| geneid | 2009 |
|---|---|
| ensemblid | ENSG00000066629.19 |
| hgncid | 3330 |
| symbol | EML1 |
| name | EMAP like 1 |
| refseq_nuc | NM_004434.3 |
| refseq_prot | NP_004425.2 |
| ensembl_nuc | ENST00000262233.11 |
| ensembl_prot | ENSP00000262233.7 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 99793413 |
| end | 99942060 |
| strand | + |
| ver | v1.2 |
| region | chr14:99793413-99942060 |
| region5000 | chr14:99788413-99947060 |
| regionname0 | EML1_chr14_99793413_99942060 |
| regionname5000 | EML1_chr14_99788413_99947060 |
| 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 | 815 | 120 | 72 | 18 | 16 | 7 | 7 | 9 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0002 | 1/1 | 815 | 86 | 4 | 21 | 48 | 2 | 9 | 34 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0003 | 0/0 | 815 | 77 | 8 | 19 | 43 | 1 | 6 | 32 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0004 | 0/0 | 815 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0005 | 0/0 | 815 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0006 | 0/0 | 815 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0007 | 0/0 | 815 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2448 | 82 | 4 | 18 | 47 | 2 | 9 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| c0002 | 0/0 | 2448 | 73 | 5 | 18 | 43 | 1 | 6 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| c0003 | 0/0 | 2448 | 66 | 50 | 7 | 3 | 4 | 2 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| c0004 | 0/0 | 2448 | 42 | 12 | 9 | 13 | 3 | 5 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| c0005 | 0/0 | 2448 | 9 | 8 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| c0006 | 0/0 | 2448 | 4 | 0 | 3 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| c0007 | 0/0 | 2448 | 2 | 2 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| c0008 | 0/0 | 2448 | 2 | 2 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| c0009 | 0/0 | 2448 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| c0010 | 0/0 | 2448 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| c0011 | 0/0 | 2448 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| c0012 | 0/0 | 2448 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| c0013 | 0/0 | 2448 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| c0014 | 0/0 | 2448 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| c0015 | 0/0 | 2448 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| c0016 | 0/0 | 2448 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| 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 | 2013 | 112 | 50 | 17 | 33 | 5 | 7 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| t0002 | 1/1 | 2013 | 81 | 7 | 23 | 40 | 0 | 9 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| t0003 | 0/0 | 2013 | 52 | 4 | 13 | 25 | 4 | 6 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| t0004 | 0/0 | 1994 | 9 | 6 | 0 | 3 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| t0005 | 0/0 | 2013 | 8 | 8 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| t0006 | 0/0 | 2013 | 6 | 0 | 4 | 2 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| t0007 | 0/0 | 2013 | 3 | 3 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| t0008 | 0/0 | 1994 | 3 | 3 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| t0009 | 0/0 | 2013 | 2 | 2 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| t0010 | 0/0 | 2013 | 2 | 1 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| t0011 | 0/0 | 2013 | 2 | 0 | 0 | 2 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| t0012 | 0/0 | 2013 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| t0013 | 0/0 | 2013 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| t0014 | 0/0 | 2013 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| t0015 | 0/0 | 2013 | 1 | 0 | 0 | 0 | 1 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| t0016 | 0/0 | 2013 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| t0017 | 0/0 | 2013 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| t0018 | 0/0 | 1994 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| t0019 | 0/0 | 2013 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0051 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0071 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0003 | 0/0 | 2448 | 66 | 50 | 7 | 3 | 4 | 2 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0001c0004 | 0/0 | 2448 | 42 | 12 | 9 | 13 | 3 | 5 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0001c0005 | 0/0 | 2448 | 9 | 8 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0001c0007 | 0/0 | 2448 | 2 | 2 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0001c0013 | 0/0 | 2448 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0002c0001 | 1/1 | 2448 | 82 | 4 | 18 | 47 | 2 | 9 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0002c0006 | 0/0 | 2448 | 4 | 0 | 3 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0003c0002 | 0/0 | 2448 | 73 | 5 | 18 | 43 | 1 | 6 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0003c0010 | 0/0 | 2448 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0003c0014 | 0/0 | 2448 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0003c0015 | 0/0 | 2448 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0003c0016 | 0/0 | 2448 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0004c0008 | 0/0 | 2448 | 2 | 2 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0005c0009 | 0/0 | 2448 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0006c0011 | 0/0 | 2448 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0007c0012 | 0/0 | 2448 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0003t0001 | 0/0 | 4460 | 45 | 37 | 4 | 0 | 3 | 1 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0001c0003t0002 | 0/0 | 4460 | 5 | 3 | 2 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0001c0003t0003 | 0/0 | 4460 | 6 | 3 | 1 | 0 | 1 | 1 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0001c0003t0004 | 0/0 | 4441 | 3 | 0 | 0 | 3 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0001c0003t0005 | 0/0 | 4460 | 2 | 2 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0001c0003t0007 | 0/0 | 4460 | 3 | 3 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0001c0003t0008 | 0/0 | 4441 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0001c0003t0009 | 0/0 | 4460 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0001c0004t0001 | 0/0 | 4460 | 9 | 5 | 0 | 3 | 1 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0001c0004t0002 | 0/0 | 4460 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0001c0004t0003 | 0/0 | 4460 | 25 | 1 | 9 | 9 | 2 | 4 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0001c0004t0004 | 0/0 | 4441 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0001c0004t0005 | 0/0 | 4460 | 3 | 3 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0001c0004t0010 | 0/0 | 4460 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0001c0004t0011 | 0/0 | 4460 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0001c0004t0013 | 0/0 | 4460 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0001c0005t0001 | 0/0 | 4460 | 2 | 1 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0001c0005t0004 | 0/0 | 4441 | 2 | 2 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0001c0005t0005 | 0/0 | 4460 | 3 | 3 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0001c0005t0008 | 0/0 | 4441 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0001c0005t0009 | 0/0 | 4460 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0001c0007t0002 | 0/0 | 4460 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0001c0007t0018 | 0/0 | 4441 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0001c0013t0001 | 0/0 | 4460 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0002c0001t0001 | 0/0 | 4460 | 6 | 1 | 0 | 4 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0002c0001t0002 | 1/1 | 4460 | 63 | 2 | 17 | 35 | 0 | 7 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0002c0001t0003 | 0/0 | 4460 | 11 | 0 | 1 | 8 | 1 | 1 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0002c0001t0015 | 0/0 | 4460 | 1 | 0 | 0 | 0 | 1 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0002c0001t0019 | 0/0 | 4460 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0002c0006t0002 | 0/0 | 4460 | 2 | 0 | 2 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0002c0006t0003 | 0/0 | 4460 | 2 | 0 | 1 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0003c0002t0001 | 0/0 | 4460 | 47 | 4 | 11 | 26 | 1 | 5 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0003c0002t0002 | 0/0 | 4460 | 7 | 0 | 2 | 4 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0003c0002t0003 | 0/0 | 4460 | 8 | 0 | 1 | 7 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0003c0002t0006 | 0/0 | 4460 | 5 | 0 | 3 | 2 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0003c0002t0008 | 0/0 | 4441 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0003c0002t0010 | 0/0 | 4460 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0003c0002t0011 | 0/0 | 4460 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0003c0002t0012 | 0/0 | 4460 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0003c0002t0016 | 0/0 | 4460 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0003c0002t0017 | 0/0 | 4460 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0003c0010t0006 | 0/0 | 4460 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0003c0014t0004 | 0/0 | 4441 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0003c0015t0001 | 0/0 | 4460 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0003c0016t0014 | 0/0 | 4460 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0004c0008t0004 | 0/0 | 4441 | 2 | 2 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0005c0009t0002 | 0/0 | 4460 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0006c0011t0001 | 0/0 | 4460 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| a0007c0012t0002 | 0/0 | 4460 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | copy fasta | chr14 | 99788413 | 99947060 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0003t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0003g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0005g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0007g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0007g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0008g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0003t0009g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0003g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0010g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0011g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0004t0013g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0005t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0005t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0005t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0005t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0005t0005g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0005t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0005t0005g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0005t0008g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0005t0009g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0007t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0007t0018g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0001c0013t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0051 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0071 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0015g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0001t0019g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0006t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0006t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0006t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0002c0006t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0006g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0006g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0006g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0006g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0006g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0008g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0010g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0011g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0012g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0016g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0002t0017g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0010t0006g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0014t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0015t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0003c0016t0014g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0004c0008t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0004c0008t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0005c0009t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0006c0011t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| a0007c0012t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0004 | t0001 | g0115 | EUR | GBR | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG00140 | hp2 | a0001 | c0003 | t0003 | g0277 | EUR | GBR | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG00323 | hp1 | a0002 | c0001 | t0003 | g0142 | EUR | FIN | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG00323 | hp2 | a0001 | c0003 | t0001 | g0193 | EUR | FIN | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG00408 | hp1 | a0002 | c0001 | t0003 | g0139 | EAS | CHS | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG00408 | hp2 | a0003 | c0002 | t0001 | g0070 | EAS | CHS | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG00423 | hp1 | a0003 | c0002 | t0003 | g0212 | EAS | CHS | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG00423 | hp2 | a0002 | c0001 | t0002 | g0067 | EAS | CHS | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG00438 | hp1 | a0003 | c0002 | t0001 | g0262 | EAS | CHS | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG00438 | hp2 | a0002 | c0001 | t0002 | g0084 | EAS | CHS | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG00544 | hp1 | a0003 | c0002 | t0002 | g0138 | EAS | CHS | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG00544 | hp2 | a0002 | c0001 | t0002 | g0081 | EAS | CHS | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG00558 | hp1 | a0002 | c0001 | t0002 | g0093 | EAS | CHS | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG00558 | hp2 | a0003 | c0002 | t0001 | g0187 | EAS | CHS | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG00609 | hp1 | a0001 | c0004 | t0003 | g0048 | EAS | CHS | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG00609 | hp2 | a0001 | c0003 | t0004 | g0258 | EAS | CHS | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG00621 | hp1 | a0002 | c0001 | t0002 | g0099 | EAS | CHS | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG00621 | hp2 | a0003 | c0002 | t0010 | g0200 | EAS | CHS | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG00639 | hp1 | a0003 | c0002 | t0001 | g0002 | AMR | PUR | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG00639 | hp2 | a0001 | c0005 | t0001 | g0250 | AMR | PUR | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG00642 | hp1 | a0003 | c0002 | t0001 | g0002 | AMR | PUR | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG00642 | hp2 | a0002 | c0001 | t0002 | g0153 | AMR | PUR | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG00733 | hp1 | a0001 | c0003 | t0002 | g0252 | AMR | PUR | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG00733 | hp2 | a0002 | c0001 | t0002 | g0045 | AMR | PUR | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG00735 | hp1 | a0002 | c0001 | t0002 | g0031 | AMR | PUR | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG00735 | hp2 | a0003 | c0002 | t0003 | g0125 | AMR | PUR | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01069 | hp1 | a0001 | c0004 | t0003 | g0257 | AMR | PUR | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01069 | hp2 | a0001 | c0003 | t0001 | g0041 | AMR | PUR | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01071 | hp1 | a0001 | c0004 | t0003 | g0256 | AMR | PUR | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01071 | hp2 | a0002 | c0001 | t0002 | g0278 | AMR | PUR | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01074 | hp1 | a0001 | c0003 | t0003 | g0279 | AMR | PUR | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01074 | hp2 | a0002 | c0001 | t0002 | g0058 | AMR | PUR | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01081 | hp1 | a0003 | c0002 | t0001 | g0191 | AMR | PUR | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01081 | hp2 | a0002 | c0001 | t0002 | g0089 | AMR | PUR | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01109 | hp1 | a0003 | c0002 | t0006 | g0042 | AMR | PUR | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01109 | hp2 | a0001 | c0003 | t0001 | g0233 | AMR | PUR | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01168 | hp1 | a0002 | c0006 | t0002 | g0148 | AMR | PUR | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01168 | hp2 | a0002 | c0001 | t0002 | g0110 | AMR | PUR | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01169 | hp1 | a0002 | c0006 | t0002 | g0128 | AMR | PUR | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01169 | hp2 | a0002 | c0001 | t0002 | g0129 | AMR | PUR | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01175 | hp1 | a0003 | c0002 | t0001 | g0192 | AMR | PUR | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01175 | hp2 | a0002 | c0001 | t0002 | g0118 | AMR | PUR | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01192 | hp1 | a0003 | c0002 | t0001 | g0218 | AMR | PUR | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01192 | hp2 | a0003 | c0002 | t0001 | g0087 | AMR | PUR | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01243 | hp1 | a0001 | c0013 | t0001 | g0126 | AMR | PUR | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01243 | hp2 | a0002 | c0001 | t0002 | g0026 | AMR | PUR | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01255 | hp1 | a0002 | c0001 | t0002 | g0182 | AMR | CLM | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01255 | hp2 | a0003 | c0002 | t0001 | g0044 | AMR | CLM | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01256 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | CLM | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01256 | hp2 | a0001 | c0004 | t0003 | g0103 | AMR | CLM | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01258 | hp1 | a0001 | c0004 | t0003 | g0075 | AMR | CLM | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01258 | hp2 | a0001 | c0003 | t0001 | g0001 | AMR | CLM | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01261 | hp1 | a0001 | c0003 | t0002 | g0181 | AMR | CLM | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01261 | hp2 | a0002 | c0006 | t0003 | g0076 | AMR | CLM | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01346 | hp1 | a0002 | c0001 | t0002 | g0102 | AMR | CLM | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01346 | hp2 | a0001 | c0004 | t0003 | g0090 | AMR | CLM | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01433 | hp1 | a0003 | c0002 | t0001 | g0190 | AMR | CLM | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01433 | hp2 | a0001 | c0004 | t0003 | g0074 | AMR | CLM | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01496 | hp1 | a0001 | c0004 | t0003 | g0030 | AMR | CLM | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01496 | hp2 | a0003 | c0002 | t0001 | g0054 | AMR | CLM | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01515 | hp1 | a0002 | c0001 | t0015 | g0109 | EUR | IBS | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01515 | hp2 | a0001 | c0003 | t0001 | g0120 | EUR | IBS | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01884 | hp1 | a0002 | c0001 | t0001 | g0239 | AFR | ACB | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01884 | hp2 | a0003 | c0015 | t0001 | g0013 | AFR | ACB | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01928 | hp1 | a0002 | c0001 | t0002 | g0176 | AMR | PEL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01928 | hp2 | a0003 | c0002 | t0006 | g0088 | AMR | PEL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01943 | hp1 | a0003 | c0002 | t0001 | g0209 | AMR | PEL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01943 | hp2 | a0002 | c0001 | t0002 | g0101 | AMR | PEL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01975 | hp1 | a0001 | c0004 | t0003 | g0064 | AMR | PEL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01975 | hp2 | a0002 | c0001 | t0002 | g0063 | AMR | PEL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01981 | hp1 | a0003 | c0002 | t0017 | g0028 | AMR | PEL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01981 | hp2 | a0003 | c0002 | t0001 | g0055 | AMR | PEL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02004 | hp1 | a0003 | c0002 | t0006 | g0043 | AMR | PEL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02004 | hp2 | a0003 | c0002 | t0002 | g0222 | AMR | PEL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02015 | hp1 | a0002 | c0001 | t0002 | g0276 | EAS | KHV | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02015 | hp2 | a0003 | c0002 | t0011 | g0024 | EAS | KHV | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02040 | hp1 | a0003 | c0002 | t0003 | g0230 | EAS | KHV | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02040 | hp2 | a0002 | c0001 | t0003 | g0119 | EAS | KHV | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02055 | hp1 | a0001 | c0004 | t0013 | g0108 | AFR | ACB | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02055 | hp2 | a0004 | c0008 | t0004 | g0268 | AFR | ACB | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02071 | hp1 | a0003 | c0002 | t0001 | g0194 | EAS | KHV | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02071 | hp2 | a0002 | c0001 | t0003 | g0137 | EAS | KHV | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02074 | hp1 | a0002 | c0001 | t0003 | g0236 | EAS | KHV | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02074 | hp2 | a0001 | c0004 | t0001 | g0091 | EAS | KHV | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02083 | hp1 | a0001 | c0004 | t0011 | g0156 | EAS | KHV | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02083 | hp2 | a0001 | c0003 | t0004 | g0027 | EAS | KHV | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02132 | hp1 | a0002 | c0001 | t0002 | g0038 | EAS | KHV | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02132 | hp2 | a0001 | c0004 | t0003 | g0127 | EAS | KHV | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02145 | hp1 | a0002 | c0001 | t0002 | g0066 | AFR | ACB | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02145 | hp2 | a0001 | c0007 | t0002 | g0005 | AFR | ACB | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02155 | hp1 | a0003 | c0002 | t0003 | g0155 | EAS | CDX | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02155 | hp2 | a0002 | c0006 | t0003 | g0229 | EAS | CDX | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02257 | hp1 | a0003 | c0016 | t0014 | g0060 | AFR | ACB | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02257 | hp2 | a0001 | c0004 | t0004 | g0017 | AFR | ACB | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02273 | hp1 | a0003 | c0002 | t0002 | g0050 | AMR | PEL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02273 | hp2 | a0003 | c0010 | t0006 | g0226 | AMR | PEL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02280 | hp1 | a0001 | c0004 | t0005 | g0266 | AFR | ACB | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0012 | AFR | ACB | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02293 | hp1 | a0002 | c0001 | t0002 | g0046 | AMR | PEL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02293 | hp2 | a0001 | c0004 | t0003 | g0197 | AMR | PEL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02451 | hp1 | a0001 | c0005 | t0005 | g0003 | AFR | ACB | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02451 | hp2 | a0001 | c0004 | t0001 | g0255 | AFR | ACB | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02523 | hp1 | a0002 | c0001 | t0002 | g0157 | EAS | KHV | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02523 | hp2 | a0001 | c0004 | t0003 | g0022 | EAS | KHV | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02572 | hp1 | a0001 | c0003 | t0001 | g0158 | AFR | GWD | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02572 | hp2 | a0003 | c0002 | t0001 | g0215 | AFR | GWD | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02602 | hp1 | a0003 | c0002 | t0001 | g0036 | SAS | PJL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02602 | hp2 | a0002 | c0001 | t0002 | g0164 | SAS | PJL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02615 | hp1 | a0004 | c0008 | t0004 | g0004 | AFR | GWD | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02615 | hp2 | a0001 | c0003 | t0007 | g0281 | AFR | GWD | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02622 | hp1 | a0001 | c0004 | t0005 | g0249 | AFR | GWD | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02622 | hp2 | a0001 | c0005 | t0005 | g0265 | AFR | GWD | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02630 | hp1 | a0001 | c0003 | t0001 | g0114 | AFR | GWD | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02630 | hp2 | a0001 | c0003 | t0002 | g0106 | AFR | GWD | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02698 | hp1 | a0002 | c0001 | t0002 | g0025 | SAS | PJL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02698 | hp2 | a0001 | c0003 | t0001 | g0152 | SAS | PJL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02717 | hp1 | a0001 | c0003 | t0008 | g0271 | AFR | GWD | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0086 | AFR | GWD | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0006 | AFR | GWD | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02723 | hp2 | a0001 | c0003 | t0002 | g0116 | AFR | GWD | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0225 | AFR | GWD | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02809 | hp2 | a0001 | c0005 | t0009 | g0078 | AFR | GWD | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02818 | hp1 | a0001 | c0003 | t0001 | g0168 | AFR | GWD | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02818 | hp2 | a0001 | c0007 | t0018 | g0241 | AFR | GWD | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0282 | AFR | GWD | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02886 | hp2 | a0001 | c0003 | t0001 | g0080 | AFR | GWD | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0163 | AFR | GWD | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02895 | hp2 | a0001 | c0003 | t0003 | g0033 | AFR | GWD | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02896 | hp1 | a0001 | c0003 | t0003 | g0034 | AFR | GWD | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02896 | hp2 | a0001 | c0003 | t0005 | g0247 | AFR | GWD | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02897 | hp1 | a0001 | c0003 | t0005 | g0246 | AFR | GWD | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02897 | hp2 | a0001 | c0003 | t0003 | g0032 | AFR | GWD | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0243 | AFR | ESN | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02922 | hp2 | a0001 | c0005 | t0008 | g0077 | AFR | ESN | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0274 | AFR | ESN | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02965 | hp2 | a0006 | c0011 | t0001 | g0011 | AFR | ESN | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02970 | hp1 | a0001 | c0005 | t0005 | g0097 | AFR | ESN | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02970 | hp2 | a0001 | c0004 | t0001 | g0143 | AFR | ESN | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02976 | hp1 | a0003 | c0002 | t0001 | g0237 | AFR | ESN | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02976 | hp2 | a0001 | c0003 | t0001 | g0113 | AFR | ESN | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0015 | AFR | GWD | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03041 | hp2 | a0001 | c0003 | t0002 | g0105 | AFR | GWD | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03098 | hp1 | a0001 | c0003 | t0001 | g0007 | AFR | MSL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0112 | AFR | MSL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03130 | hp1 | a0001 | c0005 | t0004 | g0285 | AFR | ESN | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03130 | hp2 | a0001 | c0004 | t0010 | g0235 | AFR | ESN | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0240 | AFR | ESN | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0244 | AFR | ESN | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03209 | hp1 | a0001 | c0004 | t0005 | g0242 | AFR | MSL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03209 | hp2 | a0003 | c0002 | t0008 | g0238 | AFR | MSL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03225 | hp1 | a0001 | c0003 | t0001 | g0259 | AFR | MSL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03225 | hp2 | a0001 | c0004 | t0001 | g0009 | AFR | MSL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03239 | hp1 | a0001 | c0004 | t0002 | g0047 | SAS | PJL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03239 | hp2 | a0002 | c0001 | t0002 | g0133 | SAS | PJL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03453 | hp1 | a0001 | c0003 | t0007 | g0014 | AFR | MSL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03453 | hp2 | a0001 | c0003 | t0001 | g0286 | AFR | MSL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03492 | hp1 | a0003 | c0002 | t0001 | g0198 | SAS | PJL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03492 | hp2 | a0003 | c0002 | t0001 | g0104 | SAS | PJL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0221 | AFR | ESN | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03516 | hp2 | a0001 | c0003 | t0009 | g0251 | AFR | ESN | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03540 | hp1 | a0001 | c0004 | t0001 | g0123 | AFR | GWD | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0283 | AFR | GWD | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03579 | hp1 | a0001 | c0004 | t0001 | g0248 | AFR | MSL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03579 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | MSL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03654 | hp1 | a0002 | c0001 | t0002 | g0227 | SAS | PJL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03654 | hp2 | a0001 | c0004 | t0003 | g0131 | SAS | PJL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03704 | hp1 | a0003 | c0002 | t0002 | g0231 | SAS | PJL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03704 | hp2 | a0002 | c0001 | t0002 | g0083 | SAS | PJL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03834 | hp1 | a0001 | c0004 | t0003 | g0059 | SAS | BEB | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03834 | hp2 | a0001 | c0004 | t0003 | g0035 | SAS | BEB | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03927 | hp1 | a0003 | c0002 | t0001 | g0124 | SAS | BEB | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03927 | hp2 | a0002 | c0001 | t0002 | g0174 | SAS | BEB | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG04115 | hp1 | a0001 | c0003 | t0003 | g0184 | SAS | STU | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG04115 | hp2 | a0002 | c0001 | t0001 | g0092 | SAS | STU | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG04204 | hp1 | a0003 | c0002 | t0001 | g0107 | SAS | STU | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG04204 | hp2 | a0001 | c0004 | t0003 | g0195 | SAS | STU | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18522 | hp1 | a0003 | c0014 | t0004 | g0254 | AFR | YRI | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18522 | hp2 | a0001 | c0003 | t0007 | g0117 | AFR | YRI | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18747 | hp1 | a0003 | c0002 | t0001 | g0094 | EAS | CHB | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18747 | hp2 | a0002 | c0001 | t0002 | g0039 | EAS | CHB | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0008 | AFR | YRI | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18906 | hp2 | a0001 | c0003 | t0001 | g0269 | AFR | YRI | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18939 | hp1 | a0002 | c0001 | t0002 | g0150 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18939 | hp2 | a0001 | c0004 | t0001 | g0040 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18947 | hp1 | a0003 | c0002 | t0001 | g0213 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18947 | hp2 | a0002 | c0001 | t0002 | g0082 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18951 | hp1 | a0003 | c0002 | t0002 | g0203 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18951 | hp2 | a0002 | c0001 | t0002 | g0136 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18952 | hp1 | a0001 | c0003 | t0004 | g0141 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18952 | hp2 | a0003 | c0002 | t0001 | g0186 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18953 | hp1 | a0002 | c0001 | t0002 | g0056 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18953 | hp2 | a0001 | c0004 | t0003 | g0206 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18954 | hp1 | a0002 | c0001 | t0002 | g0160 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18954 | hp2 | a0003 | c0002 | t0001 | g0161 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18956 | hp1 | a0003 | c0002 | t0001 | g0205 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18956 | hp2 | a0002 | c0001 | t0002 | g0065 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18957 | hp1 | a0002 | c0001 | t0003 | g0188 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18957 | hp2 | a0003 | c0002 | t0001 | g0170 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18960 | hp1 | a0002 | c0001 | t0002 | g0179 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18960 | hp2 | a0005 | c0009 | t0002 | g0132 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18961 | hp1 | a0002 | c0001 | t0002 | g0144 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18961 | hp2 | a0003 | c0002 | t0012 | g0253 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18963 | hp1 | a0001 | c0004 | t0003 | g0149 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18963 | hp2 | a0002 | c0001 | t0003 | g0147 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18966 | hp1 | a0003 | c0002 | t0001 | g0263 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18966 | hp2 | a0002 | c0001 | t0002 | g0072 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18969 | hp1 | a0002 | c0001 | t0002 | g0177 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18969 | hp2 | a0003 | c0002 | t0016 | g0202 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18970 | hp1 | a0001 | c0004 | t0001 | g0135 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18970 | hp2 | a0002 | c0001 | t0002 | g0151 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18974 | hp1 | a0002 | c0001 | t0002 | g0018 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18974 | hp2 | a0003 | c0002 | t0001 | g0019 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18977 | hp1 | a0002 | c0001 | t0002 | g0196 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18977 | hp2 | a0003 | c0002 | t0001 | g0210 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18983 | hp1 | a0001 | c0004 | t0003 | g0180 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18983 | hp2 | a0003 | c0002 | t0002 | g0162 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18984 | hp1 | a0002 | c0001 | t0002 | g0068 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18984 | hp2 | a0001 | c0004 | t0003 | g0049 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18991 | hp1 | a0002 | c0001 | t0002 | g0095 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18991 | hp2 | a0003 | c0002 | t0006 | g0228 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18994 | hp1 | a0002 | c0001 | t0002 | g0173 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18994 | hp2 | a0003 | c0002 | t0003 | g0208 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18998 | hp1 | a0002 | c0001 | t0002 | g0224 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18998 | hp2 | a0003 | c0002 | t0003 | g0159 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18999 | hp1 | a0002 | c0001 | t0002 | g0183 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18999 | hp2 | a0002 | c0001 | t0002 | g0069 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19002 | hp1 | a0002 | c0001 | t0002 | g0175 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19002 | hp2 | a0003 | c0002 | t0001 | g0217 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19005 | hp1 | a0002 | c0001 | t0003 | g0189 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19005 | hp2 | a0003 | c0002 | t0001 | g0154 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19009 | hp1 | a0003 | c0002 | t0001 | g0166 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19009 | hp2 | a0002 | c0001 | t0001 | g0267 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19010 | hp1 | a0003 | c0002 | t0003 | g0169 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19010 | hp2 | a0003 | c0002 | t0001 | g0201 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19011 | hp1 | a0002 | c0001 | t0002 | g0057 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19011 | hp2 | a0003 | c0002 | t0001 | g0185 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19030 | hp1 | a0007 | c0012 | t0002 | g0275 | AFR | LWK | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0020 | AFR | LWK | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19060 | hp1 | a0001 | c0004 | t0003 | g0199 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19060 | hp2 | a0003 | c0002 | t0001 | g0207 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19063 | hp1 | a0002 | c0001 | t0003 | g0098 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19063 | hp2 | a0003 | c0002 | t0001 | g0171 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19064 | hp1 | a0002 | c0001 | t0002 | g0178 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19064 | hp2 | a0003 | c0002 | t0006 | g0140 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19066 | hp1 | a0003 | c0002 | t0001 | g0146 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19066 | hp2 | a0002 | c0001 | t0002 | g0023 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19074 | hp1 | a0003 | c0002 | t0003 | g0261 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19074 | hp2 | a0003 | c0002 | t0001 | g0053 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19084 | hp1 | a0003 | c0002 | t0001 | g0172 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19084 | hp2 | a0002 | c0001 | t0001 | g0216 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19085 | hp1 | a0003 | c0002 | t0001 | g0037 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19085 | hp2 | a0003 | c0002 | t0002 | g0211 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19086 | hp1 | a0003 | c0002 | t0001 | g0264 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19086 | hp2 | a0002 | c0001 | t0002 | g0073 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19088 | hp1 | a0002 | c0001 | t0001 | g0062 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19088 | hp2 | a0001 | c0004 | t0003 | g0145 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19091 | hp1 | a0002 | c0001 | t0002 | g0061 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19091 | hp2 | a0002 | c0001 | t0002 | g0165 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19240 | hp1 | a0001 | c0003 | t0001 | g0220 | AFR | YRI | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0245 | AFR | YRI | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA20129 | hp1 | a0001 | c0005 | t0004 | g0284 | AFR | ASW | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA20129 | hp2 | a0001 | c0003 | t0001 | g0167 | AFR | ASW | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA20752 | hp1 | a0003 | c0002 | t0001 | g0100 | EUR | TSI | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0085 | EUR | TSI | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA20805 | hp1 | a0001 | c0004 | t0003 | g0096 | EUR | TSI | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA20805 | hp2 | a0001 | c0004 | t0003 | g0280 | EUR | TSI | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA20905 | hp1 | a0002 | c0001 | t0003 | g0121 | SAS | GIH | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA20905 | hp2 | a0002 | c0001 | t0002 | g0052 | SAS | GIH | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01123 | hp1 | a0002 | c0001 | t0003 | g0134 | AMR | CLM | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG01123 | hp2 | a0002 | c0001 | t0002 | g0021 | AMR | CLM | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02109 | hp1 | a0001 | c0003 | t0001 | g0016 | AFR | ACB | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0232 | AFR | ACB | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02486 | hp1 | a0002 | c0001 | t0002 | g0122 | AFR | ACB | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02486 | hp2 | a0001 | c0003 | t0001 | g0214 | AFR | ACB | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02559 | hp1 | a0001 | c0004 | t0003 | g0029 | AFR | ACB | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0273 | AFR | ACB | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03471 | hp1 | a0001 | c0005 | t0001 | g0079 | AFR | MSL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG03471 | hp2 | a0001 | c0003 | t0001 | g0272 | AFR | MSL | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG06807 | hp1 | a0001 | c0003 | t0001 | g0111 | AFR | USA | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| HG06807 | hp2 | a0003 | c0002 | t0001 | g0130 | AFR | USA | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18955 | hp1 | a0003 | c0002 | t0001 | g0204 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA18955 | hp2 | a0002 | c0001 | t0001 | g0219 | EAS | JPT | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0260 | AFR | USA | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA20300 | hp2 | a0003 | c0002 | t0001 | g0223 | AFR | USA | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA21309 | hp1 | a0001 | c0003 | t0001 | g0270 | AFR | LWK | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| NA21309 | hp2 | a0002 | c0001 | t0019 | g0234 | AFR | LWK | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0001 | t0002 | g0051 | REF | REF | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| homoSapiens_grch38 | hp1 | a0002 | c0001 | t0002 | g0071 | REF | REF | EML1_chr14_99788413_99947060 | EML1 | chr14 | 99788413 | 99947060 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:99865589
|
G | A | 2 | a0004a0005 | 3 | HG02055.hp2 HG02615.hp1 NA18960.hp2 |
missense_variant | MODERATE | c.326G>A | p.Gly109Asp | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/22 | 390/4460 | 326/2448 | 109/815 | chr14 | 99865589 | ||
| chr14:99909370
|
C | T | 2 | a0003a0005 | 78 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(75): Show |
missense_variant | MODERATE | c.1130C>T | p.Ala377Val | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 11/22 | 1194/4460 | 1130/2448 | 377/815 | chr14 | 99909370 | ||
| chr14:99914611
|
T | C | 6 | a0001a0003a0004others(3): Show | 202 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(199): Show |
missense_variant | MODERATE | c.1666T>C | p.Ser556Pro | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 15/22 | 1730/4460 | 1666/2448 | 556/815 | chr14 | 99914611 | ||
| chr14:99917834
|
G | C | 1 | a0006 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.1805G>C | p.Gly602Ala | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/22 | 1869/4460 | 1805/2448 | 602/815 | chr14 | 99917834 | ||
| chr14:99939251
|
A | G | 1 | a0007 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.2246A>G | p.His749Arg | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 21/22 | 2310/4460 | 2246/2448 | 749/815 | chr14 | 99939251 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:99850935
|
C | T | 1 | a0003c0016 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.150C>T | p.Asp50Asp | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/22 | 214/4460 | 150/2448 | 50/815 | chr14 | 99850935 | ||
| chr14:99865539
|
T | C | 3 | a0001c0004a0001c0007a0002c0006 | 48 | HG00140.hp1 HG00609.hp1 HG01069.hp1 others(45): Show |
synonymous_variant | LOW | c.276T>C | p.Pro92Pro | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/22 | 340/4460 | 276/2448 | 92/815 | chr14 | 99865539 | ||
| chr14:99878497
|
G | A | 1 | a0003c0010 | 1 | HG02273.hp2 | synonymous_variant | LOW | c.396G>A | p.Arg132Arg | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/22 | 460/4460 | 396/2448 | 132/815 | chr14 | 99878497 | ||
| chr14:99894735
|
C | G | 1 | a0001c0005 | 9 | HG00639.hp2 HG02451.hp1 HG02622.hp2 others(6): Show |
synonymous_variant | LOW | c.654C>G | p.Thr218Thr | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/22 | 718/4460 | 654/2448 | 218/815 | chr14 | 99894735 | ||
| chr14:99914658
|
C | T | 1 | a0003c0015 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.1713C>T | p.Asp571Asp | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 15/22 | 1777/4460 | 1713/2448 | 571/815 | chr14 | 99914658 | ||
| chr14:99917823
|
G | A | 1 | a0001c0007 | 2 | HG02145.hp2 HG02818.hp2 |
synonymous_variant | LOW | c.1794G>A | p.Val598Val | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/22 | 1858/4460 | 1794/2448 | 598/815 | chr14 | 99917823 | ||
| chr14:99920828
|
C | T | 1 | a0001c0013 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.1860C>T | p.Thr620Thr | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/22 | 1924/4460 | 1860/2448 | 620/815 | chr14 | 99920828 | ||
| chr14:99936108
|
G | A | 1 | a0003c0014 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.1989G>A | p.Thr663Thr | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 18/22 | 2053/4460 | 1989/2448 | 663/815 | chr14 | 99936108 | ||
| chr14:99940004
|
C | T | 1 | a0007c0012 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.2340C>T | p.Tyr780Tyr | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 22/22 | 2404/4460 | 2340/2448 | 780/815 | chr14 | 99940004 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:99940526
|
C | T | 6 | a0001c0003t0005a0001c0003t0008a0001c0004t0005others(3): Show | 11 | HG02280.hp1 HG02451.hp1 HG02622.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*414C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 22/22 | 414 | chr14 | 99940526 | |||||
| chr14:99940756
|
G | A | 1 | a0003c0002t0012 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*644G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 22/22 | 644 | chr14 | 99940756 | |||||
| chr14:99940812
|
A | G | 22 | a0001c0003t0003a0001c0003t0004a0001c0003t0005others(19): Show | 80 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*700A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 22/22 | 700 | chr14 | 99940812 | |||||
| chr14:99940815
|
C | T | 1 | a0003c0002t0016 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*703C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 22/22 | 703 | chr14 | 99940815 | |||||
| chr14:99940849
|
G | A | 2 | a0001c0007t0018a0003c0002t0017 | 2 | HG01981.hp1 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*737G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 22/22 | 737 | chr14 | 99940849 | |||||
| chr14:99940917
|
C | T | 1 | a0002c0001t0015 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*805C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 22/22 | 805 | chr14 | 99940917 | |||||
| chr14:99940923
|
T | A | 2 | a0003c0002t0006a0003c0010t0006 | 6 | HG01109.hp1 HG01928.hp2 HG02004.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*811T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 22/22 | 811 | chr14 | 99940923 | |||||
| chr14:99941044
|
T | C | 22 | a0001c0003t0001a0001c0003t0007a0001c0003t0009others(19): Show | 132 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*932T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 22/22 | 932 | chr14 | 99941044 | |||||
| chr14:99941071
|
G | A | 1 | a0001c0004t0013 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*959G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 22/22 | 959 | chr14 | 99941071 | |||||
| chr14:99941164
|
C | T | 2 | a0001c0004t0010a0003c0002t0010 | 2 | HG00621.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1052C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 22/22 | 1052 | chr14 | 99941164 | |||||
| chr14:99941211
|
C | T | 1 | a0003c0016t0014 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1099C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 22/22 | 1099 | chr14 | 99941211 | |||||
| chr14:99941440
|
G | C | 1 | a0001c0003t0007 | 3 | HG02615.hp2 HG03453.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1328G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 22/22 | 1328 | chr14 | 99941440 | |||||
| chr14:99941647
|
ATTTGCAG others(12): Show |
A | 9 | a0001c0003t0004a0001c0003t0008a0001c0004t0004others(6): Show | 13 | HG00609.hp2 HG02055.hp2 HG02083.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1565_*1583delAGAC others(15): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 22/22 | 1565 | INFO_REALIGN_3_PRIME | chr14 | 99941647 | ||||
| chr14:99941694
|
T | C | 1 | a0002c0001t0019 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1582T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 22/22 | 1582 | chr14 | 99941694 | |||||
| chr14:99941770
|
T | A | 2 | a0001c0003t0009a0001c0005t0009 | 2 | HG02809.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1658T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 22/22 | 1658 | chr14 | 99941770 | |||||
| chr14:99941977
|
A | T | 3 | a0001c0003t0008a0001c0005t0008a0003c0002t0008 | 3 | HG02717.hp1 HG02922.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1865A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 22/22 | 1865 | chr14 | 99941977 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:99793637
|
C | G | 1 | a0001c0003t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.67+94C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99793637 | ||||||
| chr14:99793815
|
G | T | 1 | a0003c0002t0001g0002 | 2 | HG00639.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.67+272G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99793815 | ||||||
| chr14:99793828
|
G | A | 2 | a0001c0005t0005g0003a0004c0008t0004g0004 | 2 | HG02451.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.67+285G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99793828 | ||||||
| chr14:99793875
|
T | C | 1 | a0001c0007t0002g0005 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.67+332T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99793875 | ||||||
| chr14:99793909
|
C | T | 6 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0005t0004g0284others(3): Show | 6 | HG02451.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+366C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99793909 | ||||||
| chr14:99794187
|
A | G | 6 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0005t0004g0284others(3): Show | 6 | HG02451.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+644A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99794187 | ||||||
| chr14:99794226
|
A | T | 4 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0005t0004g0284others(1): Show | 4 | HG02886.hp1 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+683A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99794226 | ||||||
| chr14:99794334
|
C | T | 47 | a0001c0003t0001g0240a0001c0003t0001g0243a0001c0003t0001g0244others(44): Show | 48 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.67+791C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99794334 | ||||||
| chr14:99794339
|
C | CT | 7 | a0001c0003t0003g0277a0001c0003t0003g0279a0001c0003t0007g0281others(4): Show | 7 | HG00140.hp2 HG01071.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.67+810dupT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99794339 | |||||
| chr14:99794419
|
A | G | 1 | a0002c0001t0019g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.67+876A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99794419 | ||||||
| chr14:99794467
|
A | C | 1 | a0002c0001t0002g0276 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.67+924A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99794467 | ||||||
| chr14:99794569
|
A | G | 89 | a0001c0003t0001g0158a0001c0003t0001g0163a0001c0003t0001g0167others(86): Show | 89 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.67+1026A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99794569 | ||||||
| chr14:99794708
|
T | C | 1 | a0001c0004t0010g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.67+1165T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99794708 | ||||||
| chr14:99794843
|
T | C | 136 | a0001c0003t0001g0158a0001c0003t0001g0163a0001c0003t0001g0167others(133): Show | 137 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.67+1300T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99794843 | ||||||
| chr14:99794971
|
T | C | 3 | a0001c0004t0010g0235a0001c0005t0005g0003a0004c0008t0004g0004 | 3 | HG02451.hp1 HG02615.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.67+1428T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99794971 | ||||||
| chr14:99794999
|
G | A | 4 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0005t0004g0284others(1): Show | 4 | HG02886.hp1 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+1456G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99794999 | ||||||
| chr14:99795033
|
A | G | 1 | a0001c0004t0010g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.67+1490A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99795033 | ||||||
| chr14:99795203
|
C | T | 2 | a0001c0003t0001g0152a0002c0001t0002g0153 | 2 | HG00642.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.67+1660C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99795203 | ||||||
| chr14:99795285
|
G | A | 2 | a0003c0002t0001g0237a0003c0002t0008g0238 | 2 | HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.67+1742G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99795285 | ||||||
| chr14:99795345
|
T | C | 4 | a0001c0004t0011g0156a0002c0001t0002g0157a0003c0002t0001g0154others(1): Show | 4 | HG02083.hp1 HG02155.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+1802T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99795345 | ||||||
| chr14:99795510
|
A | G | 2 | a0002c0001t0002g0150a0002c0001t0002g0151 | 2 | NA18939.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.67+1967A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99795510 | ||||||
| chr14:99795584
|
T | C | 1 | a0001c0004t0010g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.67+2041T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99795584 | ||||||
| chr14:99795812
|
C | T | 2 | a0001c0005t0005g0003a0004c0008t0004g0004 | 2 | HG02451.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.67+2269C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99795812 | ||||||
| chr14:99796055
|
C | A | 3 | a0001c0004t0010g0235a0001c0005t0005g0003a0004c0008t0004g0004 | 3 | HG02451.hp1 HG02615.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.67+2512C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99796055 | ||||||
| chr14:99796072
|
A | G | 1 | a0001c0004t0003g0149 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.67+2529A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99796072 | ||||||
| chr14:99796103
|
A | C | 136 | a0001c0003t0001g0158a0001c0003t0001g0163a0001c0003t0001g0167others(133): Show | 137 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.67+2560A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99796103 | ||||||
| chr14:99796114
|
A | G | 89 | a0001c0003t0001g0158a0001c0003t0001g0163a0001c0003t0001g0167others(86): Show | 89 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.67+2571A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99796114 | ||||||
| chr14:99796186
|
C | CAG | 24 | a0001c0003t0001g0080a0001c0003t0001g0085a0001c0003t0001g0086others(21): Show | 25 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.67+2687_67+2688dup others(2): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796186 | |||||
| chr14:99796186
|
C | CAGAG | 10 | a0001c0004t0003g0096a0001c0004t0003g0103a0001c0005t0005g0097others(7): Show | 10 | HG00621.hp1 HG00642.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.67+2685_67+2688dup others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796186 | |||||
| chr14:99796186
|
C | CAGAGAG | 7 | a0001c0003t0002g0105a0001c0003t0002g0106a0001c0004t0013g0108others(4): Show | 7 | HG01168.hp2 HG01515.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.67+2683_67+2688dup others(6): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796186 | |||||
| chr14:99796186
|
C | CAGAGAGA others(1): Show |
10 | a0001c0003t0001g0111a0001c0003t0001g0112a0001c0003t0001g0113others(7): Show | 10 | HG00140.hp1 HG01175.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.67+2681_67+2688dup others(8): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796186 | |||||
| chr14:99796186
|
C | CAGAGAGA others(3): Show |
4 | a0001c0003t0001g0120a0001c0004t0001g0123a0002c0001t0002g0122others(1): Show | 4 | HG01515.hp2 HG02486.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+2679_67+2688dup others(10): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796186 | |||||
| chr14:99796186
|
C | CAGAGAGA others(5): Show |
7 | a0001c0004t0003g0127a0001c0013t0001g0126a0002c0001t0002g0129others(4): Show | 7 | HG00735.hp2 HG01169.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.67+2677_67+2688dup others(12): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796186 | |||||
| chr14:99796186
|
C | CAGAGAGA others(7): Show |
5 | a0001c0004t0001g0135a0001c0004t0003g0131a0002c0001t0002g0133others(2): Show | 5 | HG01123.hp1 HG03239.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+2675_67+2688dup others(14): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796186 | |||||
| chr14:99796186
|
C | CAGAGAGA others(9): Show |
6 | a0001c0004t0003g0149a0002c0001t0002g0136a0002c0001t0003g0137others(3): Show | 6 | HG00408.hp1 HG00544.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+2673_67+2688dup others(16): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796186 | |||||
| chr14:99796186
|
C | CAGAGAGA others(11): Show |
3 | a0001c0003t0004g0141a0001c0004t0001g0143a0002c0001t0003g0142 | 3 | HG00323.hp1 HG02970.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.67+2671_67+2688dup others(18): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796186 | |||||
| chr14:99796186
|
C | CAGAGAGA others(13): Show |
2 | a0001c0004t0003g0145a0002c0001t0002g0144 | 2 | NA18961.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.67+2669_67+2688dup others(20): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796186 | |||||
| chr14:99796186
|
C | CAGAGAGA others(15): Show |
2 | a0002c0001t0003g0147a0003c0002t0001g0146 | 2 | NA18963.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.67+2667_67+2688dup others(22): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796186 | |||||
| chr14:99796186
|
CAG | C | 6 | a0001c0003t0001g0152a0001c0004t0003g0029a0001c0004t0005g0266others(3): Show | 6 | HG01981.hp1 HG02055.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+2687_67+2688del others(2): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796186 | |||||
| chr14:99796186
|
CAGAG | C | 36 | a0001c0003t0001g0020a0001c0003t0001g0243a0001c0003t0001g0244others(33): Show | 36 | HG00438.hp1 HG00609.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.67+2685_67+2688del others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796186 | |||||
| chr14:99796186
|
CAGAGAG | C | 6 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0286others(3): Show | 6 | HG02109.hp1 HG02257.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+2683_67+2688del others(6): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796186 | |||||
| chr14:99796186
|
CAGAGAGA others(1): Show |
C | 8 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(5): Show | 8 | HG01884.hp2 HG02280.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.67+2681_67+2688del others(8): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796186 | |||||
| chr14:99796186
|
CAGAGAGA others(3): Show |
C | 4 | a0001c0003t0003g0277a0001c0003t0003g0279a0001c0004t0003g0280others(1): Show | 4 | HG00140.hp2 HG01071.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+2679_67+2688del others(10): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796186 | |||||
| chr14:99796186
|
CAGAGAGA others(5): Show |
C | 3 | a0001c0003t0001g0006a0003c0002t0001g0237a0003c0002t0008g0238 | 3 | HG02723.hp1 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.67+2677_67+2688del others(12): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796186 | |||||
| chr14:99796186
|
CAGAGAGA others(7): Show |
C | 4 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0005t0004g0284others(1): Show | 4 | HG02886.hp1 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+2675_67+2688del others(14): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796186 | |||||
| chr14:99796186
|
CAGAGAGA others(9): Show |
C | 2 | a0001c0003t0001g0232a0001c0003t0001g0233 | 2 | HG01109.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.67+2673_67+2688del others(16): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796186 | |||||
| chr14:99796186
|
CAGAGAGA others(13): Show |
C | 82 | a0001c0003t0001g0163a0001c0003t0001g0167a0001c0003t0001g0168others(79): Show | 82 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.67+2669_67+2688del others(20): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796186 | |||||
| chr14:99796186
|
CAGAGAGA others(15): Show |
C | 1 | a0001c0003t0001g0158 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.67+2667_67+2688del others(22): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796186 | |||||
| chr14:99796190
|
G | A | 1 | a0002c0001t0001g0239 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.67+2647G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99796190 | ||||||
| chr14:99796231
|
A | AGAGAGAG others(4): Show |
1 | a0002c0006t0002g0148 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.67+2688_67+2689ins others(11): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99796231 | ||||||
| chr14:99796311
|
T | C | 1 | a0002c0001t0002g0153 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.67+2768T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99796311 | ||||||
| chr14:99796381
|
A | G | 2 | a0001c0005t0005g0003a0004c0008t0004g0004 | 2 | HG02451.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.67+2838A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99796381 | ||||||
| chr14:99796409
|
T | C | 4 | a0001c0003t0001g0111a0001c0003t0001g0112a0001c0003t0001g0113others(1): Show | 4 | HG02630.hp1 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+2866T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99796409 | ||||||
| chr14:99796490
|
C | CT | 6 | a0001c0004t0003g0103a0002c0001t0002g0073a0002c0001t0002g0095others(3): Show | 6 | HG01168.hp2 HG01256.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+2963dupT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796490 | |||||
| chr14:99796490
|
CT | C | 86 | a0001c0003t0001g0158a0001c0003t0001g0163a0001c0003t0001g0167others(83): Show | 86 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.67+2963delT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796490 | |||||
| chr14:99796573
|
A | C | 88 | a0001c0003t0001g0158a0001c0003t0001g0163a0001c0003t0001g0167others(85): Show | 88 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.67+3030A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99796573 | ||||||
| chr14:99796582
|
C | T | 1 | a0001c0004t0003g0149 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.67+3039C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99796582 | ||||||
| chr14:99796677
|
G | GA | 88 | a0001c0003t0001g0158a0001c0003t0001g0163a0001c0003t0001g0167others(85): Show | 88 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.67+3146dupA | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796677 | |||||
| chr14:99796899
|
T | TGTGTG | 4 | a0002c0001t0002g0160a0003c0002t0001g0161a0003c0002t0002g0162others(1): Show | 4 | NA18954.hp1 NA18954.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+3356_67+3357ins others(5): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99796899 | ||||||
| chr14:99796907
|
GTA | G | 3 | a0001c0003t0001g0167a0001c0003t0001g0168a0002c0001t0002g0164 | 3 | HG02602.hp2 HG02818.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.67+3366_67+3367del others(2): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796907 | |||||
| chr14:99796909
|
A | ATG | 12 | a0001c0003t0004g0027a0001c0004t0001g0143a0001c0004t0013g0108others(9): Show | 12 | HG01346.hp1 HG02055.hp1 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.67+3393_67+3394dup others(2): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796909 | |||||
| chr14:99796909
|
A | ATGTG | 4 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0005t0004g0284others(1): Show | 4 | HG02886.hp1 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+3391_67+3394dup others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796909 | |||||
| chr14:99796909
|
A | G | 75 | a0001c0003t0001g0158a0001c0003t0001g0193a0001c0003t0001g0214others(72): Show | 75 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.67+3366A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99796909 | ||||||
| chr14:99796909
|
ATGTG | A | 6 | a0001c0003t0001g0240a0001c0003t0003g0277a0001c0003t0003g0279others(3): Show | 6 | HG00140.hp2 HG01071.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+3391_67+3394del others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796909 | |||||
| chr14:99796932
|
T | A | 1 | a0002c0001t0002g0164 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.67+3389T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99796932 | ||||||
| chr14:99796934
|
T | A | 3 | a0002c0001t0002g0164a0002c0001t0002g0165a0003c0002t0001g0166 | 3 | HG02602.hp2 NA19009.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.67+3391T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99796934 | ||||||
| chr14:99796934
|
T | TGAGAGA | 5 | a0002c0001t0002g0173a0003c0002t0001g0170a0003c0002t0001g0171others(2): Show | 5 | NA18957.hp2 NA18994.hp1 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+3392_67+3393ins others(6): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796934 | |||||
| chr14:99796936
|
T | A | 15 | a0001c0003t0001g0111a0001c0003t0001g0163a0001c0003t0001g0167others(12): Show | 15 | HG01109.hp2 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.67+3393T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99796936 | ||||||
| chr14:99796936
|
T | TGA | 39 | a0001c0003t0001g0112a0001c0003t0001g0113a0001c0003t0001g0114others(36): Show | 39 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.67+3399_67+3400dup others(2): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796936 | |||||
| chr14:99796936
|
T | TGAGAGA | 9 | a0002c0001t0002g0160a0002c0001t0002g0174a0002c0001t0002g0175others(6): Show | 9 | HG01928.hp1 HG03927.hp2 NA18954.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+3395_67+3400dup others(6): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796936 | |||||
| chr14:99796936
|
T | TGTGAGAG others(3): Show |
3 | a0001c0003t0003g0184a0003c0002t0001g0185a0003c0002t0001g0186 | 3 | HG04115.hp1 NA18952.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.67+3394_67+3395ins others(10): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796936 | |||||
| chr14:99796936
|
T | TGTGTGAG others(3): Show |
18 | a0001c0003t0001g0193a0001c0004t0003g0195a0001c0004t0003g0197others(15): Show | 18 | HG00323.hp2 HG01081.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.67+3394_67+3395ins others(10): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796936 | |||||
| chr14:99796936
|
T | TGTGTGAG others(5): Show |
1 | a0003c0002t0001g0187 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.67+3394_67+3395ins others(12): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796936 | |||||
| chr14:99796936
|
T | TGTGTGTG others(5): Show |
18 | a0001c0003t0001g0214a0001c0004t0003g0199a0001c0004t0003g0206others(15): Show | 18 | HG00423.hp1 HG00621.hp2 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.67+3394_67+3395ins others(12): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796936 | |||||
| chr14:99796936
|
T | TGTGTGTG others(7): Show |
10 | a0001c0003t0001g0220a0001c0003t0001g0221a0002c0001t0001g0216others(7): Show | 10 | HG01192.hp1 HG02004.hp2 HG03516.hp1 others(7): Show |
intron_variant | MODIFIER | c.67+3394_67+3395ins others(14): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796936 | |||||
| chr14:99796936
|
T | TGTGTGTG others(9): Show |
2 | a0001c0003t0001g0225a0003c0010t0006g0226 | 2 | HG02273.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.67+3394_67+3395ins others(16): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99796936 | |||||
| chr14:99796938
|
A | T | 3 | a0001c0004t0010g0235a0001c0005t0005g0003a0004c0008t0004g0004 | 3 | HG02451.hp1 HG02615.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.67+3395A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99796938 | ||||||
| chr14:99797008
|
G | A | 1 | a0001c0003t0001g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.67+3465G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99797008 | ||||||
| chr14:99797069
|
T | C | 285 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0007others(282): Show | 287 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.67+3526T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99797069 | ||||||
| chr14:99797201
|
G | A | 1 | a0002c0001t0002g0179 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.67+3658G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99797201 | ||||||
| chr14:99797235
|
C | T | 1 | a0001c0004t0010g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.67+3692C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99797235 | ||||||
| chr14:99797274
|
T | G | 203 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0008others(200): Show | 204 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.67+3731T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99797274 | ||||||
| chr14:99797322
|
A | G | 1 | a0001c0003t0001g0001 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.67+3779A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99797322 | ||||||
| chr14:99797325
|
A | G | 2 | a0003c0002t0001g0262a0003c0002t0003g0261 | 2 | HG00438.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.67+3782A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99797325 | ||||||
| chr14:99797462
|
T | C | 1 | a0002c0001t0002g0081 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.67+3919T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99797462 | ||||||
| chr14:99797471
|
A | G | 3 | a0001c0004t0010g0235a0001c0005t0005g0003a0004c0008t0004g0004 | 3 | HG02451.hp1 HG02615.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.67+3928A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99797471 | ||||||
| chr14:99797547
|
T | C | 88 | a0001c0003t0001g0158a0001c0003t0001g0163a0001c0003t0001g0167others(85): Show | 88 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.67+4004T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99797547 | ||||||
| chr14:99797566
|
A | C | 135 | a0001c0003t0001g0158a0001c0003t0001g0163a0001c0003t0001g0167others(132): Show | 136 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.67+4023A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99797566 | ||||||
| chr14:99797570
|
T | C | 3 | a0001c0004t0010g0235a0001c0005t0005g0003a0004c0008t0004g0004 | 3 | HG02451.hp1 HG02615.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.67+4027T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99797570 | ||||||
| chr14:99797697
|
C | T | 1 | a0001c0004t0001g0123 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.67+4154C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99797697 | ||||||
| chr14:99797953
|
T | C | 1 | a0001c0003t0001g0163 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.67+4410T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99797953 | ||||||
| chr14:99798109
|
G | A | 3 | a0001c0004t0010g0235a0001c0005t0005g0003a0004c0008t0004g0004 | 3 | HG02451.hp1 HG02615.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.67+4566G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99798109 | ||||||
| chr14:99798130
|
G | A | 4 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0005t0004g0284others(1): Show | 4 | HG02886.hp1 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+4587G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99798130 | ||||||
| chr14:99798392
|
C | CT | 114 | a0001c0003t0001g0007a0001c0003t0001g0158a0001c0003t0001g0167others(111): Show | 115 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.67+4866dupT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99798392 | |||||
| chr14:99798499
|
TCTC | T | 5 | a0002c0001t0002g0224a0003c0002t0001g0223a0003c0002t0002g0222others(2): Show | 5 | HG02004.hp2 HG02273.hp2 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+4959_67+4961del others(3): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99798499 | |||||
| chr14:99798593
|
TG | T | 4 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0005t0004g0284others(1): Show | 4 | HG02886.hp1 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+5051delG | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99798593 | ||||||
| chr14:99798613
|
A | G | 2 | a0001c0003t0001g0272a0001c0003t0001g0273 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.67+5070A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99798613 | ||||||
| chr14:99798613
|
A | T | 2 | a0002c0001t0002g0165a0003c0002t0001g0166 | 2 | NA19009.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.67+5070A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99798613 | ||||||
| chr14:99798806
|
C | T | 2 | a0001c0003t0002g0105a0001c0003t0002g0106 | 2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.67+5263C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99798806 | ||||||
| chr14:99798813
|
T | G | 40 | a0001c0003t0001g0240a0001c0003t0001g0243a0001c0003t0001g0244others(37): Show | 41 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.67+5270T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99798813 | ||||||
| chr14:99798859
|
G | A | 81 | a0001c0003t0001g0158a0001c0003t0001g0163a0001c0003t0001g0167others(78): Show | 81 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.67+5316G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99798859 | ||||||
| chr14:99798939
|
A | G | 1 | a0001c0004t0010g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.67+5396A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99798939 | ||||||
| chr14:99799054
|
C | T | 2 | a0003c0002t0001g0237a0003c0002t0008g0238 | 2 | HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.67+5511C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99799054 | ||||||
| chr14:99799188
|
A | G | 3 | a0001c0004t0001g0143a0001c0004t0013g0108a0003c0002t0001g0130 | 3 | HG02055.hp1 HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.67+5645A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99799188 | ||||||
| chr14:99799533
|
C | T | 1 | a0002c0001t0002g0102 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.67+5990C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99799533 | ||||||
| chr14:99799572
|
A | G | 5 | a0001c0003t0003g0277a0001c0003t0003g0279a0001c0003t0007g0281others(2): Show | 5 | HG00140.hp2 HG01071.hp2 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+6029A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99799572 | ||||||
| chr14:99799587
|
A | G | 1 | a0003c0002t0001g0104 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.67+6044A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99799587 | ||||||
| chr14:99799613
|
G | C | 3 | a0001c0004t0010g0235a0001c0005t0005g0003a0004c0008t0004g0004 | 3 | HG02451.hp1 HG02615.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.67+6070G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99799613 | ||||||
| chr14:99799750
|
C | G | 1 | a0001c0004t0010g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.67+6207C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99799750 | ||||||
| chr14:99799894
|
A | G | 5 | a0002c0001t0002g0144a0002c0001t0003g0139a0002c0001t0003g0147others(2): Show | 5 | HG00408.hp1 NA18961.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+6351A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99799894 | ||||||
| chr14:99799958
|
C | T | 2 | a0001c0003t0002g0105a0001c0003t0002g0106 | 2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.67+6415C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99799958 | ||||||
| chr14:99799965
|
T | C | 16 | a0001c0003t0001g0243a0001c0003t0001g0244a0001c0003t0001g0245others(13): Show | 16 | HG00733.hp1 HG02280.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.67+6422T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99799965 | ||||||
| chr14:99800183
|
C | G | 3 | a0001c0003t0001g0163a0001c0003t0001g0232a0001c0003t0001g0233 | 3 | HG01109.hp2 HG02109.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.67+6640C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99800183 | ||||||
| chr14:99800187
|
T | G | 4 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0005t0004g0284others(1): Show | 4 | HG02886.hp1 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+6644T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99800187 | ||||||
| chr14:99800234
|
A | C | 4 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0005t0004g0284others(1): Show | 4 | HG02886.hp1 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+6691A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99800234 | ||||||
| chr14:99800265
|
A | G | 4 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0005t0004g0284others(1): Show | 4 | HG02886.hp1 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+6722A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99800265 | ||||||
| chr14:99800301
|
A | G | 4 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0005t0004g0284others(1): Show | 4 | HG02886.hp1 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+6758A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99800301 | ||||||
| chr14:99800341
|
GT | G | 16 | a0001c0003t0001g0243a0001c0003t0001g0244a0001c0003t0001g0245others(13): Show | 16 | HG00733.hp1 HG02280.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.67+6808delT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99800341 | |||||
| chr14:99800352
|
A | T | 3 | a0001c0004t0010g0235a0001c0005t0005g0003a0004c0008t0004g0004 | 3 | HG02451.hp1 HG02615.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.67+6809A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99800352 | ||||||
| chr14:99800518
|
C | A | 4 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0005t0004g0284others(1): Show | 4 | HG02886.hp1 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+6975C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99800518 | ||||||
| chr14:99800636
|
A | G | 136 | a0001c0003t0001g0158a0001c0003t0001g0163a0001c0003t0001g0167others(133): Show | 137 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.67+7093A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99800636 | ||||||
| chr14:99800741
|
C | T | 1 | a0002c0001t0002g0026 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.67+7198C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99800741 | ||||||
| chr14:99800869
|
G | A | 1 | a0001c0004t0003g0035 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.67+7326G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99800869 | ||||||
| chr14:99800965
|
C | T | 1 | a0003c0015t0001g0013 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.67+7422C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99800965 | ||||||
| chr14:99800983
|
CAGAG | C | 3 | a0001c0004t0010g0235a0001c0005t0005g0003a0004c0008t0004g0004 | 3 | HG02451.hp1 HG02615.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.67+7441_67+7444del others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99800983 | ||||||
| chr14:99801013
|
C | T | 3 | a0001c0004t0010g0235a0001c0005t0005g0003a0004c0008t0004g0004 | 3 | HG02451.hp1 HG02615.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.67+7470C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99801013 | ||||||
| chr14:99801098
|
G | A | 1 | a0003c0002t0003g0230 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.67+7555G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99801098 | ||||||
| chr14:99801220
|
G | A | 3 | a0001c0004t0010g0235a0001c0005t0005g0003a0004c0008t0004g0004 | 3 | HG02451.hp1 HG02615.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.67+7677G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99801220 | ||||||
| chr14:99801263
|
A | G | 3 | a0001c0004t0001g0248a0001c0004t0005g0249a0001c0004t0005g0266 | 3 | HG02280.hp1 HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.67+7720A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99801263 | ||||||
| chr14:99801355
|
C | T | 1 | a0001c0007t0002g0005 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.67+7812C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99801355 | ||||||
| chr14:99801386
|
T | C | 1 | a0001c0005t0008g0077 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.67+7843T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99801386 | ||||||
| chr14:99801614
|
CA | C | 84 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0163others(81): Show | 84 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.67+8085delA | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99801614 | |||||
| chr14:99801619
|
A | C | 5 | a0001c0003t0001g0214a0001c0003t0001g0220a0001c0003t0001g0221others(2): Show | 5 | HG02486.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+8076A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99801619 | ||||||
| chr14:99801666
|
A | C | 3 | a0001c0004t0010g0235a0001c0005t0005g0003a0004c0008t0004g0004 | 3 | HG02451.hp1 HG02615.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.67+8123A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99801666 | ||||||
| chr14:99801721
|
C | T | 3 | a0001c0004t0010g0235a0001c0005t0005g0003a0004c0008t0004g0004 | 3 | HG02451.hp1 HG02615.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.67+8178C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99801721 | ||||||
| chr14:99801982
|
C | A | 1 | a0001c0004t0003g0180 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.67+8439C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99801982 | ||||||
| chr14:99802163
|
C | T | 1 | a0001c0003t0001g0158 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.67+8620C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99802163 | ||||||
| chr14:99802196
|
A | T | 3 | a0001c0004t0010g0235a0001c0005t0005g0003a0004c0008t0004g0004 | 3 | HG02451.hp1 HG02615.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.67+8653A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99802196 | ||||||
| chr14:99802366
|
G | A | 38 | a0001c0003t0001g0111a0001c0003t0001g0112a0001c0003t0001g0113others(35): Show | 38 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(35): Show |
intron_variant | MODIFIER | c.67+8823G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99802366 | ||||||
| chr14:99802391
|
G | C | 2 | a0001c0003t0001g0272a0001c0003t0001g0273 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.67+8848G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99802391 | ||||||
| chr14:99802483
|
T | G | 40 | a0001c0003t0001g0240a0001c0003t0001g0243a0001c0003t0001g0244others(37): Show | 41 | HG00438.hp1 HG00609.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.67+8940T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99802483 | ||||||
| chr14:99802534
|
A | G | 1 | a0001c0004t0010g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.67+8991A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99802534 | ||||||
| chr14:99802664
|
G | C | 3 | a0001c0004t0003g0199a0002c0001t0003g0188a0002c0001t0003g0189 | 3 | NA18957.hp1 NA19005.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.67+9121G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99802664 | ||||||
| chr14:99802669
|
G | A | 2 | a0003c0002t0001g0201a0003c0002t0010g0200 | 2 | HG00621.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.67+9126G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99802669 | ||||||
| chr14:99802719
|
G | T | 3 | a0001c0003t0001g0158a0001c0003t0001g0167a0001c0003t0001g0168 | 3 | HG02572.hp1 HG02818.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.67+9176G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99802719 | ||||||
| chr14:99802788
|
A | G | 134 | a0001c0003t0001g0012a0001c0003t0001g0163a0001c0003t0001g0193others(131): Show | 135 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.67+9245A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99802788 | ||||||
| chr14:99802855
|
C | T | 73 | a0001c0003t0001g0193a0001c0003t0001g0214a0001c0003t0001g0220others(70): Show | 73 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.67+9312C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99802855 | ||||||
| chr14:99802859
|
T | C | 4 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0005t0004g0284others(1): Show | 4 | HG02886.hp1 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+9316T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99802859 | ||||||
| chr14:99802868
|
T | A | 1 | a0001c0007t0018g0241 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.67+9325T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99802868 | ||||||
| chr14:99802913
|
A | G | 1 | a0003c0002t0001g0198 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.67+9370A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99802913 | ||||||
| chr14:99802914
|
G | A | 1 | a0003c0002t0001g0107 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.67+9371G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99802914 | ||||||
| chr14:99802926
|
C | A | 1 | a0001c0004t0010g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.67+9383C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99802926 | ||||||
| chr14:99802961
|
C | A | 72 | a0001c0003t0001g0193a0001c0003t0001g0214a0001c0003t0001g0220others(69): Show | 72 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.67+9418C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99802961 | ||||||
| chr14:99803174
|
G | T | 12 | a0001c0003t0001g0012a0001c0003t0001g0163a0001c0003t0001g0232others(9): Show | 12 | HG01109.hp2 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.67+9631G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99803174 | ||||||
| chr14:99803232
|
G | A | 3 | a0001c0003t0001g0008a0001c0003t0001g0010a0001c0004t0001g0009 | 3 | HG03225.hp2 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.67+9689G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99803232 | ||||||
| chr14:99803378
|
C | T | 3 | a0002c0001t0002g0068a0002c0001t0002g0069a0003c0002t0001g0070 | 3 | HG00408.hp2 NA18984.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.67+9835C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99803378 | ||||||
| chr14:99803450
|
A | G | 2 | a0001c0005t0001g0079a0001c0005t0009g0078 | 2 | HG02809.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.67+9907A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99803450 | ||||||
| chr14:99803550
|
A | T | 195 | a0001c0003t0001g0006a0001c0003t0001g0008a0001c0003t0001g0010others(192): Show | 196 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.67+10007A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99803550 | ||||||
| chr14:99803655
|
G | A | 4 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0005t0004g0284others(1): Show | 4 | HG02886.hp1 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+10112G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99803655 | ||||||
| chr14:99803660
|
A | G | 10 | a0001c0003t0001g0243a0001c0003t0001g0244a0001c0003t0001g0245others(7): Show | 10 | HG02280.hp1 HG02622.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.67+10117A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99803660 | ||||||
| chr14:99804195
|
G | A | 3 | a0002c0001t0001g0216a0003c0002t0001g0237a0003c0002t0008g0238 | 3 | HG02976.hp1 HG03209.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.67+10652G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99804195 | ||||||
| chr14:99804546
|
A | G | 4 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0005t0004g0284others(1): Show | 4 | HG02886.hp1 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+11003A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99804546 | ||||||
| chr14:99804601
|
G | A | 1 | a0003c0015t0001g0013 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.67+11058G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99804601 | ||||||
| chr14:99805039
|
T | C | 89 | a0001c0003t0001g0111a0001c0003t0001g0112a0001c0003t0001g0113others(86): Show | 90 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.67+11496T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99805039 | ||||||
| chr14:99805080
|
A | G | 1 | a0003c0002t0002g0231 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.67+11537A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99805080 | ||||||
| chr14:99805097
|
C | T | 3 | a0002c0001t0002g0067a0002c0001t0002g0081a0002c0001t0002g0093 | 3 | HG00423.hp2 HG00544.hp2 HG00558.hp1 |
intron_variant | MODIFIER | c.67+11554C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99805097 | ||||||
| chr14:99805162
|
G | T | 1 | a0003c0002t0002g0231 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.67+11619G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99805162 | ||||||
| chr14:99805249
|
T | C | 3 | a0001c0004t0010g0235a0001c0005t0005g0003a0004c0008t0004g0004 | 3 | HG02451.hp1 HG02615.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.67+11706T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99805249 | ||||||
| chr14:99805362
|
T | C | 1 | a0003c0002t0012g0253 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.67+11819T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99805362 | ||||||
| chr14:99805617
|
G | A | 8 | a0002c0001t0001g0267a0002c0001t0002g0276a0003c0002t0001g0002others(5): Show | 9 | HG00438.hp1 HG00639.hp1 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+12074G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99805617 | ||||||
| chr14:99805672
|
C | T | 2 | a0001c0005t0005g0003a0004c0008t0004g0004 | 2 | HG02451.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.67+12129C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99805672 | ||||||
| chr14:99805770
|
C | T | 80 | a0001c0003t0001g0012a0001c0003t0001g0158a0001c0003t0001g0163others(77): Show | 80 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.67+12227C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99805770 | ||||||
| chr14:99805870
|
G | A | 38 | a0001c0003t0001g0111a0001c0003t0001g0112a0001c0003t0001g0113others(35): Show | 38 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(35): Show |
intron_variant | MODIFIER | c.67+12327G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99805870 | ||||||
| chr14:99805979
|
G | A | 3 | a0001c0004t0010g0235a0001c0005t0005g0003a0004c0008t0004g0004 | 3 | HG02451.hp1 HG02615.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.67+12436G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99805979 | ||||||
| chr14:99806000
|
C | T | 4 | a0001c0004t0003g0030a0002c0001t0002g0031a0002c0001t0002g0122others(1): Show | 4 | HG00735.hp1 HG01123.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+12457C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99806000 | ||||||
| chr14:99806035
|
A | G | 1 | a0001c0003t0008g0271 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.67+12492A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99806035 | ||||||
| chr14:99806116
|
A | C | 40 | a0001c0003t0001g0111a0001c0003t0001g0112a0001c0003t0001g0113others(37): Show | 40 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(37): Show |
intron_variant | MODIFIER | c.67+12573A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99806116 | ||||||
| chr14:99806117
|
A | G | 2 | a0001c0005t0005g0003a0004c0008t0004g0004 | 2 | HG02451.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.67+12574A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99806117 | ||||||
| chr14:99806133
|
A | G | 1 | a0002c0001t0002g0026 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.67+12590A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99806133 | ||||||
| chr14:99806189
|
G | A | 4 | a0001c0003t0001g0012a0001c0003t0001g0163a0001c0003t0001g0232others(1): Show | 4 | HG01109.hp2 HG02109.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+12646G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99806189 | ||||||
| chr14:99806206
|
T | C | 2 | a0001c0005t0005g0003a0004c0008t0004g0004 | 2 | HG02451.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.67+12663T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99806206 | ||||||
| chr14:99806316
|
C | CT | 19 | a0001c0003t0001g0016a0001c0003t0001g0020a0001c0003t0001g0282others(16): Show | 19 | HG00423.hp2 HG00544.hp1 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.67+12797dupT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99806316 | |||||
| chr14:99806316
|
CT | C | 121 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0120others(118): Show | 122 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.67+12797delT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99806316 | |||||
| chr14:99806316
|
CTT | C | 25 | a0001c0003t0001g0006a0001c0003t0001g0008a0001c0003t0001g0080others(22): Show | 25 | HG00642.hp2 HG02040.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.67+12796_67+12797d others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99806316 | |||||
| chr14:99806316
|
CTTTTTTT others(4): Show |
C | 2 | a0003c0002t0001g0263a0003c0002t0001g0264 | 2 | NA18966.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.67+12787_67+12797d others(13): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99806316 | |||||
| chr14:99806316
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0005t0005g0265 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.67+12783_67+12797d others(17): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99806316 | |||||
| chr14:99806352
|
G | C | 4 | a0001c0003t0001g0158a0001c0003t0001g0167a0001c0003t0001g0168others(1): Show | 4 | HG02145.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+12809G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99806352 | ||||||
| chr14:99806376
|
C | T | 4 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0005t0004g0284others(1): Show | 4 | HG02886.hp1 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+12833C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99806376 | ||||||
| chr14:99806386
|
G | A | 2 | a0001c0003t0001g0270a0007c0012t0002g0275 | 2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.67+12843G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99806386 | ||||||
| chr14:99806393
|
C | T | 2 | a0001c0003t0001g0270a0007c0012t0002g0275 | 2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.67+12850C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99806393 | ||||||
| chr14:99806409
|
C | T | 2 | a0001c0005t0005g0003a0004c0008t0004g0004 | 2 | HG02451.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.67+12866C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99806409 | ||||||
| chr14:99806441
|
C | T | 1 | a0002c0001t0002g0173 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.67+12898C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99806441 | ||||||
| chr14:99806696
|
G | A | 2 | a0001c0005t0005g0003a0004c0008t0004g0004 | 2 | HG02451.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.67+13153G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99806696 | ||||||
| chr14:99806800
|
C | T | 1 | a0001c0003t0001g0158 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.67+13257C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99806800 | ||||||
| chr14:99806832
|
T | TA | 6 | a0001c0003t0001g0006a0001c0003t0001g0008a0001c0003t0001g0010others(3): Show | 6 | HG02257.hp2 HG02723.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+13290dupA | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99806832 | |||||
| chr14:99807030
|
A | C | 1 | a0003c0002t0001g0186 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.67+13487A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99807030 | ||||||
| chr14:99807034
|
A | G | 3 | a0001c0004t0010g0235a0001c0005t0005g0003a0004c0008t0004g0004 | 3 | HG02451.hp1 HG02615.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.67+13491A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99807034 | ||||||
| chr14:99807066
|
C | T | 1 | a0003c0002t0003g0212 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.67+13523C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99807066 | ||||||
| chr14:99807072
|
C | T | 1 | a0001c0004t0001g0123 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.67+13529C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99807072 | ||||||
| chr14:99807199
|
C | T | 2 | a0003c0002t0001g0237a0003c0002t0008g0238 | 2 | HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.67+13656C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99807199 | ||||||
| chr14:99807261
|
A | G | 5 | a0001c0003t0003g0277a0001c0003t0003g0279a0001c0003t0007g0281others(2): Show | 5 | HG00140.hp2 HG01071.hp2 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+13718A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99807261 | ||||||
| chr14:99807288
|
T | C | 198 | a0001c0003t0001g0006a0001c0003t0001g0008a0001c0003t0001g0010others(195): Show | 199 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.67+13745T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99807288 | ||||||
| chr14:99807294
|
A | G | 1 | a0001c0004t0010g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.67+13751A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99807294 | ||||||
| chr14:99807442
|
TG | T | 4 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0005t0004g0284others(1): Show | 4 | HG02886.hp1 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+13900delG | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99807442 | ||||||
| chr14:99807519
|
C | T | 1 | a0002c0001t0002g0176 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.67+13976C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99807519 | ||||||
| chr14:99807577
|
G | T | 1 | a0002c0001t0002g0276 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.67+14034G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99807577 | ||||||
| chr14:99807605
|
G | A | 1 | a0001c0004t0001g0123 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.67+14062G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99807605 | ||||||
| chr14:99807690
|
C | T | 1 | a0003c0002t0002g0138 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.67+14147C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99807690 | ||||||
| chr14:99807734
|
G | T | 81 | a0001c0003t0001g0012a0001c0003t0001g0158a0001c0003t0001g0167others(78): Show | 81 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.67+14191G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99807734 | ||||||
| chr14:99807742
|
G | A | 5 | a0001c0003t0001g0012a0001c0003t0001g0232a0001c0003t0001g0233others(2): Show | 5 | HG01109.hp2 HG01975.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+14199G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99807742 | ||||||
| chr14:99807778
|
C | T | 1 | a0003c0002t0001g0187 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.67+14235C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99807778 | ||||||
| chr14:99807838
|
T | C | 4 | a0001c0004t0001g0040a0001c0004t0001g0135a0002c0001t0002g0065others(1): Show | 4 | HG02015.hp2 NA18939.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+14295T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99807838 | ||||||
| chr14:99807910
|
C | T | 2 | a0001c0003t0001g0272a0001c0003t0001g0273 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.67+14367C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99807910 | ||||||
| chr14:99807953
|
A | G | 14 | a0001c0003t0001g0163a0001c0003t0001g0282a0001c0003t0001g0283others(11): Show | 14 | HG02015.hp2 HG02055.hp1 HG02886.hp1 others(11): Show |
intron_variant | MODIFIER | c.67+14410A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99807953 | ||||||
| chr14:99807979
|
C | T | 1 | a0004c0008t0004g0268 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.67+14436C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99807979 | ||||||
| chr14:99808119
|
C | G | 225 | a0001c0003t0001g0001a0001c0003t0001g0007a0001c0003t0001g0015others(222): Show | 226 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.67+14576C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99808119 | ||||||
| chr14:99808148
|
C | T | 1 | a0001c0007t0002g0005 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.67+14605C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99808148 | ||||||
| chr14:99808365
|
G | A | 1 | a0001c0003t0007g0281 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.67+14822G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99808365 | ||||||
| chr14:99808434
|
G | A | 65 | a0001c0003t0001g0041a0001c0003t0001g0085a0001c0003t0001g0152others(62): Show | 65 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.67+14891G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99808434 | ||||||
| chr14:99808513
|
G | A | 1 | a0001c0004t0003g0022 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.67+14970G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99808513 | ||||||
| chr14:99808530
|
A | G | 2 | a0002c0001t0002g0046a0002c0001t0002g0176 | 2 | HG01928.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.67+14987A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99808530 | ||||||
| chr14:99808540
|
C | A | 24 | a0001c0003t0001g0158a0001c0003t0001g0167a0001c0003t0001g0168others(21): Show | 24 | HG00140.hp2 HG01069.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.67+14997C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99808540 | ||||||
| chr14:99808565
|
T | G | 1 | a0001c0003t0004g0258 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.67+15022T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99808565 | ||||||
| chr14:99808585
|
T | C | 7 | a0001c0003t0002g0105a0001c0003t0002g0106a0001c0003t0002g0116others(4): Show | 7 | HG00609.hp2 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.67+15042T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99808585 | ||||||
| chr14:99808627
|
C | T | 6 | a0001c0003t0001g0007a0001c0003t0001g0015a0001c0003t0001g0016others(3): Show | 6 | HG02109.hp1 HG02615.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+15084C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99808627 | ||||||
| chr14:99808824
|
C | G | 7 | a0001c0003t0002g0105a0001c0003t0002g0106a0001c0003t0002g0116others(4): Show | 7 | HG01884.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.67+15281C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99808824 | ||||||
| chr14:99808829
|
C | G | 7 | a0001c0003t0002g0105a0001c0003t0002g0106a0001c0003t0002g0116others(4): Show | 7 | HG01884.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.67+15286C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99808829 | ||||||
| chr14:99808872
|
A | G | 1 | a0001c0003t0004g0258 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.67+15329A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99808872 | ||||||
| chr14:99808963
|
G | A | 2 | a0001c0003t0001g0272a0001c0003t0001g0273 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.67+15420G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99808963 | ||||||
| chr14:99808981
|
A | G | 1 | a0003c0002t0001g0094 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.67+15438A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99808981 | ||||||
| chr14:99809023
|
A | G | 115 | a0001c0003t0001g0001a0001c0003t0001g0080a0001c0003t0001g0158others(112): Show | 116 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.67+15480A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99809023 | ||||||
| chr14:99809076
|
T | C | 115 | a0001c0003t0001g0001a0001c0003t0001g0007a0001c0003t0001g0015others(112): Show | 116 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.67+15533T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99809076 | ||||||
| chr14:99809089
|
C | T | 1 | a0001c0003t0004g0258 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.67+15546C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99809089 | ||||||
| chr14:99809188
|
A | G | 3 | a0001c0003t0003g0032a0001c0003t0003g0033a0001c0003t0003g0034 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.67+15645A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99809188 | ||||||
| chr14:99809214
|
C | T | 3 | a0001c0003t0001g0272a0001c0003t0001g0273a0006c0011t0001g0011 | 3 | HG02559.hp2 HG02965.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.67+15671C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99809214 | ||||||
| chr14:99809280
|
A | G | 9 | a0001c0003t0001g0260a0001c0003t0008g0271a0001c0004t0001g0255others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.67+15737A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99809280 | ||||||
| chr14:99809334
|
T | TTTTA | 6 | a0001c0003t0001g0007a0001c0003t0001g0015a0001c0003t0001g0016others(3): Show | 6 | HG02109.hp1 HG02615.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+15808_67+15811d others(6): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99809334 | |||||
| chr14:99809361
|
C | G | 130 | a0001c0003t0001g0001a0001c0003t0001g0007a0001c0003t0001g0015others(127): Show | 131 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.67+15818C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99809361 | ||||||
| chr14:99809421
|
A | G | 7 | a0001c0003t0001g0080a0001c0003t0001g0259a0001c0003t0004g0258others(4): Show | 7 | HG00609.hp2 HG00639.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.67+15878A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99809421 | ||||||
| chr14:99809440
|
C | T | 2 | a0001c0003t0002g0105a0001c0003t0002g0106 | 2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.67+15897C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99809440 | ||||||
| chr14:99809481
|
T | C | 3 | a0001c0003t0001g0012a0001c0003t0001g0232a0001c0003t0001g0233 | 3 | HG01109.hp2 HG02109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.67+15938T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99809481 | ||||||
| chr14:99809581
|
G | T | 4 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0005t0004g0284others(1): Show | 4 | HG02886.hp1 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+16038G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99809581 | ||||||
| chr14:99809776
|
G | A | 1 | a0001c0003t0001g0163 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.67+16233G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99809776 | ||||||
| chr14:99809946
|
A | G | 1 | a0003c0002t0001g0186 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.67+16403A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99809946 | ||||||
| chr14:99810075
|
C | T | 1 | a0002c0001t0002g0063 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.67+16532C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99810075 | ||||||
| chr14:99810107
|
G | A | 1 | a0003c0002t0010g0200 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.67+16564G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99810107 | ||||||
| chr14:99810192
|
G | C | 1 | a0001c0003t0004g0258 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.67+16649G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99810192 | ||||||
| chr14:99810266
|
T | C | 2 | a0002c0001t0002g0177a0002c0001t0002g0178 | 2 | NA18969.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.67+16723T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99810266 | ||||||
| chr14:99810278
|
A | T | 1 | a0001c0003t0007g0281 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.67+16735A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99810278 | ||||||
| chr14:99810367
|
G | C | 1 | a0001c0004t0001g0255 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.67+16824G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99810367 | ||||||
| chr14:99810370
|
G | A | 109 | a0001c0003t0001g0001a0001c0003t0001g0007a0001c0003t0001g0015others(106): Show | 110 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.67+16827G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99810370 | ||||||
| chr14:99810432
|
C | T | 1 | a0006c0011t0001g0011 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.67+16889C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99810432 | ||||||
| chr14:99810439
|
G | A | 1 | a0001c0003t0004g0258 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.67+16896G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99810439 | ||||||
| chr14:99810676
|
A | G | 1 | a0001c0004t0003g0197 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.67+17133A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99810676 | ||||||
| chr14:99810746
|
G | T | 1 | a0002c0001t0002g0110 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.67+17203G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99810746 | ||||||
| chr14:99810925
|
G | T | 2 | a0001c0003t0001g0272a0001c0003t0001g0273 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.67+17382G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99810925 | ||||||
| chr14:99810989
|
A | C | 4 | a0001c0003t0003g0277a0001c0003t0003g0279a0001c0004t0003g0280others(1): Show | 4 | HG00140.hp2 HG01071.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+17446A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99810989 | ||||||
| chr14:99811139
|
A | ACAGTGAT others(45): Show |
3 | a0001c0003t0003g0277a0001c0003t0003g0279a0002c0001t0002g0278 | 3 | HG00140.hp2 HG01071.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.67+17600_67+17601i others(54): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99811139 | |||||
| chr14:99811142
|
G | T | 1 | a0001c0003t0004g0258 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.67+17599G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99811142 | ||||||
| chr14:99811162
|
AG | A | 6 | a0001c0003t0001g0007a0001c0003t0001g0015a0001c0003t0001g0016others(3): Show | 6 | HG02109.hp1 HG02615.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+17623delG | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99811162 | |||||
| chr14:99811165
|
G | GT | 3 | a0002c0001t0001g0092a0002c0001t0001g0219a0002c0001t0002g0095 | 3 | HG04115.hp2 NA18955.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.67+17622_67+17623i others(3): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99811165 | ||||||
| chr14:99811165
|
GGT | G | 3 | a0001c0003t0003g0277a0001c0003t0003g0279a0002c0001t0002g0278 | 3 | HG00140.hp2 HG01071.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.67+17623_67+17624d others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99811165 | ||||||
| chr14:99811166
|
G | T | 103 | a0001c0003t0001g0001a0001c0003t0001g0158a0001c0003t0001g0167others(100): Show | 104 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.67+17623G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99811166 | ||||||
| chr14:99811166
|
GT | G | 12 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0003t0003g0032others(9): Show | 12 | HG00609.hp2 HG02055.hp1 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.67+17633delT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99811166 | |||||
| chr14:99811328
|
GAGCCACT others(1347): Show |
G | 3 | a0001c0003t0003g0277a0001c0003t0003g0279a0002c0001t0002g0278 | 3 | HG00140.hp2 HG01071.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.67+17790_67+19143d others(2): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99811328 | |||||
| chr14:99811418
|
T | C | 6 | a0001c0003t0001g0007a0001c0003t0001g0015a0001c0003t0001g0016others(3): Show | 6 | HG02109.hp1 HG02615.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+17875T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99811418 | ||||||
| chr14:99811429
|
G | A | 4 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0005t0004g0284others(1): Show | 4 | HG02886.hp1 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+17886G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99811429 | ||||||
| chr14:99811479
|
A | C | 3 | a0001c0003t0001g0012a0001c0003t0001g0232a0001c0003t0001g0233 | 3 | HG01109.hp2 HG02109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.67+17936A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99811479 | ||||||
| chr14:99811573
|
C | T | 1 | a0001c0003t0004g0258 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.67+18030C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99811573 | ||||||
| chr14:99811607
|
A | G | 1 | a0003c0002t0001g0130 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.67+18064A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99811607 | ||||||
| chr14:99811620
|
C | T | 6 | a0001c0003t0001g0007a0001c0003t0001g0015a0001c0003t0001g0016others(3): Show | 6 | HG02109.hp1 HG02615.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+18077C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99811620 | ||||||
| chr14:99811623
|
T | C | 115 | a0001c0003t0001g0001a0001c0003t0001g0007a0001c0003t0001g0015others(112): Show | 116 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.67+18080T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99811623 | ||||||
| chr14:99811640
|
C | CA | 55 | a0001c0003t0001g0086a0001c0003t0001g0193a0001c0003t0002g0181others(52): Show | 56 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.67+18118dupA | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99811640 | |||||
| chr14:99811640
|
CA | C | 43 | a0001c0003t0001g0006a0001c0003t0001g0008a0001c0003t0001g0010others(40): Show | 43 | HG00323.hp1 HG00639.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.67+18118delA | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99811640 | |||||
| chr14:99811640
|
CAAA | C | 94 | a0001c0003t0001g0001a0001c0003t0001g0158a0001c0003t0001g0167others(91): Show | 95 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.67+18116_67+18118d others(5): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99811640 | |||||
| chr14:99811814
|
AAG | A | 100 | a0001c0003t0001g0001a0001c0003t0001g0158a0001c0003t0001g0167others(97): Show | 101 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.67+18287_67+18288d others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99811814 | |||||
| chr14:99811864
|
A | G | 1 | a0001c0003t0004g0258 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.67+18321A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99811864 | ||||||
| chr14:99811929
|
T | G | 2 | a0001c0003t0001g0286a0001c0004t0003g0280 | 2 | HG03453.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.67+18386T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99811929 | ||||||
| chr14:99812170
|
G | A | 1 | a0001c0004t0005g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.67+18627G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99812170 | ||||||
| chr14:99812237
|
G | C | 1 | a0001c0003t0004g0027 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.67+18694G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99812237 | ||||||
| chr14:99812248
|
G | A | 8 | a0001c0003t0002g0105a0001c0003t0002g0106a0001c0003t0002g0116others(5): Show | 8 | HG01884.hp1 HG02615.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.67+18705G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99812248 | ||||||
| chr14:99812389
|
C | T | 1 | a0001c0003t0007g0014 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+18846C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99812389 | ||||||
| chr14:99812489
|
T | G | 2 | a0001c0003t0001g0286a0001c0004t0003g0280 | 2 | HG03453.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.67+18946T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99812489 | ||||||
| chr14:99812518
|
A | C | 113 | a0001c0003t0001g0001a0001c0003t0001g0158a0001c0003t0001g0167others(110): Show | 114 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.67+18975A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99812518 | ||||||
| chr14:99812644
|
T | C | 1 | a0002c0001t0003g0134 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.67+19101T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99812644 | ||||||
| chr14:99812719
|
G | C | 1 | a0003c0002t0001g0154 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.67+19176G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99812719 | ||||||
| chr14:99812812
|
G | A | 7 | a0002c0001t0002g0051a0003c0002t0001g0044a0003c0002t0001g0087others(4): Show | 7 | HG01109.hp1 HG01192.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.67+19269G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99812812 | ||||||
| chr14:99813146
|
G | C | 99 | a0001c0003t0001g0001a0001c0003t0001g0158a0001c0003t0001g0167others(96): Show | 100 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.67+19603G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99813146 | ||||||
| chr14:99813155
|
G | C | 86 | a0001c0003t0004g0027a0001c0004t0001g0040a0001c0004t0001g0091others(83): Show | 86 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.67+19612G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99813155 | ||||||
| chr14:99813345
|
A | G | 2 | a0001c0003t0001g0272a0001c0003t0001g0273 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.67+19802A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99813345 | ||||||
| chr14:99813355
|
T | G | 126 | a0001c0003t0001g0001a0001c0003t0001g0007a0001c0003t0001g0015others(123): Show | 127 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.67+19812T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99813355 | ||||||
| chr14:99813431
|
A | G | 3 | a0001c0003t0001g0111a0001c0003t0001g0113a0001c0003t0001g0114 | 3 | HG02630.hp1 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.67+19888A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99813431 | ||||||
| chr14:99813556
|
A | G | 1 | a0001c0003t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.67+20013A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99813556 | ||||||
| chr14:99813659
|
A | T | 1 | a0006c0011t0001g0011 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.67+20116A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99813659 | ||||||
| chr14:99813718
|
T | A | 2 | a0001c0003t0001g0269a0001c0007t0002g0005 | 2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.67+20175T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99813718 | ||||||
| chr14:99814031
|
A | T | 2 | a0001c0003t0001g0272a0001c0003t0001g0273 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.67+20488A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99814031 | ||||||
| chr14:99814297
|
A | G | 2 | a0003c0002t0001g0237a0003c0002t0008g0238 | 2 | HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.67+20754A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99814297 | ||||||
| chr14:99814406
|
T | G | 1 | a0006c0011t0001g0011 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.67+20863T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99814406 | ||||||
| chr14:99814444
|
T | G | 3 | a0001c0003t0003g0032a0001c0003t0003g0033a0001c0003t0003g0034 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.67+20901T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99814444 | ||||||
| chr14:99814534
|
A | G | 110 | a0001c0003t0001g0001a0001c0003t0001g0007a0001c0003t0001g0015others(107): Show | 111 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.67+20991A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99814534 | ||||||
| chr14:99814668
|
AT | A | 3 | a0001c0004t0003g0195a0004c0008t0004g0268a0005c0009t0002g0132 | 3 | HG02055.hp2 HG04204.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.67+21129delT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99814668 | |||||
| chr14:99814744
|
A | C | 3 | a0001c0003t0001g0006a0001c0003t0001g0010a0001c0004t0004g0017 | 3 | HG02257.hp2 HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.67+21201A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99814744 | ||||||
| chr14:99814789
|
C | T | 13 | a0001c0003t0001g0001a0001c0003t0001g0158a0001c0003t0001g0167others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.67+21246C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99814789 | ||||||
| chr14:99814825
|
T | C | 1 | a0002c0001t0015g0109 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.67+21282T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99814825 | ||||||
| chr14:99814947
|
G | A | 13 | a0001c0003t0001g0001a0001c0003t0001g0158a0001c0003t0001g0167others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.67+21404G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99814947 | ||||||
| chr14:99814993
|
G | A | 2 | a0002c0001t0002g0068a0002c0001t0002g0069 | 2 | NA18984.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.67+21450G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99814993 | ||||||
| chr14:99815056
|
G | A | 1 | a0001c0005t0005g0097 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.67+21513G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99815056 | ||||||
| chr14:99815139
|
C | CT | 7 | a0002c0001t0001g0062a0002c0001t0001g0092a0002c0001t0002g0061others(4): Show | 7 | HG01975.hp2 HG04115.hp2 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.67+21616dupT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99815139 | |||||
| chr14:99815139
|
CT | C | 157 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0015others(154): Show | 158 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.67+21616delT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99815139 | |||||
| chr14:99815139
|
CTTT | C | 12 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0003t0003g0032others(9): Show | 12 | HG02055.hp1 HG02886.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.67+21614_67+21616d others(5): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99815139 | |||||
| chr14:99815261
|
C | G | 1 | a0001c0003t0004g0258 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.67+21718C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99815261 | ||||||
| chr14:99815302
|
C | T | 1 | a0001c0004t0003g0280 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.67+21759C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99815302 | ||||||
| chr14:99815303
|
G | A | 1 | a0002c0001t0003g0236 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.67+21760G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99815303 | ||||||
| chr14:99815435
|
C | A | 1 | a0001c0003t0001g0086 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.67+21892C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99815435 | ||||||
| chr14:99815523
|
T | A | 112 | a0001c0003t0001g0001a0001c0003t0001g0007a0001c0003t0001g0015others(109): Show | 113 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.67+21980T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99815523 | ||||||
| chr14:99815528
|
G | C | 1 | a0003c0002t0017g0028 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.67+21985G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99815528 | ||||||
| chr14:99815604
|
G | A | 1 | a0001c0003t0004g0258 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.67+22061G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99815604 | ||||||
| chr14:99815748
|
G | A | 1 | a0002c0001t0002g0061 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.67+22205G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99815748 | ||||||
| chr14:99815806
|
G | A | 1 | a0002c0001t0001g0216 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.67+22263G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99815806 | ||||||
| chr14:99815833
|
G | A | 110 | a0001c0003t0001g0001a0001c0003t0001g0007a0001c0003t0001g0015others(107): Show | 111 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.67+22290G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99815833 | ||||||
| chr14:99815836
|
G | A | 110 | a0001c0003t0001g0001a0001c0003t0001g0007a0001c0003t0001g0015others(107): Show | 111 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.67+22293G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99815836 | ||||||
| chr14:99815847
|
G | A | 122 | a0001c0003t0001g0001a0001c0003t0001g0007a0001c0003t0001g0015others(119): Show | 123 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.67+22304G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99815847 | ||||||
| chr14:99815968
|
G | C | 1 | a0002c0001t0002g0052 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.67+22425G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99815968 | ||||||
| chr14:99816090
|
G | A | 2 | a0001c0004t0003g0049a0001c0004t0003g0145 | 2 | NA18984.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.67+22547G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99816090 | ||||||
| chr14:99816186
|
C | T | 1 | a0001c0003t0007g0281 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.67+22643C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99816186 | ||||||
| chr14:99816190
|
G | T | 1 | a0003c0002t0001g0002 | 2 | HG00639.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.67+22647G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99816190 | ||||||
| chr14:99816205
|
C | T | 4 | a0001c0004t0001g0143a0001c0004t0010g0235a0001c0004t0013g0108others(1): Show | 4 | HG02055.hp1 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+22662C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99816205 | ||||||
| chr14:99816212
|
G | A | 1 | a0001c0004t0010g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.67+22669G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99816212 | ||||||
| chr14:99816253
|
T | C | 1 | a0001c0003t0001g0158 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.67+22710T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99816253 | ||||||
| chr14:99816337
|
A | G | 13 | a0001c0003t0001g0001a0001c0003t0001g0158a0001c0003t0001g0167others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.67+22794A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99816337 | ||||||
| chr14:99816351
|
T | C | 122 | a0001c0003t0001g0001a0001c0003t0001g0007a0001c0003t0001g0015others(119): Show | 123 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.67+22808T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99816351 | ||||||
| chr14:99816453
|
G | A | 110 | a0001c0003t0001g0001a0001c0003t0001g0007a0001c0003t0001g0015others(107): Show | 111 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.67+22910G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99816453 | ||||||
| chr14:99816898
|
A | C | 12 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0003t0003g0032others(9): Show | 12 | HG02055.hp1 HG02886.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.67+23355A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99816898 | ||||||
| chr14:99816911
|
G | A | 97 | a0001c0003t0001g0001a0001c0003t0001g0158a0001c0003t0001g0167others(94): Show | 98 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.67+23368G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99816911 | ||||||
| chr14:99816949
|
T | C | 4 | a0001c0004t0003g0180a0002c0001t0002g0183a0003c0002t0002g0162others(1): Show | 4 | NA18983.hp1 NA18983.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+23406T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99816949 | ||||||
| chr14:99817072
|
C | G | 5 | a0001c0003t0001g0286a0001c0003t0003g0277a0001c0003t0003g0279others(2): Show | 5 | HG00140.hp2 HG01071.hp2 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+23529C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99817072 | ||||||
| chr14:99817098
|
C | CT | 84 | a0001c0003t0004g0027a0001c0004t0001g0040a0001c0004t0001g0091others(81): Show | 84 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.67+23563dupT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99817098 | |||||
| chr14:99817213
|
G | A | 6 | a0001c0003t0001g0007a0001c0003t0001g0015a0001c0003t0001g0016others(3): Show | 6 | HG02109.hp1 HG02615.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+23670G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99817213 | ||||||
| chr14:99817358
|
G | A | 1 | a0003c0002t0012g0253 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.67+23815G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99817358 | ||||||
| chr14:99817389
|
G | A | 1 | a0003c0002t0001g0146 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.67+23846G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99817389 | ||||||
| chr14:99817437
|
C | T | 11 | a0001c0003t0001g0243a0001c0003t0001g0244a0001c0003t0001g0245others(8): Show | 11 | HG02280.hp1 HG02622.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.67+23894C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99817437 | ||||||
| chr14:99817455
|
C | A | 4 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0005t0004g0284others(1): Show | 4 | HG02886.hp1 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+23912C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99817455 | ||||||
| chr14:99817456
|
G | A | 1 | a0003c0002t0003g0212 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.67+23913G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99817456 | ||||||
| chr14:99817473
|
G | A | 1 | a0001c0003t0001g0158 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.67+23930G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99817473 | ||||||
| chr14:99817519
|
C | T | 84 | a0001c0003t0004g0027a0001c0004t0001g0040a0001c0004t0001g0091others(81): Show | 84 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.67+23976C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99817519 | ||||||
| chr14:99817700
|
C | T | 4 | a0001c0004t0001g0143a0001c0004t0010g0235a0001c0004t0013g0108others(1): Show | 4 | HG02055.hp1 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+24157C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99817700 | ||||||
| chr14:99817768
|
A | G | 1 | a0001c0003t0004g0258 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.67+24225A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99817768 | ||||||
| chr14:99817976
|
A | G | 2 | a0001c0003t0004g0258a0006c0011t0001g0011 | 2 | HG00609.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.67+24433A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99817976 | ||||||
| chr14:99818017
|
G | T | 6 | a0001c0003t0001g0007a0001c0003t0001g0015a0001c0003t0001g0016others(3): Show | 6 | HG02109.hp1 HG02615.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+24474G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99818017 | ||||||
| chr14:99818051
|
C | T | 3 | a0001c0003t0001g0120a0001c0013t0001g0126a0002c0001t0002g0133 | 3 | HG01243.hp1 HG01515.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.67+24508C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99818051 | ||||||
| chr14:99818212
|
G | T | 3 | a0001c0003t0003g0032a0001c0003t0003g0033a0001c0003t0003g0034 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.67+24669G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99818212 | ||||||
| chr14:99818236
|
G | C | 1 | a0003c0002t0001g0198 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.67+24693G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99818236 | ||||||
| chr14:99818282
|
G | A | 6 | a0001c0003t0001g0080a0001c0003t0001g0259a0001c0005t0001g0250others(3): Show | 6 | HG00639.hp2 HG02451.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+24739G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99818282 | ||||||
| chr14:99818311
|
C | T | 1 | a0001c0003t0004g0258 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.67+24768C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99818311 | ||||||
| chr14:99818342
|
C | G | 106 | a0001c0003t0001g0001a0001c0003t0001g0007a0001c0003t0001g0015others(103): Show | 107 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.67+24799C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99818342 | ||||||
| chr14:99818415
|
G | A | 8 | a0001c0003t0002g0105a0001c0003t0002g0106a0001c0003t0002g0116others(5): Show | 8 | HG01884.hp1 HG02615.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.67+24872G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99818415 | ||||||
| chr14:99818453
|
C | A | 2 | a0003c0002t0001g0237a0003c0002t0008g0238 | 2 | HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.67+24910C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99818453 | ||||||
| chr14:99818461
|
A | G | 5 | a0001c0003t0001g0286a0001c0003t0003g0277a0001c0003t0003g0279others(2): Show | 5 | HG00140.hp2 HG01071.hp2 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+24918A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99818461 | ||||||
| chr14:99818467
|
T | C | 5 | a0001c0003t0001g0286a0001c0003t0003g0277a0001c0003t0003g0279others(2): Show | 5 | HG00140.hp2 HG01071.hp2 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+24924T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99818467 | ||||||
| chr14:99818535
|
T | C | 8 | a0001c0003t0001g0272a0001c0003t0001g0273a0001c0003t0001g0286others(5): Show | 8 | HG00140.hp2 HG00609.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.67+24992T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99818535 | ||||||
| chr14:99818605
|
C | T | 1 | a0001c0003t0007g0014 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+25062C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99818605 | ||||||
| chr14:99818606
|
A | G | 285 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0007others(282): Show | 287 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.67+25063A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99818606 | ||||||
| chr14:99818668
|
C | T | 1 | a0001c0003t0004g0258 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.67+25125C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99818668 | ||||||
| chr14:99818706
|
G | C | 1 | a0002c0001t0002g0081 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.67+25163G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99818706 | ||||||
| chr14:99818819
|
G | A | 1 | a0001c0007t0002g0005 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.67+25276G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99818819 | ||||||
| chr14:99818842
|
C | T | 5 | a0001c0003t0003g0032a0001c0003t0003g0033a0001c0003t0003g0034others(2): Show | 5 | HG02895.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+25299C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99818842 | ||||||
| chr14:99818843
|
G | A | 85 | a0001c0003t0004g0027a0001c0004t0001g0040a0001c0004t0001g0091others(82): Show | 85 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.67+25300G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99818843 | ||||||
| chr14:99818925
|
A | C | 3 | a0001c0003t0003g0032a0001c0003t0003g0033a0001c0003t0003g0034 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.67+25382A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99818925 | ||||||
| chr14:99819004
|
A | T | 2 | a0001c0005t0004g0284a0001c0005t0004g0285 | 2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.67+25461A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99819004 | ||||||
| chr14:99819208
|
G | A | 12 | a0001c0003t0001g0001a0001c0003t0001g0158a0001c0003t0001g0167others(9): Show | 13 | HG01069.hp1 HG01071.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.67+25665G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99819208 | ||||||
| chr14:99819209
|
C | T | 3 | a0001c0003t0003g0032a0001c0003t0003g0033a0001c0003t0003g0034 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.67+25666C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99819209 | ||||||
| chr14:99819244
|
T | G | 5 | a0001c0003t0001g0286a0001c0003t0003g0277a0001c0003t0003g0279others(2): Show | 5 | HG00140.hp2 HG01071.hp2 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+25701T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99819244 | ||||||
| chr14:99819405
|
C | G | 8 | a0001c0003t0002g0105a0001c0003t0002g0106a0001c0003t0002g0116others(5): Show | 8 | HG01884.hp1 HG02615.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.67+25862C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99819405 | ||||||
| chr14:99819556
|
C | T | 1 | a0001c0003t0001g0152 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.67+26013C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99819556 | ||||||
| chr14:99819623
|
G | A | 1 | a0001c0003t0003g0279 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.67+26080G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99819623 | ||||||
| chr14:99819728
|
A | T | 1 | a0006c0011t0001g0011 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.67+26185A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99819728 | ||||||
| chr14:99819746
|
G | A | 2 | a0001c0003t0001g0272a0001c0003t0001g0273 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.67+26203G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99819746 | ||||||
| chr14:99819886
|
A | G | 1 | a0001c0004t0003g0149 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.67+26343A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99819886 | ||||||
| chr14:99820199
|
T | C | 34 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0158others(31): Show | 34 | HG00609.hp2 HG01074.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.67+26656T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99820199 | ||||||
| chr14:99820323
|
C | T | 2 | a0001c0003t0001g0282a0001c0003t0001g0283 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.67+26780C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99820323 | ||||||
| chr14:99820573
|
C | T | 6 | a0001c0003t0001g0080a0001c0003t0001g0259a0001c0005t0001g0250others(3): Show | 6 | HG00639.hp2 HG02451.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+27030C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99820573 | ||||||
| chr14:99820703
|
A | C | 5 | a0001c0003t0002g0116a0001c0005t0005g0265a0001c0007t0018g0241others(2): Show | 5 | HG01884.hp1 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+27160A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99820703 | ||||||
| chr14:99820712
|
C | T | 6 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0003t0003g0279others(3): Show | 6 | HG01074.hp1 HG02886.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+27169C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99820712 | ||||||
| chr14:99820955
|
A | G | 6 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0003t0003g0279others(3): Show | 6 | HG01074.hp1 HG02886.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+27412A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99820955 | ||||||
| chr14:99821023
|
C | CT | 6 | a0001c0003t0001g0001a0002c0001t0003g0098a0003c0002t0001g0146others(3): Show | 7 | HG01256.hp1 HG01258.hp2 NA19002.hp2 others(4): Show |
intron_variant | MODIFIER | c.67+27499dupT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99821023 | |||||
| chr14:99821023
|
CT | C | 41 | a0001c0003t0001g0010a0001c0003t0001g0080a0001c0003t0001g0158others(38): Show | 41 | HG00609.hp2 HG00639.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.67+27499delT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99821023 | |||||
| chr14:99821113
|
C | T | 3 | a0001c0003t0001g0012a0001c0003t0001g0232a0001c0003t0001g0233 | 3 | HG01109.hp2 HG02109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.67+27570C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99821113 | ||||||
| chr14:99821375
|
C | T | 1 | a0001c0004t0001g0091 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.67+27832C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99821375 | ||||||
| chr14:99821572
|
TG | T | 6 | a0001c0003t0001g0080a0001c0003t0001g0259a0001c0005t0001g0250others(3): Show | 6 | HG00639.hp2 HG02451.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.67+28032delG | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99821572 | |||||
| chr14:99821640
|
A | C | 3 | a0001c0003t0003g0032a0001c0003t0003g0033a0001c0003t0003g0034 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.67+28097A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99821640 | ||||||
| chr14:99821783
|
A | G | 4 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0005t0004g0284others(1): Show | 4 | HG02886.hp1 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+28240A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99821783 | ||||||
| chr14:99822102
|
T | G | 6 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0003t0003g0279others(3): Show | 6 | HG01074.hp1 HG02886.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+28559T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99822102 | ||||||
| chr14:99822118
|
G | A | 6 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0003t0003g0279others(3): Show | 6 | HG01074.hp1 HG02886.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+28575G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99822118 | ||||||
| chr14:99822137
|
A | G | 5 | a0001c0003t0002g0116a0001c0005t0005g0265a0001c0007t0018g0241others(2): Show | 5 | HG01884.hp1 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+28594A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99822137 | ||||||
| chr14:99822199
|
T | C | 4 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0005t0004g0284others(1): Show | 4 | HG02886.hp1 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-28654T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99822199 | ||||||
| chr14:99822199
|
TG | T | 22 | a0001c0003t0001g0010a0001c0003t0001g0158a0001c0003t0001g0163others(19): Show | 22 | HG02145.hp2 HG02257.hp2 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.68-28653delG | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99822199 | ||||||
| chr14:99822200
|
G | T | 7 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0003t0003g0279others(4): Show | 7 | HG00609.hp2 HG01074.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-28653G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99822200 | ||||||
| chr14:99822260
|
C | G | 1 | a0003c0002t0001g0198 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.68-28593C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99822260 | ||||||
| chr14:99822267
|
C | T | 2 | a0001c0003t0003g0279a0001c0004t0003g0280 | 2 | HG01074.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.68-28586C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99822267 | ||||||
| chr14:99822275
|
A | G | 6 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0003t0003g0279others(3): Show | 6 | HG01074.hp1 HG02886.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-28578A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99822275 | ||||||
| chr14:99822296
|
T | C | 6 | a0001c0003t0001g0282a0001c0003t0001g0283a0001c0003t0003g0279others(3): Show | 6 | HG01074.hp1 HG02886.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-28557T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99822296 | ||||||
| chr14:99822473
|
T | G | 22 | a0001c0003t0001g0010a0001c0003t0001g0158a0001c0003t0001g0163others(19): Show | 22 | HG02145.hp2 HG02257.hp2 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.68-28380T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99822473 | ||||||
| chr14:99822606
|
C | T | 3 | a0001c0003t0003g0032a0001c0003t0003g0033a0001c0003t0003g0034 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.68-28247C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99822606 | ||||||
| chr14:99822690
|
C | T | 18 | a0001c0003t0001g0010a0001c0003t0001g0163a0001c0003t0001g0214others(15): Show | 18 | HG02257.hp2 HG02451.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.68-28163C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99822690 | ||||||
| chr14:99822769
|
G | A | 13 | a0001c0003t0001g0080a0001c0003t0001g0259a0001c0003t0001g0286others(10): Show | 13 | HG00639.hp2 HG01884.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.68-28084G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99822769 | ||||||
| chr14:99822897
|
C | T | 6 | a0001c0003t0001g0080a0001c0003t0001g0259a0001c0005t0001g0250others(3): Show | 6 | HG00639.hp2 HG02451.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-27956C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99822897 | ||||||
| chr14:99823051
|
C | T | 3 | a0001c0003t0001g0158a0001c0003t0001g0167a0001c0003t0001g0168 | 3 | HG02572.hp1 HG02818.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.68-27802C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99823051 | ||||||
| chr14:99823067
|
G | A | 2 | a0002c0001t0001g0239a0004c0008t0004g0004 | 2 | HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.68-27786G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99823067 | ||||||
| chr14:99823105
|
G | C | 12 | a0001c0003t0001g0012a0001c0003t0001g0220a0001c0003t0001g0221others(9): Show | 12 | HG01109.hp2 HG02109.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.68-27748G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99823105 | ||||||
| chr14:99823301
|
G | A | 1 | a0002c0001t0003g0142 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.68-27552G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99823301 | ||||||
| chr14:99823313
|
G | A | 5 | a0001c0003t0001g0282a0001c0003t0003g0279a0001c0004t0003g0280others(2): Show | 5 | HG01074.hp1 HG02886.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-27540G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99823313 | ||||||
| chr14:99823353
|
C | G | 1 | a0001c0004t0001g0143 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.68-27500C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99823353 | ||||||
| chr14:99823406
|
G | C | 1 | a0001c0003t0001g0232 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.68-27447G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99823406 | ||||||
| chr14:99823507
|
G | A | 1 | a0001c0003t0004g0258 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.68-27346G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99823507 | ||||||
| chr14:99823568
|
C | T | 67 | a0001c0003t0001g0001a0001c0003t0004g0027a0001c0004t0001g0040others(64): Show | 68 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.68-27285C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99823568 | ||||||
| chr14:99823583
|
A | G | 29 | a0001c0003t0001g0010a0001c0003t0001g0163a0001c0003t0001g0214others(26): Show | 29 | HG00609.hp2 HG01074.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.68-27270A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99823583 | ||||||
| chr14:99823672
|
C | T | 4 | a0001c0003t0008g0271a0001c0004t0001g0255a0002c0001t0002g0083others(1): Show | 4 | HG02451.hp2 HG02602.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-27181C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99823672 | ||||||
| chr14:99823689
|
A | G | 5 | a0001c0003t0001g0282a0001c0003t0003g0279a0001c0004t0003g0280others(2): Show | 5 | HG01074.hp1 HG02886.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-27164A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99823689 | ||||||
| chr14:99823739
|
G | A | 1 | a0001c0004t0001g0091 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.68-27114G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99823739 | ||||||
| chr14:99823767
|
G | A | 3 | a0001c0003t0004g0141a0004c0008t0004g0268a0005c0009t0002g0132 | 3 | HG02055.hp2 NA18952.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.68-27086G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99823767 | ||||||
| chr14:99823789
|
A | G | 2 | a0001c0003t0003g0279a0001c0004t0003g0280 | 2 | HG01074.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.68-27064A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99823789 | ||||||
| chr14:99823955
|
T | G | 5 | a0001c0003t0002g0116a0001c0005t0005g0265a0001c0007t0018g0241others(2): Show | 5 | HG01884.hp1 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-26898T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99823955 | ||||||
| chr14:99824184
|
T | A | 2 | a0001c0003t0003g0279a0001c0004t0003g0280 | 2 | HG01074.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.68-26669T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99824184 | ||||||
| chr14:99824198
|
G | A | 5 | a0001c0003t0001g0282a0001c0003t0003g0279a0001c0004t0003g0280others(2): Show | 5 | HG01074.hp1 HG02886.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-26655G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99824198 | ||||||
| chr14:99824303
|
G | A | 6 | a0001c0003t0001g0008a0001c0003t0001g0282a0001c0003t0003g0279others(3): Show | 6 | HG01074.hp1 HG02886.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-26550G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99824303 | ||||||
| chr14:99824425
|
A | ATGTACAC others(82): Show |
10 | a0001c0003t0001g0282a0001c0003t0003g0279a0001c0003t0004g0258others(7): Show | 10 | HG00609.hp2 HG01074.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.68-26414_68-26326d others(91): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99824425 | |||||
| chr14:99824439
|
GTATGTCA others(82): Show |
G | 1 | a0002c0001t0002g0102 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.68-26394_68-26306d others(91): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99824439 | |||||
| chr14:99824454
|
G | A | 1 | a0001c0003t0001g0240 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.68-26399G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99824454 | ||||||
| chr14:99824469
|
A | G | 1 | a0001c0004t0001g0115 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.68-26384A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99824469 | ||||||
| chr14:99824552
|
C | T | 2 | a0001c0003t0001g0283a0001c0003t0001g0286 | 2 | HG03453.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.68-26301C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99824552 | ||||||
| chr14:99824589
|
C | CT | 19 | a0001c0003t0001g0010a0001c0003t0001g0163a0001c0003t0001g0214others(16): Show | 19 | HG01884.hp1 HG02257.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.68-26254dupT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99824589 | |||||
| chr14:99824602
|
T | C | 10 | a0001c0003t0001g0282a0001c0003t0003g0279a0001c0003t0004g0258others(7): Show | 10 | HG00609.hp2 HG01074.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.68-26251T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99824602 | ||||||
| chr14:99824619
|
TA | T | 3 | a0002c0001t0002g0173a0003c0002t0001g0209a0003c0002t0001g0210 | 3 | HG01943.hp1 NA18977.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.68-26233delA | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99824619 | ||||||
| chr14:99824765
|
T | TC | 10 | a0001c0003t0001g0282a0001c0003t0003g0279a0001c0003t0004g0258others(7): Show | 10 | HG00609.hp2 HG01074.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.68-26082dupC | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99824765 | |||||
| chr14:99824854
|
T | C | 7 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0015others(4): Show | 7 | HG02109.hp1 HG02615.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-25999T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99824854 | ||||||
| chr14:99824930
|
T | C | 3 | a0001c0003t0001g0282a0001c0005t0004g0284a0001c0005t0004g0285 | 3 | HG02886.hp1 HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.68-25923T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99824930 | ||||||
| chr14:99824993
|
T | C | 5 | a0001c0003t0004g0258a0001c0003t0008g0271a0001c0004t0001g0255others(2): Show | 5 | HG00609.hp2 HG02451.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-25860T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99824993 | ||||||
| chr14:99825032
|
G | A | 1 | a0003c0002t0002g0203 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.68-25821G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99825032 | ||||||
| chr14:99825238
|
G | C | 1 | a0002c0001t0002g0196 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.68-25615G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99825238 | ||||||
| chr14:99825264
|
G | A | 1 | a0001c0003t0004g0258 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.68-25589G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99825264 | ||||||
| chr14:99825299
|
A | G | 1 | a0003c0002t0002g0138 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.68-25554A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99825299 | ||||||
| chr14:99825312
|
T | C | 4 | a0001c0003t0008g0271a0001c0004t0001g0255a0002c0001t0002g0083others(1): Show | 4 | HG02451.hp2 HG02602.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-25541T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99825312 | ||||||
| chr14:99825522
|
G | C | 1 | a0003c0002t0001g0053 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.68-25331G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99825522 | ||||||
| chr14:99825638
|
C | G | 1 | a0001c0003t0001g0010 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.68-25215C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99825638 | ||||||
| chr14:99825696
|
G | A | 5 | a0001c0003t0004g0258a0001c0003t0008g0271a0001c0004t0001g0255others(2): Show | 5 | HG00609.hp2 HG02451.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-25157G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99825696 | ||||||
| chr14:99825793
|
G | A | 2 | a0001c0003t0003g0279a0001c0004t0003g0280 | 2 | HG01074.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.68-25060G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99825793 | ||||||
| chr14:99825871
|
G | A | 14 | a0001c0003t0001g0010a0001c0003t0001g0163a0001c0003t0001g0214others(11): Show | 14 | HG02257.hp2 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.68-24982G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99825871 | ||||||
| chr14:99826105
|
A | AT | 25 | a0001c0003t0001g0114a0001c0003t0001g0167a0001c0003t0001g0168others(22): Show | 25 | HG00621.hp2 HG00733.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.68-24723dupT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99826105 | |||||
| chr14:99826105
|
A | ATT | 6 | a0001c0003t0001g0158a0001c0003t0003g0279a0001c0003t0004g0258others(3): Show | 6 | HG00609.hp2 HG01074.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-24724_68-24723d others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99826105 | |||||
| chr14:99826105
|
A | ATTTTTTT others(15): Show |
1 | a0002c0001t0002g0083 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.68-24744_68-24723d others(24): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99826105 | |||||
| chr14:99826105
|
A | ATTTTTTT others(16): Show |
2 | a0001c0003t0008g0271a0003c0002t0001g0036 | 2 | HG02602.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.68-24745_68-24723d others(25): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99826105 | |||||
| chr14:99826105
|
A | ATTTTTTT others(21): Show |
1 | a0001c0004t0001g0255 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.68-24723_68-24722i others(30): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99826105 | |||||
| chr14:99826105
|
AT | A | 95 | a0001c0003t0001g0001a0001c0003t0001g0008a0001c0003t0001g0080others(92): Show | 96 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.68-24723delT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99826105 | |||||
| chr14:99826105
|
ATT | A | 11 | a0001c0003t0001g0283a0001c0003t0001g0286a0001c0003t0002g0116others(8): Show | 11 | HG01496.hp2 HG01884.hp1 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.68-24724_68-24723d others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99826105 | |||||
| chr14:99826105
|
ATTT | A | 10 | a0001c0003t0001g0010a0001c0003t0001g0259a0001c0003t0002g0105others(7): Show | 10 | HG00639.hp2 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.68-24725_68-24723d others(5): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99826105 | |||||
| chr14:99826105
|
ATTTTTTT others(3): Show |
A | 1 | a0002c0001t0002g0102 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.68-24732_68-24723d others(12): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99826105 | |||||
| chr14:99826200
|
C | T | 5 | a0001c0003t0004g0258a0001c0003t0008g0271a0001c0004t0001g0255others(2): Show | 5 | HG00609.hp2 HG02451.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-24653C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99826200 | ||||||
| chr14:99826246
|
G | A | 5 | a0001c0003t0001g0282a0001c0003t0003g0279a0001c0004t0003g0280others(2): Show | 5 | HG01074.hp1 HG02886.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-24607G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99826246 | ||||||
| chr14:99826269
|
C | T | 11 | a0001c0003t0001g0041a0001c0003t0001g0085a0001c0003t0001g0152others(8): Show | 11 | HG00140.hp1 HG00642.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.68-24584C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99826269 | ||||||
| chr14:99826302
|
A | G | 10 | a0001c0003t0001g0282a0001c0003t0003g0279a0001c0003t0004g0258others(7): Show | 10 | HG00609.hp2 HG01074.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.68-24551A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99826302 | ||||||
| chr14:99826356
|
G | A | 5 | a0001c0003t0002g0116a0001c0005t0005g0265a0001c0007t0018g0241others(2): Show | 5 | HG01884.hp1 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-24497G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99826356 | ||||||
| chr14:99826381
|
G | A | 1 | a0001c0003t0001g0008 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.68-24472G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99826381 | ||||||
| chr14:99826392
|
C | T | 2 | a0003c0002t0002g0162a0003c0002t0002g0211 | 2 | NA18983.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.68-24461C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99826392 | ||||||
| chr14:99826440
|
G | C | 5 | a0001c0003t0001g0282a0001c0003t0003g0279a0001c0004t0003g0280others(2): Show | 5 | HG01074.hp1 HG02886.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-24413G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99826440 | ||||||
| chr14:99826662
|
G | C | 1 | a0001c0003t0004g0258 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.68-24191G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99826662 | ||||||
| chr14:99826718
|
C | CA | 8 | a0001c0003t0001g0008a0001c0003t0007g0014a0001c0003t0007g0281others(5): Show | 8 | HG02055.hp1 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.68-24126dupA | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99826718 | |||||
| chr14:99826774
|
C | A | 1 | a0002c0001t0002g0018 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.68-24079C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99826774 | ||||||
| chr14:99827016
|
TACTAAGT others(13): Show |
T | 2 | a0001c0003t0003g0279a0001c0004t0003g0280 | 2 | HG01074.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.68-23835_68-23816d others(22): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99827016 | |||||
| chr14:99827090
|
G | C | 1 | a0001c0003t0001g0260 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.68-23763G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99827090 | ||||||
| chr14:99827280
|
C | T | 19 | a0001c0003t0001g0010a0001c0003t0001g0163a0001c0003t0001g0214others(16): Show | 19 | HG01884.hp1 HG02257.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.68-23573C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99827280 | ||||||
| chr14:99827305
|
C | T | 1 | a0006c0011t0001g0011 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.68-23548C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99827305 | ||||||
| chr14:99827380
|
C | T | 3 | a0001c0003t0001g0282a0001c0005t0004g0284a0001c0005t0004g0285 | 3 | HG02886.hp1 HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.68-23473C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99827380 | ||||||
| chr14:99827394
|
C | T | 4 | a0001c0003t0008g0271a0001c0004t0001g0255a0002c0001t0002g0083others(1): Show | 4 | HG02451.hp2 HG02602.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-23459C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99827394 | ||||||
| chr14:99827400
|
G | T | 3 | a0001c0003t0001g0008a0001c0003t0007g0014a0001c0003t0007g0281 | 3 | HG02615.hp2 HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.68-23453G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99827400 | ||||||
| chr14:99827411
|
T | C | 1 | a0001c0003t0004g0258 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.68-23442T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99827411 | ||||||
| chr14:99827426
|
C | G | 6 | a0001c0003t0001g0010a0001c0003t0001g0214a0001c0003t0002g0105others(3): Show | 6 | HG02257.hp2 HG02486.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-23427C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99827426 | ||||||
| chr14:99827433
|
C | T | 1 | a0001c0003t0001g0158 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.68-23420C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99827433 | ||||||
| chr14:99827667
|
G | A | 24 | a0001c0003t0001g0010a0001c0003t0001g0163a0001c0003t0001g0214others(21): Show | 24 | HG01884.hp1 HG02257.hp2 HG02486.hp2 others(21): Show |
intron_variant | MODIFIER | c.68-23186G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99827667 | ||||||
| chr14:99827693
|
G | A | 1 | a0001c0003t0001g0158 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.68-23160G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99827693 | ||||||
| chr14:99827807
|
A | T | 2 | a0001c0003t0003g0279a0001c0004t0003g0280 | 2 | HG01074.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.68-23046A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99827807 | ||||||
| chr14:99827856
|
A | G | 31 | a0001c0003t0001g0008a0001c0003t0001g0010a0001c0003t0001g0080others(28): Show | 31 | HG00609.hp2 HG00639.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.68-22997A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99827856 | ||||||
| chr14:99827961
|
G | A | 30 | a0001c0003t0001g0008a0001c0003t0001g0010a0001c0003t0001g0163others(27): Show | 30 | HG00609.hp2 HG01074.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.68-22892G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99827961 | ||||||
| chr14:99827991
|
G | A | 7 | a0001c0003t0001g0272a0001c0003t0001g0273a0001c0003t0003g0032others(4): Show | 7 | HG02559.hp2 HG02895.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-22862G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99827991 | ||||||
| chr14:99828014
|
G | C | 1 | a0003c0002t0001g0209 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.68-22839G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99828014 | ||||||
| chr14:99828254
|
T | C | 3 | a0001c0003t0001g0282a0001c0005t0004g0284a0001c0005t0004g0285 | 3 | HG02886.hp1 HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.68-22599T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99828254 | ||||||
| chr14:99828308
|
G | A | 88 | a0001c0003t0001g0001a0001c0003t0002g0181a0001c0003t0004g0027others(85): Show | 89 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.68-22545G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99828308 | ||||||
| chr14:99828312
|
A | G | 1 | a0001c0003t0004g0258 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.68-22541A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99828312 | ||||||
| chr14:99828366
|
G | A | 2 | a0001c0003t0007g0014a0001c0003t0007g0281 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.68-22487G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99828366 | ||||||
| chr14:99828399
|
C | T | 1 | a0001c0003t0001g0008 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.68-22454C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99828399 | ||||||
| chr14:99828417
|
A | T | 1 | a0001c0007t0002g0005 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.68-22436A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99828417 | ||||||
| chr14:99828536
|
T | C | 1 | a0003c0014t0004g0254 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.68-22317T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99828536 | ||||||
| chr14:99828642
|
G | T | 1 | a0002c0001t0002g0051 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.68-22211G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99828642 | ||||||
| chr14:99828794
|
A | C | 6 | a0001c0003t0001g0282a0001c0003t0003g0279a0001c0003t0004g0258others(3): Show | 6 | HG00609.hp2 HG01074.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-22059A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99828794 | ||||||
| chr14:99828867
|
A | G | 1 | a0002c0001t0002g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.68-21986A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99828867 | ||||||
| chr14:99828895
|
C | T | 1 | a0003c0002t0003g0125 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.68-21958C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99828895 | ||||||
| chr14:99828906
|
C | T | 3 | a0003c0002t0003g0159a0003c0002t0003g0169a0003c0002t0003g0208 | 3 | NA18994.hp2 NA18998.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.68-21947C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99828906 | ||||||
| chr14:99828915
|
G | T | 5 | a0001c0003t0001g0282a0001c0003t0003g0279a0001c0004t0003g0280others(2): Show | 5 | HG01074.hp1 HG02886.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-21938G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99828915 | ||||||
| chr14:99828916
|
G | T | 5 | a0001c0003t0001g0282a0001c0003t0003g0279a0001c0004t0003g0280others(2): Show | 5 | HG01074.hp1 HG02886.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-21937G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99828916 | ||||||
| chr14:99828941
|
G | A | 5 | a0001c0003t0001g0282a0001c0003t0003g0279a0001c0004t0003g0280others(2): Show | 5 | HG01074.hp1 HG02886.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-21912G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99828941 | ||||||
| chr14:99829020
|
T | C | 2 | a0001c0003t0003g0279a0001c0004t0003g0280 | 2 | HG01074.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.68-21833T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99829020 | ||||||
| chr14:99829033
|
A | G | 1 | a0001c0003t0004g0258 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.68-21820A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99829033 | ||||||
| chr14:99829048
|
G | A | 2 | a0001c0003t0001g0272a0001c0003t0001g0273 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.68-21805G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99829048 | ||||||
| chr14:99829062
|
G | T | 26 | a0001c0003t0001g0010a0001c0003t0001g0163a0001c0003t0001g0214others(23): Show | 26 | HG00609.hp2 HG01884.hp1 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.68-21791G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99829062 | ||||||
| chr14:99829081
|
G | T | 89 | a0001c0003t0001g0001a0001c0003t0002g0181a0001c0003t0004g0027others(86): Show | 90 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.68-21772G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99829081 | ||||||
| chr14:99829257
|
C | T | 2 | a0001c0003t0001g0167a0001c0003t0001g0168 | 2 | HG02818.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.68-21596C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99829257 | ||||||
| chr14:99829361
|
T | G | 3 | a0001c0003t0001g0282a0001c0005t0004g0284a0001c0005t0004g0285 | 3 | HG02886.hp1 HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.68-21492T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99829361 | ||||||
| chr14:99829372
|
T | C | 1 | a0002c0001t0002g0081 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.68-21481T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99829372 | ||||||
| chr14:99829475
|
TG | T | 3 | a0002c0006t0002g0128a0002c0006t0002g0148a0002c0006t0003g0076 | 3 | HG01168.hp1 HG01169.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.68-21377delG | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99829475 | ||||||
| chr14:99829498
|
C | A | 1 | a0001c0003t0001g0163 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.68-21355C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99829498 | ||||||
| chr14:99829622
|
C | T | 1 | a0001c0003t0001g0193 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.68-21231C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99829622 | ||||||
| chr14:99829649
|
G | C | 145 | a0001c0003t0001g0001a0001c0003t0001g0008a0001c0003t0001g0010others(142): Show | 146 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.68-21204G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99829649 | ||||||
| chr14:99829698
|
A | T | 1 | a0003c0002t0001g0171 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.68-21155A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99829698 | ||||||
| chr14:99829816
|
T | C | 1 | a0001c0003t0001g0008 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.68-21037T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99829816 | ||||||
| chr14:99829832
|
C | T | 1 | a0003c0002t0001g0171 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.68-21021C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99829832 | ||||||
| chr14:99829967
|
C | T | 26 | a0001c0003t0001g0010a0001c0003t0001g0163a0001c0003t0001g0214others(23): Show | 26 | HG00609.hp2 HG01884.hp1 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.68-20886C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99829967 | ||||||
| chr14:99829999
|
G | C | 2 | a0001c0003t0001g0272a0001c0003t0001g0273 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.68-20854G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99829999 | ||||||
| chr14:99830024
|
G | A | 1 | a0003c0014t0004g0254 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.68-20829G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99830024 | ||||||
| chr14:99830030
|
T | C | 3 | a0001c0003t0001g0008a0001c0003t0007g0014a0001c0003t0007g0281 | 3 | HG02615.hp2 HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.68-20823T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99830030 | ||||||
| chr14:99830290
|
T | G | 1 | a0001c0003t0001g0193 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.68-20563T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99830290 | ||||||
| chr14:99830511
|
C | CT | 4 | a0001c0003t0008g0271a0001c0004t0001g0255a0002c0001t0002g0083others(1): Show | 4 | HG02451.hp2 HG02602.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-20335dupT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99830511 | |||||
| chr14:99830546
|
C | CTTTTTGT others(2): Show |
24 | a0001c0003t0001g0010a0001c0003t0001g0163a0001c0003t0001g0214others(21): Show | 24 | HG00609.hp2 HG01074.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.68-20294_68-20286d others(11): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99830546 | |||||
| chr14:99830546
|
C | CTTTTTGT others(3): Show |
4 | a0001c0003t0008g0271a0001c0004t0001g0255a0002c0001t0002g0083others(1): Show | 4 | HG02451.hp2 HG02602.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-20302_68-20293d others(12): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99830546 | |||||
| chr14:99830793
|
C | T | 1 | a0003c0016t0014g0060 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.68-20060C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99830793 | ||||||
| chr14:99830847
|
A | G | 34 | a0001c0003t0001g0008a0001c0003t0001g0010a0001c0003t0001g0163others(31): Show | 34 | HG00609.hp2 HG01074.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.68-20006A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99830847 | ||||||
| chr14:99830980
|
G | A | 1 | a0001c0003t0001g0167 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.68-19873G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99830980 | ||||||
| chr14:99831037
|
G | A | 3 | a0001c0003t0001g0008a0001c0003t0007g0014a0001c0003t0007g0281 | 3 | HG02615.hp2 HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.68-19816G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99831037 | ||||||
| chr14:99831091
|
T | C | 3 | a0001c0004t0001g0040a0001c0004t0001g0135a0003c0002t0001g0070 | 3 | HG00408.hp2 NA18939.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.68-19762T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99831091 | ||||||
| chr14:99831234
|
T | G | 1 | a0003c0002t0001g0171 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.68-19619T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99831234 | ||||||
| chr14:99831235
|
G | A | 1 | a0003c0002t0001g0171 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.68-19618G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99831235 | ||||||
| chr14:99831278
|
C | T | 1 | a0003c0002t0001g0210 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.68-19575C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99831278 | ||||||
| chr14:99831304
|
G | A | 2 | a0001c0003t0001g0283a0001c0003t0001g0286 | 2 | HG03453.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.68-19549G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99831304 | ||||||
| chr14:99831389
|
A | G | 2 | a0002c0001t0002g0052a0002c0001t0002g0174 | 2 | HG03927.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.68-19464A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99831389 | ||||||
| chr14:99831415
|
T | G | 1 | a0001c0004t0003g0280 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.68-19438T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99831415 | ||||||
| chr14:99831432
|
A | G | 1 | a0001c0003t0004g0258 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.68-19421A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99831432 | ||||||
| chr14:99831441
|
G | A | 14 | a0001c0003t0001g0272a0001c0003t0001g0273a0001c0003t0001g0283others(11): Show | 14 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.68-19412G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99831441 | ||||||
| chr14:99831495
|
C | A | 1 | a0001c0003t0001g0214 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.68-19358C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99831495 | ||||||
| chr14:99831589
|
A | G | 2 | a0003c0002t0001g0237a0003c0002t0008g0238 | 2 | HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.68-19264A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99831589 | ||||||
| chr14:99831814
|
A | G | 1 | a0003c0002t0001g0185 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.68-19039A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99831814 | ||||||
| chr14:99831835
|
A | T | 1 | a0003c0002t0001g0171 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.68-19018A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99831835 | ||||||
| chr14:99831848
|
A | AT | 16 | a0001c0003t0002g0116a0001c0003t0004g0027a0001c0003t0004g0141others(13): Show | 16 | HG00609.hp2 HG01192.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.68-18991dupT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99831848 | |||||
| chr14:99831848
|
AT | A | 20 | a0001c0003t0001g0007a0001c0003t0001g0015a0001c0003t0001g0016others(17): Show | 20 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.68-18991delT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99831848 | |||||
| chr14:99831971
|
G | C | 1 | a0003c0002t0001g0087 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.68-18882G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99831971 | ||||||
| chr14:99831998
|
A | C | 1 | a0002c0001t0002g0101 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.68-18855A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99831998 | ||||||
| chr14:99832319
|
C | G | 1 | a0001c0003t0001g0163 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.68-18534C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99832319 | ||||||
| chr14:99832417
|
G | A | 1 | a0002c0001t0002g0063 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.68-18436G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99832417 | ||||||
| chr14:99832422
|
C | T | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.68-18431C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99832422 | ||||||
| chr14:99832588
|
G | A | 2 | a0001c0003t0007g0014a0001c0005t0005g0265 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.68-18265G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99832588 | ||||||
| chr14:99832936
|
C | G | 1 | a0001c0004t0001g0091 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.68-17917C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99832936 | ||||||
| chr14:99832937
|
G | T | 1 | a0001c0004t0001g0091 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.68-17916G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99832937 | ||||||
| chr14:99832938
|
G | A | 1 | a0001c0004t0001g0091 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.68-17915G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99832938 | ||||||
| chr14:99832939
|
T | C | 1 | a0001c0004t0001g0091 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.68-17914T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99832939 | ||||||
| chr14:99832940
|
T | C | 1 | a0001c0004t0001g0091 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.68-17913T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99832940 | ||||||
| chr14:99832942
|
T | A | 1 | a0001c0004t0001g0091 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.68-17911T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99832942 | ||||||
| chr14:99832947
|
T | C | 3 | a0001c0004t0004g0017a0001c0005t0004g0284a0001c0005t0004g0285 | 3 | HG02257.hp2 HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.68-17906T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99832947 | ||||||
| chr14:99832977
|
G | T | 1 | a0001c0004t0001g0255 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.68-17876G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99832977 | ||||||
| chr14:99833049
|
G | C | 4 | a0001c0003t0001g0243a0001c0003t0001g0244a0001c0003t0001g0245others(1): Show | 4 | HG02723.hp2 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-17804G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99833049 | ||||||
| chr14:99833061
|
T | C | 1 | a0001c0003t0001g0163 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.68-17792T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99833061 | ||||||
| chr14:99833136
|
A | G | 184 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(181): Show | 184 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.68-17717A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99833136 | ||||||
| chr14:99833181
|
A | C | 1 | a0001c0003t0001g0163 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.68-17672A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99833181 | ||||||
| chr14:99833209
|
T | C | 1 | a0001c0003t0001g0163 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.68-17644T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99833209 | ||||||
| chr14:99833277
|
A | G | 1 | a0001c0003t0007g0281 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.68-17576A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99833277 | ||||||
| chr14:99833558
|
A | T | 1 | a0003c0002t0003g0155 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.68-17295A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99833558 | ||||||
| chr14:99833821
|
T | A | 1 | a0002c0001t0003g0098 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.68-17032T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99833821 | ||||||
| chr14:99833875
|
G | A | 2 | a0001c0003t0001g0274a0001c0003t0008g0271 | 2 | HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.68-16978G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99833875 | ||||||
| chr14:99833906
|
A | G | 177 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(174): Show | 177 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.68-16947A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99833906 | ||||||
| chr14:99834098
|
CTGAG | C | 46 | a0001c0004t0001g0009a0001c0004t0001g0040a0001c0004t0001g0091others(43): Show | 46 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.68-16752_68-16749d others(6): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99834098 | |||||
| chr14:99834223
|
C | A | 3 | a0001c0003t0003g0032a0001c0003t0003g0033a0001c0003t0003g0034 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.68-16630C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99834223 | ||||||
| chr14:99834309
|
C | CT | 166 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(163): Show | 166 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.68-16533dupT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99834309 | |||||
| chr14:99834309
|
C | CTT | 11 | a0001c0003t0003g0279a0002c0001t0002g0025a0002c0001t0002g0026others(8): Show | 11 | HG01071.hp2 HG01074.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.68-16534_68-16533d others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99834309 | |||||
| chr14:99834339
|
A | G | 1 | a0001c0007t0018g0241 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.68-16514A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99834339 | ||||||
| chr14:99834450
|
C | T | 177 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(174): Show | 177 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.68-16403C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99834450 | ||||||
| chr14:99834769
|
T | C | 1 | a0002c0001t0002g0174 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.68-16084T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99834769 | ||||||
| chr14:99834833
|
G | C | 1 | a0001c0003t0001g0167 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.68-16020G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99834833 | ||||||
| chr14:99834920
|
A | G | 1 | a0002c0001t0002g0093 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.68-15933A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99834920 | ||||||
| chr14:99834950
|
G | A | 8 | a0001c0003t0001g0008a0001c0003t0001g0010a0001c0003t0001g0167others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-15903G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99834950 | ||||||
| chr14:99834994
|
A | AT | 175 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(172): Show | 175 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.68-15851dupT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99834994 | |||||
| chr14:99835058
|
G | A | 97 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0220others(94): Show | 97 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.68-15795G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99835058 | ||||||
| chr14:99835061
|
A | G | 1 | a0001c0004t0001g0255 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.68-15792A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99835061 | ||||||
| chr14:99835066
|
C | A | 4 | a0003c0002t0001g0154a0003c0002t0001g0262a0003c0002t0003g0155others(1): Show | 4 | HG00438.hp1 HG02155.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-15787C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99835066 | ||||||
| chr14:99835198
|
T | G | 177 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(174): Show | 177 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.68-15655T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99835198 | ||||||
| chr14:99835305
|
T | C | 1 | a0002c0001t0002g0063 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.68-15548T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99835305 | ||||||
| chr14:99835316
|
A | G | 177 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(174): Show | 177 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.68-15537A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99835316 | ||||||
| chr14:99835486
|
G | C | 177 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(174): Show | 177 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.68-15367G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99835486 | ||||||
| chr14:99835521
|
G | A | 2 | a0001c0003t0002g0105a0001c0003t0002g0106 | 2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.68-15332G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99835521 | ||||||
| chr14:99835596
|
G | A | 1 | a0003c0002t0008g0238 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.68-15257G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99835596 | ||||||
| chr14:99835664
|
T | G | 177 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(174): Show | 177 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.68-15189T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99835664 | ||||||
| chr14:99835666
|
A | G | 1 | a0003c0014t0004g0254 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.68-15187A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99835666 | ||||||
| chr14:99835989
|
C | T | 4 | a0001c0003t0001g0243a0001c0003t0001g0244a0001c0003t0001g0245others(1): Show | 4 | HG02723.hp2 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-14864C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99835989 | ||||||
| chr14:99836064
|
A | AAC | 177 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(174): Show | 177 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.68-14788_68-14787i others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99836064 | |||||
| chr14:99836098
|
T | C | 1 | a0001c0004t0001g0255 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.68-14755T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99836098 | ||||||
| chr14:99836141
|
T | G | 76 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(73): Show | 76 | HG00140.hp1 HG00609.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.68-14712T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99836141 | ||||||
| chr14:99836169
|
A | G | 177 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(174): Show | 177 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.68-14684A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99836169 | ||||||
| chr14:99836206
|
T | TTTATTA | 177 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(174): Show | 177 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.68-14645_68-14640d others(8): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99836206 | |||||
| chr14:99836264
|
G | A | 46 | a0001c0004t0001g0009a0001c0004t0001g0040a0001c0004t0001g0091others(43): Show | 46 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.68-14589G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99836264 | ||||||
| chr14:99836626
|
T | C | 1 | a0002c0001t0003g0139 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.68-14227T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99836626 | ||||||
| chr14:99836674
|
G | T | 1 | a0002c0001t0002g0175 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.68-14179G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99836674 | ||||||
| chr14:99836715
|
G | A | 176 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(173): Show | 176 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.68-14138G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99836715 | ||||||
| chr14:99836771
|
G | A | 3 | a0002c0001t0019g0234a0003c0002t0001g0237a0003c0015t0001g0013 | 3 | HG01884.hp2 HG02976.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.68-14082G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99836771 | ||||||
| chr14:99836773
|
G | T | 1 | a0003c0002t0017g0028 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.68-14080G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99836773 | ||||||
| chr14:99836786
|
G | T | 175 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(172): Show | 175 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.68-14067G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99836786 | ||||||
| chr14:99836956
|
T | A | 3 | a0001c0004t0003g0199a0002c0001t0003g0188a0002c0001t0003g0189 | 3 | NA18957.hp1 NA19005.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.68-13897T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99836956 | ||||||
| chr14:99836991
|
A | ATT | 85 | a0001c0003t0001g0012a0001c0003t0001g0221a0001c0003t0001g0232others(82): Show | 85 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.68-13848_68-13847d others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99836991 | |||||
| chr14:99836991
|
A | ATTT | 12 | a0001c0003t0001g0080a0001c0003t0001g0220a0001c0003t0001g0233others(9): Show | 12 | HG01109.hp2 HG01928.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.68-13849_68-13847d others(5): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99836991 | |||||
| chr14:99836993
|
T | A | 1 | a0003c0016t0014g0060 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.68-13860T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99836993 | ||||||
| chr14:99837173
|
C | T | 47 | a0001c0003t0001g0270a0001c0004t0001g0009a0001c0004t0001g0040others(44): Show | 47 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.68-13680C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99837173 | ||||||
| chr14:99837495
|
T | C | 3 | a0001c0004t0003g0074a0001c0004t0003g0075a0001c0004t0003g0103 | 3 | HG01256.hp2 HG01258.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.68-13358T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99837495 | ||||||
| chr14:99837514
|
T | A | 2 | a0001c0005t0004g0284a0001c0005t0004g0285 | 2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.68-13339T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99837514 | ||||||
| chr14:99837525
|
T | G | 1 | a0001c0004t0003g0180 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.68-13328T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99837525 | ||||||
| chr14:99837738
|
A | G | 1 | a0001c0003t0001g0168 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.68-13115A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99837738 | ||||||
| chr14:99837796
|
T | C | 2 | a0001c0003t0001g0274a0001c0003t0008g0271 | 2 | HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.68-13057T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99837796 | ||||||
| chr14:99837948
|
A | G | 2 | a0002c0001t0002g0021a0002c0001t0002g0066 | 2 | HG01123.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.68-12905A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99837948 | ||||||
| chr14:99837981
|
T | C | 2 | a0001c0003t0002g0105a0001c0003t0002g0106 | 2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.68-12872T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99837981 | ||||||
| chr14:99838215
|
A | G | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.68-12638A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99838215 | ||||||
| chr14:99838301
|
TTTA | T | 30 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(27): Show | 30 | HG00639.hp2 HG02109.hp1 HG02451.hp1 others(27): Show |
intron_variant | MODIFIER | c.68-12549_68-12547d others(5): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838301 | |||||
| chr14:99838359
|
C | A | 3 | a0001c0003t0003g0032a0001c0003t0003g0033a0001c0003t0003g0034 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.68-12494C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99838359 | ||||||
| chr14:99838410
|
A | G | 1 | a0001c0003t0001g0273 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.68-12443A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99838410 | ||||||
| chr14:99838545
|
A | G | 1 | a0001c0003t0001g0114 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.68-12308A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99838545 | ||||||
| chr14:99838593
|
C | T | 2 | a0001c0004t0003g0256a0001c0004t0003g0257 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.68-12260C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99838593 | ||||||
| chr14:99838629
|
G | GT | 19 | a0001c0003t0001g0007a0001c0003t0001g0015a0001c0003t0001g0016others(16): Show | 19 | HG00639.hp2 HG02055.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.68-12213dupT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838629 | |||||
| chr14:99838649
|
C | T | 12 | a0001c0003t0001g0008a0001c0003t0001g0010a0001c0003t0001g0167others(9): Show | 12 | HG02486.hp2 HG02630.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.68-12204C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99838649 | ||||||
| chr14:99838650
|
G | A | 2 | a0001c0003t0007g0014a0001c0005t0005g0265 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.68-12203G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99838650 | ||||||
| chr14:99838729
|
G | A | 77 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(74): Show | 77 | HG00140.hp1 HG00609.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.68-12124G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99838729 | ||||||
| chr14:99838792
|
CTT | C | 4 | a0001c0003t0003g0032a0001c0003t0003g0033a0001c0003t0003g0034others(1): Show | 4 | HG02055.hp1 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-12060_68-12059d others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99838792 | ||||||
| chr14:99838817
|
G | A | 3 | a0002c0001t0002g0136a0002c0001t0002g0144a0002c0001t0002g0173 | 3 | NA18951.hp2 NA18961.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.68-12036G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99838817 | ||||||
| chr14:99838820
|
G | A | 1 | a0002c0001t0002g0144 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.68-12033G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99838820 | ||||||
| chr14:99838878
|
CAA | C | 30 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(27): Show | 30 | HG00639.hp2 HG02109.hp1 HG02451.hp1 others(27): Show |
intron_variant | MODIFIER | c.68-11974_68-11973d others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99838878 | ||||||
| chr14:99838906
|
T | TGC | 90 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0111others(87): Show | 92 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.68-11935_68-11934d others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838906 | |||||
| chr14:99838906
|
T | TGCGC | 23 | a0001c0003t0003g0032a0001c0003t0003g0033a0001c0003t0003g0034others(20): Show | 23 | HG00438.hp2 HG00609.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.68-11937_68-11934d others(6): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838906 | |||||
| chr14:99838906
|
T | TGCGCGC | 9 | a0001c0003t0001g0283a0001c0004t0003g0199a0002c0001t0001g0219others(6): Show | 9 | HG02132.hp1 HG02523.hp1 HG03540.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-11939_68-11934d others(8): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838906 | |||||
| chr14:99838906
|
T | TGCGCGCG others(1): Show |
3 | a0001c0003t0001g0272a0001c0003t0001g0273a0002c0001t0003g0189 | 3 | HG02559.hp2 HG03471.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.68-11941_68-11934d others(10): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838906 | |||||
| chr14:99838918
|
C | CGCGCGCG others(21): Show |
1 | a0002c0001t0002g0021 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.68-11934_68-11933i others(30): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838918 | |||||
| chr14:99838918
|
C | CGCGCGCG others(5): Show |
2 | a0001c0003t0001g0225a0001c0005t0005g0097 | 2 | HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.68-11934_68-11933i others(14): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838918 | |||||
| chr14:99838918
|
C | CGCGCGCG others(7): Show |
4 | a0001c0003t0001g0007a0001c0003t0001g0016a0001c0003t0001g0020others(1): Show | 4 | HG02109.hp1 HG03098.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-11934_68-11933i others(16): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838918 | |||||
| chr14:99838918
|
C | CGCGCGCG others(15): Show |
1 | a0001c0003t0001g0221 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.68-11934_68-11933i others(24): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838918 | |||||
| chr14:99838918
|
C | CGCGCGCG others(17): Show |
5 | a0001c0003t0001g0012a0001c0003t0001g0233a0002c0001t0002g0118others(2): Show | 5 | HG01109.hp2 HG01175.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-11934_68-11933i others(26): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838918 | |||||
| chr14:99838918
|
C | CGCGCGCG others(21): Show |
1 | a0002c0001t0002g0066 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.68-11934_68-11933i others(30): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838918 | |||||
| chr14:99838918
|
C | CGCGCGCG others(5): Show |
6 | a0001c0003t0001g0015a0001c0003t0001g0260a0001c0005t0001g0250others(3): Show | 6 | HG00639.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-11934_68-11933i others(14): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838918 | |||||
| chr14:99838918
|
C | CGCGCGCG others(7): Show |
3 | a0001c0003t0001g0286a0001c0003t0007g0014a0001c0005t0005g0265 | 3 | HG02622.hp2 HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.68-11934_68-11933i others(16): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838918 | |||||
| chr14:99838918
|
C | CGCGCGCG others(13): Show |
2 | a0001c0003t0001g0080a0001c0003t0001g0259 | 2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.68-11934_68-11933i others(22): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838918 | |||||
| chr14:99838918
|
C | CGCGCGCG others(15): Show |
5 | a0001c0003t0001g0232a0002c0001t0002g0031a0002c0001t0002g0065others(2): Show | 5 | HG00735.hp1 HG02109.hp2 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-11934_68-11933i others(24): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838918 | |||||
| chr14:99838918
|
C | CGCGCGCG others(17): Show |
10 | a0002c0001t0001g0092a0002c0001t0002g0052a0002c0001t0002g0072others(7): Show | 10 | HG00544.hp2 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.68-11934_68-11933i others(26): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838918 | |||||
| chr14:99838918
|
C | CGCGCGCG others(19): Show |
1 | a0003c0002t0001g0055 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.68-11934_68-11933i others(28): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838918 | |||||
| chr14:99838918
|
C | CGCGCGTG others(1): Show |
4 | a0002c0001t0002g0056a0002c0001t0002g0057a0002c0001t0002g0150others(1): Show | 4 | NA18939.hp1 NA18953.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-11934_68-11933i others(10): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838918 | |||||
| chr14:99838918
|
C | CGCGCGTG others(11): Show |
1 | a0002c0001t0002g0278 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.68-11934_68-11933i others(20): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838918 | |||||
| chr14:99838918
|
C | CGCGCGTG others(13): Show |
1 | a0002c0001t0002g0018 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.68-11934_68-11933i others(22): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838918 | |||||
| chr14:99838918
|
C | CGCGCGTG others(15): Show |
22 | a0002c0001t0001g0267a0002c0001t0002g0025a0002c0001t0002g0046others(19): Show | 22 | HG00558.hp1 HG00621.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.68-11934_68-11933i others(24): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838918 | |||||
| chr14:99838918
|
C | CGCGCGTG others(17): Show |
14 | a0002c0001t0001g0062a0002c0001t0002g0026a0002c0001t0002g0045others(11): Show | 14 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(11): Show |
intron_variant | MODIFIER | c.68-11934_68-11933i others(26): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838918 | |||||
| chr14:99838918
|
C | CGCGTGTG others(5): Show |
8 | a0001c0003t0001g0008a0001c0003t0001g0010a0001c0003t0001g0167others(5): Show | 8 | HG02486.hp2 HG02717.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-11934_68-11933i others(14): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838918 | |||||
| chr14:99838918
|
C | CGCGTGTG others(9): Show |
1 | a0002c0001t0002g0089 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.68-11934_68-11933i others(18): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838918 | |||||
| chr14:99838918
|
C | CGCGTGTG others(15): Show |
1 | a0002c0001t0002g0276 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.68-11934_68-11933i others(24): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838918 | |||||
| chr14:99838918
|
C | CTGCGCGC others(14): Show |
1 | a0001c0003t0001g0220 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.68-11935_68-11934i others(23): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99838918 | ||||||
| chr14:99838918
|
C | T | 2 | a0001c0003t0007g0281a0001c0004t0013g0108 | 2 | HG02055.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.68-11935C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99838918 | ||||||
| chr14:99838920
|
T | C | 6 | a0001c0003t0001g0243a0001c0003t0001g0244a0001c0003t0001g0245others(3): Show | 6 | HG01496.hp2 HG02723.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-11933T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99838920 | ||||||
| chr14:99838928
|
T | C | 3 | a0002c0001t0002g0021a0002c0001t0002g0066a0002c0001t0002g0173 | 3 | HG01123.hp2 HG02145.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.68-11925T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99838928 | ||||||
| chr14:99838930
|
T | C | 94 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(91): Show | 94 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.68-11923T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99838930 | ||||||
| chr14:99838930
|
T | TGTGTGTG others(1): Show |
4 | a0001c0003t0002g0105a0001c0003t0002g0106a0001c0004t0003g0180others(1): Show | 4 | HG02630.hp2 HG02818.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-11922_68-11921i others(10): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838930 | |||||
| chr14:99838930
|
T | TGTGTGTG others(3): Show |
4 | a0001c0003t0001g0243a0001c0003t0001g0244a0001c0003t0001g0245others(1): Show | 4 | HG02723.hp2 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-11922_68-11921i others(12): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838930 | |||||
| chr14:99838930
|
T | TGTGTGTG others(3): Show |
38 | a0001c0004t0001g0009a0001c0004t0001g0040a0001c0004t0001g0091others(35): Show | 38 | HG00140.hp1 HG00735.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.68-11922_68-11921i others(12): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838930 | |||||
| chr14:99838930
|
T | TGTGTGTG others(5): Show |
1 | a0002c0006t0003g0076 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.68-11922_68-11921i others(14): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838930 | |||||
| chr14:99838930
|
T | TGTGTGTG others(5): Show |
4 | a0001c0003t0001g0283a0001c0004t0003g0048a0001c0004t0003g0195others(1): Show | 4 | HG00609.hp1 HG03540.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-11922_68-11921i others(14): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838930 | |||||
| chr14:99838930
|
T | TGTGTGTG others(7): Show |
2 | a0001c0003t0001g0272a0001c0003t0001g0273 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.68-11922_68-11921i others(16): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838930 | |||||
| chr14:99838930
|
T | TGTGTGTG others(9): Show |
2 | a0001c0003t0003g0032a0001c0003t0003g0033 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.68-11922_68-11921i others(18): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838930 | |||||
| chr14:99838930
|
T | TGTGTGTG others(11): Show |
18 | a0001c0003t0003g0034a0001c0003t0003g0279a0001c0004t0003g0199others(15): Show | 18 | HG01074.hp1 HG01346.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.68-11922_68-11921i others(20): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838930 | |||||
| chr14:99838930
|
T | TGTGTGTG others(13): Show |
5 | a0002c0001t0001g0239a0002c0001t0002g0023a0002c0001t0002g0084others(2): Show | 5 | HG00438.hp2 HG01884.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-11922_68-11921i others(22): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838930 | |||||
| chr14:99838930
|
T | TGTGTGTG others(17): Show |
1 | a0003c0002t0001g0054 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.68-11922_68-11921i others(26): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99838930 | |||||
| chr14:99838932
|
C | T | 4 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258others(1): Show | 4 | HG00609.hp2 HG02083.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-11921C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99838932 | ||||||
| chr14:99838943
|
G | C | 8 | a0001c0003t0001g0008a0001c0003t0001g0010a0001c0003t0001g0167others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-11910G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99838943 | ||||||
| chr14:99839088
|
CT | C | 180 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(177): Show | 180 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.68-11763delT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99839088 | |||||
| chr14:99839288
|
A | G | 1 | a0001c0004t0001g0255 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.68-11565A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99839288 | ||||||
| chr14:99839816
|
C | T | 100 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0220others(97): Show | 100 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.68-11037C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99839816 | ||||||
| chr14:99839954
|
G | A | 1 | a0001c0004t0013g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.68-10899G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99839954 | ||||||
| chr14:99840032
|
TTGTA | T | 97 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0220others(94): Show | 97 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.68-10817_68-10814d others(6): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99840032 | |||||
| chr14:99840095
|
CTA | C | 3 | a0003c0002t0001g0044a0003c0002t0001g0087a0003c0002t0002g0222 | 3 | HG01192.hp2 HG01255.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.68-10756_68-10755d others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99840095 | |||||
| chr14:99840347
|
G | A | 1 | a0002c0001t0001g0219 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.68-10506G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99840347 | ||||||
| chr14:99840380
|
G | T | 74 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(71): Show | 74 | HG00140.hp1 HG00609.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.68-10473G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99840380 | ||||||
| chr14:99840460
|
G | A | 3 | a0003c0002t0001g0044a0003c0002t0001g0087a0003c0002t0002g0222 | 3 | HG01192.hp2 HG01255.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.68-10393G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99840460 | ||||||
| chr14:99840524
|
C | T | 7 | a0003c0002t0001g0223a0003c0002t0006g0042a0003c0002t0006g0043others(4): Show | 7 | HG01109.hp1 HG01928.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-10329C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99840524 | ||||||
| chr14:99840776
|
C | G | 270 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0007others(267): Show | 272 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(269): Show |
intron_variant | MODIFIER | c.68-10077C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99840776 | ||||||
| chr14:99840796
|
G | C | 1 | a0001c0004t0013g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.68-10057G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99840796 | ||||||
| chr14:99840804
|
A | G | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.68-10049A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99840804 | ||||||
| chr14:99840891
|
T | A | 1 | a0001c0004t0001g0255 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.68-9962T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99840891 | ||||||
| chr14:99840894
|
T | G | 1 | a0001c0004t0001g0255 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.68-9959T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99840894 | ||||||
| chr14:99840938
|
TG | T | 6 | a0002c0001t0002g0056a0002c0001t0002g0057a0002c0001t0002g0150others(3): Show | 6 | HG02040.hp2 NA18939.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-9913delG | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99840938 | |||||
| chr14:99840983
|
C | G | 181 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(178): Show | 181 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.68-9870C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99840983 | ||||||
| chr14:99841130
|
C | T | 5 | a0003c0002t0001g0170a0003c0002t0001g0171a0003c0002t0001g0172others(2): Show | 5 | HG01433.hp1 NA18952.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-9723C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99841130 | ||||||
| chr14:99841140
|
G | A | 177 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(174): Show | 177 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.68-9713G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99841140 | ||||||
| chr14:99841239
|
T | C | 3 | a0001c0003t0001g0167a0001c0003t0001g0168a0006c0011t0001g0011 | 3 | HG02818.hp1 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.68-9614T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99841239 | ||||||
| chr14:99841307
|
C | T | 1 | a0001c0004t0013g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.68-9546C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99841307 | ||||||
| chr14:99841431
|
A | G | 1 | a0003c0002t0006g0043 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.68-9422A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99841431 | ||||||
| chr14:99841440
|
A | G | 5 | a0002c0001t0002g0046a0002c0001t0002g0068a0002c0001t0002g0069others(2): Show | 5 | HG01928.hp1 HG02293.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-9413A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99841440 | ||||||
| chr14:99841504
|
G | A | 177 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(174): Show | 177 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.68-9349G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99841504 | ||||||
| chr14:99841688
|
G | T | 4 | a0001c0003t0001g0243a0001c0003t0001g0244a0001c0003t0001g0245others(1): Show | 4 | HG02723.hp2 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-9165G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99841688 | ||||||
| chr14:99841724
|
G | C | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.68-9129G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99841724 | ||||||
| chr14:99841776
|
C | G | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.68-9077C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99841776 | ||||||
| chr14:99841857
|
G | A | 30 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(27): Show | 30 | HG00639.hp2 HG02109.hp1 HG02451.hp1 others(27): Show |
intron_variant | MODIFIER | c.68-8996G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99841857 | ||||||
| chr14:99841916
|
G | A | 177 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(174): Show | 177 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.68-8937G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99841916 | ||||||
| chr14:99841928
|
C | A | 1 | a0001c0003t0003g0277 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.68-8925C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99841928 | ||||||
| chr14:99842027
|
T | TAA | 146 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0220others(143): Show | 146 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.68-8822_68-8821dup others(2): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99842027 | |||||
| chr14:99842444
|
C | T | 1 | a0003c0002t0001g0217 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.68-8409C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99842444 | ||||||
| chr14:99842466
|
CATT | C | 100 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0220others(97): Show | 100 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.68-8385_68-8383del others(3): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99842466 | |||||
| chr14:99842581
|
C | T | 8 | a0001c0003t0001g0008a0001c0003t0001g0010a0001c0003t0001g0167others(5): Show | 8 | HG02486.hp2 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-8272C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99842581 | ||||||
| chr14:99842582
|
A | G | 177 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(174): Show | 177 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.68-8271A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99842582 | ||||||
| chr14:99842714
|
A | G | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.68-8139A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99842714 | ||||||
| chr14:99842869
|
C | G | 1 | a0001c0004t0013g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.68-7984C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99842869 | ||||||
| chr14:99843108
|
C | T | 4 | a0002c0001t0002g0023a0002c0001t0002g0081a0002c0001t0002g0093others(1): Show | 4 | HG00544.hp2 HG00558.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-7745C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99843108 | ||||||
| chr14:99843157
|
GAT | G | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.68-7694_68-7693del others(2): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99843157 | |||||
| chr14:99843162
|
G | A | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.68-7691G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99843162 | ||||||
| chr14:99843424
|
A | AAACAAC | 134 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(131): Show | 134 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.68-7426_68-7421dup others(6): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99843424 | |||||
| chr14:99843440
|
A | G | 134 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(131): Show | 134 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.68-7413A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99843440 | ||||||
| chr14:99843458
|
T | C | 97 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0220others(94): Show | 97 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.68-7395T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99843458 | ||||||
| chr14:99843459
|
A | G | 34 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(31): Show | 34 | HG00639.hp2 HG02055.hp1 HG02109.hp1 others(31): Show |
intron_variant | MODIFIER | c.68-7394A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99843459 | ||||||
| chr14:99843571
|
A | G | 1 | a0003c0002t0001g0209 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.68-7282A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99843571 | ||||||
| chr14:99843747
|
A | G | 1 | a0003c0002t0008g0238 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.68-7106A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99843747 | ||||||
| chr14:99843947
|
A | G | 2 | a0001c0003t0001g0274a0001c0003t0008g0271 | 2 | HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.68-6906A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99843947 | ||||||
| chr14:99844032
|
A | C | 100 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0220others(97): Show | 100 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.68-6821A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99844032 | ||||||
| chr14:99844097
|
A | G | 4 | a0002c0001t0002g0183a0003c0002t0001g0070a0003c0002t0002g0162others(1): Show | 4 | HG00408.hp2 NA18983.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-6756A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99844097 | ||||||
| chr14:99844476
|
CA | C | 39 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(36): Show | 39 | HG00609.hp2 HG00639.hp2 HG01433.hp1 others(36): Show |
intron_variant | MODIFIER | c.68-6359delA | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99844476 | |||||
| chr14:99844476
|
CAA | C | 47 | a0001c0003t0003g0032a0001c0003t0003g0033a0001c0003t0003g0034others(44): Show | 47 | HG00140.hp1 HG00735.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.68-6360_68-6359del others(2): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99844476 | |||||
| chr14:99844476
|
CAAA | C | 13 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0220others(10): Show | 13 | HG00609.hp1 HG01109.hp2 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.68-6361_68-6359del others(3): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99844476 | |||||
| chr14:99844476
|
CAAAA | C | 85 | a0001c0003t0003g0279a0001c0004t0003g0199a0002c0001t0001g0062others(82): Show | 85 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.68-6362_68-6359del others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99844476 | |||||
| chr14:99844480
|
A | C | 1 | a0003c0002t0001g0190 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.68-6373A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99844480 | ||||||
| chr14:99844532
|
T | C | 146 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0220others(143): Show | 146 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.68-6321T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99844532 | ||||||
| chr14:99844546
|
CTTTAT | C | 46 | a0001c0004t0001g0009a0001c0004t0001g0040a0001c0004t0001g0091others(43): Show | 46 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.68-6301_68-6297del others(5): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99844546 | |||||
| chr14:99844599
|
A | G | 9 | a0003c0002t0001g0198a0003c0002t0001g0217a0003c0002t0001g0223others(6): Show | 9 | HG01109.hp1 HG01928.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-6254A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99844599 | ||||||
| chr14:99844819
|
C | G | 1 | a0001c0004t0003g0280 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.68-6034C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99844819 | ||||||
| chr14:99845330
|
T | C | 1 | a0003c0016t0014g0060 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.68-5523T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99845330 | ||||||
| chr14:99845786
|
C | T | 39 | a0001c0004t0001g0009a0001c0004t0001g0040a0001c0004t0001g0091others(36): Show | 39 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.68-5067C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99845786 | ||||||
| chr14:99845919
|
A | G | 269 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0007others(266): Show | 271 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.68-4934A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99845919 | ||||||
| chr14:99845982
|
G | A | 1 | a0003c0002t0001g0201 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.68-4871G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99845982 | ||||||
| chr14:99846049
|
C | CA | 9 | a0001c0003t0003g0032a0001c0003t0003g0033a0001c0003t0003g0034others(6): Show | 9 | HG02071.hp1 HG02145.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-4788dupA | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99846049 | |||||
| chr14:99846281
|
A | AT | 49 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0086others(46): Show | 49 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.68-4553dupT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99846281 | |||||
| chr14:99846281
|
A | ATT | 7 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0001g0220others(4): Show | 7 | HG02818.hp1 HG02965.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-4554_68-4553dup others(2): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99846281 | |||||
| chr14:99846281
|
A | ATTT | 11 | a0001c0003t0005g0246a0001c0003t0005g0247a0001c0004t0001g0009others(8): Show | 11 | HG02280.hp1 HG02451.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.68-4555_68-4553dup others(3): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99846281 | |||||
| chr14:99846281
|
A | ATTTT | 31 | a0001c0004t0001g0040a0001c0004t0001g0091a0001c0004t0001g0115others(28): Show | 31 | HG00140.hp1 HG00735.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.68-4556_68-4553dup others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99846281 | |||||
| chr14:99846385
|
C | T | 10 | a0001c0003t0007g0014a0001c0005t0001g0079a0001c0005t0001g0250others(7): Show | 10 | HG00639.hp2 HG02451.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.68-4468C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99846385 | ||||||
| chr14:99846698
|
T | G | 2 | a0003c0002t0001g0263a0003c0002t0001g0264 | 2 | NA18966.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.68-4155T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99846698 | ||||||
| chr14:99846707
|
A | G | 1 | a0001c0003t0001g0163 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.68-4146A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99846707 | ||||||
| chr14:99846720
|
G | A | 3 | a0003c0002t0001g0044a0003c0002t0001g0087a0003c0002t0002g0222 | 3 | HG01192.hp2 HG01255.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.68-4133G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99846720 | ||||||
| chr14:99847072
|
A | AAAATTTT | 71 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0001g0225others(68): Show | 71 | HG00140.hp1 HG00609.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.68-3781_68-3780ins others(7): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99847072 | ||||||
| chr14:99847212
|
A | G | 1 | a0001c0004t0001g0115 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.68-3641A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99847212 | ||||||
| chr14:99847256
|
G | A | 1 | a0001c0003t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.68-3597G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99847256 | ||||||
| chr14:99847291
|
C | T | 1 | a0003c0002t0001g0130 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.68-3562C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99847291 | ||||||
| chr14:99847357
|
T | C | 3 | a0001c0003t0001g0167a0001c0003t0001g0168a0006c0011t0001g0011 | 3 | HG02818.hp1 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.68-3496T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99847357 | ||||||
| chr14:99847590
|
T | C | 1 | a0001c0005t0001g0250 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.68-3263T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99847590 | ||||||
| chr14:99847644
|
C | G | 1 | a0005c0009t0002g0132 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.68-3209C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99847644 | ||||||
| chr14:99847686
|
T | G | 1 | a0005c0009t0002g0132 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.68-3167T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99847686 | ||||||
| chr14:99847718
|
T | G | 1 | a0002c0001t0002g0063 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.68-3135T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99847718 | ||||||
| chr14:99847942
|
T | A | 1 | a0002c0001t0002g0058 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.68-2911T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99847942 | ||||||
| chr14:99847943
|
A | T | 49 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0005g0246others(46): Show | 49 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.68-2910A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99847943 | ||||||
| chr14:99848548
|
C | A | 49 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0005g0246others(46): Show | 49 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.68-2305C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99848548 | ||||||
| chr14:99848646
|
A | G | 22 | a0001c0003t0001g0225a0001c0003t0001g0260a0001c0003t0001g0274others(19): Show | 22 | HG00639.hp2 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.68-2207A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99848646 | ||||||
| chr14:99848724
|
G | T | 1 | a0002c0001t0003g0098 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.68-2129G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99848724 | ||||||
| chr14:99848824
|
G | A | 4 | a0001c0005t0001g0250a0001c0005t0005g0003a0001c0005t0005g0097others(1): Show | 4 | HG00639.hp2 HG02451.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-2029G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99848824 | ||||||
| chr14:99848839
|
T | C | 13 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0220others(10): Show | 13 | HG01109.hp2 HG01123.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.68-2014T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99848839 | ||||||
| chr14:99848859
|
A | C | 1 | a0002c0001t0002g0153 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.68-1994A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99848859 | ||||||
| chr14:99848945
|
G | A | 177 | a0001c0003t0001g0008a0001c0003t0001g0010a0001c0003t0001g0012others(174): Show | 177 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.68-1908G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99848945 | ||||||
| chr14:99848960
|
CA | C | 178 | a0001c0003t0001g0008a0001c0003t0001g0010a0001c0003t0001g0012others(175): Show | 178 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.68-1879delA | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99848960 | |||||
| chr14:99849027
|
G | A | 49 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0005g0246others(46): Show | 49 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.68-1826G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99849027 | ||||||
| chr14:99849125
|
A | G | 5 | a0001c0004t0004g0017a0001c0005t0004g0284a0001c0005t0004g0285others(2): Show | 5 | HG02145.hp2 HG02257.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-1728A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99849125 | ||||||
| chr14:99849132
|
T | G | 22 | a0001c0003t0001g0225a0001c0003t0001g0260a0001c0003t0001g0274others(19): Show | 22 | HG00639.hp2 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.68-1721T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99849132 | ||||||
| chr14:99849505
|
T | TTG | 25 | a0001c0003t0001g0006a0001c0003t0001g0080a0001c0003t0001g0111others(22): Show | 25 | HG00639.hp2 HG01109.hp2 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.68-1324_68-1323dup others(2): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99849505 | |||||
| chr14:99849505
|
T | TTGTG | 6 | a0001c0003t0002g0105a0001c0003t0002g0106a0002c0001t0002g0089others(3): Show | 6 | HG01081.hp2 HG01496.hp2 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-1326_68-1323dup others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99849505 | |||||
| chr14:99849505
|
T | TTGTGTGT others(3): Show |
1 | a0001c0004t0013g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.68-1332_68-1323dup others(10): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99849505 | |||||
| chr14:99849505
|
TTG | T | 5 | a0001c0003t0009g0251a0003c0002t0001g0044a0003c0002t0001g0087others(2): Show | 5 | HG01192.hp2 HG01255.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-1324_68-1323del others(2): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99849505 | |||||
| chr14:99849517
|
G | A | 1 | a0001c0004t0003g0197 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.68-1336G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99849517 | ||||||
| chr14:99849525
|
GTGTGTA | G | 7 | a0001c0003t0005g0246a0001c0003t0005g0247a0001c0004t0001g0123others(4): Show | 7 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-1326_68-1321del others(6): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99849525 | |||||
| chr14:99849527
|
GTGTA | G | 43 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0004g0027others(40): Show | 43 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.68-1324_68-1321del others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99849527 | |||||
| chr14:99849529
|
GTA | G | 10 | a0001c0003t0001g0007a0001c0003t0001g0015a0001c0003t0001g0016others(7): Show | 10 | HG02109.hp1 HG02486.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.68-1316_68-1315del others(2): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99849529 | |||||
| chr14:99849531
|
A | G | 121 | a0001c0003t0001g0008a0001c0003t0001g0010a0001c0003t0001g0012others(118): Show | 121 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.68-1322A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99849531 | ||||||
| chr14:99849533
|
A | G | 97 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0220others(94): Show | 97 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.68-1320A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99849533 | ||||||
| chr14:99849534
|
T | C | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.68-1319T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99849534 | ||||||
| chr14:99849535
|
A | G | 1 | a0002c0001t0001g0092 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.68-1318A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99849535 | ||||||
| chr14:99849553
|
A | G | 49 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0005g0246others(46): Show | 49 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.68-1300A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99849553 | ||||||
| chr14:99849557
|
G | A | 49 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0005g0246others(46): Show | 49 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.68-1296G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99849557 | ||||||
| chr14:99849729
|
G | A | 1 | a0003c0002t0001g0107 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.68-1124G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99849729 | ||||||
| chr14:99849750
|
A | G | 17 | a0001c0003t0001g0225a0001c0003t0001g0260a0001c0003t0007g0014others(14): Show | 17 | HG00639.hp2 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.68-1103A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99849750 | ||||||
| chr14:99849809
|
G | A | 183 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(180): Show | 183 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.68-1044G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99849809 | ||||||
| chr14:99849811
|
G | C | 6 | a0002c0001t0002g0061a0002c0001t0002g0063a0002c0001t0002g0073others(3): Show | 6 | HG00438.hp2 HG01975.hp2 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-1042G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99849811 | ||||||
| chr14:99849818
|
G | T | 49 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0005g0246others(46): Show | 49 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.68-1035G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99849818 | ||||||
| chr14:99849837
|
G | A | 1 | a0003c0002t0001g0218 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.68-1016G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99849837 | ||||||
| chr14:99849917
|
G | A | 1 | a0001c0003t0007g0281 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.68-936G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99849917 | ||||||
| chr14:99849917
|
G | C | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.68-936G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99849917 | ||||||
| chr14:99849925
|
G | A | 49 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0005g0246others(46): Show | 49 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.68-928G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99849925 | ||||||
| chr14:99849978
|
G | A | 13 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0220others(10): Show | 13 | HG01109.hp2 HG01123.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.68-875G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99849978 | ||||||
| chr14:99850008
|
A | G | 1 | a0002c0001t0002g0058 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.68-845A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99850008 | ||||||
| chr14:99850096
|
A | AT | 22 | a0001c0003t0001g0225a0001c0003t0001g0260a0001c0003t0007g0014others(19): Show | 22 | HG00639.hp2 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.68-742dupT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99850096 | |||||
| chr14:99850096
|
AT | A | 6 | a0001c0003t0001g0163a0001c0003t0001g0193a0001c0004t0003g0064others(3): Show | 6 | HG00323.hp2 HG01975.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-742delT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr14 | 99850096 | |||||
| chr14:99850218
|
C | T | 20 | a0001c0003t0001g0225a0001c0003t0001g0260a0001c0003t0003g0032others(17): Show | 20 | HG00639.hp2 HG02145.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.68-635C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99850218 | ||||||
| chr14:99850352
|
A | G | 3 | a0001c0003t0005g0246a0001c0003t0005g0247a0001c0004t0005g0242 | 3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.68-501A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99850352 | ||||||
| chr14:99850737
|
C | T | 1 | a0001c0004t0003g0195 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.68-116C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 1/21 | chr14 | 99850737 | ||||||
| chr14:99851039
|
G | A | 39 | a0001c0004t0001g0009a0001c0004t0001g0040a0001c0004t0001g0091others(36): Show | 39 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(36): Show |
splice_region_variant&intron_variant | LOW | c.250+4G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99851039 | ||||||
| chr14:99851079
|
G | A | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.250+44G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99851079 | ||||||
| chr14:99851135
|
G | A | 39 | a0001c0004t0001g0009a0001c0004t0001g0040a0001c0004t0001g0091others(36): Show | 39 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.250+100G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99851135 | ||||||
| chr14:99851265
|
G | T | 1 | a0002c0001t0019g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.250+230G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99851265 | ||||||
| chr14:99851330
|
CAG | C | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.250+298_250+299del others(2): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr14 | 99851330 | |||||
| chr14:99851456
|
C | T | 1 | a0003c0014t0004g0254 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.250+421C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99851456 | ||||||
| chr14:99851509
|
G | A | 1 | a0001c0003t0001g0163 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.250+474G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99851509 | ||||||
| chr14:99851524
|
G | A | 1 | a0001c0004t0003g0022 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.250+489G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99851524 | ||||||
| chr14:99851546
|
A | T | 96 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0220others(93): Show | 96 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.250+511A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99851546 | ||||||
| chr14:99851663
|
T | C | 1 | a0002c0001t0002g0276 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.250+628T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99851663 | ||||||
| chr14:99851751
|
A | T | 12 | a0001c0003t0007g0014a0001c0005t0001g0079a0001c0005t0001g0250others(9): Show | 12 | HG00639.hp2 HG02451.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.250+716A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99851751 | ||||||
| chr14:99851828
|
CG | C | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.250+796delG | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr14 | 99851828 | |||||
| chr14:99852147
|
T | C | 1 | a0002c0006t0003g0229 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.250+1112T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99852147 | ||||||
| chr14:99852167
|
G | A | 49 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0005g0246others(46): Show | 49 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.250+1132G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99852167 | ||||||
| chr14:99852182
|
T | C | 7 | a0003c0002t0001g0223a0003c0002t0006g0042a0003c0002t0006g0043others(4): Show | 7 | HG01109.hp1 HG01928.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.250+1147T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99852182 | ||||||
| chr14:99852226
|
G | C | 95 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0220others(92): Show | 95 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.250+1191G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99852226 | ||||||
| chr14:99852390
|
A | G | 1 | a0003c0002t0001g0087 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.250+1355A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99852390 | ||||||
| chr14:99852781
|
A | G | 2 | a0003c0002t0002g0162a0003c0002t0002g0211 | 2 | NA18983.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.250+1746A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99852781 | ||||||
| chr14:99852836
|
C | T | 1 | a0003c0002t0006g0140 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.250+1801C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99852836 | ||||||
| chr14:99853256
|
A | T | 2 | a0002c0001t0003g0098a0002c0001t0003g0119 | 2 | HG02040.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.250+2221A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99853256 | ||||||
| chr14:99853261
|
C | T | 2 | a0001c0004t0003g0059a0001c0004t0003g0197 | 2 | HG02293.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.250+2226C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99853261 | ||||||
| chr14:99853429
|
C | A | 2 | a0001c0003t0002g0105a0001c0003t0002g0106 | 2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.250+2394C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99853429 | ||||||
| chr14:99853723
|
G | A | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.250+2688G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99853723 | ||||||
| chr14:99853818
|
C | T | 1 | a0003c0002t0008g0238 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.250+2783C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99853818 | ||||||
| chr14:99853914
|
G | A | 39 | a0001c0004t0001g0009a0001c0004t0001g0040a0001c0004t0001g0091others(36): Show | 39 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.250+2879G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99853914 | ||||||
| chr14:99853923
|
G | A | 2 | a0001c0003t0001g0243a0001c0007t0002g0005 | 2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.250+2888G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99853923 | ||||||
| chr14:99854427
|
G | A | 1 | a0002c0001t0002g0129 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.250+3392G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99854427 | ||||||
| chr14:99854640
|
A | G | 22 | a0001c0003t0001g0225a0001c0003t0001g0260a0001c0003t0001g0274others(19): Show | 22 | HG00639.hp2 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.250+3605A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99854640 | ||||||
| chr14:99854732
|
A | C | 32 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0001g0225others(29): Show | 32 | HG00639.hp2 HG02145.hp2 HG02257.hp2 others(29): Show |
intron_variant | MODIFIER | c.250+3697A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99854732 | ||||||
| chr14:99854822
|
T | C | 39 | a0001c0004t0001g0009a0001c0004t0001g0040a0001c0004t0001g0091others(36): Show | 39 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.250+3787T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99854822 | ||||||
| chr14:99854981
|
G | A | 74 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0001g0225others(71): Show | 74 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.250+3946G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99854981 | ||||||
| chr14:99854996
|
T | C | 1 | a0003c0002t0017g0028 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.250+3961T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99854996 | ||||||
| chr14:99855265
|
A | G | 2 | a0002c0006t0002g0128a0002c0006t0002g0148 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.250+4230A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99855265 | ||||||
| chr14:99855474
|
A | G | 107 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(104): Show | 107 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.250+4439A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99855474 | ||||||
| chr14:99855636
|
G | T | 49 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0005g0246others(46): Show | 49 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.250+4601G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99855636 | ||||||
| chr14:99855660
|
C | T | 1 | a0003c0002t0001g0205 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.250+4625C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99855660 | ||||||
| chr14:99855668
|
C | T | 49 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0005g0246others(46): Show | 49 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.250+4633C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99855668 | ||||||
| chr14:99856148
|
G | A | 1 | a0002c0001t0002g0099 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.250+5113G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99856148 | ||||||
| chr14:99856302
|
GAATAT | G | 14 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0220others(11): Show | 14 | HG01109.hp2 HG01123.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.250+5271_250+5275d others(7): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr14 | 99856302 | |||||
| chr14:99856409
|
C | A | 49 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0005g0246others(46): Show | 49 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.250+5374C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99856409 | ||||||
| chr14:99856656
|
C | T | 1 | a0004c0008t0004g0004 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.250+5621C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99856656 | ||||||
| chr14:99856718
|
A | G | 1 | a0003c0002t0002g0138 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.250+5683A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99856718 | ||||||
| chr14:99856854
|
T | C | 1 | a0002c0001t0001g0239 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.250+5819T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99856854 | ||||||
| chr14:99856874
|
T | G | 62 | a0001c0003t0001g0001a0001c0003t0001g0120a0001c0013t0001g0126others(59): Show | 64 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.250+5839T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99856874 | ||||||
| chr14:99856918
|
G | A | 49 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0005g0246others(46): Show | 49 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.250+5883G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99856918 | ||||||
| chr14:99857014
|
G | A | 35 | a0002c0001t0002g0083a0002c0001t0002g0183a0003c0002t0001g0019others(32): Show | 35 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.250+5979G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99857014 | ||||||
| chr14:99857041
|
G | A | 5 | a0001c0004t0001g0009a0001c0004t0001g0143a0001c0004t0005g0249others(2): Show | 5 | HG02280.hp1 HG02622.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.250+6006G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99857041 | ||||||
| chr14:99857108
|
C | T | 1 | a0002c0001t0003g0134 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.250+6073C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99857108 | ||||||
| chr14:99857140
|
C | T | 2 | a0003c0002t0001g0263a0003c0002t0001g0264 | 2 | NA18966.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.250+6105C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99857140 | ||||||
| chr14:99857270
|
C | CA | 6 | a0001c0004t0001g0009a0001c0004t0001g0143a0001c0004t0003g0131others(3): Show | 6 | HG02280.hp1 HG02622.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.250+6245dupA | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr14 | 99857270 | |||||
| chr14:99857277
|
AAAAT | A | 22 | a0001c0003t0001g0225a0001c0003t0001g0260a0001c0003t0001g0274others(19): Show | 22 | HG00639.hp2 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.250+6254_250+6257d others(6): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr14 | 99857277 | |||||
| chr14:99857329
|
C | T | 4 | a0001c0004t0003g0199a0002c0001t0002g0065a0002c0001t0003g0188others(1): Show | 4 | NA18956.hp2 NA18957.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.250+6294C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99857329 | ||||||
| chr14:99857890
|
A | G | 1 | a0002c0001t0002g0175 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.250+6855A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99857890 | ||||||
| chr14:99857974
|
G | A | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.250+6939G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99857974 | ||||||
| chr14:99857987
|
A | G | 2 | a0001c0005t0004g0284a0001c0005t0004g0285 | 2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.250+6952A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99857987 | ||||||
| chr14:99858097
|
T | G | 1 | a0001c0003t0001g0163 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.250+7062T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99858097 | ||||||
| chr14:99858201
|
TAGG | T | 21 | a0001c0003t0001g0225a0001c0003t0001g0260a0001c0003t0001g0274others(18): Show | 21 | HG00639.hp2 HG02145.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.250+7167_250+7169d others(5): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99858201 | ||||||
| chr14:99858205
|
C | T | 21 | a0001c0003t0001g0225a0001c0003t0001g0260a0001c0003t0001g0274others(18): Show | 21 | HG00639.hp2 HG02145.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.250+7170C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99858205 | ||||||
| chr14:99858221
|
G | A | 4 | a0002c0001t0002g0061a0002c0001t0002g0063a0002c0001t0002g0073others(1): Show | 4 | HG01975.hp2 NA19086.hp2 NA19091.hp1 others(1): Show |
intron_variant | MODIFIER | c.250+7186G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99858221 | ||||||
| chr14:99858238
|
A | G | 2 | a0001c0004t0003g0048a0001c0004t0003g0206 | 2 | HG00609.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.250+7203A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99858238 | ||||||
| chr14:99858250
|
T | A | 4 | a0002c0001t0002g0056a0002c0001t0002g0057a0002c0001t0002g0150others(1): Show | 4 | NA18939.hp1 NA18953.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.250+7215T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99858250 | ||||||
| chr14:99858702
|
A | T | 171 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0167others(168): Show | 171 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.251-6812A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99858702 | ||||||
| chr14:99858929
|
G | A | 3 | a0001c0003t0001g0167a0001c0003t0001g0168a0006c0011t0001g0011 | 3 | HG02818.hp1 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.251-6585G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99858929 | ||||||
| chr14:99858938
|
A | C | 1 | a0001c0004t0001g0123 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.251-6576A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99858938 | ||||||
| chr14:99859128
|
T | G | 175 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(172): Show | 175 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.251-6386T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99859128 | ||||||
| chr14:99859263
|
C | G | 5 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258others(2): Show | 5 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.251-6251C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99859263 | ||||||
| chr14:99859374
|
T | G | 9 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(6): Show | 9 | HG02109.hp1 HG02486.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.251-6140T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99859374 | ||||||
| chr14:99859380
|
C | T | 2 | a0001c0005t0001g0079a0001c0005t0009g0078 | 2 | HG02809.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.251-6134C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99859380 | ||||||
| chr14:99859610
|
G | A | 1 | a0002c0001t0002g0136 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.251-5904G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99859610 | ||||||
| chr14:99859710
|
A | G | 18 | a0001c0003t0001g0008a0001c0003t0001g0010a0001c0003t0001g0158others(15): Show | 18 | HG00639.hp2 HG02451.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.251-5804A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99859710 | ||||||
| chr14:99859956
|
G | A | 1 | a0003c0002t0001g0198 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.251-5558G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99859956 | ||||||
| chr14:99860035
|
C | T | 1 | a0001c0004t0003g0022 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.251-5479C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99860035 | ||||||
| chr14:99860036
|
G | A | 1 | a0003c0002t0001g0154 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.251-5478G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99860036 | ||||||
| chr14:99860044
|
T | C | 171 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(168): Show | 171 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.251-5470T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99860044 | ||||||
| chr14:99860122
|
T | TA | 3 | a0001c0003t0003g0032a0001c0003t0003g0033a0001c0003t0003g0034 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.251-5391dupA | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr14 | 99860122 | |||||
| chr14:99860183
|
A | G | 1 | a0002c0001t0002g0083 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.251-5331A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99860183 | ||||||
| chr14:99860263
|
G | T | 37 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(34): Show | 37 | HG00609.hp2 HG00639.hp2 HG02083.hp2 others(34): Show |
intron_variant | MODIFIER | c.251-5251G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99860263 | ||||||
| chr14:99860464
|
T | C | 4 | a0003c0002t0001g0170a0003c0002t0001g0171a0003c0002t0001g0172others(1): Show | 4 | NA18952.hp2 NA18957.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.251-5050T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99860464 | ||||||
| chr14:99860575
|
A | G | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.251-4939A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99860575 | ||||||
| chr14:99860769
|
T | C | 1 | a0002c0001t0002g0058 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.251-4745T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99860769 | ||||||
| chr14:99860847
|
T | A | 1 | a0001c0003t0004g0141 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.251-4667T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99860847 | ||||||
| chr14:99860905
|
A | G | 1 | a0002c0001t0002g0278 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.251-4609A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99860905 | ||||||
| chr14:99860997
|
A | G | 1 | a0002c0001t0002g0276 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.251-4517A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99860997 | ||||||
| chr14:99861005
|
T | C | 8 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(5): Show | 8 | HG02109.hp1 HG02486.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.251-4509T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99861005 | ||||||
| chr14:99861129
|
C | T | 14 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0220others(11): Show | 14 | HG01109.hp2 HG01123.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.251-4385C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99861129 | ||||||
| chr14:99861264
|
C | T | 4 | a0001c0004t0001g0009a0001c0004t0001g0143a0001c0004t0005g0249others(1): Show | 4 | HG02280.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.251-4250C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99861264 | ||||||
| chr14:99861293
|
C | T | 1 | a0002c0001t0001g0216 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.251-4221C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99861293 | ||||||
| chr14:99861574
|
C | T | 47 | a0001c0004t0001g0009a0001c0004t0001g0040a0001c0004t0001g0091others(44): Show | 47 | HG00140.hp1 HG00609.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.251-3940C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99861574 | ||||||
| chr14:99861862
|
A | G | 1 | a0001c0004t0003g0022 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.251-3652A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99861862 | ||||||
| chr14:99862279
|
A | G | 12 | a0001c0003t0001g0163a0001c0003t0001g0167a0001c0003t0001g0168others(9): Show | 12 | HG02717.hp1 HG02723.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.251-3235A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99862279 | ||||||
| chr14:99862342
|
T | G | 1 | a0002c0001t0002g0133 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.251-3172T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99862342 | ||||||
| chr14:99862870
|
G | C | 2 | a0001c0003t0002g0105a0001c0003t0002g0106 | 2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.251-2644G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99862870 | ||||||
| chr14:99862969
|
G | A | 88 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(85): Show | 88 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.251-2545G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99862969 | ||||||
| chr14:99863095
|
G | A | 6 | a0001c0003t0003g0279a0002c0001t0002g0026a0002c0001t0002g0051others(3): Show | 6 | HG01074.hp1 HG01243.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.251-2419G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99863095 | ||||||
| chr14:99863290
|
C | T | 41 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(38): Show | 41 | HG00609.hp2 HG00639.hp2 HG02083.hp2 others(38): Show |
intron_variant | MODIFIER | c.251-2224C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99863290 | ||||||
| chr14:99863709
|
T | C | 89 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(86): Show | 89 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.251-1805T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99863709 | ||||||
| chr14:99863960
|
G | C | 1 | a0002c0001t0002g0065 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.251-1554G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99863960 | ||||||
| chr14:99864281
|
A | G | 3 | a0002c0001t0002g0025a0002c0001t0002g0052a0002c0001t0002g0174 | 3 | HG02698.hp1 HG03927.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.251-1233A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99864281 | ||||||
| chr14:99864358
|
T | C | 36 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(33): Show | 36 | HG00639.hp2 HG02109.hp1 HG02451.hp1 others(33): Show |
intron_variant | MODIFIER | c.251-1156T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99864358 | ||||||
| chr14:99864489
|
G | A | 1 | a0003c0002t0002g0231 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.251-1025G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99864489 | ||||||
| chr14:99864586
|
C | T | 1 | a0003c0002t0001g0100 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.251-928C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99864586 | ||||||
| chr14:99864748
|
T | G | 89 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(86): Show | 89 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.251-766T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99864748 | ||||||
| chr14:99864805
|
C | CAA | 10 | a0001c0003t0007g0014a0001c0005t0001g0079a0001c0005t0001g0250others(7): Show | 10 | HG00639.hp2 HG02622.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.251-691_251-690dup others(2): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr14 | 99864805 | |||||
| chr14:99864805
|
CA | C | 98 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0220others(95): Show | 98 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.251-690delA | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr14 | 99864805 | |||||
| chr14:99864820
|
A | G | 1 | a0001c0004t0010g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.251-694A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99864820 | ||||||
| chr14:99864921
|
T | C | 2 | a0001c0004t0003g0064a0001c0004t0003g0090 | 2 | HG01346.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.251-593T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99864921 | ||||||
| chr14:99865024
|
A | C | 4 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0005g0246others(1): Show | 4 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.251-490A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99865024 | ||||||
| chr14:99865137
|
G | A | 1 | a0003c0002t0001g0215 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.251-377G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99865137 | ||||||
| chr14:99865296
|
G | A | 2 | a0001c0003t0001g0274a0001c0003t0008g0271 | 2 | HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.251-218G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99865296 | ||||||
| chr14:99865318
|
G | A | 48 | a0001c0004t0001g0009a0001c0004t0001g0040a0001c0004t0001g0091others(45): Show | 48 | HG00140.hp1 HG00609.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.251-196G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 2/21 | chr14 | 99865318 | ||||||
| chr14:99865791
|
A | G | 2 | a0001c0003t0001g0225a0001c0003t0001g0260 | 2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.383+145A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99865791 | ||||||
| chr14:99866350
|
C | G | 2 | a0001c0003t0001g0274a0001c0003t0008g0271 | 2 | HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.383+704C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99866350 | ||||||
| chr14:99866399
|
A | G | 2 | a0002c0001t0002g0057a0002c0001t0002g0151 | 2 | NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.383+753A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99866399 | ||||||
| chr14:99866430
|
C | T | 6 | a0001c0003t0001g0006a0001c0003t0001g0111a0001c0003t0001g0112others(3): Show | 6 | HG02572.hp1 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.383+784C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99866430 | ||||||
| chr14:99866431
|
G | A | 2 | a0001c0003t0001g0225a0001c0003t0001g0260 | 2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.383+785G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99866431 | ||||||
| chr14:99866570
|
C | CA | 71 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0220others(68): Show | 71 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.383+950dupA | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr14 | 99866570 | |||||
| chr14:99866570
|
C | CAA | 17 | a0001c0003t0001g0233a0002c0001t0001g0092a0002c0001t0002g0018others(14): Show | 17 | HG00423.hp2 HG00733.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.383+949_383+950dup others(2): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr14 | 99866570 | |||||
| chr14:99866570
|
CAAA | C | 39 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(36): Show | 39 | HG00639.hp2 HG02055.hp1 HG02109.hp1 others(36): Show |
intron_variant | MODIFIER | c.383+948_383+950del others(3): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr14 | 99866570 | |||||
| chr14:99866570
|
CAAAA | C | 6 | a0001c0003t0001g0015a0001c0003t0001g0274a0001c0003t0004g0027others(3): Show | 6 | HG02083.hp2 HG02451.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.383+947_383+950del others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr14 | 99866570 | |||||
| chr14:99866570
|
CAAAAAAA others(7): Show |
C | 41 | a0001c0004t0001g0009a0001c0004t0001g0040a0001c0004t0001g0091others(38): Show | 41 | HG00140.hp1 HG00609.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.383+937_383+950del others(14): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr14 | 99866570 | |||||
| chr14:99866641
|
A | G | 89 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(86): Show | 89 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.383+995A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99866641 | ||||||
| chr14:99866702
|
T | TC | 87 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(84): Show | 87 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.383+1060dupC | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr14 | 99866702 | |||||
| chr14:99866747
|
T | C | 48 | a0001c0004t0001g0009a0001c0004t0001g0040a0001c0004t0001g0091others(45): Show | 48 | HG00140.hp1 HG00609.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.383+1101T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99866747 | ||||||
| chr14:99866813
|
T | C | 181 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(178): Show | 181 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.383+1167T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99866813 | ||||||
| chr14:99866979
|
A | G | 24 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(21): Show | 24 | HG00639.hp2 HG02109.hp1 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.383+1333A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99866979 | ||||||
| chr14:99867047
|
C | A | 1 | a0001c0004t0003g0090 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.383+1401C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99867047 | ||||||
| chr14:99867169
|
T | C | 1 | a0002c0001t0001g0219 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.383+1523T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99867169 | ||||||
| chr14:99867189
|
C | A | 4 | a0001c0004t0001g0009a0001c0004t0001g0143a0001c0004t0005g0249others(1): Show | 4 | HG02280.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.383+1543C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99867189 | ||||||
| chr14:99867280
|
T | C | 48 | a0001c0004t0001g0009a0001c0004t0001g0040a0001c0004t0001g0091others(45): Show | 48 | HG00140.hp1 HG00609.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.383+1634T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99867280 | ||||||
| chr14:99867376
|
G | A | 12 | a0001c0003t0001g0163a0001c0003t0001g0167a0001c0003t0001g0168others(9): Show | 12 | HG02717.hp1 HG02723.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.383+1730G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99867376 | ||||||
| chr14:99867422
|
C | T | 87 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(84): Show | 87 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.383+1776C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99867422 | ||||||
| chr14:99867463
|
A | G | 24 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(21): Show | 24 | HG00639.hp2 HG02109.hp1 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.383+1817A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99867463 | ||||||
| chr14:99867525
|
G | A | 89 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(86): Show | 89 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.383+1879G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99867525 | ||||||
| chr14:99867534
|
A | G | 1 | a0001c0003t0001g0163 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.383+1888A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99867534 | ||||||
| chr14:99867555
|
C | T | 1 | a0001c0003t0001g0270 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383+1909C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99867555 | ||||||
| chr14:99867673
|
A | AT | 89 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(86): Show | 89 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.383+2027_383+2028i others(3): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99867673 | ||||||
| chr14:99867739
|
T | C | 2 | a0001c0003t0001g0225a0001c0003t0001g0260 | 2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.383+2093T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99867739 | ||||||
| chr14:99867768
|
G | A | 2 | a0001c0003t0001g0225a0001c0003t0001g0260 | 2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.383+2122G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99867768 | ||||||
| chr14:99868032
|
A | C | 89 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(86): Show | 89 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.383+2386A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99868032 | ||||||
| chr14:99868065
|
G | A | 1 | a0002c0001t0002g0133 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.383+2419G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99868065 | ||||||
| chr14:99868167
|
T | C | 89 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(86): Show | 89 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.383+2521T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99868167 | ||||||
| chr14:99868381
|
G | A | 2 | a0002c0001t0002g0045a0002c0001t0002g0227 | 2 | HG00733.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.383+2735G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99868381 | ||||||
| chr14:99868382
|
C | G | 89 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(86): Show | 89 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.383+2736C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99868382 | ||||||
| chr14:99868389
|
A | G | 4 | a0003c0002t0001g0154a0003c0002t0001g0262a0003c0002t0003g0155others(1): Show | 4 | HG00438.hp1 HG02155.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.383+2743A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99868389 | ||||||
| chr14:99868474
|
C | T | 1 | a0003c0002t0002g0050 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.383+2828C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99868474 | ||||||
| chr14:99868533
|
A | G | 1 | a0001c0003t0003g0279 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.383+2887A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99868533 | ||||||
| chr14:99868623
|
T | C | 1 | a0002c0001t0002g0153 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.383+2977T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99868623 | ||||||
| chr14:99868753
|
A | G | 4 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0005g0246others(1): Show | 4 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.383+3107A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99868753 | ||||||
| chr14:99868938
|
A | T | 1 | a0002c0001t0002g0067 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.383+3292A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99868938 | ||||||
| chr14:99869069
|
G | C | 1 | a0001c0003t0001g0163 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.383+3423G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99869069 | ||||||
| chr14:99869117
|
T | C | 1 | a0003c0002t0011g0024 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.383+3471T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99869117 | ||||||
| chr14:99869118
|
G | C | 11 | a0001c0004t0001g0115a0001c0004t0002g0047a0001c0004t0003g0029others(8): Show | 11 | HG00140.hp1 HG01168.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.383+3472G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99869118 | ||||||
| chr14:99869123
|
C | T | 1 | a0002c0006t0003g0229 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.383+3477C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99869123 | ||||||
| chr14:99869191
|
G | A | 4 | a0001c0004t0001g0009a0001c0004t0001g0143a0001c0004t0005g0249others(1): Show | 4 | HG02280.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.383+3545G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99869191 | ||||||
| chr14:99869366
|
G | A | 1 | a0007c0012t0002g0275 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.383+3720G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99869366 | ||||||
| chr14:99869769
|
G | A | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.383+4123G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99869769 | ||||||
| chr14:99869784
|
G | C | 3 | a0003c0002t0003g0159a0003c0002t0003g0169a0003c0002t0003g0208 | 3 | NA18994.hp2 NA18998.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.383+4138G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99869784 | ||||||
| chr14:99869791
|
C | G | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.383+4145C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99869791 | ||||||
| chr14:99869843
|
T | A | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.383+4197T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99869843 | ||||||
| chr14:99869898
|
C | G | 10 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0220others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.383+4252C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99869898 | ||||||
| chr14:99869936
|
A | G | 36 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(33): Show | 36 | HG00639.hp2 HG02109.hp1 HG02451.hp1 others(33): Show |
intron_variant | MODIFIER | c.383+4290A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99869936 | ||||||
| chr14:99870004
|
T | C | 89 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(86): Show | 89 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.383+4358T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99870004 | ||||||
| chr14:99870013
|
C | A | 1 | a0003c0002t0001g0037 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.383+4367C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99870013 | ||||||
| chr14:99870084
|
G | A | 8 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(5): Show | 8 | HG02109.hp1 HG02486.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.383+4438G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99870084 | ||||||
| chr14:99870237
|
A | C | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.383+4591A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99870237 | ||||||
| chr14:99870399
|
G | A | 3 | a0004c0008t0004g0004a0004c0008t0004g0268a0005c0009t0002g0132 | 3 | HG02055.hp2 HG02615.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.383+4753G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99870399 | ||||||
| chr14:99870644
|
C | G | 1 | a0001c0013t0001g0126 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.383+4998C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99870644 | ||||||
| chr14:99870645
|
A | G | 1 | a0001c0003t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.383+4999A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99870645 | ||||||
| chr14:99870788
|
C | T | 1 | a0003c0002t0002g0138 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.383+5142C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99870788 | ||||||
| chr14:99870935
|
C | T | 2 | a0001c0003t0002g0105a0001c0003t0002g0106 | 2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.383+5289C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99870935 | ||||||
| chr14:99871008
|
G | A | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.383+5362G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99871008 | ||||||
| chr14:99871193
|
A | G | 4 | a0001c0004t0001g0009a0001c0004t0001g0143a0001c0004t0005g0249others(1): Show | 4 | HG02280.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.383+5547A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99871193 | ||||||
| chr14:99871236
|
C | T | 2 | a0001c0003t0001g0225a0001c0003t0001g0260 | 2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.383+5590C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99871236 | ||||||
| chr14:99871414
|
G | A | 9 | a0003c0002t0001g0198a0003c0002t0001g0217a0003c0002t0001g0223others(6): Show | 9 | HG01109.hp1 HG01928.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.383+5768G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99871414 | ||||||
| chr14:99871559
|
C | T | 24 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(21): Show | 24 | HG00639.hp2 HG02109.hp1 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.383+5913C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99871559 | ||||||
| chr14:99871705
|
A | T | 3 | a0001c0003t0001g0008a0001c0003t0001g0010a0001c0003t0001g0214 | 3 | HG02486.hp2 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.383+6059A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99871705 | ||||||
| chr14:99871798
|
C | T | 1 | a0002c0001t0001g0216 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.383+6152C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99871798 | ||||||
| chr14:99871905
|
G | A | 4 | a0002c0001t0002g0023a0002c0001t0002g0081a0002c0001t0002g0093others(1): Show | 4 | HG00544.hp2 HG00558.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.383+6259G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99871905 | ||||||
| chr14:99871910
|
G | A | 6 | a0001c0003t0001g0243a0001c0003t0001g0244a0001c0003t0001g0245others(3): Show | 6 | HG02717.hp1 HG02723.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.383+6264G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99871910 | ||||||
| chr14:99872165
|
G | A | 1 | a0002c0001t0002g0224 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.384-6320G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99872165 | ||||||
| chr14:99872335
|
C | T | 7 | a0001c0004t0001g0123a0001c0004t0001g0248a0001c0004t0001g0255others(4): Show | 7 | HG02055.hp1 HG02155.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.384-6150C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99872335 | ||||||
| chr14:99872358
|
A | T | 92 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0220others(89): Show | 92 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.384-6127A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99872358 | ||||||
| chr14:99872388
|
C | T | 1 | a0003c0002t0001g0037 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.384-6097C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99872388 | ||||||
| chr14:99872432
|
A | T | 4 | a0001c0003t0001g0243a0001c0003t0001g0244a0001c0003t0001g0245others(1): Show | 4 | HG02723.hp2 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.384-6053A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99872432 | ||||||
| chr14:99872865
|
T | C | 1 | a0002c0001t0002g0176 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.384-5620T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99872865 | ||||||
| chr14:99872881
|
GTA | G | 6 | a0001c0004t0001g0123a0001c0004t0001g0248a0001c0004t0001g0255others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.384-5600_384-5599d others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr14 | 99872881 | |||||
| chr14:99872884
|
T | C | 1 | a0001c0003t0004g0141 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.384-5601T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99872884 | ||||||
| chr14:99873293
|
A | C | 5 | a0002c0001t0002g0046a0002c0001t0002g0068a0002c0001t0002g0069others(2): Show | 5 | HG01928.hp1 HG02293.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.384-5192A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99873293 | ||||||
| chr14:99873384
|
C | T | 2 | a0002c0001t0002g0082a0002c0001t0002g0084 | 2 | HG00438.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.384-5101C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99873384 | ||||||
| chr14:99873432
|
G | T | 3 | a0001c0003t0001g0243a0001c0003t0001g0244a0001c0003t0001g0245 | 3 | HG02922.hp1 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.384-5053G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99873432 | ||||||
| chr14:99873492
|
A | G | 2 | a0001c0003t0001g0225a0001c0003t0001g0260 | 2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.384-4993A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99873492 | ||||||
| chr14:99873511
|
T | C | 2 | a0001c0003t0001g0225a0001c0003t0001g0260 | 2 | HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.384-4974T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99873511 | ||||||
| chr14:99873927
|
C | G | 3 | a0001c0003t0003g0032a0001c0003t0003g0033a0001c0003t0003g0034 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.384-4558C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99873927 | ||||||
| chr14:99873950
|
C | T | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.384-4535C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99873950 | ||||||
| chr14:99874080
|
A | T | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.384-4405A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99874080 | ||||||
| chr14:99874241
|
A | G | 1 | a0003c0002t0001g0124 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.384-4244A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99874241 | ||||||
| chr14:99874246
|
C | T | 88 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(85): Show | 88 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.384-4239C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99874246 | ||||||
| chr14:99874384
|
T | G | 2 | a0002c0001t0002g0057a0002c0001t0002g0151 | 2 | NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.384-4101T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99874384 | ||||||
| chr14:99874578
|
T | TGTCTTGT others(17): Show |
6 | a0001c0004t0001g0123a0001c0004t0001g0248a0001c0004t0001g0255others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.384-3906_384-3883d others(26): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr14 | 99874578 | |||||
| chr14:99874677
|
TTTTTTAT others(5): Show |
T | 13 | a0001c0003t0001g0163a0001c0003t0001g0167a0001c0003t0001g0168others(10): Show | 13 | HG02257.hp2 HG02717.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.384-3807_384-3796d others(14): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99874677 | ||||||
| chr14:99874716
|
A | T | 2 | a0001c0004t0002g0047a0001c0004t0003g0029 | 2 | HG02559.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.384-3769A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99874716 | ||||||
| chr14:99875084
|
C | T | 2 | a0001c0003t0002g0252a0001c0003t0009g0251 | 2 | HG00733.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.384-3401C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99875084 | ||||||
| chr14:99875093
|
A | G | 86 | a0001c0003t0003g0279a0001c0003t0007g0117a0001c0003t0007g0281others(83): Show | 86 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.384-3392A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99875093 | ||||||
| chr14:99875097
|
A | C | 25 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(22): Show | 25 | HG00639.hp2 HG02109.hp1 HG02451.hp1 others(22): Show |
intron_variant | MODIFIER | c.384-3388A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99875097 | ||||||
| chr14:99875645
|
A | G | 184 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(181): Show | 185 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.384-2840A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99875645 | ||||||
| chr14:99875950
|
G | A | 265 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0008others(262): Show | 266 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.384-2535G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99875950 | ||||||
| chr14:99876139
|
CAG | C | 46 | a0001c0004t0001g0009a0001c0004t0001g0040a0001c0004t0001g0091others(43): Show | 46 | HG00140.hp1 HG00609.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.384-2341_384-2340d others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr14 | 99876139 | |||||
| chr14:99876182
|
CAAG | C | 181 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(178): Show | 182 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.384-2299_384-2297d others(5): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr14 | 99876182 | |||||
| chr14:99876323
|
T | C | 7 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0001g0225others(4): Show | 7 | HG02809.hp1 HG02818.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.384-2162T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99876323 | ||||||
| chr14:99876504
|
T | C | 9 | a0001c0003t0001g0163a0001c0003t0001g0167a0001c0003t0001g0168others(6): Show | 9 | HG02257.hp2 HG02809.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.384-1981T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99876504 | ||||||
| chr14:99876518
|
C | T | 1 | a0001c0004t0010g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.384-1967C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99876518 | ||||||
| chr14:99876548
|
G | A | 2 | a0001c0003t0001g0163a0001c0004t0004g0017 | 2 | HG02257.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.384-1937G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99876548 | ||||||
| chr14:99876767
|
C | G | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.384-1718C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99876767 | ||||||
| chr14:99876815
|
T | G | 29 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(26): Show | 29 | HG00639.hp2 HG02109.hp1 HG02451.hp1 others(26): Show |
intron_variant | MODIFIER | c.384-1670T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99876815 | ||||||
| chr14:99876903
|
G | A | 268 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0008others(265): Show | 269 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.384-1582G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99876903 | ||||||
| chr14:99877006
|
G | A | 7 | a0001c0004t0001g0123a0001c0004t0001g0248a0001c0004t0001g0255others(4): Show | 7 | HG02055.hp1 HG02451.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.384-1479G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99877006 | ||||||
| chr14:99877083
|
A | G | 2 | a0002c0001t0003g0188a0002c0001t0003g0189 | 2 | NA18957.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.384-1402A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99877083 | ||||||
| chr14:99877115
|
G | A | 46 | a0001c0004t0001g0009a0001c0004t0001g0040a0001c0004t0001g0091others(43): Show | 46 | HG00140.hp1 HG00609.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.384-1370G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99877115 | ||||||
| chr14:99877348
|
A | G | 11 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(8): Show | 11 | HG02109.hp1 HG02486.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.384-1137A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99877348 | ||||||
| chr14:99877492
|
C | T | 7 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0001g0225others(4): Show | 7 | HG02809.hp1 HG02818.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.384-993C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99877492 | ||||||
| chr14:99877793
|
G | A | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.384-692G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99877793 | ||||||
| chr14:99877814
|
C | T | 96 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0220others(93): Show | 96 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.384-671C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99877814 | ||||||
| chr14:99877822
|
G | A | 2 | a0001c0003t0001g0274a0001c0003t0008g0271 | 2 | HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.384-663G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99877822 | ||||||
| chr14:99877825
|
T | C | 268 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0008others(265): Show | 269 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.384-660T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99877825 | ||||||
| chr14:99877958
|
A | G | 5 | a0003c0002t0001g0044a0003c0002t0001g0055a0003c0002t0001g0087others(2): Show | 5 | HG01192.hp2 HG01255.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.384-527A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99877958 | ||||||
| chr14:99878151
|
AAG | A | 46 | a0001c0004t0001g0009a0001c0004t0001g0040a0001c0004t0001g0091others(43): Show | 46 | HG00140.hp1 HG00609.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.384-332_384-331del others(2): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr14 | 99878151 | |||||
| chr14:99878154
|
A | T | 46 | a0001c0004t0001g0009a0001c0004t0001g0040a0001c0004t0001g0091others(43): Show | 46 | HG00140.hp1 HG00609.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.384-331A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99878154 | ||||||
| chr14:99878313
|
C | T | 11 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(8): Show | 11 | HG02109.hp1 HG02486.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.384-172C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99878313 | ||||||
| chr14:99878361
|
T | C | 265 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0008others(262): Show | 266 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.384-124T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 3/21 | chr14 | 99878361 | ||||||
| chr14:99878628
|
G | A | 2 | a0001c0003t0001g0274a0001c0003t0008g0271 | 2 | HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.518+9G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99878628 | ||||||
| chr14:99878633
|
A | G | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.518+14A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99878633 | ||||||
| chr14:99878715
|
G | C | 16 | a0001c0003t0001g0243a0001c0003t0001g0244a0001c0003t0001g0245others(13): Show | 16 | HG00639.hp2 HG02451.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.518+96G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99878715 | ||||||
| chr14:99878833
|
ACTGT | A | 46 | a0001c0004t0001g0009a0001c0004t0001g0040a0001c0004t0001g0091others(43): Show | 46 | HG00140.hp1 HG00609.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.518+216_518+219del others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr14 | 99878833 | |||||
| chr14:99878942
|
A | G | 206 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(203): Show | 207 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(204): Show |
intron_variant | MODIFIER | c.518+323A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99878942 | ||||||
| chr14:99879076
|
C | A | 219 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0008others(216): Show | 220 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.518+457C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99879076 | ||||||
| chr14:99879133
|
C | T | 1 | a0001c0004t0005g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.518+514C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99879133 | ||||||
| chr14:99879196
|
A | G | 219 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0008others(216): Show | 220 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.518+577A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99879196 | ||||||
| chr14:99879321
|
A | G | 181 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(178): Show | 182 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.518+702A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99879321 | ||||||
| chr14:99879434
|
A | T | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.518+815A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99879434 | ||||||
| chr14:99879618
|
C | T | 4 | a0001c0003t0001g0243a0001c0003t0001g0244a0001c0003t0001g0245others(1): Show | 4 | HG02723.hp2 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.518+999C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99879618 | ||||||
| chr14:99879768
|
A | C | 4 | a0001c0005t0001g0250a0001c0005t0005g0003a0001c0005t0005g0097others(1): Show | 4 | HG00639.hp2 HG02451.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.518+1149A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99879768 | ||||||
| chr14:99879778
|
G | A | 1 | a0001c0003t0001g0163 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.518+1159G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99879778 | ||||||
| chr14:99879855
|
G | T | 2 | a0001c0003t0001g0274a0001c0003t0008g0271 | 2 | HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.518+1236G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99879855 | ||||||
| chr14:99880216
|
G | A | 1 | a0003c0002t0001g0107 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.518+1597G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99880216 | ||||||
| chr14:99880302
|
A | T | 2 | a0001c0003t0001g0163a0001c0004t0004g0017 | 2 | HG02257.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.518+1683A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99880302 | ||||||
| chr14:99880327
|
A | C | 13 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(10): Show | 13 | HG02109.hp1 HG02486.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.518+1708A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99880327 | ||||||
| chr14:99880494
|
C | T | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.518+1875C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99880494 | ||||||
| chr14:99880567
|
C | T | 1 | a0003c0002t0001g0262 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.518+1948C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99880567 | ||||||
| chr14:99880568
|
G | A | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.518+1949G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99880568 | ||||||
| chr14:99880631
|
G | A | 197 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(194): Show | 198 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.518+2012G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99880631 | ||||||
| chr14:99880669
|
G | T | 2 | a0001c0003t0001g0163a0001c0004t0004g0017 | 2 | HG02257.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.518+2050G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99880669 | ||||||
| chr14:99880851
|
G | A | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.518+2232G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99880851 | ||||||
| chr14:99880852
|
C | T | 7 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0001g0225others(4): Show | 7 | HG02809.hp1 HG02818.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.518+2233C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99880852 | ||||||
| chr14:99880885
|
C | T | 2 | a0002c0001t0002g0045a0002c0001t0002g0227 | 2 | HG00733.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.518+2266C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99880885 | ||||||
| chr14:99880927
|
G | A | 3 | a0003c0002t0001g0037a0003c0002t0001g0209a0003c0002t0001g0210 | 3 | HG01943.hp1 NA18977.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.518+2308G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99880927 | ||||||
| chr14:99881008
|
C | T | 1 | a0001c0004t0003g0049 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.518+2389C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99881008 | ||||||
| chr14:99881013
|
C | T | 1 | a0001c0004t0003g0049 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.518+2394C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99881013 | ||||||
| chr14:99881015
|
C | T | 2 | a0001c0003t0001g0163a0001c0004t0004g0017 | 2 | HG02257.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.518+2396C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99881015 | ||||||
| chr14:99881076
|
A | G | 1 | a0001c0004t0003g0059 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.518+2457A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99881076 | ||||||
| chr14:99881096
|
C | T | 4 | a0001c0003t0001g0243a0001c0003t0001g0244a0001c0003t0001g0245others(1): Show | 4 | HG02723.hp2 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.518+2477C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99881096 | ||||||
| chr14:99881568
|
A | C | 196 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(193): Show | 197 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.518+2949A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99881568 | ||||||
| chr14:99881607
|
C | CT | 188 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(185): Show | 189 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.518+3000dupT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr14 | 99881607 | |||||
| chr14:99881607
|
C | CTT | 15 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0005g0246others(12): Show | 15 | HG00639.hp2 HG01928.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.518+2999_518+3000d others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr14 | 99881607 | |||||
| chr14:99881607
|
CT | C | 13 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(10): Show | 13 | HG02109.hp1 HG02486.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.518+3000delT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr14 | 99881607 | |||||
| chr14:99881792
|
G | T | 1 | a0003c0002t0002g0138 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.518+3173G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99881792 | ||||||
| chr14:99881833
|
T | C | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.518+3214T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99881833 | ||||||
| chr14:99881878
|
C | T | 7 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0001g0225others(4): Show | 7 | HG02809.hp1 HG02818.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.518+3259C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99881878 | ||||||
| chr14:99881974
|
T | C | 218 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0008others(215): Show | 219 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.518+3355T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99881974 | ||||||
| chr14:99881994
|
G | A | 8 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(5): Show | 8 | HG02109.hp1 HG02486.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.518+3375G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99881994 | ||||||
| chr14:99881999
|
C | T | 2 | a0001c0005t0001g0079a0001c0005t0009g0078 | 2 | HG02809.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.518+3380C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99881999 | ||||||
| chr14:99882052
|
T | A | 13 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(10): Show | 13 | HG02109.hp1 HG02486.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.518+3433T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99882052 | ||||||
| chr14:99882232
|
G | C | 2 | a0001c0003t0001g0163a0001c0004t0004g0017 | 2 | HG02257.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.518+3613G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99882232 | ||||||
| chr14:99882289
|
T | C | 13 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(10): Show | 13 | HG02109.hp1 HG02486.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.518+3670T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99882289 | ||||||
| chr14:99882301
|
G | C | 5 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0005g0246others(2): Show | 5 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.518+3682G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99882301 | ||||||
| chr14:99882332
|
G | A | 196 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(193): Show | 197 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.518+3713G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99882332 | ||||||
| chr14:99882338
|
T | C | 1 | a0003c0002t0002g0138 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.518+3719T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99882338 | ||||||
| chr14:99882448
|
C | G | 7 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0001g0225others(4): Show | 7 | HG02809.hp1 HG02818.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.518+3829C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99882448 | ||||||
| chr14:99882649
|
TAA | T | 13 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258others(10): Show | 13 | HG00609.hp2 HG02055.hp1 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.518+4055_518+4056d others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr14 | 99882649 | |||||
| chr14:99882649
|
TAAA | T | 39 | a0001c0003t0001g0260a0001c0004t0001g0009a0001c0004t0001g0040others(36): Show | 39 | HG00140.hp1 HG00609.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.518+4054_518+4056d others(5): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr14 | 99882649 | |||||
| chr14:99882649
|
TAAAA | T | 36 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0167others(33): Show | 36 | HG00639.hp2 HG01109.hp2 HG01943.hp2 others(33): Show |
intron_variant | MODIFIER | c.518+4053_518+4056d others(6): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr14 | 99882649 | |||||
| chr14:99882649
|
TAAAAA | T | 179 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0008others(176): Show | 180 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.518+4052_518+4056d others(7): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr14 | 99882649 | |||||
| chr14:99882669
|
A | G | 182 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0008others(179): Show | 183 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.518+4050A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99882669 | ||||||
| chr14:99882671
|
A | G | 47 | a0001c0003t0007g0014a0001c0004t0001g0009a0001c0004t0001g0040others(44): Show | 47 | HG00140.hp1 HG00609.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.518+4052A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99882671 | ||||||
| chr14:99882823
|
GA | G | 44 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0167others(41): Show | 44 | HG00639.hp2 HG01109.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.518+4216delA | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr14 | 99882823 | |||||
| chr14:99882895
|
C | A | 9 | a0001c0005t0001g0079a0001c0005t0001g0250a0001c0005t0004g0284others(6): Show | 9 | HG00639.hp2 HG02451.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.518+4276C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99882895 | ||||||
| chr14:99882923
|
G | A | 19 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0167others(16): Show | 19 | HG01109.hp2 HG02109.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.518+4304G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99882923 | ||||||
| chr14:99882946
|
A | C | 8 | a0001c0003t0007g0014a0001c0004t0001g0123a0001c0004t0001g0248others(5): Show | 8 | HG02055.hp1 HG02451.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.518+4327A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99882946 | ||||||
| chr14:99883029
|
C | T | 19 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0167others(16): Show | 19 | HG01109.hp2 HG02109.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.518+4410C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99883029 | ||||||
| chr14:99883065
|
T | C | 111 | a0001c0003t0001g0006a0001c0003t0001g0008a0001c0003t0001g0010others(108): Show | 112 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.518+4446T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99883065 | ||||||
| chr14:99883071
|
C | T | 2 | a0001c0003t0001g0041a0001c0003t0003g0184 | 2 | HG01069.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.518+4452C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99883071 | ||||||
| chr14:99883101
|
T | C | 266 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0008others(263): Show | 267 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.518+4482T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99883101 | ||||||
| chr14:99883101
|
T | G | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.518+4482T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99883101 | ||||||
| chr14:99883169
|
C | T | 2 | a0003c0002t0001g0237a0003c0015t0001g0013 | 2 | HG01884.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.518+4550C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99883169 | ||||||
| chr14:99883392
|
G | A | 49 | a0001c0003t0003g0279a0001c0003t0007g0014a0001c0004t0001g0009others(46): Show | 49 | HG00140.hp1 HG00609.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.518+4773G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99883392 | ||||||
| chr14:99883444
|
T | C | 78 | a0001c0003t0001g0163a0001c0004t0004g0017a0003c0002t0001g0002others(75): Show | 79 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.518+4825T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99883444 | ||||||
| chr14:99883531
|
C | CA | 6 | a0001c0003t0002g0252a0001c0007t0002g0005a0001c0007t0018g0241others(3): Show | 6 | HG00733.hp1 HG02071.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.518+4931dupA | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr14 | 99883531 | |||||
| chr14:99883680
|
T | C | 79 | a0001c0003t0001g0163a0001c0004t0004g0017a0003c0002t0001g0002others(76): Show | 80 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.518+5061T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99883680 | ||||||
| chr14:99883817
|
T | C | 21 | a0001c0003t0001g0006a0001c0003t0001g0111a0001c0003t0001g0112others(18): Show | 21 | HG00639.hp2 HG02451.hp1 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.518+5198T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99883817 | ||||||
| chr14:99883820
|
A | C | 1 | a0003c0002t0003g0155 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.518+5201A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99883820 | ||||||
| chr14:99883923
|
G | A | 2 | a0002c0001t0002g0065a0002c0001t0002g0183 | 2 | NA18956.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.518+5304G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99883923 | ||||||
| chr14:99883960
|
A | G | 8 | a0001c0003t0007g0014a0001c0004t0001g0123a0001c0004t0001g0248others(5): Show | 8 | HG02055.hp1 HG02451.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.518+5341A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99883960 | ||||||
| chr14:99883970
|
G | C | 2 | a0001c0003t0001g0163a0001c0004t0004g0017 | 2 | HG02257.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.518+5351G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99883970 | ||||||
| chr14:99884154
|
C | T | 19 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0167others(16): Show | 19 | HG01109.hp2 HG02109.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.518+5535C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99884154 | ||||||
| chr14:99884296
|
T | C | 202 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(199): Show | 203 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.518+5677T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99884296 | ||||||
| chr14:99884630
|
A | G | 15 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(12): Show | 15 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.518+6011A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99884630 | ||||||
| chr14:99884706
|
C | T | 21 | a0001c0003t0001g0006a0001c0003t0001g0111a0001c0003t0001g0112others(18): Show | 21 | HG00639.hp2 HG02451.hp1 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.518+6087C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99884706 | ||||||
| chr14:99884707
|
T | C | 21 | a0001c0003t0001g0006a0001c0003t0001g0111a0001c0003t0001g0112others(18): Show | 21 | HG00639.hp2 HG02451.hp1 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.518+6088T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99884707 | ||||||
| chr14:99884854
|
G | A | 2 | a0001c0003t0001g0163a0001c0004t0004g0017 | 2 | HG02257.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.518+6235G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99884854 | ||||||
| chr14:99885005
|
T | C | 1 | a0001c0004t0011g0156 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.519-6194T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99885005 | ||||||
| chr14:99885072
|
C | A | 70 | a0001c0003t0001g0006a0001c0003t0001g0111a0001c0003t0001g0112others(67): Show | 70 | HG00140.hp1 HG00609.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.519-6127C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99885072 | ||||||
| chr14:99885117
|
C | T | 14 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0220others(11): Show | 14 | HG01109.hp2 HG02109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.519-6082C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99885117 | ||||||
| chr14:99885177
|
A | G | 1 | a0002c0001t0002g0093 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.519-6022A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99885177 | ||||||
| chr14:99885235
|
T | C | 1 | a0002c0001t0002g0072 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.519-5964T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99885235 | ||||||
| chr14:99885275
|
A | G | 19 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0167others(16): Show | 19 | HG01109.hp2 HG02109.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.519-5924A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99885275 | ||||||
| chr14:99885488
|
A | G | 181 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0163others(178): Show | 182 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.519-5711A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99885488 | ||||||
| chr14:99885598
|
T | G | 1 | a0001c0005t0008g0077 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.519-5601T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99885598 | ||||||
| chr14:99885601
|
C | A | 269 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0008others(266): Show | 270 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.519-5598C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99885601 | ||||||
| chr14:99885813
|
ATATCT | A | 19 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0167others(16): Show | 19 | HG01109.hp2 HG02109.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.519-5382_519-5378d others(7): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr14 | 99885813 | |||||
| chr14:99886038
|
C | T | 77 | a0003c0002t0001g0002a0003c0002t0001g0019a0003c0002t0001g0036others(74): Show | 78 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.519-5161C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99886038 | ||||||
| chr14:99886263
|
T | C | 21 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0163others(18): Show | 21 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.519-4936T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99886263 | ||||||
| chr14:99886489
|
A | G | 2 | a0002c0001t0002g0095a0002c0001t0002g0224 | 2 | NA18991.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.519-4710A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99886489 | ||||||
| chr14:99886515
|
A | C | 2 | a0002c0001t0003g0139a0002c0001t0003g0147 | 2 | HG00408.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.519-4684A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99886515 | ||||||
| chr14:99886615
|
C | T | 19 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0167others(16): Show | 19 | HG01109.hp2 HG02109.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.519-4584C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99886615 | ||||||
| chr14:99886682
|
C | A | 18 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(15): Show | 18 | HG00609.hp2 HG02055.hp2 HG02083.hp2 others(15): Show |
intron_variant | MODIFIER | c.519-4517C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99886682 | ||||||
| chr14:99886697
|
C | T | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.519-4502C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99886697 | ||||||
| chr14:99886718
|
C | T | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.519-4481C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99886718 | ||||||
| chr14:99886740
|
A | T | 1 | a0001c0004t0004g0017 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.519-4459A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99886740 | ||||||
| chr14:99886778
|
A | C | 1 | a0002c0001t0002g0133 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.519-4421A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99886778 | ||||||
| chr14:99886798
|
C | T | 82 | a0002c0001t0001g0062a0002c0001t0001g0092a0002c0001t0001g0216others(79): Show | 82 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.519-4401C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99886798 | ||||||
| chr14:99886946
|
A | G | 1 | a0001c0004t0003g0280 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.519-4253A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99886946 | ||||||
| chr14:99887012
|
C | T | 21 | a0001c0003t0001g0006a0001c0003t0001g0111a0001c0003t0001g0112others(18): Show | 21 | HG00639.hp2 HG02451.hp1 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.519-4187C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99887012 | ||||||
| chr14:99887052
|
G | C | 2 | a0001c0003t0001g0163a0001c0004t0004g0017 | 2 | HG02257.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.519-4147G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99887052 | ||||||
| chr14:99887224
|
C | T | 2 | a0001c0004t0003g0049a0001c0004t0003g0145 | 2 | NA18984.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.519-3975C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99887224 | ||||||
| chr14:99887284
|
T | C | 2 | a0001c0004t0001g0040a0001c0004t0001g0135 | 2 | NA18939.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.519-3915T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99887284 | ||||||
| chr14:99887289
|
A | G | 1 | a0001c0003t0002g0116 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.519-3910A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99887289 | ||||||
| chr14:99887300
|
T | C | 181 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0163others(178): Show | 182 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.519-3899T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99887300 | ||||||
| chr14:99887323
|
T | C | 49 | a0001c0003t0003g0279a0001c0003t0007g0014a0001c0004t0001g0009others(46): Show | 49 | HG00140.hp1 HG00609.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.519-3876T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99887323 | ||||||
| chr14:99887427
|
G | T | 1 | a0003c0002t0003g0212 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.519-3772G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99887427 | ||||||
| chr14:99887488
|
G | C | 1 | a0002c0001t0001g0092 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.519-3711G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99887488 | ||||||
| chr14:99887529
|
AT | A | 49 | a0001c0003t0003g0279a0001c0003t0007g0014a0001c0004t0001g0009others(46): Show | 49 | HG00140.hp1 HG00609.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.519-3668delT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr14 | 99887529 | |||||
| chr14:99887699
|
G | A | 1 | a0003c0002t0003g0230 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.519-3500G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99887699 | ||||||
| chr14:99887704
|
A | C | 21 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0163others(18): Show | 21 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.519-3495A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99887704 | ||||||
| chr14:99887789
|
A | T | 82 | a0002c0001t0001g0062a0002c0001t0001g0092a0002c0001t0001g0216others(79): Show | 82 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.519-3410A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99887789 | ||||||
| chr14:99887880
|
A | G | 161 | a0001c0003t0001g0286a0001c0004t0003g0206a0002c0001t0001g0062others(158): Show | 162 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.519-3319A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99887880 | ||||||
| chr14:99888072
|
G | A | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.519-3127G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99888072 | ||||||
| chr14:99888080
|
A | C | 1 | a0001c0003t0003g0184 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.519-3119A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99888080 | ||||||
| chr14:99888592
|
T | C | 1 | a0001c0003t0003g0184 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.519-2607T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99888592 | ||||||
| chr14:99888823
|
G | GGCTCCCC others(4): Show |
15 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(12): Show | 15 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.519-2376_519-2375i others(13): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99888823 | ||||||
| chr14:99888824
|
A | T | 15 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(12): Show | 15 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.519-2375A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99888824 | ||||||
| chr14:99888859
|
G | C | 269 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0008others(266): Show | 270 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.519-2340G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99888859 | ||||||
| chr14:99888951
|
C | T | 77 | a0003c0002t0001g0002a0003c0002t0001g0019a0003c0002t0001g0036others(74): Show | 78 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.519-2248C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99888951 | ||||||
| chr14:99888958
|
C | T | 5 | a0001c0004t0003g0149a0001c0005t0001g0250a0001c0005t0005g0003others(2): Show | 5 | HG00639.hp2 HG02451.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.519-2241C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99888958 | ||||||
| chr14:99888978
|
T | G | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.519-2221T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99888978 | ||||||
| chr14:99889028
|
C | T | 19 | a0001c0003t0001g0006a0001c0003t0001g0111a0001c0003t0001g0112others(16): Show | 19 | HG00639.hp2 HG02451.hp1 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.519-2171C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99889028 | ||||||
| chr14:99889118
|
C | T | 2 | a0003c0002t0001g0237a0003c0015t0001g0013 | 2 | HG01884.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.519-2081C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99889118 | ||||||
| chr14:99889240
|
GCAGCAGC | G | 19 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0167others(16): Show | 19 | HG01109.hp2 HG02109.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.519-1958_519-1952d others(9): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99889240 | ||||||
| chr14:99889260
|
G | A | 77 | a0003c0002t0001g0002a0003c0002t0001g0019a0003c0002t0001g0036others(74): Show | 78 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.519-1939G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99889260 | ||||||
| chr14:99889678
|
G | A | 19 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0167others(16): Show | 19 | HG01109.hp2 HG02109.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.519-1521G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99889678 | ||||||
| chr14:99889721
|
G | A | 1 | a0007c0012t0002g0275 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.519-1478G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99889721 | ||||||
| chr14:99889744
|
T | C | 1 | a0001c0003t0001g0214 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.519-1455T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99889744 | ||||||
| chr14:99889767
|
A | G | 1 | a0001c0003t0001g0283 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.519-1432A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99889767 | ||||||
| chr14:99890029
|
C | T | 4 | a0002c0001t0002g0038a0002c0001t0002g0039a0002c0001t0002g0099others(1): Show | 4 | HG00621.hp1 HG02132.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.519-1170C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99890029 | ||||||
| chr14:99890141
|
A | G | 1 | a0001c0004t0001g0255 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.519-1058A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99890141 | ||||||
| chr14:99890178
|
G | A | 19 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0167others(16): Show | 19 | HG01109.hp2 HG02109.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.519-1021G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99890178 | ||||||
| chr14:99890235
|
G | A | 1 | a0002c0001t0001g0092 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.519-964G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99890235 | ||||||
| chr14:99890295
|
G | A | 83 | a0001c0003t0001g0286a0002c0001t0001g0062a0002c0001t0001g0092others(80): Show | 83 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.519-904G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99890295 | ||||||
| chr14:99890340
|
C | T | 39 | a0001c0003t0003g0279a0001c0004t0001g0009a0001c0004t0001g0040others(36): Show | 39 | HG00140.hp1 HG00609.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.519-859C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99890340 | ||||||
| chr14:99890481
|
C | A | 2 | a0001c0003t0002g0105a0001c0003t0002g0106 | 2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.519-718C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99890481 | ||||||
| chr14:99890601
|
G | A | 19 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0167others(16): Show | 19 | HG01109.hp2 HG02109.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.519-598G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99890601 | ||||||
| chr14:99890712
|
G | C | 269 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0008others(266): Show | 270 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.519-487G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99890712 | ||||||
| chr14:99890894
|
G | A | 2 | a0003c0002t0001g0263a0003c0002t0001g0264 | 2 | NA18966.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.519-305G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99890894 | ||||||
| chr14:99890898
|
G | A | 1 | a0001c0005t0009g0078 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.519-301G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99890898 | ||||||
| chr14:99890966
|
A | G | 1 | a0002c0001t0002g0021 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.519-233A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 4/21 | chr14 | 99890966 | ||||||
| chr14:99891306
|
C | T | 77 | a0002c0001t0001g0062a0002c0001t0001g0092a0002c0001t0001g0216others(74): Show | 77 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.547+79C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99891306 | ||||||
| chr14:99891401
|
C | G | 2 | a0001c0003t0001g0274a0001c0003t0008g0271 | 2 | HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.547+174C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99891401 | ||||||
| chr14:99891748
|
G | A | 1 | a0002c0001t0002g0069 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.547+521G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99891748 | ||||||
| chr14:99891846
|
C | T | 4 | a0003c0002t0001g0037a0003c0002t0001g0094a0003c0002t0001g0209others(1): Show | 4 | HG01943.hp1 NA18747.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.547+619C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99891846 | ||||||
| chr14:99891939
|
A | G | 14 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0220others(11): Show | 14 | HG01109.hp2 HG02109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.547+712A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99891939 | ||||||
| chr14:99892002
|
G | T | 1 | a0001c0005t0001g0250 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.547+775G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99892002 | ||||||
| chr14:99892038
|
G | C | 1 | a0001c0004t0004g0017 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.547+811G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99892038 | ||||||
| chr14:99892043
|
G | A | 1 | a0003c0002t0001g0130 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.547+816G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99892043 | ||||||
| chr14:99892125
|
G | A | 8 | a0001c0003t0007g0014a0001c0004t0001g0123a0001c0004t0001g0248others(5): Show | 8 | HG02055.hp1 HG02451.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.547+898G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99892125 | ||||||
| chr14:99892341
|
A | G | 1 | a0002c0001t0002g0133 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.547+1114A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99892341 | ||||||
| chr14:99892342
|
C | T | 1 | a0003c0002t0001g0104 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.547+1115C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99892342 | ||||||
| chr14:99892401
|
T | C | 1 | a0002c0001t0019g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.547+1174T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99892401 | ||||||
| chr14:99892529
|
G | A | 77 | a0003c0002t0001g0002a0003c0002t0001g0019a0003c0002t0001g0036others(74): Show | 78 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.547+1302G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99892529 | ||||||
| chr14:99892769
|
A | G | 1 | a0003c0002t0002g0050 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.547+1542A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99892769 | ||||||
| chr14:99892834
|
G | A | 1 | a0001c0004t0003g0035 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.547+1607G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99892834 | ||||||
| chr14:99892942
|
C | A | 2 | a0001c0007t0002g0005a0001c0007t0018g0241 | 2 | HG02145.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.548-1687C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99892942 | ||||||
| chr14:99892957
|
T | C | 121 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(118): Show | 122 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.548-1672T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99892957 | ||||||
| chr14:99892986
|
T | TTGGTTGT others(2): Show |
121 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(118): Show | 122 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.548-1641_548-1633d others(11): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr14 | 99892986 | |||||
| chr14:99892994
|
G | A | 4 | a0001c0004t0001g0009a0001c0004t0001g0143a0001c0004t0005g0249others(1): Show | 4 | HG02280.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.548-1635G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99892994 | ||||||
| chr14:99893083
|
C | T | 19 | a0001c0003t0001g0006a0001c0003t0001g0111a0001c0003t0001g0112others(16): Show | 19 | HG00639.hp2 HG02451.hp1 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.548-1546C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99893083 | ||||||
| chr14:99893116
|
A | T | 1 | a0002c0001t0002g0179 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.548-1513A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99893116 | ||||||
| chr14:99893119
|
C | T | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.548-1510C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99893119 | ||||||
| chr14:99893137
|
A | T | 39 | a0001c0003t0003g0279a0001c0004t0001g0009a0001c0004t0001g0040others(36): Show | 39 | HG00140.hp1 HG00609.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.548-1492A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99893137 | ||||||
| chr14:99893246
|
G | C | 1 | a0001c0004t0005g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.548-1383G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99893246 | ||||||
| chr14:99893254
|
G | A | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.548-1375G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99893254 | ||||||
| chr14:99893259
|
C | T | 15 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(12): Show | 15 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.548-1370C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99893259 | ||||||
| chr14:99893261
|
T | TA | 269 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0008others(266): Show | 270 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.548-1365dupA | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr14 | 99893261 | |||||
| chr14:99893426
|
A | G | 41 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(38): Show | 41 | HG00639.hp2 HG01109.hp2 HG02109.hp2 others(38): Show |
intron_variant | MODIFIER | c.548-1203A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99893426 | ||||||
| chr14:99893552
|
G | A | 3 | a0001c0003t0001g0007a0001c0003t0001g0015a0001c0003t0001g0016 | 3 | HG02109.hp1 HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.548-1077G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99893552 | ||||||
| chr14:99893757
|
A | G | 39 | a0001c0003t0003g0279a0001c0004t0001g0009a0001c0004t0001g0040others(36): Show | 39 | HG00140.hp1 HG00609.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.548-872A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99893757 | ||||||
| chr14:99893911
|
C | T | 2 | a0001c0003t0001g0274a0001c0003t0008g0271 | 2 | HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.548-718C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99893911 | ||||||
| chr14:99893912
|
G | T | 1 | a0001c0003t0001g0163 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.548-717G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99893912 | ||||||
| chr14:99893925
|
G | A | 171 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(168): Show | 172 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.548-704G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99893925 | ||||||
| chr14:99894130
|
A | C | 2 | a0001c0003t0002g0252a0001c0003t0009g0251 | 2 | HG00733.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.548-499A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99894130 | ||||||
| chr14:99894150
|
G | A | 282 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0007others(279): Show | 284 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.548-479G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99894150 | ||||||
| chr14:99894401
|
G | A | 1 | a0001c0003t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.548-228G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99894401 | ||||||
| chr14:99894503
|
A | G | 4 | a0001c0003t0007g0014a0001c0004t0001g0123a0001c0004t0001g0248others(1): Show | 4 | HG03209.hp1 HG03453.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.548-126A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99894503 | ||||||
| chr14:99894518
|
A | G | 83 | a0001c0003t0001g0286a0002c0001t0001g0062a0002c0001t0001g0092others(80): Show | 83 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.548-111A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99894518 | ||||||
| chr14:99894584
|
G | C | 2 | a0002c0001t0002g0056a0002c0001t0002g0150 | 2 | NA18939.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.548-45G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 5/21 | chr14 | 99894584 | ||||||
| chr14:99894968
|
C | T | 87 | a0002c0001t0001g0062a0002c0001t0001g0092a0002c0001t0001g0216others(84): Show | 87 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.677+210C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | chr14 | 99894968 | ||||||
| chr14:99895095
|
T | TA | 9 | a0001c0005t0001g0079a0001c0005t0001g0250a0001c0005t0004g0284others(6): Show | 9 | HG00639.hp2 HG02451.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.677+337_677+338ins others(1): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | chr14 | 99895095 | ||||||
| chr14:99895096
|
C | T | 9 | a0001c0005t0001g0079a0001c0005t0001g0250a0001c0005t0004g0284others(6): Show | 9 | HG00639.hp2 HG02451.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.677+338C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | chr14 | 99895096 | ||||||
| chr14:99895300
|
C | T | 172 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(169): Show | 173 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.677+542C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | chr14 | 99895300 | ||||||
| chr14:99895315
|
C | T | 39 | a0001c0003t0003g0279a0001c0004t0001g0009a0001c0004t0001g0040others(36): Show | 39 | HG00140.hp1 HG00609.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.677+557C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | chr14 | 99895315 | ||||||
| chr14:99895338
|
G | A | 8 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(5): Show | 8 | HG02109.hp1 HG02486.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.677+580G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | chr14 | 99895338 | ||||||
| chr14:99895404
|
C | T | 172 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(169): Show | 173 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.677+646C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | chr14 | 99895404 | ||||||
| chr14:99895549
|
A | T | 73 | a0003c0002t0001g0002a0003c0002t0001g0019a0003c0002t0001g0036others(70): Show | 74 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.677+791A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | chr14 | 99895549 | ||||||
| chr14:99895765
|
T | TA | 109 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0008others(106): Show | 109 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.677+1020dupA | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr14 | 99895765 | |||||
| chr14:99895765
|
T | TAA | 157 | a0002c0001t0001g0062a0002c0001t0001g0092a0002c0001t0001g0216others(154): Show | 158 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.677+1019_677+1020d others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr14 | 99895765 | |||||
| chr14:99895892
|
A | G | 2 | a0002c0001t0001g0267a0002c0001t0002g0061 | 2 | NA19009.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.677+1134A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | chr14 | 99895892 | ||||||
| chr14:99895964
|
C | T | 82 | a0002c0001t0001g0062a0002c0001t0001g0092a0002c0001t0001g0216others(79): Show | 82 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.678-1181C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | chr14 | 99895964 | ||||||
| chr14:99896019
|
C | T | 82 | a0002c0001t0001g0062a0002c0001t0001g0092a0002c0001t0001g0216others(79): Show | 82 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.678-1126C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | chr14 | 99896019 | ||||||
| chr14:99896080
|
T | A | 82 | a0002c0001t0001g0062a0002c0001t0001g0092a0002c0001t0001g0216others(79): Show | 82 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.678-1065T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | chr14 | 99896080 | ||||||
| chr14:99896108
|
A | G | 1 | a0001c0004t0003g0145 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.678-1037A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | chr14 | 99896108 | ||||||
| chr14:99896170
|
A | T | 5 | a0002c0001t0002g0063a0002c0001t0002g0073a0002c0001t0002g0082others(2): Show | 5 | HG00438.hp2 HG01975.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.678-975A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | chr14 | 99896170 | ||||||
| chr14:99896209
|
G | A | 82 | a0002c0001t0001g0062a0002c0001t0001g0092a0002c0001t0001g0216others(79): Show | 82 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.678-936G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | chr14 | 99896209 | ||||||
| chr14:99896359
|
C | CT | 13 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(10): Show | 13 | HG01928.hp2 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.678-775dupT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr14 | 99896359 | |||||
| chr14:99896359
|
CT | C | 82 | a0002c0001t0001g0062a0002c0001t0001g0092a0002c0001t0001g0216others(79): Show | 82 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.678-775delT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr14 | 99896359 | |||||
| chr14:99896390
|
G | A | 1 | a0003c0002t0001g0104 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.678-755G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | chr14 | 99896390 | ||||||
| chr14:99896478
|
A | G | 1 | a0001c0003t0001g0086 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.678-667A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | chr14 | 99896478 | ||||||
| chr14:99896486
|
A | G | 39 | a0001c0003t0003g0279a0001c0004t0001g0009a0001c0004t0001g0040others(36): Show | 39 | HG00140.hp1 HG00609.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.678-659A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | chr14 | 99896486 | ||||||
| chr14:99896615
|
G | A | 82 | a0002c0001t0001g0062a0002c0001t0001g0092a0002c0001t0001g0216others(79): Show | 82 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.678-530G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | chr14 | 99896615 | ||||||
| chr14:99896667
|
A | C | 2 | a0003c0002t0001g0053a0003c0002t0001g0262 | 2 | HG00438.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.678-478A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | chr14 | 99896667 | ||||||
| chr14:99896740
|
A | AT | 117 | a0001c0003t0003g0279a0001c0003t0004g0027a0001c0003t0004g0141others(114): Show | 118 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.678-392dupT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr14 | 99896740 | |||||
| chr14:99896740
|
A | ATT | 50 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(47): Show | 50 | HG00639.hp2 HG01109.hp2 HG02055.hp1 others(47): Show |
intron_variant | MODIFIER | c.678-393_678-392dup others(2): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr14 | 99896740 | |||||
| chr14:99896768
|
T | C | 82 | a0002c0001t0001g0062a0002c0001t0001g0092a0002c0001t0001g0216others(79): Show | 82 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.678-377T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | chr14 | 99896768 | ||||||
| chr14:99896777
|
ATGTG | A | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.678-360_678-357del others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr14 | 99896777 | |||||
| chr14:99896855
|
C | T | 172 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(169): Show | 173 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.678-290C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | chr14 | 99896855 | ||||||
| chr14:99896917
|
A | C | 172 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(169): Show | 173 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.678-228A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | chr14 | 99896917 | ||||||
| chr14:99896929
|
T | C | 79 | a0002c0001t0001g0062a0002c0001t0001g0092a0002c0001t0001g0216others(76): Show | 79 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.678-216T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | chr14 | 99896929 | ||||||
| chr14:99896999
|
T | C | 187 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0008others(184): Show | 188 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.678-146T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | chr14 | 99896999 | ||||||
| chr14:99897076
|
C | T | 2 | a0001c0007t0002g0005a0001c0007t0018g0241 | 2 | HG02145.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.678-69C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 6/21 | chr14 | 99897076 | ||||||
| chr14:99897334
|
G | C | 172 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(169): Show | 173 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.827+40G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 7/21 | chr14 | 99897334 | ||||||
| chr14:99897335
|
A | G | 172 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(169): Show | 173 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.827+41A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 7/21 | chr14 | 99897335 | ||||||
| chr14:99897340
|
A | T | 1 | a0001c0007t0002g0005 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.827+46A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 7/21 | chr14 | 99897340 | ||||||
| chr14:99897473
|
T | C | 4 | a0001c0005t0001g0250a0001c0005t0005g0003a0001c0005t0005g0097others(1): Show | 4 | HG00639.hp2 HG02451.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.827+179T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 7/21 | chr14 | 99897473 | ||||||
| chr14:99897501
|
G | A | 1 | a0003c0002t0001g0217 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.827+207G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 7/21 | chr14 | 99897501 | ||||||
| chr14:99897622
|
T | C | 8 | a0001c0003t0007g0014a0001c0004t0001g0123a0001c0004t0001g0248others(5): Show | 8 | HG02055.hp1 HG02451.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.827+328T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 7/21 | chr14 | 99897622 | ||||||
| chr14:99897687
|
A | G | 2 | a0001c0004t0001g0040a0001c0004t0001g0135 | 2 | NA18939.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.827+393A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 7/21 | chr14 | 99897687 | ||||||
| chr14:99897826
|
C | T | 77 | a0003c0002t0001g0002a0003c0002t0001g0019a0003c0002t0001g0036others(74): Show | 78 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.828-407C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 7/21 | chr14 | 99897826 | ||||||
| chr14:99897927
|
A | G | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.828-306A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 7/21 | chr14 | 99897927 | ||||||
| chr14:99898066
|
T | C | 172 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(169): Show | 173 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.828-167T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 7/21 | chr14 | 99898066 | ||||||
| chr14:99898084
|
G | A | 5 | a0001c0003t0001g0225a0001c0003t0001g0260a0001c0003t0004g0027others(2): Show | 5 | HG00609.hp2 HG02083.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.828-149G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 7/21 | chr14 | 99898084 | ||||||
| chr14:99898161
|
A | C | 1 | a0001c0003t0001g0113 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.828-72A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 7/21 | chr14 | 99898161 | ||||||
| chr14:99898435
|
G | A | 1 | a0001c0003t0001g0270 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.897+133G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 8/21 | chr14 | 99898435 | ||||||
| chr14:99898443
|
T | A | 3 | a0001c0004t0004g0017a0001c0007t0002g0005a0001c0007t0018g0241 | 3 | HG02145.hp2 HG02257.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.897+141T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 8/21 | chr14 | 99898443 | ||||||
| chr14:99898464
|
T | C | 3 | a0001c0004t0004g0017a0001c0007t0002g0005a0001c0007t0018g0241 | 3 | HG02145.hp2 HG02257.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.897+162T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 8/21 | chr14 | 99898464 | ||||||
| chr14:99898479
|
C | T | 1 | a0002c0001t0002g0150 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.897+177C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 8/21 | chr14 | 99898479 | ||||||
| chr14:99898629
|
G | A | 1 | a0002c0001t0003g0137 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.897+327G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 8/21 | chr14 | 99898629 | ||||||
| chr14:99898644
|
C | T | 1 | a0003c0015t0001g0013 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.897+342C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 8/21 | chr14 | 99898644 | ||||||
| chr14:99898676
|
C | T | 19 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0167others(16): Show | 19 | HG01109.hp2 HG02109.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.897+374C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 8/21 | chr14 | 99898676 | ||||||
| chr14:99898751
|
C | CA | 7 | a0001c0003t0001g0233a0001c0003t0004g0027a0001c0003t0004g0141others(4): Show | 7 | HG00609.hp2 HG01109.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.897+467dupA | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr14 | 99898751 | |||||
| chr14:99898751
|
CA | C | 99 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(96): Show | 99 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.897+467delA | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr14 | 99898751 | |||||
| chr14:99898899
|
A | T | 8 | a0001c0003t0007g0014a0001c0004t0001g0123a0001c0004t0001g0248others(5): Show | 8 | HG02055.hp1 HG02451.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.897+597A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 8/21 | chr14 | 99898899 | ||||||
| chr14:99899020
|
G | A | 269 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0008others(266): Show | 270 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.897+718G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 8/21 | chr14 | 99899020 | ||||||
| chr14:99899176
|
A | G | 1 | a0003c0002t0001g0054 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.897+874A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 8/21 | chr14 | 99899176 | ||||||
| chr14:99899197
|
A | ATTTC | 254 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(251): Show | 255 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.897+898_897+899ins others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr14 | 99899197 | |||||
| chr14:99899243
|
G | T | 1 | a0001c0003t0001g0016 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.897+941G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 8/21 | chr14 | 99899243 | ||||||
| chr14:99899317
|
AT | A | 80 | a0001c0003t0001g0008a0001c0003t0004g0027a0001c0003t0004g0141others(77): Show | 81 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.897+1028delT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr14 | 99899317 | |||||
| chr14:99899375
|
GCA | G | 3 | a0001c0004t0004g0017a0001c0007t0002g0005a0001c0007t0018g0241 | 3 | HG02145.hp2 HG02257.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.897+1076_897+1077d others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr14 | 99899375 | |||||
| chr14:99899489
|
G | C | 1 | a0002c0001t0019g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.897+1187G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 8/21 | chr14 | 99899489 | ||||||
| chr14:99899704
|
G | A | 4 | a0001c0003t0001g0243a0001c0003t0001g0244a0001c0003t0001g0245others(1): Show | 4 | HG02723.hp2 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.898-1225G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 8/21 | chr14 | 99899704 | ||||||
| chr14:99899714
|
AT | A | 172 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(169): Show | 173 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.898-1202delT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr14 | 99899714 | |||||
| chr14:99899771
|
C | T | 39 | a0001c0003t0003g0279a0001c0004t0001g0009a0001c0004t0001g0040others(36): Show | 39 | HG00140.hp1 HG00609.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.898-1158C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 8/21 | chr14 | 99899771 | ||||||
| chr14:99899843
|
G | T | 1 | a0002c0001t0002g0276 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.898-1086G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 8/21 | chr14 | 99899843 | ||||||
| chr14:99899887
|
A | G | 172 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(169): Show | 173 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.898-1042A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 8/21 | chr14 | 99899887 | ||||||
| chr14:99900181
|
CTT | C | 11 | a0001c0003t0007g0014a0001c0004t0001g0123a0001c0004t0001g0248others(8): Show | 11 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.898-725_898-724del others(2): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr14 | 99900181 | |||||
| chr14:99900181
|
CTTT | C | 41 | a0001c0003t0003g0279a0001c0003t0004g0027a0001c0003t0004g0141others(38): Show | 41 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.898-726_898-724del others(3): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr14 | 99900181 | |||||
| chr14:99900181
|
CTTTTTTT | C | 118 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(115): Show | 119 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.898-730_898-724del others(7): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr14 | 99900181 | |||||
| chr14:99900247
|
A | G | 172 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(169): Show | 173 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.898-682A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 8/21 | chr14 | 99900247 | ||||||
| chr14:99900260
|
C | G | 1 | a0001c0003t0003g0277 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.898-669C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 8/21 | chr14 | 99900260 | ||||||
| chr14:99900291
|
C | T | 1 | a0001c0003t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.898-638C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 8/21 | chr14 | 99900291 | ||||||
| chr14:99900349
|
G | A | 172 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(169): Show | 173 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.898-580G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 8/21 | chr14 | 99900349 | ||||||
| chr14:99900430
|
A | C | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.898-499A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 8/21 | chr14 | 99900430 | ||||||
| chr14:99901294
|
T | C | 1 | a0002c0001t0003g0147 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1008+255T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99901294 | ||||||
| chr14:99901379
|
C | T | 1 | a0001c0004t0003g0064 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1008+340C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99901379 | ||||||
| chr14:99901707
|
A | G | 5 | a0001c0003t0003g0032a0001c0003t0003g0033a0001c0003t0003g0034others(2): Show | 5 | HG02055.hp2 HG02615.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1008+668A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99901707 | ||||||
| chr14:99901769
|
G | A | 2 | a0001c0003t0007g0117a0001c0003t0007g0281 | 2 | HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1008+730G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99901769 | ||||||
| chr14:99901784
|
G | A | 39 | a0001c0003t0003g0279a0001c0004t0001g0009a0001c0004t0001g0040others(36): Show | 39 | HG00140.hp1 HG00609.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.1008+745G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99901784 | ||||||
| chr14:99901869
|
T | C | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.1008+830T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99901869 | ||||||
| chr14:99901940
|
C | A | 1 | a0002c0001t0002g0164 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1008+901C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99901940 | ||||||
| chr14:99901971
|
T | A | 172 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(169): Show | 173 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.1008+932T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99901971 | ||||||
| chr14:99902021
|
A | G | 172 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(169): Show | 173 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.1008+982A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99902021 | ||||||
| chr14:99902339
|
C | T | 8 | a0001c0003t0007g0014a0001c0004t0001g0123a0001c0004t0001g0248others(5): Show | 8 | HG02055.hp1 HG02451.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.1008+1300C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99902339 | ||||||
| chr14:99902345
|
T | C | 15 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(12): Show | 15 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1008+1306T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99902345 | ||||||
| chr14:99902345
|
T | G | 42 | a0001c0003t0003g0279a0001c0003t0004g0027a0001c0003t0004g0141others(39): Show | 42 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.1008+1306T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99902345 | ||||||
| chr14:99902377
|
G | A | 1 | a0001c0004t0003g0127 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1008+1338G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99902377 | ||||||
| chr14:99902690
|
G | C | 1 | a0007c0012t0002g0275 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1008+1651G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99902690 | ||||||
| chr14:99902723
|
A | G | 172 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(169): Show | 173 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.1008+1684A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99902723 | ||||||
| chr14:99902733
|
T | C | 172 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(169): Show | 173 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.1008+1694T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99902733 | ||||||
| chr14:99902840
|
C | G | 9 | a0002c0001t0001g0216a0002c0001t0001g0219a0002c0001t0002g0056others(6): Show | 9 | HG02040.hp2 NA18939.hp1 NA18953.hp1 others(6): Show |
intron_variant | MODIFIER | c.1008+1801C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99902840 | ||||||
| chr14:99903202
|
T | A | 3 | a0001c0004t0004g0017a0001c0007t0002g0005a0001c0007t0018g0241 | 3 | HG02145.hp2 HG02257.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1008+2163T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99903202 | ||||||
| chr14:99903418
|
C | T | 8 | a0001c0003t0007g0014a0001c0004t0001g0123a0001c0004t0001g0248others(5): Show | 8 | HG02055.hp1 HG02451.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.1008+2379C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99903418 | ||||||
| chr14:99903419
|
A | G | 285 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0007others(282): Show | 287 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.1008+2380A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99903419 | ||||||
| chr14:99903641
|
C | T | 1 | a0001c0004t0001g0123 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1008+2602C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99903641 | ||||||
| chr14:99903760
|
C | T | 203 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0007others(200): Show | 205 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.1008+2721C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99903760 | ||||||
| chr14:99903784
|
C | CT | 7 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258others(4): Show | 7 | HG00609.hp2 HG02055.hp1 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.1008+2745_1008+274 others(5): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99903784 | ||||||
| chr14:99903784
|
C | CTT | 42 | a0001c0003t0003g0279a0001c0003t0007g0014a0001c0004t0001g0040others(39): Show | 42 | HG00140.hp1 HG00609.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.1008+2745_1008+274 others(6): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99903784 | ||||||
| chr14:99903784
|
CA | C | 9 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0001g0233others(6): Show | 9 | HG01109.hp2 HG02818.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1008+2746delA | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99903784 | ||||||
| chr14:99903784
|
CAT | C | 110 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(107): Show | 111 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.1008+2746_1008+274 others(6): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99903784 | ||||||
| chr14:99903784
|
CATT | C | 3 | a0001c0003t0001g0274a0001c0003t0008g0271a0003c0002t0002g0050 | 3 | HG02273.hp1 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1008+2746_1008+274 others(7): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99903784 | ||||||
| chr14:99903785
|
A | AT | 30 | a0001c0003t0001g0001a0001c0003t0001g0007a0001c0003t0001g0008others(27): Show | 31 | HG00323.hp2 HG00733.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.1008+2762dupT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr14 | 99903785 | |||||
| chr14:99903785
|
A | T | 50 | a0001c0003t0003g0279a0001c0003t0004g0027a0001c0003t0004g0141others(47): Show | 50 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1008+2746A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99903785 | ||||||
| chr14:99903983
|
G | C | 122 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(119): Show | 123 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.1008+2944G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99903983 | ||||||
| chr14:99904084
|
A | G | 15 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(12): Show | 15 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1008+3045A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99904084 | ||||||
| chr14:99904272
|
A | G | 119 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(116): Show | 120 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.1008+3233A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99904272 | ||||||
| chr14:99904375
|
C | CA | 11 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258others(8): Show | 11 | HG00609.hp2 HG02055.hp1 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.1009-3254dupA | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr14 | 99904375 | |||||
| chr14:99904375
|
CA | C | 10 | a0001c0003t0001g0006a0001c0003t0001g0111a0001c0003t0001g0112others(7): Show | 10 | HG02572.hp1 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1009-3254delA | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr14 | 99904375 | |||||
| chr14:99904519
|
C | CT | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.1009-3115dupT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr14 | 99904519 | |||||
| chr14:99904546
|
CTTATTA | C | 50 | a0001c0003t0003g0279a0001c0003t0004g0027a0001c0003t0004g0141others(47): Show | 50 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1009-3082_1009-307 others(10): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr14 | 99904546 | |||||
| chr14:99904666
|
C | G | 119 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(116): Show | 120 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.1009-2972C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99904666 | ||||||
| chr14:99904746
|
A | G | 122 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(119): Show | 123 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.1009-2892A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99904746 | ||||||
| chr14:99904778
|
T | C | 35 | a0001c0003t0003g0279a0001c0004t0001g0040a0001c0004t0001g0091others(32): Show | 35 | HG00140.hp1 HG00609.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.1009-2860T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99904778 | ||||||
| chr14:99904783
|
T | C | 8 | a0001c0003t0007g0014a0001c0004t0001g0123a0001c0004t0001g0248others(5): Show | 8 | HG02055.hp1 HG02451.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.1009-2855T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99904783 | ||||||
| chr14:99904821
|
T | C | 50 | a0001c0003t0003g0279a0001c0003t0004g0027a0001c0003t0004g0141others(47): Show | 50 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1009-2817T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99904821 | ||||||
| chr14:99904873
|
C | G | 2 | a0002c0001t0002g0057a0002c0001t0002g0151 | 2 | NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1009-2765C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99904873 | ||||||
| chr14:99905040
|
C | CAG | 12 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258others(9): Show | 12 | HG00609.hp2 HG02055.hp1 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1009-2582_1009-258 others(6): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr14 | 99905040 | |||||
| chr14:99905349
|
A | G | 39 | a0001c0003t0003g0279a0001c0004t0001g0009a0001c0004t0001g0040others(36): Show | 39 | HG00140.hp1 HG00609.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.1009-2289A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99905349 | ||||||
| chr14:99905529
|
C | T | 3 | a0001c0003t0001g0001a0001c0003t0001g0120a0001c0013t0001g0126 | 4 | HG01243.hp1 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1009-2109C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99905529 | ||||||
| chr14:99905539
|
C | T | 122 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(119): Show | 123 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.1009-2099C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99905539 | ||||||
| chr14:99905626
|
A | G | 122 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(119): Show | 123 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.1009-2012A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99905626 | ||||||
| chr14:99905675
|
A | T | 172 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(169): Show | 173 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.1009-1963A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99905675 | ||||||
| chr14:99905722
|
G | A | 50 | a0001c0003t0003g0279a0001c0003t0004g0027a0001c0003t0004g0141others(47): Show | 50 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1009-1916G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99905722 | ||||||
| chr14:99905928
|
G | C | 2 | a0001c0003t0002g0105a0001c0003t0002g0106 | 2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1009-1710G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99905928 | ||||||
| chr14:99905930
|
C | A | 172 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(169): Show | 173 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.1009-1708C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99905930 | ||||||
| chr14:99905935
|
C | A | 172 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(169): Show | 173 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.1009-1703C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99905935 | ||||||
| chr14:99905935
|
C | CA | 15 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(12): Show | 15 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1009-1703_1009-170 others(5): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99905935 | ||||||
| chr14:99905956
|
C | T | 172 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(169): Show | 173 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.1009-1682C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99905956 | ||||||
| chr14:99906022
|
A | G | 16 | a0002c0001t0001g0267a0002c0001t0002g0018a0002c0001t0002g0038others(13): Show | 16 | HG00621.hp1 HG01928.hp1 HG02132.hp1 others(13): Show |
intron_variant | MODIFIER | c.1009-1616A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99906022 | ||||||
| chr14:99906094
|
C | T | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.1009-1544C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99906094 | ||||||
| chr14:99906215
|
C | T | 3 | a0003c0002t0001g0191a0003c0002t0001g0192a0003c0002t0003g0125 | 3 | HG00735.hp2 HG01081.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1009-1423C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99906215 | ||||||
| chr14:99906366
|
T | C | 172 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(169): Show | 173 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.1009-1272T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99906366 | ||||||
| chr14:99906622
|
C | T | 77 | a0003c0002t0001g0002a0003c0002t0001g0019a0003c0002t0001g0036others(74): Show | 78 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1009-1016C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99906622 | ||||||
| chr14:99906635
|
C | T | 2 | a0001c0003t0001g0193a0001c0003t0002g0181 | 2 | HG00323.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1009-1003C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99906635 | ||||||
| chr14:99906660
|
T | C | 3 | a0002c0001t0002g0021a0002c0001t0002g0066a0002c0001t0002g0153 | 3 | HG00642.hp2 HG01123.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1009-978T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99906660 | ||||||
| chr14:99906747
|
C | T | 2 | a0003c0002t0001g0237a0003c0015t0001g0013 | 2 | HG01884.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1009-891C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99906747 | ||||||
| chr14:99907019
|
G | A | 1 | a0001c0004t0001g0255 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1009-619G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99907019 | ||||||
| chr14:99907041
|
G | T | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.1009-597G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99907041 | ||||||
| chr14:99907120
|
C | G | 1 | a0001c0003t0002g0116 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1009-518C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99907120 | ||||||
| chr14:99907344
|
C | T | 5 | a0003c0002t0001g0044a0003c0002t0001g0055a0003c0002t0001g0087others(2): Show | 5 | HG01192.hp2 HG01255.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1009-294C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99907344 | ||||||
| chr14:99907485
|
A | C | 1 | a0002c0001t0002g0150 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1009-153A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 9/21 | chr14 | 99907485 | ||||||
| chr14:99907822
|
A | T | 1 | a0003c0002t0001g0154 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1104+89A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 10/21 | chr14 | 99907822 | ||||||
| chr14:99907846
|
G | A | 15 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(12): Show | 15 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1104+113G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 10/21 | chr14 | 99907846 | ||||||
| chr14:99907967
|
T | C | 31 | a0001c0003t0001g0001a0001c0003t0001g0007a0001c0003t0001g0008others(28): Show | 32 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.1104+234T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 10/21 | chr14 | 99907967 | ||||||
| chr14:99908067
|
A | G | 187 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0012others(184): Show | 189 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.1104+334A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 10/21 | chr14 | 99908067 | ||||||
| chr14:99908138
|
G | A | 119 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(116): Show | 120 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.1104+405G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 10/21 | chr14 | 99908138 | ||||||
| chr14:99908151
|
G | A | 2 | a0001c0003t0001g0274a0001c0003t0008g0271 | 2 | HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1104+418G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 10/21 | chr14 | 99908151 | ||||||
| chr14:99908165
|
G | A | 10 | a0001c0003t0001g0163a0001c0003t0007g0014a0001c0004t0001g0123others(7): Show | 10 | HG02055.hp1 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1104+432G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 10/21 | chr14 | 99908165 | ||||||
| chr14:99908177
|
A | G | 1 | a0001c0007t0002g0005 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1104+444A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 10/21 | chr14 | 99908177 | ||||||
| chr14:99908206
|
G | A | 1 | a0001c0003t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1104+473G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 10/21 | chr14 | 99908206 | ||||||
| chr14:99908227
|
A | G | 4 | a0002c0001t0002g0068a0002c0001t0002g0069a0002c0001t0002g0160others(1): Show | 4 | HG01928.hp1 NA18954.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.1104+494A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 10/21 | chr14 | 99908227 | ||||||
| chr14:99908231
|
C | G | 2 | a0001c0007t0002g0005a0001c0007t0018g0241 | 2 | HG02145.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1104+498C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 10/21 | chr14 | 99908231 | ||||||
| chr14:99908612
|
T | A | 2 | a0001c0004t0003g0256a0001c0004t0003g0257 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1105-733T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 10/21 | chr14 | 99908612 | ||||||
| chr14:99908728
|
G | T | 19 | a0001c0003t0001g0006a0001c0003t0001g0111a0001c0003t0001g0112others(16): Show | 19 | HG00639.hp2 HG02451.hp1 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.1105-617G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 10/21 | chr14 | 99908728 | ||||||
| chr14:99908803
|
C | A | 1 | a0001c0003t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1105-542C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 10/21 | chr14 | 99908803 | ||||||
| chr14:99908809
|
G | A | 2 | a0001c0007t0002g0005a0001c0007t0018g0241 | 2 | HG02145.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1105-536G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 10/21 | chr14 | 99908809 | ||||||
| chr14:99909246
|
T | C | 2 | a0001c0004t0003g0049a0001c0004t0003g0145 | 2 | NA18984.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1105-99T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 10/21 | chr14 | 99909246 | ||||||
| chr14:99909780
|
G | C | 1 | a0001c0004t0010g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1239+301G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 11/21 | chr14 | 99909780 | ||||||
| chr14:99909846
|
A | C | 1 | a0002c0001t0002g0182 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1239+367A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 11/21 | chr14 | 99909846 | ||||||
| chr14:99910145
|
G | A | 1 | a0003c0002t0003g0230 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1240-97G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 11/21 | chr14 | 99910145 | ||||||
| chr14:99910165
|
C | T | 122 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(119): Show | 123 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.1240-77C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 11/21 | chr14 | 99910165 | ||||||
| chr14:99910378
|
G | A | 12 | a0001c0003t0003g0279a0001c0004t0001g0115a0001c0004t0002g0047others(9): Show | 12 | HG00140.hp1 HG01074.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.1339+37G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 12/21 | chr14 | 99910378 | ||||||
| chr14:99910673
|
T | G | 1 | a0005c0009t0002g0132 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1339+332T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 12/21 | chr14 | 99910673 | ||||||
| chr14:99910721
|
A | AGCTAATT others(4): Show |
2 | a0001c0007t0002g0005a0001c0007t0018g0241 | 2 | HG02145.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1339+385_1339+395d others(13): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr14 | 99910721 | |||||
| chr14:99910834
|
G | A | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.1339+493G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 12/21 | chr14 | 99910834 | ||||||
| chr14:99911023
|
C | T | 1 | a0003c0014t0004g0254 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1340-399C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 12/21 | chr14 | 99911023 | ||||||
| chr14:99911038
|
C | G | 1 | a0001c0003t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1340-384C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 12/21 | chr14 | 99911038 | ||||||
| chr14:99911202
|
G | T | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.1340-220G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 12/21 | chr14 | 99911202 | ||||||
| chr14:99911211
|
A | G | 21 | a0001c0003t0003g0279a0001c0004t0001g0091a0001c0004t0001g0115others(18): Show | 21 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.1340-211A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 12/21 | chr14 | 99911211 | ||||||
| chr14:99911896
|
C | T | 1 | a0001c0004t0003g0059 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1494+320C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 13/21 | chr14 | 99911896 | ||||||
| chr14:99911932
|
C | CTG | 200 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0007others(197): Show | 202 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.1494+357_1494+358i others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr14 | 99911932 | |||||
| chr14:99911984
|
C | T | 1 | a0003c0014t0004g0254 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1494+408C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 13/21 | chr14 | 99911984 | ||||||
| chr14:99912030
|
C | T | 1 | a0001c0004t0001g0255 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1494+454C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 13/21 | chr14 | 99912030 | ||||||
| chr14:99912502
|
G | A | 1 | a0003c0002t0001g0053 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1494+926G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 13/21 | chr14 | 99912502 | ||||||
| chr14:99912604
|
G | A | 71 | a0003c0002t0001g0002a0003c0002t0001g0019a0003c0002t0001g0036others(68): Show | 72 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.1494+1028G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 13/21 | chr14 | 99912604 | ||||||
| chr14:99912829
|
G | C | 122 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(119): Show | 123 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.1494+1253G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 13/21 | chr14 | 99912829 | ||||||
| chr14:99912875
|
C | T | 5 | a0003c0002t0001g0044a0003c0002t0001g0055a0003c0002t0001g0087others(2): Show | 5 | HG01192.hp2 HG01255.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1494+1299C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 13/21 | chr14 | 99912875 | ||||||
| chr14:99912944
|
C | T | 8 | a0001c0003t0007g0014a0001c0004t0001g0123a0001c0004t0001g0248others(5): Show | 8 | HG02055.hp1 HG02451.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.1495-1235C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 13/21 | chr14 | 99912944 | ||||||
| chr14:99913058
|
T | C | 2 | a0001c0003t0002g0105a0001c0003t0002g0106 | 2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1495-1121T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 13/21 | chr14 | 99913058 | ||||||
| chr14:99913099
|
G | A | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.1495-1080G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 13/21 | chr14 | 99913099 | ||||||
| chr14:99913164
|
G | GTTATA | 31 | a0001c0003t0001g0001a0001c0003t0001g0007a0001c0003t0001g0008others(28): Show | 32 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.1495-1011_1495-101 others(9): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr14 | 99913164 | |||||
| chr14:99913165
|
T | TTA | 169 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(166): Show | 170 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.1495-1012_1495-101 others(6): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr14 | 99913165 | |||||
| chr14:99913186
|
A | T | 2 | a0001c0004t0003g0049a0001c0004t0003g0145 | 2 | NA18984.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1495-993A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 13/21 | chr14 | 99913186 | ||||||
| chr14:99913188
|
T | A | 2 | a0001c0004t0003g0049a0001c0004t0003g0145 | 2 | NA18984.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1495-991T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 13/21 | chr14 | 99913188 | ||||||
| chr14:99913212
|
G | T | 8 | a0001c0003t0007g0014a0001c0004t0001g0123a0001c0004t0001g0248others(5): Show | 8 | HG02055.hp1 HG02451.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.1495-967G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 13/21 | chr14 | 99913212 | ||||||
| chr14:99913320
|
C | T | 2 | a0003c0002t0001g0237a0003c0015t0001g0013 | 2 | HG01884.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1495-859C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 13/21 | chr14 | 99913320 | ||||||
| chr14:99913396
|
A | G | 200 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0007others(197): Show | 202 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.1495-783A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 13/21 | chr14 | 99913396 | ||||||
| chr14:99913505
|
A | G | 13 | a0001c0003t0001g0001a0001c0003t0001g0041a0001c0003t0001g0085others(10): Show | 14 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.1495-674A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 13/21 | chr14 | 99913505 | ||||||
| chr14:99913629
|
T | A | 2 | a0001c0003t0001g0163a0001c0004t0004g0017 | 2 | HG02257.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1495-550T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 13/21 | chr14 | 99913629 | ||||||
| chr14:99913701
|
TTTTTTGA others(77): Show |
T | 1 | a0003c0002t0001g0201 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1495-475_1495-392d others(86): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr14 | 99913701 | |||||
| chr14:99913710
|
A | G | 1 | a0001c0007t0018g0241 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1495-469A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 13/21 | chr14 | 99913710 | ||||||
| chr14:99913723
|
C | G | 1 | a0001c0003t0001g0111 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1495-456C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 13/21 | chr14 | 99913723 | ||||||
| chr14:99913840
|
C | T | 19 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0167others(16): Show | 19 | HG01109.hp2 HG02109.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.1495-339C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 13/21 | chr14 | 99913840 | ||||||
| chr14:99913953
|
G | A | 103 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0163others(100): Show | 104 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.1495-226G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 13/21 | chr14 | 99913953 | ||||||
| chr14:99913997
|
G | GTATC | 168 | a0001c0003t0001g0006a0001c0003t0001g0012a0001c0003t0001g0080others(165): Show | 169 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.1495-178_1495-175d others(6): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr14 | 99913997 | |||||
| chr14:99914005
|
G | C | 1 | a0003c0002t0001g0201 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1495-174G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 13/21 | chr14 | 99914005 | ||||||
| chr14:99914006
|
T | TATGTTTT others(82): Show |
1 | a0003c0002t0001g0201 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1495-173_1495-172i others(91): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 13/21 | chr14 | 99914006 | ||||||
| chr14:99914007
|
G | T | 1 | a0003c0002t0001g0201 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1495-172G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 13/21 | chr14 | 99914007 | ||||||
| chr14:99914008
|
A | G | 1 | a0003c0002t0001g0201 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1495-171A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 13/21 | chr14 | 99914008 | ||||||
| chr14:99914059
|
A | T | 31 | a0001c0003t0001g0001a0001c0003t0001g0007a0001c0003t0001g0008others(28): Show | 32 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.1495-120A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 13/21 | chr14 | 99914059 | ||||||
| chr14:99914480
|
T | C | 1 | a0001c0003t0001g0015 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1621-86T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 14/21 | chr14 | 99914480 | ||||||
| chr14:99914518
|
C | T | 1 | a0001c0003t0004g0141 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1621-48C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 14/21 | chr14 | 99914518 | ||||||
| chr14:99914522
|
C | T | 2 | a0001c0003t0001g0274a0001c0003t0008g0271 | 2 | HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1621-44C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 14/21 | chr14 | 99914522 | ||||||
| chr14:99914713
|
A | G | 3 | a0001c0004t0004g0017a0001c0007t0002g0005a0001c0007t0018g0241 | 3 | HG02145.hp2 HG02257.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1752+16A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 15/21 | chr14 | 99914713 | ||||||
| chr14:99915070
|
A | G | 15 | a0001c0003t0001g0001a0001c0003t0001g0041a0001c0003t0001g0085others(12): Show | 16 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.1752+373A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 15/21 | chr14 | 99915070 | ||||||
| chr14:99915234
|
G | A | 13 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0010others(10): Show | 13 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1752+537G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 15/21 | chr14 | 99915234 | ||||||
| chr14:99915276
|
G | A | 1 | a0001c0003t0001g0111 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1752+579G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 15/21 | chr14 | 99915276 | ||||||
| chr14:99915346
|
A | AGG | 6 | a0002c0001t0002g0025a0002c0001t0002g0026a0002c0001t0002g0051others(3): Show | 6 | HG01243.hp2 HG01943.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1752+650_1752+651d others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr14 | 99915346 | |||||
| chr14:99915368
|
C | T | 1 | a0003c0002t0001g0198 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1752+671C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 15/21 | chr14 | 99915368 | ||||||
| chr14:99915386
|
T | C | 15 | a0001c0003t0001g0001a0001c0003t0001g0041a0001c0003t0001g0085others(12): Show | 16 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.1752+689T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 15/21 | chr14 | 99915386 | ||||||
| chr14:99915412
|
C | CA | 48 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0012others(45): Show | 49 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.1752+737dupA | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr14 | 99915412 | |||||
| chr14:99915412
|
CA | C | 120 | a0001c0003t0001g0163a0001c0003t0001g0274a0001c0003t0001g0286others(117): Show | 121 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.1752+737delA | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr14 | 99915412 | |||||
| chr14:99915506
|
C | T | 38 | a0001c0003t0003g0184a0001c0003t0003g0279a0001c0004t0001g0009others(35): Show | 38 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1752+809C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 15/21 | chr14 | 99915506 | ||||||
| chr14:99915539
|
C | G | 19 | a0001c0003t0001g0006a0001c0003t0001g0111a0001c0003t0001g0112others(16): Show | 19 | HG00639.hp2 HG02451.hp1 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.1752+842C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 15/21 | chr14 | 99915539 | ||||||
| chr14:99915697
|
A | G | 2 | a0001c0004t0003g0059a0001c0004t0003g0197 | 2 | HG02293.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1752+1000A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 15/21 | chr14 | 99915697 | ||||||
| chr14:99915699
|
A | G | 154 | a0001c0003t0001g0006a0001c0003t0001g0111a0001c0003t0001g0112others(151): Show | 155 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.1752+1002A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 15/21 | chr14 | 99915699 | ||||||
| chr14:99915828
|
C | G | 3 | a0001c0004t0003g0074a0001c0004t0003g0075a0001c0004t0003g0103 | 3 | HG01256.hp2 HG01258.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1752+1131C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 15/21 | chr14 | 99915828 | ||||||
| chr14:99915917
|
T | G | 1 | a0001c0004t0003g0180 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1752+1220T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 15/21 | chr14 | 99915917 | ||||||
| chr14:99916063
|
C | T | 38 | a0001c0003t0003g0184a0001c0003t0003g0279a0001c0004t0001g0009others(35): Show | 38 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1752+1366C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 15/21 | chr14 | 99916063 | ||||||
| chr14:99916533
|
A | C | 169 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0008others(166): Show | 170 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.1753-1249A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 15/21 | chr14 | 99916533 | ||||||
| chr14:99916658
|
G | A | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.1753-1124G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 15/21 | chr14 | 99916658 | ||||||
| chr14:99916828
|
G | A | 1 | a0003c0002t0006g0140 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1753-954G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 15/21 | chr14 | 99916828 | ||||||
| chr14:99916855
|
C | T | 85 | a0001c0003t0001g0163a0001c0003t0001g0274a0001c0003t0001g0286others(82): Show | 86 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1753-927C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 15/21 | chr14 | 99916855 | ||||||
| chr14:99916953
|
C | T | 1 | a0001c0007t0018g0241 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1753-829C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 15/21 | chr14 | 99916953 | ||||||
| chr14:99917224
|
G | A | 1 | a0001c0007t0002g0005 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1753-558G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 15/21 | chr14 | 99917224 | ||||||
| chr14:99917339
|
A | G | 171 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0041others(168): Show | 173 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.1753-443A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 15/21 | chr14 | 99917339 | ||||||
| chr14:99917458
|
C | T | 1 | a0001c0004t0003g0199 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1753-324C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 15/21 | chr14 | 99917458 | ||||||
| chr14:99917626
|
C | G | 79 | a0002c0001t0002g0110a0002c0001t0002g0118a0002c0001t0015g0109others(76): Show | 80 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.1753-156C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 15/21 | chr14 | 99917626 | ||||||
| chr14:99917695
|
TTGTG | T | 38 | a0001c0003t0003g0184a0001c0003t0003g0279a0001c0004t0001g0009others(35): Show | 38 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1753-82_1753-79del others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr14 | 99917695 | |||||
| chr14:99917743
|
A | G | 1 | a0007c0012t0002g0275 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1753-39A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 15/21 | chr14 | 99917743 | ||||||
| chr14:99917865
|
C | T | 2 | a0001c0003t0002g0105a0001c0003t0002g0106 | 2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1820+16C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | chr14 | 99917865 | ||||||
| chr14:99917895
|
A | C | 120 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0041others(117): Show | 122 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1820+46A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | chr14 | 99917895 | ||||||
| chr14:99917896
|
G | A | 1 | a0001c0005t0005g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1820+47G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | chr14 | 99917896 | ||||||
| chr14:99917994
|
C | T | 1 | a0003c0002t0001g0107 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1820+145C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | chr14 | 99917994 | ||||||
| chr14:99918064
|
C | T | 1 | a0002c0001t0002g0066 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1820+215C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | chr14 | 99918064 | ||||||
| chr14:99918110
|
T | G | 4 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0005g0246others(1): Show | 4 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1820+261T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | chr14 | 99918110 | ||||||
| chr14:99918127
|
C | T | 1 | a0003c0002t0001g0217 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1820+278C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | chr14 | 99918127 | ||||||
| chr14:99918175
|
C | CT | 5 | a0003c0002t0001g0187a0003c0002t0002g0162a0003c0002t0002g0211others(2): Show | 5 | HG00558.hp2 HG02040.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.1820+328dupT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr14 | 99918175 | |||||
| chr14:99918238
|
C | G | 3 | a0001c0004t0004g0017a0001c0007t0002g0005a0001c0007t0018g0241 | 3 | HG02145.hp2 HG02257.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1820+389C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | chr14 | 99918238 | ||||||
| chr14:99918466
|
G | A | 1 | a0001c0004t0003g0096 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1820+617G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | chr14 | 99918466 | ||||||
| chr14:99918763
|
T | C | 1 | a0003c0002t0001g0044 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1820+914T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | chr14 | 99918763 | ||||||
| chr14:99918801
|
C | T | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.1820+952C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | chr14 | 99918801 | ||||||
| chr14:99919004
|
G | A | 56 | a0001c0003t0001g0001a0001c0003t0001g0041a0001c0003t0001g0085others(53): Show | 57 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.1820+1155G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | chr14 | 99919004 | ||||||
| chr14:99919010
|
A | G | 3 | a0001c0004t0004g0017a0001c0007t0002g0005a0001c0007t0018g0241 | 3 | HG02145.hp2 HG02257.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1820+1161A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | chr14 | 99919010 | ||||||
| chr14:99919398
|
CCACACAC others(21): Show |
C | 5 | a0003c0002t0001g0053a0003c0002t0001g0192a0003c0002t0001g0209others(2): Show | 5 | HG00438.hp1 HG01175.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.1821-1378_1821-135 others(32): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr14 | 99919398 | |||||
| chr14:99919398
|
CCACACAC others(23): Show |
C | 2 | a0003c0002t0001g0154a0003c0002t0003g0155 | 2 | HG02155.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1821-1378_1821-134 others(34): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr14 | 99919398 | |||||
| chr14:99919398
|
CCACACAC others(25): Show |
C | 2 | a0002c0001t0002g0110a0002c0001t0002g0118 | 2 | HG01168.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.1821-1378_1821-134 others(36): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr14 | 99919398 | |||||
| chr14:99919399
|
CACACACA others(19): Show |
C | 60 | a0003c0002t0001g0019a0003c0002t0001g0036a0003c0002t0001g0037others(57): Show | 60 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.1821-1378_1821-135 others(30): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr14 | 99919399 | |||||
| chr14:99919401
|
CACACACA others(17): Show |
C | 7 | a0002c0001t0015g0109a0003c0002t0001g0002a0003c0002t0001g0107others(4): Show | 8 | HG00639.hp1 HG00642.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.1821-1378_1821-135 others(28): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr14 | 99919401 | |||||
| chr14:99919403
|
CACACACA others(15): Show |
C | 3 | a0001c0003t0001g0163a0003c0002t0006g0042a0003c0002t0006g0088 | 3 | HG01109.hp1 HG01928.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1821-1378_1821-135 others(26): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr14 | 99919403 | |||||
| chr14:99919406
|
A | G | 1 | a0002c0001t0002g0182 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1821-1383A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | chr14 | 99919406 | ||||||
| chr14:99919409
|
CATACGCA others(9): Show |
C | 1 | a0003c0002t0001g0130 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1821-1378_1821-136 others(20): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr14 | 99919409 | |||||
| chr14:99919418
|
G | GCACACAG others(5): Show |
30 | a0001c0004t0001g0009a0001c0004t0001g0040a0001c0004t0001g0091others(27): Show | 30 | HG00609.hp1 HG00735.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.1821-1364_1821-135 others(16): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr14 | 99919418 | |||||
| chr14:99919418
|
GCACACAG others(3): Show |
G | 3 | a0001c0004t0001g0123a0001c0004t0001g0248a0001c0004t0005g0242 | 3 | HG03209.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1821-1364_1821-135 others(14): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr14 | 99919418 | |||||
| chr14:99919419
|
CACACAG | C | 3 | a0001c0003t0007g0014a0001c0004t0001g0255a0001c0004t0010g0235 | 3 | HG02451.hp2 HG03130.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1821-1364_1821-135 others(10): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr14 | 99919419 | |||||
| chr14:99919425
|
G | GAC | 22 | a0001c0003t0001g0008a0001c0003t0001g0010a0001c0003t0001g0012others(19): Show | 22 | HG00423.hp2 HG01109.hp2 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.1821-1327_1821-132 others(6): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr14 | 99919425 | |||||
| chr14:99919425
|
G | GACAC | 22 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0015others(19): Show | 22 | HG02055.hp2 HG02109.hp1 HG02293.hp1 others(19): Show |
intron_variant | MODIFIER | c.1821-1329_1821-132 others(8): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr14 | 99919425 | |||||
| chr14:99919425
|
G | GACACAC | 4 | a0001c0003t0001g0168a0001c0003t0005g0246a0001c0003t0005g0247others(1): Show | 4 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1821-1331_1821-132 others(10): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr14 | 99919425 | |||||
| chr14:99919425
|
G | GACACACA others(7): Show |
2 | a0001c0003t0001g0270a0001c0004t0003g0180 | 2 | NA18983.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1821-1353_1821-135 others(18): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr14 | 99919425 | |||||
| chr14:99919425
|
G | GACACACA others(9): Show |
10 | a0001c0003t0001g0001a0001c0003t0001g0041a0001c0003t0001g0085others(7): Show | 11 | HG00140.hp2 HG00733.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.1821-1353_1821-135 others(20): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr14 | 99919425 | |||||
| chr14:99919425
|
G | GACACACA others(11): Show |
5 | a0001c0003t0001g0086a0001c0003t0001g0193a0001c0003t0001g0269others(2): Show | 5 | HG00323.hp2 HG01243.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.1821-1353_1821-135 others(22): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr14 | 99919425 | |||||
| chr14:99919425
|
GAC | G | 7 | a0001c0003t0001g0274a0001c0003t0001g0286a0001c0003t0008g0271others(4): Show | 7 | HG00639.hp2 HG02132.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1821-1327_1821-132 others(6): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr14 | 99919425 | |||||
| chr14:99919425
|
GACAC | G | 5 | a0001c0003t0001g0214a0002c0001t0002g0039a0002c0001t0002g0099others(2): Show | 5 | HG00621.hp1 HG02071.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1821-1329_1821-132 others(8): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr14 | 99919425 | |||||
| chr14:99919425
|
GACACACA others(15): Show |
G | 2 | a0001c0007t0002g0005a0001c0007t0018g0241 | 2 | HG02145.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1821-1347_1821-132 others(26): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr14 | 99919425 | |||||
| chr14:99919427
|
C | CACACACA others(3): Show |
5 | a0001c0003t0003g0184a0001c0004t0001g0115a0001c0004t0003g0131others(2): Show | 5 | HG00140.hp1 HG02293.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.1821-1353_1821-135 others(14): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr14 | 99919427 | |||||
| chr14:99919429
|
C | CACACACA others(1): Show |
4 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258others(1): Show | 4 | HG00609.hp2 HG02083.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1821-1353_1821-135 others(12): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr14 | 99919429 | |||||
| chr14:99919659
|
A | G | 1 | a0003c0002t0001g0215 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1821-1130A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | chr14 | 99919659 | ||||||
| chr14:99919842
|
T | C | 2 | a0001c0007t0002g0005a0001c0007t0018g0241 | 2 | HG02145.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1821-947T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | chr14 | 99919842 | ||||||
| chr14:99920099
|
T | G | 1 | a0003c0002t0002g0138 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1821-690T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | chr14 | 99920099 | ||||||
| chr14:99920143
|
G | A | 1 | a0003c0002t0002g0138 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1821-646G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | chr14 | 99920143 | ||||||
| chr14:99920247
|
A | G | 170 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0041others(167): Show | 172 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.1821-542A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | chr14 | 99920247 | ||||||
| chr14:99920247
|
A | T | 1 | a0003c0002t0011g0024 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1821-542A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | chr14 | 99920247 | ||||||
| chr14:99920278
|
G | A | 8 | a0001c0003t0007g0014a0001c0004t0001g0123a0001c0004t0001g0248others(5): Show | 8 | HG02055.hp1 HG02451.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.1821-511G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | chr14 | 99920278 | ||||||
| chr14:99920321
|
T | G | 1 | a0003c0002t0001g0209 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1821-468T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | chr14 | 99920321 | ||||||
| chr14:99920369
|
T | C | 15 | a0001c0003t0001g0001a0001c0003t0001g0041a0001c0003t0001g0085others(12): Show | 16 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.1821-420T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | chr14 | 99920369 | ||||||
| chr14:99920405
|
G | A | 2 | a0003c0002t0001g0237a0003c0015t0001g0013 | 2 | HG01884.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1821-384G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | chr14 | 99920405 | ||||||
| chr14:99920469
|
G | A | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.1821-320G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | chr14 | 99920469 | ||||||
| chr14:99920722
|
C | T | 1 | a0003c0002t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1821-67C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | chr14 | 99920722 | ||||||
| chr14:99920764
|
G | C | 2 | a0003c0002t0001g0161a0003c0002t0001g0205 | 2 | NA18954.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.1821-25G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | chr14 | 99920764 | ||||||
| chr14:99920768
|
T | C | 12 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0220others(9): Show | 12 | HG01109.hp2 HG02109.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1821-21T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 16/21 | chr14 | 99920768 | ||||||
| chr14:99920905
|
A | AT | 171 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0041others(168): Show | 173 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.1909+35dupT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99920905 | |||||
| chr14:99921193
|
T | C | 1 | a0002c0001t0002g0023 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1909+316T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99921193 | ||||||
| chr14:99921256
|
TC | T | 9 | a0001c0003t0001g0008a0001c0003t0001g0010a0001c0003t0001g0214others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1909+381delC | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99921256 | |||||
| chr14:99921325
|
A | G | 5 | a0003c0002t0001g0170a0003c0002t0001g0171a0003c0002t0001g0172others(2): Show | 5 | HG01433.hp1 NA18952.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.1909+448A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99921325 | ||||||
| chr14:99921342
|
T | C | 62 | a0001c0003t0001g0001a0001c0003t0001g0007a0001c0003t0001g0015others(59): Show | 63 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.1909+465T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99921342 | ||||||
| chr14:99921384
|
C | G | 13 | a0001c0003t0001g0012a0001c0003t0001g0080a0001c0003t0001g0220others(10): Show | 13 | HG01109.hp2 HG02109.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1909+507C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99921384 | ||||||
| chr14:99921496
|
C | G | 3 | a0001c0003t0004g0027a0001c0003t0004g0141a0001c0003t0004g0258 | 3 | HG00609.hp2 HG02083.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.1909+619C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99921496 | ||||||
| chr14:99921667
|
G | T | 5 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0005g0246others(2): Show | 5 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1909+790G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99921667 | ||||||
| chr14:99921702
|
T | C | 1 | a0002c0001t0002g0061 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1909+825T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99921702 | ||||||
| chr14:99921780
|
A | G | 1 | a0003c0002t0001g0154 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1909+903A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99921780 | ||||||
| chr14:99922030
|
G | A | 4 | a0003c0002t0001g0104a0003c0002t0001g0191a0003c0002t0001g0192others(1): Show | 4 | HG01081.hp1 HG01175.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1909+1153G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99922030 | ||||||
| chr14:99922182
|
A | G | 15 | a0001c0003t0001g0006a0001c0003t0001g0111a0001c0003t0001g0112others(12): Show | 15 | HG00639.hp2 HG02451.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1909+1305A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99922182 | ||||||
| chr14:99922297
|
G | A | 5 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0005g0246others(2): Show | 5 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1909+1420G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99922297 | ||||||
| chr14:99922387
|
T | A | 199 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0007others(196): Show | 201 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.1909+1510T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99922387 | ||||||
| chr14:99922393
|
G | T | 1 | a0001c0013t0001g0126 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1909+1516G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99922393 | ||||||
| chr14:99922403
|
A | G | 1 | a0003c0002t0001g0210 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1909+1526A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99922403 | ||||||
| chr14:99922405
|
C | T | 1 | a0001c0005t0001g0250 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1909+1528C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99922405 | ||||||
| chr14:99922464
|
A | T | 1 | a0001c0003t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1909+1587A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99922464 | ||||||
| chr14:99922573
|
A | G | 40 | a0001c0003t0003g0184a0001c0003t0003g0279a0001c0004t0001g0009others(37): Show | 40 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.1909+1696A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99922573 | ||||||
| chr14:99922827
|
A | G | 1 | a0003c0002t0001g0107 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1909+1950A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99922827 | ||||||
| chr14:99922876
|
C | T | 1 | a0001c0003t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1909+1999C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99922876 | ||||||
| chr14:99923030
|
A | G | 4 | a0001c0004t0004g0017a0001c0005t0008g0077a0001c0007t0002g0005others(1): Show | 4 | HG02145.hp2 HG02257.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1909+2153A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923030 | ||||||
| chr14:99923056
|
C | T | 3 | a0002c0001t0002g0021a0002c0001t0002g0066a0002c0001t0002g0153 | 3 | HG00642.hp2 HG01123.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1909+2179C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923056 | ||||||
| chr14:99923154
|
C | G | 1 | a0003c0002t0001g0036 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1909+2277C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923154 | ||||||
| chr14:99923190
|
C | T | 1 | a0001c0003t0001g0233 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1909+2313C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923190 | ||||||
| chr14:99923193
|
C | T | 1 | a0003c0002t0017g0028 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1909+2316C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923193 | ||||||
| chr14:99923309
|
A | G | 163 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0007others(160): Show | 165 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1909+2432A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923309 | ||||||
| chr14:99923560
|
T | TGTTGAAT others(72): Show |
1 | a0003c0002t0001g0217 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1909+2701_1909+270 others(83): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99923560 | |||||
| chr14:99923560
|
T | TGTTGAAT others(230): Show |
1 | a0004c0008t0004g0268 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1909+2714_1909+271 others(241): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99923560 | |||||
| chr14:99923560
|
T | TGTTGAAT others(72): Show |
2 | a0001c0004t0001g0091a0001c0004t0003g0149 | 2 | HG02074.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.1909+2725_1909+272 others(83): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99923560 | |||||
| chr14:99923560
|
T | TGTTGAAT others(230): Show |
1 | a0003c0015t0001g0013 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1909+2725_1909+272 others(241): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99923560 | |||||
| chr14:99923560
|
T | TGTTGAAT others(72): Show |
1 | a0001c0005t0009g0078 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1909+2729_1909+273 others(83): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99923560 | |||||
| chr14:99923560
|
T | TGTTGAAT others(151): Show |
7 | a0001c0003t0001g0085a0001c0003t0001g0086a0001c0003t0001g0152others(4): Show | 7 | HG00140.hp2 HG00323.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.1909+2729_1909+273 others(162): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99923560 | |||||
| chr14:99923560
|
T | TGTTGAAT others(72): Show |
53 | a0002c0001t0002g0082a0002c0001t0002g0084a0002c0001t0002g0133others(50): Show | 54 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1909+2746_1909+274 others(83): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99923560 | |||||
| chr14:99923560
|
T | TGTTGAAT others(151): Show |
1 | a0003c0002t0003g0159 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1909+2746_1909+274 others(162): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99923560 | |||||
| chr14:99923560
|
T | TGTTGAAT others(230): Show |
1 | a0002c0001t0002g0196 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1909+2746_1909+274 others(241): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99923560 | |||||
| chr14:99923592
|
T | C | 2 | a0001c0004t0004g0017a0004c0008t0004g0004 | 2 | HG02257.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1909+2715T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923592 | ||||||
| chr14:99923592
|
T | TCAATCGA others(230): Show |
1 | a0003c0002t0001g0237 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1909+2729_1909+273 others(241): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99923592 | |||||
| chr14:99923598
|
G | GATCAGAA others(72): Show |
1 | a0003c0002t0001g0161 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1909+2746_1909+274 others(83): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99923598 | |||||
| chr14:99923603
|
G | A | 27 | a0001c0003t0003g0184a0001c0003t0003g0279a0001c0003t0004g0141others(24): Show | 27 | HG00140.hp1 HG00609.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1909+2726G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923603 | ||||||
| chr14:99923607
|
T | C | 51 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0015others(48): Show | 52 | HG00558.hp1 HG00639.hp2 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.1909+2730T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923607 | ||||||
| chr14:99923607
|
T | TGTAAAGG others(72): Show |
1 | a0003c0014t0004g0254 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1909+2746_1909+274 others(83): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99923607 | |||||
| chr14:99923607
|
T | TGTAAAGG others(72): Show |
2 | a0002c0001t0002g0182a0003c0002t0001g0094 | 2 | HG01255.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1909+2746_1909+274 others(83): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99923607 | |||||
| chr14:99923607
|
T | TGTAAAGG others(151): Show |
1 | a0003c0002t0008g0238 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1909+2746_1909+274 others(162): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99923607 | |||||
| chr14:99923607
|
T | TGTAAAGG others(151): Show |
1 | a0003c0002t0001g0215 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1909+2746_1909+274 others(162): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99923607 | |||||
| chr14:99923607
|
T | TGTAAAGG others(72): Show |
3 | a0001c0003t0003g0032a0001c0003t0003g0033a0001c0003t0003g0034 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1909+2762_1909+276 others(83): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99923607 | |||||
| chr14:99923607
|
T | TGTAAAGG others(467): Show |
1 | a0001c0003t0007g0281 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1909+2762_1909+276 others(478): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99923607 | |||||
| chr14:99923607
|
T | TGTAAAGG others(546): Show |
1 | a0001c0003t0007g0117 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1909+2762_1909+276 others(557): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99923607 | |||||
| chr14:99923608
|
G | C | 1 | a0001c0005t0001g0079 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1909+2731G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923608 | ||||||
| chr14:99923624
|
G | A | 60 | a0001c0003t0001g0001a0001c0003t0001g0007a0001c0003t0001g0015others(57): Show | 61 | HG00140.hp1 HG00609.hp1 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.1909+2747G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923624 | ||||||
| chr14:99923638
|
GC | G | 127 | a0001c0003t0001g0006a0001c0003t0001g0085a0001c0003t0001g0086others(124): Show | 128 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1909+2766delC | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99923638 | |||||
| chr14:99923639
|
C | CGTTGAAT others(71): Show |
1 | a0001c0004t0013g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1909+2762_1909+276 others(82): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(308): Show |
1 | a0004c0008t0004g0004 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1909+2762_1909+276 others(319): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(229): Show |
1 | a0001c0004t0001g0123 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1909+2762_1909+276 others(240): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(150): Show |
2 | a0001c0004t0005g0242a0001c0005t0005g0097 | 2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1909+2762_1909+276 others(161): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(387): Show |
1 | a0001c0004t0001g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1909+2762_1909+276 others(398): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(150): Show |
2 | a0001c0003t0002g0105a0001c0003t0002g0106 | 2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1909+2762_1909+276 others(161): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(71): Show |
2 | a0001c0003t0001g0012a0002c0001t0001g0239 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1909+2762_1909+276 others(82): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(308): Show |
2 | a0001c0005t0004g0284a0001c0005t0004g0285 | 2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1909+2762_1909+276 others(319): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(150): Show |
1 | a0001c0003t0008g0271 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1909+2762_1909+276 others(161): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(545): Show |
1 | a0001c0003t0002g0116 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1909+2762_1909+276 others(556): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(229): Show |
3 | a0001c0003t0001g0243a0001c0003t0001g0244a0001c0003t0001g0245 | 3 | HG02922.hp1 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1909+2762_1909+276 others(240): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(466): Show |
1 | a0001c0003t0001g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1909+2762_1909+276 others(477): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(71): Show |
1 | a0002c0001t0002g0175 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1909+2762_1909+276 others(82): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(229): Show |
1 | a0001c0004t0005g0266 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1909+2762_1909+276 others(240): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(229): Show |
1 | a0001c0003t0001g0015 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1909+2762_1909+276 others(240): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(229): Show |
9 | a0001c0003t0001g0080a0001c0003t0001g0220a0001c0003t0001g0221others(6): Show | 9 | HG02622.hp1 HG02886.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1909+2762_1909+276 others(240): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(308): Show |
1 | a0001c0003t0001g0273 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1909+2762_1909+276 others(319): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(71): Show |
9 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0001g0225others(6): Show | 9 | HG00639.hp2 HG02040.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1909+2762_1909+276 others(82): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(150): Show |
1 | a0001c0003t0001g0010 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1909+2762_1909+276 others(161): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(229): Show |
1 | a0001c0003t0001g0269 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1909+2762_1909+276 others(240): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(150): Show |
2 | a0001c0005t0001g0079a0001c0005t0005g0265 | 2 | HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1909+2762_1909+276 others(161): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(229): Show |
1 | a0003c0002t0001g0130 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1909+2762_1909+276 others(240): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(545): Show |
1 | a0001c0003t0007g0014 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1909+2762_1909+276 others(556): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(150): Show |
1 | a0001c0003t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1909+2762_1909+276 others(161): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(387): Show |
1 | a0001c0007t0002g0005 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1909+2762_1909+276 others(398): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(71): Show |
14 | a0001c0003t0001g0041a0001c0004t0001g0040a0001c0004t0001g0135others(11): Show | 14 | HG00733.hp2 HG01069.hp2 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.1909+2762_1909+276 others(82): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(229): Show |
1 | a0001c0005t0008g0077 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1909+2762_1909+276 others(240): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(308): Show |
1 | a0001c0003t0001g0214 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1909+2762_1909+276 others(319): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(150): Show |
5 | a0001c0003t0001g0008a0001c0003t0001g0240a0001c0003t0002g0252others(2): Show | 5 | HG00733.hp1 HG02965.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1909+2762_1909+276 others(161): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(229): Show |
1 | a0001c0003t0001g0020 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1909+2762_1909+276 others(240): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(308): Show |
1 | a0001c0003t0001g0016 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1909+2762_1909+276 others(319): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(229): Show |
4 | a0001c0003t0001g0001a0001c0003t0001g0007a0001c0003t0001g0120others(1): Show | 5 | HG01243.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1909+2762_1909+276 others(240): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(308): Show |
1 | a0001c0007t0018g0241 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1909+2762_1909+276 others(319): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923639
|
C | CGTTGAAT others(782): Show |
1 | a0001c0003t0001g0163 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1909+2762_1909+276 others(793): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923639 | ||||||
| chr14:99923656
|
T | C | 5 | a0001c0003t0004g0141a0002c0001t0003g0142a0002c0006t0002g0128others(2): Show | 5 | HG00323.hp1 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1909+2779T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923656 | ||||||
| chr14:99923663
|
G | A | 1 | a0003c0015t0001g0013 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1909+2786G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923663 | ||||||
| chr14:99923675
|
C | T | 1 | a0003c0002t0002g0050 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1909+2798C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923675 | ||||||
| chr14:99923676
|
T | C | 202 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0007others(199): Show | 204 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.1909+2799T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923676 | ||||||
| chr14:99923735
|
ATAGTGTT others(9): Show |
A | 1 | a0002c0001t0002g0176 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1909+2859_1909+287 others(20): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923735 | ||||||
| chr14:99923843
|
A | G | 1 | a0003c0002t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1909+2966A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923843 | ||||||
| chr14:99923854
|
T | C | 187 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0008others(184): Show | 189 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.1909+2977T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923854 | ||||||
| chr14:99923935
|
T | A | 143 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0015others(140): Show | 145 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.1909+3058T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923935 | ||||||
| chr14:99923958
|
C | T | 3 | a0001c0003t0002g0252a0001c0003t0008g0271a0003c0002t0008g0238 | 3 | HG00733.hp1 HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1909+3081C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923958 | ||||||
| chr14:99923963
|
A | G | 2 | a0001c0003t0001g0167a0001c0003t0001g0168 | 2 | HG02818.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1909+3086A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99923963 | ||||||
| chr14:99924072
|
A | G | 1 | a0001c0007t0002g0005 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1909+3195A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99924072 | ||||||
| chr14:99924180
|
G | GT | 50 | a0001c0003t0001g0008a0001c0003t0001g0010a0001c0003t0001g0214others(47): Show | 50 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.1909+3311dupT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99924180 | |||||
| chr14:99924190
|
T | C | 1 | a0001c0003t0001g0163 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1909+3313T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99924190 | ||||||
| chr14:99924273
|
C | T | 1 | a0002c0001t0002g0144 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1909+3396C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99924273 | ||||||
| chr14:99924429
|
T | C | 4 | a0002c0001t0002g0021a0002c0001t0002g0031a0002c0001t0002g0066others(1): Show | 4 | HG00735.hp1 HG01123.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1909+3552T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99924429 | ||||||
| chr14:99924503
|
A | T | 1 | a0001c0004t0003g0195 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1909+3626A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99924503 | ||||||
| chr14:99924572
|
C | T | 1 | a0003c0002t0001g0036 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1909+3695C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99924572 | ||||||
| chr14:99924713
|
T | C | 1 | a0002c0001t0002g0160 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1909+3836T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99924713 | ||||||
| chr14:99925184
|
GTGAAACT others(97): Show |
G | 1 | a0003c0002t0006g0043 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1909+4309_1909+441 others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99925184 | |||||
| chr14:99925189
|
A | ACTACCTG others(1): Show |
4 | a0003c0002t0001g0044a0003c0002t0001g0055a0003c0002t0001g0087others(1): Show | 4 | HG01192.hp2 HG01255.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1909+4313_1909+432 others(12): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99925189 | |||||
| chr14:99925275
|
C | CT | 9 | a0001c0003t0001g0001a0001c0003t0001g0120a0001c0003t0002g0252others(6): Show | 10 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1909+4414dupT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99925275 | |||||
| chr14:99925276
|
T | C | 1 | a0002c0001t0002g0136 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1909+4399T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99925276 | ||||||
| chr14:99925325
|
A | G | 2 | a0001c0003t0004g0027a0001c0003t0004g0258 | 2 | HG00609.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.1909+4448A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99925325 | ||||||
| chr14:99925329
|
C | T | 2 | a0001c0004t0001g0123a0001c0004t0001g0248 | 2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1909+4452C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99925329 | ||||||
| chr14:99925424
|
TAATTTTT others(36): Show |
T | 1 | a0001c0004t0001g0123 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1909+4549_1909+459 others(47): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99925424 | |||||
| chr14:99925622
|
G | T | 1 | a0001c0003t0001g0269 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1909+4745G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99925622 | ||||||
| chr14:99925682
|
G | A | 1 | a0003c0002t0001g0215 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1909+4805G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99925682 | ||||||
| chr14:99925977
|
C | T | 45 | a0001c0003t0001g0286a0001c0003t0003g0032a0001c0003t0003g0033others(42): Show | 45 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1909+5100C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99925977 | ||||||
| chr14:99925988
|
C | A | 1 | a0002c0001t0019g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1909+5111C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99925988 | ||||||
| chr14:99926037
|
G | A | 1 | a0001c0003t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1909+5160G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99926037 | ||||||
| chr14:99926240
|
C | A | 4 | a0001c0003t0009g0251a0001c0005t0009g0078a0003c0002t0001g0215others(1): Show | 4 | HG02572.hp2 HG02809.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1909+5363C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99926240 | ||||||
| chr14:99926283
|
G | GT | 34 | a0001c0003t0003g0277a0001c0003t0003g0279a0001c0004t0001g0115others(31): Show | 34 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.1909+5406_1909+540 others(5): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99926283 | ||||||
| chr14:99926283
|
G | GTT | 3 | a0001c0003t0003g0184a0001c0004t0003g0199a0003c0002t0003g0125 | 3 | HG00735.hp2 HG04115.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1909+5406_1909+540 others(6): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99926283 | ||||||
| chr14:99926284
|
G | GT | 106 | a0001c0003t0001g0001a0001c0003t0001g0015a0001c0003t0001g0041others(103): Show | 108 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.1909+5417dupT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99926284 | |||||
| chr14:99926284
|
G | GTT | 7 | a0001c0003t0001g0112a0001c0004t0010g0235a0003c0002t0001g0019others(4): Show | 7 | HG01496.hp2 HG03098.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1909+5416_1909+541 others(6): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99926284 | |||||
| chr14:99926284
|
G | T | 37 | a0001c0003t0003g0184a0001c0003t0003g0277a0001c0003t0003g0279others(34): Show | 37 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1909+5407G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99926284 | ||||||
| chr14:99926324
|
G | T | 2 | a0001c0003t0004g0027a0001c0003t0004g0258 | 2 | HG00609.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.1909+5447G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99926324 | ||||||
| chr14:99926402
|
G | A | 2 | a0001c0003t0004g0027a0001c0003t0004g0258 | 2 | HG00609.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.1909+5525G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99926402 | ||||||
| chr14:99926422
|
C | G | 5 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0016others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1909+5545C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99926422 | ||||||
| chr14:99926507
|
G | A | 186 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0007others(183): Show | 188 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1909+5630G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99926507 | ||||||
| chr14:99926515
|
C | G | 1 | a0003c0014t0004g0254 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1909+5638C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99926515 | ||||||
| chr14:99926555
|
G | A | 4 | a0001c0004t0004g0017a0001c0005t0004g0284a0001c0005t0004g0285others(1): Show | 4 | HG02145.hp2 HG02257.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1909+5678G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99926555 | ||||||
| chr14:99926559
|
A | G | 1 | a0003c0002t0012g0253 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1909+5682A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99926559 | ||||||
| chr14:99926574
|
T | C | 199 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0007others(196): Show | 201 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.1909+5697T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99926574 | ||||||
| chr14:99926608
|
T | C | 49 | a0001c0003t0001g0286a0001c0003t0003g0032a0001c0003t0003g0033others(46): Show | 49 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.1909+5731T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99926608 | ||||||
| chr14:99926658
|
T | G | 2 | a0001c0003t0004g0027a0001c0003t0004g0258 | 2 | HG00609.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.1909+5781T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99926658 | ||||||
| chr14:99926735
|
G | A | 5 | a0003c0002t0001g0223a0003c0002t0006g0042a0003c0002t0006g0043others(2): Show | 5 | HG01109.hp1 HG01928.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1909+5858G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99926735 | ||||||
| chr14:99926749
|
C | CT | 6 | a0001c0003t0001g0085a0001c0003t0002g0252a0001c0004t0003g0199others(3): Show | 6 | HG00544.hp2 HG00733.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1909+5885dupT | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99926749 | |||||
| chr14:99927032
|
G | A | 1 | a0003c0014t0004g0254 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1909+6155G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927032 | ||||||
| chr14:99927139
|
T | C | 284 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0007others(281): Show | 286 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.1909+6262T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927139 | ||||||
| chr14:99927146
|
C | A | 1 | a0003c0014t0004g0254 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1909+6269C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927146 | ||||||
| chr14:99927301
|
G | A | 1 | a0001c0003t0009g0251 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1909+6424G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927301 | ||||||
| chr14:99927535
|
A | G | 2 | a0001c0003t0004g0027a0001c0003t0004g0258 | 2 | HG00609.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.1909+6658A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927535 | ||||||
| chr14:99927563
|
T | C | 5 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0016others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1909+6686T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927563 | ||||||
| chr14:99927639
|
C | T | 1 | a0001c0003t0002g0252 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1909+6762C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927639 | ||||||
| chr14:99927643
|
GTGGTAGA others(37): Show |
G | 1 | a0001c0004t0011g0156 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1909+6768_1909+681 others(48): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927643 | |||||
| chr14:99927687
|
A | G | 2 | a0001c0005t0004g0284a0001c0005t0004g0285 | 2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1909+6810A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927687 | ||||||
| chr14:99927749
|
G | A | 117 | a0001c0003t0001g0001a0001c0003t0001g0008a0001c0003t0001g0010others(114): Show | 119 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.1909+6872G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927749 | ||||||
| chr14:99927765
|
AGTAGTGG others(5): Show |
A | 1 | a0002c0001t0002g0101 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1909+6904_1909+691 others(16): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927765 | |||||
| chr14:99927768
|
A | G | 1 | a0003c0002t0002g0203 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1909+6891A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927768 | ||||||
| chr14:99927775
|
G | A | 1 | a0003c0002t0002g0203 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1909+6898G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927775 | ||||||
| chr14:99927777
|
G | A | 1 | a0003c0002t0002g0203 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1909+6900G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927777 | ||||||
| chr14:99927780
|
A | G | 1 | a0001c0005t0004g0284 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1909+6903A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927780 | ||||||
| chr14:99927791
|
T | TCGGGGGT others(10): Show |
1 | a0003c0002t0002g0203 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1909+6914_1909+691 others(21): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927791 | ||||||
| chr14:99927792
|
A | G | 1 | a0003c0002t0002g0203 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1909+6915A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927792 | ||||||
| chr14:99927793
|
T | G | 1 | a0003c0002t0002g0203 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1909+6916T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927793 | ||||||
| chr14:99927793
|
TTGGTGGT others(22): Show |
T | 2 | a0001c0003t0004g0027a0001c0003t0004g0258 | 2 | HG00609.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.1909+6926_1909+695 others(33): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927793 | |||||
| chr14:99927797
|
T | G | 1 | a0007c0012t0002g0275 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1909+6920T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927797 | ||||||
| chr14:99927800
|
T | TG | 22 | a0001c0003t0001g0020a0001c0003t0001g0286a0001c0003t0005g0247others(19): Show | 22 | HG00642.hp2 HG01175.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.1909+6931dupG | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927800 | |||||
| chr14:99927808
|
G | A | 42 | a0001c0003t0003g0032a0001c0003t0003g0033a0001c0003t0003g0034others(39): Show | 42 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.1909+6931G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927808 | ||||||
| chr14:99927808
|
G | T | 1 | a0007c0012t0002g0275 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1909+6931G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927808 | ||||||
| chr14:99927809
|
T | G | 3 | a0001c0004t0011g0156a0001c0004t0013g0108a0007c0012t0002g0275 | 3 | HG02055.hp1 HG02083.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1909+6932T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927809 | ||||||
| chr14:99927811
|
G | T | 1 | a0007c0012t0002g0275 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1909+6934G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927811 | ||||||
| chr14:99927814
|
G | T | 1 | a0007c0012t0002g0275 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1909+6937G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927814 | ||||||
| chr14:99927814
|
GGGTGGTG others(74): Show |
G | 2 | a0002c0001t0002g0065a0002c0001t0002g0183 | 2 | NA18956.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1909+6969_1909+704 others(85): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927814 | |||||
| chr14:99927817
|
T | TGGTGGTG others(123): Show |
1 | a0001c0003t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1909+6955_1909+695 others(134): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927817 | |||||
| chr14:99927822
|
G | A | 1 | a0003c0002t0001g0054 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1909+6945G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927822 | ||||||
| chr14:99927833
|
A | G | 4 | a0001c0003t0001g0286a0001c0004t0003g0059a0001c0004t0003g0197others(1): Show | 4 | HG02293.hp2 HG03453.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1909+6956A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927833 | ||||||
| chr14:99927834
|
T | A | 2 | a0001c0004t0003g0059a0001c0004t0003g0197 | 2 | HG02293.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1909+6957T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927834 | ||||||
| chr14:99927834
|
T | G | 3 | a0001c0003t0001g0286a0003c0002t0002g0050a0003c0002t0002g0203 | 3 | HG02273.hp1 HG03453.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.1909+6957T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927834 | ||||||
| chr14:99927834
|
TTGGTGGT others(5): Show |
T | 1 | a0001c0004t0005g0249 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1909+6969_1909+698 others(16): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927834 | |||||
| chr14:99927836
|
G | A | 1 | a0003c0002t0002g0050 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1909+6959G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927836 | ||||||
| chr14:99927837
|
G | A | 1 | a0003c0002t0002g0203 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1909+6960G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927837 | ||||||
| chr14:99927838
|
T | TGGTGGTG others(305): Show |
1 | a0001c0004t0005g0266 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1909+6968_1909+696 others(316): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927838 | |||||
| chr14:99927838
|
T | TGGTGGTG others(308): Show |
1 | a0001c0004t0001g0009 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1909+6968_1909+696 others(319): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927838 | |||||
| chr14:99927844
|
T | C | 1 | a0003c0002t0002g0050 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1909+6967T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927844 | ||||||
| chr14:99927846
|
A | G | 3 | a0001c0004t0001g0009a0001c0004t0005g0266a0003c0002t0002g0050 | 3 | HG02273.hp1 HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1909+6969A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927846 | ||||||
| chr14:99927846
|
ATGGTGGT others(44): Show |
A | 1 | a0001c0003t0004g0141 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1909+6983_1909+703 others(55): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927846 | |||||
| chr14:99927846
|
ATGGTGGT others(128): Show |
A | 1 | a0002c0001t0001g0062 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1909+6978_1909+711 others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927846 | |||||
| chr14:99927849
|
G | GTGGTGGT others(569): Show |
1 | a0001c0003t0007g0281 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1909+6979_1909+698 others(580): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927849 | |||||
| chr14:99927849
|
G | GTGGTGGT others(1233): Show |
1 | a0001c0003t0007g0117 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1909+6979_1909+698 others(1244): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927849 | |||||
| chr14:99927853
|
T | TGGGGGTG others(8): Show |
1 | a0003c0002t0002g0050 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1909+6978_1909+697 others(19): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927853 | |||||
| chr14:99927855
|
G | A | 3 | a0003c0002t0001g0170a0003c0002t0001g0171a0003c0002t0001g0172 | 3 | NA18957.hp2 NA19063.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1909+6978G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927855 | ||||||
| chr14:99927857
|
G | A | 5 | a0001c0003t0007g0014a0001c0003t0009g0251a0001c0005t0009g0078others(2): Show | 5 | HG02572.hp2 HG02809.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1909+6980G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927857 | ||||||
| chr14:99927857
|
GGTA | G | 5 | a0001c0003t0002g0105a0001c0003t0002g0106a0003c0002t0001g0170others(2): Show | 5 | HG02630.hp2 HG03041.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.1909+6983_1909+698 others(7): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927857 | |||||
| chr14:99927860
|
A | G | 4 | a0001c0004t0001g0009a0001c0004t0005g0266a0003c0002t0002g0050others(1): Show | 4 | HG02273.hp1 HG02280.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1909+6983A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927860 | ||||||
| chr14:99927861
|
G | T | 1 | a0002c0001t0002g0278 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1909+6984G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927861 | ||||||
| chr14:99927862
|
T | A | 1 | a0003c0002t0002g0203 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1909+6985T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927862 | ||||||
| chr14:99927866
|
A | G | 12 | a0001c0003t0007g0014a0001c0003t0009g0251a0001c0004t0001g0009others(9): Show | 12 | HG01071.hp2 HG02280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1909+6989A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927866 | ||||||
| chr14:99927867
|
G | T | 1 | a0003c0002t0002g0050 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1909+6990G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927867 | ||||||
| chr14:99927869
|
A | AGTGGTGG others(2): Show |
5 | a0001c0003t0001g0008a0001c0003t0001g0010a0001c0003t0001g0214others(2): Show | 5 | HG02486.hp2 HG03471.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1909+6999_1909+700 others(13): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927869 | |||||
| chr14:99927869
|
A | G | 13 | a0001c0003t0007g0014a0001c0003t0009g0251a0001c0004t0001g0009others(10): Show | 13 | HG01071.hp2 HG02273.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1909+6992A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927869 | ||||||
| chr14:99927876
|
G | A | 1 | a0002c0001t0002g0278 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1909+6999G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927876 | ||||||
| chr14:99927876
|
G | GTGGTGGT others(1247): Show |
1 | a0001c0003t0001g0283 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1909+6999_1909+700 others(1258): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927876 | ||||||
| chr14:99927877
|
C | CGGTGGTG others(167): Show |
1 | a0002c0001t0002g0110 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1909+7011_1909+701 others(178): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927877 | |||||
| chr14:99927877
|
C | CGGTGGTG others(464): Show |
1 | a0001c0003t0002g0116 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1909+7011_1909+701 others(475): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927877 | |||||
| chr14:99927877
|
C | CGGTGGTG others(470): Show |
3 | a0001c0003t0001g0243a0001c0003t0001g0244a0001c0003t0001g0245 | 3 | HG02922.hp1 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1909+7011_1909+701 others(481): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927877 | |||||
| chr14:99927877
|
C | T | 7 | a0001c0003t0001g0283a0001c0004t0001g0009a0001c0004t0005g0266others(4): Show | 7 | HG01071.hp2 HG02273.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1909+7000C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927877 | ||||||
| chr14:99927879
|
G | A | 2 | a0001c0004t0001g0009a0001c0004t0005g0266 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1909+7002G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927879 | ||||||
| chr14:99927879
|
G | GTGGTGGT others(2289): Show |
1 | a0001c0004t0001g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1909+7011_1909+701 others(2300): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927879 | |||||
| chr14:99927882
|
G | A | 1 | a0003c0002t0002g0050 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1909+7005G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927882 | ||||||
| chr14:99927885
|
G | A | 2 | a0002c0001t0002g0278a0003c0002t0002g0203 | 2 | HG01071.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.1909+7008G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927885 | ||||||
| chr14:99927886
|
T | TGGG | 35 | a0001c0003t0003g0184a0001c0003t0003g0277a0001c0003t0003g0279others(32): Show | 35 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.1909+7011_1909+701 others(7): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927886 | |||||
| chr14:99927889
|
T | G | 232 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0007others(229): Show | 234 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.1909+7012T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927889 | ||||||
| chr14:99927891
|
G | A | 1 | a0003c0002t0002g0050 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1909+7014G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927891 | ||||||
| chr14:99927894
|
G | A | 2 | a0001c0003t0001g0283a0003c0002t0002g0203 | 2 | HG03540.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.1909+7017G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927894 | ||||||
| chr14:99927895
|
T | G | 250 | a0001c0003t0001g0001a0001c0003t0001g0008a0001c0003t0001g0010others(247): Show | 252 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.1909+7018T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927895 | ||||||
| chr14:99927895
|
T | TGGGGGTG others(2): Show |
15 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0016others(12): Show | 15 | HG00735.hp1 HG01123.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1909+7020_1909+702 others(13): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927895 | |||||
| chr14:99927897
|
G | A | 2 | a0001c0004t0001g0009a0001c0004t0005g0266 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1909+7020G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927897 | ||||||
| chr14:99927898
|
T | A | 1 | a0003c0002t0002g0050 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1909+7021T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927898 | ||||||
| chr14:99927898
|
T | G | 3 | a0001c0003t0004g0027a0001c0003t0004g0258a0001c0005t0004g0284 | 3 | HG00609.hp2 HG02083.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1909+7021T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927898 | ||||||
| chr14:99927900
|
GTGGTGGT others(143): Show |
G | 1 | a0001c0005t0004g0284 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1909+7037_1909+718 others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927900 | |||||
| chr14:99927901
|
T | A | 1 | a0002c0001t0002g0278 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1909+7024T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927901 | ||||||
| chr14:99927901
|
T | G | 265 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0007others(262): Show | 267 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.1909+7024T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927901 | ||||||
| chr14:99927901
|
T | TGGTGGTA others(362): Show |
1 | a0001c0003t0001g0111 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1909+7030_1909+703 others(373): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927901 | |||||
| chr14:99927904
|
T | G | 11 | a0001c0003t0004g0027a0001c0003t0004g0258a0003c0002t0001g0019others(8): Show | 11 | HG00609.hp2 HG02083.hp2 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.1909+7027T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927904 | ||||||
| chr14:99927906
|
G | C | 1 | a0001c0004t0001g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1909+7029G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927906 | ||||||
| chr14:99927906
|
GTGGTGGT others(26): Show |
G | 1 | a0002c0001t0019g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1909+7037_1909+706 others(37): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927906 | |||||
| chr14:99927907
|
T | A | 1 | a0003c0002t0002g0050 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1909+7030T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927907 | ||||||
| chr14:99927909
|
G | A | 1 | a0002c0001t0002g0110 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1909+7032G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927909 | ||||||
| chr14:99927910
|
T | G | 2 | a0001c0003t0004g0027a0001c0003t0004g0258 | 2 | HG00609.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.1909+7033T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927910 | ||||||
| chr14:99927912
|
G | A | 5 | a0001c0003t0001g0243a0001c0003t0001g0244a0001c0003t0001g0245others(2): Show | 5 | HG02723.hp2 HG02922.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1909+7035G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927912 | ||||||
| chr14:99927913
|
TATTGGTG others(203): Show |
T | 2 | a0001c0003t0004g0027a0001c0003t0004g0258 | 2 | HG00609.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.1909+7037_1909+724 others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927913 | ||||||
| chr14:99927914
|
A | G | 11 | a0001c0003t0001g0243a0001c0003t0001g0244a0001c0003t0001g0245others(8): Show | 11 | HG01168.hp2 HG02273.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1909+7037A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927914 | ||||||
| chr14:99927915
|
T | A | 1 | a0003c0002t0002g0203 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1909+7038T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927915 | ||||||
| chr14:99927915
|
T | G | 10 | a0001c0003t0001g0243a0001c0003t0001g0244a0001c0003t0001g0245others(7): Show | 10 | HG01168.hp2 HG02273.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1909+7038T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927915 | ||||||
| chr14:99927918
|
G | A | 1 | a0003c0002t0002g0050 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1909+7041G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927918 | ||||||
| chr14:99927919
|
TGGTGGTG others(80): Show |
T | 2 | a0002c0001t0002g0056a0002c0001t0002g0150 | 2 | NA18939.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.1909+7053_1909+713 others(91): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927919 | |||||
| chr14:99927921
|
G | A | 3 | a0001c0004t0001g0009a0001c0004t0005g0266a0002c0001t0002g0278 | 3 | HG01071.hp2 HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1909+7044G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927921 | ||||||
| chr14:99927921
|
G | GTGGTGGT others(1941): Show |
1 | a0001c0003t0001g0233 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1909+7052_1909+705 others(1952): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927921 | |||||
| chr14:99927921
|
G | GTGGTGGT others(1076): Show |
2 | a0001c0003t0001g0272a0001c0003t0001g0273 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1909+7052_1909+705 others(1087): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927921 | |||||
| chr14:99927921
|
G | GTGGTGGT others(1076): Show |
2 | a0001c0003t0001g0220a0001c0003t0001g0221 | 2 | HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1909+7052_1909+705 others(1087): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927921 | |||||
| chr14:99927921
|
G | GTGGTGGT others(1079): Show |
1 | a0001c0003t0001g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1909+7052_1909+705 others(1090): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927921 | |||||
| chr14:99927921
|
G | GTGGTGGT others(1076): Show |
1 | a0001c0003t0001g0232 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1909+7052_1909+705 others(1087): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927921 | |||||
| chr14:99927924
|
G | A | 1 | a0002c0001t0003g0119 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1909+7047G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927924 | ||||||
| chr14:99927924
|
G | GTGGTGGT others(751): Show |
1 | a0001c0003t0007g0014 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1909+7052_1909+705 others(762): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927924 | |||||
| chr14:99927924
|
GTGGTGAT others(278): Show |
G | 3 | a0001c0003t0001g0225a0001c0003t0001g0260a0001c0004t0001g0255 | 3 | HG02451.hp2 HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1909+7062_1909+734 others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927924 | |||||
| chr14:99927927
|
G | T | 1 | a0001c0003t0001g0163 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1909+7050G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927927 | ||||||
| chr14:99927930
|
A | ATGG | 3 | a0001c0003t0001g0008a0001c0003t0001g0010a0001c0003t0001g0214 | 3 | HG02486.hp2 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1909+7059_1909+706 others(7): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927930 | |||||
| chr14:99927930
|
A | ATGGTGGT others(276): Show |
1 | a0002c0001t0002g0031 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1909+7077_1909+707 others(287): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927930 | |||||
| chr14:99927930
|
A | ATGGTGGT others(1952): Show |
1 | a0002c0001t0001g0092 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1909+7061_1909+706 others(1963): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927930 | |||||
| chr14:99927930
|
A | ATGGTGGT others(239): Show |
1 | a0001c0003t0001g0080 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1909+7061_1909+706 others(250): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927930 | |||||
| chr14:99927930
|
A | G | 15 | a0001c0003t0001g0012a0001c0003t0001g0220a0001c0003t0001g0221others(12): Show | 15 | HG01071.hp2 HG01109.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1909+7053A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927930 | ||||||
| chr14:99927930
|
ATGGTGGT others(191): Show |
A | 1 | a0001c0003t0002g0252 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1909+7062_1909+725 others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927930 | |||||
| chr14:99927933
|
G | GTGGTGGT others(104): Show |
1 | a0001c0004t0003g0064 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1909+7061_1909+706 others(115): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927933 | |||||
| chr14:99927933
|
GTGGTGAT others(143): Show |
G | 1 | a0002c0001t0002g0151 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1909+7095_1909+724 others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927933 | |||||
| chr14:99927934
|
T | A | 1 | a0003c0014t0004g0254 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1909+7057T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927934 | ||||||
| chr14:99927934
|
T | TGGTGGTG others(56): Show |
1 | a0004c0008t0004g0004 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1909+7061_1909+706 others(67): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927934 | |||||
| chr14:99927939
|
A | ATGG | 30 | a0001c0003t0003g0032a0001c0003t0003g0033a0001c0003t0003g0034others(27): Show | 30 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.1909+7075_1909+707 others(7): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927939 | |||||
| chr14:99927939
|
A | ATGGTGGT others(764): Show |
1 | a0003c0002t0001g0198 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1909+7070_1909+707 others(775): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927939 | |||||
| chr14:99927939
|
A | ATGGTGGT others(401): Show |
1 | a0003c0002t0001g0204 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1909+7070_1909+707 others(412): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927939 | |||||
| chr14:99927939
|
A | ATGGTGGT others(386): Show |
1 | a0003c0002t0006g0043 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1909+7071_1909+707 others(397): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927939 | |||||
| chr14:99927939
|
A | ATGGTGGT others(503): Show |
1 | a0003c0002t0006g0088 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1909+7071_1909+707 others(514): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927939 | |||||
| chr14:99927939
|
A | G | 16 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0001g0243others(13): Show | 16 | HG01975.hp1 HG02055.hp2 HG02293.hp1 others(13): Show |
intron_variant | MODIFIER | c.1909+7062A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927939 | ||||||
| chr14:99927940
|
T | TGGTGGTG others(65): Show |
1 | a0001c0003t0007g0117 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1909+7070_1909+707 others(76): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927940 | |||||
| chr14:99927940
|
T | TGGTGGTG others(2): Show |
4 | a0003c0002t0001g0223a0003c0002t0006g0042a0003c0002t0006g0228others(1): Show | 4 | HG01109.hp1 HG02273.hp2 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.1909+7071_1909+707 others(13): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927940 | |||||
| chr14:99927943
|
T | C | 1 | a0002c0001t0019g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1909+7066T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927943 | ||||||
| chr14:99927943
|
T | TGGTGGTG others(5): Show |
2 | a0002c0001t0003g0188a0002c0001t0003g0189 | 2 | NA18957.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1909+7078_1909+708 others(16): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927943 | |||||
| chr14:99927944
|
G | A | 2 | a0002c0001t0002g0046a0007c0012t0002g0275 | 2 | HG02293.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1909+7067G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927944 | ||||||
| chr14:99927945
|
G | GTGGTGA | 4 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0016others(1): Show | 4 | HG02109.hp1 HG02723.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1909+7073_1909+707 others(10): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927945 | |||||
| chr14:99927945
|
G | GTGGTGGT others(86): Show |
2 | a0001c0003t0001g0167a0001c0003t0001g0168 | 2 | HG02818.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1909+7076_1909+707 others(97): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927945 | |||||
| chr14:99927945
|
G | GTGGTGGT others(5): Show |
1 | a0001c0004t0004g0017 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1909+7077_1909+707 others(16): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927945 | |||||
| chr14:99927945
|
G | GTGGTGGT others(557): Show |
1 | a0002c0001t0003g0142 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1909+7077_1909+707 others(568): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927945 | |||||
| chr14:99927945
|
GTGGTGGT others(137): Show |
G | 1 | a0007c0012t0002g0275 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1909+7078_1909+722 others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927945 | |||||
| chr14:99927946
|
T | A | 2 | a0001c0003t0002g0105a0001c0003t0002g0106 | 2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1909+7069T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927946 | ||||||
| chr14:99927946
|
TGGTGGTG others(152): Show |
T | 1 | a0002c0001t0002g0061 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1909+7078_1909+723 others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927946 | |||||
| chr14:99927946
|
TGGTGGTG others(170): Show |
T | 1 | a0002c0001t0002g0144 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1909+7078_1909+725 others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927946 | |||||
| chr14:99927948
|
G | A | 2 | a0001c0004t0013g0108a0003c0002t0002g0050 | 2 | HG02055.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1909+7071G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927948 | ||||||
| chr14:99927949
|
T | A | 3 | a0003c0002t0001g0198a0003c0002t0001g0204a0003c0002t0006g0043 | 3 | HG02004.hp1 HG03492.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.1909+7072T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927949 | ||||||
| chr14:99927949
|
T | TGGAGGTG others(863): Show |
1 | a0001c0004t0001g0040 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1909+7074_1909+707 others(874): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927949 | |||||
| chr14:99927949
|
T | TGGTGGTG others(869): Show |
1 | a0001c0004t0001g0123 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1909+7077_1909+707 others(880): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927949 | |||||
| chr14:99927949
|
T | TGGTGGTG others(143): Show |
1 | a0001c0004t0003g0145 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1909+7077_1909+707 others(154): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927949 | |||||
| chr14:99927949
|
T | TGGTGGTG others(203): Show |
1 | a0001c0004t0003g0149 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1909+7077_1909+707 others(214): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927949 | |||||
| chr14:99927949
|
T | TGGTGGTG others(422): Show |
1 | a0001c0004t0003g0030 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1909+7077_1909+707 others(433): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927949 | |||||
| chr14:99927949
|
T | TGGTGGTG others(839): Show |
1 | a0003c0002t0017g0028 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1909+7077_1909+707 others(850): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927949 | |||||
| chr14:99927949
|
T | TGGTGGTG others(728): Show |
1 | a0003c0002t0001g0192 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1909+7077_1909+707 others(739): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927949 | |||||
| chr14:99927950
|
G | A | 1 | a0002c0001t0002g0046 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1909+7073G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927950 | ||||||
| chr14:99927951
|
G | A | 1 | a0003c0002t0006g0088 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1909+7074G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927951 | ||||||
| chr14:99927951
|
G | GTGGTGGA others(194): Show |
1 | a0001c0004t0003g0280 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1909+7077_1909+707 others(205): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927951 | |||||
| chr14:99927952
|
TGGA | T | 3 | a0001c0004t0013g0108a0001c0005t0004g0285a0001c0007t0002g0005 | 3 | HG02055.hp1 HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1909+7078_1909+708 others(7): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927952 | |||||
| chr14:99927953
|
G | A | 1 | a0002c0001t0002g0046 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1909+7076G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927953 | ||||||
| chr14:99927953
|
G | GATGGTGG others(286): Show |
1 | a0004c0008t0004g0268 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1909+7076_1909+707 others(297): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927953 | ||||||
| chr14:99927954
|
G | A | 6 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0016others(3): Show | 6 | HG02109.hp1 HG02280.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1909+7077G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927954 | ||||||
| chr14:99927954
|
G | GGGGTGGG others(103): Show |
1 | a0002c0001t0002g0176 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1909+7077_1909+707 others(114): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927954 | ||||||
| chr14:99927954
|
G | GGTGGAGG others(4): Show |
1 | a0001c0004t0011g0156 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1909+7077_1909+707 others(15): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927954 | ||||||
| chr14:99927954
|
G | GTGGAGGT others(383): Show |
1 | a0001c0004t0003g0127 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1909+7077_1909+707 others(394): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927954 | ||||||
| chr14:99927955
|
A | AGGTGGTG others(404): Show |
1 | a0003c0002t0001g0146 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1909+7088_1909+708 others(415): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927955 | |||||
| chr14:99927955
|
A | AGGTGGTG others(368): Show |
1 | a0003c0002t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1909+7088_1909+708 others(379): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927955 | |||||
| chr14:99927955
|
A | AGGTGGTG others(476): Show |
1 | a0001c0003t0008g0271 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1909+7092_1909+709 others(487): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927955 | |||||
| chr14:99927955
|
A | AGGTGGTG others(371): Show |
1 | a0001c0005t0008g0077 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1909+7092_1909+709 others(382): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927955 | |||||
| chr14:99927955
|
A | AGGTGGTG others(419): Show |
1 | a0003c0002t0008g0238 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1909+7092_1909+709 others(430): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927955 | |||||
| chr14:99927955
|
A | AGGTGGTG others(1925): Show |
1 | a0003c0002t0001g0036 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1909+7094_1909+709 others(1936): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927955 | |||||
| chr14:99927955
|
A | AGGTGGTG others(542): Show |
1 | a0001c0005t0001g0250 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1909+7094_1909+709 others(553): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927955 | |||||
| chr14:99927955
|
A | AGGTGGTG others(98): Show |
1 | a0003c0002t0001g0161 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1909+7094_1909+709 others(109): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927955 | |||||
| chr14:99927955
|
A | AGGTGGTG others(404): Show |
1 | a0003c0002t0001g0186 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1909+7094_1909+709 others(415): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927955 | |||||
| chr14:99927955
|
A | AGGTGGTG others(611): Show |
1 | a0003c0002t0001g0100 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1909+7094_1909+709 others(622): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927955 | |||||
| chr14:99927955
|
A | AGGTGGTG others(530): Show |
2 | a0003c0002t0001g0055a0003c0002t0002g0222 | 2 | HG01981.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1909+7094_1909+709 others(541): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927955 | |||||
| chr14:99927955
|
A | AGGTGGTG others(704): Show |
1 | a0003c0002t0001g0044 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1909+7094_1909+709 others(715): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927955 | |||||
| chr14:99927955
|
A | AGGTGGTG others(353): Show |
4 | a0001c0004t0003g0049a0003c0002t0003g0159a0003c0002t0003g0169others(1): Show | 4 | NA18984.hp2 NA18994.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.1909+7094_1909+709 others(364): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927955 | |||||
| chr14:99927955
|
A | G | 2 | a0001c0004t0011g0156a0002c0001t0019g0234 | 2 | HG02083.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1909+7078A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927955 | ||||||
| chr14:99927955
|
A | T | 48 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0016others(45): Show | 48 | HG00323.hp1 HG01074.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.1909+7078A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927955 | ||||||
| chr14:99927957
|
G | A | 2 | a0001c0004t0004g0017a0004c0008t0004g0004 | 2 | HG02257.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1909+7080G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927957 | ||||||
| chr14:99927957
|
G | GAGGTGGT others(195): Show |
3 | a0002c0001t0002g0021a0002c0001t0002g0066a0002c0001t0002g0129 | 3 | HG01123.hp2 HG01169.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1909+7080_1909+708 others(206): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927957 | ||||||
| chr14:99927957
|
G | GAGGTGGT others(1904): Show |
1 | a0001c0004t0003g0096 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1909+7080_1909+708 others(1915): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927957 | ||||||
| chr14:99927957
|
G | GAGGTGGT others(350): Show |
1 | a0001c0003t0003g0279 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1909+7080_1909+708 others(361): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927957 | ||||||
| chr14:99927958
|
T | A | 2 | a0001c0003t0001g0286a0001c0003t0007g0281 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1909+7081T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927958 | ||||||
| chr14:99927960
|
G | A | 3 | a0001c0004t0003g0064a0001c0005t0004g0285a0001c0007t0002g0005 | 3 | HG01975.hp1 HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1909+7083G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927960 | ||||||
| chr14:99927960
|
G | GTGGTGGT others(1004): Show |
1 | a0001c0004t0003g0048 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1909+7094_1909+709 others(1015): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927960 | |||||
| chr14:99927961
|
T | C | 1 | a0002c0001t0002g0046 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1909+7084T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927961 | ||||||
| chr14:99927963
|
G | A | 9 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0004t0001g0009others(6): Show | 9 | HG00323.hp1 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1909+7086G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927963 | ||||||
| chr14:99927963
|
G | GTGA | 4 | a0001c0003t0009g0251a0001c0005t0009g0078a0003c0002t0001g0215others(1): Show | 4 | HG02572.hp2 HG02809.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1909+7088_1909+708 others(7): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927963 | |||||
| chr14:99927963
|
G | GTGATGGT others(320): Show |
1 | a0003c0002t0012g0253 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1909+7088_1909+708 others(331): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927963 | |||||
| chr14:99927963
|
G | GTGGTGGT others(732): Show |
1 | a0001c0004t0003g0074 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1909+7094_1909+709 others(743): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927963 | |||||
| chr14:99927963
|
G | GTGGTGGT others(449): Show |
3 | a0001c0003t0003g0184a0001c0004t0001g0115a0001c0004t0003g0131 | 3 | HG00140.hp1 HG03654.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1909+7094_1909+709 others(460): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927963 | |||||
| chr14:99927963
|
G | GTGGTGGT others(185): Show |
10 | a0001c0004t0003g0035a0001c0004t0003g0090a0001c0004t0003g0180others(7): Show | 10 | HG01069.hp1 HG01071.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.1909+7094_1909+709 others(196): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927963 | |||||
| chr14:99927963
|
G | GTGGTGGT others(428): Show |
1 | a0002c0001t0003g0121 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1909+7094_1909+709 others(439): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927963 | |||||
| chr14:99927963
|
G | GTGGTGGT others(506): Show |
2 | a0003c0002t0001g0263a0003c0002t0001g0264 | 2 | NA18966.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1909+7094_1909+709 others(517): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927963 | |||||
| chr14:99927963
|
G | GTGGTGGT others(320): Show |
1 | a0003c0002t0010g0200 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1909+7094_1909+709 others(331): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927963 | |||||
| chr14:99927963
|
G | GTGGTGGT others(347): Show |
1 | a0003c0002t0001g0002 | 2 | HG00639.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.1909+7094_1909+709 others(358): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927963 | |||||
| chr14:99927963
|
G | GTGGTGGT others(1085): Show |
1 | a0001c0013t0001g0126 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1909+7094_1909+709 others(1096): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927963 | |||||
| chr14:99927963
|
G | GTGGTGGT others(329): Show |
1 | a0001c0003t0001g0085 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1909+7094_1909+709 others(340): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927963 | |||||
| chr14:99927963
|
G | GTGGTGGT others(359): Show |
1 | a0001c0003t0001g0152 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1909+7094_1909+709 others(370): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927963 | |||||
| chr14:99927963
|
G | GTGGTGGT others(1016): Show |
1 | a0001c0003t0001g0259 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1909+7094_1909+709 others(1027): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927963 | |||||
| chr14:99927964
|
T | G | 1 | a0002c0001t0019g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1909+7087T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927964 | ||||||
| chr14:99927965
|
G | A | 1 | a0001c0003t0004g0141 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1909+7088G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927965 | ||||||
| chr14:99927966
|
G | A | 1 | a0005c0009t0002g0132 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1909+7089G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927966 | ||||||
| chr14:99927966
|
GTGGTGAT others(77): Show |
G | 1 | a0002c0001t0002g0081 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1909+7095_1909+717 others(88): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927966 | |||||
| chr14:99927967
|
T | TGGTGGTG others(584): Show |
1 | a0002c0001t0015g0109 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1909+7094_1909+709 others(595): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927967 | |||||
| chr14:99927969
|
G | A | 1 | a0003c0002t0002g0050 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1909+7092G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927969 | ||||||
| chr14:99927969
|
G | GTGGTGGT others(485): Show |
1 | a0002c0001t0002g0182 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1909+7094_1909+709 others(496): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927969 | |||||
| chr14:99927969
|
G | GTGGTGGT others(578): Show |
1 | a0001c0003t0001g0015 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1909+7094_1909+709 others(589): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927969 | |||||
| chr14:99927969
|
G | GTGGTGGT others(446): Show |
1 | a0001c0005t0005g0265 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1909+7094_1909+709 others(457): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927969 | |||||
| chr14:99927969
|
G | GTGGTGGT others(575): Show |
3 | a0003c0002t0001g0170a0003c0002t0001g0171a0003c0002t0001g0172 | 3 | NA18957.hp2 NA19063.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1909+7094_1909+709 others(586): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927969 | |||||
| chr14:99927969
|
G | GTGGTGGT others(485): Show |
1 | a0003c0002t0001g0187 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1909+7094_1909+709 others(496): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927969 | |||||
| chr14:99927969
|
G | GTGGTGGT others(494): Show |
1 | a0001c0003t0001g0086 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1909+7094_1909+709 others(505): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927969 | |||||
| chr14:99927969
|
G | GTGGTGGT others(122): Show |
1 | a0001c0003t0001g0111 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1909+7094_1909+709 others(133): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927969 | |||||
| chr14:99927969
|
GTGA | G | 34 | a0001c0003t0001g0001a0001c0003t0001g0041a0001c0003t0001g0163others(31): Show | 35 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.1909+7095_1909+709 others(7): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927969 | |||||
| chr14:99927970
|
T | G | 1 | a0002c0001t0019g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1909+7093T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927970 | ||||||
| chr14:99927971
|
G | A | 1 | a0001c0003t0004g0141 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1909+7094G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927971 | ||||||
| chr14:99927972
|
A | ATGGTGGT others(380): Show |
1 | a0002c0001t0002g0084 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1909+7110_1909+711 others(391): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927972 | |||||
| chr14:99927972
|
A | G | 99 | a0001c0003t0001g0008a0001c0003t0001g0010a0001c0003t0001g0012others(96): Show | 100 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.1909+7095A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927972 | ||||||
| chr14:99927972
|
ATGGTGGT others(128): Show |
A | 2 | a0002c0001t0003g0098a0002c0001t0003g0119 | 2 | HG02040.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1909+7111_1909+724 others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927972 | |||||
| chr14:99927972
|
ATGGTGGT others(161): Show |
A | 1 | a0002c0001t0002g0093 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1909+7164_1909+733 others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927972 | |||||
| chr14:99927973
|
T | A | 1 | a0001c0004t0002g0047 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1909+7096T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927973 | ||||||
| chr14:99927973
|
T | G | 1 | a0002c0001t0002g0046 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1909+7096T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927973 | ||||||
| chr14:99927973
|
T | TGGTGGTG others(272): Show |
1 | a0002c0001t0002g0082 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1909+7110_1909+711 others(283): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927973 | |||||
| chr14:99927973
|
T | TGGTGGTG others(1613): Show |
1 | a0003c0014t0004g0254 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1909+7112_1909+711 others(1624): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927973 | |||||
| chr14:99927974
|
G | A | 1 | a0001c0003t0004g0141 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1909+7097G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927974 | ||||||
| chr14:99927975
|
G | A | 1 | a0001c0004t0003g0022 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1909+7098G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927975 | ||||||
| chr14:99927975
|
G | GTGGTGGA others(698): Show |
1 | a0003c0002t0003g0125 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1909+7104_1909+710 others(709): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927975 | |||||
| chr14:99927975
|
G | GTGGTGGT others(248): Show |
2 | a0001c0003t0005g0246a0001c0003t0005g0247 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1909+7109_1909+711 others(259): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927975 | |||||
| chr14:99927975
|
G | GTGGTGGT others(26): Show |
1 | a0001c0003t0001g0158 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1909+7109_1909+711 others(37): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927975 | |||||
| chr14:99927975
|
G | GTGGTGGT others(41): Show |
5 | a0001c0003t0001g0113a0001c0003t0001g0114a0001c0003t0001g0120others(2): Show | 5 | HG01515.hp2 HG01884.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1909+7109_1909+711 others(52): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927975 | |||||
| chr14:99927975
|
G | GTGGTGGT others(179): Show |
1 | a0003c0002t0001g0210 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1909+7109_1909+711 others(190): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927975 | |||||
| chr14:99927975
|
G | GTGGTGGT others(347): Show |
1 | a0003c0016t0014g0060 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1909+7109_1909+711 others(358): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927975 | |||||
| chr14:99927975
|
G | GTGGTGGT others(506): Show |
1 | a0001c0003t0001g0112 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1909+7109_1909+711 others(517): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927975 | |||||
| chr14:99927975
|
G | GTGGTGGT others(674): Show |
1 | a0003c0002t0003g0155 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1909+7109_1909+711 others(685): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927975 | |||||
| chr14:99927975
|
G | GTGGTGGT others(8): Show |
1 | a0001c0004t0005g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1909+7113_1909+712 others(19): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927975 | |||||
| chr14:99927976
|
T | G | 1 | a0002c0001t0019g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1909+7099T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927976 | ||||||
| chr14:99927976
|
T | TGGTGATG others(257): Show |
2 | a0002c0001t0002g0052a0002c0001t0002g0174 | 2 | HG03927.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1909+7103_1909+710 others(268): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927976 | |||||
| chr14:99927976
|
T | TGGTGGTG others(758): Show |
1 | a0003c0002t0001g0154 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1909+7106_1909+710 others(769): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927976 | |||||
| chr14:99927976
|
T | TGGTGGTG others(431): Show |
1 | a0003c0002t0001g0217 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1909+7109_1909+711 others(442): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927976 | |||||
| chr14:99927977
|
G | A | 1 | a0005c0009t0002g0132 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1909+7100G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927977 | ||||||
| chr14:99927978
|
G | C | 1 | a0005c0009t0002g0132 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1909+7101G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927978 | ||||||
| chr14:99927978
|
G | GTGGTGGT others(1148): Show |
1 | a0001c0004t0001g0135 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1909+7109_1909+711 others(1159): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927978 | |||||
| chr14:99927978
|
G | GTGGTGGT others(791): Show |
1 | a0001c0007t0018g0241 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1909+7109_1909+711 others(802): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927978 | |||||
| chr14:99927979
|
T | A | 1 | a0001c0004t0003g0064 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1909+7102T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927979 | ||||||
| chr14:99927979
|
T | TGGAGGTG others(128): Show |
1 | a0001c0003t0003g0277 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1909+7104_1909+710 others(139): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927979 | |||||
| chr14:99927979
|
T | TGGAGGTG others(83): Show |
3 | a0001c0004t0003g0059a0001c0004t0003g0197a0002c0001t0003g0137 | 3 | HG02071.hp2 HG02293.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1909+7104_1909+710 others(94): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927979 | |||||
| chr14:99927979
|
T | TGGTGGTG others(14): Show |
1 | a0002c0001t0002g0224 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1909+7112_1909+711 others(25): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927979 | |||||
| chr14:99927981
|
G | A | 16 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0016others(13): Show | 16 | HG01123.hp2 HG01169.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1909+7104G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927981 | ||||||
| chr14:99927982
|
T | A | 6 | a0001c0003t0001g0008a0001c0004t0003g0029a0001c0004t0003g0075others(3): Show | 6 | HG01123.hp1 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1909+7105T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927982 | ||||||
| chr14:99927982
|
T | C | 1 | a0001c0003t0004g0141 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1909+7105T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927982 | ||||||
| chr14:99927982
|
T | G | 1 | a0002c0001t0002g0046 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1909+7105T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927982 | ||||||
| chr14:99927984
|
G | A | 1 | a0003c0015t0001g0013 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1909+7107G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927984 | ||||||
| chr14:99927985
|
T | G | 1 | a0001c0004t0011g0156 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1909+7108T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927985 | ||||||
| chr14:99927985
|
T | TATTGGTG others(139): Show |
1 | a0001c0003t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1909+7108_1909+710 others(150): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927985 | ||||||
| chr14:99927987
|
G | A | 10 | a0001c0003t0001g0012a0001c0003t0001g0220a0001c0003t0001g0221others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1909+7110G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927987 | ||||||
| chr14:99927988
|
T | A | 1 | a0003c0002t0001g0044 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1909+7111T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927988 | ||||||
| chr14:99927989
|
G | A | 1 | a0002c0001t0019g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1909+7112G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927989 | ||||||
| chr14:99927990
|
A | ATGG | 3 | a0001c0004t0003g0149a0001c0005t0001g0079a0003c0002t0001g0130 | 3 | HG03471.hp1 HG06807.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.1909+7126_1909+712 others(7): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927990 | |||||
| chr14:99927990
|
A | G | 33 | a0001c0003t0001g0008a0001c0003t0001g0012a0001c0003t0001g0220others(30): Show | 33 | HG01109.hp2 HG01123.hp1 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1909+7113A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927990 | ||||||
| chr14:99927990
|
A | T | 1 | a0002c0001t0019g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1909+7113A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927990 | ||||||
| chr14:99927990
|
ATGGTGGT others(68): Show |
A | 1 | a0002c0001t0002g0173 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1909+7129_1909+720 others(79): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927990 | |||||
| chr14:99927990
|
ATGGTGGT others(110): Show |
A | 1 | a0002c0001t0002g0089 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1909+7164_1909+728 others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927990 | |||||
| chr14:99927993
|
G | A | 1 | a0005c0009t0002g0132 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1909+7116G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927993 | ||||||
| chr14:99927993
|
G | GTGGTGGT others(380): Show |
1 | a0003c0002t0001g0185 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1909+7128_1909+712 others(391): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927993 | |||||
| chr14:99927994
|
T | G | 1 | a0001c0003t0004g0141 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1909+7117T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927994 | ||||||
| chr14:99927996
|
G | A | 6 | a0001c0003t0001g0220a0001c0003t0001g0221a0001c0003t0001g0272others(3): Show | 6 | HG01928.hp1 HG02523.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1909+7119G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927996 | ||||||
| chr14:99927997
|
T | A | 4 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0016others(1): Show | 4 | HG02109.hp1 HG02723.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1909+7120T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927997 | ||||||
| chr14:99927999
|
G | A | 8 | a0001c0003t0007g0281a0001c0004t0013g0108a0001c0013t0001g0126others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1909+7122G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99927999 | ||||||
| chr14:99927999
|
G | GTGGTGAT others(446): Show |
1 | a0003c0010t0006g0226 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1909+7127_1909+712 others(457): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927999 | |||||
| chr14:99927999
|
G | GTGGTGAT others(533): Show |
1 | a0003c0002t0006g0228 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1909+7127_1909+712 others(544): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927999 | |||||
| chr14:99927999
|
G | GTGGTGAT others(533): Show |
1 | a0003c0002t0006g0140 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1909+7127_1909+712 others(544): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927999 | |||||
| chr14:99927999
|
G | GTGGTGAT others(416): Show |
2 | a0003c0002t0001g0223a0003c0002t0006g0042 | 2 | HG01109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1909+7127_1909+712 others(427): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99927999 | |||||
| chr14:99928000
|
T | G | 2 | a0001c0003t0004g0141a0003c0002t0002g0050 | 2 | HG02273.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.1909+7123T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928000 | ||||||
| chr14:99928001
|
G | A | 1 | a0002c0001t0002g0046 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1909+7124G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928001 | ||||||
| chr14:99928002
|
G | A | 2 | a0001c0003t0001g0010a0003c0002t0001g0054 | 2 | HG01496.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1909+7125G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928002 | ||||||
| chr14:99928002
|
G | T | 2 | a0001c0003t0001g0008a0002c0001t0002g0046 | 2 | HG02293.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1909+7125G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928002 | ||||||
| chr14:99928002
|
GTGGAGGT others(200): Show |
G | 1 | a0001c0007t0002g0005 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1909+7129_1909+733 others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928002 | |||||
| chr14:99928003
|
TGGA | T | 5 | a0001c0003t0007g0014a0002c0001t0001g0062a0002c0001t0002g0031others(2): Show | 5 | HG00735.hp1 HG01192.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1909+7129_1909+713 others(7): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928003 | |||||
| chr14:99928004
|
G | A | 1 | a0001c0004t0003g0048 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1909+7127G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928004 | ||||||
| chr14:99928005
|
G | A | 10 | a0001c0003t0008g0271a0001c0004t0003g0029a0001c0004t0003g0075others(7): Show | 10 | HG01123.hp1 HG01256.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1909+7128G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928005 | ||||||
| chr14:99928005
|
G | GTGGTATT others(1049): Show |
1 | a0001c0003t0001g0274 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1909+7128_1909+712 others(1060): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928005 | ||||||
| chr14:99928006
|
A | AGGTGGTG others(341): Show |
1 | a0001c0005t0001g0079 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1909+7149_1909+715 others(352): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928006 | |||||
| chr14:99928006
|
A | AGGTGGTG others(95): Show |
2 | a0002c0001t0003g0188a0002c0001t0003g0189 | 2 | NA18957.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1909+7158_1909+715 others(106): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928006 | |||||
| chr14:99928006
|
A | AGGTGGTG others(500): Show |
1 | a0002c0001t0002g0101 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1909+7163_1909+716 others(511): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928006 | |||||
| chr14:99928006
|
A | G | 2 | a0001c0003t0004g0141a0003c0002t0002g0050 | 2 | HG02273.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.1909+7129A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928006 | ||||||
| chr14:99928006
|
A | T | 105 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0007others(102): Show | 106 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.1909+7129A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928006 | ||||||
| chr14:99928008
|
G | A | 25 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0016others(22): Show | 25 | HG01109.hp1 HG01255.hp2 HG01515.hp1 others(22): Show |
intron_variant | MODIFIER | c.1909+7131G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928008 | ||||||
| chr14:99928008
|
G | GTGATGGT others(482): Show |
1 | a0003c0002t0001g0190 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1909+7133_1909+713 others(493): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928008 | |||||
| chr14:99928008
|
G | GTGATGGT others(362): Show |
1 | a0003c0002t0001g0019 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1909+7133_1909+713 others(373): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928008 | |||||
| chr14:99928008
|
G | GTGATGGT others(1061): Show |
1 | a0001c0004t0001g0143 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1909+7133_1909+713 others(1072): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928008 | |||||
| chr14:99928008
|
G | GTGATGGT others(1052): Show |
1 | a0001c0004t0010g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1909+7133_1909+713 others(1063): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928008 | |||||
| chr14:99928008
|
G | GTGATGGT others(467): Show |
1 | a0003c0002t0001g0104 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1909+7133_1909+713 others(478): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928008 | |||||
| chr14:99928008
|
G | GTGATGGT others(434): Show |
1 | a0003c0002t0003g0212 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1909+7133_1909+713 others(445): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928008 | |||||
| chr14:99928008
|
G | GTGATGGT others(455): Show |
1 | a0001c0003t0001g0193 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1909+7133_1909+713 others(466): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928008 | |||||
| chr14:99928008
|
G | GTGATGGT others(434): Show |
1 | a0001c0004t0001g0091 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1909+7133_1909+713 others(445): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928008 | |||||
| chr14:99928008
|
G | GTGATGGT others(953): Show |
1 | a0001c0003t0001g0282 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1909+7133_1909+713 others(964): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928008 | |||||
| chr14:99928008
|
G | GTGATGGT others(839): Show |
1 | a0001c0003t0001g0270 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1909+7133_1909+713 others(850): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928008 | |||||
| chr14:99928008
|
G | GTGATGGT others(437): Show |
5 | a0003c0002t0001g0166a0003c0002t0001g0201a0003c0002t0001g0207others(2): Show | 5 | HG02015.hp2 NA18969.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.1909+7133_1909+713 others(448): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928008 | |||||
| chr14:99928008
|
G | GTGATGGT others(803): Show |
1 | a0003c0002t0001g0070 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1909+7133_1909+713 others(814): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928008 | |||||
| chr14:99928008
|
G | GTGATGGT others(1277): Show |
1 | a0001c0003t0001g0001 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1909+7133_1909+713 others(1288): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928008 | |||||
| chr14:99928008
|
G | GTGATGGT others(383): Show |
1 | a0003c0002t0001g0213 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1909+7133_1909+713 others(394): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928008 | |||||
| chr14:99928008
|
G | GTGATGGT others(632): Show |
1 | a0001c0004t0005g0249 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1909+7133_1909+713 others(643): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928008 | |||||
| chr14:99928008
|
G | GTGATGGT others(1193): Show |
1 | a0001c0005t0005g0097 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1909+7133_1909+713 others(1204): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928008 | |||||
| chr14:99928008
|
G | GTGATGGT others(1238): Show |
1 | a0001c0005t0005g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1909+7133_1909+713 others(1249): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928008 | |||||
| chr14:99928008
|
G | GTGATGGT others(596): Show |
1 | a0001c0003t0001g0163 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1909+7133_1909+713 others(607): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928008 | |||||
| chr14:99928008
|
G | GTGATGGT others(425): Show |
1 | a0003c0002t0001g0205 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1909+7133_1909+713 others(436): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928008 | |||||
| chr14:99928008
|
G | GTGATGGT others(455): Show |
2 | a0003c0002t0001g0037a0003c0002t0001g0209 | 2 | HG01943.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1909+7133_1909+713 others(466): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928008 | |||||
| chr14:99928008
|
G | GTGATGGT others(854): Show |
1 | a0003c0002t0001g0191 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1909+7133_1909+713 others(865): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928008 | |||||
| chr14:99928008
|
G | GTGATGGT others(722): Show |
1 | a0001c0003t0001g0041 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1909+7133_1909+713 others(733): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928008 | |||||
| chr14:99928008
|
G | GTGATGGT others(476): Show |
1 | a0003c0002t0001g0094 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1909+7133_1909+713 others(487): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928008 | |||||
| chr14:99928008
|
G | GTGATGGT others(605): Show |
2 | a0003c0002t0001g0053a0003c0002t0001g0262 | 2 | HG00438.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1909+7133_1909+713 others(616): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928008 | |||||
| chr14:99928008
|
G | GTGGTGGT others(23): Show |
1 | a0001c0004t0001g0040 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1909+7151_1909+715 others(34): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928008 | |||||
| chr14:99928009
|
T | TGATGGTG others(704): Show |
1 | a0002c0001t0002g0133 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1909+7133_1909+713 others(715): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928009 | |||||
| chr14:99928009
|
T | TGGTGGAG others(362): Show |
1 | a0002c0001t0002g0278 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1909+7137_1909+713 others(373): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928009 | |||||
| chr14:99928009
|
T | TGGTGGTG others(167): Show |
1 | a0002c0001t0002g0025 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1909+7163_1909+716 others(178): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928009 | |||||
| chr14:99928009
|
TGGTGGTG others(158): Show |
T | 38 | a0002c0001t0001g0216a0002c0001t0001g0219a0002c0001t0001g0267others(35): Show | 38 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1909+7206_1909+737 others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928009 | |||||
| chr14:99928010
|
G | A | 2 | a0001c0003t0001g0269a0003c0002t0001g0237 | 2 | HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1909+7133G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928010 | ||||||
| chr14:99928011
|
G | A | 2 | a0001c0003t0001g0214a0001c0004t0002g0047 | 2 | HG02486.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1909+7134G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928011 | ||||||
| chr14:99928011
|
G | T | 2 | a0001c0003t0001g0269a0003c0002t0001g0237 | 2 | HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1909+7134G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928011 | ||||||
| chr14:99928012
|
T | G | 2 | a0002c0001t0002g0176a0003c0002t0002g0050 | 2 | HG01928.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1909+7135T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928012 | ||||||
| chr14:99928013
|
G | A | 1 | a0001c0003t0001g0240 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1909+7136G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928013 | ||||||
| chr14:99928014
|
G | A | 8 | a0001c0003t0001g0286a0001c0003t0002g0116a0001c0005t0004g0285others(5): Show | 8 | HG01192.hp1 HG02293.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1909+7137G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928014 | ||||||
| chr14:99928014
|
G | GTGGTGGT others(17): Show |
1 | a0003c0002t0002g0138 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1909+7145_1909+714 others(28): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928014 | |||||
| chr14:99928014
|
G | GTGGTGGT others(1076): Show |
1 | a0002c0001t0002g0051 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1909+7163_1909+716 others(1087): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928014 | |||||
| chr14:99928014
|
G | T | 1 | a0001c0003t0001g0240 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1909+7137G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928014 | ||||||
| chr14:99928015
|
T | A | 1 | a0001c0004t0013g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1909+7138T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928015 | ||||||
| chr14:99928015
|
T | TGGTGGTG others(119): Show |
1 | a0003c0002t0001g0130 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1909+7149_1909+715 others(130): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928015 | |||||
| chr14:99928017
|
G | A | 12 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0016others(9): Show | 12 | HG01243.hp1 HG01255.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1909+7140G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928017 | ||||||
| chr14:99928017
|
G | GTGGTGGT others(11): Show |
2 | a0003c0002t0001g0055a0003c0002t0002g0222 | 2 | HG01981.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1909+7148_1909+714 others(22): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928017 | |||||
| chr14:99928018
|
T | A | 1 | a0001c0003t0001g0010 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1909+7141T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928018 | ||||||
| chr14:99928018
|
T | G | 3 | a0001c0003t0002g0105a0001c0003t0002g0106a0002c0001t0002g0176 | 3 | HG01928.hp1 HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1909+7141T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928018 | ||||||
| chr14:99928019
|
G | A | 1 | a0001c0003t0004g0141 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1909+7142G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928019 | ||||||
| chr14:99928020
|
G | A | 2 | a0003c0002t0001g0100a0003c0002t0001g0198 | 2 | HG03492.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1909+7143G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928020 | ||||||
| chr14:99928020
|
G | GTGGTGGT others(119): Show |
1 | a0001c0003t0001g0080 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1909+7151_1909+715 others(130): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928020 | |||||
| chr14:99928020
|
G | GTGGTGGT others(53): Show |
1 | a0002c0001t0002g0224 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1909+7157_1909+715 others(64): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928020 | |||||
| chr14:99928020
|
G | T | 1 | a0001c0003t0004g0141 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1909+7143G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928020 | ||||||
| chr14:99928021
|
T | A | 2 | a0001c0004t0001g0248a0001c0004t0011g0156 | 2 | HG02083.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1909+7144T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928021 | ||||||
| chr14:99928023
|
G | A | 20 | a0001c0003t0001g0012a0001c0003t0001g0220a0001c0003t0001g0221others(17): Show | 20 | HG01109.hp2 HG01123.hp1 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.1909+7146G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928023 | ||||||
| chr14:99928023
|
G | GTGGTGAT others(413): Show |
1 | a0003c0002t0001g0204 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1909+7151_1909+715 others(424): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928023 | |||||
| chr14:99928024
|
T | A | 1 | a0001c0003t0001g0020 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1909+7147T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928024 | ||||||
| chr14:99928024
|
T | G | 3 | a0001c0003t0002g0105a0001c0003t0002g0106a0002c0001t0002g0176 | 3 | HG01928.hp1 HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1909+7147T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928024 | ||||||
| chr14:99928025
|
G | A | 1 | a0003c0002t0002g0050 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1909+7148G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928025 | ||||||
| chr14:99928026
|
G | A | 8 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0016others(5): Show | 8 | HG00735.hp1 HG01074.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1909+7149G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928026 | ||||||
| chr14:99928026
|
G | GTGA | 17 | a0001c0003t0001g0086a0001c0003t0001g0120a0001c0003t0001g0167others(14): Show | 18 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.1909+7151_1909+715 others(7): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928026 | |||||
| chr14:99928026
|
G | T | 1 | a0003c0002t0002g0050 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1909+7149G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928026 | ||||||
| chr14:99928027
|
T | A | 6 | a0001c0004t0001g0009a0001c0004t0005g0266a0003c0002t0001g0185others(3): Show | 6 | HG00544.hp1 HG00621.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1909+7150T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928027 | ||||||
| chr14:99928027
|
T | TGATGGTG others(20): Show |
1 | a0001c0004t0002g0047 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1909+7151_1909+715 others(31): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928027 | |||||
| chr14:99928027
|
T | TGGTGGAG others(674): Show |
1 | a0001c0004t0003g0022 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1909+7155_1909+715 others(685): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928027 | |||||
| chr14:99928028
|
G | A | 5 | a0001c0003t0001g0286a0002c0001t0001g0062a0002c0001t0002g0046others(2): Show | 5 | HG02293.hp1 HG03453.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.1909+7151G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928028 | ||||||
| chr14:99928029
|
G | A | 76 | a0001c0003t0001g0001a0001c0003t0001g0041a0001c0003t0001g0085others(73): Show | 77 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.1909+7152G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928029 | ||||||
| chr14:99928029
|
G | GTGGTGGT others(575): Show |
1 | a0003c0002t0001g0107 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1909+7160_1909+716 others(586): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928029 | |||||
| chr14:99928029
|
G | GTGGTGGT others(23): Show |
1 | a0003c0002t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1909+7160_1909+716 others(34): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928029 | |||||
| chr14:99928029
|
G | GTGGTGGT others(599): Show |
1 | a0003c0002t0001g0087 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1909+7160_1909+716 others(610): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928029 | |||||
| chr14:99928030
|
T | A | 2 | a0001c0004t0003g0145a0002c0001t0002g0082 | 2 | NA18947.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1909+7153T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928030 | ||||||
| chr14:99928030
|
T | G | 2 | a0001c0003t0002g0105a0001c0003t0002g0106 | 2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1909+7153T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928030 | ||||||
| chr14:99928032
|
G | A | 3 | a0002c0001t0002g0133a0003c0002t0001g0054a0003c0002t0017g0028 | 3 | HG01496.hp2 HG01981.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1909+7155G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928032 | ||||||
| chr14:99928032
|
G | GTGATGGT others(323): Show |
3 | a0001c0003t0003g0032a0001c0003t0003g0033a0001c0003t0003g0034 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1909+7157_1909+715 others(334): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928032 | |||||
| chr14:99928032
|
G | GTGGTGGT others(509): Show |
1 | a0001c0004t0001g0123 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1909+7166_1909+716 others(520): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928032 | |||||
| chr14:99928033
|
T | A | 4 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0016others(1): Show | 4 | HG02109.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1909+7156T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928033 | ||||||
| chr14:99928034
|
G | A | 5 | a0001c0003t0001g0286a0002c0001t0001g0062a0002c0001t0002g0046others(2): Show | 5 | HG02293.hp1 HG03453.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.1909+7157G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928034 | ||||||
| chr14:99928035
|
G | A | 10 | a0001c0003t0001g0020a0001c0003t0004g0141a0001c0004t0003g0280others(7): Show | 10 | HG01123.hp2 HG01169.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.1909+7158G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928035 | ||||||
| chr14:99928035
|
G | GTGATGGT others(74): Show |
1 | a0002c0001t0002g0095 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1909+7160_1909+716 others(85): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928035 | |||||
| chr14:99928035
|
G | GTGGTGAT others(74): Show |
1 | a0001c0003t0001g0008 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1909+7163_1909+716 others(85): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928035 | |||||
| chr14:99928035
|
G | GTGGTGAT others(413): Show |
1 | a0002c0001t0002g0058 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1909+7163_1909+716 others(424): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928035 | |||||
| chr14:99928035
|
G | GTGTTGGT others(107): Show |
1 | a0001c0003t0001g0010 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1909+7160_1909+716 others(118): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928035 | |||||
| chr14:99928036
|
T | A | 1 | a0002c0001t0019g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1909+7159T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928036 | ||||||
| chr14:99928037
|
G | A | 5 | a0001c0003t0001g0286a0002c0001t0001g0062a0002c0001t0002g0046others(2): Show | 5 | HG02293.hp1 HG03453.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.1909+7160G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928037 | ||||||
| chr14:99928038
|
G | A | 8 | a0001c0004t0003g0030a0001c0004t0003g0049a0002c0001t0001g0092others(5): Show | 8 | HG01496.hp1 HG01884.hp2 HG04115.hp2 others(5): Show |
intron_variant | MODIFIER | c.1909+7161G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928038 | ||||||
| chr14:99928038
|
G | GTGATGGT others(764): Show |
1 | a0002c0001t0002g0026 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1909+7163_1909+716 others(775): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928038 | |||||
| chr14:99928039
|
T | A | 1 | a0003c0014t0004g0254 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1909+7162T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928039 | ||||||
| chr14:99928041
|
G | A | 5 | a0001c0003t0002g0116a0001c0003t0003g0032a0001c0003t0003g0033others(2): Show | 5 | HG02273.hp1 HG02723.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1909+7164G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928041 | ||||||
| chr14:99928041
|
GTGA | G | 7 | a0001c0003t0001g0113a0001c0003t0001g0114a0001c0003t0001g0158others(4): Show | 7 | HG01884.hp1 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1909+7167_1909+716 others(7): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928041 | |||||
| chr14:99928041
|
GTGATGGT others(167): Show |
G | 1 | a0001c0005t0004g0285 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1909+7167_1909+734 others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928041 | |||||
| chr14:99928044
|
A | ATGG | 6 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0016others(3): Show | 6 | HG02109.hp1 HG02572.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.1909+7170_1909+717 others(7): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928044 | |||||
| chr14:99928044
|
A | ATGGTGGT others(383): Show |
1 | a0003c0002t0001g0036 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1909+7172_1909+717 others(394): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928044 | |||||
| chr14:99928044
|
A | ATGGTGGT others(134): Show |
1 | a0002c0001t0002g0164 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1909+7172_1909+717 others(145): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928044 | |||||
| chr14:99928044
|
A | ATGGTGGT others(455): Show |
1 | a0002c0001t0002g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1909+7172_1909+717 others(466): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928044 | |||||
| chr14:99928044
|
A | G | 144 | a0001c0003t0001g0001a0001c0003t0001g0012a0001c0003t0001g0041others(141): Show | 145 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.1909+7167A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928044 | ||||||
| chr14:99928045
|
T | C | 5 | a0001c0003t0001g0286a0002c0001t0001g0062a0002c0001t0002g0046others(2): Show | 5 | HG02293.hp1 HG03453.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.1909+7168T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928045 | ||||||
| chr14:99928045
|
TGGTGATG others(58): Show |
T | 1 | a0001c0003t0002g0106 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1909+7169_1909+723 others(69): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928045 | ||||||
| chr14:99928045
|
TGGTGATG others(61): Show |
T | 1 | a0001c0003t0002g0105 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1909+7169_1909+723 others(72): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928045 | ||||||
| chr14:99928047
|
G | A | 1 | a0003c0002t0001g0210 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1909+7170G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928047 | ||||||
| chr14:99928047
|
GTGATGGT others(104): Show |
G | 1 | a0001c0003t0004g0141 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1909+7173_1909+728 others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928047 | |||||
| chr14:99928048
|
T | A | 2 | a0002c0001t0002g0224a0003c0002t0001g0054 | 2 | HG01496.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1909+7171T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928048 | ||||||
| chr14:99928050
|
A | ATGGTGGT others(41): Show |
1 | a0002c0001t0002g0084 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1909+7182_1909+718 others(52): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928050 | |||||
| chr14:99928050
|
A | G | 80 | a0001c0003t0001g0008a0001c0003t0001g0010a0001c0003t0001g0015others(77): Show | 81 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.1909+7173A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928050 | ||||||
| chr14:99928051
|
T | A | 6 | a0001c0003t0007g0014a0001c0004t0013g0108a0002c0001t0002g0021others(3): Show | 6 | HG00735.hp1 HG01123.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.1909+7174T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928051 | ||||||
| chr14:99928053
|
G | A | 4 | a0001c0003t0007g0117a0001c0003t0009g0251a0001c0005t0009g0078others(1): Show | 4 | HG02809.hp2 HG02965.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1909+7176G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928053 | ||||||
| chr14:99928054
|
T | A | 1 | a0002c0001t0002g0081 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1909+7177T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928054 | ||||||
| chr14:99928054
|
T | G | 1 | a0001c0005t0004g0284 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1909+7177T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928054 | ||||||
| chr14:99928056
|
G | A | 2 | a0001c0003t0001g0020a0003c0002t0001g0192 | 2 | HG01175.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1909+7179G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928056 | ||||||
| chr14:99928056
|
G | GTGGTGGT others(1250): Show |
1 | a0003c0002t0001g0237 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1909+7190_1909+719 others(1261): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928056 | |||||
| chr14:99928057
|
T | G | 5 | a0001c0003t0001g0286a0002c0001t0001g0062a0002c0001t0002g0046others(2): Show | 5 | HG02293.hp1 HG03453.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.1909+7180T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928057 | ||||||
| chr14:99928059
|
G | A | 5 | a0001c0003t0007g0281a0001c0004t0003g0049a0003c0002t0003g0159others(2): Show | 5 | HG02615.hp2 NA18984.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.1909+7182G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928059 | ||||||
| chr14:99928059
|
G | GTGA | 6 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0016others(3): Show | 6 | HG02109.hp1 HG02155.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1909+7184_1909+718 others(7): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928059 | |||||
| chr14:99928060
|
T | A | 12 | a0001c0003t0001g0015a0001c0004t0003g0030a0001c0004t0011g0156others(9): Show | 13 | HG00639.hp1 HG00642.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.1909+7183T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928060 | ||||||
| chr14:99928060
|
T | G | 1 | a0001c0005t0004g0284 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1909+7183T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928060 | ||||||
| chr14:99928060
|
T | TGGTGGTG others(125): Show |
1 | a0002c0001t0003g0134 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1909+7191_1909+719 others(136): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928060 | |||||
| chr14:99928062
|
G | A | 18 | a0001c0003t0001g0111a0001c0003t0001g0112a0001c0003t0001g0120others(15): Show | 18 | HG00140.hp2 HG01515.hp2 HG01975.hp1 others(15): Show |
intron_variant | MODIFIER | c.1909+7185G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928062 | ||||||
| chr14:99928062
|
G | GTGGTGAT others(176): Show |
2 | a0001c0003t0001g0240a0001c0003t0001g0269 | 2 | HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1909+7190_1909+719 others(187): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928062 | |||||
| chr14:99928063
|
T | A | 2 | a0004c0008t0004g0004a0004c0008t0004g0268 | 2 | HG02055.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1909+7186T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928063 | ||||||
| chr14:99928063
|
T | G | 5 | a0001c0003t0001g0286a0002c0001t0001g0062a0002c0001t0002g0046others(2): Show | 5 | HG02293.hp1 HG03453.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.1909+7186T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928063 | ||||||
| chr14:99928063
|
T | TGGTGGAG others(674): Show |
2 | a0001c0004t0003g0075a0001c0004t0003g0103 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1909+7191_1909+719 others(685): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928063 | |||||
| chr14:99928065
|
G | A | 4 | a0001c0003t0001g0020a0001c0003t0001g0086a0001c0004t0003g0280others(1): Show | 4 | HG02717.hp2 NA19030.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.1909+7188G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928065 | ||||||
| chr14:99928065
|
G | GTGA | 3 | a0001c0004t0003g0096a0002c0001t0002g0182a0003c0002t0002g0231 | 3 | HG01255.hp1 HG03704.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1909+7190_1909+719 others(7): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928065 | |||||
| chr14:99928065
|
G | GTGGAGGT others(527): Show |
1 | a0001c0004t0003g0029 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1909+7191_1909+719 others(538): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928065 | |||||
| chr14:99928065
|
G | GTGGAGGT others(125): Show |
1 | a0001c0004t0003g0206 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1909+7191_1909+719 others(136): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928065 | |||||
| chr14:99928066
|
T | A | 90 | a0001c0003t0001g0001a0001c0003t0001g0012a0001c0003t0001g0041others(87): Show | 91 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1909+7189T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928066 | ||||||
| chr14:99928068
|
G | A | 11 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0016others(8): Show | 11 | HG00621.hp2 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1909+7191G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928068 | ||||||
| chr14:99928068
|
G | GTGA | 3 | a0001c0003t0001g0085a0001c0003t0001g0152a0001c0003t0003g0279 | 3 | HG01074.hp1 HG02698.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1909+7193_1909+719 others(7): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928068 | |||||
| chr14:99928068
|
G | GTGGTGAT others(707): Show |
1 | a0002c0001t0002g0083 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1909+7196_1909+719 others(718): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928068 | |||||
| chr14:99928068
|
G | GTGGTGGT others(860): Show |
1 | a0003c0002t0001g0215 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1909+7199_1909+720 others(871): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928068 | |||||
| chr14:99928069
|
T | A | 4 | a0001c0003t0003g0032a0001c0003t0003g0033a0001c0003t0003g0034others(1): Show | 4 | HG00438.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1909+7192T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928069 | ||||||
| chr14:99928069
|
T | G | 6 | a0001c0003t0001g0286a0001c0004t0002g0047a0002c0001t0001g0062others(3): Show | 6 | HG02293.hp1 HG03239.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1909+7192T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928069 | ||||||
| chr14:99928071
|
G | A | 8 | a0001c0004t0003g0049a0001c0004t0013g0108a0003c0002t0001g0146others(5): Show | 8 | HG02004.hp1 HG02055.hp1 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.1909+7194G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928071 | ||||||
| chr14:99928072
|
T | A | 2 | a0002c0001t0002g0176a0003c0014t0004g0254 | 2 | HG01928.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1909+7195T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928072 | ||||||
| chr14:99928072
|
T | TGGTGATG others(68): Show |
1 | a0002c0001t0002g0082 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1909+7199_1909+720 others(79): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928072 | |||||
| chr14:99928073
|
G | A | 1 | a0001c0005t0004g0284 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1909+7196G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928073 | ||||||
| chr14:99928074
|
G | A | 7 | a0001c0003t0007g0014a0001c0004t0003g0280a0002c0001t0002g0031others(4): Show | 7 | HG00735.hp1 HG01255.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1909+7197G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928074 | ||||||
| chr14:99928074
|
G | T | 1 | a0001c0005t0004g0284 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1909+7197G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928074 | ||||||
| chr14:99928075
|
T | A | 1 | a0001c0005t0005g0265 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1909+7198T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928075 | ||||||
| chr14:99928077
|
G | A | 2 | a0003c0002t0001g0185a0003c0002t0001g0192 | 2 | HG01175.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1909+7200G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928077 | ||||||
| chr14:99928078
|
T | A | 3 | a0001c0004t0001g0009a0001c0004t0005g0266a0001c0004t0011g0156 | 3 | HG02083.hp1 HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1909+7201T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928078 | ||||||
| chr14:99928080
|
G | A | 5 | a0001c0003t0001g0020a0001c0003t0001g0080a0001c0003t0009g0251others(2): Show | 5 | HG02809.hp2 HG02886.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1909+7203G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928080 | ||||||
| chr14:99928081
|
T | A | 4 | a0001c0004t0003g0096a0002c0001t0002g0023a0002c0001t0002g0081others(1): Show | 4 | HG00544.hp2 HG03704.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.1909+7204T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928081 | ||||||
| chr14:99928082
|
G | A | 6 | a0001c0003t0001g0286a0001c0004t0002g0047a0002c0001t0001g0062others(3): Show | 6 | HG02293.hp1 HG03239.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1909+7205G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928082 | ||||||
| chr14:99928083
|
A | ATGG | 5 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0016others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1909+7209_1909+721 others(7): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928083 | |||||
| chr14:99928083
|
A | ATGGTGGT others(29): Show |
1 | a0003c0002t0002g0050 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1909+7211_1909+721 others(40): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928083 | |||||
| chr14:99928083
|
A | G | 170 | a0001c0003t0001g0001a0001c0003t0001g0012a0001c0003t0001g0020others(167): Show | 171 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.1909+7206A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928083 | ||||||
| chr14:99928083
|
A | T | 6 | a0001c0003t0001g0286a0001c0004t0002g0047a0002c0001t0001g0062others(3): Show | 6 | HG02293.hp1 HG03239.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1909+7206A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928083 | ||||||
| chr14:99928084
|
T | A | 4 | a0001c0003t0003g0279a0002c0001t0002g0083a0003c0002t0010g0200others(1): Show | 4 | HG00621.hp2 HG01074.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.1909+7207T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928084 | ||||||
| chr14:99928086
|
G | T | 1 | a0001c0003t0001g0214 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1909+7209G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928086 | ||||||
| chr14:99928087
|
T | A | 1 | a0003c0002t0001g0215 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1909+7210T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928087 | ||||||
| chr14:99928089
|
A | ATGGTGGT others(1106): Show |
1 | a0001c0004t0003g0149 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1909+7227_1909+722 others(1117): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928089 | |||||
| chr14:99928089
|
A | ATGGTGGT others(272): Show |
1 | a0003c0002t0003g0155 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1909+7227_1909+722 others(283): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928089 | |||||
| chr14:99928089
|
A | G | 73 | a0001c0003t0001g0008a0001c0003t0001g0010a0001c0003t0001g0080others(70): Show | 74 | HG00544.hp2 HG00621.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.1909+7212A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928089 | ||||||
| chr14:99928090
|
T | A | 3 | a0002c0001t0003g0188a0002c0001t0003g0189a0003c0016t0014g0060 | 3 | HG02257.hp1 NA18957.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1909+7213T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928090 | ||||||
| chr14:99928092
|
G | A | 3 | a0001c0003t0005g0246a0001c0003t0005g0247a0002c0001t0002g0173 | 3 | HG02896.hp2 HG02897.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1909+7215G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928092 | ||||||
| chr14:99928092
|
G | GTGGTGGT others(17): Show |
2 | a0003c0002t0001g0171a0003c0002t0001g0172 | 2 | NA19063.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1909+7223_1909+722 others(28): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928092 | |||||
| chr14:99928093
|
T | A | 1 | a0003c0002t0001g0192 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1909+7216T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928093 | ||||||
| chr14:99928094
|
G | A | 1 | a0007c0012t0002g0275 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1909+7217G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928094 | ||||||
| chr14:99928095
|
G | A | 4 | a0001c0003t0001g0244a0001c0003t0001g0245a0001c0003t0001g0286others(1): Show | 4 | HG02071.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1909+7218G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928095 | ||||||
| chr14:99928095
|
G | GTGGTGGT others(479): Show |
1 | a0004c0008t0004g0268 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1909+7226_1909+722 others(490): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928095 | |||||
| chr14:99928096
|
T | A | 1 | a0001c0004t0001g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1909+7219T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928096 | ||||||
| chr14:99928097
|
G | A | 1 | a0007c0012t0002g0275 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1909+7220G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928097 | ||||||
| chr14:99928098
|
G | A | 18 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0016others(15): Show | 18 | HG00438.hp2 HG00544.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.1909+7221G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928098 | ||||||
| chr14:99928098
|
G | GAGGTGGT others(794): Show |
1 | a0003c0002t0001g0002 | 2 | HG00639.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.1909+7221_1909+722 others(805): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928098 | ||||||
| chr14:99928098
|
G | GTGATGGT others(215): Show |
1 | a0002c0001t0002g0066 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1909+7223_1909+722 others(226): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928098 | |||||
| chr14:99928098
|
G | GTGATGGT others(329): Show |
1 | a0002c0001t0002g0021 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1909+7223_1909+722 others(340): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928098 | |||||
| chr14:99928098
|
G | GTGGTGGT others(101): Show |
1 | a0002c0001t0002g0110 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1909+7227_1909+722 others(112): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928098 | |||||
| chr14:99928099
|
T | A | 1 | a0003c0002t0001g0186 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1909+7222T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928099 | ||||||
| chr14:99928101
|
G | A | 8 | a0001c0003t0001g0243a0001c0003t0002g0116a0001c0004t0003g0030others(5): Show | 8 | HG01243.hp1 HG01496.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1909+7224G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928101 | ||||||
| chr14:99928101
|
G | GTGGTGAT others(44): Show |
1 | a0001c0004t0013g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1909+7227_1909+722 others(55): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928101 | |||||
| chr14:99928104
|
G | A | 6 | a0001c0003t0003g0032a0001c0003t0003g0033a0001c0003t0003g0034others(3): Show | 6 | HG01192.hp1 HG01255.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1909+7227G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928104 | ||||||
| chr14:99928104
|
G | GTGA | 3 | a0003c0002t0001g0054a0003c0002t0017g0028a0003c0015t0001g0013 | 3 | HG01496.hp2 HG01884.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1909+7227_1909+722 others(7): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928104 | ||||||
| chr14:99928105
|
A | AGGTGGTG others(56): Show |
1 | a0002c0001t0002g0082 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1909+7245_1909+724 others(67): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928105 | |||||
| chr14:99928105
|
A | C | 2 | a0002c0001t0019g0234a0007c0012t0002g0275 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1909+7228A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928105 | ||||||
| chr14:99928105
|
A | T | 183 | a0001c0003t0001g0001a0001c0003t0001g0008a0001c0003t0001g0010others(180): Show | 185 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.1909+7228A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928105 | ||||||
| chr14:99928107
|
G | A | 73 | a0001c0003t0001g0012a0001c0003t0001g0120a0001c0003t0001g0220others(70): Show | 73 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.1909+7230G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928107 | ||||||
| chr14:99928107
|
G | GAGGTGGT others(185): Show |
2 | a0003c0002t0001g0263a0003c0002t0001g0264 | 2 | NA18966.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1909+7230_1909+723 others(196): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928107 | ||||||
| chr14:99928107
|
G | GTGA | 54 | a0001c0003t0001g0001a0001c0003t0001g0041a0001c0003t0001g0086others(51): Show | 55 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.1909+7232_1909+723 others(7): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928107 | |||||
| chr14:99928107
|
G | GTGATGGT others(665): Show |
1 | a0001c0003t0001g0015 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1909+7232_1909+723 others(676): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928107 | |||||
| chr14:99928107
|
G | GTGGTGAT others(14): Show |
1 | a0003c0002t0001g0170 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1909+7235_1909+723 others(25): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928107 | |||||
| chr14:99928107
|
G | GTGGTGGT others(788): Show |
1 | a0003c0016t0014g0060 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1909+7245_1909+724 others(799): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928107 | |||||
| chr14:99928107
|
G | GTGGTGGT others(668): Show |
1 | a0001c0003t0001g0112 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1909+7245_1909+724 others(679): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928107 | |||||
| chr14:99928107
|
G | GTGGTGGT others(617): Show |
1 | a0001c0003t0001g0111 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1909+7245_1909+724 others(628): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928107 | |||||
| chr14:99928109
|
G | A | 1 | a0001c0003t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1909+7232G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928109 | ||||||
| chr14:99928110
|
G | A | 3 | a0001c0003t0001g0080a0001c0004t0013g0108a0003c0002t0001g0107 | 3 | HG02055.hp1 HG02886.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1909+7233G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928110 | ||||||
| chr14:99928110
|
G | GTGGTGAT others(17): Show |
4 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0016others(1): Show | 4 | HG02109.hp1 HG02723.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1909+7238_1909+723 others(28): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928110 | |||||
| chr14:99928110
|
G | GTGGTGGT others(443): Show |
1 | a0003c0002t0001g0130 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1909+7245_1909+724 others(454): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928110 | |||||
| chr14:99928111
|
T | A | 1 | a0002c0001t0003g0137 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1909+7234T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928111 | ||||||
| chr14:99928113
|
G | A | 5 | a0001c0003t0001g0244a0001c0003t0001g0245a0002c0001t0002g0021others(2): Show | 5 | HG01123.hp2 HG01255.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1909+7236G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928113 | ||||||
| chr14:99928114
|
T | A | 1 | a0003c0002t0001g0185 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1909+7237T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928114 | ||||||
| chr14:99928115
|
G | A | 1 | a0001c0003t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1909+7238G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928115 | ||||||
| chr14:99928116
|
G | A | 10 | a0001c0003t0003g0279a0001c0003t0005g0246a0001c0003t0005g0247others(7): Show | 10 | HG00621.hp2 HG01074.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.1909+7239G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928116 | ||||||
| chr14:99928116
|
G | GTGGTGAT others(8): Show |
2 | a0001c0003t0001g0008a0001c0003t0001g0010 | 2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1909+7244_1909+724 others(19): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928116 | |||||
| chr14:99928116
|
G | GTGGTGGT others(5): Show |
2 | a0001c0003t0001g0085a0001c0003t0001g0152 | 2 | HG02698.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1909+7245_1909+724 others(16): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928116 | |||||
| chr14:99928117
|
T | A | 2 | a0001c0013t0001g0126a0006c0011t0001g0011 | 2 | HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1909+7240T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928117 | ||||||
| chr14:99928117
|
T | G | 2 | a0002c0001t0019g0234a0007c0012t0002g0275 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1909+7240T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928117 | ||||||
| chr14:99928118
|
G | A | 1 | a0001c0003t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1909+7241G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928118 | ||||||
| chr14:99928119
|
G | A | 12 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0016others(9): Show | 12 | HG00544.hp1 HG01884.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1909+7242G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928119 | ||||||
| chr14:99928119
|
G | GTGATGGT others(14): Show |
2 | a0001c0003t0001g0167a0001c0003t0001g0168 | 2 | HG02818.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1909+7244_1909+724 others(25): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928119 | |||||
| chr14:99928121
|
G | A | 1 | a0001c0004t0003g0030 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1909+7244G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928121 | ||||||
| chr14:99928121
|
G | GGTGGTGG others(392): Show |
1 | a0003c0002t0002g0203 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1909+7245_1909+724 others(403): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928121 | |||||
| chr14:99928122
|
G | A | 7 | a0002c0001t0002g0058a0002c0001t0002g0083a0003c0002t0001g0054others(4): Show | 7 | HG01074.hp2 HG01192.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.1909+7245G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928122 | ||||||
| chr14:99928122
|
G | C | 1 | a0001c0004t0003g0030 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1909+7245G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928122 | ||||||
| chr14:99928122
|
G | GTGATGGT others(305): Show |
1 | a0003c0002t0001g0187 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1909+7245_1909+724 others(316): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928122 | ||||||
| chr14:99928123
|
A | AGGTGGTG others(92): Show |
1 | a0003c0002t0006g0088 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1909+7257_1909+725 others(103): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928123 | |||||
| chr14:99928123
|
A | AGGTGGTG others(725): Show |
1 | a0001c0003t0009g0251 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1909+7268_1909+726 others(736): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928123 | |||||
| chr14:99928123
|
A | AGGTGGTG others(728): Show |
1 | a0001c0005t0009g0078 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1909+7268_1909+726 others(739): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928123 | |||||
| chr14:99928123
|
A | G | 3 | a0002c0001t0019g0234a0003c0002t0001g0002a0007c0012t0002g0275 | 4 | HG00639.hp1 HG00642.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1909+7246A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928123 | ||||||
| chr14:99928123
|
A | T | 102 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0008others(99): Show | 102 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.1909+7246A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928123 | ||||||
| chr14:99928125
|
G | A | 6 | a0001c0003t0001g0008a0001c0003t0001g0010a0001c0003t0002g0106others(3): Show | 6 | HG01123.hp1 HG02630.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1909+7248G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928125 | ||||||
| chr14:99928125
|
G | GAGGTGGT others(140): Show |
1 | a0001c0003t0001g0214 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1909+7248_1909+724 others(151): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928125 | ||||||
| chr14:99928125
|
G | GTGA | 3 | a0001c0003t0001g0240a0001c0003t0001g0269a0001c0005t0001g0079 | 3 | HG03195.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1909+7250_1909+725 others(7): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928125 | |||||
| chr14:99928126
|
T | A | 1 | a0003c0002t0001g0107 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1909+7249T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928126 | ||||||
| chr14:99928126
|
T | C | 1 | a0001c0003t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1909+7249T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928126 | ||||||
| chr14:99928128
|
G | A | 21 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0016others(18): Show | 21 | HG01884.hp1 HG02004.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1909+7251G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928128 | ||||||
| chr14:99928129
|
T | G | 4 | a0001c0003t0004g0027a0001c0003t0004g0258a0002c0001t0019g0234others(1): Show | 4 | HG00609.hp2 HG02083.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1909+7252T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928129 | ||||||
| chr14:99928131
|
G | A | 1 | a0002c0001t0002g0182 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1909+7254G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928131 | ||||||
| chr14:99928133
|
G | A | 2 | a0001c0003t0004g0027a0001c0003t0004g0258 | 2 | HG00609.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.1909+7256G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928133 | ||||||
| chr14:99928134
|
G | A | 11 | a0001c0003t0001g0012a0001c0003t0001g0220a0001c0003t0001g0221others(8): Show | 11 | HG00558.hp2 HG01109.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1909+7257G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928134 | ||||||
| chr14:99928134
|
G | T | 2 | a0001c0003t0004g0027a0001c0003t0004g0258 | 2 | HG00609.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.1909+7257G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928134 | ||||||
| chr14:99928135
|
T | A | 11 | a0001c0003t0001g0167a0001c0003t0001g0168a0001c0003t0001g0244others(8): Show | 12 | HG00639.hp1 HG00642.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1909+7258T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928135 | ||||||
| chr14:99928135
|
T | TGGTGGTG others(392): Show |
1 | a0001c0004t0003g0195 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1909+7271_1909+727 others(403): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928135 | |||||
| chr14:99928137
|
G | A | 24 | a0001c0003t0001g0085a0001c0003t0001g0152a0001c0003t0007g0014others(21): Show | 24 | HG00621.hp2 HG00735.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.1909+7260G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928137 | ||||||
| chr14:99928137
|
G | GTGGTGGT others(1022): Show |
2 | a0001c0003t0001g0113a0001c0003t0001g0114 | 2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1909+7268_1909+726 others(1033): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928137 | |||||
| chr14:99928137
|
G | GTGGTGGT others(1022): Show |
1 | a0001c0003t0001g0158 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1909+7268_1909+726 others(1033): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928137 | |||||
| chr14:99928137
|
G | GTGGTGGT others(1106): Show |
1 | a0001c0004t0005g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1909+7268_1909+726 others(1117): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928137 | |||||
| chr14:99928138
|
T | A | 1 | a0002c0001t0002g0082 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1909+7261T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928138 | ||||||
| chr14:99928138
|
T | C | 1 | a0002c0001t0019g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1909+7261T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928138 | ||||||
| chr14:99928138
|
T | G | 1 | a0001c0003t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1909+7261T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928138 | ||||||
| chr14:99928140
|
G | A | 26 | a0001c0003t0001g0080a0001c0003t0001g0240a0001c0003t0003g0032others(23): Show | 26 | HG00544.hp2 HG01074.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.1909+7263G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928140 | ||||||
| chr14:99928140
|
G | GTGGTGA | 5 | a0001c0003t0001g0243a0001c0003t0001g0259a0001c0003t0002g0116others(2): Show | 5 | HG00609.hp1 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1909+7268_1909+726 others(10): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928140 | |||||
| chr14:99928140
|
G | GTGGTGAT others(38): Show |
1 | a0001c0004t0003g0074 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1909+7268_1909+726 others(49): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928140 | |||||
| chr14:99928140
|
G | GTGGTGAT others(665): Show |
1 | a0001c0004t0003g0059 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1909+7268_1909+726 others(676): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928140 | |||||
| chr14:99928140
|
G | GTGGTGGT others(5): Show |
1 | a0003c0002t0017g0028 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1909+7274_1909+727 others(16): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928140 | |||||
| chr14:99928141
|
T | A | 3 | a0001c0003t0002g0106a0001c0005t0001g0079a0002c0001t0002g0084 | 3 | HG00438.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1909+7264T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928141 | ||||||
| chr14:99928141
|
T | TGGTGGTG others(110): Show |
1 | a0002c0001t0002g0095 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1909+7277_1909+727 others(121): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928141 | |||||
| chr14:99928142
|
G | A | 1 | a0007c0012t0002g0275 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1909+7265G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928142 | ||||||
| chr14:99928143
|
G | A | 15 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0016others(12): Show | 15 | HG00735.hp1 HG01123.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1909+7266G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928143 | ||||||
| chr14:99928143
|
G | GTGA | 6 | a0001c0004t0003g0022a0001c0004t0003g0029a0001c0004t0003g0096others(3): Show | 6 | HG02523.hp2 HG02559.hp1 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.1909+7268_1909+726 others(7): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928143 | |||||
| chr14:99928143
|
G | GTGATGGT others(272): Show |
1 | a0002c0001t0002g0101 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1909+7268_1909+726 others(283): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928143 | |||||
| chr14:99928143
|
G | GTGATGGT others(134): Show |
1 | a0001c0003t0003g0277 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1909+7268_1909+726 others(145): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928143 | |||||
| chr14:99928143
|
G | GTGGTGAT others(65): Show |
2 | a0002c0001t0003g0142a0003c0002t0003g0125 | 2 | HG00323.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.1909+7271_1909+727 others(76): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928143 | |||||
| chr14:99928143
|
G | GTGGTGAT others(38): Show |
13 | a0001c0003t0003g0184a0001c0004t0001g0115a0001c0004t0003g0035others(10): Show | 13 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1909+7271_1909+727 others(49): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928143 | |||||
| chr14:99928143
|
G | GTGGTGGT others(662): Show |
1 | a0001c0004t0003g0197 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1909+7274_1909+727 others(673): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928143 | |||||
| chr14:99928143
|
G | T | 1 | a0007c0012t0002g0275 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1909+7266G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928143 | ||||||
| chr14:99928143
|
GTGGTGGT others(8): Show |
G | 1 | a0002c0001t0019g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1909+7281_1909+729 others(19): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928143 | |||||
| chr14:99928144
|
T | A | 3 | a0001c0003t0002g0105a0002c0001t0003g0188a0002c0001t0003g0189 | 3 | HG03041.hp2 NA18957.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1909+7267T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928144 | ||||||
| chr14:99928144
|
T | G | 1 | a0001c0003t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1909+7267T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928144 | ||||||
| chr14:99928146
|
G | A | 73 | a0001c0003t0001g0001a0001c0003t0001g0015a0001c0003t0001g0041others(70): Show | 74 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1909+7269G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928146 | ||||||
| chr14:99928147
|
T | A | 1 | a0002c0001t0003g0134 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1909+7270T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928147 | ||||||
| chr14:99928149
|
G | A | 6 | a0001c0003t0004g0027a0001c0003t0004g0258a0001c0004t0003g0090others(3): Show | 6 | HG00544.hp1 HG00609.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.1909+7272G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928149 | ||||||
| chr14:99928152
|
G | A | 1 | a0002c0001t0002g0083 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1909+7275G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928152 | ||||||
| chr14:99928152
|
GTGGTGAT others(56): Show |
G | 1 | a0002c0001t0002g0102 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1909+7281_1909+734 others(67): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928152 | |||||
| chr14:99928155
|
G | A | 5 | a0001c0003t0002g0252a0001c0004t0011g0156a0002c0001t0002g0023others(2): Show | 5 | HG00544.hp1 HG00733.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.1909+7278G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928155 | ||||||
| chr14:99928158
|
A | G | 112 | a0001c0003t0001g0001a0001c0003t0001g0015a0001c0003t0001g0041others(109): Show | 113 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.1909+7281A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928158 | ||||||
| chr14:99928161
|
G | A | 27 | a0001c0003t0003g0184a0001c0003t0003g0277a0001c0004t0001g0115others(24): Show | 27 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.1909+7284G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928161 | ||||||
| chr14:99928162
|
T | A | 1 | a0001c0004t0004g0017 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1909+7285T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928162 | ||||||
| chr14:99928162
|
T | TGGTGGTG others(170): Show |
1 | a0001c0004t0003g0049 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1909+7296_1909+729 others(181): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928162 | |||||
| chr14:99928164
|
G | A | 61 | a0001c0003t0001g0001a0001c0003t0001g0015a0001c0003t0001g0041others(58): Show | 62 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.1909+7287G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928164 | ||||||
| chr14:99928165
|
T | A | 2 | a0003c0014t0004g0254a0007c0012t0002g0275 | 2 | NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1909+7288T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928165 | ||||||
| chr14:99928165
|
T | G | 1 | a0002c0001t0019g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1909+7288T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928165 | ||||||
| chr14:99928166
|
G | C | 2 | a0001c0003t0004g0027a0001c0003t0004g0258 | 2 | HG00609.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.1909+7289G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928166 | ||||||
| chr14:99928167
|
G | A | 6 | a0001c0003t0001g0008a0001c0003t0001g0010a0001c0003t0001g0214others(3): Show | 6 | HG02486.hp2 HG02818.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1909+7290G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928167 | ||||||
| chr14:99928168
|
T | TGGTATTG others(141): Show |
1 | a0001c0003t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1909+7294_1909+729 others(152): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928168 | |||||
| chr14:99928170
|
G | A | 2 | a0002c0001t0002g0023a0003c0002t0002g0138 | 2 | HG00544.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1909+7293G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928170 | ||||||
| chr14:99928173
|
G | A | 1 | a0003c0014t0004g0254 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1909+7296G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928173 | ||||||
| chr14:99928174
|
A | AGGT | 17 | a0001c0004t0002g0047a0002c0001t0001g0062a0002c0001t0002g0046others(14): Show | 17 | HG01081.hp2 HG01168.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.1909+7329_1909+733 others(7): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928174 | |||||
| chr14:99928174
|
A | G | 2 | a0001c0003t0001g0286a0002c0001t0019g0234 | 2 | HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1909+7297A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928174 | ||||||
| chr14:99928174
|
A | T | 140 | a0001c0003t0001g0001a0001c0003t0001g0008a0001c0003t0001g0010others(137): Show | 142 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.1909+7297A>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928174 | ||||||
| chr14:99928176
|
G | A | 17 | a0001c0003t0001g0244a0001c0003t0001g0245a0001c0003t0008g0271others(14): Show | 18 | HG00639.hp1 HG00642.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1909+7299G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928176 | ||||||
| chr14:99928176
|
G | GTGA | 4 | a0001c0005t0005g0265a0003c0002t0003g0159a0003c0002t0003g0169others(1): Show | 4 | HG02622.hp2 NA18994.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.1909+7301_1909+730 others(7): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928176 | |||||
| chr14:99928176
|
G | GTGGTGGT others(791): Show |
1 | a0002c0001t0002g0129 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1909+7313_1909+731 others(802): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928176 | |||||
| chr14:99928177
|
T | TGGTGGTG others(761): Show |
1 | a0001c0004t0011g0156 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1909+7323_1909+732 others(772): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928177 | |||||
| chr14:99928179
|
G | A | 30 | a0001c0003t0003g0032a0001c0003t0003g0033a0001c0003t0003g0034others(27): Show | 30 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.1909+7302G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928179 | ||||||
| chr14:99928179
|
G | GTGATGGT others(92): Show |
1 | a0003c0002t0008g0238 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1909+7304_1909+730 others(103): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928179 | |||||
| chr14:99928179
|
G | GTGGTGGT others(416): Show |
1 | a0002c0001t0002g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1909+7322_1909+732 others(427): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928179 | |||||
| chr14:99928180
|
T | G | 1 | a0002c0001t0019g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1909+7303T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928180 | ||||||
| chr14:99928182
|
G | A | 61 | a0001c0003t0001g0001a0001c0003t0001g0015a0001c0003t0001g0041others(58): Show | 62 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.1909+7305G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928182 | ||||||
| chr14:99928183
|
T | A | 2 | a0001c0003t0004g0027a0001c0003t0004g0258 | 2 | HG00609.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.1909+7306T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928183 | ||||||
| chr14:99928185
|
G | A | 2 | a0001c0003t0001g0259a0001c0004t0004g0017 | 2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1909+7308G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928185 | ||||||
| chr14:99928186
|
T | A | 10 | a0001c0003t0001g0008a0001c0003t0001g0010a0001c0003t0001g0214others(7): Show | 10 | HG00544.hp1 HG02486.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.1909+7309T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928186 | ||||||
| chr14:99928186
|
T | G | 1 | a0002c0001t0019g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1909+7309T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928186 | ||||||
| chr14:99928186
|
T | TGGTGATG others(149): Show |
1 | a0001c0003t0007g0117 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1909+7313_1909+731 others(160): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928186 | |||||
| chr14:99928186
|
T | TGGTGATG others(150): Show |
1 | a0001c0003t0007g0281 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1909+7313_1909+731 others(161): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928186 | |||||
| chr14:99928187
|
G | A | 1 | a0001c0003t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1909+7310G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928187 | ||||||
| chr14:99928188
|
G | A | 10 | a0001c0003t0001g0283a0001c0003t0002g0105a0001c0003t0002g0106others(7): Show | 10 | HG01433.hp2 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1909+7311G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928188 | ||||||
| chr14:99928188
|
G | T | 1 | a0001c0003t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1909+7311G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928188 | ||||||
| chr14:99928189
|
T | A | 1 | a0001c0004t0003g0049 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1909+7312T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928189 | ||||||
| chr14:99928191
|
G | A | 24 | a0001c0003t0003g0184a0001c0003t0003g0277a0001c0004t0001g0115others(21): Show | 24 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.1909+7314G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928191 | ||||||
| chr14:99928191
|
G | GAGGTGGT others(107): Show |
1 | a0001c0004t0003g0064 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1909+7314_1909+731 others(118): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928191 | ||||||
| chr14:99928191
|
G | GTGATGGT others(526): Show |
1 | a0002c0001t0002g0164 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1909+7316_1909+731 others(537): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928191 | |||||
| chr14:99928191
|
G | GTGATGGT others(527): Show |
1 | a0002c0001t0002g0025 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1909+7316_1909+731 others(538): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928191 | |||||
| chr14:99928191
|
G | GTGGTGAT others(866): Show |
1 | a0001c0003t0002g0116 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1909+7319_1909+732 others(877): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928191 | |||||
| chr14:99928191
|
G | GTGGTGAT others(863): Show |
1 | a0001c0003t0001g0243 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1909+7319_1909+732 others(874): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928191 | |||||
| chr14:99928191
|
G | GTGGTGAT others(560): Show |
1 | a0001c0004t0003g0280 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1909+7319_1909+732 others(571): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928191 | |||||
| chr14:99928191
|
G | GTGGTGAT others(197): Show |
1 | a0001c0004t0003g0048 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1909+7319_1909+732 others(208): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928191 | |||||
| chr14:99928191
|
G | GTGGTGAT others(86): Show |
5 | a0001c0003t0001g0080a0001c0003t0008g0271a0001c0004t0003g0075others(2): Show | 5 | HG01256.hp2 HG01258.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1909+7319_1909+732 others(97): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928191 | |||||
| chr14:99928191
|
G | GTGGTGAT others(143): Show |
1 | a0002c0001t0003g0137 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1909+7319_1909+732 others(154): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928191 | |||||
| chr14:99928191
|
G | GTGGTGAT others(134): Show |
1 | a0001c0003t0003g0279 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1909+7319_1909+732 others(145): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928191 | |||||
| chr14:99928191
|
G | GTGGTGAT others(146): Show |
1 | a0001c0004t0003g0206 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1909+7319_1909+732 others(157): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928191 | |||||
| chr14:99928191
|
G | GTGGTGAT others(131): Show |
1 | a0001c0013t0001g0126 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1909+7319_1909+732 others(142): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928191 | |||||
| chr14:99928191
|
G | GTGGTGGT others(482): Show |
1 | a0001c0004t0003g0090 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1909+7322_1909+732 others(493): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928191 | |||||
| chr14:99928191
|
G | GTGGTGGT others(89): Show |
1 | a0001c0004t0003g0145 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1909+7322_1909+732 others(100): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928191 | |||||
| chr14:99928191
|
G | GTGGTGGT others(410): Show |
1 | a0002c0001t0002g0278 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1909+7325_1909+732 others(421): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928191 | |||||
| chr14:99928191
|
G | GTGGTGGT others(1085): Show |
1 | a0001c0003t0001g0269 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1909+7328_1909+732 others(1096): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928191 | |||||
| chr14:99928191
|
G | GTGGTGGT others(296): Show |
1 | a0002c0001t0002g0058 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1909+7331_1909+733 others(307): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928191 | |||||
| chr14:99928192
|
T | A | 8 | a0001c0003t0001g0244a0001c0003t0001g0245a0001c0005t0005g0265others(5): Show | 8 | HG01169.hp2 HG01496.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1909+7315T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928192 | ||||||
| chr14:99928194
|
G | A | 65 | a0001c0003t0001g0001a0001c0003t0001g0015a0001c0003t0001g0041others(62): Show | 67 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.1909+7317G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928194 | ||||||
| chr14:99928194
|
G | GTGA | 3 | a0001c0004t0001g0009a0001c0004t0001g0135a0001c0004t0005g0266 | 3 | HG02280.hp1 HG03225.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1909+7319_1909+732 others(7): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928194 | |||||
| chr14:99928197
|
G | A | 33 | a0001c0003t0001g0012a0001c0003t0001g0085a0001c0003t0001g0113others(30): Show | 33 | HG00621.hp2 HG01109.hp2 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.1909+7320G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928197 | ||||||
| chr14:99928197
|
GTGGTGGT others(11): Show |
G | 1 | a0002c0001t0002g0031 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1909+7332_1909+734 others(22): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928197 | |||||
| chr14:99928198
|
T | A | 3 | a0001c0003t0003g0032a0001c0003t0003g0033a0001c0003t0003g0034 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1909+7321T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928198 | ||||||
| chr14:99928199
|
G | A | 1 | a0002c0001t0019g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1909+7322G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928199 | ||||||
| chr14:99928200
|
G | T | 1 | a0002c0001t0019g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1909+7323G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928200 | ||||||
| chr14:99928203
|
G | A | 2 | a0001c0003t0002g0252a0007c0012t0002g0275 | 2 | HG00733.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1909+7326G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928203 | ||||||
| chr14:99928203
|
GTGGTGAT others(5): Show |
G | 3 | a0001c0003t0007g0014a0002c0001t0002g0021a0002c0001t0002g0066 | 3 | HG01123.hp2 HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1909+7332_1909+734 others(16): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928203 | |||||
| chr14:99928206
|
G | A | 2 | a0001c0004t0003g0059a0001c0004t0003g0074 | 2 | HG01433.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1909+7329G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928206 | ||||||
| chr14:99928207
|
T | TGGTGGTG others(2): Show |
5 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0016others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1909+7331_1909+733 others(13): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928207 | |||||
| chr14:99928209
|
A | G | 150 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0007others(147): Show | 152 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.1909+7332A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928209 | ||||||
| chr14:99928215
|
A | ATGGTGGT others(143): Show |
1 | a0003c0002t0017g0028 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1909+7353_1909+735 others(154): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928215 | |||||
| chr14:99928215
|
A | ATGGTGGT others(311): Show |
1 | a0002c0001t0003g0134 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1909+7355_1909+735 others(322): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928215 | |||||
| chr14:99928215
|
A | G | 150 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0007others(147): Show | 152 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.1909+7338A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928215 | ||||||
| chr14:99928216
|
T | A | 3 | a0001c0003t0001g0286a0001c0005t0004g0285a0001c0007t0002g0005 | 3 | HG02145.hp2 HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1909+7339T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928216 | ||||||
| chr14:99928216
|
T | TATTGGTG others(116): Show |
1 | a0001c0004t0004g0017 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1909+7339_1909+734 others(127): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928216 | ||||||
| chr14:99928218
|
G | A | 86 | a0001c0003t0001g0001a0001c0003t0001g0008a0001c0003t0001g0010others(83): Show | 88 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.1909+7341G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928218 | ||||||
| chr14:99928218
|
G | GAGGTGGT others(1808): Show |
1 | a0001c0004t0001g0123 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1909+7341_1909+734 others(1819): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928218 | ||||||
| chr14:99928218
|
G | GTGATGGT others(20): Show |
1 | a0001c0004t0003g0049 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1909+7343_1909+734 others(31): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928218 | |||||
| chr14:99928218
|
G | GTGGTGAT others(101): Show |
1 | a0001c0004t0001g0135 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1909+7346_1909+734 others(112): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928218 | |||||
| chr14:99928218
|
G | GTGGTGAT others(488): Show |
1 | a0001c0003t0001g0120 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1909+7346_1909+734 others(499): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928218 | |||||
| chr14:99928218
|
G | GTGGTGAT others(881): Show |
2 | a0001c0003t0001g0244a0001c0003t0001g0245 | 2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1909+7346_1909+734 others(892): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928218 | |||||
| chr14:99928218
|
G | GTGGTGGA others(98): Show |
1 | a0001c0003t0001g0259 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1909+7347_1909+734 others(109): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928218 | |||||
| chr14:99928218
|
G | GTGGTGGA others(608): Show |
1 | a0003c0002t0001g0161 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1909+7347_1909+734 others(619): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928218 | |||||
| chr14:99928218
|
G | GTGGTGGT others(548): Show |
1 | a0003c0002t0001g0124 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1909+7349_1909+735 others(559): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928218 | |||||
| chr14:99928218
|
G | GTGGTGGT others(296): Show |
2 | a0001c0004t0001g0009a0001c0004t0005g0266 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1909+7349_1909+735 others(307): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928218 | |||||
| chr14:99928218
|
G | GTGGTGGT others(47): Show |
1 | a0001c0004t0003g0195 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1909+7349_1909+735 others(58): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928218 | |||||
| chr14:99928218
|
G | GTGGTGGT others(1010): Show |
1 | a0001c0003t0001g0240 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1909+7349_1909+735 others(1021): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928218 | |||||
| chr14:99928218
|
G | GTGGTGGT others(443): Show |
1 | a0001c0003t0001g0085 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1909+7352_1909+735 others(454): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928218 | |||||
| chr14:99928218
|
G | GTGGTGGT others(251): Show |
1 | a0003c0002t0006g0043 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1909+7353_1909+735 others(262): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928218 | |||||
| chr14:99928218
|
G | GTGGTGGT others(1454): Show |
1 | a0002c0001t0001g0239 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1909+7353_1909+735 others(1465): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928218 | |||||
| chr14:99928218
|
G | GTGGTGGT others(191): Show |
1 | a0003c0002t0001g0192 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1909+7353_1909+735 others(202): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928218 | |||||
| chr14:99928218
|
G | GTGGTGGT others(252): Show |
1 | a0002c0001t0002g0182 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1909+7353_1909+735 others(263): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928218 | |||||
| chr14:99928218
|
G | GTGGTGGT others(251): Show |
1 | a0003c0002t0001g0210 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1909+7353_1909+735 others(262): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928218 | |||||
| chr14:99928218
|
G | GTGGTGGT others(20): Show |
1 | a0003c0002t0003g0155 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1909+7355_1909+735 others(31): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928218 | |||||
| chr14:99928218
|
G | GTGGTGGT others(44): Show |
8 | a0001c0003t0001g0113a0001c0003t0001g0114a0001c0003t0001g0158others(5): Show | 8 | HG00621.hp2 HG01928.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1909+7355_1909+735 others(55): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928218 | |||||
| chr14:99928218
|
G | GTGGTGGT others(47): Show |
10 | a0001c0003t0001g0012a0001c0003t0001g0167a0001c0003t0001g0168others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1909+7355_1909+735 others(58): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928218 | |||||
| chr14:99928218
|
G | GTGGTGGT others(62): Show |
1 | a0001c0005t0005g0265 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1909+7355_1909+735 others(73): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928218 | |||||
| chr14:99928218
|
G | GTGGTGGT others(710): Show |
1 | a0003c0002t0001g0186 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1909+7355_1909+735 others(721): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928218 | |||||
| chr14:99928218
|
G | GTGGTGGT others(32): Show |
1 | a0003c0002t0001g0185 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1909+7355_1909+735 others(43): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928218 | |||||
| chr14:99928218
|
G | GTGGTGGT others(488): Show |
1 | a0003c0002t0001g0100 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1909+7355_1909+735 others(499): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928218 | |||||
| chr14:99928218
|
G | GTGGTGGT others(446): Show |
1 | a0003c0002t0001g0054 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1909+7355_1909+735 others(457): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928218 | |||||
| chr14:99928218
|
G | GTGGTGGT others(440): Show |
1 | a0001c0003t0001g0152 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1909+7355_1909+735 others(451): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928218 | |||||
| chr14:99928218
|
G | GTGGTGGT others(650): Show |
1 | a0004c0008t0004g0004 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1909+7356_1909+735 others(661): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928218 | |||||
| chr14:99928218
|
G | GTGGTGGT others(197): Show |
3 | a0003c0002t0003g0159a0003c0002t0003g0169a0003c0002t0003g0208 | 3 | NA18994.hp2 NA18998.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1909+7358_1909+735 others(208): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928218 | |||||
| chr14:99928218
|
G | GTGGTGGT others(83): Show |
1 | a0002c0001t0002g0133 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1909+7361_1909+736 others(94): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928218 | |||||
| chr14:99928218
|
G | GTGGTGGT others(539): Show |
1 | a0001c0004t0001g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1909+7364_1909+736 others(550): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928218 | |||||
| chr14:99928218
|
G | GTGGTGGT others(671): Show |
2 | a0001c0003t0005g0246a0001c0003t0005g0247 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1909+7365_1909+736 others(682): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928218 | |||||
| chr14:99928218
|
G | GTGGTGGT others(443): Show |
1 | a0001c0007t0018g0241 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1909+7371_1909+737 others(454): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928218 | |||||
| chr14:99928221
|
G | GTGGAGGT others(209): Show |
1 | a0003c0015t0001g0013 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1909+7347_1909+734 others(220): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928221 | |||||
| chr14:99928221
|
G | GTGGTGGA others(365): Show |
1 | a0003c0014t0004g0254 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1909+7350_1909+735 others(376): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928221 | |||||
| chr14:99928221
|
G | GTGGTGGT others(425): Show |
1 | a0003c0002t0001g0218 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1909+7355_1909+735 others(436): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928221 | |||||
| chr14:99928224
|
G | A | 3 | a0002c0001t0002g0031a0002c0001t0002g0129a0002c0001t0019g0234 | 3 | HG00735.hp1 HG01169.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1909+7347G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928224 | ||||||
| chr14:99928224
|
G | GTGGTGGT others(593): Show |
1 | a0006c0011t0001g0011 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1909+7369_1909+737 others(604): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928224 | |||||
| chr14:99928231
|
T | A | 3 | a0001c0003t0001g0225a0001c0003t0001g0260a0001c0004t0001g0255 | 3 | HG02451.hp2 HG02809.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1909+7354T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928231 | ||||||
| chr14:99928243
|
T | A | 1 | a0002c0001t0019g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1909+7366T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928243 | ||||||
| chr14:99928327
|
C | G | 1 | a0003c0014t0004g0254 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1909+7450C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928327 | ||||||
| chr14:99928476
|
G | A | 2 | a0001c0003t0003g0184a0001c0004t0001g0115 | 2 | HG00140.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1910-7553G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928476 | ||||||
| chr14:99928477
|
G | GA | 3 | a0001c0003t0007g0014a0001c0003t0007g0117a0001c0003t0007g0281 | 3 | HG02615.hp2 HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1910-7551dupA | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99928477 | |||||
| chr14:99928549
|
A | G | 1 | a0003c0002t0008g0238 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1910-7480A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928549 | ||||||
| chr14:99928636
|
G | A | 1 | a0001c0004t0003g0145 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1910-7393G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928636 | ||||||
| chr14:99928643
|
C | A | 2 | a0001c0003t0004g0027a0001c0003t0004g0258 | 2 | HG00609.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.1910-7386C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928643 | ||||||
| chr14:99928665
|
G | T | 2 | a0001c0003t0004g0027a0001c0003t0004g0258 | 2 | HG00609.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.1910-7364G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928665 | ||||||
| chr14:99928942
|
T | G | 3 | a0001c0003t0003g0032a0001c0003t0003g0033a0001c0003t0003g0034 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1910-7087T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928942 | ||||||
| chr14:99928989
|
C | T | 1 | a0001c0003t0001g0167 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1910-7040C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99928989 | ||||||
| chr14:99929404
|
G | A | 1 | a0002c0001t0002g0110 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1910-6625G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99929404 | ||||||
| chr14:99929409
|
C | T | 1 | a0002c0001t0019g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1910-6620C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99929409 | ||||||
| chr14:99929537
|
A | C | 2 | a0001c0003t0004g0027a0001c0003t0004g0258 | 2 | HG00609.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.1910-6492A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99929537 | ||||||
| chr14:99929547
|
G | A | 1 | a0002c0001t0002g0102 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1910-6482G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99929547 | ||||||
| chr14:99929704
|
C | A | 1 | a0003c0002t0001g0192 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1910-6325C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99929704 | ||||||
| chr14:99929755
|
G | A | 4 | a0001c0004t0003g0022a0001c0004t0003g0127a0001c0004t0003g0149others(1): Show | 4 | HG02083.hp1 HG02132.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.1910-6274G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99929755 | ||||||
| chr14:99929847
|
G | A | 1 | a0003c0014t0004g0254 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1910-6182G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99929847 | ||||||
| chr14:99929852
|
G | A | 16 | a0001c0003t0001g0012a0001c0003t0001g0220a0001c0003t0001g0221others(13): Show | 16 | HG01109.hp2 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1910-6177G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99929852 | ||||||
| chr14:99929870
|
T | G | 1 | a0002c0001t0002g0144 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1910-6159T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99929870 | ||||||
| chr14:99929964
|
G | A | 4 | a0001c0004t0004g0017a0001c0005t0004g0284a0001c0005t0004g0285others(1): Show | 4 | HG02145.hp2 HG02257.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1910-6065G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99929964 | ||||||
| chr14:99930078
|
A | G | 140 | a0001c0003t0001g0001a0001c0003t0001g0008a0001c0003t0001g0010others(137): Show | 142 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.1910-5951A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99930078 | ||||||
| chr14:99930145
|
A | G | 195 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0007others(192): Show | 197 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.1910-5884A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99930145 | ||||||
| chr14:99930184
|
C | T | 16 | a0001c0003t0001g0012a0001c0003t0001g0220a0001c0003t0001g0221others(13): Show | 16 | HG01109.hp2 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1910-5845C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99930184 | ||||||
| chr14:99930308
|
A | G | 2 | a0001c0003t0004g0141a0005c0009t0002g0132 | 2 | NA18952.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1910-5721A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99930308 | ||||||
| chr14:99930363
|
G | A | 1 | a0002c0001t0019g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1910-5666G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99930363 | ||||||
| chr14:99930377
|
C | T | 3 | a0001c0003t0003g0032a0001c0003t0003g0033a0001c0003t0003g0034 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1910-5652C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99930377 | ||||||
| chr14:99930378
|
G | A | 1 | a0002c0001t0003g0137 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1910-5651G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99930378 | ||||||
| chr14:99930784
|
A | G | 3 | a0001c0003t0002g0252a0001c0003t0004g0141a0005c0009t0002g0132 | 3 | HG00733.hp1 NA18952.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1910-5245A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99930784 | ||||||
| chr14:99931037
|
C | T | 4 | a0002c0001t0002g0021a0002c0001t0002g0031a0002c0001t0002g0066others(1): Show | 4 | HG00735.hp1 HG01123.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1910-4992C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99931037 | ||||||
| chr14:99931245
|
A | AC | 17 | a0001c0003t0001g0233a0001c0003t0001g0272a0001c0003t0004g0027others(14): Show | 17 | HG00642.hp2 HG00735.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1910-4779dupC | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99931245 | |||||
| chr14:99931248
|
C | G | 1 | a0001c0005t0004g0284 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1910-4781C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99931248 | ||||||
| chr14:99931360
|
G | C | 1 | a0003c0015t0001g0013 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1910-4669G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99931360 | ||||||
| chr14:99931480
|
C | T | 1 | a0001c0004t0011g0156 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1910-4549C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99931480 | ||||||
| chr14:99931534
|
G | A | 1 | a0002c0001t0002g0093 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1910-4495G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99931534 | ||||||
| chr14:99931610
|
C | T | 2 | a0002c0006t0003g0229a0003c0002t0001g0036 | 2 | HG02155.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1910-4419C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99931610 | ||||||
| chr14:99931746
|
C | T | 2 | a0001c0003t0004g0027a0001c0003t0004g0258 | 2 | HG00609.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.1910-4283C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99931746 | ||||||
| chr14:99931879
|
G | T | 1 | a0002c0001t0002g0021 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1910-4150G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99931879 | ||||||
| chr14:99931959
|
G | A | 2 | a0001c0004t0001g0040a0001c0004t0001g0135 | 2 | NA18939.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1910-4070G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99931959 | ||||||
| chr14:99931981
|
C | T | 53 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0016others(50): Show | 53 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.1910-4048C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99931981 | ||||||
| chr14:99932177
|
G | A | 1 | a0001c0003t0002g0252 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1910-3852G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99932177 | ||||||
| chr14:99932221
|
C | A | 2 | a0001c0003t0002g0105a0001c0003t0002g0106 | 2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1910-3808C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99932221 | ||||||
| chr14:99932236
|
G | A | 1 | a0002c0001t0002g0083 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1910-3793G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99932236 | ||||||
| chr14:99932366
|
G | A | 2 | a0001c0005t0001g0079a0003c0002t0001g0130 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1910-3663G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99932366 | ||||||
| chr14:99932424
|
G | C | 1 | a0003c0014t0004g0254 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1910-3605G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99932424 | ||||||
| chr14:99932482
|
C | T | 5 | a0002c0001t0002g0063a0002c0001t0002g0073a0002c0001t0002g0082others(2): Show | 5 | HG00438.hp2 HG01975.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.1910-3547C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99932482 | ||||||
| chr14:99932529
|
T | C | 205 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0007others(202): Show | 207 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1910-3500T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99932529 | ||||||
| chr14:99932531
|
T | A | 4 | a0003c0002t0001g0044a0003c0002t0001g0055a0003c0002t0001g0087others(1): Show | 4 | HG01192.hp2 HG01255.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1910-3498T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99932531 | ||||||
| chr14:99932548
|
A | C | 2 | a0001c0003t0003g0184a0001c0004t0001g0115 | 2 | HG00140.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1910-3481A>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99932548 | ||||||
| chr14:99932553
|
C | T | 1 | a0001c0007t0002g0005 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1910-3476C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99932553 | ||||||
| chr14:99932554
|
G | T | 6 | a0001c0003t0002g0252a0001c0003t0004g0141a0001c0004t0004g0017others(3): Show | 6 | HG00733.hp1 HG02257.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1910-3475G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99932554 | ||||||
| chr14:99932609
|
T | G | 4 | a0001c0003t0009g0251a0001c0005t0009g0078a0003c0002t0001g0215others(1): Show | 4 | HG02572.hp2 HG02809.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1910-3420T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99932609 | ||||||
| chr14:99932646
|
T | TA | 61 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0016others(58): Show | 61 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1910-3366dupA | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99932646 | |||||
| chr14:99932646
|
T | TAA | 135 | a0001c0003t0001g0001a0001c0003t0001g0008a0001c0003t0001g0010others(132): Show | 137 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1910-3367_1910-336 others(6): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99932646 | |||||
| chr14:99932646
|
T | TAAA | 6 | a0001c0003t0001g0080a0001c0003t0001g0111a0001c0003t0001g0167others(3): Show | 6 | HG00733.hp1 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1910-3368_1910-336 others(7): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99932646 | |||||
| chr14:99932646
|
TA | T | 7 | a0001c0003t0002g0105a0002c0001t0002g0063a0002c0001t0002g0101others(4): Show | 7 | HG01255.hp1 HG01943.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.1910-3366delA | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99932646 | |||||
| chr14:99932913
|
C | T | 1 | a0001c0005t0005g0265 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1910-3116C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99932913 | ||||||
| chr14:99933004
|
G | C | 1 | a0001c0003t0002g0252 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1910-3025G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99933004 | ||||||
| chr14:99933064
|
A | G | 1 | a0001c0003t0001g0015 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1910-2965A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99933064 | ||||||
| chr14:99933075
|
T | C | 201 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0007others(198): Show | 203 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.1910-2954T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99933075 | ||||||
| chr14:99933083
|
G | A | 98 | a0001c0003t0001g0001a0001c0003t0001g0015a0001c0003t0001g0041others(95): Show | 100 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1910-2946G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99933083 | ||||||
| chr14:99933156
|
G | T | 139 | a0001c0003t0001g0001a0001c0003t0001g0008a0001c0003t0001g0010others(136): Show | 141 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.1910-2873G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99933156 | ||||||
| chr14:99933268
|
C | T | 4 | a0001c0004t0004g0017a0001c0005t0004g0284a0001c0005t0004g0285others(1): Show | 4 | HG02145.hp2 HG02257.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1910-2761C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99933268 | ||||||
| chr14:99933299
|
C | G | 1 | a0001c0007t0002g0005 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1910-2730C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99933299 | ||||||
| chr14:99933612
|
G | C | 1 | a0002c0001t0019g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1910-2417G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99933612 | ||||||
| chr14:99933832
|
G | A | 2 | a0001c0003t0002g0252a0005c0009t0002g0132 | 2 | HG00733.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1910-2197G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99933832 | ||||||
| chr14:99933866
|
G | A | 4 | a0001c0003t0003g0032a0001c0003t0003g0033a0001c0003t0003g0034others(1): Show | 4 | HG02895.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1910-2163G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99933866 | ||||||
| chr14:99933911
|
A | G | 2 | a0001c0004t0003g0022a0001c0004t0003g0199 | 2 | HG02523.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1910-2118A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99933911 | ||||||
| chr14:99933923
|
C | T | 51 | a0001c0003t0001g0286a0001c0003t0003g0032a0001c0003t0003g0033others(48): Show | 51 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.1910-2106C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99933923 | ||||||
| chr14:99934043
|
T | C | 285 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0007others(282): Show | 287 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.1910-1986T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99934043 | ||||||
| chr14:99934164
|
T | G | 2 | a0004c0008t0004g0004a0004c0008t0004g0268 | 2 | HG02055.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1910-1865T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99934164 | ||||||
| chr14:99934176
|
C | T | 51 | a0001c0003t0001g0286a0001c0003t0003g0032a0001c0003t0003g0033others(48): Show | 51 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.1910-1853C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99934176 | ||||||
| chr14:99934247
|
G | A | 1 | a0003c0002t0001g0161 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1910-1782G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99934247 | ||||||
| chr14:99934301
|
C | T | 56 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0016others(53): Show | 56 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.1910-1728C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99934301 | ||||||
| chr14:99934347
|
G | A | 1 | a0002c0001t0019g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1910-1682G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99934347 | ||||||
| chr14:99934460
|
G | A | 3 | a0001c0003t0008g0271a0001c0005t0008g0077a0003c0002t0008g0238 | 3 | HG02717.hp1 HG02922.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1910-1569G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99934460 | ||||||
| chr14:99934562
|
G | A | 1 | a0003c0014t0004g0254 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1910-1467G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99934562 | ||||||
| chr14:99934677
|
C | T | 1 | a0001c0004t0004g0017 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1910-1352C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99934677 | ||||||
| chr14:99934710
|
A | G | 6 | a0001c0004t0001g0040a0001c0004t0001g0135a0001c0004t0003g0049others(3): Show | 6 | NA18939.hp2 NA18970.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.1910-1319A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99934710 | ||||||
| chr14:99934872
|
T | C | 1 | a0002c0001t0002g0046 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1910-1157T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99934872 | ||||||
| chr14:99935037
|
G | C | 1 | a0006c0011t0001g0011 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1910-992G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99935037 | ||||||
| chr14:99935071
|
C | T | 1 | a0001c0004t0003g0127 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1910-958C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99935071 | ||||||
| chr14:99935072
|
G | A | 3 | a0001c0003t0008g0271a0001c0005t0008g0077a0003c0002t0008g0238 | 3 | HG02717.hp1 HG02922.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1910-957G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99935072 | ||||||
| chr14:99935136
|
A | G | 1 | a0001c0004t0003g0035 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1910-893A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99935136 | ||||||
| chr14:99935517
|
G | T | 1 | a0001c0003t0001g0282 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1910-512G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99935517 | ||||||
| chr14:99935555
|
G | A | 1 | a0002c0001t0019g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1910-474G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99935555 | ||||||
| chr14:99935600
|
G | A | 1 | a0002c0001t0019g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1910-429G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99935600 | ||||||
| chr14:99935753
|
G | A | 2 | a0001c0003t0002g0105a0001c0003t0002g0106 | 2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1910-276G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99935753 | ||||||
| chr14:99935760
|
C | T | 4 | a0002c0001t0002g0021a0002c0001t0002g0031a0002c0001t0002g0066others(1): Show | 4 | HG00735.hp1 HG01123.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1910-269C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99935760 | ||||||
| chr14:99935761
|
G | A | 1 | a0003c0002t0008g0238 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1910-268G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99935761 | ||||||
| chr14:99935775
|
C | G | 2 | a0002c0001t0002g0179a0002c0001t0002g0224 | 2 | NA18960.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1910-254C>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | chr14 | 99935775 | ||||||
| chr14:99935781
|
C | CA | 131 | a0001c0003t0001g0001a0001c0003t0001g0010a0001c0003t0001g0012others(128): Show | 133 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.1910-224dupA | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99935781 | |||||
| chr14:99935781
|
C | CAA | 19 | a0001c0003t0001g0008a0001c0003t0001g0112a0001c0003t0001g0113others(16): Show | 19 | HG00423.hp1 HG01884.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.1910-225_1910-224d others(4): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99935781 | |||||
| chr14:99935781
|
C | CAAAAAAA others(8): Show |
1 | a0001c0004t0004g0017 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1910-238_1910-224d others(17): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99935781 | |||||
| chr14:99935781
|
C | CAAAAAAA others(10): Show |
1 | a0001c0007t0002g0005 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1910-240_1910-224d others(19): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99935781 | |||||
| chr14:99935781
|
C | CAAAAAAA others(13): Show |
2 | a0001c0005t0004g0284a0001c0005t0004g0285 | 2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1910-243_1910-224d others(22): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99935781 | |||||
| chr14:99935781
|
CA | C | 7 | a0001c0003t0003g0032a0001c0003t0004g0141a0001c0004t0003g0103others(4): Show | 7 | HG01256.hp2 HG01943.hp2 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.1910-224delA | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99935781 | |||||
| chr14:99935989
|
ATTG | A | 97 | a0001c0003t0001g0001a0001c0003t0001g0015a0001c0003t0001g0041others(94): Show | 99 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.1910-37_1910-35del others(3): Show |
EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr14 | 99935989 | |||||
| chr14:99936167
|
G | A | 1 | a0003c0014t0004g0254 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2007+41G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 18/21 | chr14 | 99936167 | ||||||
| chr14:99936216
|
A | G | 1 | a0002c0001t0002g0101 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2008-31A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 18/21 | chr14 | 99936216 | ||||||
| chr14:99936438
|
C | T | 4 | a0001c0004t0004g0017a0001c0005t0004g0284a0001c0005t0004g0285others(1): Show | 4 | HG02145.hp2 HG02257.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2095+104C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 19/21 | chr14 | 99936438 | ||||||
| chr14:99936467
|
G | A | 1 | a0001c0003t0001g0283 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2095+133G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 19/21 | chr14 | 99936467 | ||||||
| chr14:99936478
|
G | A | 47 | a0001c0003t0002g0252a0001c0003t0003g0032a0001c0003t0003g0033others(44): Show | 47 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.2095+144G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 19/21 | chr14 | 99936478 | ||||||
| chr14:99936491
|
G | T | 51 | a0001c0003t0001g0286a0001c0003t0003g0032a0001c0003t0003g0033others(48): Show | 51 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.2095+157G>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 19/21 | chr14 | 99936491 | ||||||
| chr14:99936636
|
G | A | 4 | a0001c0003t0001g0243a0001c0003t0001g0244a0001c0003t0001g0245others(1): Show | 4 | HG02723.hp2 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2095+302G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 19/21 | chr14 | 99936636 | ||||||
| chr14:99936670
|
G | A | 1 | a0001c0004t0003g0030 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2095+336G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 19/21 | chr14 | 99936670 | ||||||
| chr14:99936743
|
G | A | 10 | a0001c0003t0001g0012a0001c0003t0001g0220a0001c0003t0001g0221others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2095+409G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 19/21 | chr14 | 99936743 | ||||||
| chr14:99936846
|
G | A | 1 | a0001c0003t0001g0259 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2095+512G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 19/21 | chr14 | 99936846 | ||||||
| chr14:99936967
|
C | T | 1 | a0003c0002t0001g0036 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2095+633C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 19/21 | chr14 | 99936967 | ||||||
| chr14:99936998
|
C | T | 206 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0007others(203): Show | 208 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.2095+664C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 19/21 | chr14 | 99936998 | ||||||
| chr14:99937054
|
G | C | 4 | a0002c0001t0002g0045a0002c0001t0002g0110a0002c0001t0002g0118others(1): Show | 4 | HG00733.hp2 HG01168.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.2095+720G>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 19/21 | chr14 | 99937054 | ||||||
| chr14:99937075
|
C | T | 1 | a0007c0012t0002g0275 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2095+741C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 19/21 | chr14 | 99937075 | ||||||
| chr14:99937151
|
A | G | 3 | a0001c0003t0008g0271a0001c0005t0008g0077a0003c0002t0008g0238 | 3 | HG02717.hp1 HG02922.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2096-666A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 19/21 | chr14 | 99937151 | ||||||
| chr14:99937279
|
A | G | 206 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0007others(203): Show | 208 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.2096-538A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 19/21 | chr14 | 99937279 | ||||||
| chr14:99937483
|
G | A | 12 | a0001c0003t0001g0008a0001c0003t0001g0010a0001c0003t0001g0214others(9): Show | 12 | HG02486.hp2 HG02572.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.2096-334G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 19/21 | chr14 | 99937483 | ||||||
| chr14:99937611
|
C | T | 200 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0007others(197): Show | 202 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.2096-206C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 19/21 | chr14 | 99937611 | ||||||
| chr14:99937683
|
G | A | 1 | a0001c0004t0003g0029 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2096-134G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 19/21 | chr14 | 99937683 | ||||||
| chr14:99937730
|
A | G | 140 | a0001c0003t0001g0001a0001c0003t0001g0008a0001c0003t0001g0010others(137): Show | 142 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.2096-87A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 19/21 | chr14 | 99937730 | ||||||
| chr14:99937920
|
T | G | 1 | a0001c0005t0005g0265 | 1 | HG02622.hp2 | splice_region_variant&intron_variant | LOW | c.2191+8T>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 20/21 | chr14 | 99937920 | ||||||
| chr14:99938014
|
T | C | 207 | a0001c0003t0001g0001a0001c0003t0001g0006a0001c0003t0001g0007others(204): Show | 209 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.2191+102T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 20/21 | chr14 | 99938014 | ||||||
| chr14:99938454
|
G | A | 1 | a0002c0001t0002g0278 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2191+542G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 20/21 | chr14 | 99938454 | ||||||
| chr14:99938536
|
G | A | 3 | a0002c0001t0002g0065a0002c0001t0002g0183a0003c0002t0003g0230 | 3 | HG02040.hp1 NA18956.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.2191+624G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 20/21 | chr14 | 99938536 | ||||||
| chr14:99938724
|
A | G | 1 | a0003c0014t0004g0254 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2192-473A>G | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 20/21 | chr14 | 99938724 | ||||||
| chr14:99938750
|
G | A | 1 | a0002c0001t0001g0062 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2192-447G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 20/21 | chr14 | 99938750 | ||||||
| chr14:99939165
|
T | C | 1 | a0001c0003t0002g0252 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2192-32T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 20/21 | chr14 | 99939165 | ||||||
| chr14:99939182
|
T | C | 1 | a0003c0002t0001g0218 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2192-15T>C | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 20/21 | chr14 | 99939182 | ||||||
| chr14:99939353
|
C | A | 2 | a0001c0003t0002g0105a0001c0003t0002g0106 | 2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2322+26C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 21/21 | chr14 | 99939353 | ||||||
| chr14:99939420
|
C | T | 114 | a0001c0003t0001g0001a0001c0003t0001g0008a0001c0003t0001g0010others(111): Show | 116 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.2322+93C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 21/21 | chr14 | 99939420 | ||||||
| chr14:99939464
|
G | A | 1 | a0002c0001t0001g0092 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2322+137G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 21/21 | chr14 | 99939464 | ||||||
| chr14:99939579
|
C | A | 9 | a0001c0003t0003g0032a0001c0003t0003g0033a0001c0003t0003g0034others(6): Show | 9 | HG00609.hp2 HG02055.hp2 HG02083.hp2 others(6): Show |
intron_variant | MODIFIER | c.2322+252C>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 21/21 | chr14 | 99939579 | ||||||
| chr14:99939612
|
G | A | 1 | a0001c0004t0004g0017 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2322+285G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 21/21 | chr14 | 99939612 | ||||||
| chr14:99939613
|
C | T | 2 | a0001c0003t0002g0116a0001c0003t0004g0141 | 2 | HG02723.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.2322+286C>T | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 21/21 | chr14 | 99939613 | ||||||
| chr14:99939652
|
G | A | 1 | a0003c0002t0001g0146 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2322+325G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 21/21 | chr14 | 99939652 | ||||||
| chr14:99939758
|
G | A | 2 | a0001c0003t0002g0105a0001c0003t0002g0106 | 2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2323-229G>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 21/21 | chr14 | 99939758 | ||||||
| chr14:99939856
|
T | A | 72 | a0001c0003t0001g0008a0001c0003t0001g0010a0001c0003t0001g0214others(69): Show | 72 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.2323-131T>A | EML1 | ENSG00000066629.19 | transcript | ENST00000262233.11 | protein_coding | 21/21 | chr14 | 99939856 |