 | HG03195.hp2 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.823+11622C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221552109 | ||||||
| chr2:221552125
|
C | T | 14 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0112others(11): Show | 14 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.823+11606G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221552125 | ||||||
| chr2:221552214
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.823+11517G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221552214 | ||||||
| chr2:221552404
|
C | A | 1 | a0001c0001t0001g0042 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.823+11327G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221552404 | ||||||
| chr2:221552438
|
T | C | 1 | a0001c0001t0001g0294 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.823+11293A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221552438 | ||||||
| chr2:221552531
|
G | A | 14 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0112others(11): Show | 14 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.823+11200C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221552531 | ||||||
| chr2:221552610
|
G | A | 5 | a0001c0001t0018g0113a0001c0001t0036g0115a0001c0003t0003g0114others(2): Show | 5 | HG03195.hp2 HG03579.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.823+11121C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221552610 | ||||||
| chr2:221552622
|
C | G | 2 | a0001c0002t0001g0125a0001c0002t0001g0149 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.823+11109G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221552622 | ||||||
| chr2:221552804
|
T | C | 5 | a0001c0001t0001g0287a0001c0001t0004g0291a0001c0001t0013g0290others(2): Show | 5 | HG01891.hp1 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.823+10927A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221552804 | ||||||
| chr2:221552856
|
G | T | 14 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0112others(11): Show | 14 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.823+10875C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221552856 | ||||||
| chr2:221553008
|
G | T | 2 | a0001c0001t0001g0182a0001c0001t0001g0202 | 2 | HG01433.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.823+10723C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221553008 | ||||||
| chr2:221553214
|
T | C | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.823+10517A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221553214 | ||||||
| chr2:221553277
|
C | A | 1 | a0001c0001t0001g0200 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.823+10454G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221553277 | ||||||
| chr2:221553391
|
T | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | NA19057.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.823+10340A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221553391 | ||||||
| chr2:221553593
|
G | A | 1 | a0001c0002t0029g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.823+10138C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221553593 | ||||||
| chr2:221553634
|
T | C | 1 | a0001c0001t0001g0253 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.823+10097A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221553634 | ||||||
| chr2:221553711
|
C | T | 1 | a0001c0001t0001g0171 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.823+10020G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221553711 | ||||||
| chr2:221553723
|
A | G | 1 | a0001c0002t0001g0195 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.823+10008T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221553723 | ||||||
| chr2:221553773
|
A | G | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.823+9958T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221553773 | ||||||
| chr2:221553946
|
A | G | 1 | a0001c0002t0004g0234 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.823+9785T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221553946 | ||||||
| chr2:221554430
|
C | T | 2 | a0001c0001t0036g0115a0001c0003t0003g0114 | 2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.823+9301G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221554430 | ||||||
| chr2:221554506
|
C | T | 3 | a0001c0001t0018g0113a0001c0006t0003g0118a0001c0012t0018g0272 | 3 | HG03195.hp2 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.823+9225G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221554506 | ||||||
| chr2:221555144
|
G | A | 16 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0112others(13): Show | 16 | HG00639.hp1 HG01975.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.823+8587C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221555144 | ||||||
| chr2:221555145
|
G | C | 61 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0092others(58): Show | 61 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.823+8586C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221555145 | ||||||
| chr2:221555314
|
G | C | 1 | a0001c0001t0001g0007 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.823+8417C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221555314 | ||||||
| chr2:221555642
|
GAGGTACC others(9): Show |
G | 1 | a0001c0001t0001g0050 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.823+8073_823+8088d others(18): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221555642 | ||||||
| chr2:221555684
|
C | T | 1 | a0001c0002t0002g0053 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.823+8047G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221555684 | ||||||
| chr2:221555707
|
G | A | 1 | a0001c0001t0002g0142 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.823+8024C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221555707 | ||||||
| chr2:221555752
|
C | A | 1 | a0001c0002t0001g0054 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.823+7979G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221555752 | ||||||
| chr2:221556028
|
G | A | 5 | a0001c0001t0009g0274a0001c0001t0018g0113a0001c0002t0022g0273others(2): Show | 5 | HG03195.hp2 HG03516.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.823+7703C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221556028 | ||||||
| chr2:221556107
|
C | T | 1 | a0001c0001t0001g0062 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.823+7624G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221556107 | ||||||
| chr2:221556207
|
G | A | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.823+7524C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221556207 | ||||||
| chr2:221556424
|
G | A | 4 | a0001c0001t0001g0220a0001c0001t0001g0282a0001c0001t0002g0277others(1): Show | 4 | HG00280.hp1 HG01081.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.823+7307C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221556424 | ||||||
| chr2:221556471
|
A | AT | 8 | a0001c0001t0001g0155a0001c0001t0001g0294a0001c0001t0002g0147others(5): Show | 8 | HG00639.hp1 HG02145.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.823+7259dupA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221556471 | ||||||
| chr2:221556471
|
A | ATT | 44 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0060others(41): Show | 44 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.823+7258_823+7259d others(4): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221556471 | ||||||
| chr2:221556596
|
C | T | 27 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0060others(24): Show | 27 | HG00423.hp2 HG00544.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.823+7135G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221556596 | ||||||
| chr2:221556605
|
C | CTT | 14 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0112others(11): Show | 14 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.823+7124_823+7125d others(4): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221556605 | ||||||
| chr2:221556650
|
C | G | 1 | a0001c0001t0005g0116 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.823+7081G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221556650 | ||||||
| chr2:221556711
|
C | T | 55 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0092others(52): Show | 55 | HG00280.hp1 HG00408.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.823+7020G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221556711 | ||||||
| chr2:221556719
|
C | T | 3 | a0001c0001t0009g0274a0001c0002t0022g0273a0001c0006t0003g0118 | 3 | HG03516.hp2 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.823+7012G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221556719 | ||||||
| chr2:221556731
|
A | G | 1 | a0001c0001t0012g0275 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.823+7000T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221556731 | ||||||
| chr2:221556951
|
T | A | 71 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.823+6780A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221556951 | ||||||
| chr2:221556951
|
T | C | 15 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0112others(12): Show | 15 | HG00639.hp1 HG01975.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.823+6780A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221556951 | ||||||
| chr2:221556964
|
C | T | 1 | a0001c0002t0029g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.823+6767G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221556964 | ||||||
| chr2:221556965
|
G | A | 1 | a0001c0001t0049g0227 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.823+6766C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221556965 | ||||||
| chr2:221556965
|
G | C | 1 | a0001c0002t0029g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.823+6766C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221556965 | ||||||
| chr2:221557005
|
C | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(82): Show | 85 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.823+6726G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221557005 | ||||||
| chr2:221557097
|
T | C | 2 | a0001c0001t0001g0022a0001c0001t0004g0057 | 2 | HG02071.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.823+6634A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221557097 | ||||||
| chr2:221557107
|
A | C | 3 | a0001c0001t0001g0063a0001c0001t0002g0064a0001c0001t0002g0066 | 3 | NA18943.hp1 NA18975.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.823+6624T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221557107 | ||||||
| chr2:221557238
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.823+6493C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221557238 | ||||||
| chr2:221557404
|
T | TGAA | 71 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.823+6326_823+6327i others(5): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221557404 | ||||||
| chr2:221557406
|
A | T | 71 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.823+6325T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221557406 | ||||||
| chr2:221557407
|
C | A | 71 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.823+6324G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221557407 | ||||||
| chr2:221557464
|
C | T | 1 | a0001c0005t0001g0034 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.823+6267G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221557464 | ||||||
| chr2:221557523
|
G | A | 2 | a0001c0001t0036g0115a0001c0003t0003g0114 | 2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.823+6208C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221557523 | ||||||
| chr2:221557623
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.823+6108A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221557623 | ||||||
| chr2:221557691
|
TA | T | 55 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0092others(52): Show | 55 | HG00280.hp1 HG00408.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.823+6039delT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221557691 | ||||||
| chr2:221558027
|
G | A | 1 | a0001c0001t0002g0206 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.823+5704C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221558027 | ||||||
| chr2:221558428
|
G | A | 5 | a0001c0001t0009g0274a0001c0001t0018g0113a0001c0002t0022g0273others(2): Show | 5 | HG03195.hp2 HG03516.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.823+5303C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221558428 | ||||||
| chr2:221558599
|
T | C | 6 | a0001c0001t0008g0117a0001c0001t0008g0132a0001c0001t0008g0134others(3): Show | 6 | HG01884.hp1 HG02257.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.823+5132A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221558599 | ||||||
| chr2:221558621
|
A | G | 2 | a0001c0001t0011g0240a0001c0001t0011g0241 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.823+5110T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221558621 | ||||||
| chr2:221558669
|
G | A | 126 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(123): Show | 126 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.823+5062C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221558669 | ||||||
| chr2:221558839
|
G | A | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.823+4892C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221558839 | ||||||
| chr2:221558854
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | NA18977.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.823+4877G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221558854 | ||||||
| chr2:221558923
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.823+4808T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221558923 | ||||||
| chr2:221558956
|
C | T | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.823+4775G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221558956 | ||||||
| chr2:221559040
|
AT | A | 86 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(83): Show | 86 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.823+4690delA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221559040 | ||||||
| chr2:221559088
|
T | C | 1 | a0001c0002t0029g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.823+4643A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221559088 | ||||||
| chr2:221559305
|
T | A | 2 | a0001c0001t0033g0170a0001c0008t0003g0157 | 2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.823+4426A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221559305 | ||||||
| chr2:221559342
|
G | A | 91 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(88): Show | 91 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.823+4389C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221559342 | ||||||
| chr2:221559739
|
T | C | 1 | a0001c0002t0029g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.823+3992A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221559739 | ||||||
| chr2:221559824
|
T | C | 32 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0060others(29): Show | 32 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.823+3907A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221559824 | ||||||
| chr2:221559982
|
C | T | 1 | a0001c0002t0001g0195 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.823+3749G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221559982 | ||||||
| chr2:221560113
|
G | A | 1 | a0001c0001t0004g0235 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.823+3618C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221560113 | ||||||
| chr2:221560120
|
C | G | 1 | a0001c0002t0001g0020 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.823+3611G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221560120 | ||||||
| chr2:221560185
|
C | T | 2 | a0001c0001t0005g0165a0001c0001t0021g0156 | 2 | HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.823+3546G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221560185 | ||||||
| chr2:221560445
|
A | C | 32 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0060others(29): Show | 32 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.823+3286T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221560445 | ||||||
| chr2:221560582
|
C | T | 2 | a0001c0001t0001g0260a0001c0002t0001g0259 | 2 | HG02523.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.823+3149G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221560582 | ||||||
| chr2:221560848
|
C | T | 2 | a0001c0001t0033g0170a0001c0008t0003g0157 | 2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.823+2883G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221560848 | ||||||
| chr2:221560900
|
A | G | 9 | a0001c0001t0001g0220a0001c0001t0001g0282a0001c0001t0002g0277others(6): Show | 9 | HG00280.hp1 HG00741.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.823+2831T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221560900 | ||||||
| chr2:221560980
|
C | T | 14 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0112others(11): Show | 14 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.823+2751G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221560980 | ||||||
| chr2:221561098
|
C | T | 55 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0092others(52): Show | 55 | HG00280.hp1 HG00408.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.823+2633G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221561098 | ||||||
| chr2:221561099
|
A | G | 196 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 196 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.823+2632T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221561099 | ||||||
| chr2:221561114
|
C | T | 1 | a0001c0001t0004g0203 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.823+2617G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221561114 | ||||||
| chr2:221561119
|
G | A | 52 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0092others(49): Show | 52 | HG00280.hp1 HG00408.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.823+2612C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221561119 | ||||||
| chr2:221561128
|
G | T | 2 | a0001c0001t0001g0182a0001c0001t0001g0202 | 2 | HG01433.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.823+2603C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221561128 | ||||||
| chr2:221561242
|
A | AAAAT | 16 | a0001c0001t0001g0105a0001c0001t0001g0112a0001c0001t0002g0010others(13): Show | 16 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.823+2485_823+2488d others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221561242 | ||||||
| chr2:221561242
|
AAAAT | A | 6 | a0001c0001t0001g0294a0001c0001t0009g0274a0001c0001t0018g0113others(3): Show | 6 | HG00639.hp1 HG03195.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.823+2485_823+2488d others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221561242 | ||||||
| chr2:221561278
|
C | T | 1 | a0001c0001t0001g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.823+2453G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221561278 | ||||||
| chr2:221561296
|
T | G | 71 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.823+2435A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221561296 | ||||||
| chr2:221561299
|
G | T | 2 | a0001c0001t0004g0235a0001c0002t0004g0234 | 2 | HG02145.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.823+2432C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221561299 | ||||||
| chr2:221561611
|
C | T | 2 | a0001c0004t0019g0236a0001c0004t0019g0237 | 2 | HG01243.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.823+2120G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221561611 | ||||||
| chr2:221562008
|
T | C | 14 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0112others(11): Show | 14 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.823+1723A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221562008 | ||||||
| chr2:221562128
|
A | G | 4 | a0001c0003t0001g0085a0001c0003t0001g0086a0001c0003t0004g0084others(1): Show | 4 | HG00323.hp2 HG01169.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.823+1603T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221562128 | ||||||
| chr2:221562140
|
G | C | 5 | a0001c0001t0009g0274a0001c0001t0018g0113a0001c0002t0022g0273others(2): Show | 5 | HG03195.hp2 HG03516.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.823+1591C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221562140 | ||||||
| chr2:221562183
|
T | C | 1 | a0001c0001t0001g0065 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.823+1548A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221562183 | ||||||
| chr2:221562207
|
C | CT | 104 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(101): Show | 104 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.823+1523dupA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221562207 | ||||||
| chr2:221562207
|
C | CTT | 12 | a0001c0001t0001g0225a0001c0001t0002g0027a0001c0001t0002g0095others(9): Show | 12 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.823+1522_823+1523d others(4): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221562207 | ||||||
| chr2:221562207
|
CT | C | 9 | a0001c0001t0001g0193a0001c0001t0001g0205a0001c0001t0001g0211others(6): Show | 9 | HG00741.hp2 HG01243.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.823+1523delA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221562207 | ||||||
| chr2:221562439
|
T | C | 1 | a0001c0001t0001g0231 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.823+1292A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221562439 | ||||||
| chr2:221562714
|
T | A | 1 | a0001c0002t0023g0219 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.823+1017A>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221562714 | ||||||
| chr2:221562809
|
A | G | 1 | a0001c0001t0008g0117 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.823+922T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221562809 | ||||||
| chr2:221562873
|
G | A | 1 | a0001c0002t0001g0195 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.823+858C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221562873 | ||||||
| chr2:221562936
|
G | C | 1 | a0001c0001t0013g0290 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.823+795C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221562936 | ||||||
| chr2:221563034
|
T | G | 1 | a0001c0001t0001g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.823+697A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221563034 | ||||||
| chr2:221563151
|
T | C | 191 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(188): Show | 191 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.823+580A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221563151 | ||||||
| chr2:221563200
|
C | T | 2 | a0001c0001t0009g0274a0001c0002t0022g0273 | 2 | HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.823+531G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221563200 | ||||||
| chr2:221563208
|
C | G | 1 | a0001c0001t0006g0238 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.823+523G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221563208 | ||||||
| chr2:221563419
|
G | A | 1 | a0001c0001t0002g0146 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.823+312C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221563419 | ||||||
| chr2:221563533
|
C | G | 2 | a0001c0001t0004g0285a0001c0001t0005g0284 | 2 | HG03704.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.823+198G>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221563533 | ||||||
| chr2:221563612
|
G | A | 125 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(122): Show | 125 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.823+119C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221563612 | ||||||
| chr2:221563710
|
C | A | 1 | a0001c0001t0002g0160 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.823+21G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 3/17 | chr2 | 221563710 | ||||||
| chr2:221564576
|
G | GT | 85 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(82): Show | 85 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.160-183dupA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221564576 | ||||||
| chr2:221564648
|
G | T | 2 | a0001c0001t0036g0115a0001c0003t0003g0114 | 2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.160-254C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221564648 | ||||||
| chr2:221564887
|
C | CA | 59 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0001g0063others(56): Show | 59 | HG00323.hp2 HG00733.hp2 HG01106.hp1 others(56): Show |
intron_variant | MODIFIER | c.160-494dupT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221564887 | ||||||
| chr2:221564887
|
C | CAA | 21 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(18): Show | 21 | HG00423.hp2 HG00544.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.160-495_160-494dup others(2): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221564887 | ||||||
| chr2:221564887
|
CA | C | 7 | a0001c0001t0001g0221a0001c0001t0001g0294a0001c0001t0002g0158others(4): Show | 7 | HG00558.hp2 HG00639.hp1 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.160-494delT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221564887 | ||||||
| chr2:221564887
|
CAAA | C | 20 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0112others(17): Show | 20 | HG00423.hp1 HG01975.hp2 HG02129.hp1 others(17): Show |
intron_variant | MODIFIER | c.160-496_160-494del others(3): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221564887 | ||||||
| chr2:221564887
|
CAAAA | C | 35 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(32): Show | 35 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.160-497_160-494del others(4): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221564887 | ||||||
| chr2:221564887
|
CAAAAA | C | 27 | a0001c0001t0001g0033a0001c0001t0001g0038a0001c0001t0001g0041others(24): Show | 27 | HG00544.hp2 HG00738.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.160-498_160-494del others(5): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221564887 | ||||||
| chr2:221565382
|
G | T | 81 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(78): Show | 81 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.160-988C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221565382 | ||||||
| chr2:221565448
|
AGCTTAAG others(28): Show |
A | 1 | a0001c0001t0004g0057 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.160-1089_160-1055d others(37): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221565448 | ||||||
| chr2:221565507
|
A | T | 1 | a0001c0003t0003g0082 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.160-1113T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221565507 | ||||||
| chr2:221565776
|
T | C | 1 | a0001c0001t0002g0160 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.160-1382A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221565776 | ||||||
| chr2:221565914
|
T | C | 1 | a0001c0001t0004g0074 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.160-1520A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221565914 | ||||||
| chr2:221566110
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.160-1716A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566110 | ||||||
| chr2:221566204
|
C | T | 3 | a0001c0001t0009g0274a0001c0002t0022g0273a0001c0006t0003g0118 | 3 | HG03516.hp2 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.160-1810G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566204 | ||||||
| chr2:221566263
|
T | C | 30 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0001g0063others(27): Show | 30 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.160-1869A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566263 | ||||||
| chr2:221566271
|
A | G | 1 | a0001c0012t0018g0272 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.160-1877T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566271 | ||||||
| chr2:221566455
|
C | A | 1 | a0001c0002t0023g0219 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.160-2061G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566455 | ||||||
| chr2:221566722
|
G | T | 1 | a0001c0001t0001g0187 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.159+1996C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566722 | ||||||
| chr2:221566755
|
G | A | 1 | a0001c0006t0003g0118 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.159+1963C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566755 | ||||||
| chr2:221566787
|
G | T | 39 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0001g0063others(36): Show | 39 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.159+1931C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566787 | ||||||
| chr2:221566801
|
G | A | 145 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(142): Show | 145 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.159+1917C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566801 | ||||||
| chr2:221566836
|
A | AAGAAGG | 6 | a0001c0001t0001g0092a0001c0001t0018g0113a0001c0001t0036g0115others(3): Show | 6 | HG02723.hp1 HG03195.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.159+1876_159+1881d others(8): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566836 | ||||||
| chr2:221566836
|
A | AAGAAGGA others(5): Show |
1 | a0001c0001t0001g0172 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.159+1870_159+1881d others(14): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566836 | ||||||
| chr2:221566836
|
A | G | 1 | a0001c0002t0029g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.159+1882T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566836 | ||||||
| chr2:221566836
|
AAGAAGG | A | 139 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(136): Show | 139 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.159+1876_159+1881d others(8): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566836 | ||||||
| chr2:221566845
|
A | G | 6 | a0001c0001t0001g0245a0001c0001t0011g0240a0001c0001t0011g0241others(3): Show | 6 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.159+1873T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566845 | ||||||
| chr2:221566848
|
GAGA | G | 19 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0001g0063others(16): Show | 19 | HG00733.hp2 HG01123.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.159+1867_159+1869d others(5): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566848 | ||||||
| chr2:221566848
|
GAGAAGGA others(11): Show |
G | 1 | a0001c0001t0044g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.159+1852_159+1869d others(20): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566848 | ||||||
| chr2:221566851
|
A | G | 12 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(9): Show | 12 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.159+1867T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566851 | ||||||
| chr2:221566854
|
G | A | 20 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0069others(17): Show | 20 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(17): Show |
intron_variant | MODIFIER | c.159+1864C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566854 | ||||||
| chr2:221566854
|
G | GAGAAGA | 19 | a0001c0001t0001g0168a0001c0001t0001g0177a0001c0001t0001g0187others(16): Show | 19 | HG00642.hp1 HG01071.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.159+1858_159+1863d others(8): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566854 | ||||||
| chr2:221566854
|
G | GAGAAGAA others(11): Show |
1 | a0001c0001t0002g0169 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.159+1846_159+1863d others(20): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566854 | ||||||
| chr2:221566854
|
GAGAAGA | G | 3 | a0001c0001t0001g0139a0001c0001t0006g0238a0001c0001t0006g0246 | 3 | HG02129.hp2 HG03098.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.159+1858_159+1863d others(8): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566854 | ||||||
| chr2:221566860
|
A | G | 2 | a0001c0001t0001g0294a0001c0001t0009g0274 | 2 | HG00639.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.159+1858T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566860 | ||||||
| chr2:221566866
|
A | G | 2 | a0001c0001t0001g0294a0001c0001t0006g0250 | 2 | HG00639.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.159+1852T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566866 | ||||||
| chr2:221566872
|
A | AAGAAGAA others(8): Show |
1 | a0001c0002t0001g0195 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.159+1845_159+1846i others(17): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566872 | ||||||
| chr2:221566872
|
A | AAGAAGAA others(5): Show |
23 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0144others(20): Show | 23 | HG00408.hp2 HG01074.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.159+1845_159+1846i others(14): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566872 | ||||||
| chr2:221566872
|
A | AAGAAGAA others(11): Show |
2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02523.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.159+1845_159+1846i others(20): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566872 | ||||||
| chr2:221566872
|
A | AAGAAGAA others(8): Show |
1 | a0001c0001t0002g0206 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.159+1845_159+1846i others(17): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566872 | ||||||
| chr2:221566872
|
A | AAGAAGG | 3 | a0001c0001t0001g0154a0001c0001t0008g0135a0001c0001t0042g0153 | 3 | HG03486.hp1 NA18968.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.159+1840_159+1845d others(8): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566872 | ||||||
| chr2:221566872
|
A | AAGAAGGA others(5): Show |
3 | a0001c0001t0005g0116a0001c0001t0008g0134a0001c0001t0011g0138 | 3 | HG02145.hp2 HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.159+1834_159+1845d others(14): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566872 | ||||||
| chr2:221566872
|
A | AAGAAGGA others(11): Show |
1 | a0001c0001t0027g0137 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.159+1828_159+1845d others(20): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566872 | ||||||
| chr2:221566872
|
A | G | 31 | a0001c0001t0001g0249a0001c0001t0001g0253a0001c0001t0001g0255others(28): Show | 31 | HG00408.hp1 HG00639.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.159+1846T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566872 | ||||||
| chr2:221566875
|
AAGGAGAA others(2): Show |
A | 3 | a0001c0001t0001g0065a0001c0001t0002g0064a0001c0001t0002g0066 | 3 | NA18975.hp1 NA19068.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.159+1834_159+1842d others(11): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566875 | ||||||
| chr2:221566875
|
AAGGAGAA others(8): Show |
A | 5 | a0001c0001t0001g0282a0001c0001t0012g0275a0001c0001t0016g0058others(2): Show | 5 | HG01169.hp1 HG01257.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.159+1828_159+1842d others(17): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566875 | ||||||
| chr2:221566875
|
AAGGAGAA others(14): Show |
A | 2 | a0001c0001t0002g0280a0001c0003t0003g0281 | 2 | HG01081.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.159+1822_159+1842d others(23): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566875 | ||||||
| chr2:221566875
|
AAGGAGAA others(20): Show |
A | 8 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0121others(5): Show | 8 | HG00544.hp1 HG02300.hp2 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.159+1816_159+1842d others(29): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566875 | ||||||
| chr2:221566875
|
AAGGAGAA others(26): Show |
A | 2 | a0001c0001t0001g0070a0001c0001t0001g0081 | 2 | HG00423.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.159+1810_159+1842d others(35): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566875 | ||||||
| chr2:221566875
|
AAGGAGAA others(32): Show |
A | 1 | a0001c0003t0003g0226 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.159+1804_159+1842d others(41): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566875 | ||||||
| chr2:221566878
|
G | A | 165 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(162): Show | 165 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.159+1840C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566878 | ||||||
| chr2:221566884
|
G | A | 127 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(124): Show | 127 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.159+1834C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566884 | ||||||
| chr2:221566890
|
G | A | 128 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.159+1828C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566890 | ||||||
| chr2:221566896
|
G | A | 132 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(129): Show | 132 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.159+1822C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566896 | ||||||
| chr2:221566901
|
G | A | 1 | a0001c0003t0003g0093 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.159+1817C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566901 | ||||||
| chr2:221566902
|
G | A | 134 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(131): Show | 134 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.159+1816C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566902 | ||||||
| chr2:221566907
|
G | A | 3 | a0001c0001t0018g0113a0001c0001t0036g0115a0001c0003t0003g0114 | 3 | HG03195.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.159+1811C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566907 | ||||||
| chr2:221566908
|
G | A | 142 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(139): Show | 142 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.159+1810C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566908 | ||||||
| chr2:221566912
|
AG | A | 3 | a0001c0001t0002g0123a0001c0003t0001g0085a0001c0003t0004g0084 | 3 | HG00323.hp2 HG01261.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.159+1805delC | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566912 | ||||||
| chr2:221566912
|
AGGAGAAG others(38): Show |
A | 3 | a0001c0001t0004g0285a0001c0001t0011g0240a0001c0001t0011g0241 | 3 | HG02896.hp2 HG02897.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.159+1761_159+1805d others(47): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566912 | ||||||
| chr2:221566913
|
G | A | 1 | a0001c0002t0022g0273 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.159+1805C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566913 | ||||||
| chr2:221566913
|
GGAGAAGG others(3): Show |
G | 2 | a0001c0001t0004g0074a0001c0007t0005g0061 | 2 | NA18948.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.159+1795_159+1804d others(12): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566913 | ||||||
| chr2:221566914
|
G | A | 134 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(131): Show | 134 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.159+1804C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566914 | ||||||
| chr2:221566915
|
A | G | 1 | a0001c0002t0029g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.159+1803T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566915 | ||||||
| chr2:221566915
|
A | T | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0002g0067 | 3 | HG00544.hp1 NA18981.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.159+1803T>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566915 | ||||||
| chr2:221566915
|
AGAAGGAG others(35): Show |
A | 1 | a0001c0001t0034g0243 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.159+1761_159+1802d others(44): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566915 | ||||||
| chr2:221566916
|
GAAGGAGA others(16): Show |
G | 3 | a0001c0001t0002g0123a0001c0003t0001g0085a0001c0003t0004g0084 | 3 | HG00323.hp2 HG01261.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.159+1779_159+1801d others(25): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566916 | ||||||
| chr2:221566918
|
AGGAGAAG others(32): Show |
A | 4 | a0001c0001t0001g0225a0001c0001t0002g0277a0001c0001t0015g0244others(1): Show | 4 | HG00741.hp1 HG01106.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.159+1761_159+1799d others(41): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566918 | ||||||
| chr2:221566919
|
G | A | 1 | a0001c0001t0009g0274 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.159+1799C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566919 | ||||||
| chr2:221566919
|
GGAGAAGG others(3): Show |
G | 3 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0007g0078 | 3 | NA18986.hp1 NA18989.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.159+1789_159+1798d others(12): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566919 | ||||||
| chr2:221566919
|
GGAGAAGG others(9): Show |
G | 6 | a0001c0001t0001g0063a0001c0001t0002g0075a0001c0001t0007g0076others(3): Show | 6 | HG00733.hp2 HG01123.hp1 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.159+1783_159+1798d others(18): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566919 | ||||||
| chr2:221566920
|
G | A | 117 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(114): Show | 117 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.159+1798C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566920 | ||||||
| chr2:221566921
|
A | G | 1 | a0001c0002t0029g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.159+1797T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566921 | ||||||
| chr2:221566921
|
AGAAGGAG others(29): Show |
A | 2 | a0001c0001t0001g0220a0001c0001t0001g0245 | 2 | HG00280.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.159+1761_159+1796d others(38): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566921 | ||||||
| chr2:221566923
|
A | G | 3 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0004g0057 | 3 | HG02071.hp1 HG02165.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.159+1795T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566923 | ||||||
| chr2:221566924
|
A | AGAGGAGG others(5): Show |
2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | NA19057.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.159+1793_159+1794i others(14): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566924 | ||||||
| chr2:221566924
|
A | AGAGGAGG others(11): Show |
1 | a0001c0002t0001g0055 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.159+1793_159+1794i others(20): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566924 | ||||||
| chr2:221566924
|
A | G | 6 | a0001c0001t0001g0270a0001c0001t0017g0103a0001c0002t0012g0099others(3): Show | 6 | HG00280.hp2 HG00323.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.159+1794T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566924 | ||||||
| chr2:221566924
|
AG | A | 6 | a0001c0001t0001g0002a0001c0001t0002g0014a0001c0001t0004g0003others(3): Show | 6 | HG00423.hp1 HG00558.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.159+1793delC | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566924 | ||||||
| chr2:221566924
|
AGGAGAAG others(26): Show |
A | 1 | a0001c0001t0005g0284 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.159+1761_159+1793d others(35): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566924 | ||||||
| chr2:221566925
|
G | GAA | 3 | a0001c0001t0001g0024a0001c0001t0005g0023a0001c0001t0037g0100 | 3 | NA19009.hp1 NA19043.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.159+1792_159+1793i others(4): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566925 | ||||||
| chr2:221566925
|
G | GAGGAGGA others(7): Show |
1 | a0001c0002t0001g0052 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.159+1792_159+1793i others(16): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566925 | ||||||
| chr2:221566925
|
GGA | G | 4 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0004g0074others(1): Show | 4 | HG02165.hp2 NA18944.hp1 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.159+1791_159+1792d others(4): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566925 | ||||||
| chr2:221566925
|
GGAGAAGG others(3): Show |
G | 1 | a0001c0001t0025g0233 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.159+1783_159+1792d others(12): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566925 | ||||||
| chr2:221566926
|
G | A | 100 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(97): Show | 100 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.159+1792C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566926 | ||||||
| chr2:221566927
|
A | AG | 4 | a0001c0001t0001g0112a0001c0001t0002g0027a0001c0001t0006g0028others(1): Show | 4 | HG01981.hp1 HG02809.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.159+1790dupC | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566927 | ||||||
| chr2:221566927
|
A | AGAGGAAG others(20): Show |
2 | a0001c0001t0036g0115a0001c0003t0003g0114 | 2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.159+1790_159+1791i others(29): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566927 | ||||||
| chr2:221566927
|
A | G | 8 | a0001c0001t0001g0270a0001c0001t0001g0294a0001c0001t0004g0057others(5): Show | 8 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(5): Show |
intron_variant | MODIFIER | c.159+1791T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566927 | ||||||
| chr2:221566927
|
AGAAGGAG others(23): Show |
A | 2 | a0001c0002t0028g0242a0001c0003t0046g0278 | 2 | HG03041.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.159+1761_159+1790d others(32): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566927 | ||||||
| chr2:221566929
|
A | AAG | 10 | a0001c0001t0001g0032a0001c0001t0001g0050a0001c0001t0001g0106others(7): Show | 10 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.159+1787_159+1788d others(4): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566929 | ||||||
| chr2:221566929
|
A | G | 9 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0002g0014others(6): Show | 9 | HG00423.hp1 HG00558.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.159+1789T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566929 | ||||||
| chr2:221566930
|
A | G | 15 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0036others(12): Show | 15 | HG01433.hp1 HG02004.hp2 HG02293.hp2 others(12): Show |
intron_variant | MODIFIER | c.159+1788T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566930 | ||||||
| chr2:221566930
|
AG | A | 3 | a0001c0001t0001g0006a0001c0002t0001g0054a0001c0002t0002g0053 | 3 | HG00738.hp1 NA18963.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.159+1787delC | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566930 | ||||||
| chr2:221566930
|
AGGAGAAG others(20): Show |
A | 1 | a0001c0001t0003g0279 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.159+1761_159+1787d others(29): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566930 | ||||||
| chr2:221566931
|
G | GAGGAGGA others(1): Show |
3 | a0001c0001t0001g0025a0001c0001t0001g0105a0001c0002t0012g0101 | 3 | HG02976.hp2 HG03139.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.159+1786_159+1787i others(10): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566931 | ||||||
| chr2:221566931
|
GGA | G | 7 | a0001c0001t0001g0002a0001c0001t0001g0060a0001c0001t0001g0062others(4): Show | 7 | HG00423.hp1 HG00558.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.159+1785_159+1786d others(4): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566931 | ||||||
| chr2:221566932
|
G | A | 90 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(87): Show | 90 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.159+1786C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566932 | ||||||
| chr2:221566933
|
A | AAGAG | 3 | a0001c0001t0001g0024a0001c0001t0005g0023a0001c0001t0037g0100 | 3 | NA19009.hp1 NA19043.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.159+1784_159+1785i others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566933 | ||||||
| chr2:221566933
|
A | AG | 13 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0050others(10): Show | 13 | HG01167.hp1 HG01169.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.159+1784dupC | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566933 | ||||||
| chr2:221566933
|
A | G | 32 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0017others(29): Show | 32 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.159+1785T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566933 | ||||||
| chr2:221566935
|
A | AAG | 5 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0119others(2): Show | 5 | HG00673.hp2 HG02129.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.159+1781_159+1782d others(4): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566935 | ||||||
| chr2:221566935
|
A | G | 5 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0002t0001g0054others(2): Show | 5 | HG00738.hp1 HG02080.hp2 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.159+1783T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566935 | ||||||
| chr2:221566936
|
A | G | 18 | a0001c0001t0001g0018a0001c0001t0001g0033a0001c0001t0001g0041others(15): Show | 18 | HG00544.hp2 HG01975.hp2 HG02004.hp1 others(15): Show |
intron_variant | MODIFIER | c.159+1782T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566936 | ||||||
| chr2:221566936
|
AGGAGAAG others(14): Show |
A | 1 | a0001c0003t0003g0082 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.159+1761_159+1781d others(23): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566936 | ||||||
| chr2:221566937
|
GGA | G | 7 | a0001c0001t0001g0006a0001c0001t0001g0063a0001c0001t0002g0075others(4): Show | 7 | HG00733.hp2 HG01123.hp1 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.159+1779_159+1780d others(4): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566937 | ||||||
| chr2:221566938
|
G | A | 118 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(115): Show | 118 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.159+1780C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566938 | ||||||
| chr2:221566938
|
G | GAGAAGAG others(8): Show |
2 | a0001c0002t0007g0239a0001c0002t0022g0090 | 2 | HG03516.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.159+1779_159+1780i others(17): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566938 | ||||||
| chr2:221566939
|
A | AAGAGGAA others(15): Show |
2 | a0001c0002t0001g0054a0001c0002t0002g0053 | 2 | HG00738.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.159+1778_159+1779i others(24): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566939 | ||||||
| chr2:221566939
|
A | AG | 7 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0119others(4): Show | 7 | HG00673.hp2 HG02129.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.159+1778dupC | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566939 | ||||||
| chr2:221566939
|
A | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(82): Show | 85 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.159+1779T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566939 | ||||||
| chr2:221566940
|
G | T | 2 | a0001c0001t0036g0115a0001c0003t0003g0114 | 2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.159+1778C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566940 | ||||||
| chr2:221566941
|
A | AAG | 3 | a0001c0001t0002g0223a0001c0001t0002g0224a0001c0003t0003g0079 | 3 | HG02895.hp2 HG02897.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.159+1775_159+1776d others(4): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566941 | ||||||
| chr2:221566941
|
A | G | 1 | a0001c0001t0002g0051 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.159+1777T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566941 | ||||||
| chr2:221566942
|
A | AGAG | 4 | a0001c0001t0001g0287a0001c0001t0015g0286a0001c0001t0032g0251others(1): Show | 4 | HG01891.hp1 HG02257.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+1775_159+1776i others(5): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566942 | ||||||
| chr2:221566942
|
A | G | 7 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0010g0107others(4): Show | 7 | HG01243.hp2 HG02004.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.159+1776T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566942 | ||||||
| chr2:221566942
|
AGGAGAAG others(8): Show |
A | 1 | a0001c0002t0029g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.159+1761_159+1775d others(17): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566942 | ||||||
| chr2:221566943
|
G | GAGGAA | 4 | a0001c0001t0001g0262a0001c0001t0002g0073a0001c0001t0003g0289others(1): Show | 4 | HG01109.hp2 HG03098.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.159+1774_159+1775i others(7): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566943 | ||||||
| chr2:221566944
|
G | A | 147 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(144): Show | 147 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.159+1774C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566944 | ||||||
| chr2:221566944
|
G | GAGAAGAG others(8): Show |
1 | a0001c0003t0003g0292 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.159+1773_159+1774i others(17): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566944 | ||||||
| chr2:221566944
|
G | GGGAAGAG others(11): Show |
1 | a0001c0001t0009g0214 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.159+1773_159+1774i others(20): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566944 | ||||||
| chr2:221566945
|
A | AAGAGGAA others(21): Show |
1 | a0001c0001t0002g0051 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.159+1772_159+1773i others(30): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566945 | ||||||
| chr2:221566945
|
A | AG | 7 | a0001c0001t0001g0262a0001c0001t0002g0073a0001c0001t0002g0223others(4): Show | 7 | HG01109.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.159+1772dupC | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566945 | ||||||
| chr2:221566945
|
A | G | 113 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(110): Show | 113 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.159+1773T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566945 | ||||||
| chr2:221566945
|
AGAAGGAG others(5): Show |
A | 1 | a0001c0001t0006g0228 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.159+1761_159+1772d others(14): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566945 | ||||||
| chr2:221566948
|
A | G | 10 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0042others(7): Show | 10 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.159+1770T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566948 | ||||||
| chr2:221566950
|
G | A | 160 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(157): Show | 160 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.159+1768C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566950 | ||||||
| chr2:221566951
|
A | AGAGGAGG others(17): Show |
1 | a0001c0003t0003g0056 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.159+1766_159+1767i others(26): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566951 | ||||||
| chr2:221566951
|
A | G | 116 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(113): Show | 116 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.159+1767T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566951 | ||||||
| chr2:221566954
|
A | G | 1 | a0001c0002t0001g0020 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.159+1764T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566954 | ||||||
| chr2:221566954
|
AGGG | A | 8 | a0001c0001t0001g0249a0001c0001t0001g0253a0001c0001t0002g0252others(5): Show | 8 | HG00408.hp1 HG02015.hp2 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.159+1761_159+1763d others(5): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566954 | ||||||
| chr2:221566956
|
G | A | 157 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(154): Show | 157 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.159+1762C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566956 | ||||||
| chr2:221566956
|
G | GAGAAGGA others(50): Show |
1 | a0001c0001t0001g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.159+1761_159+1762i others(59): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566956 | ||||||
| chr2:221566956
|
G | GAGAAGGA others(32): Show |
1 | a0001c0001t0001g0150 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.159+1761_159+1762i others(41): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566956 | ||||||
| chr2:221566956
|
G | GAGAAGGA others(35): Show |
1 | a0001c0003t0003g0161 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.159+1761_159+1762i others(44): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566956 | ||||||
| chr2:221566956
|
G | GAGAAGGA others(29): Show |
4 | a0001c0001t0001g0164a0001c0001t0002g0160a0001c0002t0001g0163others(1): Show | 4 | HG00738.hp2 HG01975.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.159+1761_159+1762i others(38): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566956 | ||||||
| chr2:221566956
|
G | GAGAAGGA others(32): Show |
3 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0002g0179 | 3 | HG03239.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.159+1761_159+1762i others(41): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566956 | ||||||
| chr2:221566956
|
G | GAGAAGGA others(35): Show |
1 | a0001c0001t0016g0191 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.159+1761_159+1762i others(44): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566956 | ||||||
| chr2:221566956
|
G | GAGAAGGA others(41): Show |
2 | a0001c0001t0001g0211a0001c0001t0014g0213 | 2 | HG01243.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.159+1761_159+1762i others(50): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566956 | ||||||
| chr2:221566956
|
G | GAGAAGGA others(47): Show |
1 | a0001c0001t0001g0217 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.159+1761_159+1762i others(56): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566956 | ||||||
| chr2:221566956
|
G | GAGAAGGA others(20): Show |
3 | a0001c0001t0008g0132a0001c0001t0030g0130a0001c0001t0039g0131 | 3 | HG01884.hp1 HG02895.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.159+1761_159+1762i others(29): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566956 | ||||||
| chr2:221566956
|
G | GAGAAGGA others(23): Show |
1 | a0001c0001t0048g0162 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.159+1761_159+1762i others(32): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566956 | ||||||
| chr2:221566956
|
G | GAGAAGGA others(26): Show |
1 | a0001c0001t0001g0120 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.159+1761_159+1762i others(35): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566956 | ||||||
| chr2:221566956
|
G | GAGAAGGA others(29): Show |
2 | a0001c0001t0001g0190a0001c0001t0001g0255 | 2 | HG00642.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.159+1761_159+1762i others(38): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566956 | ||||||
| chr2:221566956
|
G | GAGAAGGA others(35): Show |
2 | a0001c0001t0001g0230a0001c0001t0009g0212 | 2 | HG03225.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.159+1761_159+1762i others(44): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566956 | ||||||
| chr2:221566956
|
G | GAGAAGGA others(29): Show |
2 | a0001c0001t0002g0158a0001c0002t0001g0159 | 2 | HG03831.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.159+1761_159+1762i others(38): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566956 | ||||||
| chr2:221566956
|
G | GAGAAGGA others(32): Show |
2 | a0001c0001t0004g0174a0001c0001t0020g0173 | 2 | NA18612.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.159+1761_159+1762i others(41): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566956 | ||||||
| chr2:221566956
|
G | GAGAAGGG others(5): Show |
2 | a0001c0001t0008g0117a0001c0003t0003g0133 | 2 | HG02257.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.159+1761_159+1762i others(14): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566956 | ||||||
| chr2:221566956
|
G | GAGAAGGG others(26): Show |
2 | a0001c0001t0001g0222a0001c0001t0002g0175 | 2 | NA18956.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.159+1761_159+1762i others(35): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566956 | ||||||
| chr2:221566956
|
G | GAGAAGGG others(32): Show |
1 | a0001c0001t0002g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.159+1761_159+1762i others(41): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566956 | ||||||
| chr2:221566956
|
G | GAGAAGGG others(35): Show |
1 | a0001c0001t0002g0210 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.159+1761_159+1762i others(44): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566956 | ||||||
| chr2:221566957
|
G | A | 73 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0105others(70): Show | 73 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.159+1761C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566957 | ||||||
| chr2:221566957
|
G | GGAA | 4 | a0001c0001t0017g0103a0001c0001t0018g0113a0001c0003t0001g0030others(1): Show | 4 | HG00280.hp2 HG00323.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+1758_159+1760d others(5): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566957 | ||||||
| chr2:221566960
|
A | AGAAGAAG others(5): Show |
1 | a0001c0001t0049g0227 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.159+1757_159+1758i others(14): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566960 | ||||||
| chr2:221566960
|
A | G | 3 | a0001c0001t0001g0080a0001c0001t0003g0279a0001c0002t0001g0039 | 3 | HG02602.hp2 HG03927.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.159+1758T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566960 | ||||||
| chr2:221566960
|
AGAG | A | 7 | a0001c0001t0001g0017a0001c0001t0001g0081a0001c0001t0001g0139others(4): Show | 7 | HG01081.hp2 HG01257.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.159+1755_159+1757d others(5): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566960 | ||||||
| chr2:221566962
|
A | G | 9 | a0001c0001t0001g0177a0001c0001t0001g0189a0001c0001t0001g0192others(6): Show | 9 | HG00741.hp2 HG01123.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.159+1756T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566962 | ||||||
| chr2:221566963
|
G | A | 100 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0025others(97): Show | 100 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.159+1755C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566963 | ||||||
| chr2:221566963
|
G | GGAAGAAG others(2): Show |
5 | a0001c0001t0001g0032a0001c0001t0006g0004a0001c0001t0008g0117others(2): Show | 5 | HG02257.hp1 HG02896.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.159+1754_159+1755i others(11): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566963 | ||||||
| chr2:221566963
|
G | GGAAGAAG others(5): Show |
4 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0106others(1): Show | 4 | HG02922.hp2 NA18977.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.159+1754_159+1755i others(14): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566963 | ||||||
| chr2:221566963
|
G | GGAAGAAG others(8): Show |
8 | a0001c0001t0001g0045a0001c0001t0001g0050a0001c0001t0002g0044others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.159+1754_159+1755i others(17): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566963 | ||||||
| chr2:221566963
|
G | GGAAGAAG others(14): Show |
2 | a0001c0001t0001g0260a0001c0002t0001g0259 | 2 | HG02523.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.159+1754_159+1755i others(23): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566963 | ||||||
| chr2:221566963
|
GGAAGAGG others(8): Show |
G | 1 | a0001c0001t0001g0080 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.159+1740_159+1754d others(17): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566963 | ||||||
| chr2:221566964
|
G | GAAGAAGA others(5): Show |
1 | a0001c0001t0001g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.159+1753_159+1754i others(14): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566964 | ||||||
| chr2:221566966
|
AGAG | A | 11 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0220others(8): Show | 11 | HG00280.hp1 HG00558.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.159+1749_159+1751d others(5): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566966 | ||||||
| chr2:221566967
|
G | T | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.159+1751C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566967 | ||||||
| chr2:221566969
|
G | A | 140 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(137): Show | 140 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.159+1749C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566969 | ||||||
| chr2:221566969
|
G | GGAAGAAG others(2): Show |
5 | a0001c0001t0001g0018a0001c0001t0001g0119a0001c0001t0011g0138others(2): Show | 5 | HG02004.hp1 HG02129.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.159+1740_159+1748d others(11): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566969 | ||||||
| chr2:221566969
|
G | GGAAGAAG others(5): Show |
14 | a0001c0001t0001g0026a0001c0001t0001g0140a0001c0001t0001g0141others(11): Show | 14 | HG02071.hp2 HG02559.hp2 HG02698.hp1 others(11): Show |
intron_variant | MODIFIER | c.159+1737_159+1748d others(14): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566969 | ||||||
| chr2:221566969
|
G | GGAAGAAG others(8): Show |
11 | a0001c0001t0001g0033a0001c0001t0001g0151a0001c0001t0001g0152others(8): Show | 11 | HG01975.hp2 HG02523.hp2 HG04199.hp1 others(8): Show |
intron_variant | MODIFIER | c.159+1734_159+1748d others(17): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566969 | ||||||
| chr2:221566969
|
G | GGAAGAAG others(11): Show |
10 | a0001c0001t0001g0059a0001c0001t0001g0166a0001c0001t0001g0167others(7): Show | 10 | HG00408.hp2 HG02165.hp1 HG03486.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+1731_159+1748d others(20): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566969 | ||||||
| chr2:221566969
|
G | GGAAGAAG others(14): Show |
12 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(9): Show | 12 | HG00544.hp2 HG00639.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.159+1728_159+1748d others(23): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566969 | ||||||
| chr2:221566969
|
G | GGAAGAAG others(17): Show |
11 | a0001c0001t0001g0197a0001c0001t0001g0200a0001c0001t0001g0202others(8): Show | 11 | HG00558.hp2 HG00642.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.159+1725_159+1748d others(26): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566969 | ||||||
| chr2:221566969
|
G | GGAAGAAG others(20): Show |
8 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(5): Show | 8 | HG00673.hp1 HG01071.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+1722_159+1748d others(29): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566969 | ||||||
| chr2:221566969
|
G | GGAAGAAG others(23): Show |
2 | a0001c0001t0002g0111a0001c0001t0010g0110 | 2 | HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.159+1719_159+1748d others(32): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566969 | ||||||
| chr2:221566969
|
G | GGAAGAAG others(26): Show |
2 | a0001c0001t0002g0215a0001c0001t0005g0216 | 2 | HG01071.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.159+1716_159+1748d others(35): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566969 | ||||||
| chr2:221566969
|
G | GGAAGAAG others(11): Show |
2 | a0001c0001t0008g0134a0001c0001t0008g0135 | 2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.159+1748_159+1749i others(20): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566969 | ||||||
| chr2:221566969
|
G | GGAAGAAG others(26): Show |
1 | a0001c0002t0022g0273 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.159+1748_159+1749i others(35): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566969 | ||||||
| chr2:221566969
|
G | GGAAGAGG others(8): Show |
1 | a0001c0001t0002g0136 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.159+1748_159+1749i others(17): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566969 | ||||||
| chr2:221566969
|
G | GGAAGAGG others(14): Show |
1 | a0001c0003t0003g0079 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.159+1748_159+1749i others(23): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566969 | ||||||
| chr2:221566969
|
G | GGAAGAGG others(17): Show |
1 | a0001c0005t0014g0040 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.159+1748_159+1749i others(26): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566969 | ||||||
| chr2:221566969
|
G | GGAAGAGG others(20): Show |
2 | a0001c0001t0001g0177a0001c0010t0001g0176 | 2 | HG01978.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.159+1748_159+1749i others(29): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566969 | ||||||
| chr2:221566969
|
G | GGAAGAGG others(23): Show |
5 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 5 | HG00741.hp2 HG03017.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.159+1748_159+1749i others(32): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566969 | ||||||
| chr2:221566969
|
G | GGAAGAGG others(17): Show |
1 | a0001c0006t0003g0118 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.159+1748_159+1749i others(26): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566969 | ||||||
| chr2:221566969
|
G | GGAAGAGG others(35): Show |
1 | a0001c0001t0009g0274 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.159+1748_159+1749i others(44): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566969 | ||||||
| chr2:221566969
|
G | GGAAGAGG others(23): Show |
1 | a0001c0001t0001g0038 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.159+1748_159+1749i others(32): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566969 | ||||||
| chr2:221566969
|
G | GGAAGAGG others(20): Show |
1 | a0001c0002t0001g0020 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.159+1748_159+1749i others(29): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566969 | ||||||
| chr2:221566969
|
G | GGAAGAGG others(35): Show |
1 | a0001c0002t0001g0039 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.159+1748_159+1749i others(44): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566969 | ||||||
| chr2:221566969
|
G | GGAGGAAG others(23): Show |
1 | a0001c0001t0004g0203 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.159+1748_159+1749i others(32): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566969 | ||||||
| chr2:221566972
|
A | AGAAGAAG others(5): Show |
2 | a0001c0001t0024g0129a0001c0001t0040g0128 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.159+1745_159+1746i others(14): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566972 | ||||||
| chr2:221566972
|
A | G | 1 | a0001c0001t0002g0089 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.159+1746T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566972 | ||||||
| chr2:221566975
|
A | G | 30 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0001g0063others(27): Show | 30 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.159+1743T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566975 | ||||||
| chr2:221566978
|
A | G | 29 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0001g0063others(26): Show | 29 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.159+1740T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566978 | ||||||
| chr2:221566983
|
A | AAGAAGAA others(11): Show |
3 | a0001c0001t0002g0097a0001c0001t0002g0223a0001c0001t0002g0224 | 3 | HG02895.hp2 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.159+1734_159+1735i others(20): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566983 | ||||||
| chr2:221566983
|
A | AAGAAGAA others(5): Show |
2 | a0001c0001t0002g0095a0001c0009t0002g0094 | 2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.159+1734_159+1735i others(14): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566983 | ||||||
| chr2:221566983
|
A | G | 1 | a0001c0001t0045g0096 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.159+1735T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566983 | ||||||
| chr2:221566999
|
A | AGAAGAAG others(11): Show |
2 | a0001c0002t0001g0125a0001c0003t0003g0126 | 2 | HG03491.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.159+1718_159+1719i others(20): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221566999 | ||||||
| chr2:221567006
|
GAAGA | G | 4 | a0001c0001t0001g0060a0001c0001t0002g0089a0001c0001t0016g0058others(1): Show | 4 | HG01884.hp2 HG02735.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.159+1708_159+1711d others(6): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221567006 | ||||||
| chr2:221567009
|
G | GAA | 7 | a0001c0001t0001g0092a0001c0001t0009g0274a0001c0001t0018g0113others(4): Show | 7 | HG02723.hp1 HG03195.hp2 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.159+1707_159+1708d others(4): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221567009 | ||||||
| chr2:221567009
|
GA | G | 27 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(24): Show | 27 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.159+1708delT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221567009 | ||||||
| chr2:221567012
|
A | G | 4 | a0001c0001t0001g0059a0001c0001t0001g0120a0001c0001t0001g0294others(1): Show | 4 | HG00639.hp1 HG01261.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+1706T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221567012 | ||||||
| chr2:221567233
|
C | A | 2 | a0001c0002t0023g0218a0001c0002t0023g0219 | 2 | HG00673.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.159+1485G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221567233 | ||||||
| chr2:221567240
|
T | G | 2 | a0001c0002t0022g0090a0001c0003t0003g0091 | 2 | HG03041.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.159+1478A>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221567240 | ||||||
| chr2:221567600
|
T | C | 25 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0220others(22): Show | 25 | HG00280.hp1 HG00741.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.159+1118A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221567600 | ||||||
| chr2:221567769
|
C | T | 81 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(78): Show | 81 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.159+949G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221567769 | ||||||
| chr2:221567914
|
T | C | 1 | a0001c0001t0004g0074 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.159+804A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221567914 | ||||||
| chr2:221567983
|
T | C | 4 | a0001c0001t0002g0075a0001c0001t0007g0076a0001c0001t0007g0078others(1): Show | 4 | NA18989.hp1 NA18991.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.159+735A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221567983 | ||||||
| chr2:221568077
|
T | C | 1 | a0001c0001t0001g0231 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.159+641A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221568077 | ||||||
| chr2:221568112
|
C | A | 2 | a0001c0004t0019g0236a0001c0004t0019g0237 | 2 | HG01243.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.159+606G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221568112 | ||||||
| chr2:221568252
|
G | A | 1 | a0001c0003t0003g0082 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.159+466C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221568252 | ||||||
| chr2:221568300
|
T | C | 1 | a0001c0001t0001g0222 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.159+418A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221568300 | ||||||
| chr2:221568326
|
CT | C | 8 | a0001c0001t0001g0092a0001c0001t0009g0274a0001c0001t0018g0113others(5): Show | 8 | HG02723.hp1 HG03195.hp2 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+391delA | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221568326 | ||||||
| chr2:221568375
|
C | T | 1 | a0001c0001t0016g0058 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.159+343G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221568375 | ||||||
| chr2:221568395
|
A | C | 1 | a0001c0001t0001g0294 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.159+323T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221568395 | ||||||
| chr2:221568419
|
G | T | 8 | a0001c0001t0001g0092a0001c0001t0009g0274a0001c0001t0018g0113others(5): Show | 8 | HG02723.hp1 HG03195.hp2 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+299C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221568419 | ||||||
| chr2:221568677
|
C | T | 1 | a0001c0001t0008g0117 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.159+41G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 2/17 | chr2 | 221568677 | ||||||
| chr2:221569000
|
A | G | 275 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(272): Show | 275 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.92-215T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221569000 | ||||||
| chr2:221569059
|
G | T | 24 | a0001c0001t0001g0092a0001c0001t0001g0105a0001c0001t0001g0106others(21): Show | 24 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.92-274C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221569059 | ||||||
| chr2:221569189
|
T | TA | 10 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0225others(7): Show | 10 | HG01361.hp1 HG02055.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.92-405dupT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221569189 | ||||||
| chr2:221569408
|
CTCTT | C | 12 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0002g0277others(9): Show | 12 | HG00741.hp1 HG01081.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.92-627_92-624delAA others(2): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221569408 | ||||||
| chr2:221569546
|
G | A | 2 | a0001c0001t0004g0285a0001c0001t0005g0284 | 2 | HG03704.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.92-761C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221569546 | ||||||
| chr2:221569757
|
G | T | 1 | a0001c0001t0001g0112 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.92-972C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221569757 | ||||||
| chr2:221569758
|
G | C | 1 | a0001c0003t0003g0056 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.92-973C>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221569758 | ||||||
| chr2:221569787
|
C | A | 1 | a0001c0001t0001g0112 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.92-1002G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221569787 | ||||||
| chr2:221569896
|
T | C | 1 | a0001c0001t0004g0057 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.92-1111A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221569896 | ||||||
| chr2:221570178
|
T | C | 40 | a0001c0001t0001g0092a0001c0001t0001g0105a0001c0001t0001g0106others(37): Show | 40 | HG00639.hp1 HG00741.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.92-1393A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221570178 | ||||||
| chr2:221570315
|
TC | T | 62 | a0001c0001t0001g0092a0001c0001t0001g0105a0001c0001t0001g0106others(59): Show | 62 | HG00408.hp1 HG00741.hp1 HG01081.hp2 others(59): Show |
intron_variant | MODIFIER | c.92-1531delG | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221570315 | ||||||
| chr2:221570315
|
TCC | T | 134 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(131): Show | 134 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.92-1532_92-1531del others(2): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221570315 | ||||||
| chr2:221570320
|
C | A | 1 | a0001c0001t0018g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.92-1535G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221570320 | ||||||
| chr2:221570325
|
C | T | 1 | a0001c0001t0005g0116 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92-1540G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221570325 | ||||||
| chr2:221570326
|
C | A | 29 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0062others(26): Show | 29 | HG00423.hp2 HG00544.hp1 HG01361.hp1 others(26): Show |
intron_variant | MODIFIER | c.92-1541G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221570326 | ||||||
| chr2:221570326
|
C | CA | 7 | a0001c0001t0002g0089a0001c0001t0021g0083a0001c0003t0001g0085others(4): Show | 7 | HG00323.hp2 HG00733.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-1542dupT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221570326 | ||||||
| chr2:221570327
|
A | C | 4 | a0001c0001t0001g0002a0001c0001t0004g0003a0001c0001t0005g0001others(1): Show | 4 | HG02015.hp1 HG02080.hp1 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-1542T>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221570327 | ||||||
| chr2:221570328
|
A | G | 121 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(118): Show | 121 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.92-1543T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221570328 | ||||||
| chr2:221570558
|
A | G | 1 | a0001c0002t0029g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.91+1600T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221570558 | ||||||
| chr2:221570560
|
G | A | 137 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(134): Show | 137 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.91+1598C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221570560 | ||||||
| chr2:221570576
|
A | G | 1 | a0001c0002t0029g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.91+1582T>C | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221570576 | ||||||
| chr2:221570698
|
TA | T | 135 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(132): Show | 135 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.91+1459delT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221570698 | ||||||
| chr2:221570797
|
T | TGGACGGA others(77): Show |
1 | a0001c0001t0001g0294 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.91+1360_91+1361ins others(84): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221570797 | ||||||
| chr2:221570801
|
G | T | 1 | a0001c0001t0001g0294 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.91+1357C>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221570801 | ||||||
| chr2:221570809
|
T | C | 1 | a0001c0001t0001g0294 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.91+1349A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221570809 | ||||||
| chr2:221571210
|
T | TGCAGACA others(11): Show |
4 | a0001c0001t0001g0264a0001c0001t0003g0266a0001c0001t0003g0267others(1): Show | 4 | HG01071.hp1 HG01167.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+930_91+947dupGT others(16): Show |
EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221571210 | ||||||
| chr2:221571236
|
T | C | 2 | a0001c0001t0036g0115a0001c0003t0003g0114 | 2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.91+922A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221571236 | ||||||
| chr2:221571255
|
T | C | 1 | a0001c0001t0001g0294 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.91+903A>G | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221571255 | ||||||
| chr2:221571255
|
T | TAC | 119 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(116): Show | 119 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.91+901_91+902dupGT | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221571255 | ||||||
| chr2:221571426
|
C | T | 24 | a0001c0001t0001g0092a0001c0001t0001g0105a0001c0001t0001g0106others(21): Show | 24 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.91+732G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221571426 | ||||||
| chr2:221571503
|
G | A | 14 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0002g0277others(11): Show | 14 | HG00741.hp1 HG01081.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.91+655C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221571503 | ||||||
| chr2:221571815
|
C | T | 91 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(88): Show | 91 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.91+343G>A | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221571815 | ||||||
| chr2:221571915
|
G | A | 8 | a0001c0001t0001g0287a0001c0001t0003g0289a0001c0001t0004g0291others(5): Show | 8 | HG01109.hp2 HG01891.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+243C>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221571915 | ||||||
| chr2:221572023
|
C | A | 1 | a0001c0001t0001g0294 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.91+135G>T | EPHA4 | ENSG00000116106.12 | transcript | ENST00000281821.7 | protein_coding | 1/17 | chr2 | 221572023 |