Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 8411 |
|---|---|
| ensemblid | ENSG00000102189.17 |
| hgncid | 3185 |
| symbol | EEA1 |
| name | early endosome antigen 1 |
| refseq_nuc | NM_003566.4 |
| refseq_prot | NP_003557.3 |
| ensembl_nuc | ENST00000322349.13 |
| ensembl_prot | ENSP00000317955.8 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 92770637 |
| end | 92929295 |
| strand | - |
| ver | v1.2 |
| region | chr12:92770637-92929295 |
| region5000 | chr12:92765637-92934295 |
| regionname0 | EEA1_chr12_92770637_92929295 |
| regionname5000 | EEA1_chr12_92765637_92934295 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1411 | 136 | 45 | 37 | 20 | 7 | 27 | 9 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0002 | 1/1 | 1411 | 80 | 46 | 14 | 5 | 5 | 8 | 3 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0003 | 0/0 | 1411 | 10 | 1 | 2 | 6 | 1 | 0 | 2 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0004 | 0/0 | 1411 | 6 | 3 | 1 | 0 | 1 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0005 | 0/0 | 1411 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0006 | 0/0 | 1411 | 4 | 0 | 2 | 2 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0007 | 0/0 | 1411 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0008 | 0/0 | 1411 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0009 | 0/0 | 1411 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 4236 | 72 | 15 | 18 | 19 | 4 | 16 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| c0002 | 0/0 | 4236 | 56 | 24 | 18 | 1 | 3 | 10 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| c0003 | 0/1 | 4236 | 45 | 19 | 10 | 5 | 3 | 7 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| c0004 | 1/0 | 4236 | 28 | 21 | 3 | 0 | 2 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| c0005 | 0/0 | 4236 | 10 | 1 | 2 | 6 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| c0006 | 0/0 | 4236 | 6 | 3 | 1 | 0 | 1 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| c0007 | 0/0 | 4236 | 5 | 0 | 0 | 5 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| c0008 | 0/0 | 4236 | 5 | 4 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| c0009 | 0/0 | 4236 | 4 | 0 | 2 | 2 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| c0010 | 0/0 | 4236 | 4 | 4 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| c0011 | 0/0 | 4236 | 2 | 2 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| c0012 | 0/0 | 4236 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| c0013 | 0/0 | 4236 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| c0014 | 0/0 | 4236 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| c0015 | 0/0 | 4236 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| c0016 | 0/0 | 4236 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| c0017 | 0/0 | 4236 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| c0018 | 0/0 | 4236 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 5612 | 52 | 10 | 15 | 15 | 2 | 10 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0002 | 0/1 | 5610 | 25 | 2 | 8 | 5 | 3 | 6 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0003 | 0/0 | 5610 | 21 | 5 | 9 | 5 | 1 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0004 | 0/0 | 5608 | 14 | 12 | 2 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0005 | 0/0 | 5614 | 14 | 0 | 5 | 2 | 2 | 5 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0006 | 0/0 | 5610 | 13 | 9 | 4 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0007 | 0/0 | 5612 | 12 | 2 | 5 | 0 | 3 | 2 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0008 | 0/0 | 5604 | 9 | 2 | 1 | 5 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0009 | 0/0 | 5614 | 7 | 0 | 0 | 1 | 0 | 6 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0010 | 0/0 | 5605 | 6 | 6 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0011 | 1/0 | 5604 | 5 | 0 | 2 | 0 | 2 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0012 | 0/0 | 5604 | 5 | 4 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0013 | 0/0 | 5613 | 5 | 4 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0014 | 0/0 | 5605 | 4 | 4 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0015 | 0/0 | 5609 | 3 | 3 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0016 | 0/0 | 5607 | 3 | 3 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0017 | 0/0 | 5614 | 3 | 0 | 1 | 0 | 0 | 2 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0018 | 0/0 | 5606 | 3 | 3 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0019 | 0/0 | 5612 | 2 | 2 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0020 | 0/0 | 5611 | 2 | 0 | 2 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0021 | 0/0 | 5604 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0022 | 0/0 | 5605 | 1 | 0 | 0 | 0 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0023 | 0/0 | 5612 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0024 | 0/0 | 5604 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0025 | 0/0 | 5612 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0026 | 0/0 | 5610 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0027 | 0/0 | 5610 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0028 | 0/0 | 5610 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0029 | 0/0 | 5612 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0030 | 0/0 | 5610 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0031 | 0/0 | 5605 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0032 | 0/0 | 5609 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0033 | 0/0 | 5605 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0034 | 0/0 | 5605 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0035 | 0/0 | 5610 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0036 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0037 | 0/0 | 5610 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0038 | 0/0 | 5610 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0039 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0040 | 0/0 | 5614 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0041 | 0/0 | 5606 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0042 | 0/0 | 5610 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0043 | 0/0 | 5612 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0044 | 0/0 | 5611 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0045 | 0/0 | 5611 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0046 | 0/0 | 5615 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0047 | 0/0 | 5611 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0048 | 0/0 | 5604 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0049 | 0/0 | 5621 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0050 | 0/0 | 5611 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0051 | 0/0 | 5616 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0052 | 0/0 | 5610 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0053 | 0/0 | 5612 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0054 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0055 | 0/0 | 5608 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| t0056 | 0/0 | 5608 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0172 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0228 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 4236 | 72 | 15 | 18 | 19 | 4 | 16 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0002 | 0/0 | 4236 | 56 | 24 | 18 | 1 | 3 | 10 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0010 | 0/0 | 4236 | 4 | 4 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0011 | 0/0 | 4236 | 2 | 2 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0012 | 0/0 | 4236 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0018 | 0/0 | 4236 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0002c0003 | 0/1 | 4236 | 45 | 19 | 10 | 5 | 3 | 7 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0002c0004 | 1/0 | 4236 | 28 | 21 | 3 | 0 | 2 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0002c0008 | 0/0 | 4236 | 5 | 4 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0002c0015 | 0/0 | 4236 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0002c0017 | 0/0 | 4236 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0003c0005 | 0/0 | 4236 | 10 | 1 | 2 | 6 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0004c0006 | 0/0 | 4236 | 6 | 3 | 1 | 0 | 1 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0005c0007 | 0/0 | 4236 | 5 | 0 | 0 | 5 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0006c0009 | 0/0 | 4236 | 4 | 0 | 2 | 2 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0007c0016 | 0/0 | 4236 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0008c0014 | 0/0 | 4236 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0009c0013 | 0/0 | 4236 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 9847 | 47 | 9 | 13 | 13 | 2 | 10 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0001t0005 | 0/0 | 9849 | 13 | 0 | 4 | 2 | 2 | 5 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0001t0013 | 0/0 | 9848 | 5 | 4 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0001t0023 | 0/0 | 9847 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0001t0049 | 0/0 | 9856 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0001t0050 | 0/0 | 9846 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0001t0051 | 0/0 | 9851 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0001t0052 | 0/0 | 9845 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0001t0053 | 0/0 | 9847 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0001t0054 | 0/0 | 9848 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0002t0003 | 0/0 | 9845 | 12 | 4 | 7 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0002t0006 | 0/0 | 9845 | 5 | 2 | 3 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0002t0007 | 0/0 | 9847 | 12 | 2 | 5 | 0 | 3 | 2 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0002t0009 | 0/0 | 9849 | 7 | 0 | 0 | 1 | 0 | 6 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0002t0017 | 0/0 | 9849 | 2 | 0 | 1 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0002t0019 | 0/0 | 9847 | 2 | 2 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0002t0020 | 0/0 | 9846 | 2 | 0 | 2 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0002t0026 | 0/0 | 9845 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0002t0027 | 0/0 | 9845 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0002t0028 | 0/0 | 9845 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0002t0032 | 0/0 | 9844 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0002t0035 | 0/0 | 9845 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0002t0036 | 0/0 | 9851 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0002t0037 | 0/0 | 9845 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0002t0038 | 0/0 | 9845 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0002t0039 | 0/0 | 9851 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0002t0040 | 0/0 | 9849 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0002t0044 | 0/0 | 9846 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0002t0045 | 0/0 | 9846 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0002t0046 | 0/0 | 9850 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0002t0047 | 0/0 | 9846 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0010t0006 | 0/0 | 9845 | 4 | 4 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0011t0006 | 0/0 | 9845 | 2 | 2 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0012t0006 | 0/0 | 9845 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0001c0018t0017 | 0/0 | 9849 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0002c0003t0002 | 0/1 | 9845 | 25 | 2 | 8 | 5 | 3 | 6 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0002c0003t0004 | 0/0 | 9843 | 14 | 12 | 2 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0002c0003t0016 | 0/0 | 9842 | 3 | 3 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0002c0003t0043 | 0/0 | 9847 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0002c0003t0055 | 0/0 | 9843 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0002c0003t0056 | 0/0 | 9843 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0002c0004t0010 | 0/0 | 9840 | 6 | 6 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0002c0004t0011 | 1/0 | 9839 | 5 | 0 | 2 | 0 | 2 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0002c0004t0014 | 0/0 | 9840 | 4 | 4 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0002c0004t0015 | 0/0 | 9844 | 3 | 3 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0002c0004t0018 | 0/0 | 9841 | 3 | 3 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0002c0004t0024 | 0/0 | 9839 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0002c0004t0029 | 0/0 | 9847 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0002c0004t0030 | 0/0 | 9845 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0002c0004t0031 | 0/0 | 9840 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0002c0004t0033 | 0/0 | 9840 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0002c0004t0041 | 0/0 | 9841 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0002c0004t0048 | 0/0 | 9839 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0002c0008t0012 | 0/0 | 9839 | 5 | 4 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0002c0015t0001 | 0/0 | 9847 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0002c0017t0034 | 0/0 | 9840 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0003c0005t0003 | 0/0 | 9845 | 9 | 1 | 2 | 5 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0003c0005t0042 | 0/0 | 9845 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0004c0006t0008 | 0/0 | 9839 | 4 | 2 | 1 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0004c0006t0021 | 0/0 | 9839 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0004c0006t0022 | 0/0 | 9840 | 1 | 0 | 0 | 0 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0005c0007t0008 | 0/0 | 9839 | 5 | 0 | 0 | 5 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0006c0009t0001 | 0/0 | 9847 | 4 | 0 | 2 | 2 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0007c0016t0025 | 0/0 | 9847 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0008c0014t0006 | 0/0 | 9845 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| a0009c0013t0005 | 0/0 | 9849 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | copy fasta | chr12 | 92765637 | 92934295 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0005g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0005g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0005g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0005g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0005g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0005g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0005g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0005g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0005g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0005g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0005g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0013g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0013g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0013g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0013g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0013g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0023g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0049g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0050g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0051g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0052g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0053g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0001t0054g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0003g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0006g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0006g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0006g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0007g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0007g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0007g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0007g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0007g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0007g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0007g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0007g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0007g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0007g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0007g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0007g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0009g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0009g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0009g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0009g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0009g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0009g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0009g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0017g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0017g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0019g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0019g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0020g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0020g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0026g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0027g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0028g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0032g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0035g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0036g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0037g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0038g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0039g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0040g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0044g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0045g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0046g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0002t0047g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0010t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0010t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0010t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0010t0006g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0011t0006g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0011t0006g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0012t0006g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0001c0018t0017g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0002g0172 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0004g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0016g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0016g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0016g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0043g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0055g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0003t0056g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0004t0010g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0004t0010g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0004t0010g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0004t0010g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0004t0010g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0004t0010g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0004t0011g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0004t0011g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0004t0011g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0004t0011g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0004t0011g0228 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0004t0014g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0004t0014g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0004t0014g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0004t0014g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0004t0015g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0004t0015g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0004t0015g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0004t0018g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0004t0018g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0004t0018g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0004t0024g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0004t0029g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0004t0030g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0004t0031g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0004t0033g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0004t0041g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0004t0048g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0008t0012g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0008t0012g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0008t0012g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0008t0012g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0008t0012g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0015t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0002c0017t0034g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0003c0005t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0003c0005t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0003c0005t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0003c0005t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0003c0005t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0003c0005t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0003c0005t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0003c0005t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0003c0005t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0003c0005t0042g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0004c0006t0008g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0004c0006t0008g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0004c0006t0008g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0004c0006t0008g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0004c0006t0021g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0004c0006t0022g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0005c0007t0008g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0005c0007t0008g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0005c0007t0008g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0005c0007t0008g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0005c0007t0008g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0006c0009t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0006c0009t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0006c0009t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0006c0009t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0007c0016t0025g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0008c0014t0006g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| a0009c0013t0005g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0004 | t0011 | g0207 | EUR | GBR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG00099 | hp2 | a0002 | c0003 | t0002 | g0144 | EUR | GBR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG00140 | hp1 | a0003 | c0005 | t0003 | g0239 | EUR | GBR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG00140 | hp2 | a0002 | c0003 | t0002 | g0173 | EUR | GBR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG00280 | hp1 | a0001 | c0002 | t0007 | g0116 | EUR | FIN | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0214 | EUR | FIN | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG00639 | hp1 | a0001 | c0002 | t0003 | g0025 | AMR | PUR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG00639 | hp2 | a0002 | c0003 | t0004 | g0174 | AMR | PUR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG00642 | hp1 | a0007 | c0016 | t0025 | g0019 | AMR | PUR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG00642 | hp2 | a0001 | c0002 | t0003 | g0030 | AMR | PUR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG00738 | hp1 | a0004 | c0006 | t0008 | g0006 | AMR | PUR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG00738 | hp2 | a0001 | c0002 | t0003 | g0029 | AMR | PUR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG00741 | hp2 | a0002 | c0004 | t0030 | g0209 | AMR | PUR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01069 | hp2 | a0001 | c0002 | t0003 | g0028 | AMR | PUR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01071 | hp2 | a0001 | c0002 | t0017 | g0114 | AMR | PUR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01081 | hp2 | a0001 | c0002 | t0003 | g0026 | AMR | PUR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01099 | hp1 | a0006 | c0009 | t0001 | g0098 | AMR | PUR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01099 | hp2 | a0001 | c0002 | t0007 | g0048 | AMR | PUR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01106 | hp2 | a0002 | c0003 | t0002 | g0171 | AMR | PUR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01109 | hp2 | a0001 | c0002 | t0006 | g0044 | AMR | PUR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01167 | hp1 | a0002 | c0003 | t0004 | g0166 | AMR | PUR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01167 | hp2 | a0003 | c0005 | t0003 | g0034 | AMR | PUR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01168 | hp1 | a0001 | c0012 | t0006 | g0157 | AMR | PUR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01168 | hp2 | a0001 | c0002 | t0003 | g0039 | AMR | PUR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01175 | hp1 | a0001 | c0002 | t0007 | g0131 | AMR | PUR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01175 | hp2 | a0002 | c0003 | t0002 | g0153 | AMR | PUR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01192 | hp1 | a0002 | c0003 | t0002 | g0158 | AMR | PUR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01192 | hp2 | a0003 | c0005 | t0003 | g0022 | AMR | PUR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01243 | hp2 | a0002 | c0008 | t0012 | g0237 | AMR | PUR | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01255 | hp1 | a0001 | c0001 | t0052 | g0080 | AMR | CLM | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01255 | hp2 | a0001 | c0002 | t0007 | g0117 | AMR | CLM | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01256 | hp1 | a0002 | c0003 | t0002 | g0169 | AMR | CLM | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01256 | hp2 | a0001 | c0002 | t0020 | g0123 | AMR | CLM | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01257 | hp1 | a0002 | c0003 | t0002 | g0145 | AMR | CLM | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01257 | hp2 | a0001 | c0002 | t0006 | g0195 | AMR | CLM | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01258 | hp1 | a0001 | c0002 | t0020 | g0122 | AMR | CLM | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01258 | hp2 | a0002 | c0003 | t0002 | g0146 | AMR | CLM | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01261 | hp2 | a0002 | c0004 | t0011 | g0206 | AMR | CLM | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0186 | AMR | CLM | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01346 | hp2 | a0001 | c0002 | t0007 | g0118 | AMR | CLM | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01361 | hp2 | a0002 | c0004 | t0011 | g0205 | AMR | CLM | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01433 | hp1 | a0009 | c0013 | t0005 | g0064 | AMR | CLM | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01433 | hp2 | a0001 | c0002 | t0003 | g0024 | AMR | CLM | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0085 | AMR | CLM | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | IBS | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01516 | hp2 | a0001 | c0002 | t0007 | g0119 | EUR | IBS | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01517 | hp1 | a0001 | c0002 | t0007 | g0125 | EUR | IBS | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01517 | hp2 | a0002 | c0003 | t0002 | g0161 | EUR | IBS | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01884 | hp1 | a0002 | c0003 | t0004 | g0152 | AFR | ACB | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01891 | hp1 | a0001 | c0002 | t0044 | g0139 | AFR | ACB | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01891 | hp2 | a0002 | c0003 | t0002 | g0160 | AFR | ACB | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01934 | hp1 | a0002 | c0003 | t0002 | g0149 | AMR | PEL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0052 | AMR | PEL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01975 | hp1 | a0001 | c0002 | t0006 | g0192 | AMR | PEL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG01978 | hp2 | a0002 | c0003 | t0002 | g0159 | AMR | PEL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02015 | hp2 | a0002 | c0003 | t0002 | g0001 | EAS | KHV | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02055 | hp1 | a0002 | c0004 | t0018 | g0210 | AFR | ACB | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02055 | hp2 | a0001 | c0002 | t0035 | g0188 | AFR | ACB | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02071 | hp1 | a0003 | c0005 | t0003 | g0035 | EAS | KHV | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02071 | hp2 | a0001 | c0001 | t0049 | g0018 | EAS | KHV | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02083 | hp2 | a0002 | c0003 | t0002 | g0001 | EAS | KHV | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02129 | hp1 | a0003 | c0005 | t0003 | g0021 | EAS | KHV | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02129 | hp2 | a0001 | c0001 | t0005 | g0077 | EAS | KHV | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02135 | hp1 | a0001 | c0002 | t0009 | g0113 | EAS | KHV | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02135 | hp2 | a0001 | c0001 | t0013 | g0050 | EAS | KHV | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02145 | hp2 | a0001 | c0002 | t0047 | g0187 | AFR | ACB | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02165 | hp1 | a0003 | c0005 | t0042 | g0038 | EAS | CDX | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CDX | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02257 | hp1 | a0001 | c0002 | t0045 | g0036 | AFR | ACB | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02257 | hp2 | a0002 | c0004 | t0018 | g0211 | AFR | ACB | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02258 | hp1 | a0001 | c0001 | t0013 | g0070 | AFR | ACB | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02258 | hp2 | a0001 | c0002 | t0036 | g0140 | AFR | ACB | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02273 | hp1 | a0006 | c0009 | t0001 | g0096 | AMR | PEL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02280 | hp1 | a0001 | c0001 | t0013 | g0092 | AFR | ACB | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02280 | hp2 | a0003 | c0005 | t0003 | g0020 | AFR | ACB | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02300 | hp1 | a0001 | c0001 | t0005 | g0053 | AMR | PEL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02300 | hp2 | a0001 | c0002 | t0007 | g0130 | AMR | PEL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02451 | hp1 | a0002 | c0004 | t0033 | g0233 | AFR | ACB | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02451 | hp2 | a0008 | c0014 | t0006 | g0204 | AFR | ACB | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02523 | hp1 | a0006 | c0009 | t0001 | g0086 | EAS | KHV | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02572 | hp1 | a0001 | c0002 | t0032 | g0045 | AFR | GWD | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02572 | hp2 | a0002 | c0004 | t0041 | g0201 | AFR | GWD | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02602 | hp1 | a0001 | c0002 | t0017 | g0115 | SAS | PJL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0182 | SAS | PJL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02615 | hp1 | a0001 | c0002 | t0007 | g0126 | AFR | GWD | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02615 | hp2 | a0002 | c0015 | t0001 | g0073 | AFR | GWD | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02622 | hp1 | a0002 | c0004 | t0015 | g0213 | AFR | GWD | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02622 | hp2 | a0001 | c0002 | t0038 | g0043 | AFR | GWD | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02630 | hp1 | a0001 | c0002 | t0040 | g0223 | AFR | GWD | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02630 | hp2 | a0002 | c0003 | t0004 | g0227 | AFR | GWD | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02647 | hp1 | a0001 | c0002 | t0026 | g0212 | AFR | GWD | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02647 | hp2 | a0001 | c0010 | t0006 | g0218 | AFR | GWD | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02698 | hp1 | a0001 | c0018 | t0017 | g0197 | SAS | PJL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02717 | hp1 | a0002 | c0008 | t0012 | g0015 | AFR | GWD | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02717 | hp2 | a0001 | c0001 | t0013 | g0138 | AFR | GWD | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02723 | hp1 | a0004 | c0006 | t0008 | g0002 | AFR | GWD | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02723 | hp2 | a0001 | c0002 | t0039 | g0215 | AFR | GWD | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02735 | hp1 | a0002 | c0004 | t0029 | g0200 | SAS | PJL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02809 | hp1 | a0002 | c0004 | t0015 | g0203 | AFR | GWD | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02809 | hp2 | a0002 | c0004 | t0031 | g0199 | AFR | GWD | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02818 | hp1 | a0002 | c0003 | t0016 | g0143 | AFR | GWD | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02818 | hp2 | a0002 | c0003 | t0056 | g0178 | AFR | GWD | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02886 | hp1 | a0002 | c0003 | t0004 | g0165 | AFR | GWD | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02886 | hp2 | a0001 | c0002 | t0028 | g0190 | AFR | GWD | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02895 | hp1 | a0002 | c0004 | t0014 | g0242 | AFR | GWD | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02896 | hp1 | a0002 | c0003 | t0016 | g0141 | AFR | GWD | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02896 | hp2 | a0002 | c0004 | t0014 | g0243 | AFR | GWD | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02897 | hp1 | a0002 | c0004 | t0014 | g0241 | AFR | GWD | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02922 | hp1 | a0002 | c0004 | t0010 | g0229 | AFR | ESN | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02922 | hp2 | a0002 | c0003 | t0004 | g0175 | AFR | ESN | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02965 | hp1 | a0002 | c0017 | t0034 | g0016 | AFR | ESN | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02965 | hp2 | a0002 | c0003 | t0004 | g0226 | AFR | ESN | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02970 | hp1 | a0002 | c0004 | t0015 | g0198 | AFR | ESN | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02970 | hp2 | a0001 | c0002 | t0007 | g0137 | AFR | ESN | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02976 | hp1 | a0002 | c0004 | t0010 | g0230 | AFR | ESN | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02976 | hp2 | a0002 | c0003 | t0055 | g0150 | AFR | ESN | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03017 | hp1 | a0002 | c0003 | t0002 | g0148 | SAS | PJL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0093 | SAS | PJL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03041 | hp1 | a0004 | c0006 | t0021 | g0012 | AFR | GWD | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03041 | hp2 | a0002 | c0003 | t0016 | g0142 | AFR | GWD | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03098 | hp1 | a0001 | c0002 | t0027 | g0189 | AFR | MSL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03098 | hp2 | a0001 | c0011 | t0006 | g0216 | AFR | MSL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03139 | hp1 | a0002 | c0004 | t0010 | g0231 | AFR | ESN | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03139 | hp2 | a0002 | c0003 | t0004 | g0147 | AFR | ESN | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03195 | hp1 | a0002 | c0004 | t0010 | g0232 | AFR | ESN | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03195 | hp2 | a0001 | c0002 | t0019 | g0127 | AFR | ESN | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03209 | hp1 | a0002 | c0004 | t0014 | g0240 | AFR | MSL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03209 | hp2 | a0001 | c0002 | t0003 | g0037 | AFR | MSL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03225 | hp1 | a0001 | c0001 | t0013 | g0075 | AFR | MSL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03225 | hp2 | a0001 | c0002 | t0003 | g0041 | AFR | MSL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03239 | hp1 | a0001 | c0002 | t0003 | g0027 | SAS | PJL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03453 | hp1 | a0001 | c0002 | t0003 | g0023 | AFR | MSL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03453 | hp2 | a0001 | c0011 | t0006 | g0222 | AFR | MSL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03486 | hp1 | a0002 | c0004 | t0018 | g0202 | AFR | MSL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03486 | hp2 | a0001 | c0002 | t0037 | g0194 | AFR | MSL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03491 | hp2 | a0001 | c0002 | t0009 | g0120 | SAS | PJL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03492 | hp1 | a0001 | c0002 | t0009 | g0121 | SAS | PJL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03492 | hp2 | a0001 | c0001 | t0005 | g0184 | SAS | PJL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03516 | hp1 | a0002 | c0004 | t0048 | g0017 | AFR | ESN | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03516 | hp2 | a0002 | c0008 | t0012 | g0238 | AFR | ESN | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03540 | hp1 | a0001 | c0010 | t0006 | g0219 | AFR | GWD | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03540 | hp2 | a0001 | c0002 | t0006 | g0042 | AFR | GWD | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03579 | hp1 | a0001 | c0002 | t0006 | g0191 | AFR | MSL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03579 | hp2 | a0002 | c0004 | t0010 | g0235 | AFR | MSL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03654 | hp2 | a0002 | c0003 | t0002 | g0013 | SAS | PJL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03669 | hp2 | a0002 | c0003 | t0002 | g0162 | SAS | PJL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03688 | hp1 | a0002 | c0003 | t0002 | g0164 | SAS | STU | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03688 | hp2 | a0004 | c0006 | t0008 | g0011 | SAS | STU | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03710 | hp1 | a0001 | c0001 | t0005 | g0183 | SAS | PJL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03710 | hp2 | a0002 | c0003 | t0002 | g0224 | SAS | PJL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03831 | hp1 | a0001 | c0002 | t0009 | g0129 | SAS | BEB | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0225 | SAS | BEB | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03834 | hp2 | a0001 | c0002 | t0007 | g0196 | SAS | BEB | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03927 | hp1 | a0001 | c0001 | t0051 | g0107 | SAS | BEB | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03927 | hp2 | a0001 | c0002 | t0009 | g0133 | SAS | BEB | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03942 | hp1 | a0002 | c0003 | t0043 | g0155 | SAS | BEB | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG04115 | hp1 | a0001 | c0002 | t0009 | g0124 | SAS | STU | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | STU | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG04204 | hp1 | a0001 | c0002 | t0009 | g0136 | SAS | STU | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG04204 | hp2 | a0002 | c0003 | t0002 | g0154 | SAS | STU | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA18522 | hp1 | a0002 | c0003 | t0004 | g0167 | AFR | YRI | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA18522 | hp2 | a0001 | c0002 | t0046 | g0217 | AFR | YRI | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA18747 | hp1 | a0003 | c0005 | t0003 | g0032 | EAS | CHB | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHB | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA18906 | hp1 | a0002 | c0003 | t0004 | g0151 | AFR | YRI | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA18906 | hp2 | a0001 | c0002 | t0003 | g0040 | AFR | YRI | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA18939 | hp1 | a0001 | c0001 | t0023 | g0051 | EAS | JPT | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA18939 | hp2 | a0005 | c0007 | t0008 | g0005 | EAS | JPT | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA18964 | hp1 | a0005 | c0007 | t0008 | g0009 | EAS | JPT | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA18967 | hp1 | a0002 | c0003 | t0002 | g0180 | EAS | JPT | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA18977 | hp1 | a0002 | c0003 | t0002 | g0163 | EAS | JPT | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA18977 | hp2 | a0006 | c0009 | t0001 | g0097 | EAS | JPT | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA19004 | hp2 | a0003 | c0005 | t0003 | g0031 | EAS | JPT | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | LWK | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA19030 | hp2 | a0002 | c0003 | t0004 | g0179 | AFR | LWK | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | LWK | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA19043 | hp2 | a0001 | c0002 | t0019 | g0128 | AFR | LWK | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA19054 | hp1 | a0001 | c0001 | t0050 | g0062 | EAS | JPT | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA19054 | hp2 | a0005 | c0007 | t0008 | g0003 | EAS | JPT | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA19062 | hp2 | a0005 | c0007 | t0008 | g0010 | EAS | JPT | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA19068 | hp1 | a0001 | c0001 | t0005 | g0181 | EAS | JPT | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA19068 | hp2 | a0005 | c0007 | t0008 | g0008 | EAS | JPT | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA19080 | hp2 | a0002 | c0003 | t0002 | g0177 | EAS | JPT | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA19084 | hp2 | a0003 | c0005 | t0003 | g0033 | EAS | JPT | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA19240 | hp1 | a0001 | c0001 | t0053 | g0083 | AFR | YRI | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA19240 | hp2 | a0004 | c0006 | t0008 | g0007 | AFR | YRI | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA20129 | hp1 | a0002 | c0008 | t0012 | g0014 | AFR | ASW | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA20129 | hp2 | a0002 | c0004 | t0010 | g0234 | AFR | ASW | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA20752 | hp1 | a0002 | c0004 | t0011 | g0208 | EUR | TSI | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0185 | EUR | TSI | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA20805 | hp1 | a0004 | c0006 | t0022 | g0004 | EUR | TSI | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0061 | EUR | TSI | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA20905 | hp1 | a0001 | c0002 | t0007 | g0193 | SAS | GIH | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | GIH | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02109 | hp1 | a0001 | c0010 | t0006 | g0221 | AFR | ACB | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02109 | hp2 | a0002 | c0008 | t0012 | g0236 | AFR | ACB | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02486 | hp1 | a0002 | c0003 | t0004 | g0170 | AFR | ACB | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02486 | hp2 | a0001 | c0001 | t0054 | g0071 | AFR | ACB | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02559 | hp1 | a0002 | c0003 | t0004 | g0176 | AFR | ACB | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03471 | hp1 | a0002 | c0003 | t0004 | g0168 | AFR | MSL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG03471 | hp2 | a0001 | c0010 | t0006 | g0220 | AFR | MSL | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG06807 | hp1 | a0002 | c0003 | t0002 | g0156 | AFR | USA | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | USA | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | USA | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| NA20300 | hp2 | a0002 | c0004 | t0024 | g0046 | AFR | USA | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0003 | t0002 | g0172 | REF | REF | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| homoSapiens_grch38 | hp1 | a0002 | c0004 | t0011 | g0228 | REF | REF | EEA1_chr12_92765637_92934295 | EEA1 | chr12 | 92765637 | 92934295 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:92778050
|
G | A | 1 | a0005 | 5 | NA18939.hp2 NA18964.hp1 NA19054.hp2 others(2): Show |
missense_variant | MODERATE | c.3784C>T | p.Arg1262Trp | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 26/29 | 4013/9839 | 3784/4236 | 1262/1411 | chr12 | 92778050 | ||
| chr12:92782014
|
G | A | 1 | a0007 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.3272C>T | p.Ser1091Leu | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 23/29 | 3501/9839 | 3272/4236 | 1091/1411 | chr12 | 92782014 | ||
| chr12:92782070
|
A | T | 1 | a0006 | 4 | HG01099.hp1 HG02273.hp1 HG02523.hp1 others(1): Show |
missense_variant | MODERATE | c.3216T>A | p.Asn1072Lys | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 23/29 | 3445/9839 | 3216/4236 | 1072/1411 | chr12 | 92782070 | ||
| chr12:92787992
|
C | A | 1 | a0003 | 10 | HG00140.hp1 HG01167.hp2 HG01192.hp2 others(7): Show |
missense_variant | MODERATE | c.3025G>T | p.Ala1009Ser | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/29 | 3254/9839 | 3025/4236 | 1009/1411 | chr12 | 92787992 | ||
| chr12:92801659
|
T | A | 2 | a0004a0005 | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
missense_variant | MODERATE | c.2713A>T | p.Met905Leu | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 20/29 | 2942/9839 | 2713/4236 | 905/1411 | chr12 | 92801659 | ||
| chr12:92802646
|
T | G | 5 | a0001a0003a0006others(2): Show | 152 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
missense_variant | MODERATE | c.2428A>C | p.Lys810Gln | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 19/29 | 2657/9839 | 2428/4236 | 810/1411 | chr12 | 92802646 | ||
| chr12:92832621
|
G | T | 1 | a0008 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.1145C>A | p.Ser382Tyr | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/29 | 1374/9839 | 1145/4236 | 382/1411 | chr12 | 92832621 | ||
| chr12:92857322
|
C | G | 1 | a0009 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.319G>C | p.Glu107Gln | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 5/29 | 548/9839 | 319/4236 | 107/1411 | chr12 | 92857322 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:92779232
|
C | T | 1 | a0002c0015 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.3537G>A | p.Ala1179Ala | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 25/29 | 3766/9839 | 3537/4236 | 1179/1411 | chr12 | 92779232 | ||
| chr12:92801672
|
T | C | 1 | a0001c0011 | 2 | HG03098.hp2 HG03453.hp2 |
synonymous_variant | LOW | c.2700A>G | p.Gln900Gln | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 20/29 | 2929/9839 | 2700/4236 | 900/1411 | chr12 | 92801672 | ||
| chr12:92809025
|
C | T | 4 | a0001c0001a0002c0015a0006c0009others(1): Show | 78 | HG00280.hp2 HG00741.hp1 HG01069.hp1 others(75): Show |
synonymous_variant | LOW | c.2331G>A | p.Glu777Glu | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/29 | 2560/9839 | 2331/4236 | 777/1411 | chr12 | 92809025 | ||
| chr12:92811324
|
G | A | 1 | a0002c0008 | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
synonymous_variant | LOW | c.2154C>T | p.Tyr718Tyr | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 17/29 | 2383/9839 | 2154/4236 | 718/1411 | chr12 | 92811324 | ||
| chr12:92832530
|
G | A | 2 | a0001c0010a0001c0011 | 6 | HG02109.hp1 HG02647.hp2 HG03098.hp2 others(3): Show |
synonymous_variant | LOW | c.1236C>T | p.Leu412Leu | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/29 | 1465/9839 | 1236/4236 | 412/1411 | chr12 | 92832530 | ||
| chr12:92832536
|
T | C | 1 | a0002c0017 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.1230A>G | p.Leu410Leu | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/29 | 1459/9839 | 1230/4236 | 410/1411 | chr12 | 92832536 | ||
| chr12:92832743
|
T | C | 1 | a0001c0018 | 1 | HG02698.hp1 | synonymous_variant | LOW | c.1023A>G | p.Gln341Gln | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/29 | 1252/9839 | 1023/4236 | 341/1411 | chr12 | 92832743 | ||
| chr12:92864889
|
A | G | 2 | a0001c0012a0002c0003 | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
synonymous_variant | LOW | c.216T>C | p.His72His | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/29 | 445/9839 | 216/4236 | 72/1411 | chr12 | 92864889 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:92770726
|
A | T | 2 | a0002c0004t0010a0002c0004t0033 | 7 | HG02451.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5285T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 5285 | chr12 | 92770726 | |||||
| chr12:92770782
|
C | T | 1 | a0002c0004t0014 | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5229G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 5229 | chr12 | 92770782 | |||||
| chr12:92770833
|
GA | G | 10 | a0001c0002t0020a0002c0003t0002a0002c0003t0004others(7): Show | 54 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*5177delT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 5177 | chr12 | 92770833 | |||||
| chr12:92770872
|
A | G | 2 | a0002c0008t0012a0004c0006t0021 | 6 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5139T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 5139 | chr12 | 92770872 | |||||
| chr12:92770996
|
G | GGT | 4 | a0002c0003t0004a0002c0003t0016a0002c0003t0055others(1): Show | 19 | HG00639.hp2 HG01167.hp1 HG01884.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*5013_*5014dupAC | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 5014 | chr12 | 92770996 | |||||
| chr12:92770996
|
G | GGTGT | 22 | a0001c0001t0052a0001c0002t0003a0001c0002t0006others(19): Show | 76 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*5011_*5014dupACAC | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 5014 | chr12 | 92770996 | |||||
| chr12:92770996
|
G | GGTGTGT | 14 | a0001c0001t0001a0001c0001t0013a0001c0001t0023others(11): Show | 85 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*5009_*5014dupACAC others(2): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 5014 | chr12 | 92770996 | |||||
| chr12:92770996
|
G | GGTGTGTG others(1): Show |
7 | a0001c0001t0005a0001c0002t0017a0001c0002t0040others(4): Show | 20 | HG01071.hp2 HG01346.hp1 HG01433.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*5007_*5014dupACAC others(4): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 5014 | chr12 | 92770996 | |||||
| chr12:92770996
|
G | GGTGTGTG others(3): Show |
3 | a0001c0001t0051a0001c0002t0036a0001c0002t0039 | 3 | HG02258.hp2 HG02723.hp2 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5005_*5014dupACAC others(6): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 5014 | chr12 | 92770996 | |||||
| chr12:92770996
|
G | GGTGTGTG others(9): Show |
1 | a0001c0001t0049 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4999_*5014dupACAC others(12): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 5014 | chr12 | 92770996 | |||||
| chr12:92771116
|
G | T | 4 | a0001c0002t0003a0001c0002t0045a0003c0005t0003others(1): Show | 23 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*4895C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 4895 | chr12 | 92771116 | |||||
| chr12:92771160
|
G | A | 6 | a0001c0002t0003a0001c0002t0032a0001c0002t0035others(3): Show | 25 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*4851C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 4851 | chr12 | 92771160 | |||||
| chr12:92771772
|
T | C | 1 | a0001c0001t0053 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4239A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 4239 | chr12 | 92771772 | |||||
| chr12:92771843
|
C | T | 8 | a0001c0002t0003a0001c0002t0019a0001c0002t0032others(5): Show | 28 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*4168G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 4168 | chr12 | 92771843 | |||||
| chr12:92771874
|
T | C | 2 | a0001c0002t0037a0002c0004t0041 | 2 | HG02572.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4137A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 4137 | chr12 | 92771874 | |||||
| chr12:92772413
|
A | T | 1 | a0002c0008t0012 | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3598T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 3598 | chr12 | 92772413 | |||||
| chr12:92772520
|
G | A | 1 | a0001c0002t0038 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3491C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 3491 | chr12 | 92772520 | |||||
| chr12:92772552
|
A | T | 1 | a0001c0002t0027 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3459T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 3459 | chr12 | 92772552 | |||||
| chr12:92772617
|
G | A | 2 | a0002c0004t0048a0002c0008t0012 | 6 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3394C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 3394 | chr12 | 92772617 | |||||
| chr12:92772762
|
A | G | 39 | a0001c0001t0001a0001c0001t0005a0001c0001t0013others(36): Show | 151 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*3249T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 3249 | chr12 | 92772762 | |||||
| chr12:92772942
|
A | C | 1 | a0002c0004t0033 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3069T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 3069 | chr12 | 92772942 | |||||
| chr12:92773036
|
C | T | 1 | a0002c0008t0012 | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2975G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 2975 | chr12 | 92773036 | |||||
| chr12:92773152
|
T | A | 1 | a0003c0005t0042 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2859A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 2859 | chr12 | 92773152 | |||||
| chr12:92773395
|
A | C | 2 | a0001c0002t0032a0002c0004t0015 | 4 | HG02572.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2616T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 2616 | chr12 | 92773395 | |||||
| chr12:92773659
|
G | C | 9 | a0002c0003t0002a0002c0003t0004a0002c0003t0016others(6): Show | 52 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*2352C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 2352 | chr12 | 92773659 | |||||
| chr12:92773931
|
A | AT | 9 | a0002c0003t0002a0002c0003t0004a0002c0003t0016others(6): Show | 52 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*2079dupA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 2079 | chr12 | 92773931 | |||||
| chr12:92773939
|
G | T | 1 | a0001c0002t0026 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2072C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 2072 | chr12 | 92773939 | |||||
| chr12:92773943
|
G | A | 9 | a0002c0003t0002a0002c0003t0004a0002c0003t0016others(6): Show | 52 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*2068C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 2068 | chr12 | 92773943 | |||||
| chr12:92774051
|
C | CA | 13 | a0001c0001t0049a0001c0001t0050a0001c0002t0032others(10): Show | 32 | HG00738.hp1 HG02071.hp2 HG02451.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1959dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 1959 | chr12 | 92774051 | |||||
| chr12:92774051
|
C | CAA | 39 | a0001c0001t0001a0001c0001t0005a0001c0001t0023others(36): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*1958_*1959dupTT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 1959 | chr12 | 92774051 | |||||
| chr12:92774051
|
C | CAAA | 6 | a0001c0001t0013a0001c0001t0054a0001c0002t0044others(3): Show | 10 | HG01891.hp1 HG02135.hp2 HG02145.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1957_*1959dupTTT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 1959 | chr12 | 92774051 | |||||
| chr12:92774051
|
C | CAAAA | 2 | a0001c0002t0009a0001c0002t0020 | 9 | HG01256.hp2 HG01258.hp1 HG02135.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1956_*1959dupTTTT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 1959 | chr12 | 92774051 | |||||
| chr12:92774083
|
T | C | 62 | a0001c0001t0001a0001c0001t0005a0001c0001t0013others(59): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
3_prime_UTR_variant | MODIFIER | c.*1928A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 1928 | chr12 | 92774083 | |||||
| chr12:92774166
|
T | C | 1 | a0001c0001t0054 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1845A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 1845 | chr12 | 92774166 | |||||
| chr12:92774389
|
T | C | 1 | a0002c0004t0048 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1622A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 1622 | chr12 | 92774389 | |||||
| chr12:92774768
|
T | C | 3 | a0002c0004t0024a0002c0004t0048a0002c0008t0012 | 7 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1243A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 1243 | chr12 | 92774768 | |||||
| chr12:92774989
|
A | T | 3 | a0001c0002t0026a0001c0002t0027a0001c0002t0028 | 3 | HG02647.hp1 HG02886.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1022T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 1022 | chr12 | 92774989 | |||||
| chr12:92775153
|
C | T | 1 | a0007c0016t0025 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*858G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 858 | chr12 | 92775153 | |||||
| chr12:92775285
|
T | C | 1 | a0002c0004t0024 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*726A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 726 | chr12 | 92775285 | |||||
| chr12:92775348
|
G | A | 13 | a0001c0001t0001a0001c0001t0005a0001c0001t0013others(10): Show | 78 | HG00280.hp2 HG00741.hp1 HG01069.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*663C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 663 | chr12 | 92775348 | |||||
| chr12:92775353
|
T | A | 1 | a0002c0003t0055 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*658A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 658 | chr12 | 92775353 | |||||
| chr12:92775453
|
C | G | 1 | a0002c0004t0024 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*558G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 558 | chr12 | 92775453 | |||||
| chr12:92775519
|
C | A | 1 | a0002c0003t0056 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*492G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 492 | chr12 | 92775519 | |||||
| chr12:92775819
|
A | G | 1 | a0001c0001t0023 | 1 | NA18939.hp1 | 3_prime_UTR_variant | MODIFIER | c.*192T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 29/29 | 192 | chr12 | 92775819 | |||||
| chr12:92929071
|
TA | T | 4 | a0004c0006t0008a0004c0006t0021a0004c0006t0022others(1): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-6delT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/29 | 6 | chr12 | 92929071 | |||||
| chr12:92929152
|
G | C | 1 | a0002c0004t0014 | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-86C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/29 | 86 | chr12 | 92929152 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:92776348
|
A | G | 53 | a0001c0001t0005g0085a0001c0012t0006g0157a0002c0003t0002g0001others(50): Show | 54 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.4114-215T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 28/28 | chr12 | 92776348 | ||||||
| chr12:92776723
|
A | G | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.4113+121T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 28/28 | chr12 | 92776723 | ||||||
| chr12:92776798
|
G | C | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.4113+46C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 28/28 | chr12 | 92776798 | ||||||
| chr12:92777235
|
A | G | 7 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.4015-293T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 27/28 | chr12 | 92777235 | ||||||
| chr12:92777502
|
T | G | 46 | a0001c0001t0005g0085a0001c0012t0006g0157a0002c0003t0002g0001others(43): Show | 47 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.4014+41A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 27/28 | chr12 | 92777502 | ||||||
| chr12:92777518
|
T | G | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.4014+25A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 27/28 | chr12 | 92777518 | ||||||
| chr12:92777733
|
A | T | 1 | a0003c0005t0003g0022 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3894-70T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 26/28 | chr12 | 92777733 | ||||||
| chr12:92778292
|
A | C | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.3655-113T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 25/28 | chr12 | 92778292 | ||||||
| chr12:92778443
|
C | A | 1 | a0002c0015t0001g0073 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3655-264G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 25/28 | chr12 | 92778443 | ||||||
| chr12:92778735
|
T | C | 1 | a0001c0002t0044g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3654+380A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 25/28 | chr12 | 92778735 | ||||||
| chr12:92778882
|
T | A | 8 | a0001c0002t0007g0137a0001c0002t0044g0139a0001c0002t0046g0217others(5): Show | 8 | HG01243.hp2 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.3654+233A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 25/28 | chr12 | 92778882 | ||||||
| chr12:92778945
|
A | G | 1 | a0002c0017t0034g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3654+170T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 25/28 | chr12 | 92778945 | ||||||
| chr12:92779336
|
T | C | 7 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.3469-36A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 24/28 | chr12 | 92779336 | ||||||
| chr12:92779660
|
C | T | 1 | a0001c0002t0044g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3469-360G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 24/28 | chr12 | 92779660 | ||||||
| chr12:92779704
|
GA | G | 44 | a0002c0003t0002g0001a0002c0003t0002g0013a0002c0003t0002g0144others(41): Show | 45 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.3469-405delT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 24/28 | chr12 | 92779704 | ||||||
| chr12:92779866
|
A | AACAG | 26 | a0001c0002t0003g0023a0001c0002t0003g0024a0001c0002t0003g0025others(23): Show | 26 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.3468+410_3468+413d others(6): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 24/28 | chr12 | 92779866 | ||||||
| chr12:92779919
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3468+361A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 24/28 | chr12 | 92779919 | ||||||
| chr12:92780065
|
T | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0112 | 2 | HG01261.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.3468+215A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 24/28 | chr12 | 92780065 | ||||||
| chr12:92780577
|
T | C | 1 | a0002c0004t0031g0199 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3337-166A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 23/28 | chr12 | 92780577 | ||||||
| chr12:92780643
|
T | C | 2 | a0001c0001t0001g0078a0001c0001t0001g0081 | 2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3337-232A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 23/28 | chr12 | 92780643 | ||||||
| chr12:92780709
|
A | G | 1 | a0001c0012t0006g0157 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.3337-298T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 23/28 | chr12 | 92780709 | ||||||
| chr12:92780737
|
A | C | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.3337-326T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 23/28 | chr12 | 92780737 | ||||||
| chr12:92780792
|
T | A | 1 | a0001c0018t0017g0197 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3337-381A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 23/28 | chr12 | 92780792 | ||||||
| chr12:92780837
|
T | A | 1 | a0001c0001t0001g0076 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.3337-426A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 23/28 | chr12 | 92780837 | ||||||
| chr12:92780885
|
C | T | 1 | a0004c0006t0022g0004 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3337-474G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 23/28 | chr12 | 92780885 | ||||||
| chr12:92780980
|
C | A | 129 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(126): Show | 129 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(126): Show |
intron_variant | MODIFIER | c.3337-569G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 23/28 | chr12 | 92780980 | ||||||
| chr12:92781055
|
T | C | 52 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(49): Show | 53 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.3337-644A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 23/28 | chr12 | 92781055 | ||||||
| chr12:92781067
|
T | C | 1 | a0002c0003t0055g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3337-656A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 23/28 | chr12 | 92781067 | ||||||
| chr12:92781319
|
G | C | 3 | a0002c0004t0015g0198a0002c0004t0015g0203a0002c0004t0015g0213 | 3 | HG02622.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.3336+631C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 23/28 | chr12 | 92781319 | ||||||
| chr12:92781337
|
A | G | 23 | a0001c0002t0007g0048a0001c0002t0007g0116a0001c0002t0007g0117others(20): Show | 23 | HG00280.hp1 HG00642.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.3336+613T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 23/28 | chr12 | 92781337 | ||||||
| chr12:92781639
|
G | A | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.3336+311C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 23/28 | chr12 | 92781639 | ||||||
| chr12:92781728
|
A | AAAG | 242 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(239): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.3336+219_3336+221d others(5): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 23/28 | chr12 | 92781728 | ||||||
| chr12:92782402
|
A | G | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.3151-267T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92782402 | ||||||
| chr12:92782429
|
A | T | 44 | a0002c0003t0002g0001a0002c0003t0002g0013a0002c0003t0002g0144others(41): Show | 45 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.3151-294T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92782429 | ||||||
| chr12:92782468
|
G | A | 3 | a0001c0002t0039g0215a0001c0002t0040g0223a0001c0002t0046g0217 | 3 | HG02630.hp1 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3151-333C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92782468 | ||||||
| chr12:92782603
|
C | T | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.3151-468G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92782603 | ||||||
| chr12:92782981
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3151-846G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92782981 | ||||||
| chr12:92783047
|
T | C | 15 | a0001c0002t0006g0042a0001c0002t0006g0044a0001c0002t0006g0191others(12): Show | 15 | HG01109.hp2 HG01168.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.3151-912A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92783047 | ||||||
| chr12:92783091
|
A | G | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3151-956T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92783091 | ||||||
| chr12:92783377
|
G | C | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.3151-1242C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92783377 | ||||||
| chr12:92783560
|
T | C | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.3151-1425A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92783560 | ||||||
| chr12:92783568
|
G | A | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3151-1433C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92783568 | ||||||
| chr12:92783599
|
C | A | 1 | a0002c0015t0001g0073 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3151-1464G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92783599 | ||||||
| chr12:92783747
|
G | T | 7 | a0001c0001t0005g0181a0001c0001t0005g0182a0001c0001t0005g0183others(4): Show | 7 | HG01346.hp1 HG02602.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.3151-1612C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92783747 | ||||||
| chr12:92783758
|
G | C | 1 | a0002c0003t0004g0151 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3151-1623C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92783758 | ||||||
| chr12:92783916
|
TA | T | 7 | a0002c0004t0024g0046a0002c0004t0048g0017a0002c0008t0012g0014others(4): Show | 7 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3151-1782delT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92783916 | ||||||
| chr12:92784013
|
C | T | 1 | a0002c0003t0055g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3151-1878G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92784013 | ||||||
| chr12:92784072
|
C | T | 7 | a0002c0004t0024g0046a0002c0004t0048g0017a0002c0008t0012g0014others(4): Show | 7 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3151-1937G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92784072 | ||||||
| chr12:92784231
|
T | C | 3 | a0002c0004t0015g0198a0002c0004t0015g0203a0002c0004t0015g0213 | 3 | HG02622.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.3151-2096A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92784231 | ||||||
| chr12:92784510
|
C | A | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.3151-2375G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92784510 | ||||||
| chr12:92784564
|
A | G | 26 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(23): Show | 27 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.3151-2429T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92784564 | ||||||
| chr12:92784598
|
T | C | 1 | a0001c0002t0007g0118 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3151-2463A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92784598 | ||||||
| chr12:92784873
|
C | T | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3151-2738G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92784873 | ||||||
| chr12:92784916
|
T | C | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.3151-2781A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92784916 | ||||||
| chr12:92785027
|
T | TA | 196 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(193): Show | 197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.3150+2839dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92785027 | ||||||
| chr12:92785027
|
T | TAA | 18 | a0002c0003t0004g0147a0002c0003t0004g0151a0002c0003t0004g0152others(15): Show | 18 | HG00639.hp2 HG01167.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.3150+2838_3150+283 others(6): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92785027 | ||||||
| chr12:92785089
|
T | TAGAG | 52 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(49): Show | 53 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.3150+2774_3150+277 others(8): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92785089 | ||||||
| chr12:92785383
|
T | C | 3 | a0002c0004t0010g0231a0002c0004t0010g0232a0002c0004t0010g0234 | 3 | HG03139.hp1 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3150+2484A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92785383 | ||||||
| chr12:92785550
|
A | G | 1 | a0002c0004t0024g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3150+2317T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92785550 | ||||||
| chr12:92785624
|
C | A | 1 | a0001c0001t0005g0183 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3150+2243G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92785624 | ||||||
| chr12:92785876
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3150+1991C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92785876 | ||||||
| chr12:92786098
|
T | C | 23 | a0001c0002t0007g0048a0001c0002t0007g0116a0001c0002t0007g0117others(20): Show | 23 | HG00280.hp1 HG00642.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.3150+1769A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92786098 | ||||||
| chr12:92786138
|
C | T | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.3150+1729G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92786138 | ||||||
| chr12:92786334
|
GACTTTCA others(2): Show |
G | 6 | a0001c0010t0006g0218a0001c0010t0006g0219a0001c0010t0006g0220others(3): Show | 6 | HG02109.hp1 HG02647.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.3150+1524_3150+153 others(13): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92786334 | ||||||
| chr12:92786363
|
G | A | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.3150+1504C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92786363 | ||||||
| chr12:92786756
|
A | G | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.3150+1111T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92786756 | ||||||
| chr12:92786849
|
A | G | 1 | a0002c0004t0041g0201 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3150+1018T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92786849 | ||||||
| chr12:92786970
|
C | G | 22 | a0001c0002t0007g0048a0001c0002t0007g0116a0001c0002t0007g0117others(19): Show | 22 | HG00280.hp1 HG00642.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.3150+897G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92786970 | ||||||
| chr12:92787031
|
C | T | 1 | a0002c0003t0004g0226 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3150+836G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92787031 | ||||||
| chr12:92787287
|
C | G | 71 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(68): Show | 71 | HG00280.hp2 HG00741.hp1 HG01069.hp1 others(68): Show |
intron_variant | MODIFIER | c.3150+580G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92787287 | ||||||
| chr12:92787319
|
C | G | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.3150+548G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92787319 | ||||||
| chr12:92787692
|
C | T | 3 | a0002c0003t0016g0141a0002c0003t0016g0142a0002c0003t0016g0143 | 3 | HG02818.hp1 HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3150+175G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92787692 | ||||||
| chr12:92787736
|
CAATTT | C | 5 | a0002c0004t0018g0202a0002c0004t0018g0210a0002c0004t0018g0211others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.3150+126_3150+130d others(7): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92787736 | ||||||
| chr12:92787815
|
A | C | 1 | a0002c0003t0002g0163 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3150+52T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 22/28 | chr12 | 92787815 | ||||||
| chr12:92788268
|
A | AT | 14 | a0001c0002t0006g0042a0001c0002t0006g0044a0001c0002t0006g0191others(11): Show | 14 | HG01109.hp2 HG01257.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.2968-220dupA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92788268 | ||||||
| chr12:92788268
|
AT | A | 14 | a0001c0001t0001g0049a0001c0001t0001g0068a0001c0001t0001g0069others(11): Show | 14 | HG01069.hp1 HG01081.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.2968-220delA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92788268 | ||||||
| chr12:92788284
|
A | T | 4 | a0001c0001t0001g0047a0001c0001t0001g0102a0001c0001t0001g0103others(1): Show | 4 | HG02129.hp2 HG02698.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.2968-235T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92788284 | ||||||
| chr12:92788321
|
G | A | 3 | a0001c0001t0001g0057a0001c0001t0005g0061a0009c0013t0005g0064 | 3 | HG01433.hp1 HG03834.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2968-272C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92788321 | ||||||
| chr12:92788331
|
T | C | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2968-282A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92788331 | ||||||
| chr12:92788333
|
A | G | 2 | a0001c0001t0001g0060a0001c0001t0013g0050 | 2 | HG02015.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.2968-284T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92788333 | ||||||
| chr12:92788670
|
G | C | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2968-621C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92788670 | ||||||
| chr12:92788728
|
T | C | 2 | a0001c0002t0020g0122a0001c0002t0020g0123 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2968-679A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92788728 | ||||||
| chr12:92788996
|
A | G | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2968-947T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92788996 | ||||||
| chr12:92789119
|
G | A | 15 | a0001c0002t0006g0042a0001c0002t0006g0044a0001c0002t0006g0191others(12): Show | 15 | HG01109.hp2 HG01168.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2968-1070C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92789119 | ||||||
| chr12:92789226
|
G | A | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2968-1177C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92789226 | ||||||
| chr12:92789287
|
C | CA | 115 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(112): Show | 115 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(112): Show |
intron_variant | MODIFIER | c.2968-1239dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92789287 | ||||||
| chr12:92789287
|
C | CAAA | 15 | a0001c0002t0006g0042a0001c0002t0006g0044a0001c0002t0006g0191others(12): Show | 15 | HG01109.hp2 HG01168.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2968-1241_2968-123 others(7): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92789287 | ||||||
| chr12:92789335
|
G | GA | 5 | a0002c0004t0018g0202a0002c0004t0018g0210a0002c0004t0018g0211others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2968-1287dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92789335 | ||||||
| chr12:92789490
|
C | T | 181 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(178): Show | 182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.2968-1441G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92789490 | ||||||
| chr12:92789570
|
G | A | 1 | a0002c0017t0034g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2968-1521C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92789570 | ||||||
| chr12:92789722
|
T | C | 1 | a0001c0002t0007g0116 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2968-1673A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92789722 | ||||||
| chr12:92789784
|
C | T | 11 | a0001c0002t0007g0048a0001c0002t0007g0116a0001c0002t0007g0117others(8): Show | 11 | HG00280.hp1 HG00642.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.2968-1735G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92789784 | ||||||
| chr12:92789912
|
G | A | 1 | a0002c0017t0034g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2968-1863C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92789912 | ||||||
| chr12:92790030
|
T | G | 9 | a0001c0002t0039g0215a0001c0002t0040g0223a0001c0002t0046g0217others(6): Show | 9 | HG02109.hp1 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2968-1981A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92790030 | ||||||
| chr12:92790080
|
C | T | 1 | a0002c0003t0004g0147 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2968-2031G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92790080 | ||||||
| chr12:92790261
|
C | T | 2 | a0001c0001t0001g0056a0001c0001t0001g0066 | 2 | HG01243.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2968-2212G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92790261 | ||||||
| chr12:92790264
|
A | G | 1 | a0002c0004t0041g0201 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2968-2215T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92790264 | ||||||
| chr12:92790325
|
C | T | 44 | a0002c0003t0002g0001a0002c0003t0002g0013a0002c0003t0002g0144others(41): Show | 45 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.2968-2276G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92790325 | ||||||
| chr12:92790326
|
G | A | 1 | a0002c0004t0024g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2968-2277C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92790326 | ||||||
| chr12:92790347
|
G | A | 10 | a0003c0005t0003g0020a0003c0005t0003g0021a0003c0005t0003g0022others(7): Show | 10 | HG00140.hp1 HG01167.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.2968-2298C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92790347 | ||||||
| chr12:92790485
|
T | C | 1 | a0002c0003t0002g0013 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2968-2436A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92790485 | ||||||
| chr12:92790492
|
G | C | 5 | a0002c0004t0018g0202a0002c0004t0018g0210a0002c0004t0018g0211others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2968-2443C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92790492 | ||||||
| chr12:92790592
|
T | C | 52 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(49): Show | 53 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.2968-2543A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92790592 | ||||||
| chr12:92790780
|
A | G | 6 | a0001c0010t0006g0218a0001c0010t0006g0219a0001c0010t0006g0220others(3): Show | 6 | HG02109.hp1 HG02647.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2968-2731T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92790780 | ||||||
| chr12:92790782
|
G | T | 44 | a0002c0003t0002g0001a0002c0003t0002g0013a0002c0003t0002g0144others(41): Show | 45 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.2968-2733C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92790782 | ||||||
| chr12:92791086
|
C | T | 6 | a0002c0004t0011g0205a0002c0004t0011g0206a0002c0004t0011g0207others(3): Show | 6 | HG00099.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.2968-3037G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92791086 | ||||||
| chr12:92791236
|
G | A | 44 | a0002c0003t0002g0001a0002c0003t0002g0013a0002c0003t0002g0144others(41): Show | 45 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.2968-3187C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92791236 | ||||||
| chr12:92791296
|
G | T | 1 | a0003c0005t0003g0032 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2968-3247C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92791296 | ||||||
| chr12:92791371
|
A | G | 1 | a0002c0003t0004g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2968-3322T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92791371 | ||||||
| chr12:92791374
|
G | A | 1 | a0002c0003t0004g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2968-3325C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92791374 | ||||||
| chr12:92791386
|
A | G | 1 | a0002c0003t0004g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2968-3337T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92791386 | ||||||
| chr12:92791391
|
A | G | 1 | a0002c0003t0004g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2968-3342T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92791391 | ||||||
| chr12:92791395
|
C | T | 1 | a0002c0017t0034g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2968-3346G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92791395 | ||||||
| chr12:92791396
|
G | A | 1 | a0002c0003t0004g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2968-3347C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92791396 | ||||||
| chr12:92791399
|
T | C | 1 | a0002c0003t0004g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2968-3350A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92791399 | ||||||
| chr12:92791416
|
G | A | 1 | a0002c0003t0004g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2968-3367C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92791416 | ||||||
| chr12:92791824
|
T | C | 1 | a0002c0004t0031g0199 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2968-3775A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92791824 | ||||||
| chr12:92792133
|
G | A | 151 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(148): Show | 151 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.2968-4084C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92792133 | ||||||
| chr12:92792416
|
A | G | 5 | a0002c0004t0018g0202a0002c0004t0018g0210a0002c0004t0018g0211others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2968-4367T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92792416 | ||||||
| chr12:92792455
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2968-4406G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92792455 | ||||||
| chr12:92792456
|
G | A | 5 | a0001c0001t0001g0094a0002c0004t0014g0240a0002c0004t0014g0241others(2): Show | 5 | HG02273.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2968-4407C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92792456 | ||||||
| chr12:92792564
|
T | C | 1 | a0002c0004t0010g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2968-4515A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92792564 | ||||||
| chr12:92792577
|
C | A | 1 | a0001c0002t0007g0048 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2968-4528G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92792577 | ||||||
| chr12:92792626
|
G | A | 3 | a0001c0001t0001g0090a0001c0001t0001g0095a0001c0001t0001g0214 | 3 | HG00280.hp2 HG02074.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.2968-4577C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92792626 | ||||||
| chr12:92792703
|
C | G | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2968-4654G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92792703 | ||||||
| chr12:92792728
|
T | G | 1 | a0002c0003t0056g0178 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2968-4679A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92792728 | ||||||
| chr12:92792869
|
G | A | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2968-4820C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92792869 | ||||||
| chr12:92792889
|
T | C | 16 | a0002c0003t0004g0147a0002c0003t0004g0151a0002c0003t0004g0152others(13): Show | 16 | HG00639.hp2 HG01167.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.2968-4840A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92792889 | ||||||
| chr12:92792895
|
C | T | 16 | a0002c0003t0004g0147a0002c0003t0004g0151a0002c0003t0004g0152others(13): Show | 16 | HG00639.hp2 HG01167.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.2968-4846G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92792895 | ||||||
| chr12:92792927
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2968-4878T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92792927 | ||||||
| chr12:92792954
|
C | T | 9 | a0001c0002t0009g0113a0001c0002t0009g0120a0001c0002t0009g0121others(6): Show | 9 | HG01256.hp2 HG01258.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.2968-4905G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92792954 | ||||||
| chr12:92793121
|
G | T | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2968-5072C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92793121 | ||||||
| chr12:92793141
|
A | T | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2968-5092T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92793141 | ||||||
| chr12:92793152
|
T | C | 7 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2968-5103A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92793152 | ||||||
| chr12:92793182
|
T | C | 1 | a0004c0006t0008g0011 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2968-5133A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92793182 | ||||||
| chr12:92793276
|
G | A | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2968-5227C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92793276 | ||||||
| chr12:92793354
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2968-5305C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92793354 | ||||||
| chr12:92793566
|
A | G | 1 | a0002c0004t0048g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2967+5326T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92793566 | ||||||
| chr12:92793703
|
T | C | 1 | a0004c0006t0008g0007 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2967+5189A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92793703 | ||||||
| chr12:92793704
|
G | A | 2 | a0003c0005t0003g0020a0003c0005t0003g0022 | 2 | HG01192.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.2967+5188C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92793704 | ||||||
| chr12:92793790
|
T | G | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.2967+5102A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92793790 | ||||||
| chr12:92793904
|
C | T | 1 | a0001c0001t0001g0074 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2967+4988G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92793904 | ||||||
| chr12:92793905
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2967+4987G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92793905 | ||||||
| chr12:92793945
|
C | T | 3 | a0001c0002t0006g0042a0001c0002t0006g0044a0001c0002t0038g0043 | 3 | HG01109.hp2 HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2967+4947G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92793945 | ||||||
| chr12:92793970
|
A | C | 2 | a0001c0002t0006g0191a0001c0002t0037g0194 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2967+4922T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92793970 | ||||||
| chr12:92794049
|
C | T | 1 | a0002c0004t0031g0199 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2967+4843G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92794049 | ||||||
| chr12:92794131
|
G | A | 44 | a0002c0003t0002g0001a0002c0003t0002g0013a0002c0003t0002g0144others(41): Show | 45 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.2967+4761C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92794131 | ||||||
| chr12:92794515
|
A | G | 1 | a0002c0015t0001g0073 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2967+4377T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92794515 | ||||||
| chr12:92794652
|
G | A | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2967+4240C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92794652 | ||||||
| chr12:92794666
|
G | A | 1 | a0009c0013t0005g0064 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2967+4226C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92794666 | ||||||
| chr12:92794735
|
G | GGGGGGGC | 17 | a0001c0002t0003g0023a0001c0002t0003g0024a0001c0002t0003g0025others(14): Show | 17 | HG00140.hp1 HG00639.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.2967+4156_2967+415 others(11): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92794735 | ||||||
| chr12:92794879
|
G | GA | 16 | a0002c0003t0004g0147a0002c0003t0004g0151a0002c0003t0004g0152others(13): Show | 16 | HG00639.hp2 HG01167.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.2967+4012dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92794879 | ||||||
| chr12:92794904
|
C | A | 1 | a0002c0003t0004g0167 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2967+3988G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92794904 | ||||||
| chr12:92794921
|
A | G | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2967+3971T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92794921 | ||||||
| chr12:92795105
|
A | C | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2967+3787T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92795105 | ||||||
| chr12:92795281
|
T | A | 78 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(75): Show | 78 | HG00280.hp2 HG00741.hp1 HG01069.hp1 others(75): Show |
intron_variant | MODIFIER | c.2967+3611A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92795281 | ||||||
| chr12:92795295
|
C | G | 1 | a0002c0004t0048g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2967+3597G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92795295 | ||||||
| chr12:92795323
|
G | C | 1 | a0002c0004t0048g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2967+3569C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92795323 | ||||||
| chr12:92795347
|
T | C | 1 | a0002c0004t0029g0200 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2967+3545A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92795347 | ||||||
| chr12:92795366
|
G | A | 8 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(5): Show | 8 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.2967+3526C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92795366 | ||||||
| chr12:92795435
|
C | T | 1 | a0001c0002t0007g0137 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2967+3457G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92795435 | ||||||
| chr12:92795470
|
A | G | 1 | a0002c0017t0034g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2967+3422T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92795470 | ||||||
| chr12:92795667
|
T | C | 4 | a0006c0009t0001g0086a0006c0009t0001g0096a0006c0009t0001g0097others(1): Show | 4 | HG01099.hp1 HG02273.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.2967+3225A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92795667 | ||||||
| chr12:92795784
|
C | T | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2967+3108G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92795784 | ||||||
| chr12:92796234
|
G | A | 1 | a0002c0004t0024g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2967+2658C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92796234 | ||||||
| chr12:92796445
|
T | C | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2967+2447A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92796445 | ||||||
| chr12:92796463
|
T | TTA | 71 | a0001c0001t0001g0047a0001c0001t0001g0069a0001c0001t0001g0084others(68): Show | 72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.2967+2427_2967+242 others(6): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92796463 | ||||||
| chr12:92796533
|
A | G | 7 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2967+2359T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92796533 | ||||||
| chr12:92796537
|
C | T | 1 | a0002c0003t0056g0178 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2967+2355G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92796537 | ||||||
| chr12:92796564
|
T | C | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2967+2328A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92796564 | ||||||
| chr12:92796701
|
G | C | 1 | a0001c0001t0053g0083 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2967+2191C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92796701 | ||||||
| chr12:92796938
|
T | C | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2967+1954A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92796938 | ||||||
| chr12:92797053
|
T | C | 6 | a0001c0010t0006g0218a0001c0010t0006g0219a0001c0010t0006g0220others(3): Show | 6 | HG02109.hp1 HG02647.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2967+1839A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92797053 | ||||||
| chr12:92797212
|
G | A | 44 | a0002c0003t0002g0001a0002c0003t0002g0013a0002c0003t0002g0144others(41): Show | 45 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.2967+1680C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92797212 | ||||||
| chr12:92797244
|
T | C | 7 | a0002c0004t0024g0046a0002c0004t0048g0017a0002c0008t0012g0014others(4): Show | 7 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2967+1648A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92797244 | ||||||
| chr12:92797304
|
T | C | 1 | a0002c0017t0034g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2967+1588A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92797304 | ||||||
| chr12:92797308
|
G | A | 1 | a0002c0004t0024g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2967+1584C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92797308 | ||||||
| chr12:92797550
|
C | T | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.2967+1342G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92797550 | ||||||
| chr12:92797610
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2967+1282G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92797610 | ||||||
| chr12:92797647
|
T | C | 1 | a0001c0012t0006g0157 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2967+1245A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92797647 | ||||||
| chr12:92798231
|
T | C | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.2967+661A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92798231 | ||||||
| chr12:92798345
|
A | AT | 40 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(37): Show | 41 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.2967+546dupA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92798345 | ||||||
| chr12:92798345
|
A | ATT | 4 | a0002c0003t0004g0165a0002c0003t0004g0166a0002c0003t0004g0174others(1): Show | 4 | HG00639.hp2 HG01167.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2967+545_2967+546d others(4): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92798345 | ||||||
| chr12:92798345
|
A | T | 1 | a0002c0003t0004g0226 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2967+547T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92798345 | ||||||
| chr12:92798348
|
A | T | 67 | a0001c0002t0009g0124a0001c0002t0019g0127a0001c0012t0006g0157others(64): Show | 68 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.2967+544T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92798348 | ||||||
| chr12:92798351
|
A | T | 96 | a0001c0001t0001g0091a0001c0002t0009g0113a0001c0002t0009g0120others(93): Show | 97 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.2967+541T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92798351 | ||||||
| chr12:92798387
|
C | T | 2 | a0002c0003t0004g0167a0002c0003t0004g0170 | 2 | HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2967+505G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92798387 | ||||||
| chr12:92798542
|
G | C | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2967+350C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92798542 | ||||||
| chr12:92798782
|
C | G | 1 | a0001c0002t0032g0045 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2967+110G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92798782 | ||||||
| chr12:92798845
|
A | G | 1 | a0002c0015t0001g0073 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2967+47T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 21/28 | chr12 | 92798845 | ||||||
| chr12:92799093
|
G | GA | 26 | a0001c0002t0003g0023a0001c0002t0003g0024a0001c0002t0003g0025others(23): Show | 26 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(23): Show |
splice_region_variant&intron_variant | LOW | c.2773-8dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 20/28 | chr12 | 92799093 | ||||||
| chr12:92799378
|
G | A | 51 | a0002c0003t0002g0001a0002c0003t0002g0013a0002c0003t0002g0144others(48): Show | 52 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.2773-292C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 20/28 | chr12 | 92799378 | ||||||
| chr12:92799537
|
A | T | 1 | a0001c0001t0001g0095 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2773-451T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 20/28 | chr12 | 92799537 | ||||||
| chr12:92799566
|
C | T | 1 | a0001c0002t0032g0045 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2773-480G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 20/28 | chr12 | 92799566 | ||||||
| chr12:92799651
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2773-565C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 20/28 | chr12 | 92799651 | ||||||
| chr12:92799681
|
G | T | 1 | a0006c0009t0001g0086 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2773-595C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 20/28 | chr12 | 92799681 | ||||||
| chr12:92799835
|
A | G | 1 | a0008c0014t0006g0204 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2773-749T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 20/28 | chr12 | 92799835 | ||||||
| chr12:92799933
|
A | C | 1 | a0002c0003t0002g0156 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2773-847T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 20/28 | chr12 | 92799933 | ||||||
| chr12:92800136
|
C | T | 1 | a0001c0002t0032g0045 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2773-1050G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 20/28 | chr12 | 92800136 | ||||||
| chr12:92800179
|
G | A | 5 | a0002c0004t0018g0202a0002c0004t0018g0210a0002c0004t0018g0211others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2773-1093C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 20/28 | chr12 | 92800179 | ||||||
| chr12:92800223
|
A | T | 1 | a0001c0002t0003g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2773-1137T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 20/28 | chr12 | 92800223 | ||||||
| chr12:92800518
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2772+1082G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 20/28 | chr12 | 92800518 | ||||||
| chr12:92801907
|
GATC | G | 6 | a0001c0010t0006g0218a0001c0010t0006g0219a0001c0010t0006g0220others(3): Show | 6 | HG02109.hp1 HG02647.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2671-209_2671-207d others(5): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 19/28 | chr12 | 92801907 | ||||||
| chr12:92802941
|
C | T | 1 | a0002c0003t0002g0153 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2340-207G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92802941 | ||||||
| chr12:92803008
|
C | T | 3 | a0001c0002t0026g0212a0001c0002t0027g0189a0001c0002t0028g0190 | 3 | HG02647.hp1 HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2340-274G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92803008 | ||||||
| chr12:92803219
|
A | T | 236 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(233): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.2340-485T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92803219 | ||||||
| chr12:92803236
|
T | C | 15 | a0001c0002t0006g0042a0001c0002t0006g0044a0001c0002t0006g0191others(12): Show | 15 | HG01109.hp2 HG01168.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2340-502A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92803236 | ||||||
| chr12:92803578
|
A | G | 1 | a0001c0002t0007g0137 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2340-844T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92803578 | ||||||
| chr12:92803605
|
TG | T | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2340-872delC | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92803605 | ||||||
| chr12:92803796
|
T | G | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2340-1062A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92803796 | ||||||
| chr12:92803931
|
A | G | 5 | a0002c0004t0018g0202a0002c0004t0018g0210a0002c0004t0018g0211others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2340-1197T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92803931 | ||||||
| chr12:92804113
|
A | G | 1 | a0005c0007t0008g0003 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2340-1379T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92804113 | ||||||
| chr12:92804299
|
A | G | 235 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(232): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.2340-1565T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92804299 | ||||||
| chr12:92804326
|
A | G | 78 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(75): Show | 78 | HG00280.hp2 HG00741.hp1 HG01069.hp1 others(75): Show |
intron_variant | MODIFIER | c.2340-1592T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92804326 | ||||||
| chr12:92804384
|
A | C | 8 | a0001c0002t0039g0215a0001c0002t0040g0223a0001c0002t0046g0217others(5): Show | 8 | HG02109.hp1 HG02630.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2340-1650T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92804384 | ||||||
| chr12:92804397
|
C | G | 24 | a0001c0002t0007g0048a0001c0002t0007g0116a0001c0002t0007g0117others(21): Show | 24 | HG00280.hp1 HG00642.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.2340-1663G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92804397 | ||||||
| chr12:92804557
|
G | C | 39 | a0001c0001t0001g0049a0001c0001t0001g0054a0001c0001t0001g0055others(36): Show | 39 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.2340-1823C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92804557 | ||||||
| chr12:92804566
|
T | C | 236 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(233): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.2340-1832A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92804566 | ||||||
| chr12:92804571
|
C | CA | 36 | a0001c0001t0001g0063a0001c0001t0001g0081a0001c0001t0001g0108others(33): Show | 36 | HG00099.hp2 HG00642.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.2340-1838dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92804571 | ||||||
| chr12:92804571
|
C | CAA | 5 | a0001c0010t0006g0218a0002c0008t0012g0014a0002c0008t0012g0015others(2): Show | 5 | HG01243.hp2 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2340-1839_2340-183 others(6): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92804571 | ||||||
| chr12:92804571
|
CA | C | 12 | a0001c0001t0001g0099a0001c0001t0005g0186a0001c0002t0046g0217others(9): Show | 12 | HG01346.hp1 HG02559.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.2340-1838delT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92804571 | ||||||
| chr12:92804703
|
C | T | 2 | a0001c0002t0039g0215a0001c0002t0040g0223 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2340-1969G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92804703 | ||||||
| chr12:92804713
|
A | G | 6 | a0003c0005t0003g0021a0003c0005t0003g0031a0003c0005t0003g0032others(3): Show | 6 | HG02071.hp1 HG02129.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.2340-1979T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92804713 | ||||||
| chr12:92805031
|
T | C | 1 | a0002c0004t0011g0205 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2340-2297A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92805031 | ||||||
| chr12:92805116
|
C | G | 203 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(200): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.2340-2382G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92805116 | ||||||
| chr12:92805277
|
T | A | 1 | a0002c0017t0034g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2340-2543A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92805277 | ||||||
| chr12:92805464
|
T | C | 1 | a0002c0003t0056g0178 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2340-2730A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92805464 | ||||||
| chr12:92805607
|
G | C | 3 | a0002c0003t0016g0141a0002c0003t0016g0142a0002c0003t0016g0143 | 3 | HG02818.hp1 HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2340-2873C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92805607 | ||||||
| chr12:92805743
|
C | T | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2340-3009G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92805743 | ||||||
| chr12:92806443
|
A | T | 1 | a0001c0001t0001g0090 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2339+2574T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92806443 | ||||||
| chr12:92806645
|
T | C | 3 | a0001c0001t0001g0068a0001c0001t0001g0072a0001c0001t0013g0092 | 3 | HG01069.hp1 HG01071.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2339+2372A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92806645 | ||||||
| chr12:92806781
|
T | G | 204 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(201): Show | 205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.2339+2236A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92806781 | ||||||
| chr12:92806921
|
G | A | 4 | a0001c0002t0003g0037a0001c0002t0003g0040a0001c0002t0003g0041others(1): Show | 4 | HG02257.hp1 HG03209.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2339+2096C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92806921 | ||||||
| chr12:92806931
|
C | CTTTTTTT others(6): Show |
2 | a0002c0004t0015g0203a0002c0004t0015g0213 | 2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2339+2085_2339+208 others(17): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92806931 | ||||||
| chr12:92806931
|
C | CTTTTTTT others(7): Show |
1 | a0002c0004t0015g0198 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2339+2085_2339+208 others(18): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92806931 | ||||||
| chr12:92806938
|
A | T | 3 | a0002c0004t0015g0198a0002c0004t0015g0203a0002c0004t0015g0213 | 3 | HG02622.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2339+2079T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92806938 | ||||||
| chr12:92806939
|
A | T | 3 | a0002c0004t0015g0198a0002c0004t0015g0203a0002c0004t0015g0213 | 3 | HG02622.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2339+2078T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92806939 | ||||||
| chr12:92806941
|
A | T | 3 | a0002c0004t0015g0198a0002c0004t0015g0203a0002c0004t0015g0213 | 3 | HG02622.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2339+2076T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92806941 | ||||||
| chr12:92806942
|
A | AT | 51 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(48): Show | 52 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.2339+2074dupA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92806942 | ||||||
| chr12:92806942
|
A | T | 3 | a0002c0004t0015g0198a0002c0004t0015g0203a0002c0004t0015g0213 | 3 | HG02622.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2339+2075T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92806942 | ||||||
| chr12:92806943
|
T | A | 1 | a0001c0001t0001g0063 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2339+2074A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92806943 | ||||||
| chr12:92806977
|
G | A | 1 | a0001c0002t0006g0044 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2339+2040C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92806977 | ||||||
| chr12:92806984
|
T | C | 3 | a0002c0004t0015g0198a0002c0004t0015g0203a0002c0004t0015g0213 | 3 | HG02622.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2339+2033A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92806984 | ||||||
| chr12:92807079
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2339+1938C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92807079 | ||||||
| chr12:92807239
|
C | T | 23 | a0001c0002t0007g0048a0001c0002t0007g0116a0001c0002t0007g0117others(20): Show | 23 | HG00280.hp1 HG00642.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.2339+1778G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92807239 | ||||||
| chr12:92807253
|
A | AT | 49 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(46): Show | 50 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.2339+1763dupA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92807253 | ||||||
| chr12:92807264
|
A | T | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2339+1753T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92807264 | ||||||
| chr12:92807308
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2339+1709C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92807308 | ||||||
| chr12:92807349
|
T | C | 1 | a0002c0004t0024g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2339+1668A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92807349 | ||||||
| chr12:92807409
|
G | A | 52 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(49): Show | 53 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.2339+1608C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92807409 | ||||||
| chr12:92807878
|
T | A | 1 | a0004c0006t0008g0007 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2339+1139A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92807878 | ||||||
| chr12:92808283
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2339+734A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92808283 | ||||||
| chr12:92808303
|
C | T | 242 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(239): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.2339+714G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92808303 | ||||||
| chr12:92808469
|
G | A | 44 | a0002c0003t0002g0001a0002c0003t0002g0013a0002c0003t0002g0144others(41): Show | 45 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.2339+548C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92808469 | ||||||
| chr12:92808478
|
AT | A | 28 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0072others(25): Show | 28 | HG01069.hp1 HG01071.hp1 HG02258.hp1 others(25): Show |
intron_variant | MODIFIER | c.2339+538delA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92808478 | ||||||
| chr12:92808563
|
A | G | 1 | a0001c0002t0006g0192 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2339+454T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92808563 | ||||||
| chr12:92808574
|
A | G | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2339+443T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92808574 | ||||||
| chr12:92808612
|
A | G | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2339+405T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92808612 | ||||||
| chr12:92808930
|
C | T | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2339+87G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92808930 | ||||||
| chr12:92808947
|
T | A | 7 | a0002c0004t0024g0046a0002c0004t0048g0017a0002c0008t0012g0014others(4): Show | 7 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2339+70A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92808947 | ||||||
| chr12:92808950
|
G | T | 44 | a0002c0003t0002g0001a0002c0003t0002g0013a0002c0003t0002g0144others(41): Show | 45 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.2339+67C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 18/28 | chr12 | 92808950 | ||||||
| chr12:92809250
|
G | C | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2200-94C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 17/28 | chr12 | 92809250 | ||||||
| chr12:92809260
|
C | CA | 7 | a0002c0004t0024g0046a0002c0004t0048g0017a0002c0008t0012g0014others(4): Show | 7 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2200-105dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 17/28 | chr12 | 92809260 | ||||||
| chr12:92809260
|
C | CAA | 44 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(41): Show | 45 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.2200-106_2200-105d others(4): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 17/28 | chr12 | 92809260 | ||||||
| chr12:92809295
|
G | C | 1 | a0002c0003t0002g0149 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2200-139C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 17/28 | chr12 | 92809295 | ||||||
| chr12:92809361
|
A | G | 1 | a0001c0002t0046g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2200-205T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 17/28 | chr12 | 92809361 | ||||||
| chr12:92809483
|
C | T | 3 | a0001c0001t0001g0068a0001c0001t0001g0072a0001c0001t0013g0092 | 3 | HG01069.hp1 HG01071.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2200-327G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 17/28 | chr12 | 92809483 | ||||||
| chr12:92809523
|
T | TA | 7 | a0001c0001t0001g0089a0001c0001t0001g0132a0001c0002t0047g0187others(4): Show | 7 | HG01978.hp1 HG02074.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.2200-368dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 17/28 | chr12 | 92809523 | ||||||
| chr12:92809523
|
T | TAA | 38 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(35): Show | 39 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.2200-369_2200-368d others(4): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 17/28 | chr12 | 92809523 | ||||||
| chr12:92809523
|
T | TAAA | 12 | a0002c0003t0002g0153a0002c0003t0002g0159a0002c0003t0002g0180others(9): Show | 12 | HG01175.hp2 HG01243.hp2 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.2200-370_2200-368d others(5): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 17/28 | chr12 | 92809523 | ||||||
| chr12:92809523
|
TA | T | 13 | a0001c0001t0001g0068a0001c0001t0001g0079a0001c0002t0003g0028others(10): Show | 13 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.2200-368delT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 17/28 | chr12 | 92809523 | ||||||
| chr12:92809552
|
A | G | 219 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(216): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.2200-396T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 17/28 | chr12 | 92809552 | ||||||
| chr12:92809596
|
G | A | 1 | a0003c0005t0003g0022 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2200-440C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 17/28 | chr12 | 92809596 | ||||||
| chr12:92809694
|
CA | C | 5 | a0001c0002t0044g0139a0002c0003t0004g0152a0002c0004t0018g0202others(2): Show | 5 | HG01884.hp1 HG01891.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2200-539delT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 17/28 | chr12 | 92809694 | ||||||
| chr12:92810411
|
T | C | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2199+868A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 17/28 | chr12 | 92810411 | ||||||
| chr12:92810452
|
C | A | 1 | a0001c0001t0001g0106 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2199+827G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 17/28 | chr12 | 92810452 | ||||||
| chr12:92810453
|
G | A | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2199+826C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 17/28 | chr12 | 92810453 | ||||||
| chr12:92810591
|
A | G | 152 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(149): Show | 152 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.2199+688T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 17/28 | chr12 | 92810591 | ||||||
| chr12:92810620
|
T | G | 5 | a0001c0002t0003g0023a0001c0002t0003g0037a0001c0002t0003g0040others(2): Show | 5 | HG02257.hp1 HG03209.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2199+659A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 17/28 | chr12 | 92810620 | ||||||
| chr12:92810650
|
T | A | 1 | a0001c0001t0005g0085 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2199+629A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 17/28 | chr12 | 92810650 | ||||||
| chr12:92810655
|
A | AT | 7 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(4): Show | 7 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.2199+623dupA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 17/28 | chr12 | 92810655 | ||||||
| chr12:92810655
|
A | T | 1 | a0002c0003t0016g0141 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2199+624T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 17/28 | chr12 | 92810655 | ||||||
| chr12:92810699
|
G | C | 1 | a0002c0004t0014g0242 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2199+580C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 17/28 | chr12 | 92810699 | ||||||
| chr12:92810811
|
T | C | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2199+468A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 17/28 | chr12 | 92810811 | ||||||
| chr12:92811091
|
G | A | 1 | a0001c0002t0046g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2199+188C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 17/28 | chr12 | 92811091 | ||||||
| chr12:92811126
|
A | G | 2 | a0001c0002t0020g0122a0001c0002t0020g0123 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2199+153T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 17/28 | chr12 | 92811126 | ||||||
| chr12:92811155
|
A | G | 1 | a0002c0004t0024g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2199+124T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 17/28 | chr12 | 92811155 | ||||||
| chr12:92811530
|
A | T | 1 | a0004c0006t0022g0004 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2044-96T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 16/28 | chr12 | 92811530 | ||||||
| chr12:92811572
|
T | C | 1 | a0002c0004t0010g0234 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2044-138A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 16/28 | chr12 | 92811572 | ||||||
| chr12:92811863
|
A | T | 1 | a0001c0001t0005g0181 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2044-429T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 16/28 | chr12 | 92811863 | ||||||
| chr12:92811866
|
A | T | 1 | a0002c0017t0034g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2044-432T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 16/28 | chr12 | 92811866 | ||||||
| chr12:92811868
|
A | T | 153 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(150): Show | 153 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.2044-434T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 16/28 | chr12 | 92811868 | ||||||
| chr12:92811869
|
A | T | 1 | a0008c0014t0006g0204 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2044-435T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 16/28 | chr12 | 92811869 | ||||||
| chr12:92812026
|
T | C | 44 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(41): Show | 45 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.2044-592A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 16/28 | chr12 | 92812026 | ||||||
| chr12:92812031
|
T | A | 1 | a0002c0003t0043g0155 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2044-597A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 16/28 | chr12 | 92812031 | ||||||
| chr12:92812121
|
G | A | 9 | a0001c0002t0039g0215a0001c0002t0040g0223a0001c0002t0046g0217others(6): Show | 9 | HG02109.hp1 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2044-687C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 16/28 | chr12 | 92812121 | ||||||
| chr12:92812282
|
T | C | 9 | a0001c0002t0009g0113a0001c0002t0009g0120a0001c0002t0009g0121others(6): Show | 9 | HG01256.hp2 HG01258.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.2043+698A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 16/28 | chr12 | 92812282 | ||||||
| chr12:92812458
|
T | C | 13 | a0001c0002t0003g0023a0001c0002t0003g0024a0001c0002t0003g0025others(10): Show | 13 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.2043+522A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 16/28 | chr12 | 92812458 | ||||||
| chr12:92812505
|
C | A | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2043+475G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 16/28 | chr12 | 92812505 | ||||||
| chr12:92812767
|
T | C | 3 | a0002c0003t0016g0141a0002c0003t0016g0142a0002c0003t0016g0143 | 3 | HG02818.hp1 HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2043+213A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 16/28 | chr12 | 92812767 | ||||||
| chr12:92812922
|
AATTT | A | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2043+54_2043+57del others(4): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 16/28 | chr12 | 92812922 | ||||||
| chr12:92812950
|
G | A | 1 | a0001c0001t0005g0225 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2043+30C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 16/28 | chr12 | 92812950 | ||||||
| chr12:92813102
|
G | A | 208 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(205): Show | 209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.1930-9C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92813102 | ||||||
| chr12:92813288
|
A | G | 1 | a0001c0001t0001g0100 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1930-195T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92813288 | ||||||
| chr12:92813376
|
T | C | 1 | a0002c0003t0004g0170 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1930-283A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92813376 | ||||||
| chr12:92813384
|
A | G | 4 | a0001c0002t0003g0037a0001c0002t0003g0040a0001c0002t0003g0041others(1): Show | 4 | HG02257.hp1 HG03209.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1930-291T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92813384 | ||||||
| chr12:92813465
|
T | C | 1 | a0002c0004t0011g0205 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1930-372A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92813465 | ||||||
| chr12:92813466
|
T | A | 1 | a0001c0001t0013g0138 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1930-373A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92813466 | ||||||
| chr12:92813631
|
A | T | 1 | a0004c0006t0008g0011 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1930-538T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92813631 | ||||||
| chr12:92813664
|
A | T | 1 | a0001c0001t0005g0181 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1930-571T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92813664 | ||||||
| chr12:92813675
|
C | T | 51 | a0002c0003t0002g0001a0002c0003t0002g0013a0002c0003t0002g0144others(48): Show | 52 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1930-582G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92813675 | ||||||
| chr12:92813684
|
T | C | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1930-591A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92813684 | ||||||
| chr12:92813699
|
T | A | 1 | a0006c0009t0001g0096 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1930-606A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92813699 | ||||||
| chr12:92813711
|
C | T | 3 | a0002c0004t0015g0198a0002c0004t0015g0203a0002c0004t0015g0213 | 3 | HG02622.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1930-618G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92813711 | ||||||
| chr12:92813752
|
C | T | 7 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1930-659G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92813752 | ||||||
| chr12:92813755
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1930-662G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92813755 | ||||||
| chr12:92813773
|
G | C | 44 | a0002c0003t0002g0001a0002c0003t0002g0013a0002c0003t0002g0144others(41): Show | 45 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1930-680C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92813773 | ||||||
| chr12:92813968
|
G | A | 5 | a0001c0010t0006g0220a0002c0004t0014g0240a0002c0004t0014g0241others(2): Show | 5 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1930-875C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92813968 | ||||||
| chr12:92814135
|
G | T | 44 | a0002c0003t0002g0001a0002c0003t0002g0013a0002c0003t0002g0144others(41): Show | 45 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1930-1042C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92814135 | ||||||
| chr12:92814147
|
G | T | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1930-1054C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92814147 | ||||||
| chr12:92814293
|
T | C | 1 | a0001c0002t0007g0118 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1930-1200A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92814293 | ||||||
| chr12:92814561
|
T | A | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.1930-1468A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92814561 | ||||||
| chr12:92814606
|
C | T | 1 | a0001c0002t0007g0137 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1930-1513G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92814606 | ||||||
| chr12:92814664
|
C | T | 5 | a0001c0001t0001g0090a0001c0001t0001g0095a0001c0001t0001g0099others(2): Show | 5 | HG00280.hp2 HG02074.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.1929+1536G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92814664 | ||||||
| chr12:92814803
|
AGGAAGTA others(4): Show |
A | 1 | a0001c0001t0051g0107 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1929+1386_1929+139 others(15): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92814803 | ||||||
| chr12:92815175
|
T | C | 1 | a0002c0003t0002g0159 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1929+1025A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92815175 | ||||||
| chr12:92815211
|
C | CA | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1929+988dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92815211 | ||||||
| chr12:92815246
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1929+954A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92815246 | ||||||
| chr12:92815305
|
G | C | 44 | a0002c0003t0002g0001a0002c0003t0002g0013a0002c0003t0002g0144others(41): Show | 45 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1929+895C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92815305 | ||||||
| chr12:92815358
|
T | A | 3 | a0002c0004t0015g0198a0002c0004t0015g0203a0002c0004t0015g0213 | 3 | HG02622.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1929+842A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92815358 | ||||||
| chr12:92815393
|
T | A | 1 | a0001c0001t0001g0069 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1929+807A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92815393 | ||||||
| chr12:92815481
|
C | G | 41 | a0002c0003t0002g0001a0002c0003t0002g0013a0002c0003t0002g0144others(38): Show | 42 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.1929+719G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92815481 | ||||||
| chr12:92815496
|
GTTATATT others(1): Show |
G | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1929+696_1929+703d others(10): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92815496 | ||||||
| chr12:92815589
|
T | C | 235 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(232): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1929+611A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92815589 | ||||||
| chr12:92815783
|
T | C | 1 | a0002c0004t0024g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1929+417A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92815783 | ||||||
| chr12:92815882
|
G | A | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1929+318C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92815882 | ||||||
| chr12:92815894
|
G | A | 3 | a0002c0004t0015g0198a0002c0004t0015g0203a0002c0004t0015g0213 | 3 | HG02622.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1929+306C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92815894 | ||||||
| chr12:92815951
|
G | C | 7 | a0002c0004t0024g0046a0002c0004t0048g0017a0002c0008t0012g0014others(4): Show | 7 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1929+249C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92815951 | ||||||
| chr12:92816156
|
G | A | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1929+44C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 15/28 | chr12 | 92816156 | ||||||
| chr12:92816442
|
A | G | 1 | a0001c0012t0006g0157 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1729-42T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 14/28 | chr12 | 92816442 | ||||||
| chr12:92816536
|
A | C | 23 | a0001c0002t0007g0048a0001c0002t0007g0116a0001c0002t0007g0117others(20): Show | 23 | HG00280.hp1 HG00642.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.1729-136T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 14/28 | chr12 | 92816536 | ||||||
| chr12:92816556
|
A | G | 78 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(75): Show | 78 | HG00280.hp2 HG00741.hp1 HG01069.hp1 others(75): Show |
intron_variant | MODIFIER | c.1729-156T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 14/28 | chr12 | 92816556 | ||||||
| chr12:92816559
|
G | T | 2 | a0002c0003t0002g0144a0002c0003t0002g0161 | 2 | HG00099.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1729-159C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 14/28 | chr12 | 92816559 | ||||||
| chr12:92816626
|
TA | T | 3 | a0002c0004t0015g0198a0002c0004t0015g0203a0002c0004t0015g0213 | 3 | HG02622.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1729-227delT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 14/28 | chr12 | 92816626 | ||||||
| chr12:92816781
|
CCATCTCT others(517): Show |
C | 9 | a0001c0002t0039g0215a0001c0002t0040g0223a0001c0002t0046g0217others(6): Show | 9 | HG02109.hp1 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1729-905_1729-382d others(2): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 14/28 | chr12 | 92816781 | ||||||
| chr12:92816867
|
C | T | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.1729-467G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 14/28 | chr12 | 92816867 | ||||||
| chr12:92817044
|
G | T | 209 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(206): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1729-644C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 14/28 | chr12 | 92817044 | ||||||
| chr12:92817063
|
T | C | 25 | a0001c0002t0003g0023a0001c0002t0003g0024a0001c0002t0003g0025others(22): Show | 25 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.1729-663A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 14/28 | chr12 | 92817063 | ||||||
| chr12:92817189
|
T | C | 145 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(142): Show | 145 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1729-789A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 14/28 | chr12 | 92817189 | ||||||
| chr12:92817195
|
T | C | 1 | a0002c0017t0034g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1729-795A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 14/28 | chr12 | 92817195 | ||||||
| chr12:92817419
|
C | T | 1 | a0005c0007t0008g0008 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1729-1019G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 14/28 | chr12 | 92817419 | ||||||
| chr12:92817661
|
C | T | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.1729-1261G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 14/28 | chr12 | 92817661 | ||||||
| chr12:92817694
|
C | T | 1 | a0001c0001t0005g0061 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1729-1294G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 14/28 | chr12 | 92817694 | ||||||
| chr12:92817696
|
T | C | 1 | a0001c0002t0044g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1729-1296A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 14/28 | chr12 | 92817696 | ||||||
| chr12:92818295
|
A | G | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1728+1013T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 14/28 | chr12 | 92818295 | ||||||
| chr12:92818336
|
C | T | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1728+972G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 14/28 | chr12 | 92818336 | ||||||
| chr12:92818378
|
A | T | 7 | a0002c0004t0024g0046a0002c0004t0048g0017a0002c0008t0012g0014others(4): Show | 7 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1728+930T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 14/28 | chr12 | 92818378 | ||||||
| chr12:92818606
|
G | A | 13 | a0001c0002t0007g0048a0001c0002t0007g0116a0001c0002t0007g0117others(10): Show | 13 | HG00280.hp1 HG00642.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.1728+702C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 14/28 | chr12 | 92818606 | ||||||
| chr12:92818663
|
T | C | 1 | a0001c0002t0028g0190 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1728+645A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 14/28 | chr12 | 92818663 | ||||||
| chr12:92818707
|
T | C | 15 | a0001c0002t0006g0042a0001c0002t0006g0044a0001c0002t0006g0191others(12): Show | 15 | HG01109.hp2 HG01168.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1728+601A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 14/28 | chr12 | 92818707 | ||||||
| chr12:92819180
|
C | A | 1 | a0001c0002t0007g0126 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1728+128G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 14/28 | chr12 | 92819180 | ||||||
| chr12:92819704
|
T | C | 1 | a0001c0001t0013g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1525-193A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92819704 | ||||||
| chr12:92819734
|
C | T | 1 | a0002c0004t0029g0200 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1525-223G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92819734 | ||||||
| chr12:92819743
|
G | GT | 8 | a0002c0003t0002g0158a0002c0004t0010g0229a0002c0004t0010g0230others(5): Show | 8 | HG01192.hp1 HG02451.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1525-233dupA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92819743 | ||||||
| chr12:92819828
|
C | G | 1 | a0009c0013t0005g0064 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1525-317G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92819828 | ||||||
| chr12:92820235
|
C | T | 3 | a0002c0004t0014g0241a0002c0004t0014g0242a0002c0004t0014g0243 | 3 | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1525-724G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92820235 | ||||||
| chr12:92820291
|
C | A | 1 | a0001c0002t0003g0028 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1525-780G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92820291 | ||||||
| chr12:92820332
|
G | A | 1 | a0002c0003t0002g0159 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1525-821C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92820332 | ||||||
| chr12:92820389
|
C | T | 1 | a0001c0002t0006g0042 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1525-878G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92820389 | ||||||
| chr12:92820390
|
T | G | 236 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(233): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1525-879A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92820390 | ||||||
| chr12:92820590
|
T | G | 153 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(150): Show | 153 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1525-1079A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92820590 | ||||||
| chr12:92820593
|
T | C | 235 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(232): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1525-1082A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92820593 | ||||||
| chr12:92820594
|
G | A | 44 | a0002c0003t0002g0001a0002c0003t0002g0013a0002c0003t0002g0144others(41): Show | 45 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1525-1083C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92820594 | ||||||
| chr12:92820646
|
C | A | 1 | a0001c0002t0017g0114 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1525-1135G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92820646 | ||||||
| chr12:92820647
|
G | A | 1 | a0001c0002t0032g0045 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1525-1136C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92820647 | ||||||
| chr12:92820755
|
G | GTA | 8 | a0002c0004t0010g0234a0002c0004t0018g0202a0002c0004t0018g0210others(5): Show | 8 | HG02055.hp1 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1525-1246_1525-124 others(6): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92820755 | ||||||
| chr12:92820755
|
GTA | G | 199 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(196): Show | 200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.1525-1246_1525-124 others(6): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92820755 | ||||||
| chr12:92820755
|
GTATA | G | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525-1248_1525-124 others(8): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92820755 | ||||||
| chr12:92820774
|
T | C | 2 | a0001c0002t0019g0127a0001c0002t0019g0128 | 2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1525-1263A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92820774 | ||||||
| chr12:92820784
|
C | T | 23 | a0001c0002t0007g0048a0001c0002t0007g0116a0001c0002t0007g0117others(20): Show | 23 | HG00280.hp1 HG00642.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.1525-1273G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92820784 | ||||||
| chr12:92820872
|
C | T | 78 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(75): Show | 78 | HG00280.hp2 HG00741.hp1 HG01069.hp1 others(75): Show |
intron_variant | MODIFIER | c.1525-1361G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92820872 | ||||||
| chr12:92820942
|
T | A | 5 | a0002c0004t0018g0202a0002c0004t0018g0210a0002c0004t0018g0211others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525-1431A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92820942 | ||||||
| chr12:92820961
|
T | C | 51 | a0002c0003t0002g0001a0002c0003t0002g0013a0002c0003t0002g0144others(48): Show | 52 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1525-1450A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92820961 | ||||||
| chr12:92820978
|
G | A | 1 | a0001c0002t0007g0137 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1525-1467C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92820978 | ||||||
| chr12:92821270
|
A | T | 1 | a0001c0012t0006g0157 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1525-1759T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92821270 | ||||||
| chr12:92821392
|
T | C | 1 | a0002c0003t0004g0227 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1525-1881A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92821392 | ||||||
| chr12:92821632
|
T | C | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1525-2121A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92821632 | ||||||
| chr12:92821985
|
C | CAT | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.1525-2476_1525-247 others(6): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92821985 | ||||||
| chr12:92821993
|
T | C | 7 | a0002c0004t0024g0046a0002c0004t0048g0017a0002c0008t0012g0014others(4): Show | 7 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1525-2482A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92821993 | ||||||
| chr12:92822046
|
A | G | 5 | a0002c0004t0018g0202a0002c0004t0018g0210a0002c0004t0018g0211others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525-2535T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92822046 | ||||||
| chr12:92822090
|
T | C | 1 | a0001c0002t0035g0188 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1525-2579A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92822090 | ||||||
| chr12:92822196
|
C | G | 1 | a0002c0004t0031g0199 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1525-2685G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92822196 | ||||||
| chr12:92822411
|
T | C | 2 | a0003c0005t0003g0034a0003c0005t0003g0239 | 2 | HG00140.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.1525-2900A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92822411 | ||||||
| chr12:92822480
|
T | C | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.1525-2969A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92822480 | ||||||
| chr12:92822537
|
C | T | 52 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(49): Show | 53 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1525-3026G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92822537 | ||||||
| chr12:92822570
|
A | AC | 52 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(49): Show | 53 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1525-3060_1525-305 others(5): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92822570 | ||||||
| chr12:92822643
|
A | C | 236 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(233): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1525-3132T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92822643 | ||||||
| chr12:92822830
|
C | T | 1 | a0001c0001t0005g0185 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1525-3319G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92822830 | ||||||
| chr12:92823833
|
C | T | 1 | a0001c0002t0035g0188 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1524+2333G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92823833 | ||||||
| chr12:92823998
|
T | G | 6 | a0001c0002t0006g0192a0001c0002t0006g0195a0001c0002t0007g0193others(3): Show | 6 | HG01168.hp1 HG01257.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1524+2168A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92823998 | ||||||
| chr12:92824267
|
C | T | 6 | a0003c0005t0003g0021a0003c0005t0003g0031a0003c0005t0003g0032others(3): Show | 6 | HG02071.hp1 HG02129.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.1524+1899G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92824267 | ||||||
| chr12:92824497
|
T | C | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1524+1669A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92824497 | ||||||
| chr12:92824561
|
T | C | 3 | a0002c0003t0016g0141a0002c0003t0016g0142a0002c0003t0016g0143 | 3 | HG02818.hp1 HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1524+1605A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92824561 | ||||||
| chr12:92824625
|
T | C | 1 | a0001c0001t0001g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1524+1541A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92824625 | ||||||
| chr12:92824833
|
G | C | 1 | a0001c0001t0001g0079 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1524+1333C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92824833 | ||||||
| chr12:92825058
|
C | T | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1524+1108G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92825058 | ||||||
| chr12:92825218
|
G | A | 1 | a0002c0004t0048g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1524+948C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92825218 | ||||||
| chr12:92825308
|
G | A | 3 | a0002c0004t0014g0241a0002c0004t0014g0242a0002c0004t0014g0243 | 3 | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1524+858C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92825308 | ||||||
| chr12:92825385
|
C | T | 9 | a0001c0001t0001g0068a0001c0001t0001g0072a0001c0001t0001g0078others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1524+781G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92825385 | ||||||
| chr12:92825396
|
G | A | 1 | a0002c0017t0034g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1524+770C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92825396 | ||||||
| chr12:92825459
|
C | CA | 52 | a0001c0002t0035g0188a0001c0012t0006g0157a0002c0003t0002g0001others(49): Show | 53 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1524+706dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92825459 | ||||||
| chr12:92825506
|
C | T | 242 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(239): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1524+660G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92825506 | ||||||
| chr12:92825642
|
T | G | 219 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(216): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.1524+524A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92825642 | ||||||
| chr12:92825850
|
T | C | 2 | a0001c0001t0005g0085a0001c0001t0051g0107 | 2 | HG01496.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1524+316A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92825850 | ||||||
| chr12:92826008
|
G | A | 1 | a0001c0002t0007g0048 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1524+158C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92826008 | ||||||
| chr12:92826072
|
T | A | 1 | a0001c0001t0001g0063 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1524+94A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 13/28 | chr12 | 92826072 | ||||||
| chr12:92826326
|
T | G | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1405-41A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 12/28 | chr12 | 92826326 | ||||||
| chr12:92826337
|
T | C | 3 | a0001c0002t0026g0212a0001c0002t0027g0189a0001c0002t0028g0190 | 3 | HG02647.hp1 HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1405-52A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 12/28 | chr12 | 92826337 | ||||||
| chr12:92826464
|
C | A | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1405-179G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 12/28 | chr12 | 92826464 | ||||||
| chr12:92826479
|
A | G | 52 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(49): Show | 53 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1405-194T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 12/28 | chr12 | 92826479 | ||||||
| chr12:92826536
|
T | C | 3 | a0002c0003t0002g0148a0002c0003t0002g0163a0002c0003t0002g0173 | 3 | HG00140.hp2 HG03017.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1405-251A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 12/28 | chr12 | 92826536 | ||||||
| chr12:92826545
|
T | TA | 29 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(26): Show | 30 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.1405-261dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 12/28 | chr12 | 92826545 | ||||||
| chr12:92826560
|
C | A | 1 | a0001c0002t0044g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1405-275G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 12/28 | chr12 | 92826560 | ||||||
| chr12:92826589
|
C | T | 1 | a0006c0009t0001g0098 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1405-304G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 12/28 | chr12 | 92826589 | ||||||
| chr12:92826709
|
C | T | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.1405-424G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 12/28 | chr12 | 92826709 | ||||||
| chr12:92826714
|
C | CA | 13 | a0001c0001t0001g0056a0001c0001t0001g0108a0001c0001t0001g0134others(10): Show | 13 | HG01243.hp1 HG01261.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.1405-430dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 12/28 | chr12 | 92826714 | ||||||
| chr12:92826714
|
CA | C | 5 | a0001c0002t0003g0025a0003c0005t0003g0020a0003c0005t0003g0022others(2): Show | 5 | HG00140.hp1 HG00639.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.1405-430delT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 12/28 | chr12 | 92826714 | ||||||
| chr12:92826726
|
AAAAAAG | A | 44 | a0002c0003t0002g0001a0002c0003t0002g0013a0002c0003t0002g0144others(41): Show | 45 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1405-447_1405-442d others(8): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 12/28 | chr12 | 92826726 | ||||||
| chr12:92826807
|
G | T | 2 | a0001c0001t0001g0067a0001c0001t0001g0132 | 2 | HG01496.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1405-522C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 12/28 | chr12 | 92826807 | ||||||
| chr12:92826912
|
T | C | 1 | a0002c0003t0056g0178 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1405-627A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 12/28 | chr12 | 92826912 | ||||||
| chr12:92827121
|
C | T | 2 | a0002c0004t0011g0205a0002c0004t0011g0208 | 2 | HG01361.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1404+791G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 12/28 | chr12 | 92827121 | ||||||
| chr12:92827185
|
G | A | 25 | a0002c0003t0002g0001a0002c0003t0002g0013a0002c0003t0002g0144others(22): Show | 26 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.1404+727C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 12/28 | chr12 | 92827185 | ||||||
| chr12:92827202
|
T | C | 219 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(216): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.1404+710A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 12/28 | chr12 | 92827202 | ||||||
| chr12:92827286
|
G | A | 1 | a0001c0002t0019g0127 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1404+626C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 12/28 | chr12 | 92827286 | ||||||
| chr12:92827487
|
G | C | 72 | a0001c0002t0003g0023a0001c0002t0003g0024a0001c0002t0003g0025others(69): Show | 72 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1404+425C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 12/28 | chr12 | 92827487 | ||||||
| chr12:92827487
|
G | T | 79 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(76): Show | 79 | HG00280.hp2 HG00642.hp1 HG00741.hp1 others(76): Show |
intron_variant | MODIFIER | c.1404+425C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 12/28 | chr12 | 92827487 | ||||||
| chr12:92827762
|
T | G | 1 | a0001c0002t0007g0048 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1404+150A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 12/28 | chr12 | 92827762 | ||||||
| chr12:92827875
|
C | G | 1 | a0002c0004t0048g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1404+37G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 12/28 | chr12 | 92827875 | ||||||
| chr12:92828081
|
A | C | 1 | a0002c0004t0018g0202 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1255-20T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92828081 | ||||||
| chr12:92828176
|
C | T | 1 | a0002c0003t0002g0156 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1255-115G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92828176 | ||||||
| chr12:92828177
|
G | A | 1 | a0001c0002t0044g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1255-116C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92828177 | ||||||
| chr12:92828275
|
C | T | 1 | a0001c0002t0044g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1255-214G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92828275 | ||||||
| chr12:92828355
|
C | T | 242 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(239): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1255-294G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92828355 | ||||||
| chr12:92828493
|
C | T | 7 | a0002c0004t0024g0046a0002c0004t0048g0017a0002c0008t0012g0014others(4): Show | 7 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1255-432G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92828493 | ||||||
| chr12:92828586
|
T | C | 1 | a0002c0004t0024g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1255-525A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92828586 | ||||||
| chr12:92828619
|
C | CAT | 46 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(43): Show | 47 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.1255-560_1255-559d others(4): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92828619 | ||||||
| chr12:92828650
|
A | T | 1 | a0002c0004t0048g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1255-589T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92828650 | ||||||
| chr12:92828668
|
A | C | 2 | a0001c0002t0020g0122a0001c0002t0020g0123 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1255-607T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92828668 | ||||||
| chr12:92828747
|
A | C | 5 | a0002c0004t0018g0202a0002c0004t0018g0210a0002c0004t0018g0211others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1255-686T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92828747 | ||||||
| chr12:92828989
|
A | G | 1 | a0002c0017t0034g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1255-928T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92828989 | ||||||
| chr12:92829065
|
G | A | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1255-1004C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92829065 | ||||||
| chr12:92829211
|
G | A | 9 | a0001c0002t0009g0113a0001c0002t0009g0120a0001c0002t0009g0121others(6): Show | 9 | HG01256.hp2 HG01258.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.1255-1150C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92829211 | ||||||
| chr12:92829235
|
C | T | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.1255-1174G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92829235 | ||||||
| chr12:92829457
|
T | C | 2 | a0001c0002t0019g0127a0001c0002t0019g0128 | 2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1255-1396A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92829457 | ||||||
| chr12:92829590
|
G | A | 153 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(150): Show | 153 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1255-1529C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92829590 | ||||||
| chr12:92829778
|
T | TA | 14 | a0002c0003t0016g0141a0002c0003t0016g0142a0002c0003t0016g0143others(11): Show | 14 | HG00738.hp1 HG02723.hp1 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.1255-1718dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92829778 | ||||||
| chr12:92829778
|
TA | T | 16 | a0002c0004t0011g0205a0002c0004t0011g0206a0002c0004t0011g0207others(13): Show | 16 | HG00099.hp1 HG00741.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.1255-1718delT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92829778 | ||||||
| chr12:92829792
|
A | C | 24 | a0002c0003t0002g0001a0002c0003t0002g0013a0002c0003t0002g0144others(21): Show | 25 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.1255-1731T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92829792 | ||||||
| chr12:92829796
|
AC | A | 132 | a0001c0001t0001g0049a0001c0001t0001g0054a0001c0001t0001g0055others(129): Show | 132 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1255-1736delG | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92829796 | ||||||
| chr12:92829797
|
C | A | 72 | a0001c0001t0001g0063a0001c0001t0001g0082a0001c0001t0001g0106others(69): Show | 73 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.1255-1736G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92829797 | ||||||
| chr12:92829861
|
G | A | 3 | a0001c0001t0001g0065a0001c0001t0001g0088a0001c0001t0001g0111 | 3 | HG00741.hp1 HG02145.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1255-1800C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92829861 | ||||||
| chr12:92829893
|
A | T | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1255-1832T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92829893 | ||||||
| chr12:92830011
|
T | TG | 24 | a0001c0001t0001g0055a0001c0001t0001g0065a0001c0001t0001g0081others(21): Show | 24 | HG00642.hp2 HG01175.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.1255-1951dupC | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92830011 | ||||||
| chr12:92830011
|
TG | T | 51 | a0002c0003t0002g0001a0002c0003t0002g0013a0002c0003t0002g0144others(48): Show | 52 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1255-1951delC | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92830011 | ||||||
| chr12:92830383
|
T | C | 51 | a0002c0003t0002g0001a0002c0003t0002g0013a0002c0003t0002g0144others(48): Show | 52 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1254+2129A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92830383 | ||||||
| chr12:92830415
|
C | T | 5 | a0001c0001t0001g0090a0001c0001t0001g0095a0001c0001t0001g0099others(2): Show | 5 | HG00280.hp2 HG02074.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.1254+2097G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92830415 | ||||||
| chr12:92830483
|
T | C | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1254+2029A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92830483 | ||||||
| chr12:92830516
|
A | G | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1254+1996T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92830516 | ||||||
| chr12:92830523
|
T | A | 22 | a0001c0002t0007g0048a0001c0002t0007g0116a0001c0002t0007g0117others(19): Show | 22 | HG00280.hp1 HG01071.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.1254+1989A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92830523 | ||||||
| chr12:92830704
|
T | C | 79 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(76): Show | 79 | HG00280.hp2 HG00642.hp1 HG00741.hp1 others(76): Show |
intron_variant | MODIFIER | c.1254+1808A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92830704 | ||||||
| chr12:92830831
|
T | C | 1 | a0001c0002t0007g0137 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1254+1681A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92830831 | ||||||
| chr12:92830909
|
A | G | 236 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(233): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1254+1603T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92830909 | ||||||
| chr12:92830926
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1254+1586A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92830926 | ||||||
| chr12:92831048
|
A | G | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.1254+1464T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92831048 | ||||||
| chr12:92831059
|
A | G | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.1254+1453T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92831059 | ||||||
| chr12:92831239
|
C | T | 219 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(216): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.1254+1273G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92831239 | ||||||
| chr12:92831362
|
T | G | 1 | a0001c0001t0054g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1254+1150A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92831362 | ||||||
| chr12:92831368
|
C | A | 6 | a0001c0010t0006g0218a0001c0010t0006g0219a0001c0010t0006g0220others(3): Show | 6 | HG02109.hp1 HG02647.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1254+1144G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92831368 | ||||||
| chr12:92831493
|
TATATA | T | 3 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0094 | 3 | HG01081.hp1 HG02273.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1254+1014_1254+101 others(9): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92831493 | ||||||
| chr12:92831516
|
T | C | 1 | a0002c0003t0016g0141 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1254+996A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92831516 | ||||||
| chr12:92831587
|
A | AAATATAT others(23): Show |
4 | a0001c0002t0003g0037a0001c0002t0003g0040a0001c0002t0003g0041others(1): Show | 4 | HG02257.hp1 HG03209.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+895_1254+924d others(32): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92831587 | ||||||
| chr12:92831799
|
A | G | 5 | a0002c0004t0018g0202a0002c0004t0018g0210a0002c0004t0018g0211others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1254+713T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92831799 | ||||||
| chr12:92832004
|
G | A | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1254+508C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92832004 | ||||||
| chr12:92832014
|
G | A | 1 | a0002c0004t0048g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1254+498C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92832014 | ||||||
| chr12:92832019
|
G | C | 1 | a0002c0003t0004g0179 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1254+493C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92832019 | ||||||
| chr12:92832073
|
G | A | 1 | a0002c0003t0002g0173 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1254+439C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92832073 | ||||||
| chr12:92832087
|
C | T | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1254+425G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92832087 | ||||||
| chr12:92832093
|
C | CA | 16 | a0001c0001t0001g0105a0001c0001t0001g0134a0001c0001t0001g0135others(13): Show | 16 | HG01109.hp1 HG01109.hp2 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.1254+418dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92832093 | ||||||
| chr12:92832093
|
CA | C | 19 | a0001c0002t0007g0126a0001c0002t0007g0193a0001c0002t0020g0123others(16): Show | 19 | HG00738.hp1 HG01256.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1254+418delT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92832093 | ||||||
| chr12:92832237
|
C | T | 1 | a0006c0009t0001g0086 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1254+275G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92832237 | ||||||
| chr12:92832238
|
C | T | 1 | a0006c0009t0001g0086 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1254+274G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 11/28 | chr12 | 92832238 | ||||||
| chr12:92832890
|
T | C | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.916-40A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92832890 | ||||||
| chr12:92832945
|
T | C | 1 | a0001c0001t0053g0083 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.916-95A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92832945 | ||||||
| chr12:92832978
|
G | A | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.916-128C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92832978 | ||||||
| chr12:92833262
|
A | G | 5 | a0005c0007t0008g0003a0005c0007t0008g0005a0005c0007t0008g0008others(2): Show | 5 | NA18939.hp2 NA18964.hp1 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.916-412T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92833262 | ||||||
| chr12:92833338
|
C | G | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.916-488G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92833338 | ||||||
| chr12:92833527
|
A | G | 13 | a0001c0002t0003g0023a0001c0002t0003g0024a0001c0002t0003g0025others(10): Show | 13 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.916-677T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92833527 | ||||||
| chr12:92833532
|
G | A | 8 | a0001c0002t0009g0113a0001c0002t0009g0120a0001c0002t0009g0121others(5): Show | 8 | HG01256.hp2 HG01258.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.916-682C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92833532 | ||||||
| chr12:92833677
|
T | G | 4 | a0001c0002t0009g0120a0001c0002t0009g0121a0001c0002t0009g0129others(1): Show | 4 | HG03491.hp2 HG03492.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.916-827A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92833677 | ||||||
| chr12:92833714
|
C | T | 44 | a0002c0003t0002g0001a0002c0003t0002g0013a0002c0003t0002g0144others(41): Show | 45 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.916-864G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92833714 | ||||||
| chr12:92833899
|
A | C | 1 | a0001c0002t0003g0027 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.916-1049T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92833899 | ||||||
| chr12:92833950
|
A | C | 1 | a0004c0006t0021g0012 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.916-1100T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92833950 | ||||||
| chr12:92834284
|
C | G | 3 | a0001c0001t0001g0090a0001c0001t0001g0095a0001c0001t0001g0214 | 3 | HG00280.hp2 HG02074.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.916-1434G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92834284 | ||||||
| chr12:92834305
|
A | C | 8 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(5): Show | 8 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.916-1455T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92834305 | ||||||
| chr12:92834315
|
A | G | 5 | a0001c0001t0005g0182a0001c0001t0005g0183a0001c0001t0005g0184others(2): Show | 5 | HG01346.hp1 HG02602.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.916-1465T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92834315 | ||||||
| chr12:92834334
|
A | G | 1 | a0001c0001t0005g0077 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.916-1484T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92834334 | ||||||
| chr12:92834544
|
A | G | 219 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(216): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.916-1694T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92834544 | ||||||
| chr12:92834546
|
T | TA | 53 | a0001c0001t0001g0049a0001c0002t0003g0023a0001c0002t0003g0024others(50): Show | 53 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.916-1697dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92834546 | ||||||
| chr12:92834546
|
T | TAA | 130 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0055others(127): Show | 131 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.916-1698_916-1697d others(4): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92834546 | ||||||
| chr12:92834546
|
T | TAAA | 20 | a0001c0001t0001g0065a0001c0001t0001g0089a0001c0001t0001g0106others(17): Show | 20 | HG01175.hp1 HG01192.hp1 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.916-1699_916-1697d others(5): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92834546 | ||||||
| chr12:92834558
|
AAAAAAAA others(19): Show |
A | 1 | a0002c0003t0002g0173 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.916-1734_916-1709d others(28): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92834558 | ||||||
| chr12:92834578
|
A | G | 2 | a0002c0003t0002g0154a0002c0003t0002g0164 | 2 | HG03688.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.916-1728T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92834578 | ||||||
| chr12:92834600
|
C | G | 1 | a0001c0002t0028g0190 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.916-1750G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92834600 | ||||||
| chr12:92834603
|
A | C | 1 | a0001c0002t0003g0040 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.916-1753T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92834603 | ||||||
| chr12:92834643
|
G | A | 1 | a0004c0006t0021g0012 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.916-1793C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92834643 | ||||||
| chr12:92834723
|
T | C | 1 | a0002c0004t0048g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.916-1873A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92834723 | ||||||
| chr12:92834755
|
C | A | 2 | a0002c0003t0002g0154a0002c0003t0002g0164 | 2 | HG03688.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.916-1905G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92834755 | ||||||
| chr12:92834918
|
C | T | 25 | a0001c0002t0003g0023a0001c0002t0003g0024a0001c0002t0003g0025others(22): Show | 25 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.916-2068G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92834918 | ||||||
| chr12:92834940
|
C | T | 1 | a0002c0004t0048g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.916-2090G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92834940 | ||||||
| chr12:92835072
|
G | C | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.916-2222C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92835072 | ||||||
| chr12:92835090
|
C | T | 3 | a0002c0003t0016g0141a0002c0003t0016g0142a0002c0003t0016g0143 | 3 | HG02818.hp1 HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.916-2240G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92835090 | ||||||
| chr12:92835164
|
A | G | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.916-2314T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92835164 | ||||||
| chr12:92835326
|
T | A | 4 | a0001c0002t0003g0037a0001c0002t0003g0040a0001c0002t0003g0041others(1): Show | 4 | HG02257.hp1 HG03209.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.916-2476A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92835326 | ||||||
| chr12:92835400
|
C | CTTTTTTT | 7 | a0002c0003t0004g0151a0002c0003t0004g0152a0002c0003t0004g0167others(4): Show | 7 | HG00639.hp2 HG01884.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.916-2557_916-2551d others(9): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92835400 | ||||||
| chr12:92835400
|
C | CTTTTTTT others(1): Show |
7 | a0002c0003t0002g0173a0002c0003t0004g0165a0002c0003t0004g0166others(4): Show | 7 | HG00140.hp2 HG01167.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.916-2558_916-2551d others(10): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92835400 | ||||||
| chr12:92835400
|
C | CTTTTTTT others(2): Show |
18 | a0002c0003t0002g0145a0002c0003t0002g0146a0002c0003t0002g0149others(15): Show | 18 | HG01192.hp1 HG01256.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.916-2559_916-2551d others(11): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92835400 | ||||||
| chr12:92835400
|
C | CTTTTTTT others(3): Show |
8 | a0002c0003t0002g0013a0002c0003t0002g0144a0002c0003t0002g0148others(5): Show | 8 | HG00099.hp2 HG01106.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.916-2560_916-2551d others(12): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92835400 | ||||||
| chr12:92835400
|
C | CTTTTTTT others(8): Show |
1 | a0001c0012t0006g0157 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.916-2565_916-2551d others(17): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92835400 | ||||||
| chr12:92835400
|
CT | C | 10 | a0001c0002t0026g0212a0001c0002t0028g0190a0002c0004t0011g0205others(7): Show | 10 | HG00099.hp1 HG00741.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.916-2551delA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92835400 | ||||||
| chr12:92835400
|
CTT | C | 28 | a0001c0001t0001g0054a0001c0001t0001g0082a0001c0001t0001g0105others(25): Show | 28 | HG01081.hp1 HG01109.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.916-2552_916-2551d others(4): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92835400 | ||||||
| chr12:92835400
|
CTTT | C | 130 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0058others(127): Show | 130 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.916-2553_916-2551d others(5): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92835400 | ||||||
| chr12:92835400
|
CTTTT | C | 18 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0100others(15): Show | 18 | HG01069.hp2 HG01516.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.916-2554_916-2551d others(6): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92835400 | ||||||
| chr12:92835400
|
CTTTTTTT others(5): Show |
C | 1 | a0002c0003t0002g0001 | 2 | HG02015.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.916-2562_916-2551d others(14): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92835400 | ||||||
| chr12:92835450
|
C | T | 7 | a0002c0004t0024g0046a0002c0004t0048g0017a0002c0008t0012g0014others(4): Show | 7 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.916-2600G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92835450 | ||||||
| chr12:92835495
|
T | G | 1 | a0001c0002t0006g0191 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.916-2645A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92835495 | ||||||
| chr12:92835702
|
C | T | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.916-2852G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92835702 | ||||||
| chr12:92835821
|
T | C | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.916-2971A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92835821 | ||||||
| chr12:92835898
|
T | C | 3 | a0002c0004t0015g0198a0002c0004t0015g0203a0002c0004t0015g0213 | 3 | HG02622.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.916-3048A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92835898 | ||||||
| chr12:92836091
|
A | G | 1 | a0001c0002t0009g0133 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.916-3241T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92836091 | ||||||
| chr12:92836168
|
A | G | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.916-3318T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92836168 | ||||||
| chr12:92836173
|
G | A | 1 | a0002c0003t0004g0147 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.916-3323C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92836173 | ||||||
| chr12:92836413
|
T | C | 27 | a0001c0001t0001g0049a0001c0001t0001g0054a0001c0001t0001g0055others(24): Show | 27 | HG00741.hp1 HG01081.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.916-3563A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92836413 | ||||||
| chr12:92836500
|
A | C | 23 | a0001c0002t0003g0023a0001c0002t0003g0024a0001c0002t0003g0025others(20): Show | 23 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.916-3650T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92836500 | ||||||
| chr12:92836672
|
C | T | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.916-3822G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92836672 | ||||||
| chr12:92836938
|
T | C | 1 | a0001c0010t0006g0221 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.916-4088A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92836938 | ||||||
| chr12:92836995
|
C | T | 1 | a0002c0017t0034g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.916-4145G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92836995 | ||||||
| chr12:92837046
|
G | A | 1 | a0001c0002t0006g0192 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.916-4196C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92837046 | ||||||
| chr12:92837124
|
TA | T | 91 | a0001c0001t0001g0134a0001c0002t0003g0023a0001c0002t0003g0024others(88): Show | 92 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.916-4275delT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92837124 | ||||||
| chr12:92837124
|
TAA | T | 113 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(110): Show | 113 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(110): Show |
intron_variant | MODIFIER | c.916-4276_916-4275d others(4): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92837124 | ||||||
| chr12:92837137
|
A | C | 7 | a0002c0004t0024g0046a0002c0004t0048g0017a0002c0008t0012g0014others(4): Show | 7 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.916-4287T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92837137 | ||||||
| chr12:92837220
|
G | A | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.916-4370C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92837220 | ||||||
| chr12:92837291
|
G | A | 6 | a0001c0001t0001g0069a0001c0001t0001g0084a0001c0001t0001g0104others(3): Show | 6 | HG01106.hp1 HG01109.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.916-4441C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92837291 | ||||||
| chr12:92837404
|
G | A | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.916-4554C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92837404 | ||||||
| chr12:92837451
|
C | A | 1 | a0001c0001t0053g0083 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.916-4601G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92837451 | ||||||
| chr12:92837549
|
A | G | 1 | a0001c0001t0005g0053 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.916-4699T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92837549 | ||||||
| chr12:92838217
|
C | T | 7 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.915+4248G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92838217 | ||||||
| chr12:92838301
|
A | G | 2 | a0002c0003t0002g0177a0002c0003t0002g0180 | 2 | NA18967.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.915+4164T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92838301 | ||||||
| chr12:92838492
|
C | T | 2 | a0001c0002t0006g0044a0002c0004t0048g0017 | 2 | HG01109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.915+3973G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92838492 | ||||||
| chr12:92838553
|
C | A | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.915+3912G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92838553 | ||||||
| chr12:92838883
|
T | C | 24 | a0001c0002t0007g0048a0001c0002t0007g0116a0001c0002t0007g0117others(21): Show | 24 | HG00280.hp1 HG01071.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.915+3582A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92838883 | ||||||
| chr12:92838898
|
C | T | 1 | a0001c0002t0035g0188 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.915+3567G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92838898 | ||||||
| chr12:92838915
|
T | C | 7 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.915+3550A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92838915 | ||||||
| chr12:92838968
|
C | T | 1 | a0004c0006t0008g0006 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.915+3497G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92838968 | ||||||
| chr12:92839168
|
T | C | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.915+3297A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92839168 | ||||||
| chr12:92839201
|
C | T | 1 | a0002c0003t0055g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.915+3264G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92839201 | ||||||
| chr12:92839355
|
G | A | 6 | a0002c0004t0011g0205a0002c0004t0011g0206a0002c0004t0011g0207others(3): Show | 6 | HG00099.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.915+3110C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92839355 | ||||||
| chr12:92839357
|
C | A | 236 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(233): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.915+3108G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92839357 | ||||||
| chr12:92839397
|
A | G | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.915+3068T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92839397 | ||||||
| chr12:92839473
|
G | C | 7 | a0002c0004t0024g0046a0002c0004t0048g0017a0002c0008t0012g0014others(4): Show | 7 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.915+2992C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92839473 | ||||||
| chr12:92839589
|
T | C | 1 | a0001c0002t0046g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.915+2876A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92839589 | ||||||
| chr12:92839637
|
T | A | 1 | a0001c0010t0006g0221 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.915+2828A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92839637 | ||||||
| chr12:92839660
|
T | A | 1 | a0002c0017t0034g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.915+2805A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92839660 | ||||||
| chr12:92839734
|
A | G | 1 | a0001c0002t0017g0114 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.915+2731T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92839734 | ||||||
| chr12:92840159
|
C | A | 3 | a0002c0003t0016g0141a0002c0003t0016g0142a0002c0003t0016g0143 | 3 | HG02818.hp1 HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.915+2306G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92840159 | ||||||
| chr12:92840199
|
A | G | 6 | a0001c0001t0001g0069a0001c0001t0001g0084a0001c0001t0001g0104others(3): Show | 6 | HG01106.hp1 HG01109.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.915+2266T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92840199 | ||||||
| chr12:92840369
|
G | A | 10 | a0003c0005t0003g0020a0003c0005t0003g0021a0003c0005t0003g0022others(7): Show | 10 | HG00140.hp1 HG01167.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.915+2096C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92840369 | ||||||
| chr12:92840559
|
G | A | 1 | a0001c0001t0051g0107 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.915+1906C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92840559 | ||||||
| chr12:92840686
|
T | A | 3 | a0001c0001t0001g0068a0001c0001t0001g0072a0001c0001t0013g0092 | 3 | HG01069.hp1 HG01071.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.915+1779A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92840686 | ||||||
| chr12:92840687
|
C | G | 3 | a0001c0001t0001g0068a0001c0001t0001g0072a0001c0001t0013g0092 | 3 | HG01069.hp1 HG01071.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.915+1778G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92840687 | ||||||
| chr12:92840788
|
G | GA | 7 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.915+1676dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92840788 | ||||||
| chr12:92840803
|
A | G | 1 | a0002c0004t0031g0199 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.915+1662T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92840803 | ||||||
| chr12:92841029
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.915+1436A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92841029 | ||||||
| chr12:92841212
|
G | A | 1 | a0001c0002t0006g0042 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.915+1253C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92841212 | ||||||
| chr12:92841644
|
T | G | 1 | a0002c0004t0048g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.915+821A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92841644 | ||||||
| chr12:92841710
|
T | A | 22 | a0001c0002t0007g0048a0001c0002t0007g0116a0001c0002t0007g0117others(19): Show | 22 | HG00280.hp1 HG01071.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.915+755A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92841710 | ||||||
| chr12:92841817
|
G | T | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.915+648C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92841817 | ||||||
| chr12:92842285
|
A | G | 14 | a0001c0002t0006g0042a0001c0002t0006g0044a0001c0002t0006g0191others(11): Show | 14 | HG01109.hp2 HG01257.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.915+180T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92842285 | ||||||
| chr12:92842348
|
TA | T | 19 | a0001c0002t0006g0042a0001c0002t0006g0044a0001c0002t0006g0191others(16): Show | 19 | HG01109.hp2 HG01256.hp1 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.915+116delT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92842348 | ||||||
| chr12:92842361
|
TAA | T | 16 | a0002c0003t0004g0147a0002c0003t0004g0151a0002c0003t0004g0152others(13): Show | 16 | HG00639.hp2 HG01167.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.915+102_915+103del others(2): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92842361 | ||||||
| chr12:92842400
|
T | C | 4 | a0001c0002t0007g0117a0001c0002t0007g0118a0001c0002t0007g0119others(1): Show | 4 | HG01255.hp2 HG01346.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.915+65A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92842400 | ||||||
| chr12:92842420
|
T | A | 2 | a0002c0004t0011g0205a0002c0004t0011g0208 | 2 | HG01361.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.915+45A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 10/28 | chr12 | 92842420 | ||||||
| chr12:92842583
|
TAACAA | T | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.799-7_799-3delTTGT others(1): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92842583 | ||||||
| chr12:92842626
|
C | T | 229 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(226): Show | 230 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.799-45G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92842626 | ||||||
| chr12:92842643
|
T | G | 80 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(77): Show | 80 | HG00280.hp2 HG00642.hp1 HG00741.hp1 others(77): Show |
intron_variant | MODIFIER | c.799-62A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92842643 | ||||||
| chr12:92842750
|
C | T | 1 | a0002c0004t0031g0199 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.799-169G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92842750 | ||||||
| chr12:92842784
|
C | T | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.799-203G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92842784 | ||||||
| chr12:92843126
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0112 | 2 | HG01261.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.799-545G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92843126 | ||||||
| chr12:92843159
|
T | A | 3 | a0002c0003t0016g0141a0002c0003t0016g0142a0002c0003t0016g0143 | 3 | HG02818.hp1 HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.799-578A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92843159 | ||||||
| chr12:92843208
|
A | G | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.799-627T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92843208 | ||||||
| chr12:92843251
|
C | T | 2 | a0002c0003t0002g0153a0002c0003t0002g0159 | 2 | HG01175.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.799-670G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92843251 | ||||||
| chr12:92843311
|
A | G | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.799-730T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92843311 | ||||||
| chr12:92843357
|
C | T | 2 | a0002c0004t0011g0206a0002c0004t0011g0207 | 2 | HG00099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.799-776G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92843357 | ||||||
| chr12:92843433
|
G | A | 1 | a0001c0002t0007g0137 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.799-852C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92843433 | ||||||
| chr12:92843518
|
A | C | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.799-937T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92843518 | ||||||
| chr12:92843570
|
G | A | 7 | a0001c0002t0044g0139a0001c0010t0006g0218a0001c0010t0006g0219others(4): Show | 7 | HG01891.hp1 HG02109.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.799-989C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92843570 | ||||||
| chr12:92843614
|
T | C | 1 | a0001c0002t0007g0193 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.799-1033A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92843614 | ||||||
| chr12:92843692
|
G | A | 1 | a0001c0002t0006g0192 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.799-1111C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92843692 | ||||||
| chr12:92843803
|
AATACTT | A | 7 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.799-1228_799-1223d others(8): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92843803 | ||||||
| chr12:92843888
|
C | T | 1 | a0001c0001t0051g0107 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.799-1307G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92843888 | ||||||
| chr12:92843940
|
C | T | 1 | a0002c0004t0011g0205 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.799-1359G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92843940 | ||||||
| chr12:92844027
|
T | C | 1 | a0001c0002t0046g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.799-1446A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92844027 | ||||||
| chr12:92844031
|
G | A | 1 | a0002c0004t0024g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.799-1450C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92844031 | ||||||
| chr12:92844039
|
A | C | 235 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(232): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.799-1458T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92844039 | ||||||
| chr12:92844307
|
T | C | 13 | a0001c0002t0003g0023a0001c0002t0003g0024a0001c0002t0003g0025others(10): Show | 13 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.799-1726A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92844307 | ||||||
| chr12:92844801
|
G | A | 1 | a0004c0006t0022g0004 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.799-2220C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92844801 | ||||||
| chr12:92844912
|
A | G | 1 | a0001c0001t0001g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.799-2331T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92844912 | ||||||
| chr12:92845165
|
T | C | 1 | a0001c0002t0046g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.799-2584A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92845165 | ||||||
| chr12:92845186
|
T | C | 2 | a0004c0006t0008g0006a0004c0006t0022g0004 | 2 | HG00738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.799-2605A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92845186 | ||||||
| chr12:92845209
|
G | C | 1 | a0002c0003t0055g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.799-2628C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92845209 | ||||||
| chr12:92845397
|
G | A | 1 | a0002c0015t0001g0073 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.799-2816C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92845397 | ||||||
| chr12:92845430
|
A | T | 52 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(49): Show | 53 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.799-2849T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92845430 | ||||||
| chr12:92845484
|
CCTT | C | 3 | a0002c0003t0004g0151a0002c0003t0004g0152a0002c0003t0055g0150 | 3 | HG01884.hp1 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.799-2906_799-2904d others(5): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92845484 | ||||||
| chr12:92845629
|
A | G | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-3048T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92845629 | ||||||
| chr12:92845723
|
A | T | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.799-3142T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92845723 | ||||||
| chr12:92845739
|
C | T | 16 | a0002c0003t0004g0147a0002c0003t0004g0151a0002c0003t0004g0152others(13): Show | 16 | HG00639.hp2 HG01167.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.799-3158G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92845739 | ||||||
| chr12:92846357
|
C | T | 42 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(39): Show | 43 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.799-3776G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92846357 | ||||||
| chr12:92847001
|
G | A | 1 | a0002c0004t0014g0240 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.798+4110C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92847001 | ||||||
| chr12:92847158
|
G | T | 1 | a0001c0001t0001g0106 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.798+3953C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92847158 | ||||||
| chr12:92847295
|
T | G | 1 | a0002c0003t0004g0147 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.798+3816A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92847295 | ||||||
| chr12:92847319
|
T | C | 1 | a0002c0003t0004g0151 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.798+3792A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92847319 | ||||||
| chr12:92847590
|
T | C | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.798+3521A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92847590 | ||||||
| chr12:92848018
|
A | G | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.798+3093T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92848018 | ||||||
| chr12:92848174
|
A | G | 52 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(49): Show | 53 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.798+2937T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92848174 | ||||||
| chr12:92848231
|
G | GA | 14 | a0001c0002t0006g0042a0001c0002t0006g0044a0001c0002t0006g0191others(11): Show | 14 | HG01109.hp2 HG01257.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.798+2879dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92848231 | ||||||
| chr12:92848286
|
T | C | 1 | a0002c0003t0004g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.798+2825A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92848286 | ||||||
| chr12:92848323
|
T | G | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.798+2788A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92848323 | ||||||
| chr12:92848465
|
A | C | 1 | a0001c0002t0044g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.798+2646T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92848465 | ||||||
| chr12:92848722
|
C | CT | 51 | a0001c0002t0046g0217a0001c0010t0006g0221a0001c0012t0006g0157others(48): Show | 52 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.798+2388dupA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92848722 | ||||||
| chr12:92848722
|
C | CTT | 6 | a0001c0002t0044g0139a0002c0003t0002g0153a0002c0003t0002g0156others(3): Show | 6 | HG01175.hp2 HG01891.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.798+2387_798+2388d others(4): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92848722 | ||||||
| chr12:92848722
|
CT | C | 69 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0065others(66): Show | 69 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.798+2388delA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92848722 | ||||||
| chr12:92848722
|
CTT | C | 73 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(70): Show | 73 | HG00280.hp2 HG00741.hp1 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.798+2387_798+2388d others(4): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92848722 | ||||||
| chr12:92848722
|
CTTTTTTT others(3): Show |
C | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.798+2379_798+2388d others(12): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92848722 | ||||||
| chr12:92848751
|
G | A | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.798+2360C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92848751 | ||||||
| chr12:92848879
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.798+2232G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92848879 | ||||||
| chr12:92848889
|
C | T | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.798+2222G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92848889 | ||||||
| chr12:92849253
|
G | A | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.798+1858C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92849253 | ||||||
| chr12:92849262
|
T | G | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.798+1849A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92849262 | ||||||
| chr12:92849471
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.798+1640A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92849471 | ||||||
| chr12:92849554
|
T | A | 1 | a0001c0002t0003g0039 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.798+1557A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92849554 | ||||||
| chr12:92849692
|
C | G | 2 | a0002c0003t0004g0168a0002c0003t0004g0227 | 2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.798+1419G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92849692 | ||||||
| chr12:92849849
|
G | A | 22 | a0001c0002t0007g0048a0001c0002t0007g0116a0001c0002t0007g0117others(19): Show | 22 | HG00280.hp1 HG01071.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.798+1262C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92849849 | ||||||
| chr12:92849985
|
A | G | 1 | a0008c0014t0006g0204 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.798+1126T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92849985 | ||||||
| chr12:92849996
|
T | C | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+1115A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92849996 | ||||||
| chr12:92850055
|
C | G | 3 | a0002c0004t0015g0198a0002c0004t0015g0203a0002c0004t0015g0213 | 3 | HG02622.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.798+1056G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92850055 | ||||||
| chr12:92850332
|
C | T | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.798+779G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92850332 | ||||||
| chr12:92850337
|
C | G | 1 | a0002c0004t0048g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.798+774G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92850337 | ||||||
| chr12:92850501
|
C | G | 1 | a0001c0012t0006g0157 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.798+610G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92850501 | ||||||
| chr12:92850548
|
A | G | 52 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(49): Show | 53 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.798+563T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92850548 | ||||||
| chr12:92850625
|
T | G | 235 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(232): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.798+486A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92850625 | ||||||
| chr12:92850646
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.798+465G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92850646 | ||||||
| chr12:92850657
|
T | C | 3 | a0002c0004t0015g0198a0002c0004t0015g0203a0002c0004t0015g0213 | 3 | HG02622.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.798+454A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92850657 | ||||||
| chr12:92850669
|
G | A | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.798+442C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92850669 | ||||||
| chr12:92850689
|
C | CA | 45 | a0001c0002t0003g0023a0001c0002t0006g0044a0001c0002t0009g0133others(42): Show | 45 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.798+421dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92850689 | ||||||
| chr12:92850689
|
C | CAA | 11 | a0002c0003t0002g0001a0002c0003t0002g0153a0002c0003t0002g0159others(8): Show | 12 | HG01175.hp2 HG01884.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.798+420_798+421dup others(2): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92850689 | ||||||
| chr12:92850689
|
C | CAAA | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.798+419_798+421dup others(3): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92850689 | ||||||
| chr12:92850689
|
CA | C | 111 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(108): Show | 111 | HG00280.hp2 HG00642.hp1 HG00741.hp1 others(108): Show |
intron_variant | MODIFIER | c.798+421delT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92850689 | ||||||
| chr12:92850689
|
CAA | C | 16 | a0001c0001t0005g0061a0002c0004t0018g0202a0002c0004t0018g0211others(13): Show | 16 | HG00738.hp1 HG02257.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.798+420_798+421del others(2): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92850689 | ||||||
| chr12:92850808
|
T | A | 2 | a0002c0004t0011g0205a0002c0004t0011g0208 | 2 | HG01361.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.798+303A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92850808 | ||||||
| chr12:92851097
|
A | G | 4 | a0001c0001t0001g0047a0001c0001t0001g0102a0001c0001t0001g0103others(1): Show | 4 | HG02698.hp2 HG03491.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+14T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 9/28 | chr12 | 92851097 | ||||||
| chr12:92851396
|
T | C | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.643-130A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 8/28 | chr12 | 92851396 | ||||||
| chr12:92851606
|
G | A | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.643-340C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 8/28 | chr12 | 92851606 | ||||||
| chr12:92851700
|
A | G | 14 | a0001c0002t0006g0042a0001c0002t0006g0044a0001c0002t0006g0191others(11): Show | 14 | HG01109.hp2 HG01257.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.643-434T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 8/28 | chr12 | 92851700 | ||||||
| chr12:92852423
|
T | C | 1 | a0002c0003t0002g0148 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.521-127A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 7/28 | chr12 | 92852423 | ||||||
| chr12:92852594
|
C | A | 1 | a0001c0018t0017g0197 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.521-298G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 7/28 | chr12 | 92852594 | ||||||
| chr12:92852653
|
T | A | 1 | a0001c0002t0036g0140 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.520+259A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 7/28 | chr12 | 92852653 | ||||||
| chr12:92852658
|
C | T | 16 | a0002c0003t0004g0147a0002c0003t0004g0151a0002c0003t0004g0152others(13): Show | 16 | HG00639.hp2 HG01167.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.520+254G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 7/28 | chr12 | 92852658 | ||||||
| chr12:92853999
|
G | GATA | 151 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(148): Show | 151 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.367-48_367-46dupTA others(1): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 5/28 | chr12 | 92853999 | ||||||
| chr12:92854020
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.367-66T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 5/28 | chr12 | 92854020 | ||||||
| chr12:92854100
|
A | G | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.367-146T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 5/28 | chr12 | 92854100 | ||||||
| chr12:92854683
|
T | G | 52 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(49): Show | 53 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.367-729A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 5/28 | chr12 | 92854683 | ||||||
| chr12:92854954
|
T | C | 218 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(215): Show | 219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.367-1000A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 5/28 | chr12 | 92854954 | ||||||
| chr12:92855212
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.367-1258C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 5/28 | chr12 | 92855212 | ||||||
| chr12:92855354
|
T | C | 52 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(49): Show | 53 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.367-1400A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 5/28 | chr12 | 92855354 | ||||||
| chr12:92855385
|
G | A | 1 | a0001c0001t0005g0061 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.367-1431C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 5/28 | chr12 | 92855385 | ||||||
| chr12:92855385
|
G | C | 1 | a0001c0002t0007g0048 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.367-1431C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 5/28 | chr12 | 92855385 | ||||||
| chr12:92855431
|
C | CA | 44 | a0001c0001t0001g0065a0001c0001t0001g0067a0001c0002t0003g0023others(41): Show | 44 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.367-1478dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 5/28 | chr12 | 92855431 | ||||||
| chr12:92855431
|
C | CAA | 5 | a0001c0002t0035g0188a0001c0002t0038g0043a0001c0002t0047g0187others(2): Show | 5 | HG01243.hp2 HG02055.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.367-1479_367-1478d others(4): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 5/28 | chr12 | 92855431 | ||||||
| chr12:92855431
|
CA | C | 65 | a0001c0001t0001g0099a0001c0001t0001g0109a0001c0001t0051g0107others(62): Show | 66 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.367-1478delT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 5/28 | chr12 | 92855431 | ||||||
| chr12:92855618
|
T | C | 1 | a0002c0003t0004g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.366+1657A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 5/28 | chr12 | 92855618 | ||||||
| chr12:92855654
|
C | G | 7 | a0002c0004t0024g0046a0002c0004t0048g0017a0002c0008t0012g0014others(4): Show | 7 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.366+1621G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 5/28 | chr12 | 92855654 | ||||||
| chr12:92855755
|
T | C | 1 | a0002c0003t0002g0156 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.366+1520A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 5/28 | chr12 | 92855755 | ||||||
| chr12:92855868
|
T | C | 1 | a0001c0002t0032g0045 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.366+1407A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 5/28 | chr12 | 92855868 | ||||||
| chr12:92855886
|
C | T | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.366+1389G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 5/28 | chr12 | 92855886 | ||||||
| chr12:92856021
|
A | G | 6 | a0001c0010t0006g0218a0001c0010t0006g0219a0001c0010t0006g0220others(3): Show | 6 | HG02109.hp1 HG02647.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.366+1254T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 5/28 | chr12 | 92856021 | ||||||
| chr12:92856218
|
T | C | 1 | a0002c0004t0048g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.366+1057A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 5/28 | chr12 | 92856218 | ||||||
| chr12:92856245
|
G | A | 10 | a0003c0005t0003g0020a0003c0005t0003g0021a0003c0005t0003g0022others(7): Show | 10 | HG00140.hp1 HG01167.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.366+1030C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 5/28 | chr12 | 92856245 | ||||||
| chr12:92856334
|
C | A | 1 | a0002c0017t0034g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.366+941G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 5/28 | chr12 | 92856334 | ||||||
| chr12:92856439
|
T | C | 3 | a0001c0001t0001g0067a0001c0001t0001g0087a0001c0001t0001g0132 | 3 | HG01496.hp1 HG01978.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.366+836A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 5/28 | chr12 | 92856439 | ||||||
| chr12:92856693
|
C | A | 152 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(149): Show | 152 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.366+582G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 5/28 | chr12 | 92856693 | ||||||
| chr12:92856767
|
C | CT | 156 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(153): Show | 156 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(153): Show |
intron_variant | MODIFIER | c.366+507dupA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 5/28 | chr12 | 92856767 | ||||||
| chr12:92856767
|
C | CTT | 35 | a0001c0001t0001g0065a0001c0001t0001g0079a0001c0001t0001g0081others(32): Show | 35 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.366+506_366+507dup others(2): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 5/28 | chr12 | 92856767 | ||||||
| chr12:92856767
|
CTTTTTTT others(4): Show |
C | 3 | a0001c0002t0020g0122a0001c0002t0020g0123a0002c0003t0004g0168 | 3 | HG01256.hp2 HG01258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.366+497_366+507del others(11): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 5/28 | chr12 | 92856767 | ||||||
| chr12:92856922
|
G | C | 2 | a0003c0005t0003g0020a0003c0005t0003g0022 | 2 | HG01192.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.366+353C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 5/28 | chr12 | 92856922 | ||||||
| chr12:92857092
|
T | A | 52 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(49): Show | 53 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.366+183A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 5/28 | chr12 | 92857092 | ||||||
| chr12:92857120
|
A | T | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.366+155T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 5/28 | chr12 | 92857120 | ||||||
| chr12:92857174
|
A | G | 1 | a0001c0002t0038g0043 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.366+101T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 5/28 | chr12 | 92857174 | ||||||
| chr12:92857184
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.366+91C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 5/28 | chr12 | 92857184 | ||||||
| chr12:92857497
|
T | C | 3 | a0006c0009t0001g0096a0006c0009t0001g0097a0006c0009t0001g0098 | 3 | HG01099.hp1 HG02273.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.246-12A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92857497 | ||||||
| chr12:92857535
|
C | T | 13 | a0001c0002t0003g0023a0001c0002t0003g0024a0001c0002t0003g0025others(10): Show | 13 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.246-50G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92857535 | ||||||
| chr12:92857596
|
C | A | 25 | a0001c0002t0003g0023a0001c0002t0003g0024a0001c0002t0003g0025others(22): Show | 25 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.246-111G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92857596 | ||||||
| chr12:92857599
|
A | G | 1 | a0001c0002t0044g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.246-114T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92857599 | ||||||
| chr12:92857732
|
T | C | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.246-247A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92857732 | ||||||
| chr12:92857824
|
C | T | 5 | a0002c0004t0018g0202a0002c0004t0018g0210a0002c0004t0018g0211others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.246-339G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92857824 | ||||||
| chr12:92857949
|
T | C | 236 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(233): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.246-464A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92857949 | ||||||
| chr12:92857958
|
A | C | 52 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(49): Show | 53 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.246-473T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92857958 | ||||||
| chr12:92857959
|
T | C | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.246-474A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92857959 | ||||||
| chr12:92857974
|
T | C | 1 | a0001c0002t0007g0196 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.246-489A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92857974 | ||||||
| chr12:92857979
|
C | T | 1 | a0002c0003t0004g0174 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.246-494G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92857979 | ||||||
| chr12:92858127
|
C | A | 152 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(149): Show | 152 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.246-642G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92858127 | ||||||
| chr12:92858139
|
C | A | 1 | a0002c0004t0048g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.246-654G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92858139 | ||||||
| chr12:92858340
|
T | C | 1 | a0001c0001t0051g0107 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.246-855A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92858340 | ||||||
| chr12:92858412
|
A | T | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.246-927T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92858412 | ||||||
| chr12:92858450
|
G | A | 1 | a0001c0002t0009g0113 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.246-965C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92858450 | ||||||
| chr12:92858607
|
G | T | 204 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(201): Show | 205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.246-1122C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92858607 | ||||||
| chr12:92858715
|
G | T | 152 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(149): Show | 152 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.246-1230C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92858715 | ||||||
| chr12:92858724
|
C | T | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.246-1239G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92858724 | ||||||
| chr12:92858751
|
A | G | 151 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(148): Show | 151 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.246-1266T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92858751 | ||||||
| chr12:92858893
|
G | T | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.246-1408C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92858893 | ||||||
| chr12:92858912
|
G | A | 5 | a0002c0004t0018g0202a0002c0004t0018g0210a0002c0004t0018g0211others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.246-1427C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92858912 | ||||||
| chr12:92858941
|
A | G | 42 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(39): Show | 43 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.246-1456T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92858941 | ||||||
| chr12:92859058
|
T | C | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.246-1573A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92859058 | ||||||
| chr12:92859115
|
G | C | 79 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(76): Show | 79 | HG00280.hp2 HG00642.hp1 HG00741.hp1 others(76): Show |
intron_variant | MODIFIER | c.246-1630C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92859115 | ||||||
| chr12:92859516
|
G | A | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.246-2031C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92859516 | ||||||
| chr12:92859573
|
G | C | 1 | a0004c0006t0008g0006 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.246-2088C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92859573 | ||||||
| chr12:92859632
|
A | G | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.246-2147T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92859632 | ||||||
| chr12:92859651
|
G | A | 1 | a0002c0003t0004g0170 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.246-2166C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92859651 | ||||||
| chr12:92859696
|
G | A | 7 | a0002c0004t0024g0046a0002c0004t0048g0017a0002c0008t0012g0014others(4): Show | 7 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.246-2211C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92859696 | ||||||
| chr12:92859990
|
C | T | 2 | a0004c0006t0008g0002a0004c0006t0021g0012 | 2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.246-2505G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92859990 | ||||||
| chr12:92860267
|
T | G | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.246-2782A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92860267 | ||||||
| chr12:92860541
|
A | T | 2 | a0001c0002t0017g0114a0001c0002t0017g0115 | 2 | HG01071.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.246-3056T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92860541 | ||||||
| chr12:92860562
|
T | G | 1 | a0002c0004t0029g0200 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.246-3077A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92860562 | ||||||
| chr12:92860662
|
G | A | 1 | a0002c0003t0004g0166 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.246-3177C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92860662 | ||||||
| chr12:92860692
|
G | A | 1 | a0001c0002t0046g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.246-3207C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92860692 | ||||||
| chr12:92860883
|
T | TA | 6 | a0002c0004t0048g0017a0002c0008t0012g0014a0002c0008t0012g0015others(3): Show | 6 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.246-3399dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92860883 | ||||||
| chr12:92860910
|
A | AGAG | 52 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(49): Show | 53 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.246-3428_246-3426d others(5): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92860910 | ||||||
| chr12:92860978
|
C | A | 1 | a0002c0003t0002g0162 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.246-3493G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92860978 | ||||||
| chr12:92861213
|
T | G | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.245+3647A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92861213 | ||||||
| chr12:92861312
|
G | A | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.245+3548C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92861312 | ||||||
| chr12:92861337
|
C | G | 42 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(39): Show | 43 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.245+3523G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92861337 | ||||||
| chr12:92861380
|
A | T | 1 | a0001c0001t0001g0082 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.245+3480T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92861380 | ||||||
| chr12:92861395
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.245+3465G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92861395 | ||||||
| chr12:92861521
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.245+3339G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92861521 | ||||||
| chr12:92861534
|
A | C | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.245+3326T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92861534 | ||||||
| chr12:92861606
|
T | C | 3 | a0001c0002t0039g0215a0001c0002t0040g0223a0001c0002t0046g0217 | 3 | HG02630.hp1 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.245+3254A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92861606 | ||||||
| chr12:92861698
|
CAG | C | 6 | a0001c0010t0006g0218a0001c0010t0006g0219a0001c0010t0006g0220others(3): Show | 6 | HG02109.hp1 HG02647.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.245+3160_245+3161d others(4): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92861698 | ||||||
| chr12:92861714
|
A | G | 1 | a0001c0002t0044g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.245+3146T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92861714 | ||||||
| chr12:92861832
|
C | T | 7 | a0002c0004t0024g0046a0002c0004t0048g0017a0002c0008t0012g0014others(4): Show | 7 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.245+3028G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92861832 | ||||||
| chr12:92861833
|
G | A | 9 | a0001c0002t0039g0215a0001c0002t0040g0223a0001c0002t0046g0217others(6): Show | 9 | HG02109.hp1 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.245+3027C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92861833 | ||||||
| chr12:92861881
|
G | A | 1 | a0002c0004t0048g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.245+2979C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92861881 | ||||||
| chr12:92861988
|
G | A | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.245+2872C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92861988 | ||||||
| chr12:92862187
|
G | A | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.245+2673C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92862187 | ||||||
| chr12:92862233
|
C | CTA | 236 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(233): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.245+2626_245+2627i others(4): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92862233 | ||||||
| chr12:92862364
|
G | C | 1 | a0001c0002t0044g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.245+2496C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92862364 | ||||||
| chr12:92862365
|
G | A | 5 | a0001c0002t0007g0117a0001c0002t0007g0118a0001c0002t0007g0119others(2): Show | 5 | HG01255.hp2 HG01346.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.245+2495C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92862365 | ||||||
| chr12:92862382
|
G | A | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.245+2478C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92862382 | ||||||
| chr12:92862587
|
A | G | 2 | a0001c0001t0001g0078a0001c0001t0001g0081 | 2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.245+2273T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92862587 | ||||||
| chr12:92862656
|
T | C | 1 | a0002c0017t0034g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.245+2204A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92862656 | ||||||
| chr12:92862742
|
T | C | 1 | a0002c0003t0004g0167 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.245+2118A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92862742 | ||||||
| chr12:92862930
|
C | T | 2 | a0001c0002t0039g0215a0001c0002t0040g0223 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.245+1930G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92862930 | ||||||
| chr12:92863253
|
A | T | 16 | a0002c0003t0004g0147a0002c0003t0004g0151a0002c0003t0004g0152others(13): Show | 16 | HG00639.hp2 HG01167.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.245+1607T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92863253 | ||||||
| chr12:92863418
|
T | G | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.245+1442A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92863418 | ||||||
| chr12:92863603
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.245+1257A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92863603 | ||||||
| chr12:92863612
|
T | C | 1 | a0001c0002t0044g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.245+1248A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92863612 | ||||||
| chr12:92863674
|
A | T | 1 | a0001c0001t0001g0105 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.245+1186T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92863674 | ||||||
| chr12:92863826
|
G | C | 1 | a0001c0002t0044g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.245+1034C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92863826 | ||||||
| chr12:92864022
|
A | C | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.245+838T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92864022 | ||||||
| chr12:92864133
|
A | T | 235 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(232): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.245+727T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92864133 | ||||||
| chr12:92864349
|
C | T | 236 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(233): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.245+511G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92864349 | ||||||
| chr12:92864363
|
T | G | 26 | a0001c0002t0003g0023a0001c0002t0003g0024a0001c0002t0003g0025others(23): Show | 26 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.245+497A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92864363 | ||||||
| chr12:92864631
|
C | T | 1 | a0005c0007t0008g0003 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.245+229G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92864631 | ||||||
| chr12:92864654
|
C | T | 2 | a0001c0002t0019g0127a0001c0002t0019g0128 | 2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.245+206G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92864654 | ||||||
| chr12:92864663
|
C | G | 52 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(49): Show | 53 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.245+197G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92864663 | ||||||
| chr12:92864677
|
T | C | 151 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(148): Show | 151 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.245+183A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92864677 | ||||||
| chr12:92864722
|
A | G | 79 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(76): Show | 79 | HG00280.hp2 HG00642.hp1 HG00741.hp1 others(76): Show |
intron_variant | MODIFIER | c.245+138T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92864722 | ||||||
| chr12:92864842
|
A | C | 1 | a0007c0016t0025g0019 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.245+18T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92864842 | ||||||
| chr12:92864856
|
G | A | 5 | a0002c0004t0018g0202a0002c0004t0018g0210a0002c0004t0018g0211others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02451.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.245+4C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 3/28 | chr12 | 92864856 | ||||||
| chr12:92865032
|
T | C | 26 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(23): Show | 27 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.118-45A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92865032 | ||||||
| chr12:92865093
|
C | A | 1 | a0001c0002t0007g0116 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.118-106G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92865093 | ||||||
| chr12:92865205
|
C | A | 3 | a0002c0003t0016g0141a0002c0003t0016g0142a0002c0003t0016g0143 | 3 | HG02818.hp1 HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.118-218G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92865205 | ||||||
| chr12:92865224
|
C | T | 2 | a0001c0002t0020g0122a0001c0002t0020g0123 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.118-237G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92865224 | ||||||
| chr12:92865339
|
AAAT | A | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.118-355_118-353del others(3): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92865339 | ||||||
| chr12:92865378
|
GA | G | 10 | a0001c0002t0039g0215a0001c0002t0040g0223a0001c0002t0046g0217others(7): Show | 10 | HG02109.hp1 HG02630.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.118-392delT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92865378 | ||||||
| chr12:92865500
|
A | G | 226 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(223): Show | 227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.118-513T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92865500 | ||||||
| chr12:92865612
|
G | A | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.118-625C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92865612 | ||||||
| chr12:92865714
|
T | TTTTTA | 7 | a0001c0001t0001g0076a0001c0001t0001g0091a0001c0001t0005g0052others(4): Show | 7 | HG01071.hp2 HG01934.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-732_118-728dup others(5): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92865714 | ||||||
| chr12:92865714
|
T | TTTTTATT others(3): Show |
1 | a0001c0002t0007g0131 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.118-737_118-728dup others(10): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92865714 | ||||||
| chr12:92865714
|
TTTTTA | T | 81 | a0001c0001t0001g0056a0001c0001t0001g0066a0001c0001t0001g0074others(78): Show | 81 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.118-732_118-728del others(5): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92865714 | ||||||
| chr12:92865714
|
TTTTTATT others(3): Show |
T | 15 | a0001c0001t0013g0138a0001c0002t0003g0039a0002c0004t0031g0199others(12): Show | 15 | HG00738.hp1 HG01168.hp2 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.118-737_118-728del others(10): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92865714 | ||||||
| chr12:92865714
|
TTTTTATT others(8): Show |
T | 46 | a0001c0001t0001g0081a0001c0012t0006g0157a0002c0003t0002g0001others(43): Show | 47 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.118-742_118-728del others(15): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92865714 | ||||||
| chr12:92865903
|
A | G | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.118-916T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92865903 | ||||||
| chr12:92865958
|
C | T | 152 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(149): Show | 152 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.118-971G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92865958 | ||||||
| chr12:92865961
|
G | C | 1 | a0002c0004t0031g0199 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.118-974C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92865961 | ||||||
| chr12:92866029
|
A | G | 14 | a0001c0002t0006g0042a0001c0002t0006g0044a0001c0002t0006g0191others(11): Show | 14 | HG01109.hp2 HG01257.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.118-1042T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92866029 | ||||||
| chr12:92866087
|
G | A | 1 | a0001c0002t0044g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.118-1100C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92866087 | ||||||
| chr12:92866191
|
CA | C | 91 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(88): Show | 91 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(88): Show |
intron_variant | MODIFIER | c.118-1205delT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92866191 | ||||||
| chr12:92866191
|
CAA | C | 139 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0074others(136): Show | 140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.118-1206_118-1205d others(4): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92866191 | ||||||
| chr12:92866402
|
T | C | 1 | a0003c0005t0003g0022 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.118-1415A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92866402 | ||||||
| chr12:92866536
|
T | TA | 41 | a0001c0001t0001g0108a0001c0001t0001g0112a0001c0002t0003g0023others(38): Show | 41 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.118-1550dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92866536 | ||||||
| chr12:92866537
|
A | T | 43 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(40): Show | 44 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.118-1550T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92866537 | ||||||
| chr12:92866577
|
C | T | 3 | a0002c0004t0014g0241a0002c0004t0014g0242a0002c0004t0014g0243 | 3 | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.118-1590G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92866577 | ||||||
| chr12:92866643
|
A | G | 1 | a0003c0005t0003g0022 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.118-1656T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92866643 | ||||||
| chr12:92866816
|
C | T | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.118-1829G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92866816 | ||||||
| chr12:92867001
|
A | G | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.118-2014T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92867001 | ||||||
| chr12:92867062
|
CCAGAGGA others(12): Show |
C | 23 | a0001c0002t0003g0023a0001c0002t0003g0024a0001c0002t0003g0025others(20): Show | 23 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.118-2094_118-2076d others(21): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92867062 | ||||||
| chr12:92867082
|
C | T | 52 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(49): Show | 53 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.118-2095G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92867082 | ||||||
| chr12:92867406
|
T | C | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.118-2419A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92867406 | ||||||
| chr12:92867468
|
A | G | 1 | a0001c0001t0053g0083 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.118-2481T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92867468 | ||||||
| chr12:92867774
|
A | G | 1 | a0003c0005t0003g0021 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.118-2787T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92867774 | ||||||
| chr12:92867865
|
TGA | T | 219 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(216): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.118-2880_118-2879d others(4): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92867865 | ||||||
| chr12:92867903
|
C | T | 3 | a0001c0002t0039g0215a0001c0002t0040g0223a0001c0002t0046g0217 | 3 | HG02630.hp1 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.118-2916G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92867903 | ||||||
| chr12:92868070
|
A | T | 3 | a0001c0002t0039g0215a0001c0002t0040g0223a0001c0002t0046g0217 | 3 | HG02630.hp1 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.118-3083T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92868070 | ||||||
| chr12:92868140
|
C | T | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.118-3153G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92868140 | ||||||
| chr12:92868178
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.118-3191C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92868178 | ||||||
| chr12:92868256
|
C | T | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.118-3269G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92868256 | ||||||
| chr12:92868274
|
T | A | 16 | a0002c0003t0004g0147a0002c0003t0004g0151a0002c0003t0004g0152others(13): Show | 16 | HG00639.hp2 HG01167.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.118-3287A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92868274 | ||||||
| chr12:92868443
|
A | T | 2 | a0002c0003t0002g0177a0002c0003t0002g0180 | 2 | NA18967.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.118-3456T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92868443 | ||||||
| chr12:92868446
|
C | T | 3 | a0002c0004t0015g0198a0002c0004t0015g0203a0002c0004t0015g0213 | 3 | HG02622.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.118-3459G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92868446 | ||||||
| chr12:92868641
|
A | G | 3 | a0002c0004t0015g0198a0002c0004t0015g0203a0002c0004t0015g0213 | 3 | HG02622.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.118-3654T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92868641 | ||||||
| chr12:92868725
|
T | C | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-3738A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92868725 | ||||||
| chr12:92868822
|
CT | C | 22 | a0001c0002t0007g0048a0001c0002t0007g0116a0001c0002t0007g0117others(19): Show | 22 | HG00280.hp1 HG01071.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.118-3836delA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92868822 | ||||||
| chr12:92868841
|
A | C | 2 | a0001c0001t0001g0088a0001c0001t0001g0111 | 2 | HG00741.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.118-3854T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92868841 | ||||||
| chr12:92868842
|
T | A | 79 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(76): Show | 79 | HG00280.hp2 HG00642.hp1 HG00741.hp1 others(76): Show |
intron_variant | MODIFIER | c.118-3855A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92868842 | ||||||
| chr12:92868934
|
C | T | 1 | a0001c0001t0023g0051 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.118-3947G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92868934 | ||||||
| chr12:92869005
|
T | TA | 152 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(149): Show | 152 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.118-4019dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92869005 | ||||||
| chr12:92869097
|
T | C | 7 | a0002c0004t0024g0046a0002c0004t0048g0017a0002c0008t0012g0014others(4): Show | 7 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-4110A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92869097 | ||||||
| chr12:92869214
|
A | C | 1 | a0002c0004t0031g0199 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.118-4227T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92869214 | ||||||
| chr12:92869437
|
C | T | 3 | a0002c0004t0018g0210a0002c0004t0018g0211a0008c0014t0006g0204 | 3 | HG02055.hp1 HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.118-4450G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92869437 | ||||||
| chr12:92869752
|
C | CA | 24 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0058others(21): Show | 25 | HG01081.hp1 HG01261.hp2 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.118-4766dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92869752 | ||||||
| chr12:92869752
|
C | CAA | 27 | a0001c0001t0001g0056a0001c0001t0001g0063a0001c0001t0001g0088others(24): Show | 27 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.118-4767_118-4766d others(4): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92869752 | ||||||
| chr12:92869752
|
C | CAAA | 22 | a0001c0001t0001g0065a0001c0001t0001g0111a0001c0001t0005g0053others(19): Show | 22 | HG00639.hp2 HG00741.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.118-4768_118-4766d others(5): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92869752 | ||||||
| chr12:92869752
|
C | CAAAA | 7 | a0001c0001t0005g0052a0002c0003t0002g0145a0002c0003t0002g0160others(4): Show | 7 | HG01257.hp1 HG01891.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.118-4769_118-4766d others(6): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92869752 | ||||||
| chr12:92869752
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0023g0051 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.118-4778_118-4766d others(15): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92869752 | ||||||
| chr12:92869752
|
C | CAAAAAAA others(15): Show |
1 | a0002c0003t0002g0149 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.118-4787_118-4766d others(24): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92869752 | ||||||
| chr12:92869752
|
CA | C | 25 | a0001c0001t0001g0069a0001c0001t0001g0078a0001c0001t0001g0081others(22): Show | 25 | HG00280.hp2 HG00738.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.118-4766delT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92869752 | ||||||
| chr12:92869752
|
CAA | C | 26 | a0001c0001t0001g0047a0001c0001t0001g0091a0001c0001t0001g0105others(23): Show | 26 | HG00639.hp1 HG00642.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.118-4767_118-4766d others(4): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92869752 | ||||||
| chr12:92869752
|
CAAA | C | 45 | a0001c0001t0001g0108a0001c0001t0001g0112a0001c0001t0005g0181others(42): Show | 45 | HG01071.hp2 HG01081.hp2 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.118-4768_118-4766d others(5): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92869752 | ||||||
| chr12:92869752
|
CAAAA | C | 24 | a0001c0002t0003g0029a0001c0002t0003g0030a0001c0002t0003g0037others(21): Show | 24 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.118-4769_118-4766d others(6): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92869752 | ||||||
| chr12:92869752
|
CAAAAA | C | 5 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(2): Show | 5 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.118-4770_118-4766d others(7): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92869752 | ||||||
| chr12:92869752
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0074 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.118-4775_118-4766d others(12): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92869752 | ||||||
| chr12:92869752
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0076 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.118-4776_118-4766d others(13): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92869752 | ||||||
| chr12:92869752
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0060 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.118-4778_118-4766d others(15): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92869752 | ||||||
| chr12:92869752
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0050g0062 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.118-4779_118-4766d others(16): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92869752 | ||||||
| chr12:92869752
|
CAAAAAAA others(10): Show |
C | 3 | a0001c0001t0001g0079a0001c0001t0052g0080a0001c0002t0007g0137 | 3 | HG01255.hp1 HG01975.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.118-4782_118-4766d others(19): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92869752 | ||||||
| chr12:92869752
|
CAAAAAAA others(12): Show |
C | 6 | a0001c0001t0001g0068a0001c0001t0001g0072a0001c0001t0013g0070others(3): Show | 6 | HG01069.hp1 HG01071.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.118-4784_118-4766d others(21): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92869752 | ||||||
| chr12:92869752
|
CAAAAAAA others(16): Show |
C | 1 | a0001c0002t0003g0023 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.118-4788_118-4766d others(25): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92869752 | ||||||
| chr12:92870080
|
C | T | 7 | a0002c0004t0024g0046a0002c0004t0048g0017a0002c0008t0012g0014others(4): Show | 7 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-5093G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92870080 | ||||||
| chr12:92870441
|
C | T | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.118-5454G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92870441 | ||||||
| chr12:92870615
|
A | G | 7 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-5628T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92870615 | ||||||
| chr12:92870989
|
G | A | 1 | a0001c0018t0017g0197 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.118-6002C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92870989 | ||||||
| chr12:92871114
|
T | C | 1 | a0002c0003t0002g0149 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.118-6127A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92871114 | ||||||
| chr12:92871154
|
A | G | 2 | a0001c0002t0019g0127a0001c0002t0019g0128 | 2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.118-6167T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92871154 | ||||||
| chr12:92871237
|
C | T | 1 | a0001c0002t0003g0023 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.118-6250G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92871237 | ||||||
| chr12:92871287
|
A | G | 1 | a0001c0001t0005g0181 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.118-6300T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92871287 | ||||||
| chr12:92871303
|
A | G | 152 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(149): Show | 152 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.118-6316T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92871303 | ||||||
| chr12:92871460
|
G | A | 152 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(149): Show | 152 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.118-6473C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92871460 | ||||||
| chr12:92871833
|
A | G | 1 | a0002c0003t0004g0152 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.118-6846T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92871833 | ||||||
| chr12:92871944
|
C | A | 2 | a0003c0005t0003g0020a0003c0005t0003g0022 | 2 | HG01192.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.118-6957G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92871944 | ||||||
| chr12:92872043
|
G | A | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.118-7056C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92872043 | ||||||
| chr12:92872047
|
A | AT | 103 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(100): Show | 103 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.118-7061dupA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92872047 | ||||||
| chr12:92872047
|
A | ATT | 7 | a0001c0001t0001g0065a0001c0001t0001g0082a0001c0001t0001g0111others(4): Show | 7 | HG00280.hp2 HG00741.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.118-7062_118-7061d others(4): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92872047 | ||||||
| chr12:92872111
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.118-7124G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92872111 | ||||||
| chr12:92872217
|
T | A | 1 | a0001c0002t0003g0041 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.118-7230A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92872217 | ||||||
| chr12:92872523
|
C | T | 14 | a0001c0002t0006g0042a0001c0002t0006g0044a0001c0002t0006g0191others(11): Show | 14 | HG01109.hp2 HG01257.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.118-7536G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92872523 | ||||||
| chr12:92872580
|
T | A | 24 | a0001c0002t0003g0023a0001c0002t0003g0024a0001c0002t0003g0025others(21): Show | 24 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.118-7593A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92872580 | ||||||
| chr12:92872626
|
T | A | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.118-7639A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92872626 | ||||||
| chr12:92872662
|
A | C | 1 | a0002c0003t0002g0001 | 2 | HG02015.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.118-7675T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92872662 | ||||||
| chr12:92872751
|
G | C | 1 | a0002c0004t0018g0202 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.118-7764C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92872751 | ||||||
| chr12:92872824
|
G | A | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.118-7837C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92872824 | ||||||
| chr12:92872883
|
G | T | 1 | a0004c0006t0021g0012 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.118-7896C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92872883 | ||||||
| chr12:92872988
|
A | T | 1 | a0002c0017t0034g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.118-8001T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92872988 | ||||||
| chr12:92873081
|
T | C | 2 | a0002c0003t0004g0165a0002c0003t0004g0166 | 2 | HG01167.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.118-8094A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92873081 | ||||||
| chr12:92873287
|
A | C | 11 | a0001c0002t0039g0215a0001c0002t0040g0223a0001c0002t0046g0217others(8): Show | 11 | HG02109.hp1 HG02630.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.118-8300T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92873287 | ||||||
| chr12:92873397
|
G | A | 46 | a0001c0002t0035g0188a0001c0012t0006g0157a0002c0003t0002g0001others(43): Show | 47 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.118-8410C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92873397 | ||||||
| chr12:92873462
|
T | C | 14 | a0001c0002t0006g0042a0001c0002t0006g0044a0001c0002t0006g0191others(11): Show | 14 | HG01109.hp2 HG01257.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.118-8475A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92873462 | ||||||
| chr12:92873622
|
G | A | 151 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(148): Show | 151 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.118-8635C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92873622 | ||||||
| chr12:92873727
|
T | C | 6 | a0003c0005t0003g0021a0003c0005t0003g0031a0003c0005t0003g0032others(3): Show | 6 | HG02071.hp1 HG02129.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.118-8740A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92873727 | ||||||
| chr12:92874093
|
G | A | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.118-9106C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92874093 | ||||||
| chr12:92874105
|
G | C | 21 | a0001c0002t0007g0048a0001c0002t0007g0116a0001c0002t0007g0117others(18): Show | 21 | HG00280.hp1 HG01071.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.118-9118C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92874105 | ||||||
| chr12:92874168
|
A | AC | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.118-9182_118-9181i others(3): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92874168 | ||||||
| chr12:92874213
|
T | C | 1 | a0002c0003t0004g0226 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.118-9226A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92874213 | ||||||
| chr12:92874424
|
G | A | 1 | a0001c0002t0007g0116 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.118-9437C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92874424 | ||||||
| chr12:92874679
|
C | G | 1 | a0001c0001t0013g0138 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.118-9692G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92874679 | ||||||
| chr12:92874820
|
A | G | 26 | a0001c0001t0001g0047a0001c0001t0001g0069a0001c0001t0001g0084others(23): Show | 26 | HG00280.hp2 HG01099.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.118-9833T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92874820 | ||||||
| chr12:92874972
|
T | A | 46 | a0001c0002t0035g0188a0001c0012t0006g0157a0002c0003t0002g0001others(43): Show | 47 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.118-9985A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92874972 | ||||||
| chr12:92874993
|
A | T | 1 | a0002c0003t0002g0148 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.118-10006T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92874993 | ||||||
| chr12:92874999
|
T | C | 46 | a0001c0002t0035g0188a0001c0012t0006g0157a0002c0003t0002g0001others(43): Show | 47 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.118-10012A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92874999 | ||||||
| chr12:92875113
|
C | T | 1 | a0002c0004t0011g0206 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.118-10126G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92875113 | ||||||
| chr12:92875122
|
G | A | 1 | a0002c0004t0031g0199 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.118-10135C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92875122 | ||||||
| chr12:92875123
|
A | T | 1 | a0002c0004t0031g0199 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.118-10136T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92875123 | ||||||
| chr12:92875250
|
G | A | 46 | a0001c0002t0035g0188a0001c0012t0006g0157a0002c0003t0002g0001others(43): Show | 47 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.118-10263C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92875250 | ||||||
| chr12:92875259
|
G | A | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.118-10272C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92875259 | ||||||
| chr12:92875351
|
T | G | 53 | a0001c0002t0035g0188a0001c0012t0006g0157a0002c0003t0002g0001others(50): Show | 54 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.118-10364A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92875351 | ||||||
| chr12:92875432
|
T | C | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-10445A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92875432 | ||||||
| chr12:92875461
|
C | T | 8 | a0001c0002t0007g0137a0002c0004t0024g0046a0002c0004t0048g0017others(5): Show | 8 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-10474G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92875461 | ||||||
| chr12:92875786
|
C | A | 46 | a0001c0002t0035g0188a0001c0012t0006g0157a0002c0003t0002g0001others(43): Show | 47 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.118-10799G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92875786 | ||||||
| chr12:92875804
|
C | G | 219 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(216): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.118-10817G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92875804 | ||||||
| chr12:92875837
|
A | G | 236 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(233): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.118-10850T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92875837 | ||||||
| chr12:92876042
|
A | C | 1 | a0002c0003t0004g0226 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.118-11055T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92876042 | ||||||
| chr12:92876147
|
C | G | 1 | a0004c0006t0008g0007 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.118-11160G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92876147 | ||||||
| chr12:92876275
|
C | G | 2 | a0001c0002t0019g0127a0001c0002t0019g0128 | 2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.118-11288G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92876275 | ||||||
| chr12:92876313
|
A | T | 219 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(216): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.118-11326T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92876313 | ||||||
| chr12:92876544
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.118-11557G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92876544 | ||||||
| chr12:92876663
|
C | T | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-11676G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92876663 | ||||||
| chr12:92876830
|
C | CA | 54 | a0001c0001t0001g0056a0001c0002t0009g0129a0001c0002t0035g0188others(51): Show | 55 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.118-11844dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92876830 | ||||||
| chr12:92876830
|
CA | C | 8 | a0001c0002t0006g0191a0001c0002t0009g0120a0001c0002t0036g0140others(5): Show | 8 | HG02258.hp2 HG03491.hp2 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-11844delT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92876830 | ||||||
| chr12:92876943
|
G | GT | 49 | a0001c0001t0001g0111a0001c0002t0007g0048a0001c0002t0009g0129others(46): Show | 50 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.118-11957dupA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92876943 | ||||||
| chr12:92876950
|
T | G | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-11963A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92876950 | ||||||
| chr12:92876952
|
T | G | 1 | a0002c0017t0034g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.118-11965A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92876952 | ||||||
| chr12:92877009
|
A | G | 53 | a0001c0002t0035g0188a0001c0012t0006g0157a0002c0003t0002g0001others(50): Show | 54 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.118-12022T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92877009 | ||||||
| chr12:92877030
|
G | A | 1 | a0002c0003t0004g0174 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.118-12043C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92877030 | ||||||
| chr12:92877104
|
C | T | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-12117G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92877104 | ||||||
| chr12:92877113
|
TTTTTTTC | T | 4 | a0002c0008t0012g0014a0002c0008t0012g0236a0002c0008t0012g0237others(1): Show | 4 | HG01243.hp2 HG02109.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-12133_118-1212 others(11): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92877113 | ||||||
| chr12:92877134
|
C | CT | 5 | a0001c0001t0001g0082a0002c0003t0002g0001a0002c0003t0002g0177others(2): Show | 6 | HG02015.hp2 HG02083.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.118-12148dupA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92877134 | ||||||
| chr12:92877222
|
G | A | 7 | a0002c0004t0048g0017a0003c0005t0003g0021a0003c0005t0003g0031others(4): Show | 7 | HG02071.hp1 HG02129.hp1 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-12235C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92877222 | ||||||
| chr12:92877413
|
G | A | 150 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(147): Show | 150 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.118-12426C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92877413 | ||||||
| chr12:92877525
|
A | G | 1 | a0001c0002t0035g0188 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.118-12538T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92877525 | ||||||
| chr12:92877534
|
A | AT | 23 | a0001c0001t0001g0068a0001c0001t0001g0072a0001c0001t0013g0070others(20): Show | 23 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.118-12548dupA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92877534 | ||||||
| chr12:92877904
|
G | A | 1 | a0002c0017t0034g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.118-12917C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92877904 | ||||||
| chr12:92878044
|
G | C | 1 | a0001c0002t0035g0188 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.118-13057C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92878044 | ||||||
| chr12:92878107
|
A | G | 46 | a0001c0002t0035g0188a0001c0012t0006g0157a0002c0003t0002g0001others(43): Show | 47 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.118-13120T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92878107 | ||||||
| chr12:92878210
|
G | A | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.118-13223C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92878210 | ||||||
| chr12:92878231
|
C | T | 2 | a0002c0003t0002g0145a0002c0003t0002g0146 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.118-13244G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92878231 | ||||||
| chr12:92878458
|
C | G | 2 | a0001c0002t0019g0127a0001c0002t0019g0128 | 2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.117+13171G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92878458 | ||||||
| chr12:92878612
|
T | G | 1 | a0001c0001t0001g0076 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.117+13017A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92878612 | ||||||
| chr12:92878631
|
T | G | 7 | a0002c0004t0024g0046a0002c0004t0048g0017a0002c0008t0012g0014others(4): Show | 7 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+12998A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92878631 | ||||||
| chr12:92878705
|
A | C | 1 | a0001c0002t0006g0191 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.117+12924T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92878705 | ||||||
| chr12:92878923
|
G | A | 1 | a0002c0004t0011g0206 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.117+12706C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92878923 | ||||||
| chr12:92878981
|
A | T | 10 | a0004c0006t0008g0002a0004c0006t0008g0007a0004c0006t0008g0011others(7): Show | 10 | HG02723.hp1 HG03041.hp1 HG03688.hp2 others(7): Show |
intron_variant | MODIFIER | c.117+12648T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92878981 | ||||||
| chr12:92879099
|
C | A | 2 | a0003c0005t0003g0034a0003c0005t0003g0239 | 2 | HG00140.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.117+12530G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92879099 | ||||||
| chr12:92879201
|
A | AT | 26 | a0001c0002t0003g0024a0001c0002t0007g0048a0001c0002t0007g0116others(23): Show | 26 | HG00280.hp1 HG01071.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.117+12427dupA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92879201 | ||||||
| chr12:92879201
|
A | ATT | 123 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0055others(120): Show | 123 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(120): Show |
intron_variant | MODIFIER | c.117+12426_117+1242 others(6): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92879201 | ||||||
| chr12:92879201
|
A | ATTT | 8 | a0001c0001t0001g0049a0001c0001t0001g0059a0001c0001t0001g0106others(5): Show | 8 | HG00639.hp1 HG02055.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+12425_117+1242 others(7): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92879201 | ||||||
| chr12:92879250
|
T | G | 1 | a0001c0001t0001g0069 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.117+12379A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92879250 | ||||||
| chr12:92879283
|
G | A | 1 | a0002c0003t0002g0160 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.117+12346C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92879283 | ||||||
| chr12:92879476
|
T | C | 1 | a0002c0015t0001g0073 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.117+12153A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92879476 | ||||||
| chr12:92879568
|
G | A | 7 | a0002c0004t0024g0046a0002c0004t0048g0017a0002c0008t0012g0014others(4): Show | 7 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+12061C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92879568 | ||||||
| chr12:92879625
|
GA | G | 7 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+12003delT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92879625 | ||||||
| chr12:92879774
|
G | A | 1 | a0001c0002t0007g0048 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.117+11855C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92879774 | ||||||
| chr12:92879785
|
A | G | 1 | a0002c0003t0002g0013 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.117+11844T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92879785 | ||||||
| chr12:92880225
|
C | T | 22 | a0001c0002t0007g0048a0001c0002t0007g0116a0001c0002t0007g0117others(19): Show | 22 | HG00280.hp1 HG01071.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.117+11404G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92880225 | ||||||
| chr12:92880341
|
G | A | 2 | a0002c0003t0002g0144a0002c0003t0002g0161 | 2 | HG00099.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.117+11288C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92880341 | ||||||
| chr12:92880385
|
G | T | 1 | a0003c0005t0042g0038 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.117+11244C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92880385 | ||||||
| chr12:92880418
|
C | T | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.117+11211G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92880418 | ||||||
| chr12:92880447
|
C | T | 3 | a0002c0003t0016g0141a0002c0003t0016g0142a0002c0003t0016g0143 | 3 | HG02818.hp1 HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.117+11182G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92880447 | ||||||
| chr12:92880477
|
T | G | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+11152A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92880477 | ||||||
| chr12:92880495
|
G | T | 2 | a0001c0001t0001g0056a0001c0001t0001g0066 | 2 | HG01243.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.117+11134C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92880495 | ||||||
| chr12:92880661
|
G | C | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.117+10968C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92880661 | ||||||
| chr12:92880964
|
G | C | 3 | a0001c0002t0026g0212a0001c0002t0027g0189a0001c0002t0028g0190 | 3 | HG02647.hp1 HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.117+10665C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92880964 | ||||||
| chr12:92881084
|
C | T | 151 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(148): Show | 151 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.117+10545G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92881084 | ||||||
| chr12:92881174
|
C | T | 1 | a0001c0002t0007g0193 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.117+10455G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92881174 | ||||||
| chr12:92881550
|
C | A | 1 | a0001c0002t0035g0188 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.117+10079G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92881550 | ||||||
| chr12:92881733
|
G | C | 1 | a0001c0001t0051g0107 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.117+9896C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92881733 | ||||||
| chr12:92881917
|
C | T | 24 | a0001c0002t0003g0023a0001c0002t0003g0024a0001c0002t0003g0025others(21): Show | 24 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.117+9712G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92881917 | ||||||
| chr12:92882238
|
G | A | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+9391C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92882238 | ||||||
| chr12:92882421
|
T | C | 111 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(108): Show | 111 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(108): Show |
intron_variant | MODIFIER | c.117+9208A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92882421 | ||||||
| chr12:92882631
|
C | T | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+8998G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92882631 | ||||||
| chr12:92882733
|
C | G | 226 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(223): Show | 227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.117+8896G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92882733 | ||||||
| chr12:92883034
|
G | A | 236 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(233): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.117+8595C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92883034 | ||||||
| chr12:92883105
|
T | C | 1 | a0002c0003t0002g0149 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.117+8524A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92883105 | ||||||
| chr12:92883276
|
T | A | 46 | a0001c0002t0035g0188a0001c0012t0006g0157a0002c0003t0002g0001others(43): Show | 47 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.117+8353A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92883276 | ||||||
| chr12:92883330
|
C | T | 6 | a0001c0010t0006g0218a0001c0010t0006g0219a0001c0010t0006g0220others(3): Show | 6 | HG02109.hp1 HG02647.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.117+8299G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92883330 | ||||||
| chr12:92883643
|
TTAA | T | 151 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(148): Show | 151 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.117+7983_117+7985d others(5): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92883643 | ||||||
| chr12:92883699
|
T | G | 1 | a0001c0002t0036g0140 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.117+7930A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92883699 | ||||||
| chr12:92883814
|
G | A | 2 | a0002c0003t0002g0153a0002c0003t0002g0159 | 2 | HG01175.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.117+7815C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92883814 | ||||||
| chr12:92884013
|
T | C | 1 | a0001c0002t0044g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.117+7616A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92884013 | ||||||
| chr12:92884099
|
T | C | 7 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+7530A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92884099 | ||||||
| chr12:92884242
|
C | G | 1 | a0001c0002t0009g0124 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.117+7387G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92884242 | ||||||
| chr12:92884247
|
A | G | 7 | a0002c0004t0024g0046a0002c0004t0048g0017a0002c0008t0012g0014others(4): Show | 7 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+7382T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92884247 | ||||||
| chr12:92884284
|
C | T | 150 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(147): Show | 150 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.117+7345G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92884284 | ||||||
| chr12:92884385
|
G | A | 1 | a0002c0004t0024g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.117+7244C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92884385 | ||||||
| chr12:92884522
|
A | G | 33 | a0001c0002t0003g0023a0001c0002t0003g0024a0001c0002t0003g0025others(30): Show | 33 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.117+7107T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92884522 | ||||||
| chr12:92884537
|
T | G | 7 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+7092A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92884537 | ||||||
| chr12:92884543
|
A | C | 2 | a0001c0002t0019g0127a0001c0002t0019g0128 | 2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.117+7086T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92884543 | ||||||
| chr12:92884647
|
A | G | 151 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(148): Show | 151 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.117+6982T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92884647 | ||||||
| chr12:92884660
|
G | T | 7 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+6969C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92884660 | ||||||
| chr12:92884812
|
T | C | 1 | a0001c0002t0046g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.117+6817A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92884812 | ||||||
| chr12:92884960
|
A | AT | 69 | a0001c0001t0013g0138a0001c0002t0019g0127a0001c0002t0019g0128others(66): Show | 70 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.117+6668dupA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92884960 | ||||||
| chr12:92884960
|
A | ATT | 119 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(116): Show | 119 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(116): Show |
intron_variant | MODIFIER | c.117+6667_117+6668d others(4): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92884960 | ||||||
| chr12:92884960
|
A | ATTT | 28 | a0001c0001t0001g0104a0001c0001t0005g0052a0001c0001t0005g0053others(25): Show | 28 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.117+6666_117+6668d others(5): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92884960 | ||||||
| chr12:92884960
|
AT | A | 10 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(7): Show | 10 | HG02451.hp1 HG02622.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.117+6668delA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92884960 | ||||||
| chr12:92885037
|
T | C | 1 | a0002c0003t0004g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.117+6592A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92885037 | ||||||
| chr12:92885061
|
C | T | 1 | a0004c0006t0022g0004 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.117+6568G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92885061 | ||||||
| chr12:92885151
|
T | C | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.117+6478A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92885151 | ||||||
| chr12:92885538
|
T | C | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+6091A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92885538 | ||||||
| chr12:92885545
|
G | A | 1 | a0002c0003t0004g0226 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.117+6084C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92885545 | ||||||
| chr12:92885649
|
C | T | 1 | a0002c0017t0034g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.117+5980G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92885649 | ||||||
| chr12:92885663
|
T | C | 5 | a0002c0004t0018g0202a0002c0004t0018g0210a0002c0004t0018g0211others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+5966A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92885663 | ||||||
| chr12:92885913
|
C | T | 6 | a0001c0001t0001g0069a0001c0001t0001g0084a0001c0001t0001g0104others(3): Show | 6 | HG01106.hp1 HG01109.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.117+5716G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92885913 | ||||||
| chr12:92886074
|
C | T | 1 | a0002c0004t0048g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.117+5555G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92886074 | ||||||
| chr12:92886109
|
C | T | 142 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(139): Show | 142 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.117+5520G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92886109 | ||||||
| chr12:92886120
|
G | A | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.117+5509C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92886120 | ||||||
| chr12:92886192
|
T | G | 5 | a0002c0004t0018g0202a0002c0004t0018g0210a0002c0004t0018g0211others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+5437A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92886192 | ||||||
| chr12:92886194
|
G | GA | 6 | a0001c0001t0001g0081a0001c0001t0001g0132a0001c0001t0001g0135others(3): Show | 6 | HG01109.hp1 HG01978.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.117+5434dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92886194 | ||||||
| chr12:92886194
|
GA | G | 42 | a0001c0001t0001g0058a0001c0002t0003g0023a0001c0002t0003g0024others(39): Show | 42 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.117+5434delT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92886194 | ||||||
| chr12:92886229
|
T | C | 152 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(149): Show | 152 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.117+5400A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92886229 | ||||||
| chr12:92886443
|
C | CG | 240 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(237): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.117+5185dupC | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92886443 | ||||||
| chr12:92886443
|
C | CGGCCAGG others(86): Show |
2 | a0002c0003t0002g0177a0002c0003t0002g0180 | 2 | NA18967.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.117+5185_117+5186i others(95): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92886443 | ||||||
| chr12:92886557
|
GGAAGGGA others(7): Show |
G | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.117+5058_117+5071d others(16): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92886557 | ||||||
| chr12:92886560
|
AGGGAGGG others(12): Show |
A | 5 | a0002c0004t0018g0202a0002c0004t0018g0210a0002c0004t0018g0211others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+5050_117+5068d others(21): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92886560 | ||||||
| chr12:92886598
|
A | G | 1 | a0002c0017t0034g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.117+5031T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92886598 | ||||||
| chr12:92886630
|
G | A | 1 | a0002c0003t0004g0167 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.117+4999C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92886630 | ||||||
| chr12:92886749
|
A | C | 1 | a0001c0001t0005g0085 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.117+4880T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92886749 | ||||||
| chr12:92886770
|
G | A | 2 | a0001c0002t0003g0029a0001c0002t0003g0030 | 2 | HG00642.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.117+4859C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92886770 | ||||||
| chr12:92886891
|
G | T | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+4738C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92886891 | ||||||
| chr12:92886923
|
G | C | 154 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(151): Show | 154 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.117+4706C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92886923 | ||||||
| chr12:92886986
|
G | A | 6 | a0001c0001t0001g0069a0001c0001t0001g0084a0001c0001t0001g0104others(3): Show | 6 | HG01106.hp1 HG01109.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.117+4643C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92886986 | ||||||
| chr12:92886998
|
C | CAAA | 153 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(150): Show | 153 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.117+4630_117+4631i others(5): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92886998 | ||||||
| chr12:92887035
|
G | GA | 222 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(219): Show | 223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.117+4593dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92887035 | ||||||
| chr12:92887045
|
A | G | 2 | a0001c0002t0019g0127a0001c0002t0019g0128 | 2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.117+4584T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92887045 | ||||||
| chr12:92887047
|
G | A | 2 | a0001c0002t0019g0127a0001c0002t0019g0128 | 2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.117+4582C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92887047 | ||||||
| chr12:92887118
|
T | C | 235 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(232): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.117+4511A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92887118 | ||||||
| chr12:92887145
|
A | G | 6 | a0003c0005t0003g0021a0003c0005t0003g0031a0003c0005t0003g0032others(3): Show | 6 | HG02071.hp1 HG02129.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.117+4484T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92887145 | ||||||
| chr12:92887295
|
G | C | 219 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(216): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.117+4334C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92887295 | ||||||
| chr12:92887345
|
AT | A | 236 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(233): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.117+4283delA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92887345 | ||||||
| chr12:92887366
|
G | A | 1 | a0002c0004t0048g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.117+4263C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92887366 | ||||||
| chr12:92887511
|
A | G | 27 | a0001c0002t0003g0023a0001c0002t0003g0024a0001c0002t0003g0025others(24): Show | 27 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.117+4118T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92887511 | ||||||
| chr12:92887619
|
G | T | 1 | a0002c0004t0024g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.117+4010C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92887619 | ||||||
| chr12:92887660
|
T | TA | 7 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+3968dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92887660 | ||||||
| chr12:92887798
|
A | G | 219 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(216): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.117+3831T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92887798 | ||||||
| chr12:92887852
|
A | T | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.117+3777T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92887852 | ||||||
| chr12:92887917
|
AG | A | 7 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+3711delC | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92887917 | ||||||
| chr12:92888155
|
G | A | 1 | a0001c0002t0044g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.117+3474C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92888155 | ||||||
| chr12:92888316
|
T | C | 236 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(233): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.117+3313A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92888316 | ||||||
| chr12:92888347
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.117+3282C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92888347 | ||||||
| chr12:92888349
|
A | G | 235 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(232): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.117+3280T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92888349 | ||||||
| chr12:92888446
|
G | A | 1 | a0001c0001t0005g0052 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.117+3183C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92888446 | ||||||
| chr12:92888453
|
T | C | 1 | a0002c0008t0012g0015 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.117+3176A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92888453 | ||||||
| chr12:92888556
|
G | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0081 | 2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.117+3073C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92888556 | ||||||
| chr12:92888579
|
AAAAC | A | 8 | a0001c0002t0039g0215a0001c0002t0040g0223a0001c0002t0046g0217others(5): Show | 8 | HG02109.hp1 HG02630.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.117+3046_117+3049d others(6): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92888579 | ||||||
| chr12:92888591
|
C | A | 3 | a0001c0001t0001g0078a0001c0001t0001g0081a0006c0009t0001g0097 | 3 | HG02559.hp2 NA18977.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.117+3038G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92888591 | ||||||
| chr12:92888594
|
AC | A | 21 | a0001c0001t0005g0053a0001c0002t0007g0048a0001c0002t0007g0118others(18): Show | 21 | HG01071.hp2 HG01099.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.117+3034delG | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92888594 | ||||||
| chr12:92888595
|
C | A | 83 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0056others(80): Show | 83 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.117+3034G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92888595 | ||||||
| chr12:92888617
|
C | T | 1 | a0001c0002t0032g0045 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.117+3012G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92888617 | ||||||
| chr12:92888645
|
A | G | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.117+2984T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92888645 | ||||||
| chr12:92888750
|
A | C | 235 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(232): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.117+2879T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92888750 | ||||||
| chr12:92888808
|
G | A | 9 | a0001c0002t0009g0113a0001c0002t0009g0120a0001c0002t0009g0121others(6): Show | 9 | HG01256.hp2 HG01258.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.117+2821C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92888808 | ||||||
| chr12:92888910
|
G | C | 1 | a0003c0005t0003g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.117+2719C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92888910 | ||||||
| chr12:92888925
|
G | A | 7 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+2704C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92888925 | ||||||
| chr12:92889005
|
C | T | 2 | a0002c0003t0004g0175a0002c0003t0004g0176 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.117+2624G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92889005 | ||||||
| chr12:92889156
|
T | TA | 14 | a0001c0001t0001g0135a0002c0003t0004g0175a0002c0003t0004g0176others(11): Show | 14 | HG01109.hp1 HG02451.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.117+2472dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92889156 | ||||||
| chr12:92889530
|
C | CA | 9 | a0001c0002t0026g0212a0001c0010t0006g0218a0001c0010t0006g0219others(6): Show | 9 | HG02109.hp1 HG02280.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.117+2098dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92889530 | ||||||
| chr12:92889595
|
C | T | 1 | a0002c0003t0056g0178 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.117+2034G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92889595 | ||||||
| chr12:92889621
|
G | A | 1 | a0002c0017t0034g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.117+2008C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92889621 | ||||||
| chr12:92889673
|
C | A | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+1956G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92889673 | ||||||
| chr12:92889862
|
C | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | NA18747.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.117+1767G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92889862 | ||||||
| chr12:92890115
|
A | C | 1 | a0001c0002t0047g0187 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.117+1514T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92890115 | ||||||
| chr12:92890393
|
T | C | 152 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(149): Show | 152 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.117+1236A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92890393 | ||||||
| chr12:92890409
|
C | A | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+1220G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92890409 | ||||||
| chr12:92890477
|
G | C | 1 | a0001c0002t0009g0113 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.117+1152C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92890477 | ||||||
| chr12:92890584
|
A | G | 1 | a0001c0001t0001g0058 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.117+1045T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92890584 | ||||||
| chr12:92890784
|
C | T | 1 | a0001c0002t0044g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.117+845G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92890784 | ||||||
| chr12:92890855
|
C | T | 1 | a0002c0003t0055g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.117+774G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92890855 | ||||||
| chr12:92890867
|
C | T | 2 | a0001c0002t0019g0127a0001c0002t0019g0128 | 2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.117+762G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92890867 | ||||||
| chr12:92890868
|
G | A | 1 | a0002c0003t0002g0177 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.117+761C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92890868 | ||||||
| chr12:92891116
|
A | G | 1 | a0001c0002t0006g0044 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.117+513T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92891116 | ||||||
| chr12:92891187
|
A | ATTTATAT others(13): Show |
4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+422_117+441dup others(20): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92891187 | ||||||
| chr12:92891306
|
C | T | 163 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(160): Show | 163 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.117+323G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 2/28 | chr12 | 92891306 | ||||||
| chr12:92891846
|
C | T | 1 | a0002c0004t0048g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.25-125G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92891846 | ||||||
| chr12:92891941
|
T | C | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.25-220A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92891941 | ||||||
| chr12:92892308
|
T | C | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.25-587A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92892308 | ||||||
| chr12:92892438
|
T | C | 5 | a0001c0001t0005g0182a0001c0001t0005g0183a0001c0001t0005g0184others(2): Show | 5 | HG01346.hp1 HG02602.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.25-717A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92892438 | ||||||
| chr12:92892500
|
G | C | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.25-779C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92892500 | ||||||
| chr12:92892557
|
C | CT | 10 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(7): Show | 10 | HG02451.hp1 HG02622.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.25-837dupA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92892557 | ||||||
| chr12:92892557
|
CT | C | 204 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(201): Show | 205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.25-837delA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92892557 | ||||||
| chr12:92892583
|
GCTCTGTC others(16): Show |
G | 42 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(39): Show | 43 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.25-885_25-863delTG others(21): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92892583 | ||||||
| chr12:92892629
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.25-908A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92892629 | ||||||
| chr12:92892776
|
C | A | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.25-1055G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92892776 | ||||||
| chr12:92892860
|
C | T | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.25-1139G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92892860 | ||||||
| chr12:92892871
|
C | A | 3 | a0002c0003t0016g0141a0002c0003t0016g0142a0002c0003t0016g0143 | 3 | HG02818.hp1 HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.25-1150G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92892871 | ||||||
| chr12:92892872
|
C | G | 44 | a0002c0003t0002g0001a0002c0003t0002g0013a0002c0003t0002g0144others(41): Show | 45 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.25-1151G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92892872 | ||||||
| chr12:92892873
|
C | G | 1 | a0001c0012t0006g0157 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.25-1152G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92892873 | ||||||
| chr12:92893565
|
A | G | 1 | a0001c0002t0009g0113 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.25-1844T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92893565 | ||||||
| chr12:92893678
|
C | T | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.25-1957G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92893678 | ||||||
| chr12:92894305
|
A | G | 1 | a0001c0002t0044g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.25-2584T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92894305 | ||||||
| chr12:92894431
|
T | C | 53 | a0001c0002t0035g0188a0001c0012t0006g0157a0002c0003t0002g0001others(50): Show | 54 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.25-2710A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92894431 | ||||||
| chr12:92894452
|
A | C | 1 | a0001c0012t0006g0157 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.25-2731T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92894452 | ||||||
| chr12:92894826
|
TTAAG | T | 42 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(39): Show | 43 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.25-3109_25-3106del others(4): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92894826 | ||||||
| chr12:92894916
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.25-3195G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92894916 | ||||||
| chr12:92894978
|
T | C | 1 | a0001c0001t0001g0074 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.25-3257A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92894978 | ||||||
| chr12:92895034
|
C | T | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.25-3313G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92895034 | ||||||
| chr12:92895070
|
G | T | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.25-3349C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92895070 | ||||||
| chr12:92895133
|
AT | A | 6 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0232others(3): Show | 6 | HG00741.hp2 HG01361.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.25-3413delA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92895133 | ||||||
| chr12:92895133
|
ATTTTTTT others(3): Show |
A | 20 | a0001c0012t0006g0157a0002c0003t0002g0013a0002c0003t0002g0153others(17): Show | 20 | HG01106.hp2 HG01168.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.25-3422_25-3413del others(10): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92895133 | ||||||
| chr12:92895133
|
ATTTTTTT others(4): Show |
A | 29 | a0001c0002t0035g0188a0002c0003t0002g0001a0002c0003t0002g0144others(26): Show | 30 | HG00099.hp2 HG00639.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.25-3423_25-3413del others(11): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92895133 | ||||||
| chr12:92895133
|
ATTTTTTT others(5): Show |
A | 4 | a0002c0003t0002g0148a0002c0003t0002g0173a0002c0003t0004g0226others(1): Show | 4 | HG00140.hp2 HG02055.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.25-3424_25-3413del others(12): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92895133 | ||||||
| chr12:92895133
|
ATTTTTTT others(6): Show |
A | 12 | a0002c0004t0018g0211a0004c0006t0008g0002a0004c0006t0008g0006others(9): Show | 12 | HG00738.hp1 HG02257.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.25-3425_25-3413del others(13): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92895133 | ||||||
| chr12:92895133
|
ATTTTTTT others(10): Show |
A | 1 | a0002c0017t0034g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.25-3429_25-3413del others(17): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92895133 | ||||||
| chr12:92895133
|
ATTTTTTT others(12): Show |
A | 6 | a0001c0002t0003g0023a0001c0002t0040g0223a0002c0004t0014g0240others(3): Show | 6 | HG02630.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.25-3431_25-3413del others(19): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92895133 | ||||||
| chr12:92895133
|
ATTTTTTT others(13): Show |
A | 141 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(138): Show | 141 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.25-3432_25-3413del others(20): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92895133 | ||||||
| chr12:92895133
|
ATTTTTTT others(14): Show |
A | 7 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0087others(4): Show | 7 | HG01069.hp1 HG01256.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.25-3433_25-3413del others(21): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92895133 | ||||||
| chr12:92895133
|
ATTTTTTT others(15): Show |
A | 1 | a0001c0002t0036g0140 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.25-3434_25-3413del others(22): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92895133 | ||||||
| chr12:92895133
|
ATTTTTTT others(20): Show |
A | 1 | a0002c0004t0033g0233 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.25-3439_25-3413del others(27): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92895133 | ||||||
| chr12:92895179
|
G | A | 1 | a0002c0017t0034g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.25-3458C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92895179 | ||||||
| chr12:92895194
|
C | CT | 78 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(75): Show | 78 | HG00280.hp2 HG00642.hp1 HG00741.hp1 others(75): Show |
intron_variant | MODIFIER | c.25-3474_25-3473ins others(1): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92895194 | ||||||
| chr12:92895331
|
G | GT | 7 | a0002c0004t0024g0046a0002c0004t0048g0017a0002c0008t0012g0014others(4): Show | 7 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.25-3611dupA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92895331 | ||||||
| chr12:92895508
|
GA | G | 231 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(228): Show | 232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.25-3788delT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92895508 | ||||||
| chr12:92895719
|
T | C | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.25-3998A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92895719 | ||||||
| chr12:92895962
|
G | A | 4 | a0001c0002t0009g0120a0001c0002t0009g0121a0001c0002t0009g0129others(1): Show | 4 | HG03491.hp2 HG03492.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.25-4241C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92895962 | ||||||
| chr12:92895995
|
G | C | 4 | a0001c0002t0009g0120a0001c0002t0009g0121a0001c0002t0009g0129others(1): Show | 4 | HG03491.hp2 HG03492.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.25-4274C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92895995 | ||||||
| chr12:92896059
|
C | A | 7 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.25-4338G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92896059 | ||||||
| chr12:92896099
|
G | A | 151 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(148): Show | 151 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.25-4378C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92896099 | ||||||
| chr12:92896130
|
C | T | 2 | a0002c0004t0015g0203a0002c0004t0015g0213 | 2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.25-4409G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92896130 | ||||||
| chr12:92896316
|
C | G | 7 | a0002c0004t0024g0046a0002c0004t0048g0017a0002c0008t0012g0014others(4): Show | 7 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.25-4595G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92896316 | ||||||
| chr12:92896361
|
G | A | 219 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(216): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.25-4640C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92896361 | ||||||
| chr12:92896454
|
C | T | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.25-4733G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92896454 | ||||||
| chr12:92896674
|
G | C | 1 | a0002c0017t0034g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.25-4953C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92896674 | ||||||
| chr12:92896726
|
G | A | 23 | a0001c0002t0003g0023a0001c0002t0003g0024a0001c0002t0003g0025others(20): Show | 23 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.25-5005C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92896726 | ||||||
| chr12:92896772
|
A | G | 1 | a0001c0012t0006g0157 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.25-5051T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92896772 | ||||||
| chr12:92896773
|
G | A | 1 | a0001c0012t0006g0157 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.25-5052C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92896773 | ||||||
| chr12:92896781
|
G | GA | 7 | a0001c0002t0019g0127a0001c0002t0019g0128a0002c0008t0012g0014others(4): Show | 7 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.25-5061dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92896781 | ||||||
| chr12:92896941
|
A | G | 204 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(201): Show | 205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.25-5220T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92896941 | ||||||
| chr12:92896953
|
T | C | 45 | a0001c0002t0035g0188a0001c0012t0006g0157a0002c0003t0002g0001others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.25-5232A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92896953 | ||||||
| chr12:92897036
|
G | T | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.25-5315C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92897036 | ||||||
| chr12:92897046
|
G | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0081 | 2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.25-5325C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92897046 | ||||||
| chr12:92897049
|
C | T | 1 | a0002c0003t0004g0168 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.25-5328G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92897049 | ||||||
| chr12:92897269
|
G | A | 2 | a0002c0004t0018g0202a0002c0004t0041g0201 | 2 | HG02572.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.25-5548C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92897269 | ||||||
| chr12:92897688
|
G | A | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.25-5967C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92897688 | ||||||
| chr12:92897759
|
C | T | 1 | a0002c0003t0002g0169 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.25-6038G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92897759 | ||||||
| chr12:92897826
|
A | G | 19 | a0001c0001t0001g0069a0001c0001t0001g0084a0001c0001t0001g0090others(16): Show | 19 | HG00280.hp2 HG01099.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.25-6105T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92897826 | ||||||
| chr12:92898058
|
ATATGCCT others(9): Show |
A | 1 | a0001c0002t0007g0137 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.25-6353_25-6338del others(16): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92898058 | ||||||
| chr12:92898336
|
T | C | 1 | a0002c0003t0004g0151 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.25-6615A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92898336 | ||||||
| chr12:92898432
|
G | C | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.25-6711C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92898432 | ||||||
| chr12:92898516
|
T | C | 14 | a0001c0002t0006g0042a0001c0002t0006g0044a0001c0002t0006g0191others(11): Show | 14 | HG01109.hp2 HG01257.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.25-6795A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92898516 | ||||||
| chr12:92898653
|
G | A | 1 | a0002c0003t0004g0167 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.25-6932C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92898653 | ||||||
| chr12:92898663
|
C | CA | 53 | a0001c0001t0001g0063a0001c0012t0006g0157a0002c0003t0002g0001others(50): Show | 54 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.25-6943dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92898663 | ||||||
| chr12:92898722
|
TTTTTTTC others(2): Show |
T | 10 | a0004c0006t0008g0002a0004c0006t0008g0007a0004c0006t0008g0011others(7): Show | 10 | HG02723.hp1 HG03041.hp1 HG03688.hp2 others(7): Show |
intron_variant | MODIFIER | c.25-7010_25-7002del others(9): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92898722 | ||||||
| chr12:92898731
|
C | CT | 31 | a0001c0001t0001g0049a0001c0001t0001g0054a0001c0001t0001g0056others(28): Show | 31 | HG01071.hp1 HG01081.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.25-7011dupA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92898731 | ||||||
| chr12:92898731
|
CT | C | 46 | a0001c0002t0006g0042a0001c0002t0006g0191a0001c0002t0006g0192others(43): Show | 46 | HG00099.hp1 HG00280.hp1 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.25-7011delA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92898731 | ||||||
| chr12:92898731
|
CTT | C | 36 | a0001c0002t0020g0123a0001c0012t0006g0157a0002c0003t0002g0001others(33): Show | 37 | HG00099.hp2 HG00140.hp2 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.25-7012_25-7011del others(2): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92898731 | ||||||
| chr12:92898731
|
CTTT | C | 18 | a0002c0003t0004g0147a0002c0003t0004g0165a0002c0003t0004g0166others(15): Show | 18 | HG00639.hp2 HG01167.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.25-7013_25-7011del others(3): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92898731 | ||||||
| chr12:92898731
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0005g0181 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.25-7020_25-7011del others(10): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92898731 | ||||||
| chr12:92898805
|
T | G | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.25-7084A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92898805 | ||||||
| chr12:92898852
|
A | ATAGTGCT others(5): Show |
1 | a0001c0012t0006g0157 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.25-7132_25-7131ins others(12): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92898852 | ||||||
| chr12:92898911
|
C | G | 4 | a0001c0002t0003g0037a0001c0002t0003g0040a0001c0002t0003g0041others(1): Show | 4 | HG02257.hp1 HG03209.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.25-7190G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92898911 | ||||||
| chr12:92898954
|
G | GA | 5 | a0001c0001t0001g0068a0001c0001t0001g0072a0001c0001t0001g0103others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.25-7234dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92898954 | ||||||
| chr12:92898954
|
GA | G | 10 | a0001c0002t0006g0195a0001c0012t0006g0157a0002c0003t0004g0167others(7): Show | 10 | HG01168.hp1 HG01243.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.25-7234delT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92898954 | ||||||
| chr12:92898954
|
GAA | G | 43 | a0002c0003t0002g0001a0002c0003t0002g0013a0002c0003t0002g0144others(40): Show | 44 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.25-7235_25-7234del others(2): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92898954 | ||||||
| chr12:92898956
|
A | G | 1 | a0002c0004t0024g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.25-7235T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92898956 | ||||||
| chr12:92898971
|
C | T | 152 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(149): Show | 152 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.25-7250G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92898971 | ||||||
| chr12:92899075
|
A | G | 1 | a0001c0002t0003g0040 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.25-7354T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92899075 | ||||||
| chr12:92899107
|
A | G | 2 | a0002c0003t0002g0163a0002c0003t0002g0173 | 2 | HG00140.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.25-7386T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92899107 | ||||||
| chr12:92899129
|
CA | C | 20 | a0001c0002t0007g0048a0002c0004t0014g0240a0002c0004t0014g0241others(17): Show | 20 | HG00738.hp1 HG01099.hp2 HG02622.hp1 others(17): Show |
intron_variant | MODIFIER | c.25-7409delT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92899129 | ||||||
| chr12:92899129
|
CAA | C | 206 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(203): Show | 207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.25-7410_25-7409del others(2): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92899129 | ||||||
| chr12:92899238
|
T | C | 1 | a0001c0002t0006g0191 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.25-7517A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92899238 | ||||||
| chr12:92899426
|
C | T | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.25-7705G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92899426 | ||||||
| chr12:92899563
|
G | T | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.25-7842C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92899563 | ||||||
| chr12:92899722
|
G | A | 1 | a0001c0002t0044g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.25-8001C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92899722 | ||||||
| chr12:92899765
|
G | A | 3 | a0002c0003t0016g0141a0002c0003t0016g0142a0002c0003t0016g0143 | 3 | HG02818.hp1 HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.25-8044C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92899765 | ||||||
| chr12:92899888
|
T | C | 1 | a0003c0005t0003g0035 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.25-8167A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92899888 | ||||||
| chr12:92899962
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.25-8241C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92899962 | ||||||
| chr12:92900209
|
T | A | 219 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(216): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.25-8488A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92900209 | ||||||
| chr12:92900271
|
C | A | 9 | a0001c0001t0001g0068a0001c0001t0001g0072a0001c0001t0001g0078others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.25-8550G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92900271 | ||||||
| chr12:92900303
|
G | A | 26 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(23): Show | 27 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.25-8582C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92900303 | ||||||
| chr12:92900372
|
C | T | 219 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(216): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.25-8651G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92900372 | ||||||
| chr12:92900434
|
GT | G | 44 | a0002c0003t0002g0001a0002c0003t0002g0013a0002c0003t0002g0144others(41): Show | 45 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.25-8714delA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92900434 | ||||||
| chr12:92900435
|
T | TG | 15 | a0001c0002t0006g0042a0001c0002t0006g0044a0001c0002t0006g0191others(12): Show | 15 | HG01109.hp2 HG01257.hp2 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.25-8715_25-8714ins others(1): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92900435 | ||||||
| chr12:92900436
|
T | G | 1 | a0001c0002t0032g0045 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.25-8715A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92900436 | ||||||
| chr12:92900686
|
T | C | 1 | a0002c0008t0012g0015 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.25-8965A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92900686 | ||||||
| chr12:92900825
|
C | A | 1 | a0001c0001t0001g0082 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.25-9104G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92900825 | ||||||
| chr12:92900996
|
G | A | 1 | a0001c0001t0013g0138 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.25-9275C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92900996 | ||||||
| chr12:92901073
|
G | T | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.25-9352C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92901073 | ||||||
| chr12:92901108
|
G | T | 1 | a0001c0012t0006g0157 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.25-9387C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92901108 | ||||||
| chr12:92901301
|
C | T | 3 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0094 | 3 | HG01081.hp1 HG02273.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.25-9580G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92901301 | ||||||
| chr12:92901550
|
T | C | 1 | a0001c0002t0003g0023 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.25-9829A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92901550 | ||||||
| chr12:92901718
|
C | T | 3 | a0002c0004t0015g0198a0002c0004t0015g0203a0002c0004t0015g0213 | 3 | HG02622.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.25-9997G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92901718 | ||||||
| chr12:92901978
|
A | C | 1 | a0002c0003t0002g0153 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.25-10257T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92901978 | ||||||
| chr12:92902022
|
T | C | 1 | a0002c0003t0004g0226 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.25-10301A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92902022 | ||||||
| chr12:92902058
|
A | G | 1 | a0002c0004t0011g0206 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.25-10337T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92902058 | ||||||
| chr12:92902338
|
G | T | 1 | a0001c0002t0036g0140 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.25-10617C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92902338 | ||||||
| chr12:92902417
|
T | C | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.25-10696A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92902417 | ||||||
| chr12:92902547
|
C | T | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.25-10826G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92902547 | ||||||
| chr12:92902596
|
C | T | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.25-10875G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92902596 | ||||||
| chr12:92902609
|
C | T | 9 | a0001c0002t0039g0215a0001c0002t0040g0223a0001c0002t0046g0217others(6): Show | 9 | HG02109.hp1 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.25-10888G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92902609 | ||||||
| chr12:92902639
|
G | A | 1 | a0002c0004t0024g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.25-10918C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92902639 | ||||||
| chr12:92902719
|
C | A | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.25-10998G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92902719 | ||||||
| chr12:92902740
|
T | TA | 32 | a0001c0001t0001g0047a0001c0001t0001g0065a0001c0001t0001g0069others(29): Show | 32 | HG00280.hp2 HG01099.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.25-11020dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92902740 | ||||||
| chr12:92902740
|
T | TAA | 45 | a0001c0001t0001g0135a0001c0012t0006g0157a0002c0003t0002g0001others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.25-11021_25-11020d others(4): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92902740 | ||||||
| chr12:92902740
|
TA | T | 35 | a0001c0002t0007g0048a0001c0002t0007g0116a0001c0002t0007g0117others(32): Show | 35 | HG00280.hp1 HG01071.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.25-11020delT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92902740 | ||||||
| chr12:92902758
|
A | AG | 5 | a0001c0002t0006g0192a0001c0002t0006g0195a0001c0002t0007g0193others(2): Show | 5 | HG01257.hp2 HG01975.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.25-11038dupC | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92902758 | ||||||
| chr12:92902758
|
A | G | 9 | a0001c0002t0006g0042a0001c0002t0006g0044a0001c0002t0006g0191others(6): Show | 9 | HG01109.hp2 HG02622.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.25-11037T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92902758 | ||||||
| chr12:92902936
|
C | CT | 5 | a0001c0001t0001g0134a0001c0001t0013g0070a0001c0002t0007g0130others(2): Show | 5 | HG01891.hp1 HG02258.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.25-11216dupA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92902936 | ||||||
| chr12:92902936
|
CT | C | 52 | a0001c0002t0032g0045a0002c0003t0002g0001a0002c0003t0002g0013others(49): Show | 53 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.25-11216delA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92902936 | ||||||
| chr12:92903028
|
G | A | 14 | a0001c0002t0006g0042a0001c0002t0006g0044a0001c0002t0006g0191others(11): Show | 14 | HG01109.hp2 HG01257.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.25-11307C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92903028 | ||||||
| chr12:92903081
|
C | A | 1 | a0002c0017t0034g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.25-11360G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92903081 | ||||||
| chr12:92903083
|
C | T | 8 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(5): Show | 8 | HG02451.hp1 HG02922.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.25-11362G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92903083 | ||||||
| chr12:92903102
|
T | A | 152 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(149): Show | 152 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.25-11381A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92903102 | ||||||
| chr12:92903130
|
G | T | 1 | a0002c0004t0024g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.25-11409C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92903130 | ||||||
| chr12:92903138
|
C | T | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.25-11417G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92903138 | ||||||
| chr12:92903227
|
G | A | 2 | a0002c0003t0004g0168a0002c0003t0004g0227 | 2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.25-11506C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92903227 | ||||||
| chr12:92903232
|
C | T | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.25-11511G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92903232 | ||||||
| chr12:92903260
|
T | C | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.25-11539A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92903260 | ||||||
| chr12:92903312
|
A | G | 3 | a0006c0009t0001g0096a0006c0009t0001g0097a0006c0009t0001g0098 | 3 | HG01099.hp1 HG02273.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.25-11591T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92903312 | ||||||
| chr12:92903320
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.25-11599C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92903320 | ||||||
| chr12:92903468
|
C | T | 7 | a0002c0003t0004g0147a0002c0003t0004g0167a0002c0003t0004g0168others(4): Show | 7 | HG02486.hp1 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.25-11747G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92903468 | ||||||
| chr12:92903469
|
G | A | 1 | a0001c0001t0005g0077 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.25-11748C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92903469 | ||||||
| chr12:92903800
|
T | G | 1 | a0001c0012t0006g0157 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.25-12079A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92903800 | ||||||
| chr12:92903820
|
T | C | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.25-12099A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92903820 | ||||||
| chr12:92903842
|
C | T | 152 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(149): Show | 152 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.25-12121G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92903842 | ||||||
| chr12:92904610
|
T | C | 1 | a0002c0003t0002g0153 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.25-12889A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92904610 | ||||||
| chr12:92904632
|
G | A | 1 | a0001c0002t0035g0188 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.25-12911C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92904632 | ||||||
| chr12:92904672
|
C | T | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.25-12951G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92904672 | ||||||
| chr12:92904923
|
T | C | 7 | a0002c0004t0024g0046a0002c0004t0048g0017a0002c0008t0012g0014others(4): Show | 7 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.25-13202A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92904923 | ||||||
| chr12:92904926
|
T | C | 7 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.25-13205A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92904926 | ||||||
| chr12:92905002
|
C | T | 7 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.25-13281G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92905002 | ||||||
| chr12:92905057
|
C | T | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.25-13336G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92905057 | ||||||
| chr12:92905188
|
A | C | 152 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(149): Show | 152 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.25-13467T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92905188 | ||||||
| chr12:92905441
|
T | TAC | 4 | a0002c0003t0002g0149a0002c0003t0004g0152a0002c0004t0024g0046others(1): Show | 4 | HG00741.hp2 HG01884.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.25-13722_25-13721d others(4): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92905441 | ||||||
| chr12:92905441
|
TAC | T | 155 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(152): Show | 155 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.25-13722_25-13721d others(4): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92905441 | ||||||
| chr12:92905597
|
C | G | 1 | a0004c0006t0008g0007 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.25-13876G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92905597 | ||||||
| chr12:92905652
|
T | C | 1 | a0002c0003t0043g0155 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.25-13931A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92905652 | ||||||
| chr12:92905809
|
A | G | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.25-14088T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92905809 | ||||||
| chr12:92905870
|
C | G | 1 | a0001c0002t0047g0187 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.25-14149G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92905870 | ||||||
| chr12:92905901
|
CAT | C | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.25-14182_25-14181d others(4): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92905901 | ||||||
| chr12:92905918
|
T | A | 7 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.25-14197A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92905918 | ||||||
| chr12:92905964
|
G | A | 1 | a0001c0010t0006g0220 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.25-14243C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92905964 | ||||||
| chr12:92905965
|
G | C | 3 | a0002c0004t0015g0198a0002c0004t0015g0203a0002c0004t0015g0213 | 3 | HG02622.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.25-14244C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92905965 | ||||||
| chr12:92906019
|
G | A | 79 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(76): Show | 79 | HG00280.hp2 HG00642.hp1 HG00741.hp1 others(76): Show |
intron_variant | MODIFIER | c.25-14298C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92906019 | ||||||
| chr12:92906093
|
CT | C | 45 | a0002c0003t0002g0001a0002c0003t0002g0013a0002c0003t0002g0144others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.25-14373delA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92906093 | ||||||
| chr12:92906241
|
G | A | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.25-14520C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92906241 | ||||||
| chr12:92906431
|
T | C | 1 | a0001c0002t0044g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.25-14710A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92906431 | ||||||
| chr12:92906484
|
G | C | 1 | a0001c0002t0032g0045 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.25-14763C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92906484 | ||||||
| chr12:92906579
|
G | A | 1 | a0001c0002t0003g0040 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.25-14858C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92906579 | ||||||
| chr12:92906810
|
T | C | 1 | a0002c0004t0048g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.25-15089A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92906810 | ||||||
| chr12:92906821
|
A | G | 3 | a0001c0002t0039g0215a0001c0002t0040g0223a0001c0002t0046g0217 | 3 | HG02630.hp1 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.25-15100T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92906821 | ||||||
| chr12:92906941
|
A | G | 2 | a0001c0002t0019g0127a0001c0002t0019g0128 | 2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.25-15220T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92906941 | ||||||
| chr12:92906997
|
A | G | 2 | a0001c0002t0020g0122a0001c0002t0020g0123 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.25-15276T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92906997 | ||||||
| chr12:92907047
|
G | A | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.25-15326C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92907047 | ||||||
| chr12:92907053
|
TATAG | T | 7 | a0002c0003t0004g0147a0002c0003t0004g0167a0002c0003t0004g0168others(4): Show | 7 | HG02486.hp1 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.25-15336_25-15333d others(6): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92907053 | ||||||
| chr12:92907094
|
T | C | 3 | a0002c0003t0002g0001a0002c0003t0002g0177a0002c0003t0002g0180 | 4 | HG02015.hp2 HG02083.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.25-15373A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92907094 | ||||||
| chr12:92907531
|
C | T | 1 | a0001c0002t0007g0116 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.25-15810G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92907531 | ||||||
| chr12:92907565
|
C | G | 3 | a0002c0004t0015g0198a0002c0004t0015g0203a0002c0004t0015g0213 | 3 | HG02622.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.25-15844G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92907565 | ||||||
| chr12:92907588
|
G | A | 1 | a0002c0003t0002g0162 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.25-15867C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92907588 | ||||||
| chr12:92907589
|
G | A | 1 | a0002c0003t0002g0162 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.25-15868C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92907589 | ||||||
| chr12:92907717
|
C | A | 1 | a0001c0001t0013g0092 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.25-15996G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92907717 | ||||||
| chr12:92907753
|
A | G | 2 | a0004c0006t0008g0002a0004c0006t0021g0012 | 2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.25-16032T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92907753 | ||||||
| chr12:92908062
|
CAT | C | 9 | a0001c0002t0039g0215a0001c0002t0040g0223a0001c0002t0046g0217others(6): Show | 9 | HG02109.hp1 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.25-16343_25-16342d others(4): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92908062 | ||||||
| chr12:92908089
|
G | A | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.25-16368C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92908089 | ||||||
| chr12:92908121
|
A | G | 1 | a0002c0004t0031g0199 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.25-16400T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92908121 | ||||||
| chr12:92908178
|
C | T | 2 | a0001c0002t0020g0122a0001c0002t0020g0123 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.25-16457G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92908178 | ||||||
| chr12:92908240
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.25-16519C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92908240 | ||||||
| chr12:92908285
|
G | A | 1 | a0002c0004t0024g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.25-16564C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92908285 | ||||||
| chr12:92908382
|
A | T | 14 | a0001c0002t0006g0042a0001c0002t0006g0044a0001c0002t0006g0191others(11): Show | 14 | HG01109.hp2 HG01257.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.25-16661T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92908382 | ||||||
| chr12:92908389
|
C | T | 52 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(49): Show | 53 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.25-16668G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92908389 | ||||||
| chr12:92908431
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.25-16710C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92908431 | ||||||
| chr12:92908456
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.25-16735C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92908456 | ||||||
| chr12:92908612
|
A | C | 1 | a0001c0001t0051g0107 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.25-16891T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92908612 | ||||||
| chr12:92908617
|
T | TA | 151 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(148): Show | 151 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.25-16897dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92908617 | ||||||
| chr12:92908795
|
A | G | 152 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(149): Show | 152 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.25-17074T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92908795 | ||||||
| chr12:92909004
|
G | C | 1 | a0001c0002t0044g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.25-17283C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92909004 | ||||||
| chr12:92909009
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.25-17288G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92909009 | ||||||
| chr12:92909099
|
C | T | 1 | a0002c0003t0004g0151 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.25-17378G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92909099 | ||||||
| chr12:92909100
|
G | A | 1 | a0001c0002t0040g0223 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.25-17379C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92909100 | ||||||
| chr12:92909115
|
T | C | 1 | a0001c0001t0051g0107 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.25-17394A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92909115 | ||||||
| chr12:92909184
|
G | A | 151 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(148): Show | 151 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.25-17463C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92909184 | ||||||
| chr12:92909267
|
G | A | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.25-17546C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92909267 | ||||||
| chr12:92909696
|
G | C | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.25-17975C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92909696 | ||||||
| chr12:92909721
|
A | G | 1 | a0002c0003t0043g0155 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.25-18000T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92909721 | ||||||
| chr12:92909783
|
G | A | 2 | a0002c0003t0002g0163a0002c0003t0002g0173 | 2 | HG00140.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.25-18062C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92909783 | ||||||
| chr12:92909813
|
C | T | 1 | a0007c0016t0025g0019 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.25-18092G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92909813 | ||||||
| chr12:92909925
|
C | T | 1 | a0002c0004t0024g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.25-18204G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92909925 | ||||||
| chr12:92909929
|
G | A | 14 | a0001c0002t0006g0042a0001c0002t0006g0044a0001c0002t0006g0191others(11): Show | 14 | HG01109.hp2 HG01257.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.25-18208C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92909929 | ||||||
| chr12:92909953
|
G | A | 1 | a0002c0004t0048g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.25-18232C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92909953 | ||||||
| chr12:92910014
|
C | T | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.25-18293G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92910014 | ||||||
| chr12:92910072
|
G | C | 1 | a0001c0002t0003g0023 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.25-18351C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92910072 | ||||||
| chr12:92910118
|
C | T | 3 | a0002c0004t0018g0210a0002c0004t0018g0211a0008c0014t0006g0204 | 3 | HG02055.hp1 HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.25-18397G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92910118 | ||||||
| chr12:92910159
|
A | ATTAAAT | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.25-18444_25-18439d others(8): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92910159 | ||||||
| chr12:92910162
|
A | AAATTTT | 229 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(226): Show | 230 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.25-18447_25-18442d others(8): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92910162 | ||||||
| chr12:92910162
|
A | T | 1 | a0001c0002t0040g0223 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.25-18441T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92910162 | ||||||
| chr12:92910198
|
G | A | 151 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(148): Show | 151 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.25-18477C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92910198 | ||||||
| chr12:92910343
|
C | T | 9 | a0001c0002t0039g0215a0001c0002t0040g0223a0001c0002t0046g0217others(6): Show | 9 | HG02109.hp1 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.25-18622G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92910343 | ||||||
| chr12:92910447
|
C | T | 41 | a0001c0001t0001g0049a0001c0001t0001g0054a0001c0001t0001g0055others(38): Show | 41 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.24+18596G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92910447 | ||||||
| chr12:92910448
|
G | A | 11 | a0001c0002t0007g0048a0001c0002t0007g0116a0001c0002t0007g0117others(8): Show | 11 | HG00280.hp1 HG01099.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.24+18595C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92910448 | ||||||
| chr12:92910478
|
T | A | 199 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(196): Show | 200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.24+18565A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92910478 | ||||||
| chr12:92910621
|
G | T | 1 | a0001c0002t0044g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.24+18422C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92910621 | ||||||
| chr12:92910859
|
C | G | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.24+18184G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92910859 | ||||||
| chr12:92910998
|
G | A | 7 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.24+18045C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92910998 | ||||||
| chr12:92911085
|
C | CAAAACTA others(322): Show |
1 | a0002c0004t0014g0242 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.24+17957_24+17958i others(331): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92911085 | ||||||
| chr12:92911085
|
C | CAAAACTA others(323): Show |
1 | a0002c0004t0014g0243 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.24+17957_24+17958i others(332): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92911085 | ||||||
| chr12:92911085
|
C | CAAAACTA others(324): Show |
2 | a0002c0004t0014g0240a0002c0004t0014g0241 | 2 | HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.24+17957_24+17958i others(333): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92911085 | ||||||
| chr12:92911183
|
T | C | 2 | a0002c0004t0018g0202a0002c0004t0041g0201 | 2 | HG02572.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.24+17860A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92911183 | ||||||
| chr12:92911395
|
A | G | 3 | a0002c0004t0018g0210a0002c0004t0018g0211a0008c0014t0006g0204 | 3 | HG02055.hp1 HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.24+17648T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92911395 | ||||||
| chr12:92911524
|
C | T | 1 | a0002c0004t0018g0210 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.24+17519G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92911524 | ||||||
| chr12:92911525
|
A | G | 235 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(232): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.24+17518T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92911525 | ||||||
| chr12:92911557
|
G | A | 3 | a0002c0004t0015g0198a0002c0004t0015g0203a0002c0004t0015g0213 | 3 | HG02622.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.24+17486C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92911557 | ||||||
| chr12:92911668
|
A | C | 5 | a0002c0004t0018g0202a0002c0004t0018g0210a0002c0004t0018g0211others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.24+17375T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92911668 | ||||||
| chr12:92911809
|
T | TTC | 235 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(232): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.24+17233_24+17234i others(4): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92911809 | ||||||
| chr12:92911864
|
A | T | 1 | a0001c0001t0001g0090 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.24+17179T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92911864 | ||||||
| chr12:92911903
|
G | A | 1 | a0001c0010t0006g0221 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.24+17140C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92911903 | ||||||
| chr12:92912009
|
G | A | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.24+17034C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92912009 | ||||||
| chr12:92912111
|
A | G | 1 | a0001c0001t0005g0182 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.24+16932T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92912111 | ||||||
| chr12:92912247
|
A | C | 7 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.24+16796T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92912247 | ||||||
| chr12:92912257
|
T | C | 204 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(201): Show | 205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.24+16786A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92912257 | ||||||
| chr12:92912323
|
TCCTCCCC others(2): Show |
T | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.24+16711_24+16719d others(11): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92912323 | ||||||
| chr12:92912363
|
C | G | 1 | a0001c0001t0005g0225 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.24+16680G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92912363 | ||||||
| chr12:92912370
|
A | G | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.24+16673T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92912370 | ||||||
| chr12:92912404
|
T | C | 1 | a0001c0002t0007g0137 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.24+16639A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92912404 | ||||||
| chr12:92912449
|
G | A | 1 | a0002c0003t0004g0176 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.24+16594C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92912449 | ||||||
| chr12:92912504
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.24+16539A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92912504 | ||||||
| chr12:92912581
|
T | G | 1 | a0002c0004t0033g0233 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.24+16462A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92912581 | ||||||
| chr12:92912591
|
C | T | 1 | a0001c0002t0037g0194 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.24+16452G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92912591 | ||||||
| chr12:92912725
|
T | C | 52 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(49): Show | 53 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.24+16318A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92912725 | ||||||
| chr12:92912759
|
T | C | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.24+16284A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92912759 | ||||||
| chr12:92912766
|
G | A | 1 | a0001c0002t0044g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.24+16277C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92912766 | ||||||
| chr12:92912990
|
G | A | 1 | a0001c0002t0007g0137 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.24+16053C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92912990 | ||||||
| chr12:92913172
|
C | T | 152 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(149): Show | 152 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.24+15871G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92913172 | ||||||
| chr12:92913341
|
C | T | 236 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(233): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.24+15702G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92913341 | ||||||
| chr12:92913407
|
C | T | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.24+15636G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92913407 | ||||||
| chr12:92913722
|
G | A | 1 | a0002c0004t0048g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.24+15321C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92913722 | ||||||
| chr12:92913723
|
C | T | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.24+15320G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92913723 | ||||||
| chr12:92913739
|
C | A | 42 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(39): Show | 43 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.24+15304G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92913739 | ||||||
| chr12:92913903
|
C | T | 1 | a0002c0004t0031g0199 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.24+15140G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92913903 | ||||||
| chr12:92913908
|
G | A | 1 | a0002c0004t0024g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.24+15135C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92913908 | ||||||
| chr12:92914060
|
C | A | 1 | a0002c0004t0033g0233 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.24+14983G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92914060 | ||||||
| chr12:92914231
|
T | A | 1 | a0001c0002t0009g0124 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.24+14812A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92914231 | ||||||
| chr12:92914476
|
G | A | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.24+14567C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92914476 | ||||||
| chr12:92914551
|
T | C | 219 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(216): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.24+14492A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92914551 | ||||||
| chr12:92914585
|
G | A | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.24+14458C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92914585 | ||||||
| chr12:92914665
|
A | AT | 6 | a0001c0002t0007g0137a0001c0002t0017g0115a0001c0002t0036g0140others(3): Show | 6 | HG02258.hp2 HG02602.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.24+14377dupA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92914665 | ||||||
| chr12:92914665
|
AT | A | 7 | a0001c0001t0001g0110a0001c0002t0039g0215a0001c0002t0040g0223others(4): Show | 7 | HG02630.hp1 HG02723.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.24+14377delA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92914665 | ||||||
| chr12:92914763
|
G | A | 1 | a0001c0002t0035g0188 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.24+14280C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92914763 | ||||||
| chr12:92914809
|
G | A | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.24+14234C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92914809 | ||||||
| chr12:92914848
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.24+14195G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92914848 | ||||||
| chr12:92915309
|
A | G | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.24+13734T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92915309 | ||||||
| chr12:92915319
|
G | T | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.24+13724C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92915319 | ||||||
| chr12:92915329
|
G | A | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.24+13714C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92915329 | ||||||
| chr12:92915381
|
C | T | 226 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(223): Show | 227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.24+13662G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92915381 | ||||||
| chr12:92915395
|
A | T | 1 | a0001c0002t0007g0126 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.24+13648T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92915395 | ||||||
| chr12:92915490
|
C | CA | 22 | a0001c0002t0007g0048a0001c0002t0007g0116a0001c0002t0007g0117others(19): Show | 22 | HG00280.hp1 HG01071.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.24+13552dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92915490 | ||||||
| chr12:92915517
|
C | G | 1 | a0002c0003t0043g0155 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.24+13526G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92915517 | ||||||
| chr12:92915838
|
T | A | 1 | a0001c0002t0007g0126 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.24+13205A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92915838 | ||||||
| chr12:92916066
|
A | T | 1 | a0002c0004t0011g0205 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.24+12977T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916066 | ||||||
| chr12:92916107
|
C | T | 1 | a0001c0002t0003g0040 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.24+12936G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916107 | ||||||
| chr12:92916244
|
C | A | 23 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(20): Show | 23 | HG00099.hp1 HG00741.hp2 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.24+12799G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916244 | ||||||
| chr12:92916377
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.24+12666C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916377 | ||||||
| chr12:92916382
|
C | T | 7 | a0002c0004t0024g0046a0002c0004t0048g0017a0002c0008t0012g0014others(4): Show | 7 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.24+12661G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916382 | ||||||
| chr12:92916513
|
C | T | 1 | a0002c0004t0024g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.24+12530G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916513 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3339): Show |
23 | a0002c0003t0002g0001a0002c0003t0002g0013a0002c0003t0002g0144others(20): Show | 24 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.24+12443_24+12444i others(3348): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3338): Show |
1 | a0002c0003t0043g0155 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.24+12443_24+12444i others(3347): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3337): Show |
1 | a0001c0012t0006g0157 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.24+12443_24+12444i others(3346): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3338): Show |
7 | a0002c0003t0004g0147a0002c0003t0004g0167a0002c0003t0004g0168others(4): Show | 7 | HG02486.hp1 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.24+12443_24+12444i others(3347): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3338): Show |
11 | a0002c0003t0002g0145a0002c0003t0004g0151a0002c0003t0004g0152others(8): Show | 11 | HG00639.hp2 HG01167.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.24+12443_24+12444i others(3347): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3337): Show |
1 | a0002c0003t0016g0141 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.24+12443_24+12444i others(3346): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3337): Show |
1 | a0002c0004t0048g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.24+12443_24+12444i others(3346): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3336): Show |
1 | a0001c0002t0035g0188 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.24+12443_24+12444i others(3345): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3339): Show |
1 | a0002c0008t0012g0238 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.24+12443_24+12444i others(3348): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3338): Show |
1 | a0002c0008t0012g0237 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.24+12443_24+12444i others(3347): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3338): Show |
3 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236 | 3 | HG02109.hp2 HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.24+12443_24+12444i others(3347): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3337): Show |
1 | a0002c0004t0024g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.24+12443_24+12444i others(3346): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3341): Show |
1 | a0002c0004t0018g0210 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.24+12443_24+12444i others(3350): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3340): Show |
1 | a0002c0017t0034g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.24+12443_24+12444i others(3349): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3339): Show |
1 | a0002c0004t0014g0243 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.24+12443_24+12444i others(3348): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3338): Show |
1 | a0002c0004t0014g0241 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.24+12443_24+12444i others(3347): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3336): Show |
1 | a0002c0003t0055g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.24+12443_24+12444i others(3345): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3340): Show |
3 | a0002c0004t0018g0202a0002c0004t0041g0201a0008c0014t0006g0204 | 3 | HG02451.hp2 HG02572.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.24+12443_24+12444i others(3349): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3340): Show |
1 | a0002c0004t0018g0211 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.24+12443_24+12444i others(3349): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3340): Show |
1 | a0002c0004t0030g0209 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.24+12443_24+12444i others(3349): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3340): Show |
6 | a0002c0004t0011g0205a0002c0004t0011g0206a0002c0004t0011g0207others(3): Show | 6 | HG00099.hp1 HG01261.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.24+12443_24+12444i others(3349): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3338): Show |
2 | a0002c0004t0014g0242a0005c0007t0008g0009 | 2 | HG02895.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.24+12443_24+12444i others(3347): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3337): Show |
1 | a0001c0002t0037g0194 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.24+12443_24+12444i others(3346): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3337): Show |
8 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(5): Show | 8 | HG00738.hp1 HG02723.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.24+12443_24+12444i others(3346): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3337): Show |
1 | a0005c0007t0008g0010 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.24+12443_24+12444i others(3346): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3336): Show |
1 | a0004c0006t0021g0012 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.24+12443_24+12444i others(3345): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3337): Show |
7 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.24+12443_24+12444i others(3346): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3336): Show |
3 | a0001c0002t0026g0212a0001c0002t0027g0189a0001c0002t0028g0190 | 3 | HG02647.hp1 HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.24+12443_24+12444i others(3345): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3336): Show |
10 | a0001c0002t0006g0042a0001c0002t0006g0044a0001c0002t0006g0191others(7): Show | 10 | HG01109.hp2 HG01257.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.24+12443_24+12444i others(3345): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3336): Show |
1 | a0001c0002t0044g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.24+12443_24+12444i others(3345): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3335): Show |
3 | a0001c0002t0003g0037a0001c0002t0003g0041a0001c0002t0045g0036 | 3 | HG02257.hp1 HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.24+12443_24+12444i others(3344): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3335): Show |
1 | a0001c0002t0003g0040 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.24+12443_24+12444i others(3344): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3335): Show |
19 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0026others(16): Show | 19 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.24+12443_24+12444i others(3344): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3335): Show |
1 | a0001c0002t0003g0023 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.24+12443_24+12444i others(3344): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3339): Show |
1 | a0002c0004t0014g0240 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.24+12443_24+12444i others(3348): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916599
|
G | GCCAAGAT others(3339): Show |
3 | a0002c0004t0015g0198a0002c0004t0015g0203a0002c0004t0015g0213 | 3 | HG02622.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.24+12443_24+12444i others(3348): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916599 | ||||||
| chr12:92916648
|
A | G | 3 | a0001c0002t0039g0215a0001c0002t0040g0223a0001c0002t0046g0217 | 3 | HG02630.hp1 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.24+12395T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916648 | ||||||
| chr12:92916684
|
C | T | 7 | a0002c0004t0024g0046a0002c0004t0048g0017a0002c0008t0012g0014others(4): Show | 7 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.24+12359G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916684 | ||||||
| chr12:92916735
|
C | G | 1 | a0002c0008t0012g0014 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.24+12308G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916735 | ||||||
| chr12:92916784
|
T | C | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.24+12259A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916784 | ||||||
| chr12:92916935
|
T | A | 2 | a0002c0003t0002g0154a0002c0003t0002g0164 | 2 | HG03688.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.24+12108A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916935 | ||||||
| chr12:92916946
|
C | T | 3 | a0002c0004t0024g0046a0002c0004t0031g0199a0002c0004t0048g0017 | 3 | HG02809.hp2 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.24+12097G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916946 | ||||||
| chr12:92916973
|
CAACTGGA others(4): Show |
C | 1 | a0001c0001t0005g0093 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.24+12059_24+12069d others(13): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916973 | ||||||
| chr12:92916990
|
G | A | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.24+12053C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92916990 | ||||||
| chr12:92917146
|
T | C | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.24+11897A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92917146 | ||||||
| chr12:92917155
|
G | A | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.24+11888C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92917155 | ||||||
| chr12:92917244
|
C | T | 1 | a0004c0006t0008g0002 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.24+11799G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92917244 | ||||||
| chr12:92917333
|
T | G | 163 | a0001c0002t0003g0023a0001c0002t0003g0024a0001c0002t0003g0025others(160): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.24+11710A>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92917333 | ||||||
| chr12:92917340
|
G | A | 23 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(20): Show | 23 | HG00099.hp1 HG00741.hp2 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.24+11703C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92917340 | ||||||
| chr12:92917389
|
G | A | 16 | a0002c0004t0011g0205a0002c0004t0011g0206a0002c0004t0011g0207others(13): Show | 16 | HG00099.hp1 HG00741.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.24+11654C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92917389 | ||||||
| chr12:92917398
|
G | A | 7 | a0002c0004t0011g0205a0002c0004t0011g0206a0002c0004t0011g0207others(4): Show | 7 | HG00099.hp1 HG00741.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.24+11645C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92917398 | ||||||
| chr12:92917398
|
G | C | 4 | a0002c0004t0015g0198a0002c0004t0015g0203a0002c0004t0015g0213others(1): Show | 4 | HG02622.hp1 HG02809.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.24+11645C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92917398 | ||||||
| chr12:92917432
|
C | G | 6 | a0002c0004t0011g0205a0002c0004t0011g0206a0002c0004t0011g0207others(3): Show | 6 | HG00099.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.24+11611G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92917432 | ||||||
| chr12:92917501
|
A | G | 9 | a0001c0002t0009g0113a0001c0002t0009g0120a0001c0002t0009g0121others(6): Show | 9 | HG01256.hp2 HG01258.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.24+11542T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92917501 | ||||||
| chr12:92917545
|
G | A | 5 | a0001c0001t0005g0182a0001c0001t0005g0183a0001c0001t0005g0184others(2): Show | 5 | HG01346.hp1 HG02602.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.24+11498C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92917545 | ||||||
| chr12:92917619
|
A | G | 1 | a0004c0006t0021g0012 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.24+11424T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92917619 | ||||||
| chr12:92917890
|
A | C | 6 | a0001c0001t0001g0068a0001c0001t0001g0072a0001c0001t0013g0070others(3): Show | 6 | HG01069.hp1 HG01071.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.24+11153T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92917890 | ||||||
| chr12:92917901
|
T | C | 1 | a0002c0003t0004g0226 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.24+11142A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92917901 | ||||||
| chr12:92918078
|
C | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0081 | 2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.24+10965G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92918078 | ||||||
| chr12:92918084
|
G | C | 2 | a0002c0003t0004g0175a0002c0003t0004g0176 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.24+10959C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92918084 | ||||||
| chr12:92918117
|
G | A | 1 | a0002c0004t0048g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.24+10926C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92918117 | ||||||
| chr12:92918375
|
C | T | 1 | a0001c0002t0046g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.24+10668G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92918375 | ||||||
| chr12:92918415
|
G | C | 24 | a0001c0001t0005g0181a0001c0001t0005g0182a0001c0001t0005g0183others(21): Show | 24 | HG01109.hp2 HG01257.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.24+10628C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92918415 | ||||||
| chr12:92918508
|
C | T | 1 | a0001c0001t0005g0181 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.24+10535G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92918508 | ||||||
| chr12:92918613
|
T | C | 2 | a0001c0001t0001g0067a0001c0001t0001g0132 | 2 | HG01496.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.24+10430A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92918613 | ||||||
| chr12:92918705
|
G | C | 84 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(81): Show | 85 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.24+10338C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92918705 | ||||||
| chr12:92918808
|
C | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0111 | 2 | HG00741.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.24+10235G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92918808 | ||||||
| chr12:92918820
|
A | G | 1 | a0002c0004t0048g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.24+10223T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92918820 | ||||||
| chr12:92918848
|
G | C | 1 | a0002c0004t0048g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.24+10195C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92918848 | ||||||
| chr12:92918973
|
C | T | 50 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(47): Show | 51 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.24+10070G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92918973 | ||||||
| chr12:92919189
|
C | T | 7 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.24+9854G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92919189 | ||||||
| chr12:92919427
|
C | T | 1 | a0004c0006t0008g0002 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.24+9616G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92919427 | ||||||
| chr12:92919442
|
A | T | 1 | a0002c0003t0002g0169 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.24+9601T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92919442 | ||||||
| chr12:92919495
|
C | A | 1 | a0002c0003t0056g0178 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.24+9548G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92919495 | ||||||
| chr12:92919511
|
A | T | 1 | a0002c0003t0056g0178 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.24+9532T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92919511 | ||||||
| chr12:92919755
|
G | T | 1 | a0002c0004t0024g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.24+9288C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92919755 | ||||||
| chr12:92919795
|
G | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0112 | 2 | HG01261.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.24+9248C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92919795 | ||||||
| chr12:92919832
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.24+9211C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92919832 | ||||||
| chr12:92919853
|
G | T | 3 | a0001c0002t0003g0039a0001c0002t0007g0137a0002c0003t0016g0141 | 3 | HG01168.hp2 HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.24+9190C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92919853 | ||||||
| chr12:92919875
|
A | C | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.24+9168T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92919875 | ||||||
| chr12:92920075
|
C | G | 46 | a0001c0002t0009g0129a0001c0012t0006g0157a0002c0003t0002g0001others(43): Show | 47 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.24+8968G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92920075 | ||||||
| chr12:92920241
|
A | G | 42 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(39): Show | 43 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.24+8802T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92920241 | ||||||
| chr12:92920278
|
C | T | 23 | a0001c0002t0003g0023a0001c0002t0003g0024a0001c0002t0003g0025others(20): Show | 23 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.24+8765G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92920278 | ||||||
| chr12:92920333
|
T | C | 99 | a0001c0002t0039g0215a0001c0002t0040g0223a0001c0002t0046g0217others(96): Show | 100 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.24+8710A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92920333 | ||||||
| chr12:92920349
|
A | C | 1 | a0002c0004t0011g0205 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.24+8694T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92920349 | ||||||
| chr12:92920403
|
T | C | 1 | a0001c0002t0006g0195 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.24+8640A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92920403 | ||||||
| chr12:92920408
|
A | C | 9 | a0001c0001t0005g0052a0001c0001t0005g0053a0001c0002t0009g0133others(6): Show | 9 | HG01934.hp2 HG02109.hp1 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.24+8635T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92920408 | ||||||
| chr12:92920443
|
G | A | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.24+8600C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92920443 | ||||||
| chr12:92920468
|
GA | G | 14 | a0001c0002t0006g0042a0001c0002t0006g0044a0001c0002t0006g0191others(11): Show | 14 | HG01109.hp2 HG01257.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.24+8574delT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92920468 | ||||||
| chr12:92920489
|
A | C | 1 | a0001c0001t0023g0051 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.24+8554T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92920489 | ||||||
| chr12:92920579
|
C | T | 1 | a0001c0002t0006g0192 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.24+8464G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92920579 | ||||||
| chr12:92920614
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.24+8429A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92920614 | ||||||
| chr12:92920621
|
G | A | 1 | a0002c0004t0010g0230 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.24+8422C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92920621 | ||||||
| chr12:92920679
|
T | C | 1 | a0001c0002t0017g0115 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.24+8364A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92920679 | ||||||
| chr12:92920807
|
A | G | 2 | a0004c0006t0008g0002a0004c0006t0021g0012 | 2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.24+8236T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92920807 | ||||||
| chr12:92920820
|
A | C | 1 | a0002c0004t0048g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.24+8223T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92920820 | ||||||
| chr12:92920890
|
C | A | 1 | a0002c0003t0004g0170 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.24+8153G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92920890 | ||||||
| chr12:92921012
|
T | C | 16 | a0002c0003t0004g0147a0002c0003t0004g0151a0002c0003t0004g0152others(13): Show | 16 | HG00639.hp2 HG01167.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.24+8031A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92921012 | ||||||
| chr12:92921098
|
G | A | 1 | a0001c0010t0006g0221 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.24+7945C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92921098 | ||||||
| chr12:92921312
|
C | T | 2 | a0001c0001t0013g0138a0002c0004t0024g0046 | 2 | HG02717.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.24+7731G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92921312 | ||||||
| chr12:92921347
|
C | T | 21 | a0001c0002t0007g0048a0001c0002t0007g0116a0001c0002t0007g0117others(18): Show | 21 | HG00280.hp1 HG01071.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.24+7696G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92921347 | ||||||
| chr12:92921392
|
A | G | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.24+7651T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92921392 | ||||||
| chr12:92921439
|
A | G | 162 | a0001c0002t0003g0023a0001c0002t0003g0024a0001c0002t0003g0025others(159): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.24+7604T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92921439 | ||||||
| chr12:92921471
|
T | C | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.24+7572A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92921471 | ||||||
| chr12:92921516
|
G | A | 1 | a0001c0002t0007g0196 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.24+7527C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92921516 | ||||||
| chr12:92921750
|
A | T | 1 | a0002c0004t0048g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.24+7293T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92921750 | ||||||
| chr12:92921759
|
G | GA | 13 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0002t0003g0041others(10): Show | 13 | HG00738.hp1 HG01109.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.24+7283dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92921759 | ||||||
| chr12:92921759
|
GA | G | 43 | a0001c0001t0001g0091a0002c0003t0002g0001a0002c0003t0002g0013others(40): Show | 44 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.24+7283delT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92921759 | ||||||
| chr12:92921759
|
GAA | G | 8 | a0001c0012t0006g0157a0002c0004t0010g0229a0002c0004t0010g0230others(5): Show | 8 | HG01168.hp1 HG02451.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.24+7282_24+7283del others(2): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92921759 | ||||||
| chr12:92921803
|
G | T | 4 | a0002c0004t0014g0240a0002c0004t0014g0241a0002c0004t0014g0242others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.24+7240C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92921803 | ||||||
| chr12:92921866
|
C | CA | 29 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0108others(26): Show | 29 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.24+7176dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92921866 | ||||||
| chr12:92921866
|
CA | C | 90 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0002t0006g0042others(87): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.24+7176delT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92921866 | ||||||
| chr12:92921866
|
CAA | C | 5 | a0002c0003t0002g0224a0002c0004t0014g0240a0002c0004t0014g0241others(2): Show | 5 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.24+7175_24+7176del others(2): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92921866 | ||||||
| chr12:92921879
|
AAAAAAAA others(1): Show |
A | 10 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(7): Show | 10 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.24+7156_24+7163del others(8): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92921879 | ||||||
| chr12:92921880
|
A | G | 3 | a0002c0004t0014g0241a0002c0004t0014g0242a0002c0004t0014g0243 | 3 | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.24+7163T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92921880 | ||||||
| chr12:92921882
|
AAAAAGAA others(6): Show |
A | 1 | a0006c0009t0001g0086 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.24+7148_24+7160del others(13): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92921882 | ||||||
| chr12:92921883
|
AAAAGAAA others(18): Show |
A | 1 | a0001c0001t0001g0087 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.24+7135_24+7159del others(25): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92921883 | ||||||
| chr12:92921897
|
A | G | 1 | a0006c0009t0001g0086 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.24+7146T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92921897 | ||||||
| chr12:92922023
|
CT | C | 6 | a0001c0001t0001g0109a0001c0001t0001g0110a0002c0004t0014g0240others(3): Show | 6 | HG02895.hp1 HG02895.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.24+7019delA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92922023 | ||||||
| chr12:92922189
|
C | T | 3 | a0002c0004t0015g0198a0002c0004t0015g0203a0002c0004t0015g0213 | 3 | HG02622.hp1 HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.24+6854G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92922189 | ||||||
| chr12:92922201
|
G | A | 1 | a0001c0002t0044g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.24+6842C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92922201 | ||||||
| chr12:92922319
|
C | T | 1 | a0002c0004t0031g0199 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.24+6724G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92922319 | ||||||
| chr12:92922357
|
T | C | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.24+6686A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92922357 | ||||||
| chr12:92922728
|
G | A | 1 | a0002c0004t0014g0240 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.24+6315C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92922728 | ||||||
| chr12:92922959
|
A | AAAAAT | 67 | a0001c0001t0001g0049a0001c0001t0001g0054a0001c0001t0001g0055others(64): Show | 67 | HG00099.hp1 HG00639.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.24+6079_24+6083dup others(5): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92922959 | ||||||
| chr12:92922959
|
A | AAAAATAA others(3): Show |
14 | a0001c0001t0001g0087a0001c0002t0006g0042a0001c0002t0006g0044others(11): Show | 14 | HG01109.hp2 HG02109.hp1 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.24+6074_24+6083dup others(10): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92922959 | ||||||
| chr12:92922959
|
A | AAAAATAA others(8): Show |
8 | a0002c0004t0015g0198a0002c0004t0015g0203a0002c0004t0015g0213others(5): Show | 8 | HG02055.hp1 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.24+6069_24+6083dup others(15): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92922959 | ||||||
| chr12:92922959
|
A | AAAAATAA others(13): Show |
4 | a0002c0004t0010g0231a0002c0004t0010g0232a0002c0004t0010g0234others(1): Show | 4 | HG02451.hp1 HG03139.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.24+6064_24+6083dup others(20): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92922959 | ||||||
| chr12:92922959
|
A | AAAAATAA others(18): Show |
5 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0235others(2): Show | 5 | HG02572.hp2 HG02922.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.24+6059_24+6083dup others(25): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92922959 | ||||||
| chr12:92922959
|
AAAAAT | A | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.24+6079_24+6083del others(5): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92922959 | ||||||
| chr12:92922959
|
AAAAATAA others(3): Show |
A | 1 | a0001c0002t0003g0023 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.24+6074_24+6083del others(10): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92922959 | ||||||
| chr12:92923070
|
G | A | 25 | a0001c0002t0003g0023a0001c0002t0003g0024a0001c0002t0003g0025others(22): Show | 25 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.24+5973C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92923070 | ||||||
| chr12:92923143
|
C | T | 1 | a0002c0004t0024g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.24+5900G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92923143 | ||||||
| chr12:92923203
|
C | T | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.24+5840G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92923203 | ||||||
| chr12:92923221
|
G | A | 1 | a0002c0003t0004g0147 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.24+5822C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92923221 | ||||||
| chr12:92923448
|
A | G | 1 | a0001c0012t0006g0157 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.24+5595T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92923448 | ||||||
| chr12:92923562
|
T | A | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.24+5481A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92923562 | ||||||
| chr12:92923596
|
G | A | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.24+5447C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92923596 | ||||||
| chr12:92923635
|
T | C | 1 | a0001c0001t0053g0083 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.24+5408A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92923635 | ||||||
| chr12:92923845
|
C | CA | 19 | a0001c0001t0005g0181a0001c0001t0005g0183a0001c0001t0049g0018others(16): Show | 19 | HG01109.hp2 HG01257.hp2 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.24+5197dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92923845 | ||||||
| chr12:92923845
|
CA | C | 26 | a0001c0002t0007g0048a0001c0002t0007g0116a0001c0002t0007g0117others(23): Show | 26 | HG00280.hp1 HG01071.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.24+5197delT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92923845 | ||||||
| chr12:92923846
|
A | C | 1 | a0001c0001t0005g0085 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.24+5197T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92923846 | ||||||
| chr12:92924059
|
G | A | 1 | a0001c0002t0044g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.24+4984C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92924059 | ||||||
| chr12:92924201
|
C | CT | 25 | a0001c0001t0001g0084a0001c0001t0001g0134a0001c0001t0005g0183others(22): Show | 25 | HG01106.hp1 HG01175.hp2 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.24+4841dupA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92924201 | ||||||
| chr12:92924201
|
CT | C | 12 | a0001c0001t0001g0082a0002c0004t0014g0240a0002c0004t0014g0241others(9): Show | 12 | HG00642.hp1 HG00738.hp1 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.24+4841delA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92924201 | ||||||
| chr12:92924248
|
C | T | 3 | a0002c0003t0004g0151a0002c0003t0004g0152a0002c0003t0055g0150 | 3 | HG01884.hp1 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.24+4795G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92924248 | ||||||
| chr12:92924369
|
A | C | 1 | a0001c0001t0053g0083 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.24+4674T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92924369 | ||||||
| chr12:92924398
|
G | A | 14 | a0001c0002t0006g0042a0001c0002t0006g0044a0001c0002t0006g0191others(11): Show | 14 | HG01109.hp2 HG01257.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.24+4645C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92924398 | ||||||
| chr12:92924499
|
G | A | 2 | a0001c0002t0019g0127a0001c0002t0019g0128 | 2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.24+4544C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92924499 | ||||||
| chr12:92924502
|
C | G | 2 | a0002c0004t0024g0046a0002c0004t0048g0017 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.24+4541G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92924502 | ||||||
| chr12:92924562
|
A | G | 1 | a0001c0002t0007g0137 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.24+4481T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92924562 | ||||||
| chr12:92924643
|
C | T | 1 | a0001c0001t0005g0182 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.24+4400G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92924643 | ||||||
| chr12:92924840
|
T | TA | 8 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0135others(5): Show | 8 | HG00741.hp1 HG01109.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.24+4202dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92924840 | ||||||
| chr12:92924840
|
TA | T | 94 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.24+4202delT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92924840 | ||||||
| chr12:92924840
|
TAA | T | 36 | a0001c0001t0001g0049a0001c0001t0005g0181a0001c0001t0013g0138others(33): Show | 36 | HG00140.hp2 HG00280.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.24+4201_24+4202del others(2): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92924840 | ||||||
| chr12:92924840
|
TAAA | T | 41 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(38): Show | 42 | HG00099.hp2 HG01167.hp1 HG01168.hp1 others(39): Show |
intron_variant | MODIFIER | c.24+4200_24+4202del others(3): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92924840 | ||||||
| chr12:92924841
|
A | T | 1 | a0002c0004t0031g0199 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.24+4202T>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92924841 | ||||||
| chr12:92925032
|
T | C | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.24+4011A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92925032 | ||||||
| chr12:92925181
|
C | CA | 66 | a0001c0001t0001g0132a0001c0001t0001g0134a0001c0001t0001g0135others(63): Show | 66 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.24+3861dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92925181 | ||||||
| chr12:92925181
|
C | CAA | 41 | a0001c0002t0009g0136a0001c0002t0026g0212a0001c0002t0032g0045others(38): Show | 41 | HG00099.hp1 HG00738.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.24+3860_24+3861dup others(2): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92925181 | ||||||
| chr12:92925181
|
C | CAAA | 10 | a0001c0002t0039g0215a0001c0002t0040g0223a0001c0002t0046g0217others(7): Show | 10 | HG02109.hp1 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.24+3859_24+3861dup others(3): Show |
EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92925181 | ||||||
| chr12:92925181
|
CA | C | 6 | a0002c0003t0002g0149a0002c0008t0012g0014a0002c0008t0012g0015others(3): Show | 6 | HG01243.hp2 HG01934.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.24+3861delT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92925181 | ||||||
| chr12:92925426
|
A | C | 1 | a0001c0001t0001g0047 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.24+3617T>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92925426 | ||||||
| chr12:92925811
|
T | C | 1 | a0001c0002t0007g0137 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.24+3232A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92925811 | ||||||
| chr12:92925851
|
C | G | 139 | a0001c0002t0003g0023a0001c0002t0003g0024a0001c0002t0003g0025others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.24+3192G>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92925851 | ||||||
| chr12:92925935
|
A | G | 1 | a0002c0003t0002g0148 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.24+3108T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92925935 | ||||||
| chr12:92925993
|
T | A | 1 | a0001c0002t0044g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.24+3050A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92925993 | ||||||
| chr12:92925995
|
A | AT | 7 | a0001c0001t0049g0018a0001c0002t0039g0215a0001c0002t0047g0187others(4): Show | 7 | HG00642.hp1 HG01257.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.24+3047dupA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92925995 | ||||||
| chr12:92925995
|
AT | A | 7 | a0001c0001t0013g0138a0002c0004t0014g0243a0002c0008t0012g0014others(4): Show | 7 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.24+3047delA | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92925995 | ||||||
| chr12:92926015
|
C | T | 1 | a0002c0004t0048g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.24+3028G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92926015 | ||||||
| chr12:92926353
|
A | G | 1 | a0002c0017t0034g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.24+2690T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92926353 | ||||||
| chr12:92926478
|
G | C | 1 | a0001c0002t0044g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.24+2565C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92926478 | ||||||
| chr12:92926748
|
C | T | 1 | a0001c0001t0005g0225 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.24+2295G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92926748 | ||||||
| chr12:92926813
|
GC | G | 5 | a0002c0008t0012g0014a0002c0008t0012g0015a0002c0008t0012g0236others(2): Show | 5 | HG01243.hp2 HG02109.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.24+2229delG | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92926813 | ||||||
| chr12:92926894
|
A | G | 1 | a0002c0003t0002g0144 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.24+2149T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92926894 | ||||||
| chr12:92926898
|
C | T | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.24+2145G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92926898 | ||||||
| chr12:92927068
|
GA | G | 3 | a0002c0003t0016g0141a0002c0003t0016g0142a0002c0003t0016g0143 | 3 | HG02818.hp1 HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.24+1974delT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92927068 | ||||||
| chr12:92927410
|
T | C | 9 | a0001c0002t0039g0215a0001c0002t0040g0223a0001c0002t0046g0217others(6): Show | 9 | HG02109.hp1 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.24+1633A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92927410 | ||||||
| chr12:92927446
|
G | C | 1 | a0001c0002t0036g0140 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.24+1597C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92927446 | ||||||
| chr12:92927769
|
T | C | 45 | a0001c0012t0006g0157a0002c0003t0002g0001a0002c0003t0002g0013others(42): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.24+1274A>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92927769 | ||||||
| chr12:92927861
|
G | C | 7 | a0001c0001t0005g0181a0001c0001t0005g0182a0001c0001t0005g0183others(4): Show | 7 | HG01346.hp1 HG02602.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.24+1182C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92927861 | ||||||
| chr12:92927952
|
G | T | 11 | a0004c0006t0008g0002a0004c0006t0008g0006a0004c0006t0008g0007others(8): Show | 11 | HG00738.hp1 HG02723.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.24+1091C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92927952 | ||||||
| chr12:92928143
|
G | T | 1 | a0002c0003t0002g0013 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.24+900C>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92928143 | ||||||
| chr12:92928162
|
C | CA | 40 | a0001c0001t0001g0214a0001c0001t0005g0225a0001c0002t0006g0191others(37): Show | 40 | HG00099.hp1 HG00280.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.24+880dupT | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92928162 | ||||||
| chr12:92928257
|
T | A | 1 | a0002c0003t0004g0226 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.24+786A>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92928257 | ||||||
| chr12:92928368
|
G | A | 1 | a0002c0003t0004g0227 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.24+675C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92928368 | ||||||
| chr12:92928583
|
G | C | 7 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.24+460C>G | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92928583 | ||||||
| chr12:92928584
|
C | T | 7 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.24+459G>A | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92928584 | ||||||
| chr12:92928585
|
A | G | 242 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0054others(239): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.24+458T>C | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92928585 | ||||||
| chr12:92928741
|
G | A | 7 | a0002c0004t0010g0229a0002c0004t0010g0230a0002c0004t0010g0231others(4): Show | 7 | HG02451.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.24+302C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92928741 | ||||||
| chr12:92928926
|
G | A | 3 | a0002c0008t0012g0236a0002c0008t0012g0237a0002c0008t0012g0238 | 3 | HG01243.hp2 HG02109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.24+117C>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92928926 | ||||||
| chr12:92928954
|
C | A | 1 | a0003c0005t0003g0239 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.24+89G>T | EEA1 | ENSG00000102189.17 | transcript | ENST00000322349.13 | protein_coding | 1/28 | chr12 | 92928954 |