| geneid | 5604 |
|---|---|
| ensemblid | ENSG00000169032.11 |
| hgncid | 6840 |
| symbol | MAP2K1 |
| name | mitogen-activated protein kinase kinase 1 |
| refseq_nuc | NM_002755.4 |
| refseq_prot | NP_002746.1 |
| ensembl_nuc | ENST00000307102.10 |
| ensembl_prot | ENSP00000302486.5 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 66386912 |
| end | 66491544 |
| strand | + |
| ver | v1.2 |
| region | chr15:66386912-66491544 |
| region5000 | chr15:66381912-66496544 |
| regionname0 | MAP2K1_chr15_66386912_66491544 |
| regionname5000 | MAP2K1_chr15_66381912_66496544 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 393 | 372 | 92 | 72 | 152 | 16 | 38 | 122 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| 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 | 1182 | 367 | 89 | 72 | 150 | 16 | 38 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| c0002 | 0/0 | 1182 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| c0003 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| c0004 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| c0005 | 0/0 | 1182 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| c0006 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 1366 | 217 | 77 | 49 | 70 | 2 | 18 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| t0002 | 0/0 | 1367 | 59 | 6 | 5 | 41 | 3 | 4 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| t0003 | 0/1 | 1366 | 51 | 3 | 13 | 17 | 7 | 10 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| t0004 | 0/0 | 1366 | 19 | 1 | 0 | 17 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| t0005 | 0/0 | 1366 | 10 | 0 | 2 | 5 | 1 | 2 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| t0006 | 0/0 | 1366 | 7 | 0 | 2 | 0 | 3 | 2 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| t0007 | 0/0 | 1367 | 2 | 1 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| t0008 | 0/0 | 1367 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| t0009 | 0/0 | 1367 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| t0010 | 0/0 | 1366 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| t0011 | 0/0 | 1366 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| t0012 | 0/0 | 1366 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| t0013 | 0/0 | 1366 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| t0014 | 0/0 | 1366 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0104 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0182 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0371 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1182 | 367 | 89 | 72 | 150 | 16 | 38 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| a0001c0002 | 0/0 | 1182 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| a0001c0003 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| a0001c0004 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| a0001c0005 | 0/0 | 1182 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| a0001c0006 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2547 | 213 | 74 | 49 | 69 | 2 | 18 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| a0001c0001t0002 | 0/0 | 2548 | 58 | 6 | 5 | 40 | 3 | 4 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| a0001c0001t0003 | 0/1 | 2547 | 51 | 3 | 13 | 17 | 7 | 10 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| a0001c0001t0004 | 0/0 | 2547 | 19 | 1 | 0 | 17 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| a0001c0001t0005 | 0/0 | 2547 | 10 | 0 | 2 | 5 | 1 | 2 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| a0001c0001t0006 | 0/0 | 2547 | 7 | 0 | 2 | 0 | 3 | 2 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| a0001c0001t0007 | 0/0 | 2548 | 2 | 1 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| a0001c0001t0008 | 0/0 | 2548 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| a0001c0001t0009 | 0/0 | 2548 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| a0001c0001t0010 | 0/0 | 2547 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| a0001c0001t0011 | 0/0 | 2547 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| a0001c0001t0012 | 0/0 | 2547 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| a0001c0001t0013 | 0/0 | 2547 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| a0001c0001t0014 | 0/0 | 2547 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| a0001c0002t0001 | 0/0 | 2547 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| a0001c0003t0001 | 0/0 | 2547 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| a0001c0004t0001 | 0/0 | 2547 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| a0001c0005t0002 | 0/0 | 2548 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| a0001c0006t0001 | 0/0 | 2547 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | copy fasta | chr15 | 66381912 | 66496544 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0104 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0182 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0371 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0003g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0005g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0005g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0005g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0005g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0005g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0005g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0005g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0005g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0006g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0006g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0006g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0006g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0006g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0006g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0006g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0007g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0007g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0008g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0009g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0010g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0011g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0012g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0013g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0001t0014g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0003t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0004t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0005t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| a0001c0006t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0192 | EUR | GBR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0055 | EUR | GBR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0188 | EUR | GBR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0063 | EUR | GBR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0157 | EUR | FIN | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00280 | hp2 | a0001 | c0001 | t0006 | g0006 | EUR | FIN | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0187 | EUR | FIN | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0371 | EUR | FIN | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0016 | EAS | CHS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | CHS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | CHS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00438 | hp2 | a0001 | c0001 | t0005 | g0243 | EAS | CHS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0311 | EAS | CHS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | CHS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | CHS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | CHS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | CHS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | CHS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | CHS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | CHS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | CHS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00639 | hp1 | a0001 | c0001 | t0006 | g0009 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0185 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | CHS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00673 | hp2 | a0001 | c0005 | t0002 | g0077 | EAS | CHS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0348 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0191 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0170 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0347 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0167 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0160 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0372 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0168 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0161 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0334 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0201 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0359 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0184 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0169 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01255 | hp2 | a0001 | c0001 | t0007 | g0114 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0178 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0208 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0204 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01515 | hp1 | a0001 | c0001 | t0006 | g0008 | EUR | IBS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0205 | EUR | IBS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0166 | EUR | IBS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0257 | EUR | IBS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0256 | EUR | IBS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01517 | hp2 | a0001 | c0001 | t0006 | g0007 | EUR | IBS | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0344 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0361 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01978 | hp1 | a0001 | c0001 | t0006 | g0002 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0190 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0336 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | KHV | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | KHV | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02040 | hp2 | a0001 | c0001 | t0011 | g0265 | EAS | KHV | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0358 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | KHV | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | KHV | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | KHV | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02145 | hp2 | a0001 | c0001 | t0012 | g0005 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | CDX | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | CDX | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | CDX | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CDX | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0345 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02280 | hp2 | a0001 | c0001 | t0013 | g0351 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | PEL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0194 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02572 | hp2 | a0001 | c0001 | t0014 | g0213 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02602 | hp1 | a0001 | c0001 | t0006 | g0003 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0181 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0339 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0357 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0155 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0341 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0096 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0177 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02735 | hp2 | a0001 | c0001 | t0005 | g0159 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0354 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0068 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0363 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0350 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0367 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | ESN | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0349 | AFR | ESN | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0164 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0343 | AFR | MSL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0352 | AFR | ESN | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0365 | AFR | ESN | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | MSL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03209 | hp2 | a0001 | c0006 | t0001 | g0368 | AFR | MSL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0355 | AFR | MSL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0094 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0333 | AFR | MSL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | MSL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03486 | hp2 | a0001 | c0004 | t0001 | g0015 | AFR | MSL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0176 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0162 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0369 | AFR | ESN | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | MSL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | MSL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03669 | hp1 | a0001 | c0001 | t0005 | g0158 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03688 | hp1 | a0001 | c0001 | t0006 | g0004 | SAS | STU | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | STU | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03704 | hp2 | a0001 | c0001 | t0010 | g0186 | SAS | PJL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | BEB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | BEB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0244 | SAS | BEB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0044 | SAS | BEB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0203 | SAS | BEB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0069 | SAS | BEB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0209 | SAS | STU | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | STU | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0335 | SAS | BEB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | STU | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | STU | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | STU | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0175 | SAS | STU | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | STU | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0180 | SAS | STU | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | YRI | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | YRI | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | CHB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CHB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0195 | AFR | YRI | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0364 | AFR | YRI | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18963 | hp2 | a0001 | c0001 | t0005 | g0242 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18977 | hp2 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18981 | hp2 | a0001 | c0001 | t0005 | g0241 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19006 | hp1 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0240 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19012 | hp2 | a0001 | c0001 | t0004 | g0147 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | LWK | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0362 | AFR | LWK | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0346 | AFR | LWK | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | LWK | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19057 | hp1 | a0001 | c0001 | t0005 | g0239 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19067 | hp2 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19091 | hp1 | a0001 | c0001 | t0009 | g0163 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | YRI | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0340 | AFR | YRI | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0353 | AFR | ASW | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | ASW | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0051 | EUR | TSI | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0171 | EUR | TSI | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0332 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0207 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0370 | AFR | ACB | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0356 | AFR | MSL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0360 | AFR | USA | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | USA | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0366 | AFR | USA | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | LWK | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | LWK | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0182 | REF | REF | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0104 | REF | REF | MAP2K1_chr15_66381912_66496544 | MAP2K1 | chr15 | 66381912 | 66496544 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:66387410
|
C | T | 1 | a0001c0006 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.63C>T | p.Asn21Asn | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/11 | 499/2547 | 63/1182 | 21/393 | chr15 | 66387410 | ||
| chr15:66481810
|
C | T | 1 | a0001c0005 | 1 | HG00673.hp2 | synonymous_variant | LOW | c.624C>T | p.Asp208Asp | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/11 | 1060/2547 | 624/1182 | 208/393 | chr15 | 66481810 | ||
| chr15:66487259
|
A | T | 1 | a0001c0004 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.927A>T | p.Ala309Ala | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 8/11 | 1363/2547 | 927/1182 | 309/393 | chr15 | 66487259 | ||
| chr15:66490531
|
T | C | 1 | a0001c0002 | 1 | HG00544.hp1 | synonymous_variant | LOW | c.1098T>C | p.Ala366Ala | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 11/11 | 1534/2547 | 1098/1182 | 366/393 | chr15 | 66490531 | ||
| chr15:66490570
|
C | T | 1 | a0001c0003 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.1137C>T | p.Ile379Ile | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 11/11 | 1573/2547 | 1137/1182 | 379/393 | chr15 | 66490570 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:66386940
|
G | T | 1 | a0001c0001t0014 | 1 | HG02572.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-408G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/11 | chr15 | 66386940 | ||||||
| chr15:66387148
|
G | A | 1 | a0001c0001t0008 | 1 | HG02886.hp1 | 5_prime_UTR_variant | MODIFIER | c.-200G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/11 | 200 | chr15 | 66387148 | |||||
| chr15:66387179
|
A | G | 1 | a0001c0001t0013 | 1 | HG02280.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-169A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/11 | chr15 | 66387179 | ||||||
| chr15:66387217
|
C | T | 1 | a0001c0001t0012 | 1 | HG02145.hp2 | 5_prime_UTR_variant | MODIFIER | c.-131C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/11 | 131 | chr15 | 66387217 | |||||
| chr15:66387263
|
G | C | 3 | a0001c0001t0003a0001c0001t0009a0001c0001t0010 | 53 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(50): Show |
5_prime_UTR_variant | MODIFIER | c.-85G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/11 | 85 | chr15 | 66387263 | |||||
| chr15:66387311
|
T | TC | 5 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(2): Show | 63 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(60): Show |
5_prime_UTR_variant | MODIFIER | c.-31dupC | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/11 | 30 | INFO_REALIGN_3_PRIME | chr15 | 66387311 | ||||
| chr15:66387346
|
A | G | 1 | a0001c0001t0004 | 19 | HG00423.hp1 HG03927.hp2 NA18941.hp1 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-2A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/11 | 2 | chr15 | 66387346 | |||||
| chr15:66490923
|
C | A | 3 | a0001c0001t0003a0001c0001t0005a0001c0001t0009 | 62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*308C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 11/11 | 308 | chr15 | 66490923 | |||||
| chr15:66491272
|
G | A | 2 | a0001c0001t0006a0001c0001t0012 | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*657G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 11/11 | 657 | chr15 | 66491272 | |||||
| chr15:66491375
|
G | A | 1 | a0001c0001t0011 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*760G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 11/11 | 760 | chr15 | 66491375 | |||||
| chr15:66491431
|
A | C | 1 | a0001c0001t0007 | 2 | HG01255.hp2 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*816A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 11/11 | 816 | chr15 | 66491431 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:66387455
|
G | C | 1 | a0001c0001t0001g0001 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.80+28G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66387455 | ||||||
| chr15:66387460
|
C | G | 2 | a0001c0001t0003g0371a0001c0001t0003g0372 | 2 | HG00323.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.80+33C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66387460 | ||||||
| chr15:66387481
|
G | C | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+54G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66387481 | ||||||
| chr15:66387512
|
TG | T | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+87delG | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66387512 | |||||
| chr15:66387619
|
TC | T | 29 | a0001c0001t0001g0342a0001c0001t0001g0343a0001c0001t0001g0344others(26): Show | 29 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.80+195delC | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66387619 | |||||
| chr15:66387814
|
G | C | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.80+387G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66387814 | ||||||
| chr15:66387937
|
G | A | 1 | a0001c0001t0002g0011 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.80+510G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66387937 | ||||||
| chr15:66387967
|
C | T | 1 | a0001c0001t0002g0341 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.80+540C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66387967 | ||||||
| chr15:66388052
|
C | G | 2 | a0001c0001t0001g0339a0001c0001t0001g0340 | 2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.80+625C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66388052 | ||||||
| chr15:66388181
|
C | G | 1 | a0001c0001t0001g0338 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.80+754C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66388181 | ||||||
| chr15:66388213
|
CG | C | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+787delG | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66388213 | ||||||
| chr15:66388214
|
G | C | 1 | a0001c0001t0001g0012 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.80+787G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66388214 | ||||||
| chr15:66388248
|
T | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.80+821T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66388248 | ||||||
| chr15:66388307
|
A | G | 1 | a0001c0001t0001g0337 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80+880A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66388307 | ||||||
| chr15:66388402
|
C | T | 3 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0336 | 3 | HG01099.hp2 HG02004.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.80+975C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66388402 | ||||||
| chr15:66388422
|
C | T | 40 | a0001c0001t0001g0010a0001c0001t0001g0326a0001c0001t0001g0327others(37): Show | 40 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.80+995C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66388422 | ||||||
| chr15:66388596
|
C | G | 3 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0325 | 3 | HG02055.hp1 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.80+1169C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66388596 | ||||||
| chr15:66388689
|
A | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(78): Show | 81 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.80+1262A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66388689 | ||||||
| chr15:66388747
|
C | T | 1 | a0001c0001t0001g0370 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.80+1320C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66388747 | ||||||
| chr15:66388793
|
C | T | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | NA18946.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.80+1366C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66388793 | ||||||
| chr15:66388904
|
C | CT | 73 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(70): Show | 73 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.80+1496dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66388904 | |||||
| chr15:66388904
|
C | CTT | 79 | a0001c0001t0001g0010a0001c0001t0001g0212a0001c0001t0001g0214others(76): Show | 79 | HG00280.hp2 HG00438.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.80+1495_80+1496dup others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66388904 | |||||
| chr15:66388904
|
CT | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(76): Show | 79 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.80+1496delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66388904 | |||||
| chr15:66389064
|
G | T | 63 | a0001c0001t0003g0162a0001c0001t0003g0164a0001c0001t0003g0165others(60): Show | 63 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.80+1637G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66389064 | ||||||
| chr15:66389114
|
C | T | 1 | a0001c0001t0001g0318 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.80+1687C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66389114 | ||||||
| chr15:66389176
|
G | A | 10 | a0001c0001t0005g0157a0001c0001t0005g0158a0001c0001t0005g0159others(7): Show | 10 | HG00280.hp1 HG00438.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.80+1749G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66389176 | ||||||
| chr15:66389191
|
C | G | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.80+1764C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66389191 | ||||||
| chr15:66389307
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.80+1880G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66389307 | ||||||
| chr15:66389354
|
T | C | 1 | a0001c0004t0001g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80+1927T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66389354 | ||||||
| chr15:66389440
|
A | T | 2 | a0001c0001t0001g0339a0001c0001t0001g0340 | 2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.80+2013A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66389440 | ||||||
| chr15:66389571
|
GGTT | G | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+2145_80+2147del others(3): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66389571 | ||||||
| chr15:66389572
|
G | GT | 38 | a0001c0001t0001g0113a0001c0001t0001g0154a0001c0001t0001g0283others(35): Show | 38 | HG00423.hp2 HG00609.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.80+2169dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66389572 | |||||
| chr15:66389572
|
G | GTT | 33 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0118others(30): Show | 33 | HG00438.hp1 HG00544.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.80+2168_80+2169dup others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66389572 | |||||
| chr15:66389572
|
G | GTTT | 29 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(26): Show | 29 | HG00609.hp2 HG01257.hp1 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.80+2167_80+2169dup others(3): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66389572 | |||||
| chr15:66389572
|
G | GTTTT | 6 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 6 | HG00733.hp1 HG01934.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.80+2166_80+2169dup others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66389572 | |||||
| chr15:66389572
|
GT | G | 162 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.80+2169delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66389572 | |||||
| chr15:66389573
|
T | G | 6 | a0001c0001t0004g0041a0001c0001t0004g0042a0001c0001t0004g0043others(3): Show | 6 | HG03927.hp2 NA18977.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.80+2146T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66389573 | ||||||
| chr15:66389574
|
T | G | 31 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(28): Show | 31 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.80+2147T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66389574 | ||||||
| chr15:66389647
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.80+2220T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66389647 | ||||||
| chr15:66389667
|
C | T | 113 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(110): Show | 113 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.80+2240C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66389667 | ||||||
| chr15:66389669
|
G | T | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.80+2242G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66389669 | ||||||
| chr15:66389832
|
A | G | 1 | a0001c0001t0001g0340 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.80+2405A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66389832 | ||||||
| chr15:66390121
|
A | G | 4 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(1): Show | 4 | HG02970.hp2 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.80+2694A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66390121 | ||||||
| chr15:66390234
|
C | T | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+2807C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66390234 | ||||||
| chr15:66390237
|
G | C | 2 | a0001c0001t0001g0339a0001c0001t0001g0340 | 2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.80+2810G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66390237 | ||||||
| chr15:66390271
|
C | T | 1 | a0001c0001t0001g0339 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.80+2844C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66390271 | ||||||
| chr15:66390371
|
A | G | 31 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(28): Show | 31 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.80+2944A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66390371 | ||||||
| chr15:66390603
|
A | G | 1 | a0001c0001t0014g0213 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.80+3176A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66390603 | ||||||
| chr15:66390613
|
T | C | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+3186T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66390613 | ||||||
| chr15:66390883
|
C | T | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+3456C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66390883 | ||||||
| chr15:66391057
|
CT | C | 269 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.80+3646delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66391057 | |||||
| chr15:66391057
|
CTT | C | 44 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(41): Show | 44 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.80+3645_80+3646del others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66391057 | |||||
| chr15:66391066
|
T | C | 1 | a0001c0001t0003g0205 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.80+3639T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66391066 | ||||||
| chr15:66391123
|
C | T | 2 | a0001c0001t0001g0331a0001c0001t0001g0333 | 2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.80+3696C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66391123 | ||||||
| chr15:66391134
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.80+3707C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66391134 | ||||||
| chr15:66391267
|
C | G | 1 | a0001c0001t0001g0340 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.80+3840C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66391267 | ||||||
| chr15:66391319
|
C | T | 1 | a0001c0001t0002g0090 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.80+3892C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66391319 | ||||||
| chr15:66391357
|
C | T | 1 | a0001c0001t0001g0282 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.80+3930C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66391357 | ||||||
| chr15:66391382
|
A | G | 1 | a0001c0001t0002g0089 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.80+3955A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66391382 | ||||||
| chr15:66391655
|
G | A | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+4228G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66391655 | ||||||
| chr15:66391777
|
C | T | 1 | a0001c0003t0001g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.80+4350C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66391777 | ||||||
| chr15:66392052
|
C | T | 89 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(86): Show | 89 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.80+4625C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392052 | ||||||
| chr15:66392207
|
A | G | 6 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(3): Show | 6 | HG02486.hp2 HG02572.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.80+4780A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392207 | ||||||
| chr15:66392248
|
T | C | 1 | a0001c0001t0001g0283 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.80+4821T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392248 | ||||||
| chr15:66392253
|
G | T | 1 | a0001c0001t0001g0312 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.80+4826G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392253 | ||||||
| chr15:66392254
|
G | GTT | 6 | a0001c0001t0001g0156a0001c0001t0001g0247a0001c0001t0001g0250others(3): Show | 6 | HG02273.hp1 HG02622.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.80+4827_80+4828ins others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392254 | ||||||
| chr15:66392254
|
G | GTTT | 47 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(44): Show | 47 | HG00735.hp1 HG00741.hp1 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.80+4827_80+4828ins others(3): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392254 | ||||||
| chr15:66392254
|
G | GTTTT | 85 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(82): Show | 85 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.80+4827_80+4828ins others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392254 | ||||||
| chr15:66392254
|
G | GTTTTT | 76 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0297others(73): Show | 76 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(73): Show |
intron_variant | MODIFIER | c.80+4827_80+4828ins others(5): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392254 | ||||||
| chr15:66392254
|
G | GTTTTTT | 20 | a0001c0001t0001g0212a0001c0001t0001g0217a0001c0001t0001g0218others(17): Show | 20 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.80+4827_80+4828ins others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392254 | ||||||
| chr15:66392254
|
G | GTTTTTTT | 15 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0219others(12): Show | 15 | HG00642.hp2 HG01071.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.80+4827_80+4828ins others(7): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392254 | ||||||
| chr15:66392254
|
G | GTTTTTTT others(1): Show |
6 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0229others(3): Show | 6 | HG01069.hp2 HG02165.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.80+4827_80+4828ins others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392254 | ||||||
| chr15:66392254
|
G | GTTTTTTT others(3): Show |
2 | a0001c0001t0002g0117a0001c0001t0002g0341 | 2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.80+4827_80+4828ins others(10): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392254 | ||||||
| chr15:66392254
|
G | GTTTTTTT others(5): Show |
1 | a0001c0001t0002g0120 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.80+4827_80+4828ins others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392254 | ||||||
| chr15:66392254
|
GGTTTTTT others(1): Show |
G | 12 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0232others(9): Show | 12 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.80+4828_80+4835del others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392254 | ||||||
| chr15:66392255
|
G | GTTTTTTT others(4): Show |
2 | a0001c0001t0001g0331a0001c0001t0001g0333 | 2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.80+4842_80+4852dup others(11): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66392255 | |||||
| chr15:66392255
|
G | GTTTTTTT others(5): Show |
3 | a0001c0001t0001g0326a0001c0001t0001g0347a0001c0001t0001g0348 | 3 | HG00733.hp2 HG01069.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.80+4841_80+4852dup others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66392255 | |||||
| chr15:66392255
|
G | GTTTTTTT others(6): Show |
11 | a0001c0001t0001g0010a0001c0001t0001g0327a0001c0001t0001g0328others(8): Show | 11 | HG02280.hp2 HG02896.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.80+4840_80+4852dup others(13): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66392255 | |||||
| chr15:66392255
|
G | GTTTTTTT others(7): Show |
9 | a0001c0001t0001g0329a0001c0001t0001g0332a0001c0001t0001g0354others(6): Show | 9 | HG01109.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.80+4839_80+4852dup others(14): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66392255 | |||||
| chr15:66392255
|
G | GTTTTTTT others(8): Show |
4 | a0001c0001t0001g0330a0001c0001t0001g0360a0001c0001t0001g0361others(1): Show | 4 | HG01891.hp2 HG02886.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.80+4838_80+4852dup others(15): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66392255 | |||||
| chr15:66392255
|
G | GTTTTTTT others(17): Show |
1 | a0001c0001t0001g0363 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.80+4829_80+4852dup others(24): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66392255 | |||||
| chr15:66392255
|
G | GTTTTTTT others(18): Show |
2 | a0001c0001t0001g0364a0001c0001t0001g0370 | 2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.80+4852_80+4853ins others(25): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66392255 | |||||
| chr15:66392255
|
G | T | 305 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.80+4828G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392255 | ||||||
| chr15:66392279
|
T | TTA | 33 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(30): Show | 33 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.80+4852_80+4853ins others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392279 | ||||||
| chr15:66392279
|
T | TTTA | 7 | a0001c0001t0001g0039a0001c0001t0001g0336a0001c0001t0004g0037others(4): Show | 7 | HG01243.hp2 HG02004.hp2 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.80+4852_80+4853ins others(3): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392279 | ||||||
| chr15:66392293
|
G | A | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.80+4866G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392293 | ||||||
| chr15:66392335
|
C | T | 15 | a0001c0001t0001g0218a0001c0001t0001g0225a0001c0001t0001g0226others(12): Show | 15 | HG00280.hp2 HG00639.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.80+4908C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392335 | ||||||
| chr15:66392408
|
G | C | 2 | a0001c0001t0001g0216a0001c0001t0001g0227 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.80+4981G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392408 | ||||||
| chr15:66392434
|
T | C | 364 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(361): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.80+5007T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392434 | ||||||
| chr15:66392524
|
A | G | 2 | a0001c0001t0001g0276a0001c0001t0001g0288 | 2 | HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.80+5097A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392524 | ||||||
| chr15:66392554
|
C | CT | 50 | a0001c0001t0001g0010a0001c0001t0001g0275a0001c0001t0001g0280others(47): Show | 50 | HG00280.hp2 HG00639.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.80+5143dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66392554 | |||||
| chr15:66392554
|
CT | C | 23 | a0001c0001t0001g0219a0001c0001t0001g0252a0001c0001t0002g0047others(20): Show | 23 | HG00423.hp1 HG01256.hp1 HG03491.hp1 others(20): Show |
intron_variant | MODIFIER | c.80+5143delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66392554 | |||||
| chr15:66392600
|
C | T | 38 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(35): Show | 38 | HG00323.hp1 HG00423.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.80+5173C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392600 | ||||||
| chr15:66392639
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.80+5212C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392639 | ||||||
| chr15:66392697
|
G | A | 6 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(3): Show | 6 | HG00738.hp2 HG01106.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.80+5270G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392697 | ||||||
| chr15:66392897
|
A | G | 2 | a0001c0001t0001g0339a0001c0001t0001g0340 | 2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.80+5470A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392897 | ||||||
| chr15:66392957
|
C | T | 37 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(34): Show | 37 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.80+5530C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66392957 | ||||||
| chr15:66393182
|
C | CT | 12 | a0001c0001t0001g0118a0001c0001t0001g0138a0001c0001t0001g0156others(9): Show | 12 | HG00280.hp2 HG00639.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.80+5768dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66393182 | |||||
| chr15:66393309
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.80+5882C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66393309 | ||||||
| chr15:66393470
|
C | T | 28 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(25): Show | 28 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.80+6043C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66393470 | ||||||
| chr15:66393581
|
T | C | 2 | a0001c0001t0001g0225a0001c0001t0001g0230 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.80+6154T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66393581 | ||||||
| chr15:66393634
|
A | G | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+6207A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66393634 | ||||||
| chr15:66393896
|
G | T | 1 | a0001c0001t0006g0009 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.80+6469G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66393896 | ||||||
| chr15:66393896
|
GT | G | 5 | a0001c0001t0002g0117a0001c0001t0002g0120a0001c0001t0002g0341others(2): Show | 5 | HG01255.hp2 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.80+6470delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66393896 | ||||||
| chr15:66394229
|
G | A | 1 | a0001c0001t0006g0003 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.80+6802G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66394229 | ||||||
| chr15:66394389
|
A | G | 2 | a0001c0001t0002g0078a0001c0005t0002g0077 | 2 | HG00673.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.80+6962A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66394389 | ||||||
| chr15:66394390
|
C | CAGGTTGA others(34): Show |
8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+6964_80+7004dup others(41): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66394390 | |||||
| chr15:66394432
|
G | A | 62 | a0001c0001t0003g0162a0001c0001t0003g0164a0001c0001t0003g0165others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.80+7005G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66394432 | ||||||
| chr15:66394454
|
A | C | 1 | a0001c0004t0001g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80+7027A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66394454 | ||||||
| chr15:66394459
|
C | CT | 7 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0306others(4): Show | 7 | HG00642.hp1 HG01168.hp2 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.80+7053dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66394459 | |||||
| chr15:66394459
|
C | CTT | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+7052_80+7053dup others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66394459 | |||||
| chr15:66394459
|
CT | C | 13 | a0001c0001t0001g0101a0001c0001t0001g0118a0001c0001t0001g0121others(10): Show | 13 | HG00621.hp1 HG00642.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.80+7053delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66394459 | |||||
| chr15:66394491
|
G | A | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+7064G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66394491 | ||||||
| chr15:66394648
|
G | A | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+7221G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66394648 | ||||||
| chr15:66394690
|
A | G | 2 | a0001c0001t0001g0347a0001c0001t0001g0348 | 2 | HG00733.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.80+7263A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66394690 | ||||||
| chr15:66394745
|
T | A | 1 | a0001c0003t0001g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.80+7318T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66394745 | ||||||
| chr15:66394840
|
A | G | 5 | a0001c0001t0002g0051a0001c0001t0002g0076a0001c0001t0002g0085others(2): Show | 5 | HG00597.hp2 NA18962.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.80+7413A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66394840 | ||||||
| chr15:66394919
|
C | T | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+7492C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66394919 | ||||||
| chr15:66394989
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.80+7562A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66394989 | ||||||
| chr15:66395229
|
T | C | 1 | a0001c0001t0001g0339 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.80+7802T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66395229 | ||||||
| chr15:66395484
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.80+8057A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66395484 | ||||||
| chr15:66395573
|
A | ATTTT | 7 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0006others(4): Show | 7 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.80+8162_80+8165dup others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66395573 | |||||
| chr15:66395573
|
AT | A | 50 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0001g0101others(47): Show | 50 | HG00733.hp2 HG00735.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.80+8165delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66395573 | |||||
| chr15:66395573
|
ATT | A | 296 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.80+8164_80+8165del others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66395573 | |||||
| chr15:66395573
|
ATTT | A | 6 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(3): Show | 6 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.80+8163_80+8165del others(3): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66395573 | |||||
| chr15:66395686
|
C | T | 37 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(34): Show | 37 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.80+8259C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66395686 | ||||||
| chr15:66395696
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.80+8269C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66395696 | ||||||
| chr15:66395736
|
C | T | 4 | a0001c0001t0004g0025a0001c0001t0004g0043a0001c0001t0004g0045others(1): Show | 4 | NA19006.hp1 NA19009.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.80+8309C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66395736 | ||||||
| chr15:66395753
|
T | C | 1 | a0001c0001t0002g0085 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.80+8326T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66395753 | ||||||
| chr15:66395766
|
C | G | 1 | a0001c0001t0001g0328 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.80+8339C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66395766 | ||||||
| chr15:66395812
|
A | G | 5 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(2): Show | 5 | HG01255.hp1 HG01261.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.80+8385A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66395812 | ||||||
| chr15:66395857
|
G | A | 4 | a0001c0001t0001g0280a0001c0001t0002g0117a0001c0001t0002g0120others(1): Show | 4 | HG00735.hp2 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.80+8430G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66395857 | ||||||
| chr15:66396091
|
A | G | 3 | a0001c0001t0001g0216a0001c0001t0001g0227a0001c0001t0003g0162 | 3 | HG03453.hp2 HG03491.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.80+8664A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396091 | ||||||
| chr15:66396133
|
A | G | 3 | a0001c0001t0006g0004a0001c0001t0006g0007a0001c0001t0006g0008 | 3 | HG01515.hp1 HG01517.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.80+8706A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396133 | ||||||
| chr15:66396273
|
G | A | 3 | a0001c0001t0001g0250a0001c0001t0001g0253a0001c0001t0001g0284 | 3 | HG01891.hp1 HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.80+8846G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396273 | ||||||
| chr15:66396315
|
C | G | 361 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(358): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.80+8888C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396315 | ||||||
| chr15:66396415
|
A | C | 2 | a0001c0001t0001g0303a0001c0001t0001g0305 | 2 | HG01952.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.80+8988A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396415 | ||||||
| chr15:66396428
|
G | C | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+9001G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396428 | ||||||
| chr15:66396443
|
T | A | 30 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(27): Show | 30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.80+9016T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396443 | ||||||
| chr15:66396469
|
C | T | 2 | a0001c0001t0001g0331a0001c0001t0001g0333 | 2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.80+9042C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396469 | ||||||
| chr15:66396617
|
G | A | 3 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0325 | 3 | HG02055.hp1 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.80+9190G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396617 | ||||||
| chr15:66396660
|
A | G | 2 | a0001c0001t0001g0118a0001c0001t0001g0138 | 2 | NA19074.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.80+9233A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396660 | ||||||
| chr15:66396878
|
T | G | 4 | a0001c0001t0001g0010a0001c0001t0001g0327a0001c0001t0001g0332others(1): Show | 4 | HG02109.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.80+9451T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396878 | ||||||
| chr15:66396888
|
T | C | 62 | a0001c0001t0003g0162a0001c0001t0003g0164a0001c0001t0003g0165others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.80+9461T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396888 | ||||||
| chr15:66396930
|
C | T | 54 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(51): Show | 54 | HG00735.hp1 HG00735.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.80+9503C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396930 | ||||||
| chr15:66396952
|
T | G | 1 | a0001c0001t0001g0141 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.80+9525T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396952 | ||||||
| chr15:66396964
|
C | T | 62 | a0001c0001t0003g0162a0001c0001t0003g0164a0001c0001t0003g0165others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.80+9537C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396964 | ||||||
| chr15:66396967
|
G | A | 30 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(27): Show | 30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.80+9540G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396967 | ||||||
| chr15:66396968
|
A | G | 2 | a0001c0001t0001g0135a0001c0001t0001g0137 | 2 | NA18968.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.80+9541A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66396968 | ||||||
| chr15:66396995
|
C | CT | 15 | a0001c0001t0001g0033a0001c0001t0001g0101a0001c0001t0001g0106others(12): Show | 15 | HG01433.hp1 HG02027.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.80+9595dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66396995 | |||||
| chr15:66396995
|
CT | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(178): Show | 181 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.80+9595delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66396995 | |||||
| chr15:66396995
|
CTT | C | 46 | a0001c0001t0001g0010a0001c0001t0001g0251a0001c0001t0001g0326others(43): Show | 46 | HG00280.hp2 HG00639.hp1 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.80+9594_80+9595del others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66396995 | |||||
| chr15:66396995
|
CTTTTTT | C | 57 | a0001c0001t0002g0011a0001c0001t0002g0048a0001c0001t0002g0049others(54): Show | 57 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.80+9590_80+9595del others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66396995 | |||||
| chr15:66396995
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0337 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80+9584_80+9595del others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66396995 | |||||
| chr15:66397076
|
C | T | 1 | a0001c0001t0014g0213 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.80+9649C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397076 | ||||||
| chr15:66397133
|
T | C | 1 | a0001c0001t0001g0306 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.80+9706T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397133 | ||||||
| chr15:66397145
|
C | T | 3 | a0001c0001t0001g0250a0001c0001t0001g0253a0001c0001t0001g0284 | 3 | HG01891.hp1 HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.80+9718C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397145 | ||||||
| chr15:66397196
|
A | G | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+9769A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397196 | ||||||
| chr15:66397291
|
C | T | 1 | a0001c0001t0003g0203 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.80+9864C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397291 | ||||||
| chr15:66397294
|
C | T | 2 | a0001c0001t0005g0160a0001c0001t0005g0161 | 2 | HG01074.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.80+9867C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397294 | ||||||
| chr15:66397442
|
C | T | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.80+10015C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397442 | ||||||
| chr15:66397462
|
A | C | 2 | a0001c0001t0003g0179a0001c0001t0003g0183 | 2 | NA18747.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.80+10035A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397462 | ||||||
| chr15:66397535
|
C | T | 1 | a0001c0001t0001g0337 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80+10108C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397535 | ||||||
| chr15:66397536
|
G | A | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+10109G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397536 | ||||||
| chr15:66397684
|
T | G | 1 | a0001c0001t0001g0334 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.80+10257T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397684 | ||||||
| chr15:66397773
|
T | G | 62 | a0001c0001t0003g0162a0001c0001t0003g0164a0001c0001t0003g0165others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.80+10346T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397773 | ||||||
| chr15:66397797
|
C | T | 2 | a0001c0001t0001g0356a0001c0001t0001g0357 | 2 | HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.80+10370C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397797 | ||||||
| chr15:66397846
|
G | A | 5 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.80+10419G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397846 | ||||||
| chr15:66397862
|
G | A | 31 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(28): Show | 31 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.80+10435G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397862 | ||||||
| chr15:66397931
|
A | G | 1 | a0001c0001t0001g0274 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.80+10504A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397931 | ||||||
| chr15:66397972
|
C | G | 1 | a0001c0001t0001g0301 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.80+10545C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66397972 | ||||||
| chr15:66398100
|
T | TA | 6 | a0001c0001t0001g0312a0001c0001t0002g0054a0001c0001t0002g0074others(3): Show | 6 | HG02056.hp2 NA18940.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.80+10685dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66398100 | |||||
| chr15:66398110
|
A | G | 31 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(28): Show | 31 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.80+10683A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398110 | ||||||
| chr15:66398145
|
C | G | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.80+10718C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398145 | ||||||
| chr15:66398152
|
C | T | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+10725C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398152 | ||||||
| chr15:66398173
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.80+10746G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398173 | ||||||
| chr15:66398178
|
C | A | 1 | a0001c0001t0001g0231 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.80+10751C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398178 | ||||||
| chr15:66398255
|
A | G | 1 | a0001c0001t0001g0224 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.80+10828A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398255 | ||||||
| chr15:66398291
|
G | C | 1 | a0001c0001t0001g0254 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.80+10864G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398291 | ||||||
| chr15:66398369
|
C | T | 1 | a0001c0001t0014g0213 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.80+10942C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398369 | ||||||
| chr15:66398386
|
G | T | 1 | a0001c0001t0001g0337 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80+10959G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398386 | ||||||
| chr15:66398438
|
A | G | 58 | a0001c0001t0002g0011a0001c0001t0002g0048a0001c0001t0002g0049others(55): Show | 58 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.80+11011A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398438 | ||||||
| chr15:66398447
|
A | G | 1 | a0001c0001t0006g0004 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.80+11020A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398447 | ||||||
| chr15:66398453
|
G | T | 1 | a0001c0001t0001g0269 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.80+11026G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398453 | ||||||
| chr15:66398454
|
C | T | 1 | a0001c0001t0001g0269 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.80+11027C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398454 | ||||||
| chr15:66398490
|
C | G | 1 | a0001c0001t0001g0030 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.80+11063C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398490 | ||||||
| chr15:66398514
|
T | C | 361 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(358): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.80+11087T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398514 | ||||||
| chr15:66398568
|
T | C | 364 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(361): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.80+11141T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398568 | ||||||
| chr15:66398693
|
TTG | T | 3 | a0001c0001t0001g0250a0001c0001t0001g0253a0001c0001t0001g0284 | 3 | HG01891.hp1 HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.80+11270_80+11271d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66398693 | |||||
| chr15:66398768
|
A | AT | 10 | a0001c0001t0003g0211a0001c0001t0005g0157a0001c0001t0005g0158others(7): Show | 10 | HG00280.hp1 HG00438.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.80+11353dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66398768 | |||||
| chr15:66398779
|
TTC | T | 26 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(23): Show | 26 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.80+11354_80+11355d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66398779 | |||||
| chr15:66398781
|
C | T | 52 | a0001c0001t0003g0162a0001c0001t0003g0164a0001c0001t0003g0165others(49): Show | 52 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.80+11354C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398781 | ||||||
| chr15:66398781
|
CT | C | 233 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(230): Show | 233 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.80+11365delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66398781 | |||||
| chr15:66398782
|
T | C | 78 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(75): Show | 78 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.80+11355T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398782 | ||||||
| chr15:66398837
|
G | A | 2 | a0001c0001t0002g0048a0001c0001t0002g0093 | 2 | NA19065.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.80+11410G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398837 | ||||||
| chr15:66398939
|
A | C | 1 | a0001c0001t0009g0163 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.80+11512A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66398939 | ||||||
| chr15:66399136
|
A | G | 4 | a0001c0001t0002g0078a0001c0001t0002g0100a0001c0001t0002g0150others(1): Show | 4 | HG00673.hp2 HG02165.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.80+11709A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66399136 | ||||||
| chr15:66399357
|
A | C | 1 | a0001c0001t0003g0207 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.80+11930A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66399357 | ||||||
| chr15:66399455
|
CT | C | 37 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(34): Show | 37 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.80+12037delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66399455 | |||||
| chr15:66399519
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.80+12092G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66399519 | ||||||
| chr15:66399588
|
G | A | 1 | a0001c0005t0002g0077 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.80+12161G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66399588 | ||||||
| chr15:66399612
|
A | G | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+12185A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66399612 | ||||||
| chr15:66399636
|
G | A | 1 | a0001c0001t0014g0213 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.80+12209G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66399636 | ||||||
| chr15:66399837
|
C | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(112): Show | 115 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.80+12410C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66399837 | ||||||
| chr15:66399838
|
G | T | 1 | a0001c0001t0014g0213 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.80+12411G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66399838 | ||||||
| chr15:66399872
|
G | A | 1 | a0001c0001t0001g0342 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.80+12445G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66399872 | ||||||
| chr15:66400036
|
A | G | 2 | a0001c0001t0001g0339a0001c0001t0001g0340 | 2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.80+12609A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400036 | ||||||
| chr15:66400107
|
G | A | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+12680G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400107 | ||||||
| chr15:66400174
|
A | C | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+12747A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400174 | ||||||
| chr15:66400183
|
G | T | 1 | a0001c0001t0002g0073 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.80+12756G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400183 | ||||||
| chr15:66400184
|
C | T | 1 | a0001c0001t0002g0073 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.80+12757C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400184 | ||||||
| chr15:66400238
|
G | A | 1 | a0001c0001t0001g0212 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.80+12811G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400238 | ||||||
| chr15:66400283
|
CA | C | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+12859delA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66400283 | |||||
| chr15:66400317
|
C | G | 83 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(80): Show | 83 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.80+12890C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400317 | ||||||
| chr15:66400396
|
A | G | 1 | a0001c0001t0003g0178 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.80+12969A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400396 | ||||||
| chr15:66400441
|
A | G | 3 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0325 | 3 | HG02055.hp1 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.80+13014A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400441 | ||||||
| chr15:66400501
|
A | G | 364 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(361): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.80+13074A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400501 | ||||||
| chr15:66400506
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.80+13079C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400506 | ||||||
| chr15:66400540
|
C | T | 5 | a0001c0001t0003g0177a0001c0001t0003g0182a0001c0001t0003g0201others(2): Show | 5 | HG01106.hp2 HG01515.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.80+13113C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400540 | ||||||
| chr15:66400657
|
A | G | 1 | a0001c0001t0001g0338 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.80+13230A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400657 | ||||||
| chr15:66400790
|
A | G | 324 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.80+13363A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400790 | ||||||
| chr15:66400848
|
C | T | 364 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(361): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.80+13421C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400848 | ||||||
| chr15:66400904
|
T | G | 1 | a0001c0001t0001g0214 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.80+13477T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400904 | ||||||
| chr15:66400940
|
T | C | 3 | a0001c0001t0001g0343a0001c0001t0001g0344a0001c0001t0001g0366 | 3 | HG01884.hp2 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.80+13513T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400940 | ||||||
| chr15:66400976
|
A | G | 31 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(28): Show | 31 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.80+13549A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400976 | ||||||
| chr15:66400977
|
T | C | 1 | a0001c0001t0001g0340 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.80+13550T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66400977 | ||||||
| chr15:66401017
|
G | A | 364 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(361): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.80+13590G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66401017 | ||||||
| chr15:66401022
|
T | C | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+13595T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66401022 | ||||||
| chr15:66401027
|
T | C | 1 | a0001c0001t0001g0339 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.80+13600T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66401027 | ||||||
| chr15:66401321
|
T | A | 1 | a0001c0001t0001g0119 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.80+13894T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66401321 | ||||||
| chr15:66401435
|
G | A | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+14008G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66401435 | ||||||
| chr15:66401530
|
G | C | 40 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(37): Show | 40 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.80+14103G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66401530 | ||||||
| chr15:66401532
|
A | C | 1 | a0001c0004t0001g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80+14105A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66401532 | ||||||
| chr15:66401543
|
G | A | 1 | a0001c0001t0002g0055 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.80+14116G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66401543 | ||||||
| chr15:66401792
|
G | A | 2 | a0001c0001t0001g0220a0001c0001t0001g0237 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.80+14365G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66401792 | ||||||
| chr15:66402082
|
A | T | 26 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(23): Show | 26 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.80+14655A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66402082 | ||||||
| chr15:66402093
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(112): Show | 115 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.80+14666A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66402093 | ||||||
| chr15:66402198
|
C | T | 6 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(3): Show | 6 | HG02486.hp2 HG02572.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.80+14771C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66402198 | ||||||
| chr15:66402220
|
A | C | 321 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(318): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.80+14793A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66402220 | ||||||
| chr15:66402229
|
G | A | 5 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0232others(2): Show | 5 | HG02145.hp1 HG02280.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.80+14802G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66402229 | ||||||
| chr15:66402308
|
T | C | 1 | a0001c0004t0001g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80+14881T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66402308 | ||||||
| chr15:66402360
|
G | A | 2 | a0001c0001t0001g0276a0001c0001t0001g0288 | 2 | HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.80+14933G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66402360 | ||||||
| chr15:66402536
|
G | A | 1 | a0001c0001t0001g0340 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.80+15109G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66402536 | ||||||
| chr15:66402636
|
C | T | 1 | a0001c0001t0014g0213 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.80+15209C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66402636 | ||||||
| chr15:66402696
|
A | G | 40 | a0001c0001t0001g0010a0001c0001t0001g0326a0001c0001t0001g0327others(37): Show | 40 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.80+15269A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66402696 | ||||||
| chr15:66402889
|
G | T | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+15462G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66402889 | ||||||
| chr15:66402922
|
G | T | 2 | a0001c0001t0006g0007a0001c0001t0006g0008 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.80+15495G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66402922 | ||||||
| chr15:66403154
|
C | G | 1 | a0001c0001t0001g0344 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.80+15727C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66403154 | ||||||
| chr15:66403296
|
T | C | 1 | a0001c0001t0001g0140 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.80+15869T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66403296 | ||||||
| chr15:66403301
|
A | G | 1 | a0001c0001t0001g0140 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.80+15874A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66403301 | ||||||
| chr15:66403358
|
G | C | 1 | a0001c0001t0001g0339 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.80+15931G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66403358 | ||||||
| chr15:66403705
|
C | T | 1 | a0001c0001t0003g0198 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.80+16278C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66403705 | ||||||
| chr15:66403713
|
T | C | 3 | a0001c0001t0002g0053a0001c0001t0002g0056a0001c0001t0002g0092 | 3 | HG02148.hp2 HG02273.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.80+16286T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66403713 | ||||||
| chr15:66403716
|
A | G | 2 | a0001c0001t0001g0347a0001c0001t0001g0348 | 2 | HG00733.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.80+16289A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66403716 | ||||||
| chr15:66403725
|
C | T | 321 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(318): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.80+16298C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66403725 | ||||||
| chr15:66403743
|
A | G | 321 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(318): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.80+16316A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66403743 | ||||||
| chr15:66403829
|
C | G | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.80+16402C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66403829 | ||||||
| chr15:66403854
|
T | C | 3 | a0001c0001t0002g0057a0001c0001t0002g0058a0001c0001t0002g0059 | 3 | NA18946.hp2 NA19056.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.80+16427T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66403854 | ||||||
| chr15:66403994
|
T | G | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+16567T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66403994 | ||||||
| chr15:66403999
|
C | G | 1 | a0001c0001t0001g0268 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.80+16572C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66403999 | ||||||
| chr15:66404003
|
A | G | 3 | a0001c0001t0002g0117a0001c0001t0002g0120a0001c0001t0002g0341 | 3 | HG02109.hp1 HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.80+16576A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66404003 | ||||||
| chr15:66404021
|
GCTC | G | 3 | a0001c0001t0001g0334a0001c0001t0001g0335a0001c0001t0001g0336 | 3 | HG01099.hp2 HG02004.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.80+16598_80+16600d others(5): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66404021 | |||||
| chr15:66404245
|
C | T | 1 | a0001c0001t0003g0198 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.80+16818C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66404245 | ||||||
| chr15:66404397
|
A | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(161): Show | 164 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.80+16970A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66404397 | ||||||
| chr15:66404604
|
A | G | 1 | a0001c0001t0002g0090 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.80+17177A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66404604 | ||||||
| chr15:66404720
|
G | A | 320 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(317): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.80+17293G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66404720 | ||||||
| chr15:66404775
|
G | A | 2 | a0001c0001t0005g0160a0001c0001t0005g0161 | 2 | HG01074.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.80+17348G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66404775 | ||||||
| chr15:66404813
|
A | C | 1 | a0001c0001t0003g0204 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.80+17386A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66404813 | ||||||
| chr15:66404889
|
T | C | 361 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(358): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.80+17462T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66404889 | ||||||
| chr15:66404945
|
G | A | 1 | a0001c0001t0003g0187 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.80+17518G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66404945 | ||||||
| chr15:66405060
|
T | A | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0309 | 3 | HG00438.hp1 HG02155.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.80+17633T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66405060 | ||||||
| chr15:66405405
|
T | C | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+17978T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66405405 | ||||||
| chr15:66405499
|
T | A | 1 | a0001c0001t0001g0291 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.80+18072T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66405499 | ||||||
| chr15:66405539
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.80+18112A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66405539 | ||||||
| chr15:66405603
|
G | A | 3 | a0001c0001t0001g0250a0001c0001t0001g0253a0001c0001t0001g0284 | 3 | HG01891.hp1 HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.80+18176G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66405603 | ||||||
| chr15:66405721
|
C | A | 2 | a0001c0001t0001g0339a0001c0001t0001g0340 | 2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.80+18294C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66405721 | ||||||
| chr15:66405782
|
G | A | 2 | a0001c0001t0001g0135a0001c0001t0001g0137 | 2 | NA18968.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.80+18355G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66405782 | ||||||
| chr15:66405794
|
T | C | 1 | a0001c0001t0004g0016 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.80+18367T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66405794 | ||||||
| chr15:66405834
|
G | A | 40 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(37): Show | 40 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.80+18407G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66405834 | ||||||
| chr15:66406001
|
T | C | 1 | a0001c0001t0001g0304 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.80+18574T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66406001 | ||||||
| chr15:66406242
|
T | C | 40 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(37): Show | 40 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.80+18815T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66406242 | ||||||
| chr15:66406375
|
A | G | 1 | a0001c0001t0002g0095 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.80+18948A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66406375 | ||||||
| chr15:66406575
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.80+19148A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66406575 | ||||||
| chr15:66406805
|
C | T | 6 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0174others(3): Show | 6 | HG00558.hp1 HG00673.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.80+19378C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66406805 | ||||||
| chr15:66406884
|
T | G | 1 | a0001c0001t0002g0097 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.80+19457T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66406884 | ||||||
| chr15:66406905
|
G | C | 2 | a0001c0001t0001g0091a0001c0001t0001g0102 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.80+19478G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66406905 | ||||||
| chr15:66407016
|
A | C | 1 | a0001c0001t0001g0134 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.80+19589A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66407016 | ||||||
| chr15:66407020
|
A | G | 2 | a0001c0001t0001g0216a0001c0001t0001g0227 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.80+19593A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66407020 | ||||||
| chr15:66407107
|
C | G | 4 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(1): Show | 4 | HG01261.hp2 HG01433.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.80+19680C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66407107 | ||||||
| chr15:66407380
|
C | T | 38 | a0001c0001t0001g0010a0001c0001t0001g0326a0001c0001t0001g0327others(35): Show | 38 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.80+19953C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66407380 | ||||||
| chr15:66407390
|
T | C | 38 | a0001c0001t0001g0010a0001c0001t0001g0326a0001c0001t0001g0327others(35): Show | 38 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.80+19963T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66407390 | ||||||
| chr15:66407416
|
A | G | 2 | a0001c0001t0001g0267a0001c0001t0001g0321 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.80+19989A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66407416 | ||||||
| chr15:66407605
|
C | A | 364 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(361): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.80+20178C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66407605 | ||||||
| chr15:66407629
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.80+20202G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66407629 | ||||||
| chr15:66407957
|
C | T | 2 | a0001c0001t0003g0175a0001c0001t0003g0176 | 2 | HG03490.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.80+20530C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66407957 | ||||||
| chr15:66408219
|
G | A | 1 | a0001c0001t0002g0097 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.80+20792G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66408219 | ||||||
| chr15:66408238
|
T | G | 321 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(318): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.80+20811T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66408238 | ||||||
| chr15:66408341
|
AG | A | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.80+20916delG | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66408341 | |||||
| chr15:66408419
|
C | T | 3 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0325 | 3 | HG02055.hp1 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.80+20992C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66408419 | ||||||
| chr15:66408859
|
T | C | 366 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(363): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.80+21432T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66408859 | ||||||
| chr15:66409162
|
G | A | 63 | a0001c0001t0001g0360a0001c0001t0003g0162a0001c0001t0003g0164others(60): Show | 63 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.80+21735G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66409162 | ||||||
| chr15:66409490
|
G | A | 1 | a0001c0001t0002g0051 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.80+22063G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66409490 | ||||||
| chr15:66409766
|
A | C | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+22339A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66409766 | ||||||
| chr15:66409862
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.80+22435A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66409862 | ||||||
| chr15:66409928
|
C | T | 37 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(34): Show | 37 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.80+22501C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66409928 | ||||||
| chr15:66409974
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.80+22547A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66409974 | ||||||
| chr15:66409981
|
C | A | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+22554C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66409981 | ||||||
| chr15:66410007
|
C | A | 52 | a0001c0001t0003g0162a0001c0001t0003g0164a0001c0001t0003g0165others(49): Show | 52 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.80+22580C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66410007 | ||||||
| chr15:66410122
|
C | A | 3 | a0001c0001t0002g0076a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | NA18962.hp2 NA19002.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.80+22695C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66410122 | ||||||
| chr15:66410185
|
C | A | 61 | a0001c0001t0002g0011a0001c0001t0002g0048a0001c0001t0002g0049others(58): Show | 61 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.80+22758C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66410185 | ||||||
| chr15:66410208
|
T | C | 61 | a0001c0001t0002g0011a0001c0001t0002g0048a0001c0001t0002g0049others(58): Show | 61 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.80+22781T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66410208 | ||||||
| chr15:66410423
|
AAGAG | A | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+23000_80+23003d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66410423 | |||||
| chr15:66410586
|
T | C | 1 | a0001c0001t0012g0005 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.80+23159T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66410586 | ||||||
| chr15:66410604
|
T | A | 1 | a0001c0001t0002g0060 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.80+23177T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66410604 | ||||||
| chr15:66410620
|
GA | G | 26 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(23): Show | 26 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.80+23199delA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66410620 | |||||
| chr15:66410770
|
G | A | 2 | a0001c0001t0001g0276a0001c0001t0001g0288 | 2 | HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.80+23343G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66410770 | ||||||
| chr15:66410873
|
C | G | 40 | a0001c0001t0001g0010a0001c0001t0001g0326a0001c0001t0001g0327others(37): Show | 40 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.80+23446C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66410873 | ||||||
| chr15:66410989
|
A | C | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.80+23562A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66410989 | ||||||
| chr15:66411041
|
A | G | 2 | a0001c0001t0001g0331a0001c0001t0001g0333 | 2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.80+23614A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411041 | ||||||
| chr15:66411094
|
T | G | 5 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.80+23667T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411094 | ||||||
| chr15:66411138
|
A | T | 61 | a0001c0001t0002g0011a0001c0001t0002g0048a0001c0001t0002g0049others(58): Show | 61 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.80+23711A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411138 | ||||||
| chr15:66411173
|
G | A | 6 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0023others(3): Show | 6 | NA18941.hp1 NA18944.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.80+23746G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411173 | ||||||
| chr15:66411199
|
G | C | 1 | a0001c0001t0001g0255 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.80+23772G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411199 | ||||||
| chr15:66411287
|
G | T | 3 | a0001c0001t0005g0157a0001c0001t0005g0158a0001c0001t0005g0159 | 3 | HG00280.hp1 HG02735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.81-23740G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411287 | ||||||
| chr15:66411288
|
T | C | 3 | a0001c0001t0005g0157a0001c0001t0005g0158a0001c0001t0005g0159 | 3 | HG00280.hp1 HG02735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.81-23739T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411288 | ||||||
| chr15:66411290
|
G | T | 3 | a0001c0001t0005g0157a0001c0001t0005g0158a0001c0001t0005g0159 | 3 | HG00280.hp1 HG02735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.81-23737G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411290 | ||||||
| chr15:66411291
|
G | T | 3 | a0001c0001t0005g0157a0001c0001t0005g0158a0001c0001t0005g0159 | 3 | HG00280.hp1 HG02735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.81-23736G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411291 | ||||||
| chr15:66411343
|
CCT | C | 5 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.81-23680_81-23679d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66411343 | |||||
| chr15:66411352
|
A | G | 3 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110 | 3 | HG02970.hp2 HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.81-23675A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411352 | ||||||
| chr15:66411359
|
A | G | 6 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(3): Show | 6 | HG02486.hp2 HG02572.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.81-23668A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411359 | ||||||
| chr15:66411421
|
C | T | 30 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(27): Show | 30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.81-23606C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411421 | ||||||
| chr15:66411534
|
T | G | 1 | a0001c0001t0001g0142 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.81-23493T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411534 | ||||||
| chr15:66411626
|
A | G | 5 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.81-23401A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411626 | ||||||
| chr15:66411686
|
T | C | 3 | a0001c0001t0002g0057a0001c0001t0002g0058a0001c0001t0002g0059 | 3 | NA18946.hp2 NA19056.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.81-23341T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411686 | ||||||
| chr15:66411769
|
T | C | 2 | a0001c0001t0001g0113a0001c0001t0001g0115 | 2 | HG02486.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.81-23258T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411769 | ||||||
| chr15:66411928
|
T | G | 1 | a0001c0001t0002g0061 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.81-23099T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66411928 | ||||||
| chr15:66412051
|
A | G | 1 | a0001c0001t0002g0149 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.81-22976A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66412051 | ||||||
| chr15:66412111
|
G | A | 38 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(35): Show | 38 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.81-22916G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66412111 | ||||||
| chr15:66412270
|
C | T | 1 | a0001c0001t0003g0206 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.81-22757C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66412270 | ||||||
| chr15:66412668
|
C | T | 1 | a0001c0001t0006g0002 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.81-22359C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66412668 | ||||||
| chr15:66412705
|
G | A | 92 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.81-22322G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66412705 | ||||||
| chr15:66412837
|
C | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(81): Show | 84 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.81-22190C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66412837 | ||||||
| chr15:66412966
|
G | A | 2 | a0001c0001t0001g0342a0001c0001t0001g0345 | 2 | HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.81-22061G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66412966 | ||||||
| chr15:66413053
|
G | A | 3 | a0001c0001t0002g0117a0001c0001t0002g0120a0001c0001t0002g0341 | 3 | HG02109.hp1 HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.81-21974G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413053 | ||||||
| chr15:66413096
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.81-21931A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413096 | ||||||
| chr15:66413123
|
T | C | 1 | a0001c0001t0014g0213 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.81-21904T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413123 | ||||||
| chr15:66413150
|
C | T | 38 | a0001c0001t0001g0010a0001c0001t0001g0326a0001c0001t0001g0327others(35): Show | 38 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.81-21877C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413150 | ||||||
| chr15:66413191
|
T | C | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-21836T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413191 | ||||||
| chr15:66413239
|
A | G | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-21788A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413239 | ||||||
| chr15:66413249
|
A | C | 1 | a0001c0001t0001g0326 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.81-21778A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413249 | ||||||
| chr15:66413278
|
C | G | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-21749C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413278 | ||||||
| chr15:66413398
|
G | C | 1 | a0001c0001t0003g0172 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.81-21629G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413398 | ||||||
| chr15:66413618
|
G | A | 1 | a0001c0001t0003g0199 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.81-21409G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413618 | ||||||
| chr15:66413624
|
AT | A | 353 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(350): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.81-21392delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66413624 | |||||
| chr15:66413624
|
ATT | A | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-21393_81-21392d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66413624 | |||||
| chr15:66413673
|
G | C | 1 | a0001c0001t0002g0061 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.81-21354G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413673 | ||||||
| chr15:66413698
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.81-21329T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413698 | ||||||
| chr15:66413786
|
G | A | 2 | a0001c0001t0002g0062a0001c0001t0002g0080 | 2 | NA18943.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.81-21241G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413786 | ||||||
| chr15:66413832
|
T | C | 1 | a0001c0001t0001g0306 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.81-21195T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413832 | ||||||
| chr15:66413878
|
C | A | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-21149C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413878 | ||||||
| chr15:66413886
|
T | C | 62 | a0001c0001t0002g0011a0001c0001t0002g0047a0001c0001t0002g0048others(59): Show | 62 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.81-21141T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413886 | ||||||
| chr15:66413911
|
C | CT | 297 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(294): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.81-21100dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66413911 | |||||
| chr15:66413911
|
C | CTT | 6 | a0001c0001t0001g0291a0001c0001t0001g0300a0001c0001t0002g0089others(3): Show | 6 | HG00280.hp1 HG02735.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.81-21101_81-21100d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66413911 | |||||
| chr15:66413911
|
C | CTTT | 35 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(32): Show | 35 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.81-21102_81-21100d others(5): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66413911 | |||||
| chr15:66413955
|
C | CT | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-21060dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66413955 | |||||
| chr15:66413967
|
T | A | 2 | a0001c0001t0003g0201a0001c0001t0003g0207 | 2 | HG01106.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.81-21060T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66413967 | ||||||
| chr15:66414010
|
C | A | 1 | a0001c0001t0002g0064 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.81-21017C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66414010 | ||||||
| chr15:66414167
|
G | A | 38 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(35): Show | 38 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.81-20860G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66414167 | ||||||
| chr15:66414198
|
GAGTCAGG others(140): Show |
G | 40 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(37): Show | 40 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.81-20825_81-20679d others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66414198 | |||||
| chr15:66414366
|
A | G | 46 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(43): Show | 46 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.81-20661A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66414366 | ||||||
| chr15:66414407
|
A | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(81): Show | 84 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.81-20620A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66414407 | ||||||
| chr15:66414539
|
T | C | 2 | a0001c0001t0006g0007a0001c0001t0006g0008 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.81-20488T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66414539 | ||||||
| chr15:66414574
|
C | T | 1 | a0001c0001t0002g0074 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.81-20453C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66414574 | ||||||
| chr15:66414781
|
C | CT | 40 | a0001c0001t0001g0010a0001c0001t0001g0139a0001c0001t0001g0326others(37): Show | 40 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.81-20231dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66414781 | |||||
| chr15:66414781
|
CT | C | 6 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(3): Show | 6 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.81-20231delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66414781 | |||||
| chr15:66414796
|
T | C | 37 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(34): Show | 37 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.81-20231T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66414796 | ||||||
| chr15:66414846
|
G | C | 1 | a0001c0001t0002g0085 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.81-20181G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66414846 | ||||||
| chr15:66414850
|
C | T | 40 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(37): Show | 40 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.81-20177C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66414850 | ||||||
| chr15:66415269
|
CT | C | 10 | a0001c0001t0001g0349a0001c0001t0001g0350a0001c0001t0001g0354others(7): Show | 10 | HG01891.hp2 HG02055.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.81-19756delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66415269 | |||||
| chr15:66415280
|
A | G | 1 | a0001c0001t0003g0182 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.81-19747A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66415280 | ||||||
| chr15:66415353
|
C | T | 2 | a0001c0001t0001g0220a0001c0001t0001g0237 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.81-19674C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66415353 | ||||||
| chr15:66415458
|
C | T | 1 | a0001c0001t0002g0117 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.81-19569C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66415458 | ||||||
| chr15:66415459
|
C | T | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | HG00735.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.81-19568C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66415459 | ||||||
| chr15:66415460
|
T | C | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-19567T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66415460 | ||||||
| chr15:66415523
|
G | T | 82 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(79): Show | 82 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.81-19504G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66415523 | ||||||
| chr15:66415987
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.81-19040C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66415987 | ||||||
| chr15:66416002
|
C | T | 5 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.81-19025C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66416002 | ||||||
| chr15:66416004
|
C | A | 1 | a0001c0001t0003g0244 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.81-19023C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66416004 | ||||||
| chr15:66416005
|
C | T | 1 | a0001c0001t0003g0244 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.81-19022C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66416005 | ||||||
| chr15:66416025
|
G | C | 4 | a0001c0001t0001g0248a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | HG00735.hp1 HG01167.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.81-19002G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66416025 | ||||||
| chr15:66416181
|
T | TAGGGAGT others(23): Show |
1 | a0001c0001t0001g0216 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.81-18845_81-18816d others(32): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66416181 | |||||
| chr15:66416259
|
ATTG | A | 4 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0325others(1): Show | 4 | HG00140.hp1 HG02055.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.81-18762_81-18760d others(5): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66416259 | |||||
| chr15:66416271
|
C | CTTG | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-18754_81-18752d others(5): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66416271 | |||||
| chr15:66416370
|
C | A | 1 | a0001c0001t0003g0189 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.81-18657C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66416370 | ||||||
| chr15:66416409
|
A | G | 1 | a0001c0003t0001g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.81-18618A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66416409 | ||||||
| chr15:66416437
|
C | A | 28 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(25): Show | 28 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.81-18590C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66416437 | ||||||
| chr15:66416467
|
A | C | 38 | a0001c0001t0001g0010a0001c0001t0001g0326a0001c0001t0001g0327others(35): Show | 38 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.81-18560A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66416467 | ||||||
| chr15:66416557
|
G | C | 2 | a0001c0001t0001g0347a0001c0001t0001g0348 | 2 | HG00733.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.81-18470G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66416557 | ||||||
| chr15:66416601
|
C | A | 62 | a0001c0001t0003g0162a0001c0001t0003g0164a0001c0001t0003g0165others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.81-18426C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66416601 | ||||||
| chr15:66416602
|
A | G | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-18425A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66416602 | ||||||
| chr15:66416623
|
A | G | 1 | a0001c0001t0001g0140 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.81-18404A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66416623 | ||||||
| chr15:66417033
|
C | T | 59 | a0001c0001t0002g0011a0001c0001t0002g0047a0001c0001t0002g0048others(56): Show | 59 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.81-17994C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66417033 | ||||||
| chr15:66417048
|
C | G | 313 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(310): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.81-17979C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66417048 | ||||||
| chr15:66417316
|
T | C | 2 | a0001c0001t0001g0118a0001c0001t0001g0138 | 2 | NA19074.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.81-17711T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66417316 | ||||||
| chr15:66417320
|
C | T | 2 | a0001c0001t0003g0162a0001c0001t0003g0171 | 2 | HG03491.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.81-17707C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66417320 | ||||||
| chr15:66417342
|
G | A | 1 | a0001c0001t0003g0210 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.81-17685G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66417342 | ||||||
| chr15:66417407
|
C | T | 83 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(80): Show | 83 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.81-17620C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66417407 | ||||||
| chr15:66417819
|
A | G | 1 | a0001c0001t0006g0009 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.81-17208A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66417819 | ||||||
| chr15:66417921
|
C | G | 93 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(90): Show | 93 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.81-17106C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66417921 | ||||||
| chr15:66417938
|
C | T | 23 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(20): Show | 23 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.81-17089C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66417938 | ||||||
| chr15:66418313
|
C | G | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-16714C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66418313 | ||||||
| chr15:66418345
|
T | C | 3 | a0001c0001t0001g0250a0001c0001t0001g0253a0001c0001t0001g0284 | 3 | HG01891.hp1 HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.81-16682T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66418345 | ||||||
| chr15:66418447
|
T | C | 4 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0316others(1): Show | 4 | NA18967.hp1 NA18969.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.81-16580T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66418447 | ||||||
| chr15:66418552
|
G | C | 1 | a0001c0001t0001g0001 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.81-16475G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66418552 | ||||||
| chr15:66418555
|
C | T | 1 | a0001c0001t0001g0326 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.81-16472C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66418555 | ||||||
| chr15:66418556
|
G | A | 313 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(310): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.81-16471G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66418556 | ||||||
| chr15:66418888
|
C | T | 1 | a0001c0001t0003g0196 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.81-16139C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66418888 | ||||||
| chr15:66418945
|
C | CT | 55 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0033others(52): Show | 55 | HG00597.hp1 HG00673.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.81-16060dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66418945 | |||||
| chr15:66418945
|
C | CTT | 9 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0001g0330others(6): Show | 9 | HG00733.hp2 HG01109.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.81-16061_81-16060d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66418945 | |||||
| chr15:66418945
|
CT | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(105): Show | 108 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.81-16060delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66418945 | |||||
| chr15:66419242
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.81-15785G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66419242 | ||||||
| chr15:66419349
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.81-15678G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66419349 | ||||||
| chr15:66419520
|
CA | C | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-15494delA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66419520 | |||||
| chr15:66419531
|
A | C | 4 | a0001c0001t0001g0010a0001c0001t0001g0327a0001c0001t0001g0332others(1): Show | 4 | HG02109.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.81-15496A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66419531 | ||||||
| chr15:66419543
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.81-15484C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66419543 | ||||||
| chr15:66419673
|
G | T | 38 | a0001c0001t0001g0010a0001c0001t0001g0326a0001c0001t0001g0327others(35): Show | 38 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.81-15354G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66419673 | ||||||
| chr15:66419704
|
C | G | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.81-15323C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66419704 | ||||||
| chr15:66419784
|
CTGTT | C | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-15240_81-15237d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66419784 | |||||
| chr15:66419899
|
C | CA | 313 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(310): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.81-15119dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66419899 | |||||
| chr15:66419913
|
G | A | 2 | a0001c0001t0001g0352a0001c0001t0001g0353 | 2 | HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.81-15114G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66419913 | ||||||
| chr15:66419981
|
AC | A | 62 | a0001c0001t0003g0162a0001c0001t0003g0164a0001c0001t0003g0165others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.81-15045delC | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66419981 | ||||||
| chr15:66420042
|
G | A | 30 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(27): Show | 30 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.81-14985G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420042 | ||||||
| chr15:66420154
|
G | A | 1 | a0001c0004t0001g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.81-14873G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420154 | ||||||
| chr15:66420167
|
C | T | 8 | a0001c0001t0003g0164a0001c0001t0003g0170a0001c0001t0003g0184others(5): Show | 8 | HG00323.hp2 HG00642.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.81-14860C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420167 | ||||||
| chr15:66420190
|
A | G | 361 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(358): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.81-14837A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420190 | ||||||
| chr15:66420376
|
G | T | 1 | a0001c0001t0003g0193 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.81-14651G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420376 | ||||||
| chr15:66420384
|
TG | T | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-14641delG | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420384 | |||||
| chr15:66420451
|
G | A | 2 | a0001c0001t0001g0276a0001c0001t0001g0288 | 2 | HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.81-14576G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420451 | ||||||
| chr15:66420468
|
A | C | 90 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(87): Show | 90 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.81-14559A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420468 | ||||||
| chr15:66420547
|
T | A | 1 | a0001c0001t0005g0160 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.81-14480T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420547 | ||||||
| chr15:66420553
|
AAAAAT | A | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-14460_81-14456d others(7): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420553 | |||||
| chr15:66420643
|
A | G | 1 | a0001c0001t0003g0199 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.81-14384A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420643 | ||||||
| chr15:66420706
|
C | CAT | 25 | a0001c0001t0001g0001a0001c0001t0001g0134a0001c0001t0001g0140others(22): Show | 25 | HG00323.hp2 HG00597.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.81-14306_81-14305d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420706 | |||||
| chr15:66420706
|
C | CATAT | 19 | a0001c0001t0001g0111a0001c0001t0001g0130a0001c0001t0001g0146others(16): Show | 19 | HG00423.hp2 HG00609.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.81-14308_81-14305d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420706 | |||||
| chr15:66420706
|
C | CATATAT | 13 | a0001c0001t0001g0112a0001c0001t0001g0131a0001c0001t0001g0132others(10): Show | 13 | HG00621.hp2 HG02155.hp1 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.81-14310_81-14305d others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420706 | |||||
| chr15:66420706
|
C | CATATATA others(1): Show |
9 | a0001c0001t0001g0138a0001c0001t0001g0143a0001c0001t0003g0173others(6): Show | 9 | HG00099.hp1 HG00558.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.81-14312_81-14305d others(10): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420706 | |||||
| chr15:66420706
|
C | CATATATA others(3): Show |
2 | a0001c0001t0001g0121a0001c0001t0003g0205 | 2 | HG01515.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.81-14314_81-14305d others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420706 | |||||
| chr15:66420706
|
C | CATATATA others(5): Show |
2 | a0001c0001t0002g0065a0001c0001t0008g0068 | 2 | HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.81-14316_81-14305d others(14): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420706 | |||||
| chr15:66420706
|
C | CATATATA others(7): Show |
2 | a0001c0001t0001g0231a0001c0001t0003g0165 | 2 | HG01123.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.81-14318_81-14305d others(16): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420706 | |||||
| chr15:66420706
|
C | CATATATA others(9): Show |
4 | a0001c0001t0001g0275a0001c0001t0003g0182a0001c0001t0003g0201others(1): Show | 4 | HG01106.hp2 HG03927.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.81-14320_81-14305d others(18): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420706 | |||||
| chr15:66420706
|
C | CATATATA others(11): Show |
1 | a0001c0001t0003g0177 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.81-14305_81-14304i others(20): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420706 | |||||
| chr15:66420706
|
C | CATATATA others(17): Show |
1 | a0001c0001t0001g0113 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(26): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420706 | |||||
| chr15:66420706
|
C | CATATATA others(19): Show |
1 | a0001c0001t0001g0340 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(28): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420706 | |||||
| chr15:66420706
|
C | CATATATA others(21): Show |
3 | a0001c0001t0001g0010a0001c0001t0001g0326a0001c0001t0003g0207 | 3 | HG02486.hp1 HG02723.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(30): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420706 | |||||
| chr15:66420706
|
C | CATATATA others(25): Show |
1 | a0001c0001t0009g0163 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.81-14305_81-14304i others(34): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420706 | |||||
| chr15:66420715
|
A | ATATATAT others(45): Show |
2 | a0001c0001t0001g0029a0001c0001t0004g0043 | 2 | HG04204.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(54): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420715 | |||||
| chr15:66420715
|
A | ATATATAT others(39): Show |
2 | a0001c0001t0004g0025a0001c0001t0004g0041 | 2 | NA18995.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(48): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420715 | |||||
| chr15:66420715
|
A | ATATATAT others(37): Show |
3 | a0001c0001t0004g0018a0001c0001t0004g0023a0001c0001t0004g0024 | 3 | NA18944.hp1 NA18969.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(46): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420715 | |||||
| chr15:66420715
|
A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0335 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(42): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420715 | |||||
| chr15:66420715
|
A | ATATATAT others(31): Show |
2 | a0001c0001t0001g0246a0001c0001t0004g0022 | 2 | NA18967.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(40): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420715 | |||||
| chr15:66420715
|
A | ATATATAT others(29): Show |
2 | a0001c0001t0001g0336a0001c0001t0004g0044 | 2 | HG02004.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(38): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420715 | |||||
| chr15:66420715
|
ATATATAT others(1): Show |
A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0007others(2): Show | 5 | HG01515.hp1 HG01517.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.81-14310_81-14303d others(10): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420715 | |||||
| chr15:66420717
|
A | ATATATAT others(43): Show |
2 | a0001c0001t0001g0312a0001c0001t0004g0046 | 2 | NA19006.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(52): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420717 | |||||
| chr15:66420717
|
A | ATATATAT others(37): Show |
1 | a0001c0001t0001g0036 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(46): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420717 | |||||
| chr15:66420717
|
A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0035 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(42): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420717 | |||||
| chr15:66420719
|
A | ATATATAT others(35): Show |
2 | a0001c0001t0001g0027a0001c0001t0001g0039 | 2 | HG00738.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(44): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420719 | |||||
| chr15:66420719
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0323 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(24): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420719 | |||||
| chr15:66420719
|
A | ATATATAT others(13): Show |
2 | a0001c0001t0001g0324a0001c0001t0001g0325 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(22): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420719 | |||||
| chr15:66420721
|
A | ATATATAT others(43): Show |
7 | a0001c0001t0001g0026a0001c0001t0004g0016a0001c0001t0004g0017others(4): Show | 7 | HG00423.hp1 HG01106.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.81-14305_81-14304i others(52): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0108 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.81-14305_81-14304i others(42): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(43): Show |
3 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0147 | 3 | NA18959.hp2 NA19012.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(52): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(39): Show |
1 | a0001c0001t0001g0028 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(48): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(37): Show |
1 | a0001c0001t0001g0334 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(46): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(35): Show |
1 | a0001c0001t0004g0042 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(44): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(37): Show |
1 | a0001c0001t0001g0369 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(46): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0245 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.81-14305_81-14304i others(42): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0109 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.81-14305_81-14304i others(36): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(31): Show |
2 | a0001c0001t0001g0030a0001c0001t0001g0034 | 2 | HG01123.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(40): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(27): Show |
4 | a0001c0001t0001g0329a0001c0001t0001g0332a0001c0001t0001g0344others(1): Show | 4 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.81-14305_81-14304i others(36): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(29): Show |
3 | a0001c0001t0001g0327a0001c0001t0001g0350a0001c0001t0001g0367 | 3 | HG02896.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(38): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(31): Show |
1 | a0001c0006t0001g0368 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(40): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0330 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(42): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(35): Show |
1 | a0001c0001t0001g0360 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.81-14305_81-14304i others(44): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(25): Show |
1 | a0001c0001t0001g0366 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(34): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(27): Show |
2 | a0001c0001t0001g0354a0001c0001t0014g0213 | 2 | HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(36): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(29): Show |
1 | a0001c0001t0013g0351 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(38): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(23): Show |
1 | a0001c0001t0001g0361 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(32): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(27): Show |
4 | a0001c0001t0001g0343a0001c0001t0001g0347a0001c0001t0001g0348others(1): Show | 4 | HG00733.hp2 HG01069.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.81-14305_81-14304i others(36): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(29): Show |
1 | a0001c0001t0001g0331 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.81-14305_81-14304i others(38): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0362 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(42): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0339 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.81-14305_81-14304i others(26): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(25): Show |
4 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(1): Show | 4 | HG01261.hp2 HG01433.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.81-14305_81-14304i others(34): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0328 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.81-14305_81-14304i others(28): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(23): Show |
1 | a0001c0001t0001g0359 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.81-14305_81-14304i others(32): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(25): Show |
1 | a0001c0001t0001g0333 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.81-14305_81-14304i others(34): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0110 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(24): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0352 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(30): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(25): Show |
1 | a0001c0001t0001g0365 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.81-14305_81-14304i others(34): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(13): Show |
1 | a0001c0004t0001g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(22): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0353 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.81-14305_81-14304i others(26): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0358 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(28): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(21): Show |
2 | a0001c0001t0001g0346a0001c0001t0001g0363 | 2 | HG02895.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(30): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(23): Show |
2 | a0001c0001t0001g0364a0001c0001t0001g0370 | 2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(32): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(25): Show |
1 | a0001c0001t0001g0345 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.81-14305_81-14304i others(34): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(23): Show |
1 | a0001c0001t0001g0342 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.81-14305_81-14304i others(32): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(5): Show |
4 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0136others(1): Show | 4 | HG02622.hp1 NA18956.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.81-14305_81-14304i others(14): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(3): Show |
2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG01993.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(5): Show |
11 | a0001c0001t0001g0122a0001c0001t0001g0125a0001c0001t0001g0126others(8): Show | 11 | HG00733.hp1 HG01257.hp1 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.81-14305_81-14304i others(14): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(15): Show |
2 | a0001c0001t0001g0356a0001c0001t0001g0357 | 2 | HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.81-14305_81-14304i others(24): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0139 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.81-14305_81-14304i others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420721
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.81-14306A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420721 | ||||||
| chr15:66420721
|
ATG | A | 23 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(20): Show | 23 | HG01069.hp2 HG01071.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.81-14268_81-14267d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420721 | |||||
| chr15:66420723
|
G | A | 224 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(221): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.81-14304G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420723 | ||||||
| chr15:66420725
|
G | A | 236 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(233): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.81-14302G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420725 | ||||||
| chr15:66420727
|
G | A | 227 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(224): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.81-14300G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420727 | ||||||
| chr15:66420729
|
G | A | 218 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(215): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.81-14298G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420729 | ||||||
| chr15:66420731
|
G | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.81-14296G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420731 | ||||||
| chr15:66420733
|
G | A | 158 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(155): Show | 158 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.81-14294G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420733 | ||||||
| chr15:66420735
|
G | A | 135 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(132): Show | 135 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.81-14292G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420735 | ||||||
| chr15:66420737
|
G | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(87): Show | 90 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.81-14290G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420737 | ||||||
| chr15:66420739
|
G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(73): Show | 76 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.81-14288G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420739 | ||||||
| chr15:66420741
|
G | A | 53 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0247others(50): Show | 53 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.81-14286G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420741 | ||||||
| chr15:66420743
|
G | A | 18 | a0001c0001t0001g0001a0001c0001t0001g0251a0001c0001t0001g0253others(15): Show | 18 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(15): Show |
intron_variant | MODIFIER | c.81-14284G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420743 | ||||||
| chr15:66420745
|
G | A | 4 | a0001c0001t0001g0231a0001c0001t0001g0251a0001c0001t0001g0258others(1): Show | 4 | HG00544.hp1 HG01123.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.81-14282G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420745 | ||||||
| chr15:66420747
|
G | A | 2 | a0001c0001t0001g0231a0001c0002t0001g0311 | 2 | HG00544.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.81-14280G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420747 | ||||||
| chr15:66420749
|
G | A | 1 | a0001c0002t0001g0311 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.81-14278G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420749 | ||||||
| chr15:66420755
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.81-14272G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420755 | ||||||
| chr15:66420757
|
G | A | 45 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(42): Show | 45 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.81-14270G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420757 | ||||||
| chr15:66420757
|
GTGTA | G | 3 | a0001c0001t0005g0157a0001c0001t0005g0239a0001c0001t0005g0242 | 3 | HG00280.hp1 NA18963.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.81-14266_81-14263d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420757 | |||||
| chr15:66420759
|
G | A | 111 | a0001c0001t0001g0010a0001c0001t0001g0026a0001c0001t0001g0027others(108): Show | 111 | HG00423.hp1 HG00733.hp2 HG00738.hp2 others(108): Show |
intron_variant | MODIFIER | c.81-14268G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420759 | ||||||
| chr15:66420759
|
G | GTATA | 20 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0121others(17): Show | 20 | HG00733.hp1 HG01257.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.81-14265_81-14264i others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420759 | |||||
| chr15:66420759
|
GTA | G | 23 | a0001c0001t0001g0248a0001c0001t0001g0252a0001c0001t0001g0255others(20): Show | 23 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.81-14266_81-14265d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420759 | |||||
| chr15:66420759
|
GTATGTGT others(3): Show |
G | 40 | a0001c0001t0001g0232a0001c0001t0002g0011a0001c0001t0002g0048others(37): Show | 40 | HG00099.hp2 HG00140.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.81-14264_81-14255d others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420759 | |||||
| chr15:66420759
|
GTATGTGT others(5): Show |
G | 1 | a0001c0001t0006g0002 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.81-14264_81-14253d others(14): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420759 | |||||
| chr15:66420759
|
GTATGTGT others(9): Show |
G | 1 | a0001c0001t0001g0305 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.81-14266_81-14251d others(18): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420759 | |||||
| chr15:66420761
|
A | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(150): Show | 153 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.81-14266A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420761 | ||||||
| chr15:66420763
|
G | A | 2 | a0001c0001t0002g0065a0001c0001t0008g0068 | 2 | HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.81-14264G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420763 | ||||||
| chr15:66420763
|
GTGTGTAT others(1): Show |
G | 12 | a0001c0001t0002g0047a0001c0001t0002g0051a0001c0001t0002g0066others(9): Show | 12 | HG00544.hp2 HG00597.hp2 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.81-14262_81-14255d others(10): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420763 | |||||
| chr15:66420765
|
GTGTATA | G | 4 | a0001c0001t0002g0086a0001c0001t0002g0090a0001c0001t0002g0148others(1): Show | 4 | HG00558.hp2 HG01074.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.81-14260_81-14255d others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420765 | |||||
| chr15:66420765
|
GTGTATAT others(3): Show |
G | 1 | a0001c0001t0001g0297 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.81-14258_81-14249d others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420765 | |||||
| chr15:66420767
|
GTATA | G | 26 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0263others(23): Show | 26 | HG00609.hp1 HG00639.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.81-14254_81-14251d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420767 | |||||
| chr15:66420767
|
GTATATA | G | 12 | a0001c0001t0001g0012a0001c0001t0001g0262a0001c0001t0001g0276others(9): Show | 12 | HG00280.hp2 HG00639.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.81-14256_81-14251d others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420767 | |||||
| chr15:66420767
|
GTATATAT others(1): Show |
G | 3 | a0001c0001t0001g0299a0001c0001t0003g0207a0001c0001t0009g0163 | 3 | HG02486.hp1 NA19088.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.81-14258_81-14251d others(10): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420767 | |||||
| chr15:66420769
|
A | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(101): Show | 104 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.81-14258A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420769 | ||||||
| chr15:66420771
|
A | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.81-14256A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420771 | ||||||
| chr15:66420773
|
A | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(121): Show | 124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.81-14254A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420773 | ||||||
| chr15:66420775
|
A | G | 150 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(147): Show | 150 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.81-14252A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420775 | ||||||
| chr15:66420777
|
G | A | 2 | a0001c0001t0002g0065a0001c0001t0008g0068 | 2 | HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.81-14250G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420777 | ||||||
| chr15:66420779
|
G | GTA | 28 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(25): Show | 28 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.81-14240_81-14239d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420779 | |||||
| chr15:66420779
|
G | GTATATAT others(23): Show |
1 | a0001c0001t0001g0339 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.81-14240_81-14239i others(32): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420779 | |||||
| chr15:66420779
|
G | GTATATAT others(79): Show |
1 | a0001c0001t0001g0340 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.81-14240_81-14239i others(88): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420779 | |||||
| chr15:66420781
|
A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.81-14246A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420781 | ||||||
| chr15:66420783
|
A | G | 6 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0174others(3): Show | 6 | HG00558.hp1 HG00673.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.81-14244A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420783 | ||||||
| chr15:66420787
|
ATG | A | 13 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(10): Show | 13 | HG00280.hp1 HG00438.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.81-14234_81-14233d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420787 | |||||
| chr15:66420789
|
G | A | 119 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(116): Show | 119 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.81-14238G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420789 | ||||||
| chr15:66420791
|
G | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(78): Show | 81 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.81-14236G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420791 | ||||||
| chr15:66420793
|
G | A | 48 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0115others(45): Show | 48 | HG00609.hp2 HG01069.hp2 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.81-14234G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420793 | ||||||
| chr15:66420793
|
G | GTATATAT others(7): Show |
36 | a0001c0001t0001g0010a0001c0001t0001g0326a0001c0001t0001g0327others(33): Show | 36 | HG00733.hp2 HG01069.hp1 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.81-14226_81-14213d others(16): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420793 | |||||
| chr15:66420801
|
A | ATG | 21 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0121others(18): Show | 21 | HG00733.hp1 HG01257.hp1 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.81-14222_81-14221d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420801 | |||||
| chr15:66420801
|
A | G | 2 | a0001c0001t0001g0337a0001c0001t0002g0097 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.81-14226A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420801 | ||||||
| chr15:66420803
|
G | A | 3 | a0001c0001t0001g0220a0001c0001t0001g0226a0001c0001t0001g0237 | 3 | HG02451.hp2 HG02970.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.81-14224G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420803 | ||||||
| chr15:66420805
|
G | A | 39 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(36): Show | 39 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.81-14222G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420805 | ||||||
| chr15:66420805
|
G | GTA | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.81-14214_81-14213d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420805 | |||||
| chr15:66420807
|
A | G | 2 | a0001c0001t0001g0220a0001c0001t0001g0237 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.81-14220A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420807 | ||||||
| chr15:66420809
|
A | G | 2 | a0001c0001t0001g0226a0001c0001t0002g0097 | 2 | HG01243.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.81-14218A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420809 | ||||||
| chr15:66420815
|
G | A | 4 | a0001c0001t0001g0339a0001c0001t0001g0340a0001c0001t0001g0359others(1): Show | 4 | HG01109.hp1 HG02615.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.81-14212G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420815 | ||||||
| chr15:66420817
|
GTA | G | 6 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(3): Show | 6 | HG00280.hp2 HG00639.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.81-14200_81-14199d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420817 | |||||
| chr15:66420819
|
A | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(92): Show | 95 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.81-14208A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420819 | ||||||
| chr15:66420823
|
A | G | 221 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.81-14204A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420823 | ||||||
| chr15:66420823
|
ATATATGT others(11): Show |
A | 2 | a0001c0001t0006g0007a0001c0001t0006g0008 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.81-14202_81-14185d others(20): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420823 | |||||
| chr15:66420833
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0362 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.81-14187_81-14186i others(14): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420833 | |||||
| chr15:66420833
|
A | ATATGTAT others(5): Show |
10 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0130others(7): Show | 10 | HG00609.hp2 HG01361.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.81-14191_81-14190i others(14): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420833 | |||||
| chr15:66420833
|
A | G | 1 | a0001c0001t0001g0339 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.81-14194A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420833 | ||||||
| chr15:66420837
|
A | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(78): Show | 81 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.81-14190A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420837 | ||||||
| chr15:66420837
|
ATATG | A | 6 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(3): Show | 6 | HG00280.hp2 HG00639.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.81-14188_81-14185d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420837 | |||||
| chr15:66420839
|
ATG | A | 80 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0121others(77): Show | 80 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.81-14182_81-14181d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420839 | |||||
| chr15:66420841
|
G | A | 229 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(226): Show | 229 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(226): Show |
intron_variant | MODIFIER | c.81-14186G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420841 | ||||||
| chr15:66420847
|
A | G | 1 | a0001c0001t0002g0097 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.81-14180A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420847 | ||||||
| chr15:66420853
|
A | G | 3 | a0001c0001t0002g0117a0001c0001t0002g0120a0001c0001t0002g0341 | 3 | HG02109.hp1 HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.81-14174A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420853 | ||||||
| chr15:66420855
|
G | A | 1 | a0001c0001t0001g0359 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.81-14172G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420855 | ||||||
| chr15:66420855
|
GTGTGTAT others(27): Show |
G | 1 | a0001c0001t0002g0097 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.81-14170_81-14137d others(36): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420855 | |||||
| chr15:66420857
|
GTGTATA | G | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-14168_81-14163d others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420857 | |||||
| chr15:66420859
|
GTA | G | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.81-14160_81-14159d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420859 | |||||
| chr15:66420861
|
A | G | 312 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(309): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.81-14166A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420861 | ||||||
| chr15:66420867
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.81-14160A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420867 | ||||||
| chr15:66420873
|
G | A | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-14154G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420873 | ||||||
| chr15:66420874
|
T | C | 1 | a0001c0001t0003g0190 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.81-14153T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420874 | ||||||
| chr15:66420875
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0359 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.81-14141_81-14140i others(14): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420875 | |||||
| chr15:66420881
|
A | G | 1 | a0001c0001t0001g0340 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.81-14146A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420881 | ||||||
| chr15:66420881
|
ATGTG | A | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-14144_81-14141d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420881 | |||||
| chr15:66420886
|
T | C | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-14141T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420886 | ||||||
| chr15:66420894
|
CACAT | C | 15 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0233others(12): Show | 15 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.81-14121_81-14118d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420894 | |||||
| chr15:66420896
|
C | T | 1 | a0001c0001t0002g0149 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.81-14131C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420896 | ||||||
| chr15:66420906
|
T | C | 2 | a0001c0001t0001g0264a0001c0001t0001g0283 | 2 | HG01978.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.81-14121T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420906 | ||||||
| chr15:66420912
|
CACAT | C | 109 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(106): Show | 109 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.81-14105_81-14102d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420912 | |||||
| chr15:66420916
|
T | C | 2 | a0001c0001t0002g0069a0001c0001t0002g0087 | 2 | HG00597.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.81-14111T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420916 | ||||||
| chr15:66420922
|
CAT | C | 5 | a0001c0001t0001g0352a0001c0001t0001g0353a0001c0001t0003g0165others(2): Show | 5 | HG03130.hp2 NA18940.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.81-14097_81-14096d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420922 | |||||
| chr15:66420940
|
C | CAT | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-14081_81-14080d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420940 | |||||
| chr15:66420950
|
TACAC | T | 3 | a0001c0001t0002g0057a0001c0001t0002g0058a0001c0001t0002g0059 | 3 | NA18946.hp2 NA19056.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.81-14075_81-14072d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420950 | |||||
| chr15:66420958
|
C | CAT | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-14063_81-14062d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420958 | |||||
| chr15:66420962
|
TATACAC | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(107): Show | 110 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.81-14063_81-14058d others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420962 | |||||
| chr15:66420962
|
TATACACA others(7): Show |
T | 1 | a0001c0001t0003g0168 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.81-14045_81-14032d others(16): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420962 | |||||
| chr15:66420970
|
CACAT | C | 161 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.81-14049_81-14046d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420970 | |||||
| chr15:66420974
|
T | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(108): Show | 111 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.81-14053T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420974 | ||||||
| chr15:66420974
|
TACATACA others(1): Show |
T | 40 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(37): Show | 40 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.81-14049_81-14042d others(10): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420974 | |||||
| chr15:66420976
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.81-14051C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420976 | ||||||
| chr15:66420984
|
C | T | 2 | a0001c0001t0002g0055a0001c0001t0002g0063 | 2 | HG00099.hp2 HG00140.hp2 |
intron_variant | MODIFIER | c.81-14043C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420984 | ||||||
| chr15:66420984
|
CACAT | C | 4 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(1): Show | 4 | HG03041.hp2 HG03471.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.81-14033_81-14030d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66420984 | |||||
| chr15:66420988
|
T | C | 2 | a0001c0001t0001g0119a0001c0001t0003g0193 | 2 | HG01993.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.81-14039T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420988 | ||||||
| chr15:66420995
|
A | G | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-14032A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66420995 | ||||||
| chr15:66421005
|
G | T | 1 | a0001c0001t0001g0326 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.81-14022G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66421005 | ||||||
| chr15:66421019
|
T | TTA | 361 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(358): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.81-14005_81-14004d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421019 | |||||
| chr15:66421083
|
TACACACA others(7): Show |
T | 1 | a0001c0001t0001g0337 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.81-13934_81-13921d others(16): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421083 | |||||
| chr15:66421083
|
TACACACA others(19): Show |
T | 2 | a0001c0001t0001g0339a0001c0001t0001g0340 | 2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.81-13934_81-13909d others(28): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421083 | |||||
| chr15:66421093
|
T | C | 1 | a0001c0001t0002g0341 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.81-13934T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66421093 | ||||||
| chr15:66421093
|
T | TAC | 11 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0003g0202others(8): Show | 11 | HG00280.hp1 HG00280.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.81-13902_81-13901d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421093 | |||||
| chr15:66421093
|
T | TACAC | 6 | a0001c0001t0005g0160a0001c0001t0005g0161a0001c0001t0005g0239others(3): Show | 6 | HG01074.hp1 HG01099.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.81-13904_81-13901d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421093 | |||||
| chr15:66421093
|
T | TACACAC | 3 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0005g0243 | 3 | HG00438.hp2 HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.81-13906_81-13901d others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421093 | |||||
| chr15:66421093
|
TACAC | T | 3 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0325 | 3 | HG02055.hp1 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.81-13904_81-13901d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421093 | |||||
| chr15:66421093
|
TACACAC | T | 12 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(9): Show | 12 | HG00738.hp2 HG01106.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.81-13906_81-13901d others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421093 | |||||
| chr15:66421093
|
TACACACA others(1): Show |
T | 26 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0245others(23): Show | 26 | HG00423.hp1 HG01099.hp2 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.81-13908_81-13901d others(10): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421093 | |||||
| chr15:66421093
|
TACACACA others(3): Show |
T | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.81-13910_81-13901d others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421093 | |||||
| chr15:66421093
|
TACACACA others(7): Show |
T | 38 | a0001c0001t0001g0010a0001c0001t0001g0326a0001c0001t0001g0327others(35): Show | 38 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.81-13914_81-13901d others(16): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421093 | |||||
| chr15:66421107
|
CACACACA others(15): Show |
C | 1 | a0001c0001t0003g0162 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.81-13918_81-13897d others(24): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421107 | |||||
| chr15:66421117
|
CACACACA others(3): Show |
C | 3 | a0001c0001t0001g0232a0001c0001t0001g0268a0001c0001t0002g0089 | 3 | HG02280.hp1 HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.81-13908_81-13899d others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421117 | |||||
| chr15:66421119
|
CACACACA others(1): Show |
C | 7 | a0001c0001t0001g0272a0001c0001t0001g0285a0001c0001t0001g0286others(4): Show | 7 | HG02027.hp1 HG03834.hp2 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.81-13906_81-13899d others(10): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421119 | |||||
| chr15:66421121
|
CACACAT | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(120): Show | 123 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.81-13904_81-13899d others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421121 | |||||
| chr15:66421123
|
CACAT | C | 58 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0119others(55): Show | 58 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.81-13902_81-13899d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421123 | |||||
| chr15:66421123
|
CACATAT | C | 3 | a0001c0001t0002g0341a0001c0001t0003g0371a0001c0001t0003g0372 | 3 | HG00323.hp2 HG01074.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.81-13902_81-13897d others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421123 | |||||
| chr15:66421125
|
CAT | C | 41 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0229others(38): Show | 41 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.81-13888_81-13887d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421125 | |||||
| chr15:66421125
|
CATAT | C | 10 | a0001c0001t0002g0117a0001c0001t0002g0120a0001c0001t0003g0176others(7): Show | 10 | HG00099.hp1 HG02109.hp1 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.81-13890_81-13887d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421125 | |||||
| chr15:66421127
|
T | C | 34 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(31): Show | 34 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.81-13900T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66421127 | ||||||
| chr15:66421129
|
T | C | 51 | a0001c0001t0003g0164a0001c0001t0003g0165a0001c0001t0003g0166others(48): Show | 51 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.81-13898T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66421129 | ||||||
| chr15:66421228
|
C | T | 30 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(27): Show | 30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.81-13799C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66421228 | ||||||
| chr15:66421295
|
C | A | 30 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(27): Show | 30 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.81-13732C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66421295 | ||||||
| chr15:66421378
|
C | T | 30 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(27): Show | 30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.81-13649C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66421378 | ||||||
| chr15:66421438
|
A | G | 2 | a0001c0001t0001g0292a0001c0001t0001g0298 | 2 | HG00609.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.81-13589A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66421438 | ||||||
| chr15:66421619
|
G | T | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-13408G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66421619 | ||||||
| chr15:66421683
|
C | G | 41 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(38): Show | 41 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.81-13344C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66421683 | ||||||
| chr15:66421704
|
G | T | 30 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(27): Show | 30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.81-13323G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66421704 | ||||||
| chr15:66421883
|
C | CT | 246 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(243): Show | 246 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(243): Show |
intron_variant | MODIFIER | c.81-13131dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66421883 | |||||
| chr15:66422040
|
C | G | 59 | a0001c0001t0001g0232a0001c0001t0002g0011a0001c0001t0002g0047others(56): Show | 59 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.81-12987C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66422040 | ||||||
| chr15:66422405
|
A | G | 62 | a0001c0001t0003g0162a0001c0001t0003g0164a0001c0001t0003g0165others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.81-12622A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66422405 | ||||||
| chr15:66422507
|
C | T | 7 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0306others(4): Show | 7 | HG02027.hp1 HG02040.hp2 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.81-12520C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66422507 | ||||||
| chr15:66422584
|
C | T | 1 | a0001c0001t0001g0346 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.81-12443C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66422584 | ||||||
| chr15:66422614
|
A | G | 6 | a0001c0001t0003g0164a0001c0001t0003g0170a0001c0001t0003g0184others(3): Show | 6 | HG00323.hp2 HG00642.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.81-12413A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66422614 | ||||||
| chr15:66422645
|
G | A | 3 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0325 | 3 | HG02055.hp1 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.81-12382G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66422645 | ||||||
| chr15:66422820
|
C | T | 2 | a0001c0001t0001g0352a0001c0001t0001g0353 | 2 | HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.81-12207C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66422820 | ||||||
| chr15:66422826
|
C | T | 1 | a0001c0001t0002g0075 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.81-12201C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66422826 | ||||||
| chr15:66422867
|
C | T | 1 | a0001c0001t0003g0169 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.81-12160C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66422867 | ||||||
| chr15:66422920
|
CT | C | 13 | a0001c0001t0001g0342a0001c0001t0001g0343a0001c0001t0001g0344others(10): Show | 13 | HG01884.hp2 HG02258.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.81-12098delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66422920 | |||||
| chr15:66422962
|
T | C | 1 | a0001c0003t0001g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.81-12065T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66422962 | ||||||
| chr15:66423211
|
C | T | 30 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(27): Show | 30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.81-11816C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66423211 | ||||||
| chr15:66423284
|
A | C | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-11743A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66423284 | ||||||
| chr15:66423335
|
A | C | 1 | a0001c0001t0002g0081 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.81-11692A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66423335 | ||||||
| chr15:66423339
|
T | C | 1 | a0001c0001t0001g0135 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.81-11688T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66423339 | ||||||
| chr15:66423407
|
T | C | 364 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(361): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.81-11620T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66423407 | ||||||
| chr15:66423442
|
C | CT | 11 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(8): Show | 11 | HG01255.hp1 HG01261.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.81-11571dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66423442 | |||||
| chr15:66423442
|
CT | C | 112 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(109): Show | 112 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.81-11571delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66423442 | |||||
| chr15:66423604
|
A | AT | 283 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(280): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.81-11403dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66423604 | |||||
| chr15:66423604
|
A | ATT | 19 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0139others(16): Show | 19 | HG00642.hp2 HG00673.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.81-11404_81-11403d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66423604 | |||||
| chr15:66423604
|
A | ATTT | 42 | a0001c0001t0001g0010a0001c0001t0001g0327a0001c0001t0001g0328others(39): Show | 42 | HG00280.hp1 HG00438.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.81-11405_81-11403d others(5): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66423604 | |||||
| chr15:66423738
|
G | A | 41 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(38): Show | 41 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.81-11289G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66423738 | ||||||
| chr15:66423755
|
G | GC | 313 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(310): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.81-11271dupC | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66423755 | |||||
| chr15:66423764
|
T | C | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-11263T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66423764 | ||||||
| chr15:66423768
|
C | T | 52 | a0001c0001t0003g0162a0001c0001t0003g0164a0001c0001t0003g0165others(49): Show | 52 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.81-11259C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66423768 | ||||||
| chr15:66423807
|
A | G | 1 | a0001c0001t0010g0186 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.81-11220A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66423807 | ||||||
| chr15:66423885
|
G | A | 1 | a0001c0001t0002g0088 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.81-11142G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66423885 | ||||||
| chr15:66423983
|
C | T | 4 | a0001c0001t0001g0248a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | HG00735.hp1 HG01167.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.81-11044C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66423983 | ||||||
| chr15:66424014
|
A | C | 4 | a0001c0001t0001g0248a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | HG00735.hp1 HG01167.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.81-11013A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66424014 | ||||||
| chr15:66424043
|
G | A | 2 | a0001c0001t0001g0331a0001c0001t0001g0333 | 2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.81-10984G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66424043 | ||||||
| chr15:66424064
|
A | AT | 321 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(318): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.81-10953dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66424064 | |||||
| chr15:66424064
|
A | T | 1 | a0001c0001t0001g0328 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.81-10963A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66424064 | ||||||
| chr15:66424101
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.81-10926A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66424101 | ||||||
| chr15:66424102
|
T | G | 321 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(318): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.81-10925T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66424102 | ||||||
| chr15:66424111
|
G | T | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.81-10916G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66424111 | ||||||
| chr15:66424348
|
G | A | 1 | a0001c0001t0003g0162 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.81-10679G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66424348 | ||||||
| chr15:66424358
|
C | T | 3 | a0001c0001t0003g0165a0001c0001t0003g0202a0001c0001t0009g0163 | 3 | NA18940.hp1 NA18962.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.81-10669C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66424358 | ||||||
| chr15:66424383
|
T | G | 364 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(361): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.81-10644T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66424383 | ||||||
| chr15:66424583
|
C | T | 59 | a0001c0001t0001g0232a0001c0001t0002g0011a0001c0001t0002g0047others(56): Show | 59 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.81-10444C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66424583 | ||||||
| chr15:66424603
|
C | A | 2 | a0001c0001t0005g0160a0001c0001t0005g0161 | 2 | HG01074.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.81-10424C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66424603 | ||||||
| chr15:66424791
|
C | CT | 139 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(136): Show | 139 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.81-10213dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66424791 | |||||
| chr15:66424791
|
C | CTT | 6 | a0001c0001t0001g0297a0001c0001t0003g0198a0001c0001t0003g0244others(3): Show | 6 | HG01074.hp1 HG01099.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.81-10214_81-10213d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66424791 | |||||
| chr15:66424791
|
CT | C | 24 | a0001c0001t0001g0116a0001c0001t0001g0125a0001c0001t0001g0134others(21): Show | 24 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.81-10213delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66424791 | |||||
| chr15:66424791
|
CTT | C | 9 | a0001c0001t0001g0237a0001c0001t0002g0055a0001c0001t0002g0063others(6): Show | 9 | HG00099.hp2 HG00140.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.81-10214_81-10213d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66424791 | |||||
| chr15:66424791
|
CTTT | C | 48 | a0001c0001t0001g0232a0001c0001t0002g0011a0001c0001t0002g0047others(45): Show | 48 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.81-10215_81-10213d others(5): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66424791 | |||||
| chr15:66424791
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0250a0001c0001t0001g0253a0001c0001t0001g0284 | 3 | HG01891.hp1 HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.81-10224_81-10213d others(14): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66424791 | |||||
| chr15:66424816
|
C | A | 361 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(358): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.81-10211C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66424816 | ||||||
| chr15:66425002
|
G | A | 1 | a0001c0001t0001g0339 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.81-10025G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66425002 | ||||||
| chr15:66425042
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.81-9985C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66425042 | ||||||
| chr15:66425383
|
AT | A | 10 | a0001c0001t0001g0327a0001c0001t0003g0206a0001c0001t0006g0002others(7): Show | 10 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.81-9633delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66425383 | |||||
| chr15:66425408
|
A | G | 4 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0233others(1): Show | 4 | HG02145.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.81-9619A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66425408 | ||||||
| chr15:66425417
|
G | A | 2 | a0001c0001t0001g0334a0001c0001t0001g0335 | 2 | HG01099.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.81-9610G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66425417 | ||||||
| chr15:66425446
|
C | G | 1 | a0001c0001t0005g0159 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.81-9581C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66425446 | ||||||
| chr15:66425482
|
A | G | 1 | a0001c0001t0001g0332 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.81-9545A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66425482 | ||||||
| chr15:66425915
|
C | T | 2 | a0001c0001t0001g0369a0001c0006t0001g0368 | 2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.81-9112C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66425915 | ||||||
| chr15:66425929
|
T | A | 1 | a0001c0001t0003g0210 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.81-9098T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66425929 | ||||||
| chr15:66425931
|
G | A | 2 | a0001c0001t0001g0276a0001c0001t0001g0288 | 2 | HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.81-9096G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66425931 | ||||||
| chr15:66426049
|
A | G | 30 | a0001c0001t0001g0331a0001c0001t0001g0333a0001c0001t0001g0342others(27): Show | 30 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.81-8978A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66426049 | ||||||
| chr15:66426142
|
CT | C | 309 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(306): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.81-8869delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66426142 | |||||
| chr15:66426142
|
CTT | C | 52 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(49): Show | 52 | HG00423.hp1 HG00738.hp2 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.81-8870_81-8869del others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66426142 | |||||
| chr15:66426151
|
T | A | 89 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(86): Show | 89 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.81-8876T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66426151 | ||||||
| chr15:66426313
|
T | G | 1 | a0001c0001t0014g0213 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.81-8714T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66426313 | ||||||
| chr15:66426360
|
C | CA | 254 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(251): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.81-8653dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66426360 | |||||
| chr15:66426360
|
C | CAA | 58 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(55): Show | 58 | HG00140.hp1 HG00423.hp1 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.81-8654_81-8653dup others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66426360 | |||||
| chr15:66426360
|
C | CAAA | 8 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0108others(5): Show | 8 | HG01433.hp1 HG02055.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.81-8655_81-8653dup others(3): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66426360 | |||||
| chr15:66426375
|
C | A | 3 | a0001c0001t0001g0250a0001c0001t0001g0253a0001c0001t0001g0284 | 3 | HG01891.hp1 HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.81-8652C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66426375 | ||||||
| chr15:66426416
|
A | G | 30 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(27): Show | 30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.81-8611A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66426416 | ||||||
| chr15:66426606
|
T | G | 1 | a0001c0001t0002g0150 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.81-8421T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66426606 | ||||||
| chr15:66426643
|
G | C | 1 | a0001c0001t0001g0340 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.81-8384G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66426643 | ||||||
| chr15:66426695
|
G | A | 48 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(45): Show | 48 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.81-8332G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66426695 | ||||||
| chr15:66426792
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.81-8235T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66426792 | ||||||
| chr15:66426844
|
A | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(80): Show | 83 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.81-8183A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66426844 | ||||||
| chr15:66426880
|
T | G | 1 | a0001c0001t0002g0065 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.81-8147T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66426880 | ||||||
| chr15:66426931
|
T | C | 299 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(296): Show | 299 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.81-8096T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66426931 | ||||||
| chr15:66426943
|
G | A | 82 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(79): Show | 82 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.81-8084G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66426943 | ||||||
| chr15:66427030
|
T | G | 2 | a0001c0001t0001g0128a0001c0001t0001g0142 | 2 | NA18953.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.81-7997T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66427030 | ||||||
| chr15:66427067
|
T | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0142 | 2 | NA18953.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.81-7960T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66427067 | ||||||
| chr15:66427355
|
C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0327a0001c0001t0001g0332others(1): Show | 4 | HG02109.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.81-7672C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66427355 | ||||||
| chr15:66427386
|
C | T | 31 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(28): Show | 31 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.81-7641C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66427386 | ||||||
| chr15:66427756
|
C | T | 8 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0306others(5): Show | 8 | HG02027.hp1 HG02040.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-7271C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66427756 | ||||||
| chr15:66427970
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.81-7057C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66427970 | ||||||
| chr15:66428011
|
C | G | 1 | a0001c0001t0002g0086 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.81-7016C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428011 | ||||||
| chr15:66428075
|
C | G | 1 | a0001c0001t0003g0191 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.81-6952C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428075 | ||||||
| chr15:66428098
|
C | T | 1 | a0001c0001t0014g0213 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.81-6929C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428098 | ||||||
| chr15:66428271
|
C | CGTGTGTG others(3): Show |
1 | a0001c0001t0001g0343 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.81-6711_81-6702dup others(10): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428271 | |||||
| chr15:66428271
|
CGT | C | 31 | a0001c0001t0001g0014a0001c0001t0001g0029a0001c0001t0001g0035others(28): Show | 31 | HG01169.hp1 HG01243.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.81-6703_81-6702del others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428271 | |||||
| chr15:66428271
|
CGTGT | C | 42 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0112others(39): Show | 42 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.81-6705_81-6702del others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428271 | |||||
| chr15:66428271
|
CGTGTGT | C | 89 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(86): Show | 89 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.81-6707_81-6702del others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428271 | |||||
| chr15:66428271
|
CGTGTGTG others(1): Show |
C | 76 | a0001c0001t0001g0001a0001c0001t0001g0031a0001c0001t0001g0032others(73): Show | 76 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.81-6709_81-6702del others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428271 | |||||
| chr15:66428271
|
CGTGTGTG others(3): Show |
C | 28 | a0001c0001t0001g0012a0001c0001t0001g0113a0001c0001t0001g0121others(25): Show | 28 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.81-6711_81-6702del others(10): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428271 | |||||
| chr15:66428271
|
CGTGTGTG others(5): Show |
C | 44 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(41): Show | 44 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.81-6713_81-6702del others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428271 | |||||
| chr15:66428271
|
CGTGTGTG others(7): Show |
C | 12 | a0001c0001t0001g0106a0001c0001t0001g0116a0001c0001t0001g0216others(9): Show | 12 | HG02165.hp2 HG02559.hp1 HG03453.hp2 others(9): Show |
intron_variant | MODIFIER | c.81-6715_81-6702del others(14): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428271 | |||||
| chr15:66428271
|
CGTGTGTG others(9): Show |
C | 20 | a0001c0001t0001g0115a0001c0001t0001g0212a0001c0001t0001g0217others(17): Show | 20 | HG00558.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.81-6717_81-6702del others(16): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428271 | |||||
| chr15:66428271
|
CGTGTGTG others(21): Show |
C | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.81-6729_81-6702del others(28): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428271 | |||||
| chr15:66428271
|
CGTGTGTG others(27): Show |
C | 2 | a0001c0001t0005g0157a0001c0001t0005g0159 | 2 | HG00280.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.81-6735_81-6702del others(34): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428271 | |||||
| chr15:66428275
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.81-6752T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428275 | ||||||
| chr15:66428279
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.81-6748T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428279 | ||||||
| chr15:66428281
|
T | C | 4 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0136others(1): Show | 4 | NA18953.hp1 NA18956.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.81-6746T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428281 | ||||||
| chr15:66428283
|
T | C | 2 | a0001c0001t0001g0135a0001c0001t0001g0137 | 2 | NA18968.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.81-6744T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428283 | ||||||
| chr15:66428285
|
T | C | 1 | a0001c0001t0001g0121 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.81-6742T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428285 | ||||||
| chr15:66428388
|
G | T | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-6639G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428388 | ||||||
| chr15:66428699
|
T | C | 30 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(27): Show | 30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.81-6328T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428699 | ||||||
| chr15:66428773
|
C | CT | 31 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0091others(28): Show | 31 | HG00609.hp1 HG00673.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.81-6228dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428773 | |||||
| chr15:66428773
|
C | CTT | 9 | a0001c0001t0001g0010a0001c0001t0001g0331a0001c0001t0001g0333others(6): Show | 9 | HG00733.hp2 HG01515.hp1 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.81-6229_81-6228dup others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428773 | |||||
| chr15:66428773
|
C | CTTT | 18 | a0001c0001t0001g0326a0001c0001t0001g0328a0001c0001t0001g0343others(15): Show | 18 | HG00639.hp1 HG01109.hp1 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.81-6230_81-6228dup others(3): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428773 | |||||
| chr15:66428773
|
C | CTTTT | 10 | a0001c0001t0001g0156a0001c0001t0001g0358a0001c0001t0001g0361others(7): Show | 10 | HG00280.hp2 HG01891.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.81-6231_81-6228dup others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428773 | |||||
| chr15:66428773
|
CT | C | 148 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(145): Show | 148 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.81-6228delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428773 | |||||
| chr15:66428773
|
CTTTTTTT others(1): Show |
C | 6 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(3): Show | 6 | HG02559.hp2 HG02895.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.81-6235_81-6228del others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66428773 | |||||
| chr15:66428840
|
C | T | 10 | a0001c0001t0005g0157a0001c0001t0005g0158a0001c0001t0005g0159others(7): Show | 10 | HG00280.hp1 HG00438.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.81-6187C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428840 | ||||||
| chr15:66428865
|
C | T | 83 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(80): Show | 83 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.81-6162C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428865 | ||||||
| chr15:66428866
|
G | A | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-6161G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428866 | ||||||
| chr15:66428889
|
C | T | 2 | a0001c0001t0001g0339a0001c0001t0001g0340 | 2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.81-6138C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428889 | ||||||
| chr15:66428936
|
C | T | 2 | a0001c0001t0001g0291a0001c0001t0001g0300 | 2 | NA18947.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.81-6091C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428936 | ||||||
| chr15:66428937
|
G | A | 37 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(34): Show | 37 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.81-6090G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428937 | ||||||
| chr15:66428954
|
A | G | 36 | a0001c0001t0001g0010a0001c0001t0001g0326a0001c0001t0001g0327others(33): Show | 36 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.81-6073A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66428954 | ||||||
| chr15:66429193
|
G | A | 9 | a0001c0001t0001g0315a0001c0001t0006g0002a0001c0001t0006g0003others(6): Show | 9 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.81-5834G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429193 | ||||||
| chr15:66429278
|
CAA | C | 3 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0325 | 3 | HG02055.hp1 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.81-5748_81-5747del others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429278 | ||||||
| chr15:66429300
|
G | T | 1 | a0001c0001t0002g0151 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.81-5727G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429300 | ||||||
| chr15:66429342
|
A | G | 4 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0233others(1): Show | 4 | HG02145.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.81-5685A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429342 | ||||||
| chr15:66429350
|
ACT | A | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-5676_81-5675del others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429350 | ||||||
| chr15:66429439
|
T | C | 2 | a0001c0001t0005g0240a0001c0001t0005g0243 | 2 | HG00438.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.81-5588T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429439 | ||||||
| chr15:66429517
|
A | G | 64 | a0001c0001t0001g0232a0001c0001t0001g0356a0001c0001t0001g0357others(61): Show | 64 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.81-5510A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429517 | ||||||
| chr15:66429518
|
T | C | 1 | a0001c0001t0006g0009 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.81-5509T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429518 | ||||||
| chr15:66429666
|
CCCCCCCC others(7): Show |
C | 35 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0029others(32): Show | 35 | HG00423.hp1 HG01099.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.81-5353_81-5340del others(14): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66429666 | |||||
| chr15:66429667
|
CCCCCCCC others(6): Show |
C | 4 | a0001c0001t0001g0027a0001c0001t0001g0036a0001c0001t0001g0039others(1): Show | 4 | HG00738.hp2 HG01243.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.81-5352_81-5340del others(13): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66429667 | |||||
| chr15:66429675
|
C | G | 2 | a0001c0001t0006g0006a0001c0001t0006g0008 | 2 | HG00280.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.81-5352C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429675 | ||||||
| chr15:66429676
|
C | A | 6 | a0001c0001t0001g0349a0001c0001t0001g0350a0001c0001t0001g0355others(3): Show | 6 | HG02055.hp2 HG02280.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.81-5351C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429676 | ||||||
| chr15:66429676
|
C | G | 9 | a0001c0001t0001g0340a0001c0001t0001g0346a0001c0001t0001g0347others(6): Show | 9 | HG01069.hp1 HG01517.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.81-5351C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429676 | ||||||
| chr15:66429676
|
C | T | 42 | a0001c0001t0001g0111a0001c0001t0001g0122a0001c0001t0001g0124others(39): Show | 42 | HG00423.hp2 HG00438.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.81-5351C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429676 | ||||||
| chr15:66429677
|
C | A | 4 | a0001c0001t0001g0310a0001c0001t0001g0354a0001c0001t0001g0369others(1): Show | 4 | HG02056.hp1 HG02818.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.81-5350C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429677 | ||||||
| chr15:66429677
|
C | G | 29 | a0001c0001t0001g0010a0001c0001t0001g0108a0001c0001t0001g0109others(26): Show | 29 | HG00544.hp1 HG00733.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.81-5350C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429677 | ||||||
| chr15:66429677
|
C | T | 68 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(65): Show | 68 | HG00609.hp1 HG00609.hp2 HG00733.hp1 others(65): Show |
intron_variant | MODIFIER | c.81-5350C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429677 | ||||||
| chr15:66429678
|
C | A | 2 | a0001c0001t0001g0295a0001c0001t0001g0361 | 2 | HG01891.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.81-5349C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429678 | ||||||
| chr15:66429678
|
C | CCCCG | 19 | a0001c0001t0001g0226a0001c0001t0002g0011a0001c0001t0002g0049others(16): Show | 19 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.81-5349_81-5348ins others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429678 | ||||||
| chr15:66429678
|
C | CCCG | 24 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0237others(21): Show | 24 | HG00597.hp1 HG01074.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.81-5349_81-5348ins others(3): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429678 | ||||||
| chr15:66429678
|
C | CCG | 27 | a0001c0001t0001g0156a0001c0001t0001g0212a0001c0001t0001g0217others(24): Show | 27 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.81-5349_81-5348ins others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429678 | ||||||
| chr15:66429678
|
C | G | 59 | a0001c0001t0001g0111a0001c0001t0001g0122a0001c0001t0001g0124others(56): Show | 59 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.81-5349C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429678 | ||||||
| chr15:66429678
|
CG | C | 31 | a0001c0001t0001g0010a0001c0001t0001g0109a0001c0001t0001g0110others(28): Show | 31 | HG00733.hp2 HG01074.hp1 HG01517.hp2 others(28): Show |
intron_variant | MODIFIER | c.81-5348delG | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429678 | ||||||
| chr15:66429678
|
CGT | C | 10 | a0001c0001t0001g0346a0001c0001t0001g0347a0001c0001t0001g0349others(7): Show | 10 | HG01069.hp1 HG01515.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.81-5348_81-5347del others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429678 | ||||||
| chr15:66429679
|
G | C | 159 | a0001c0001t0001g0108a0001c0001t0001g0111a0001c0001t0001g0115others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.81-5348G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429679 | ||||||
| chr15:66429679
|
G | GC | 111 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(108): Show | 111 | HG00609.hp1 HG00609.hp2 HG00621.hp2 others(108): Show |
intron_variant | MODIFIER | c.81-5348_81-5347ins others(1): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429679 | ||||||
| chr15:66429679
|
G | GCC | 9 | a0001c0001t0001g0121a0001c0001t0001g0235a0001c0001t0001g0238others(6): Show | 9 | HG00438.hp2 HG01175.hp1 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.81-5348_81-5347ins others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429679 | ||||||
| chr15:66429680
|
T | C | 311 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.81-5347T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429680 | ||||||
| chr15:66429726
|
G | A | 2 | a0001c0001t0001g0347a0001c0001t0001g0348 | 2 | HG00733.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.81-5301G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429726 | ||||||
| chr15:66429867
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.81-5160T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429867 | ||||||
| chr15:66429913
|
A | G | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-5114A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429913 | ||||||
| chr15:66429969
|
C | T | 1 | a0001c0001t0001g0124 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.81-5058C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429969 | ||||||
| chr15:66429979
|
C | T | 3 | a0001c0001t0001g0250a0001c0001t0001g0253a0001c0001t0001g0284 | 3 | HG01891.hp1 HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.81-5048C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66429979 | ||||||
| chr15:66430005
|
C | T | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-5022C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66430005 | ||||||
| chr15:66430231
|
G | A | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-4796G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66430231 | ||||||
| chr15:66430287
|
G | T | 1 | a0001c0001t0002g0094 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.81-4740G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66430287 | ||||||
| chr15:66430534
|
G | A | 5 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.81-4493G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66430534 | ||||||
| chr15:66430549
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.81-4478C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66430549 | ||||||
| chr15:66430608
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.81-4419A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66430608 | ||||||
| chr15:66430715
|
T | C | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-4312T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66430715 | ||||||
| chr15:66430936
|
T | A | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-4091T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66430936 | ||||||
| chr15:66430971
|
C | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.81-4056C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66430971 | ||||||
| chr15:66431098
|
T | C | 1 | a0001c0001t0001g0214 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.81-3929T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66431098 | ||||||
| chr15:66431211
|
C | T | 1 | a0001c0001t0002g0084 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.81-3816C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66431211 | ||||||
| chr15:66431513
|
G | A | 9 | a0001c0001t0002g0053a0001c0001t0002g0054a0001c0001t0002g0056others(6): Show | 9 | HG00544.hp2 HG01884.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.81-3514G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66431513 | ||||||
| chr15:66431587
|
A | G | 1 | a0001c0001t0001g0359 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.81-3440A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66431587 | ||||||
| chr15:66431655
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.81-3372G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66431655 | ||||||
| chr15:66431694
|
G | T | 1 | a0001c0003t0001g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.81-3333G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66431694 | ||||||
| chr15:66431871
|
G | T | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-3156G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66431871 | ||||||
| chr15:66431890
|
C | G | 1 | a0001c0001t0001g0272 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.81-3137C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66431890 | ||||||
| chr15:66432008
|
C | G | 1 | a0001c0001t0003g0180 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.81-3019C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66432008 | ||||||
| chr15:66432012
|
A | G | 90 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(87): Show | 90 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.81-3015A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66432012 | ||||||
| chr15:66432232
|
A | G | 364 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(361): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.81-2795A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66432232 | ||||||
| chr15:66432274
|
G | A | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-2753G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66432274 | ||||||
| chr15:66432343
|
G | A | 1 | a0001c0001t0002g0062 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.81-2684G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66432343 | ||||||
| chr15:66432425
|
A | G | 2 | a0001c0001t0005g0160a0001c0001t0005g0161 | 2 | HG01074.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.81-2602A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66432425 | ||||||
| chr15:66432839
|
A | G | 1 | a0001c0001t0002g0011 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.81-2188A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66432839 | ||||||
| chr15:66432959
|
A | AGT | 23 | a0001c0001t0001g0212a0001c0001t0001g0218a0001c0001t0001g0223others(20): Show | 23 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.81-2027_81-2026dup others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66432959 | |||||
| chr15:66432959
|
A | AGTGT | 39 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(36): Show | 39 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.81-2029_81-2026dup others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66432959 | |||||
| chr15:66432959
|
A | AGTGTGT | 77 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0026others(74): Show | 77 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.81-2031_81-2026dup others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66432959 | |||||
| chr15:66432959
|
A | AGTGTGTG others(1): Show |
58 | a0001c0001t0001g0012a0001c0001t0001g0128a0001c0001t0001g0135others(55): Show | 58 | HG00280.hp2 HG00323.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.81-2033_81-2026dup others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66432959 | |||||
| chr15:66432959
|
A | AGTGTGTG others(3): Show |
44 | a0001c0001t0001g0040a0001c0001t0001g0124a0001c0001t0001g0133others(41): Show | 44 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.81-2035_81-2026dup others(10): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66432959 | |||||
| chr15:66432959
|
A | AGTGTGTG others(5): Show |
39 | a0001c0001t0001g0010a0001c0001t0001g0111a0001c0001t0001g0119others(36): Show | 39 | HG00544.hp1 HG00621.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.81-2037_81-2026dup others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66432959 | |||||
| chr15:66432959
|
A | AGTGTGTG others(7): Show |
21 | a0001c0001t0001g0001a0001c0001t0001g0109a0001c0001t0001g0126others(18): Show | 21 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.81-2039_81-2026dup others(14): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66432959 | |||||
| chr15:66432959
|
A | AGTGTGTG others(9): Show |
18 | a0001c0001t0001g0108a0001c0001t0001g0118a0001c0001t0001g0141others(15): Show | 18 | HG00140.hp1 HG00609.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.81-2041_81-2026dup others(16): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66432959 | |||||
| chr15:66432959
|
A | AGTGTGTG others(11): Show |
8 | a0001c0001t0001g0110a0001c0001t0001g0138a0001c0001t0001g0293others(5): Show | 8 | HG00423.hp2 HG00438.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-2043_81-2026dup others(18): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66432959 | |||||
| chr15:66432959
|
A | AGTGTGTG others(13): Show |
2 | a0001c0001t0001g0303a0001c0001t0003g0167 | 2 | HG01071.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.81-2045_81-2026dup others(20): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66432959 | |||||
| chr15:66432959
|
A | AGTGTGTG others(21): Show |
1 | a0001c0001t0001g0113 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.81-2053_81-2026dup others(28): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66432959 | |||||
| chr15:66432959
|
A | ATGTGTGT others(8): Show |
1 | a0001c0001t0003g0244 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.81-2068_81-2067ins others(15): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66432959 | ||||||
| chr15:66432959
|
AGT | A | 5 | a0001c0001t0001g0112a0001c0001t0001g0130a0001c0001t0001g0132others(2): Show | 5 | HG00609.hp2 HG02615.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.81-2027_81-2026del others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66432959 | |||||
| chr15:66432959
|
AGTGTGT | A | 5 | a0001c0001t0001g0131a0001c0001t0001g0344a0001c0001t0002g0117others(2): Show | 5 | HG01884.hp2 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.81-2031_81-2026del others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66432959 | |||||
| chr15:66432959
|
AGTGTGTG others(5): Show |
A | 1 | a0001c0001t0011g0265 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.81-2037_81-2026del others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 66432959 | |||||
| chr15:66433007
|
G | A | 37 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(34): Show | 37 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.81-2020G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66433007 | ||||||
| chr15:66433023
|
T | C | 2 | a0001c0001t0001g0339a0001c0001t0001g0340 | 2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.81-2004T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66433023 | ||||||
| chr15:66433066
|
C | G | 1 | a0001c0001t0001g0353 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.81-1961C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66433066 | ||||||
| chr15:66433217
|
T | C | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-1810T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66433217 | ||||||
| chr15:66433277
|
C | T | 321 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(318): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.81-1750C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66433277 | ||||||
| chr15:66433412
|
C | T | 1 | a0001c0003t0001g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.81-1615C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66433412 | ||||||
| chr15:66433558
|
T | C | 1 | a0001c0001t0001g0337 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.81-1469T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66433558 | ||||||
| chr15:66433619
|
T | G | 1 | a0001c0001t0001g0353 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.81-1408T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66433619 | ||||||
| chr15:66433676
|
A | G | 82 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(79): Show | 82 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.81-1351A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66433676 | ||||||
| chr15:66433686
|
C | G | 82 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(79): Show | 82 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.81-1341C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66433686 | ||||||
| chr15:66433740
|
A | G | 3 | a0001c0001t0005g0157a0001c0001t0005g0158a0001c0001t0005g0159 | 3 | HG00280.hp1 HG02735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.81-1287A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66433740 | ||||||
| chr15:66433767
|
T | C | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-1260T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66433767 | ||||||
| chr15:66433783
|
A | G | 1 | a0001c0001t0001g0260 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.81-1244A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66433783 | ||||||
| chr15:66433809
|
G | A | 2 | a0001c0001t0001g0299a0001c0001t0001g0302 | 2 | NA18989.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.81-1218G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66433809 | ||||||
| chr15:66433913
|
C | T | 1 | a0001c0001t0001g0337 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.81-1114C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66433913 | ||||||
| chr15:66433990
|
C | T | 3 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0001g0330 | 3 | HG02257.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.81-1037C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66433990 | ||||||
| chr15:66434027
|
A | G | 30 | a0001c0001t0001g0331a0001c0001t0001g0333a0001c0001t0001g0342others(27): Show | 30 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.81-1000A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66434027 | ||||||
| chr15:66434031
|
C | T | 50 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(47): Show | 50 | HG00735.hp1 HG00735.hp2 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.81-996C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66434031 | ||||||
| chr15:66434064
|
A | C | 30 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(27): Show | 30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.81-963A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66434064 | ||||||
| chr15:66434179
|
T | C | 321 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(318): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.81-848T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66434179 | ||||||
| chr15:66434370
|
A | G | 1 | a0001c0001t0001g0140 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.81-657A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66434370 | ||||||
| chr15:66434398
|
C | T | 1 | a0001c0001t0001g0362 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.81-629C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66434398 | ||||||
| chr15:66434472
|
G | A | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-555G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66434472 | ||||||
| chr15:66434569
|
G | A | 47 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(44): Show | 47 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(44): Show |
intron_variant | MODIFIER | c.81-458G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66434569 | ||||||
| chr15:66434987
|
C | G | 1 | a0001c0001t0001g0337 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.81-40C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | chr15 | 66434987 | ||||||
| chr15:66435259
|
G | C | 82 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(79): Show | 82 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.291+22G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 2/10 | chr15 | 66435259 | ||||||
| chr15:66435351
|
A | AT | 12 | a0001c0001t0001g0028a0001c0001t0001g0137a0001c0001t0001g0153others(9): Show | 12 | HG01069.hp2 HG01256.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.291+129dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 66435351 | |||||
| chr15:66435351
|
A | ATT | 289 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(286): Show | 289 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(286): Show |
intron_variant | MODIFIER | c.291+128_291+129dup others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 66435351 | |||||
| chr15:66435351
|
A | ATTT | 62 | a0001c0001t0001g0312a0001c0001t0002g0055a0001c0001t0002g0063others(59): Show | 62 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(59): Show |
intron_variant | MODIFIER | c.291+127_291+129dup others(3): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 66435351 | |||||
| chr15:66435419
|
G | A | 3 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0001g0330 | 3 | HG02257.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.291+182G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 2/10 | chr15 | 66435419 | ||||||
| chr15:66435433
|
C | G | 1 | a0001c0001t0002g0117 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.291+196C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 2/10 | chr15 | 66435433 | ||||||
| chr15:66435436
|
C | T | 40 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(37): Show | 40 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.291+199C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 2/10 | chr15 | 66435436 | ||||||
| chr15:66435487
|
G | A | 2 | a0001c0001t0002g0076a0001c0001t0002g0086 | 2 | NA19002.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.291+250G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 2/10 | chr15 | 66435487 | ||||||
| chr15:66435558
|
C | A | 1 | a0001c0001t0002g0090 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.291+321C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 2/10 | chr15 | 66435558 | ||||||
| chr15:66435617
|
T | C | 321 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(318): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.291+380T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 2/10 | chr15 | 66435617 | ||||||
| chr15:66435705
|
A | G | 1 | a0001c0001t0003g0204 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.291+468A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 2/10 | chr15 | 66435705 | ||||||
| chr15:66435931
|
C | T | 81 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(78): Show | 81 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.291+694C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 2/10 | chr15 | 66435931 | ||||||
| chr15:66435972
|
A | G | 52 | a0001c0001t0003g0162a0001c0001t0003g0164a0001c0001t0003g0165others(49): Show | 52 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.291+735A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 2/10 | chr15 | 66435972 | ||||||
| chr15:66436048
|
G | C | 1 | a0001c0001t0001g0346 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.292-698G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 2/10 | chr15 | 66436048 | ||||||
| chr15:66436613
|
A | C | 62 | a0001c0001t0003g0162a0001c0001t0003g0164a0001c0001t0003g0165others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.292-133A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 2/10 | chr15 | 66436613 | ||||||
| chr15:66436912
|
C | T | 10 | a0001c0001t0005g0157a0001c0001t0005g0158a0001c0001t0005g0159others(7): Show | 10 | HG00280.hp1 HG00438.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.438+20C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66436912 | ||||||
| chr15:66437084
|
C | T | 10 | a0001c0001t0005g0157a0001c0001t0005g0158a0001c0001t0005g0159others(7): Show | 10 | HG00280.hp1 HG00438.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.438+192C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66437084 | ||||||
| chr15:66437095
|
T | C | 2 | a0001c0001t0001g0339a0001c0001t0001g0340 | 2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.438+203T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66437095 | ||||||
| chr15:66437231
|
G | A | 4 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0325others(1): Show | 4 | HG00673.hp2 HG02055.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.438+339G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66437231 | ||||||
| chr15:66437295
|
G | A | 2 | a0001c0001t0001g0356a0001c0001t0001g0357 | 2 | HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.438+403G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66437295 | ||||||
| chr15:66437539
|
G | A | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.438+647G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66437539 | ||||||
| chr15:66437589
|
T | C | 62 | a0001c0001t0003g0162a0001c0001t0003g0164a0001c0001t0003g0165others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.438+697T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66437589 | ||||||
| chr15:66437638
|
C | T | 4 | a0001c0001t0003g0167a0001c0001t0003g0169a0001c0001t0003g0178others(1): Show | 4 | HG00140.hp1 HG01071.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.438+746C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66437638 | ||||||
| chr15:66437773
|
T | C | 313 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(310): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.438+881T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66437773 | ||||||
| chr15:66437844
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.438+952G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66437844 | ||||||
| chr15:66437933
|
G | T | 1 | a0001c0001t0014g0213 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.438+1041G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66437933 | ||||||
| chr15:66437969
|
C | T | 52 | a0001c0001t0003g0162a0001c0001t0003g0164a0001c0001t0003g0165others(49): Show | 52 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.438+1077C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66437969 | ||||||
| chr15:66437973
|
G | C | 4 | a0001c0001t0001g0221a0001c0001t0002g0117a0001c0001t0002g0120others(1): Show | 4 | HG02109.hp1 HG02622.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.438+1081G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66437973 | ||||||
| chr15:66437998
|
A | T | 1 | a0001c0001t0014g0213 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.438+1106A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66437998 | ||||||
| chr15:66438019
|
C | CT | 121 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0216others(118): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.438+1143dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 66438019 | |||||
| chr15:66438019
|
CT | C | 10 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0102others(7): Show | 10 | HG01169.hp2 HG01256.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.438+1143delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 66438019 | |||||
| chr15:66438035
|
T | A | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.438+1143T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66438035 | ||||||
| chr15:66438159
|
T | G | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.438+1267T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66438159 | ||||||
| chr15:66438235
|
C | T | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.438+1343C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66438235 | ||||||
| chr15:66438290
|
T | C | 6 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(3): Show | 6 | HG02486.hp2 HG02572.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.438+1398T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66438290 | ||||||
| chr15:66438338
|
C | T | 3 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0325 | 3 | HG02055.hp1 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.438+1446C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66438338 | ||||||
| chr15:66438362
|
C | T | 62 | a0001c0001t0003g0162a0001c0001t0003g0164a0001c0001t0003g0165others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.438+1470C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66438362 | ||||||
| chr15:66438442
|
T | G | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.438+1550T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66438442 | ||||||
| chr15:66438443
|
T | C | 1 | a0001c0001t0001g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.438+1551T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66438443 | ||||||
| chr15:66438628
|
A | C | 1 | a0001c0001t0006g0002 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.438+1736A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66438628 | ||||||
| chr15:66438654
|
G | GT | 16 | a0001c0001t0001g0111a0001c0001t0001g0119a0001c0001t0001g0122others(13): Show | 16 | HG00733.hp1 HG01257.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.438+1767dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 66438654 | |||||
| chr15:66438707
|
A | C | 52 | a0001c0001t0003g0162a0001c0001t0003g0164a0001c0001t0003g0165others(49): Show | 52 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.438+1815A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66438707 | ||||||
| chr15:66438947
|
G | C | 113 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(110): Show | 113 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.438+2055G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66438947 | ||||||
| chr15:66438987
|
T | C | 6 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(3): Show | 6 | HG02486.hp2 HG02572.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.438+2095T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66438987 | ||||||
| chr15:66438990
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.438+2098G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66438990 | ||||||
| chr15:66438994
|
A | C | 3 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0001g0330 | 3 | HG02257.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.438+2102A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66438994 | ||||||
| chr15:66439031
|
A | T | 1 | a0001c0001t0001g0258 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.438+2139A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66439031 | ||||||
| chr15:66439152
|
A | G | 361 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(358): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.438+2260A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66439152 | ||||||
| chr15:66439275
|
C | T | 1 | a0001c0001t0001g0325 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.438+2383C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66439275 | ||||||
| chr15:66439370
|
A | G | 364 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(361): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.438+2478A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66439370 | ||||||
| chr15:66439460
|
C | A | 31 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(28): Show | 31 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.438+2568C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66439460 | ||||||
| chr15:66439538
|
G | A | 2 | a0001c0001t0001g0339a0001c0001t0001g0340 | 2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.438+2646G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66439538 | ||||||
| chr15:66439626
|
C | T | 1 | a0001c0001t0003g0244 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.438+2734C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66439626 | ||||||
| chr15:66439661
|
G | A | 2 | a0001c0001t0001g0216a0001c0001t0001g0227 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.438+2769G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66439661 | ||||||
| chr15:66439891
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.438+2999C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66439891 | ||||||
| chr15:66439935
|
C | CA | 123 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(120): Show | 123 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.438+3061dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 66439935 | |||||
| chr15:66439935
|
CA | C | 50 | a0001c0001t0001g0010a0001c0001t0001g0101a0001c0001t0001g0102others(47): Show | 50 | HG00673.hp2 HG00733.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.438+3061delA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 66439935 | |||||
| chr15:66440042
|
A | G | 1 | a0001c0001t0001g0255 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.438+3150A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66440042 | ||||||
| chr15:66440092
|
TTTTG | T | 40 | a0001c0001t0001g0010a0001c0001t0001g0326a0001c0001t0001g0327others(37): Show | 40 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.439-3176_439-3173d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 66440092 | |||||
| chr15:66440114
|
C | T | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.439-3166C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66440114 | ||||||
| chr15:66440153
|
G | A | 1 | a0001c0001t0001g0337 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.439-3127G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66440153 | ||||||
| chr15:66440278
|
A | C | 1 | a0001c0001t0003g0209 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.439-3002A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66440278 | ||||||
| chr15:66440394
|
G | C | 2 | a0001c0001t0001g0276a0001c0001t0001g0288 | 2 | HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.439-2886G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66440394 | ||||||
| chr15:66440569
|
A | G | 2 | a0001c0001t0001g0339a0001c0001t0001g0340 | 2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.439-2711A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66440569 | ||||||
| chr15:66440776
|
T | C | 3 | a0001c0001t0001g0268a0001c0001t0001g0319a0001c0001t0001g0338 | 3 | HG02451.hp1 HG02723.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.439-2504T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66440776 | ||||||
| chr15:66440913
|
C | G | 1 | a0001c0001t0001g0339 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.439-2367C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66440913 | ||||||
| chr15:66440988
|
G | A | 30 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(27): Show | 30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.439-2292G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66440988 | ||||||
| chr15:66441067
|
G | GTCC | 4 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0312others(1): Show | 4 | NA18952.hp1 NA18993.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.439-2209_439-2207d others(5): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 66441067 | |||||
| chr15:66441189
|
C | T | 2 | a0001c0001t0001g0250a0001c0001t0001g0284 | 2 | HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.439-2091C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66441189 | ||||||
| chr15:66441300
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.439-1980C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66441300 | ||||||
| chr15:66441324
|
C | T | 2 | a0001c0001t0001g0250a0001c0001t0001g0284 | 2 | HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.439-1956C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66441324 | ||||||
| chr15:66441334
|
A | G | 1 | a0001c0001t0003g0209 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.439-1946A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66441334 | ||||||
| chr15:66441410
|
C | T | 60 | a0001c0001t0001g0232a0001c0001t0002g0011a0001c0001t0002g0047others(57): Show | 60 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.439-1870C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66441410 | ||||||
| chr15:66441550
|
G | A | 8 | a0001c0001t0005g0157a0001c0001t0005g0158a0001c0001t0005g0159others(5): Show | 8 | HG00280.hp1 HG00438.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.439-1730G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66441550 | ||||||
| chr15:66441563
|
C | T | 1 | a0001c0001t0012g0005 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.439-1717C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66441563 | ||||||
| chr15:66441685
|
A | G | 1 | a0001c0001t0002g0063 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.439-1595A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66441685 | ||||||
| chr15:66441747
|
A | T | 1 | a0001c0001t0001g0217 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.439-1533A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66441747 | ||||||
| chr15:66441752
|
C | CA | 6 | a0001c0001t0001g0010a0001c0001t0001g0218a0001c0001t0001g0327others(3): Show | 6 | HG02109.hp2 HG02257.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.439-1514dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 66441752 | |||||
| chr15:66441752
|
CA | C | 11 | a0001c0001t0001g0251a0001c0001t0001g0258a0001c0001t0003g0169others(8): Show | 11 | HG00140.hp1 HG00280.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.439-1514delA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 66441752 | |||||
| chr15:66441764
|
A | C | 5 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.439-1516A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66441764 | ||||||
| chr15:66441767
|
C | A | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.439-1513C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66441767 | ||||||
| chr15:66442308
|
T | C | 1 | a0001c0003t0001g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.439-972T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66442308 | ||||||
| chr15:66442380
|
C | A | 38 | a0001c0001t0001g0010a0001c0001t0001g0326a0001c0001t0001g0327others(35): Show | 38 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.439-900C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66442380 | ||||||
| chr15:66442547
|
G | A | 5 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.439-733G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66442547 | ||||||
| chr15:66442675
|
G | A | 2 | a0001c0001t0007g0096a0001c0001t0007g0114 | 2 | HG01255.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.439-605G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66442675 | ||||||
| chr15:66442736
|
A | G | 3 | a0001c0001t0002g0084a0001c0001t0003g0175a0001c0001t0003g0176 | 3 | HG01884.hp1 HG03490.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.439-544A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66442736 | ||||||
| chr15:66442886
|
G | A | 1 | a0001c0001t0001g0337 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.439-394G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66442886 | ||||||
| chr15:66443082
|
A | AT | 174 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0029others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.439-175dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 66443082 | |||||
| chr15:66443082
|
A | ATT | 88 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(85): Show | 88 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.439-176_439-175dup others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 66443082 | |||||
| chr15:66443082
|
A | ATTT | 16 | a0001c0001t0001g0112a0001c0001t0001g0156a0001c0001t0001g0266others(13): Show | 16 | HG00544.hp1 HG01109.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.439-177_439-175dup others(3): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 66443082 | |||||
| chr15:66443082
|
A | ATTTT | 6 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0130others(3): Show | 6 | HG00609.hp2 HG01943.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.439-178_439-175dup others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 66443082 | |||||
| chr15:66443082
|
A | ATTTTT | 20 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0121others(17): Show | 20 | HG00733.hp1 HG01257.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.439-179_439-175dup others(5): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 66443082 | |||||
| chr15:66443082
|
AT | A | 10 | a0001c0001t0001g0327a0001c0001t0001g0350a0001c0001t0006g0002others(7): Show | 10 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.439-175delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 66443082 | |||||
| chr15:66443112
|
G | A | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.439-168G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66443112 | ||||||
| chr15:66443185
|
C | T | 1 | a0001c0001t0003g0166 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.439-95C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66443185 | ||||||
| chr15:66443213
|
C | T | 313 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(310): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.439-67C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 3/10 | chr15 | 66443213 | ||||||
| chr15:66443385
|
A | G | 1 | a0001c0001t0001g0360 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.516+28A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 4/10 | chr15 | 66443385 | ||||||
| chr15:66443548
|
G | A | 48 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(45): Show | 48 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.516+191G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 4/10 | chr15 | 66443548 | ||||||
| chr15:66443587
|
C | CAG | 361 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(358): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.516+230_516+231ins others(2): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 4/10 | chr15 | 66443587 | ||||||
| chr15:66443965
|
C | T | 41 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(38): Show | 41 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.516+608C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 4/10 | chr15 | 66443965 | ||||||
| chr15:66444035
|
C | T | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.517-621C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 4/10 | chr15 | 66444035 | ||||||
| chr15:66444074
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.517-582A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 4/10 | chr15 | 66444074 | ||||||
| chr15:66444162
|
C | T | 38 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(35): Show | 38 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.517-494C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 4/10 | chr15 | 66444162 | ||||||
| chr15:66444273
|
C | T | 1 | a0001c0001t0002g0011 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.517-383C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 4/10 | chr15 | 66444273 | ||||||
| chr15:66444345
|
C | A | 38 | a0001c0001t0001g0010a0001c0001t0001g0326a0001c0001t0001g0327others(35): Show | 38 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.517-311C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 4/10 | chr15 | 66444345 | ||||||
| chr15:66444402
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.517-254G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 4/10 | chr15 | 66444402 | ||||||
| chr15:66444403
|
C | T | 113 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(110): Show | 113 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.517-253C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 4/10 | chr15 | 66444403 | ||||||
| chr15:66444410
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.517-246G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 4/10 | chr15 | 66444410 | ||||||
| chr15:66444426
|
A | C | 30 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(27): Show | 30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.517-230A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 4/10 | chr15 | 66444426 | ||||||
| chr15:66444472
|
G | T | 1 | a0001c0001t0001g0113 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.517-184G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 4/10 | chr15 | 66444472 | ||||||
| chr15:66444517
|
G | T | 3 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0325 | 3 | HG02055.hp1 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.517-139G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 4/10 | chr15 | 66444517 | ||||||
| chr15:66444795
|
C | T | 6 | a0001c0001t0003g0165a0001c0001t0003g0196a0001c0001t0003g0198others(3): Show | 6 | HG00621.hp2 HG02155.hp1 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.568+88C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66444795 | ||||||
| chr15:66444863
|
G | A | 1 | a0001c0001t0005g0242 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.568+156G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66444863 | ||||||
| chr15:66444905
|
C | T | 1 | a0001c0004t0001g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.568+198C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66444905 | ||||||
| chr15:66445145
|
A | G | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+438A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66445145 | ||||||
| chr15:66445148
|
G | T | 38 | a0001c0001t0001g0010a0001c0001t0001g0326a0001c0001t0001g0327others(35): Show | 38 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.568+441G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66445148 | ||||||
| chr15:66445157
|
T | TG | 157 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0026others(154): Show | 157 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.568+457dupG | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66445157 | |||||
| chr15:66445246
|
G | A | 1 | a0001c0001t0001g0340 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.568+539G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66445246 | ||||||
| chr15:66445352
|
G | A | 30 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(27): Show | 30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.568+645G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66445352 | ||||||
| chr15:66445370
|
T | C | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+663T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66445370 | ||||||
| chr15:66445408
|
G | C | 1 | a0001c0001t0001g0122 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.568+701G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66445408 | ||||||
| chr15:66445422
|
A | G | 3 | a0001c0001t0003g0194a0001c0001t0003g0195a0001c0001t0003g0206 | 3 | HG02572.hp1 NA18906.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.568+715A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66445422 | ||||||
| chr15:66445735
|
G | T | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.568+1028G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66445735 | ||||||
| chr15:66445877
|
T | A | 3 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0074 | 3 | NA18954.hp2 NA18986.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.568+1170T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66445877 | ||||||
| chr15:66446031
|
C | T | 62 | a0001c0001t0003g0162a0001c0001t0003g0164a0001c0001t0003g0165others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.568+1324C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66446031 | ||||||
| chr15:66446081
|
C | T | 1 | a0001c0001t0005g0241 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.568+1374C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66446081 | ||||||
| chr15:66446086
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.568+1379G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66446086 | ||||||
| chr15:66446155
|
G | A | 1 | a0001c0001t0001g0249 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.568+1448G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66446155 | ||||||
| chr15:66446204
|
G | A | 3 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033 | 3 | HG01261.hp2 HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.568+1497G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66446204 | ||||||
| chr15:66446257
|
G | A | 1 | a0001c0001t0001g0297 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.568+1550G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66446257 | ||||||
| chr15:66446382
|
C | T | 1 | a0001c0001t0001g0359 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.568+1675C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66446382 | ||||||
| chr15:66446440
|
C | CA | 8 | a0001c0001t0001g0112a0001c0001t0001g0133a0001c0001t0001g0141others(5): Show | 8 | HG01891.hp2 HG02970.hp1 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+1748dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66446440 | |||||
| chr15:66446515
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.568+1808C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66446515 | ||||||
| chr15:66446528
|
C | T | 1 | a0001c0001t0001g0352 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.568+1821C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66446528 | ||||||
| chr15:66446637
|
A | G | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | NA18946.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.568+1930A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66446637 | ||||||
| chr15:66446656
|
A | G | 1 | a0001c0001t0011g0265 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.568+1949A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66446656 | ||||||
| chr15:66446712
|
C | CAG | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.568+2005_568+2006i others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66446712 | ||||||
| chr15:66446748
|
G | A | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+2041G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66446748 | ||||||
| chr15:66446780
|
A | AT | 41 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(38): Show | 41 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.568+2074dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66446780 | |||||
| chr15:66446953
|
A | G | 30 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(27): Show | 30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.568+2246A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66446953 | ||||||
| chr15:66447074
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.568+2367C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66447074 | ||||||
| chr15:66447195
|
C | A | 1 | a0001c0001t0002g0064 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.568+2488C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66447195 | ||||||
| chr15:66447332
|
A | G | 38 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(35): Show | 38 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.568+2625A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66447332 | ||||||
| chr15:66447426
|
A | G | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | HG00735.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.568+2719A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66447426 | ||||||
| chr15:66447501
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.568+2794G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66447501 | ||||||
| chr15:66447550
|
G | A | 29 | a0001c0001t0001g0331a0001c0001t0001g0333a0001c0001t0001g0342others(26): Show | 29 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.568+2843G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66447550 | ||||||
| chr15:66447554
|
G | T | 1 | a0001c0001t0002g0088 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.568+2847G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66447554 | ||||||
| chr15:66447555
|
G | T | 1 | a0001c0001t0002g0100 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.568+2848G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66447555 | ||||||
| chr15:66447592
|
T | C | 2 | a0001c0001t0001g0303a0001c0001t0001g0305 | 2 | HG01952.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.568+2885T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66447592 | ||||||
| chr15:66447686
|
C | CA | 221 | a0001c0001t0001g0010a0001c0001t0001g0111a0001c0001t0001g0112others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.568+2994dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66447686 | |||||
| chr15:66447686
|
C | CAA | 96 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(93): Show | 96 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.568+2993_568+2994d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66447686 | |||||
| chr15:66447705
|
T | A | 82 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(79): Show | 82 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.568+2998T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66447705 | ||||||
| chr15:66447839
|
G | C | 6 | a0001c0001t0003g0164a0001c0001t0003g0170a0001c0001t0003g0184others(3): Show | 6 | HG00323.hp2 HG00642.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.568+3132G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66447839 | ||||||
| chr15:66448085
|
G | A | 1 | a0001c0001t0002g0117 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.568+3378G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66448085 | ||||||
| chr15:66448152
|
C | CA | 15 | a0001c0001t0001g0010a0001c0001t0001g0107a0001c0001t0001g0138others(12): Show | 15 | HG00544.hp2 HG00621.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.568+3466dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66448152 | |||||
| chr15:66448152
|
C | CAA | 115 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0115others(112): Show | 115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.568+3465_568+3466d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66448152 | |||||
| chr15:66448152
|
C | CAAA | 80 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(77): Show | 80 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.568+3464_568+3466d others(5): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66448152 | |||||
| chr15:66448152
|
C | CAAAA | 7 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0274others(4): Show | 7 | HG01175.hp2 HG01346.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.568+3463_568+3466d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66448152 | |||||
| chr15:66448157
|
A | AC | 48 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(45): Show | 48 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.568+3450_568+3451i others(3): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66448157 | ||||||
| chr15:66448162
|
A | AAG | 51 | a0001c0001t0003g0162a0001c0001t0003g0164a0001c0001t0003g0165others(48): Show | 51 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.568+3456_568+3457i others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66448162 | |||||
| chr15:66448162
|
A | C | 48 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(45): Show | 48 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.568+3455A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66448162 | ||||||
| chr15:66448162
|
A | G | 1 | a0001c0001t0003g0180 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.568+3455A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66448162 | ||||||
| chr15:66448166
|
A | C | 41 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(38): Show | 41 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.568+3459A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66448166 | ||||||
| chr15:66448173
|
A | C | 2 | a0001c0001t0005g0160a0001c0001t0005g0161 | 2 | HG01074.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.568+3466A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66448173 | ||||||
| chr15:66448227
|
C | A | 1 | a0001c0001t0003g0162 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.568+3520C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66448227 | ||||||
| chr15:66448502
|
A | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0039 | 2 | HG00738.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.568+3795A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66448502 | ||||||
| chr15:66448663
|
T | C | 2 | a0001c0001t0001g0218a0001c0001t0001g0236 | 2 | HG01934.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.568+3956T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66448663 | ||||||
| chr15:66448683
|
T | C | 1 | a0001c0001t0003g0189 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.568+3976T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66448683 | ||||||
| chr15:66448818
|
A | G | 2 | a0001c0001t0001g0276a0001c0001t0001g0288 | 2 | HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.568+4111A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66448818 | ||||||
| chr15:66448831
|
C | T | 1 | a0001c0001t0001g0339 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.568+4124C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66448831 | ||||||
| chr15:66448872
|
C | T | 1 | a0001c0001t0001g0249 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.568+4165C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66448872 | ||||||
| chr15:66448996
|
A | T | 321 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(318): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.568+4289A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66448996 | ||||||
| chr15:66449003
|
C | CA | 150 | a0001c0001t0001g0010a0001c0001t0001g0026a0001c0001t0001g0027others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.568+4321dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66449003 | |||||
| chr15:66449003
|
C | CAA | 77 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034others(74): Show | 77 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.568+4320_568+4321d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66449003 | |||||
| chr15:66449003
|
C | CAAA | 11 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(8): Show | 11 | HG00741.hp2 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.568+4319_568+4321d others(5): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66449003 | |||||
| chr15:66449003
|
CA | C | 9 | a0001c0001t0001g0262a0001c0001t0006g0002a0001c0001t0006g0003others(6): Show | 9 | HG00280.hp2 HG00639.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.568+4321delA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66449003 | |||||
| chr15:66449029
|
C | A | 2 | a0001c0001t0002g0051a0001c0001t0002g0087 | 2 | HG00597.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.568+4322C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66449029 | ||||||
| chr15:66449049
|
C | G | 52 | a0001c0001t0003g0162a0001c0001t0003g0164a0001c0001t0003g0165others(49): Show | 52 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.568+4342C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66449049 | ||||||
| chr15:66449124
|
T | A | 1 | a0001c0001t0001g0300 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.568+4417T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66449124 | ||||||
| chr15:66449398
|
T | G | 31 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(28): Show | 31 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.568+4691T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66449398 | ||||||
| chr15:66449477
|
AAAGTGCA others(1): Show |
A | 5 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.568+4774_568+4781d others(10): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66449477 | |||||
| chr15:66449618
|
C | T | 2 | a0001c0001t0001g0299a0001c0001t0006g0003 | 2 | HG02602.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.568+4911C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66449618 | ||||||
| chr15:66449632
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.568+4925G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66449632 | ||||||
| chr15:66449657
|
G | A | 113 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(110): Show | 113 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.568+4950G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66449657 | ||||||
| chr15:66449692
|
C | T | 55 | a0001c0001t0001g0232a0001c0001t0002g0011a0001c0001t0002g0047others(52): Show | 55 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.568+4985C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66449692 | ||||||
| chr15:66449763
|
C | T | 3 | a0001c0001t0001g0250a0001c0001t0001g0253a0001c0001t0001g0284 | 3 | HG01891.hp1 HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.568+5056C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66449763 | ||||||
| chr15:66450165
|
T | A | 364 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(361): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.568+5458T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450165 | ||||||
| chr15:66450186
|
C | T | 364 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(361): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.568+5479C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450186 | ||||||
| chr15:66450223
|
T | C | 3 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0325 | 3 | HG02055.hp1 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.568+5516T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450223 | ||||||
| chr15:66450228
|
C | G | 30 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(27): Show | 30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.568+5521C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450228 | ||||||
| chr15:66450253
|
A | G | 361 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(358): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.568+5546A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450253 | ||||||
| chr15:66450264
|
A | G | 10 | a0001c0001t0005g0157a0001c0001t0005g0158a0001c0001t0005g0159others(7): Show | 10 | HG00280.hp1 HG00438.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.568+5557A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450264 | ||||||
| chr15:66450348
|
T | G | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+5641T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450348 | ||||||
| chr15:66450393
|
T | A | 1 | a0001c0001t0001g0337 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.568+5686T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450393 | ||||||
| chr15:66450394
|
C | T | 1 | a0001c0001t0003g0199 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.568+5687C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450394 | ||||||
| chr15:66450395
|
G | A | 1 | a0001c0001t0001g0337 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.568+5688G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450395 | ||||||
| chr15:66450434
|
A | G | 4 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0233others(1): Show | 4 | HG02145.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.568+5727A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450434 | ||||||
| chr15:66450504
|
CAGAG | C | 5 | a0001c0001t0001g0215a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 5 | HG02145.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.568+5800_568+5803d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66450504 | |||||
| chr15:66450580
|
A | G | 54 | a0001c0001t0001g0232a0001c0001t0002g0011a0001c0001t0002g0047others(51): Show | 54 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.568+5873A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450580 | ||||||
| chr15:66450607
|
G | T | 41 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(38): Show | 41 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.568+5900G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450607 | ||||||
| chr15:66450695
|
G | A | 1 | a0001c0002t0001g0311 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.568+5988G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450695 | ||||||
| chr15:66450810
|
A | G | 2 | a0001c0001t0003g0177a0001c0001t0003g0205 | 2 | HG01515.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.568+6103A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450810 | ||||||
| chr15:66450874
|
AC | A | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+6169delC | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66450874 | |||||
| chr15:66450985
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.568+6278A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450985 | ||||||
| chr15:66450988
|
T | C | 21 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(18): Show | 21 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.568+6281T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66450988 | ||||||
| chr15:66451008
|
T | C | 10 | a0001c0001t0005g0157a0001c0001t0005g0158a0001c0001t0005g0159others(7): Show | 10 | HG00280.hp1 HG00438.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.568+6301T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66451008 | ||||||
| chr15:66451113
|
TC | T | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+6408delC | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66451113 | |||||
| chr15:66451175
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.568+6468A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66451175 | ||||||
| chr15:66451226
|
G | A | 9 | a0001c0001t0001g0001a0001c0001t0006g0002a0001c0001t0006g0003others(6): Show | 9 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.568+6519G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66451226 | ||||||
| chr15:66451306
|
C | A | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+6599C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66451306 | ||||||
| chr15:66451379
|
G | A | 2 | a0001c0001t0001g0339a0001c0001t0001g0340 | 2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.568+6672G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66451379 | ||||||
| chr15:66451448
|
A | AAAAC | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+6744_568+6747d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66451448 | |||||
| chr15:66451472
|
T | C | 361 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(358): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.568+6765T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66451472 | ||||||
| chr15:66451617
|
A | C | 1 | a0001c0001t0002g0056 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.568+6910A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66451617 | ||||||
| chr15:66451829
|
C | T | 81 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(78): Show | 81 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.568+7122C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66451829 | ||||||
| chr15:66451884
|
A | G | 38 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(35): Show | 38 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.568+7177A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66451884 | ||||||
| chr15:66451948
|
T | C | 2 | a0001c0001t0001g0220a0001c0001t0001g0237 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.568+7241T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66451948 | ||||||
| chr15:66451963
|
A | C | 21 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(18): Show | 21 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.568+7256A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66451963 | ||||||
| chr15:66451975
|
A | C | 1 | a0001c0001t0001g0001 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.568+7268A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66451975 | ||||||
| chr15:66452002
|
T | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(78): Show | 81 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.568+7295T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452002 | ||||||
| chr15:66452031
|
G | A | 11 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(8): Show | 11 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.568+7324G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452031 | ||||||
| chr15:66452151
|
G | C | 10 | a0001c0001t0005g0157a0001c0001t0005g0158a0001c0001t0005g0159others(7): Show | 10 | HG00280.hp1 HG00438.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.568+7444G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452151 | ||||||
| chr15:66452166
|
T | C | 5 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.568+7459T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452166 | ||||||
| chr15:66452170
|
G | T | 1 | a0001c0001t0004g0022 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.568+7463G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452170 | ||||||
| chr15:66452195
|
C | T | 1 | a0001c0001t0001g0359 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.568+7488C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452195 | ||||||
| chr15:66452210
|
C | T | 113 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(110): Show | 113 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.568+7503C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452210 | ||||||
| chr15:66452226
|
A | C | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.568+7519A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452226 | ||||||
| chr15:66452265
|
C | T | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+7558C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452265 | ||||||
| chr15:66452294
|
A | AAAG | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+7589_568+7590i others(5): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66452294 | |||||
| chr15:66452300
|
A | G | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+7593A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452300 | ||||||
| chr15:66452301
|
A | AAAAG | 120 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.568+7596_568+7597i others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66452301 | |||||
| chr15:66452302
|
A | AAAAG | 120 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(117): Show | 120 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.568+7596_568+7597i others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66452302 | |||||
| chr15:66452302
|
A | AAAG | 50 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(47): Show | 50 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.568+7596_568+7597i others(5): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66452302 | |||||
| chr15:66452303
|
A | AAG | 6 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(3): Show | 6 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.568+7596_568+7597i others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452303 | ||||||
| chr15:66452304
|
G | A | 314 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(311): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.568+7597G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452304 | ||||||
| chr15:66452304
|
G | GAA | 41 | a0001c0001t0001g0010a0001c0001t0001g0156a0001c0001t0001g0323others(38): Show | 41 | HG00733.hp2 HG01109.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.568+7606_568+7607d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66452304 | |||||
| chr15:66452349
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.568+7642A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452349 | ||||||
| chr15:66452412
|
T | G | 2 | a0001c0001t0003g0194a0001c0001t0003g0195 | 2 | HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.568+7705T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452412 | ||||||
| chr15:66452435
|
C | G | 361 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(358): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.568+7728C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452435 | ||||||
| chr15:66452559
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.568+7852T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452559 | ||||||
| chr15:66452673
|
G | A | 3 | a0001c0001t0002g0076a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | NA18962.hp2 NA19002.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.568+7966G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452673 | ||||||
| chr15:66452682
|
G | T | 3 | a0001c0001t0002g0076a0001c0001t0002g0085a0001c0001t0002g0086 | 3 | NA18962.hp2 NA19002.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.568+7975G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452682 | ||||||
| chr15:66452755
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.568+8048A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452755 | ||||||
| chr15:66452787
|
C | T | 1 | a0001c0001t0006g0006 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.568+8080C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452787 | ||||||
| chr15:66452799
|
T | C | 62 | a0001c0001t0003g0162a0001c0001t0003g0164a0001c0001t0003g0165others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.568+8092T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66452799 | ||||||
| chr15:66453174
|
C | G | 1 | a0001c0001t0003g0168 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.568+8467C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66453174 | ||||||
| chr15:66453198
|
A | T | 1 | a0001c0001t0002g0061 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.568+8491A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66453198 | ||||||
| chr15:66453390
|
A | C | 3 | a0001c0001t0005g0157a0001c0001t0005g0158a0001c0001t0005g0159 | 3 | HG00280.hp1 HG02735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.568+8683A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66453390 | ||||||
| chr15:66453552
|
G | A | 364 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(361): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.568+8845G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66453552 | ||||||
| chr15:66453591
|
G | C | 30 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(27): Show | 30 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.568+8884G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66453591 | ||||||
| chr15:66453855
|
G | A | 1 | a0001c0001t0002g0094 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.568+9148G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66453855 | ||||||
| chr15:66454122
|
G | A | 48 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(45): Show | 48 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.568+9415G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66454122 | ||||||
| chr15:66454132
|
G | A | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.568+9425G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66454132 | ||||||
| chr15:66454218
|
C | A | 3 | a0001c0001t0001g0306a0001c0001t0001g0308a0001c0001t0001g0315 | 3 | HG02027.hp1 NA19010.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.568+9511C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66454218 | ||||||
| chr15:66454296
|
T | TC | 48 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(45): Show | 48 | HG00423.hp1 HG00738.hp2 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.568+9591dupC | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66454296 | |||||
| chr15:66454553
|
C | T | 31 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(28): Show | 31 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.568+9846C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66454553 | ||||||
| chr15:66454554
|
C | T | 5 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.568+9847C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66454554 | ||||||
| chr15:66454750
|
C | T | 1 | a0001c0001t0001g0277 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.568+10043C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66454750 | ||||||
| chr15:66454815
|
G | A | 1 | a0001c0001t0003g0169 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.568+10108G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66454815 | ||||||
| chr15:66454983
|
T | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(78): Show | 81 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.568+10276T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66454983 | ||||||
| chr15:66455068
|
C | T | 5 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.568+10361C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66455068 | ||||||
| chr15:66455194
|
C | T | 1 | a0001c0001t0001g0001 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.568+10487C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66455194 | ||||||
| chr15:66455243
|
A | C | 1 | a0001c0001t0001g0121 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.568+10536A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66455243 | ||||||
| chr15:66455560
|
TC | T | 3 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0325 | 3 | HG02055.hp1 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.568+10855delC | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66455560 | |||||
| chr15:66455571
|
G | T | 113 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(110): Show | 113 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.568+10864G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66455571 | ||||||
| chr15:66455665
|
A | G | 1 | a0001c0001t0012g0005 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.568+10958A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66455665 | ||||||
| chr15:66455763
|
G | A | 1 | a0001c0001t0001g0361 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.568+11056G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66455763 | ||||||
| chr15:66455869
|
T | G | 1 | a0001c0001t0001g0275 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.568+11162T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66455869 | ||||||
| chr15:66455874
|
T | A | 20 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(17): Show | 20 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.568+11167T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66455874 | ||||||
| chr15:66455875
|
C | A | 20 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(17): Show | 20 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.568+11168C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66455875 | ||||||
| chr15:66456068
|
C | T | 1 | a0001c0001t0006g0002 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.568+11361C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66456068 | ||||||
| chr15:66456330
|
C | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0249 | 2 | HG02559.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.568+11623C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66456330 | ||||||
| chr15:66456568
|
C | T | 4 | a0001c0001t0001g0112a0001c0001t0001g0130a0001c0001t0001g0131others(1): Show | 4 | HG00609.hp2 NA18947.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.568+11861C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66456568 | ||||||
| chr15:66456606
|
A | G | 60 | a0001c0001t0001g0232a0001c0001t0002g0011a0001c0001t0002g0047others(57): Show | 60 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.568+11899A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66456606 | ||||||
| chr15:66456717
|
A | C | 11 | a0001c0001t0001g0349a0001c0001t0001g0350a0001c0001t0001g0354others(8): Show | 11 | HG01891.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.568+12010A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66456717 | ||||||
| chr15:66456921
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.568+12214C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66456921 | ||||||
| chr15:66456933
|
C | G | 1 | a0001c0001t0012g0005 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.568+12226C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66456933 | ||||||
| chr15:66457115
|
TTTA | T | 62 | a0001c0001t0003g0162a0001c0001t0003g0164a0001c0001t0003g0165others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.568+12417_568+1241 others(7): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66457115 | |||||
| chr15:66457187
|
C | T | 312 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(309): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.568+12480C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66457187 | ||||||
| chr15:66457276
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.568+12569G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66457276 | ||||||
| chr15:66457292
|
G | A | 312 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(309): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.568+12585G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66457292 | ||||||
| chr15:66457308
|
C | T | 81 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(78): Show | 81 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.568+12601C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66457308 | ||||||
| chr15:66457369
|
C | T | 2 | a0001c0001t0003g0184a0001c0001t0003g0185 | 2 | HG00642.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.568+12662C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66457369 | ||||||
| chr15:66457579
|
C | T | 81 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(78): Show | 81 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.568+12872C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66457579 | ||||||
| chr15:66457727
|
C | A | 2 | a0001c0001t0003g0162a0001c0001t0003g0171 | 2 | HG03491.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.568+13020C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66457727 | ||||||
| chr15:66457732
|
C | T | 51 | a0001c0001t0003g0162a0001c0001t0003g0164a0001c0001t0003g0165others(48): Show | 51 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.568+13025C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66457732 | ||||||
| chr15:66457756
|
G | A | 90 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(87): Show | 90 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.568+13049G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66457756 | ||||||
| chr15:66457791
|
G | A | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+13084G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66457791 | ||||||
| chr15:66457835
|
C | T | 26 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(23): Show | 26 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.568+13128C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66457835 | ||||||
| chr15:66457911
|
C | T | 1 | a0001c0001t0002g0047 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.568+13204C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66457911 | ||||||
| chr15:66457963
|
G | GA | 13 | a0001c0001t0001g0012a0001c0001t0001g0232a0001c0001t0001g0318others(10): Show | 13 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.568+13271dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66457963 | |||||
| chr15:66458186
|
A | G | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+13479A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66458186 | ||||||
| chr15:66458269
|
A | C | 1 | a0001c0001t0003g0182 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.568+13562A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66458269 | ||||||
| chr15:66458277
|
A | C | 90 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(87): Show | 90 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.568+13570A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66458277 | ||||||
| chr15:66458309
|
G | A | 2 | a0001c0001t0003g0181a0001c0001t0003g0203 | 2 | HG02602.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.568+13602G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66458309 | ||||||
| chr15:66458313
|
C | T | 312 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(309): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.568+13606C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66458313 | ||||||
| chr15:66458351
|
G | A | 3 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110 | 3 | HG02970.hp2 HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.568+13644G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66458351 | ||||||
| chr15:66458712
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.568+14005G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66458712 | ||||||
| chr15:66458730
|
A | C | 1 | a0001c0001t0002g0094 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.568+14023A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66458730 | ||||||
| chr15:66458914
|
T | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(78): Show | 81 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.568+14207T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66458914 | ||||||
| chr15:66459130
|
C | T | 1 | a0001c0001t0002g0082 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.568+14423C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66459130 | ||||||
| chr15:66459205
|
T | C | 364 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(361): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.568+14498T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66459205 | ||||||
| chr15:66459309
|
C | CA | 49 | a0001c0001t0001g0010a0001c0001t0001g0108a0001c0001t0001g0109others(46): Show | 49 | HG00280.hp2 HG00639.hp1 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.568+14619dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66459309 | |||||
| chr15:66459309
|
CA | C | 295 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(292): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.568+14619delA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66459309 | |||||
| chr15:66459383
|
A | G | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | HG00735.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.568+14676A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66459383 | ||||||
| chr15:66459441
|
A | T | 2 | a0001c0001t0005g0160a0001c0001t0005g0161 | 2 | HG01074.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.568+14734A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66459441 | ||||||
| chr15:66459541
|
A | C | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+14834A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66459541 | ||||||
| chr15:66459551
|
G | A | 1 | a0001c0001t0002g0117 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.568+14844G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66459551 | ||||||
| chr15:66459616
|
T | TG | 56 | a0001c0001t0001g0221a0001c0001t0002g0011a0001c0001t0002g0047others(53): Show | 56 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.568+14909_568+1491 others(5): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66459616 | ||||||
| chr15:66459616
|
T | TGA | 3 | a0001c0001t0002g0060a0001c0001t0002g0071a0001c0001t0008g0068 | 3 | HG02886.hp1 NA18949.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.568+14909_568+1491 others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66459616 | ||||||
| chr15:66459617
|
C | A | 59 | a0001c0001t0001g0221a0001c0001t0002g0011a0001c0001t0002g0047others(56): Show | 59 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.568+14910C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66459617 | ||||||
| chr15:66459617
|
C | CA | 224 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(221): Show | 224 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.568+14925dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66459617 | |||||
| chr15:66459617
|
C | CAA | 54 | a0001c0001t0001g0320a0001c0001t0001g0323a0001c0001t0001g0324others(51): Show | 54 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.568+14924_568+1492 others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66459617 | |||||
| chr15:66459617
|
C | G | 5 | a0001c0001t0001g0232a0001c0001t0002g0049a0001c0001t0002g0050others(2): Show | 5 | HG02280.hp1 NA18954.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.568+14910C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66459617 | ||||||
| chr15:66459632
|
A | AT | 10 | a0001c0001t0003g0200a0001c0001t0005g0157a0001c0001t0005g0158others(7): Show | 10 | HG00280.hp1 HG00438.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.568+14933dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66459632 | |||||
| chr15:66459632
|
A | T | 1 | a0001c0001t0005g0239 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.568+14925A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66459632 | ||||||
| chr15:66459633
|
T | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0274 | 2 | HG02683.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.568+14926T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66459633 | ||||||
| chr15:66459917
|
C | T | 2 | a0001c0001t0002g0055a0001c0001t0002g0063 | 2 | HG00099.hp2 HG00140.hp2 |
intron_variant | MODIFIER | c.568+15210C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66459917 | ||||||
| chr15:66460054
|
T | G | 1 | a0001c0001t0001g0103 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.568+15347T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66460054 | ||||||
| chr15:66460068
|
G | C | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+15361G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66460068 | ||||||
| chr15:66460155
|
G | A | 1 | a0001c0001t0003g0204 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.568+15448G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66460155 | ||||||
| chr15:66460187
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.568+15480G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66460187 | ||||||
| chr15:66460326
|
G | A | 1 | a0001c0003t0001g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.568+15619G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66460326 | ||||||
| chr15:66460452
|
A | G | 1 | a0001c0001t0001g0328 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.568+15745A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66460452 | ||||||
| chr15:66460487
|
A | T | 1 | a0001c0001t0002g0054 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.568+15780A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66460487 | ||||||
| chr15:66460580
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.568+15873G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66460580 | ||||||
| chr15:66460696
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.568+15989G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66460696 | ||||||
| chr15:66460830
|
G | C | 62 | a0001c0001t0003g0162a0001c0001t0003g0164a0001c0001t0003g0165others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.568+16123G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66460830 | ||||||
| chr15:66460872
|
G | C | 1 | a0001c0001t0001g0352 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.568+16165G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66460872 | ||||||
| chr15:66460983
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0146 | 2 | NA18949.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.568+16276C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66460983 | ||||||
| chr15:66461163
|
T | C | 1 | a0001c0002t0001g0311 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.568+16456T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66461163 | ||||||
| chr15:66461476
|
C | CTAAA | 134 | a0001c0001t0001g0010a0001c0001t0001g0026a0001c0001t0001g0027others(131): Show | 134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.568+16805_568+1680 others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66461476 | |||||
| chr15:66461476
|
C | CTAAATAA others(1): Show |
7 | a0001c0001t0001g0218a0001c0001t0001g0226a0001c0001t0003g0192others(4): Show | 7 | HG00099.hp1 HG01433.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.568+16801_568+1680 others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66461476 | |||||
| chr15:66461476
|
CTAAA | C | 149 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(146): Show | 149 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.568+16805_568+1680 others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66461476 | |||||
| chr15:66461476
|
CTAAATAA others(1): Show |
C | 13 | a0001c0001t0001g0091a0001c0001t0001g0101a0001c0001t0001g0102others(10): Show | 13 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.568+16801_568+1680 others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66461476 | |||||
| chr15:66461516
|
T | A | 2 | a0001c0001t0003g0182a0001c0001t0003g0205 | 2 | HG01515.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.568+16809T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66461516 | ||||||
| chr15:66461517
|
A | T | 2 | a0001c0001t0003g0182a0001c0001t0003g0205 | 2 | HG01515.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.568+16810A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66461517 | ||||||
| chr15:66461581
|
A | G | 1 | a0001c0003t0001g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.568+16874A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66461581 | ||||||
| chr15:66461765
|
C | T | 2 | a0001c0001t0001g0344a0001c0001t0001g0366 | 2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.568+17058C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66461765 | ||||||
| chr15:66461791
|
T | C | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | HG00735.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.568+17084T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66461791 | ||||||
| chr15:66461816
|
G | A | 1 | a0001c0001t0002g0086 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.568+17109G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66461816 | ||||||
| chr15:66461872
|
A | G | 2 | a0001c0001t0003g0194a0001c0001t0003g0195 | 2 | HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.568+17165A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66461872 | ||||||
| chr15:66462216
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.568+17509T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66462216 | ||||||
| chr15:66462314
|
A | G | 1 | a0001c0001t0002g0117 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.568+17607A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66462314 | ||||||
| chr15:66462359
|
G | C | 5 | a0001c0001t0005g0239a0001c0001t0005g0240a0001c0001t0005g0241others(2): Show | 5 | HG00438.hp2 NA18963.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.568+17652G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66462359 | ||||||
| chr15:66462399
|
C | T | 1 | a0001c0001t0001g0223 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.568+17692C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66462399 | ||||||
| chr15:66462422
|
G | A | 1 | a0001c0001t0001g0304 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.568+17715G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66462422 | ||||||
| chr15:66462446
|
G | A | 1 | a0001c0006t0001g0368 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.568+17739G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66462446 | ||||||
| chr15:66462496
|
C | CA | 117 | a0001c0001t0001g0010a0001c0001t0001g0091a0001c0001t0001g0101others(114): Show | 117 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.568+17809dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66462496 | |||||
| chr15:66462496
|
C | CAA | 35 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0156others(32): Show | 35 | HG00642.hp2 HG01069.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.568+17808_568+1780 others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66462496 | |||||
| chr15:66462496
|
CA | C | 7 | a0001c0001t0001g0118a0001c0001t0001g0267a0001c0001t0001g0277others(4): Show | 7 | HG00738.hp1 HG01516.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.568+17809delA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66462496 | |||||
| chr15:66462593
|
A | G | 2 | a0001c0001t0004g0037a0001c0001t0004g0042 | 2 | NA18977.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.568+17886A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66462593 | ||||||
| chr15:66462603
|
G | GA | 29 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(26): Show | 29 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.568+17907dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66462603 | |||||
| chr15:66462603
|
G | GAAAA | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+17904_568+1790 others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66462603 | |||||
| chr15:66462603
|
GA | G | 108 | a0001c0001t0001g0010a0001c0001t0001g0091a0001c0001t0001g0101others(105): Show | 108 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.568+17907delA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66462603 | |||||
| chr15:66462722
|
G | C | 1 | a0001c0001t0004g0045 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.568+18015G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66462722 | ||||||
| chr15:66462884
|
C | T | 3 | a0001c0001t0002g0052a0001c0001t0002g0072a0001c0001t0002g0099 | 3 | NA18972.hp1 NA19057.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.568+18177C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66462884 | ||||||
| chr15:66462896
|
G | A | 4 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0233others(1): Show | 4 | HG02145.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.568+18189G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66462896 | ||||||
| chr15:66462907
|
G | A | 51 | a0001c0001t0001g0010a0001c0001t0001g0091a0001c0001t0001g0101others(48): Show | 51 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.568+18200G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66462907 | ||||||
| chr15:66463115
|
T | C | 3 | a0001c0001t0001g0306a0001c0001t0001g0308a0001c0001t0001g0315 | 3 | HG02027.hp1 NA19010.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.568+18408T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66463115 | ||||||
| chr15:66463184
|
T | G | 31 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(28): Show | 31 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.568+18477T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66463184 | ||||||
| chr15:66463277
|
C | G | 1 | a0001c0001t0001g0319 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.569-18478C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66463277 | ||||||
| chr15:66463495
|
T | A | 1 | a0001c0001t0003g0209 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.569-18260T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66463495 | ||||||
| chr15:66463512
|
AC | A | 371 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(368): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.569-18241delC | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66463512 | |||||
| chr15:66463585
|
C | T | 62 | a0001c0001t0003g0162a0001c0001t0003g0164a0001c0001t0003g0165others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.569-18170C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66463585 | ||||||
| chr15:66463597
|
G | A | 25 | a0001c0001t0001g0342a0001c0001t0001g0343a0001c0001t0001g0344others(22): Show | 25 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.569-18158G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66463597 | ||||||
| chr15:66463627
|
C | T | 2 | a0001c0001t0001g0339a0001c0001t0001g0340 | 2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.569-18128C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66463627 | ||||||
| chr15:66463635
|
A | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.569-18120A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66463635 | ||||||
| chr15:66463830
|
T | C | 1 | a0001c0001t0006g0009 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.569-17925T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66463830 | ||||||
| chr15:66463832
|
T | C | 1 | a0001c0001t0001g0337 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.569-17923T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66463832 | ||||||
| chr15:66464132
|
G | A | 51 | a0001c0001t0001g0010a0001c0001t0001g0091a0001c0001t0001g0101others(48): Show | 51 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.569-17623G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66464132 | ||||||
| chr15:66464181
|
C | T | 82 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(79): Show | 82 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.569-17574C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66464181 | ||||||
| chr15:66464501
|
G | GGAAAA | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-17249_569-1724 others(9): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66464501 | |||||
| chr15:66464503
|
A | G | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.569-17252A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66464503 | ||||||
| chr15:66464559
|
T | C | 1 | a0001c0001t0002g0148 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.569-17196T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66464559 | ||||||
| chr15:66464585
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.569-17170C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66464585 | ||||||
| chr15:66464587
|
T | C | 334 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(331): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.569-17168T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66464587 | ||||||
| chr15:66464650
|
T | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(111): Show | 114 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.569-17105T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66464650 | ||||||
| chr15:66464672
|
T | A | 3 | a0001c0001t0001g0363a0001c0001t0001g0364a0001c0001t0001g0370 | 3 | HG02559.hp2 HG02895.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.569-17083T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66464672 | ||||||
| chr15:66464674
|
C | T | 51 | a0001c0001t0003g0162a0001c0001t0003g0164a0001c0001t0003g0165others(48): Show | 51 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.569-17081C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66464674 | ||||||
| chr15:66464675
|
G | A | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.569-17080G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66464675 | ||||||
| chr15:66464765
|
G | T | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.569-16990G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66464765 | ||||||
| chr15:66464770
|
C | T | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.569-16985C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66464770 | ||||||
| chr15:66464949
|
A | G | 331 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(328): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.569-16806A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66464949 | ||||||
| chr15:66464953
|
T | C | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-16802T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66464953 | ||||||
| chr15:66465122
|
G | A | 41 | a0001c0001t0001g0010a0001c0001t0001g0326a0001c0001t0001g0327others(38): Show | 41 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.569-16633G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66465122 | ||||||
| chr15:66465123
|
G | C | 1 | a0001c0001t0001g0339 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.569-16632G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66465123 | ||||||
| chr15:66465202
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.569-16553G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66465202 | ||||||
| chr15:66465224
|
C | T | 11 | a0001c0001t0003g0200a0001c0001t0005g0157a0001c0001t0005g0158others(8): Show | 11 | HG00280.hp1 HG00438.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.569-16531C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66465224 | ||||||
| chr15:66465349
|
C | T | 1 | a0001c0001t0002g0069 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.569-16406C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66465349 | ||||||
| chr15:66465353
|
A | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(111): Show | 114 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.569-16402A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66465353 | ||||||
| chr15:66465490
|
C | T | 1 | a0001c0001t0002g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.569-16265C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66465490 | ||||||
| chr15:66465623
|
T | A | 62 | a0001c0001t0003g0162a0001c0001t0003g0164a0001c0001t0003g0165others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.569-16132T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66465623 | ||||||
| chr15:66465708
|
A | C | 1 | a0001c0001t0001g0315 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.569-16047A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66465708 | ||||||
| chr15:66465737
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.569-16018G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66465737 | ||||||
| chr15:66465829
|
G | A | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-15926G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66465829 | ||||||
| chr15:66466045
|
C | G | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-15710C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66466045 | ||||||
| chr15:66466354
|
C | T | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-15401C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66466354 | ||||||
| chr15:66466356
|
A | G | 30 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(27): Show | 30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.569-15399A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66466356 | ||||||
| chr15:66466371
|
G | A | 1 | a0001c0001t0001g0212 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.569-15384G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66466371 | ||||||
| chr15:66466437
|
C | T | 30 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(27): Show | 30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.569-15318C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66466437 | ||||||
| chr15:66466503
|
A | T | 1 | a0001c0001t0001g0141 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.569-15252A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66466503 | ||||||
| chr15:66466579
|
C | T | 1 | a0001c0001t0002g0051 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.569-15176C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66466579 | ||||||
| chr15:66467094
|
G | A | 3 | a0001c0001t0006g0004a0001c0001t0006g0007a0001c0001t0006g0008 | 3 | HG01515.hp1 HG01517.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.569-14661G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66467094 | ||||||
| chr15:66467181
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.569-14574C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66467181 | ||||||
| chr15:66467221
|
C | T | 1 | a0001c0001t0002g0052 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.569-14534C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66467221 | ||||||
| chr15:66467229
|
C | T | 4 | a0001c0001t0003g0167a0001c0001t0003g0169a0001c0001t0003g0178others(1): Show | 4 | HG00140.hp1 HG01071.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-14526C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66467229 | ||||||
| chr15:66467266
|
A | G | 1 | a0001c0001t0007g0114 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.569-14489A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66467266 | ||||||
| chr15:66467361
|
G | A | 41 | a0001c0001t0001g0010a0001c0001t0001g0326a0001c0001t0001g0327others(38): Show | 41 | HG00733.hp2 HG01069.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.569-14394G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66467361 | ||||||
| chr15:66467543
|
C | T | 3 | a0001c0001t0001g0259a0001c0001t0001g0267a0001c0001t0001g0321 | 3 | HG02895.hp2 HG02897.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.569-14212C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66467543 | ||||||
| chr15:66467647
|
G | A | 30 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(27): Show | 30 | HG00609.hp2 HG00733.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.569-14108G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66467647 | ||||||
| chr15:66468004
|
A | G | 92 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(89): Show | 92 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.569-13751A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468004 | ||||||
| chr15:66468246
|
A | T | 1 | a0001c0001t0001g0362 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.569-13509A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468246 | ||||||
| chr15:66468269
|
CT | C | 7 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(4): Show | 7 | HG01257.hp2 HG02615.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.569-13477delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66468269 | |||||
| chr15:66468271
|
T | C | 1 | a0001c0001t0002g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.569-13484T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468271 | ||||||
| chr15:66468281
|
C | G | 2 | a0001c0001t0001g0339a0001c0004t0001g0015 | 2 | HG02615.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.569-13474C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468281 | ||||||
| chr15:66468291
|
C | T | 1 | a0001c0001t0002g0095 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.569-13464C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468291 | ||||||
| chr15:66468361
|
C | A | 1 | a0001c0001t0001g0280 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.569-13394C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468361 | ||||||
| chr15:66468377
|
A | G | 1 | a0001c0001t0003g0164 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.569-13378A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468377 | ||||||
| chr15:66468442
|
G | C | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-13313G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468442 | ||||||
| chr15:66468553
|
T | A | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-13202T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468553 | ||||||
| chr15:66468569
|
T | C | 15 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(12): Show | 15 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.569-13186T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468569 | ||||||
| chr15:66468581
|
C | T | 1 | a0001c0001t0001g0304 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.569-13174C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468581 | ||||||
| chr15:66468633
|
TA | T | 4 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0233others(1): Show | 4 | HG02145.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-13114delA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66468633 | |||||
| chr15:66468634
|
A | T | 7 | a0001c0001t0001g0091a0001c0001t0001g0101a0001c0001t0001g0102others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.569-13121A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468634 | ||||||
| chr15:66468642
|
T | A | 63 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(60): Show | 63 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.569-13113T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468642 | ||||||
| chr15:66468645
|
T | G | 1 | a0001c0001t0001g0140 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.569-13110T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468645 | ||||||
| chr15:66468708
|
G | A | 3 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0325 | 3 | HG02055.hp1 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.569-13047G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468708 | ||||||
| chr15:66468734
|
C | A | 1 | a0001c0001t0003g0199 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.569-13021C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468734 | ||||||
| chr15:66468743
|
C | T | 1 | a0001c0001t0005g0160 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.569-13012C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468743 | ||||||
| chr15:66468792
|
G | A | 1 | a0001c0001t0001g0001 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.569-12963G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468792 | ||||||
| chr15:66468807
|
T | C | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-12948T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468807 | ||||||
| chr15:66468868
|
TTGCAGTG others(17): Show |
T | 65 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(62): Show | 65 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.569-12858_569-1283 others(28): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66468868 | |||||
| chr15:66468903
|
TG | T | 37 | a0001c0001t0001g0010a0001c0001t0001g0326a0001c0001t0001g0327others(34): Show | 37 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.569-12851delG | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468903 | ||||||
| chr15:66468949
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.569-12806G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66468949 | ||||||
| chr15:66468953
|
C | CA | 48 | a0001c0001t0003g0162a0001c0001t0003g0164a0001c0001t0003g0165others(45): Show | 48 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.569-12791dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66468953 | |||||
| chr15:66469029
|
G | T | 1 | a0001c0001t0001g0113 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.569-12726G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469029 | ||||||
| chr15:66469149
|
C | T | 2 | a0001c0001t0001g0250a0001c0001t0001g0284 | 2 | HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.569-12606C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469149 | ||||||
| chr15:66469173
|
T | C | 1 | a0001c0001t0001g0140 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.569-12582T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469173 | ||||||
| chr15:66469175
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.569-12580G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469175 | ||||||
| chr15:66469176
|
A | T | 1 | a0001c0001t0001g0140 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.569-12579A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469176 | ||||||
| chr15:66469179
|
C | A | 1 | a0001c0001t0001g0140 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.569-12576C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469179 | ||||||
| chr15:66469180
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.569-12575C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469180 | ||||||
| chr15:66469185
|
G | T | 1 | a0001c0001t0001g0140 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.569-12570G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469185 | ||||||
| chr15:66469189
|
G | T | 1 | a0001c0001t0001g0140 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.569-12566G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469189 | ||||||
| chr15:66469472
|
C | CT | 52 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0039others(49): Show | 52 | HG00544.hp2 HG00621.hp1 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.569-12256dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469472 | |||||
| chr15:66469472
|
C | CTT | 131 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(128): Show | 131 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.569-12257_569-1225 others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469472 | |||||
| chr15:66469472
|
C | CTTT | 40 | a0001c0001t0001g0112a0001c0001t0001g0125a0001c0001t0001g0130others(37): Show | 40 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.569-12258_569-1225 others(7): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469472 | |||||
| chr15:66469472
|
C | CTTTTTT | 15 | a0001c0001t0001g0328a0001c0001t0001g0333a0001c0001t0001g0342others(12): Show | 15 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.569-12261_569-1225 others(10): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469472 | |||||
| chr15:66469472
|
C | CTTTTTTT | 11 | a0001c0001t0001g0331a0001c0001t0001g0346a0001c0001t0001g0352others(8): Show | 11 | HG01891.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.569-12262_569-1225 others(11): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469472 | |||||
| chr15:66469472
|
CTT | C | 6 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(3): Show | 6 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.569-12257_569-1225 others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469472 | |||||
| chr15:66469472
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0028 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.569-12267_569-1225 others(16): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469472 | |||||
| chr15:66469472
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0299 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.569-12268_569-1225 others(17): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469472 | |||||
| chr15:66469535
|
G | A | 7 | a0001c0001t0001g0091a0001c0001t0001g0101a0001c0001t0001g0102others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.569-12220G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469535 | ||||||
| chr15:66469557
|
C | G | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.569-12198C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469557 | ||||||
| chr15:66469611
|
GAGA | G | 7 | a0001c0001t0001g0091a0001c0001t0001g0101a0001c0001t0001g0102others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.569-12136_569-1213 others(7): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469611 | |||||
| chr15:66469637
|
A | G | 4 | a0001c0001t0001g0112a0001c0001t0001g0130a0001c0001t0001g0131others(1): Show | 4 | HG00609.hp2 NA18947.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-12118A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469637 | ||||||
| chr15:66469661
|
AAAAC | A | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-12089_569-1208 others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469661 | |||||
| chr15:66469693
|
G | GAC | 8 | a0001c0001t0001g0010a0001c0001t0001g0334a0001c0001t0001g0344others(5): Show | 8 | HG01099.hp2 HG01884.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.569-12032_569-1203 others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | |||||
| chr15:66469693
|
G | GACAC | 3 | a0001c0001t0001g0326a0001c0001t0006g0007a0001c0001t0006g0008 | 3 | HG01515.hp1 HG01517.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.569-12034_569-1203 others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | |||||
| chr15:66469693
|
G | GACACACA others(1): Show |
4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG00639.hp2 NA18522.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-12038_569-1203 others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | |||||
| chr15:66469693
|
G | GACACACA others(3): Show |
48 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0247others(45): Show | 48 | HG00609.hp1 HG00735.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.569-12040_569-1203 others(14): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | |||||
| chr15:66469693
|
G | GACACACA others(5): Show |
26 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0108others(23): Show | 26 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.569-12042_569-1203 others(16): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | |||||
| chr15:66469693
|
G | GACACACA others(7): Show |
6 | a0001c0001t0001g0127a0001c0001t0001g0252a0001c0001t0001g0253others(3): Show | 6 | HG01256.hp1 HG01891.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.569-12044_569-1203 others(18): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | |||||
| chr15:66469693
|
G | GACACACA others(9): Show |
5 | a0001c0001t0001g0284a0001c0001t0001g0291a0001c0001t0001g0293others(2): Show | 5 | HG04199.hp1 NA18947.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.569-12046_569-1203 others(20): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | |||||
| chr15:66469693
|
G | GACACACA others(11): Show |
3 | a0001c0001t0001g0250a0001c0001t0001g0276a0001c0001t0001g0288 | 3 | HG02809.hp1 HG03209.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.569-12048_569-1203 others(22): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | |||||
| chr15:66469693
|
G | GACACACA others(13): Show |
3 | a0001c0001t0001g0296a0001c0001t0001g0304a0001c0001t0012g0005 | 3 | HG02145.hp2 HG04228.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.569-12050_569-1203 others(24): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | |||||
| chr15:66469693
|
G | GACACACA others(15): Show |
2 | a0001c0001t0001g0130a0001c0003t0001g0155 | 2 | HG00609.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.569-12052_569-1203 others(26): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | |||||
| chr15:66469693
|
G | GACACACA others(17): Show |
7 | a0001c0001t0001g0140a0001c0001t0001g0144a0001c0001t0001g0227others(4): Show | 7 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.569-12054_569-1203 others(28): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | |||||
| chr15:66469693
|
G | GACACACA others(19): Show |
1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.569-12056_569-1203 others(30): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | |||||
| chr15:66469693
|
G | GACACACA others(21): Show |
6 | a0001c0001t0001g0101a0001c0001t0001g0122a0001c0001t0001g0131others(3): Show | 6 | HG01952.hp1 HG02602.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.569-12058_569-1203 others(32): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | |||||
| chr15:66469693
|
G | GACACACA others(23): Show |
4 | a0001c0001t0001g0103a0001c0001t0001g0112a0001c0001t0001g0133others(1): Show | 4 | HG01934.hp1 HG02258.hp1 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.569-12060_569-1203 others(34): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | |||||
| chr15:66469693
|
G | GACACACA others(25): Show |
3 | a0001c0001t0001g0139a0001c0001t0001g0215a0001c0001t0001g0237 | 3 | HG02970.hp1 HG02976.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.569-12031_569-1203 others(36): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | |||||
| chr15:66469693
|
G | GACACACA others(27): Show |
8 | a0001c0001t0001g0119a0001c0001t0001g0125a0001c0001t0001g0129others(5): Show | 8 | HG01257.hp1 HG01993.hp1 HG03540.hp2 others(5): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(38): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | |||||
| chr15:66469693
|
G | GACACACA others(29): Show |
14 | a0001c0001t0001g0105a0001c0001t0001g0111a0001c0001t0001g0115others(11): Show | 14 | HG01069.hp2 HG01071.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(40): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | |||||
| chr15:66469693
|
G | GACACACA others(31): Show |
5 | a0001c0001t0001g0124a0001c0001t0001g0154a0001c0001t0001g0226others(2): Show | 5 | HG00642.hp2 HG02630.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(42): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | |||||
| chr15:66469693
|
G | GACACACA others(33): Show |
7 | a0001c0001t0001g0091a0001c0001t0001g0102a0001c0001t0001g0126others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(44): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | |||||
| chr15:66469693
|
G | GACACACA others(35): Show |
4 | a0001c0001t0001g0106a0001c0001t0001g0136a0001c0001t0001g0229others(1): Show | 4 | HG01123.hp1 HG02165.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(46): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | |||||
| chr15:66469693
|
G | GACACACA others(37): Show |
2 | a0001c0001t0001g0121a0001c0001t0001g0123 | 2 | NA18975.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.569-12031_569-1203 others(48): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | |||||
| chr15:66469693
|
G | GACACACA others(39): Show |
4 | a0001c0001t0001g0135a0001c0001t0001g0217a0001c0001t0001g0224others(1): Show | 4 | HG02818.hp2 NA18747.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(50): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | |||||
| chr15:66469693
|
G | GACACACA others(41): Show |
6 | a0001c0001t0001g0107a0001c0001t0001g0116a0001c0001t0001g0141others(3): Show | 6 | HG01934.hp2 HG02145.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(52): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | |||||
| chr15:66469693
|
G | GACACACA others(43): Show |
1 | a0001c0001t0001g0137 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.569-12031_569-1203 others(54): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | |||||
| chr15:66469693
|
G | GACACACA others(45): Show |
1 | a0001c0001t0001g0238 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.569-12031_569-1203 others(56): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | |||||
| chr15:66469693
|
G | GACACACA others(51): Show |
1 | a0001c0001t0001g0223 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.569-12031_569-1203 others(62): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469693 | |||||
| chr15:66469723
|
C | CACACACA others(45): Show |
1 | a0001c0001t0002g0057 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.569-12031_569-1203 others(56): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | |||||
| chr15:66469723
|
C | CACACACA others(43): Show |
2 | a0001c0001t0002g0093a0001c0001t0005g0242 | 2 | NA18963.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.569-12031_569-1203 others(54): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | |||||
| chr15:66469723
|
C | CACACACA others(41): Show |
4 | a0001c0001t0002g0054a0001c0001t0002g0074a0001c0001t0002g0081others(1): Show | 4 | HG02056.hp2 NA18993.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(52): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | |||||
| chr15:66469723
|
C | CACACACA others(39): Show |
5 | a0001c0001t0002g0069a0001c0001t0002g0083a0001c0001t0002g0085others(2): Show | 5 | HG03942.hp2 NA18962.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(50): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | |||||
| chr15:66469723
|
C | CACACACA others(41): Show |
2 | a0001c0001t0002g0049a0001c0001t0003g0200 | 2 | NA18986.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.569-12031_569-1203 others(52): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | |||||
| chr15:66469723
|
C | CACACACA others(37): Show |
3 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0097 | 3 | HG01243.hp1 NA18946.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.569-12031_569-1203 others(48): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | |||||
| chr15:66469723
|
C | CACACACA others(35): Show |
9 | a0001c0001t0002g0051a0001c0001t0002g0052a0001c0001t0002g0064others(6): Show | 9 | HG00558.hp2 HG00621.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(46): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | |||||
| chr15:66469723
|
C | CACACACA others(33): Show |
11 | a0001c0001t0001g0232a0001c0001t0002g0011a0001c0001t0002g0053others(8): Show | 11 | HG00099.hp2 HG00597.hp2 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(44): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | |||||
| chr15:66469723
|
C | CACACACA others(31): Show |
5 | a0001c0001t0002g0048a0001c0001t0002g0050a0001c0001t0002g0065others(2): Show | 5 | NA18954.hp2 NA19012.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(42): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | |||||
| chr15:66469723
|
C | CACACACA others(33): Show |
1 | a0001c0001t0005g0160 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.569-12031_569-1203 others(44): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | |||||
| chr15:66469723
|
C | CACACACA others(29): Show |
7 | a0001c0001t0002g0062a0001c0001t0002g0066a0001c0001t0002g0073others(4): Show | 7 | HG00280.hp1 HG00544.hp2 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(40): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | |||||
| chr15:66469723
|
C | CACACACA others(27): Show |
6 | a0001c0001t0002g0047a0001c0001t0002g0056a0001c0001t0002g0063others(3): Show | 6 | HG00140.hp2 HG02300.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(38): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | |||||
| chr15:66469723
|
C | CACACACA others(25): Show |
2 | a0001c0001t0005g0243a0001c0001t0008g0068 | 2 | HG00438.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.569-12031_569-1203 others(36): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | |||||
| chr15:66469723
|
C | CACACACA others(23): Show |
2 | a0001c0001t0002g0060a0001c0001t0005g0158 | 2 | HG03669.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.569-12031_569-1203 others(34): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | |||||
| chr15:66469723
|
C | CACACACA others(25): Show |
1 | a0001c0001t0005g0161 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.569-12031_569-1203 others(36): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | |||||
| chr15:66469723
|
C | CACACACA others(21): Show |
2 | a0001c0001t0002g0061a0001c0005t0002g0077 | 2 | HG00673.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.569-12031_569-1203 others(32): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | |||||
| chr15:66469723
|
C | CACACACA others(19): Show |
1 | a0001c0001t0002g0084 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.569-12031_569-1203 others(30): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | |||||
| chr15:66469723
|
C | CACACACA others(17): Show |
4 | a0001c0001t0002g0078a0001c0001t0002g0100a0001c0001t0003g0188others(1): Show | 4 | HG00140.hp1 HG02165.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(28): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | |||||
| chr15:66469723
|
C | CACACACA others(15): Show |
2 | a0001c0001t0002g0150a0001c0001t0003g0179 | 2 | NA18982.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.569-12031_569-1203 others(26): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | |||||
| chr15:66469723
|
C | CACACACA others(13): Show |
4 | a0001c0001t0003g0183a0001c0001t0003g0194a0001c0001t0003g0195others(1): Show | 4 | HG01433.hp2 HG02572.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(24): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | |||||
| chr15:66469723
|
C | CACACACA others(11): Show |
8 | a0001c0001t0002g0067a0001c0001t0003g0169a0001c0001t0003g0175others(5): Show | 8 | HG00642.hp1 HG01168.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(22): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | |||||
| chr15:66469723
|
C | CACACACA others(9): Show |
26 | a0001c0001t0003g0165a0001c0001t0003g0172a0001c0001t0003g0173others(23): Show | 26 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(20): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | |||||
| chr15:66469723
|
C | CACACACA others(7): Show |
3 | a0001c0001t0003g0170a0001c0001t0003g0171a0001c0001t0003g0192 | 3 | HG00099.hp1 HG00741.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.569-12031_569-1203 others(18): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | |||||
| chr15:66469723
|
C | CACACACA others(5): Show |
4 | a0001c0001t0003g0164a0001c0001t0003g0166a0001c0001t0003g0191others(1): Show | 4 | HG00738.hp1 HG01074.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-12031_569-1203 others(16): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | |||||
| chr15:66469723
|
C | CACACACA others(3): Show |
2 | a0001c0001t0003g0187a0001c0001t0003g0371 | 2 | HG00323.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.569-12031_569-1203 others(14): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66469723 | |||||
| chr15:66469725
|
T | C | 10 | a0001c0001t0001g0091a0001c0001t0001g0101a0001c0001t0001g0102others(7): Show | 10 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.569-12030T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469725 | ||||||
| chr15:66469829
|
T | A | 4 | a0001c0001t0005g0239a0001c0001t0005g0240a0001c0001t0005g0242others(1): Show | 4 | HG00438.hp2 NA18963.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.569-11926T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469829 | ||||||
| chr15:66469855
|
C | G | 2 | a0001c0001t0001g0339a0001c0001t0001g0340 | 2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.569-11900C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469855 | ||||||
| chr15:66469947
|
T | C | 117 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(114): Show | 117 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.569-11808T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469947 | ||||||
| chr15:66469962
|
C | A | 1 | a0001c0001t0006g0009 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.569-11793C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66469962 | ||||||
| chr15:66470091
|
CTTGT | C | 9 | a0001c0001t0003g0200a0001c0001t0005g0157a0001c0001t0005g0158others(6): Show | 9 | HG00280.hp1 HG00438.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.569-11661_569-1165 others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66470091 | |||||
| chr15:66470094
|
G | GT | 49 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(46): Show | 49 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.569-11637dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66470094 | |||||
| chr15:66470094
|
G | GTT | 12 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0003g0164others(9): Show | 12 | HG00099.hp1 HG00597.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.569-11638_569-1163 others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66470094 | |||||
| chr15:66470094
|
GT | G | 36 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0119others(33): Show | 36 | HG00609.hp2 HG00642.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.569-11637delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66470094 | |||||
| chr15:66470094
|
GTT | G | 44 | a0001c0001t0001g0001a0001c0001t0001g0108a0001c0001t0001g0109others(41): Show | 44 | HG00280.hp2 HG00544.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.569-11638_569-1163 others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66470094 | |||||
| chr15:66470094
|
GTTT | G | 98 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(95): Show | 98 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.569-11639_569-1163 others(7): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66470094 | |||||
| chr15:66470094
|
GTTTT | G | 47 | a0001c0001t0001g0115a0001c0001t0001g0219a0001c0001t0001g0220others(44): Show | 47 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.569-11640_569-1163 others(8): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66470094 | |||||
| chr15:66470094
|
GTTTTT | G | 10 | a0001c0001t0001g0091a0001c0001t0001g0101a0001c0001t0001g0102others(7): Show | 10 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.569-11641_569-1163 others(9): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66470094 | |||||
| chr15:66470094
|
GTTTTTT | G | 35 | a0001c0001t0001g0010a0001c0001t0001g0327a0001c0001t0001g0328others(32): Show | 35 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.569-11642_569-1163 others(10): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66470094 | |||||
| chr15:66470288
|
G | C | 2 | a0001c0001t0003g0179a0001c0001t0003g0183 | 2 | NA18747.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.569-11467G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66470288 | ||||||
| chr15:66470404
|
C | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(81): Show | 84 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.569-11351C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66470404 | ||||||
| chr15:66470758
|
T | C | 19 | a0001c0001t0004g0016a0001c0001t0004g0017a0001c0001t0004g0018others(16): Show | 19 | HG00423.hp1 HG03927.hp2 NA18941.hp1 others(16): Show |
intron_variant | MODIFIER | c.569-10997T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66470758 | ||||||
| chr15:66470839
|
C | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(48): Show | 51 | HG00735.hp1 HG00735.hp2 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.569-10916C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66470839 | ||||||
| chr15:66470927
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.569-10828G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66470927 | ||||||
| chr15:66471177
|
C | T | 1 | a0001c0001t0003g0204 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.569-10578C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66471177 | ||||||
| chr15:66471302
|
C | G | 7 | a0001c0001t0001g0091a0001c0001t0001g0101a0001c0001t0001g0102others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.569-10453C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66471302 | ||||||
| chr15:66471363
|
T | C | 1 | a0001c0001t0001g0272 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.569-10392T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66471363 | ||||||
| chr15:66471618
|
G | T | 1 | a0001c0001t0003g0183 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.569-10137G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66471618 | ||||||
| chr15:66471658
|
AT | A | 316 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(313): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.569-10086delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66471658 | |||||
| chr15:66471658
|
ATT | A | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-10087_569-1008 others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66471658 | |||||
| chr15:66471879
|
C | T | 2 | a0001c0001t0001g0292a0001c0001t0001g0298 | 2 | HG00609.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.569-9876C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66471879 | ||||||
| chr15:66471937
|
C | T | 2 | a0001c0001t0003g0175a0001c0001t0003g0176 | 2 | HG03490.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.569-9818C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66471937 | ||||||
| chr15:66472075
|
C | CA | 9 | a0001c0001t0001g0110a0001c0001t0001g0132a0001c0001t0001g0156others(6): Show | 9 | HG01074.hp2 HG01934.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.569-9662dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66472075 | |||||
| chr15:66472075
|
C | CAA | 181 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0111others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.569-9663_569-9662d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66472075 | |||||
| chr15:66472075
|
C | CAAA | 117 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(114): Show | 117 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.569-9664_569-9662d others(5): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66472075 | |||||
| chr15:66472075
|
C | CAAAA | 14 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0091others(11): Show | 14 | HG00438.hp1 HG01167.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.569-9665_569-9662d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66472075 | |||||
| chr15:66472075
|
C | CAAAAAAA others(2): Show |
7 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(4): Show | 7 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.569-9670_569-9662d others(11): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66472075 | |||||
| chr15:66472075
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0012g0005 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.569-9671_569-9662d others(12): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66472075 | |||||
| chr15:66472228
|
C | A | 1 | a0001c0001t0002g0097 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.569-9527C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66472228 | ||||||
| chr15:66472259
|
G | A | 1 | a0001c0001t0001g0238 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.569-9496G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66472259 | ||||||
| chr15:66472303
|
C | CA | 112 | a0001c0001t0001g0010a0001c0001t0001g0091a0001c0001t0001g0101others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.569-9437dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66472303 | |||||
| chr15:66472303
|
CA | C | 69 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(66): Show | 69 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.569-9437delA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66472303 | |||||
| chr15:66472430
|
C | T | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-9325C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66472430 | ||||||
| chr15:66472452
|
A | G | 2 | a0001c0001t0006g0007a0001c0001t0006g0008 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.569-9303A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66472452 | ||||||
| chr15:66472476
|
C | A | 20 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(17): Show | 20 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.569-9279C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66472476 | ||||||
| chr15:66472535
|
C | T | 325 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(322): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.569-9220C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66472535 | ||||||
| chr15:66472557
|
C | T | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.569-9198C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66472557 | ||||||
| chr15:66472612
|
C | T | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-9143C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66472612 | ||||||
| chr15:66472686
|
A | ATTGTCAG | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-9063_569-9062i others(9): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66472686 | |||||
| chr15:66472720
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.569-9035C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66472720 | ||||||
| chr15:66472725
|
T | C | 1 | a0001c0001t0001g0337 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.569-9030T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66472725 | ||||||
| chr15:66472852
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.569-8903A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66472852 | ||||||
| chr15:66472861
|
G | A | 1 | a0001c0001t0001g0349 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.569-8894G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66472861 | ||||||
| chr15:66472946
|
C | T | 1 | a0001c0002t0001g0311 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.569-8809C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66472946 | ||||||
| chr15:66473066
|
G | A | 36 | a0001c0001t0001g0010a0001c0001t0001g0091a0001c0001t0001g0101others(33): Show | 36 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.569-8689G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66473066 | ||||||
| chr15:66473096
|
T | A | 2 | a0001c0001t0001g0248a0001c0001t0001g0287 | 2 | HG00735.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.569-8659T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66473096 | ||||||
| chr15:66473243
|
T | C | 32 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(29): Show | 32 | HG00609.hp2 HG00642.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.569-8512T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66473243 | ||||||
| chr15:66473443
|
G | T | 1 | a0001c0003t0001g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.569-8312G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66473443 | ||||||
| chr15:66473596
|
A | C | 2 | a0001c0001t0001g0356a0001c0001t0001g0357 | 2 | HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.569-8159A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66473596 | ||||||
| chr15:66473803
|
G | C | 1 | a0001c0001t0002g0069 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.569-7952G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66473803 | ||||||
| chr15:66473921
|
A | G | 14 | a0001c0001t0001g0111a0001c0001t0001g0119a0001c0001t0001g0122others(11): Show | 14 | HG00733.hp1 HG01257.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.569-7834A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66473921 | ||||||
| chr15:66474056
|
A | T | 1 | a0001c0001t0003g0193 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.569-7699A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66474056 | ||||||
| chr15:66474209
|
G | T | 59 | a0001c0001t0001g0232a0001c0001t0002g0011a0001c0001t0002g0047others(56): Show | 59 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.569-7546G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66474209 | ||||||
| chr15:66474372
|
G | C | 1 | a0001c0001t0001g0103 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.569-7383G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66474372 | ||||||
| chr15:66474405
|
A | C | 1 | a0001c0001t0001g0296 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.569-7350A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66474405 | ||||||
| chr15:66474546
|
C | T | 2 | a0001c0001t0001g0342a0001c0001t0001g0345 | 2 | HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.569-7209C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66474546 | ||||||
| chr15:66474722
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.569-7033C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66474722 | ||||||
| chr15:66474826
|
C | G | 1 | a0001c0001t0004g0038 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.569-6929C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66474826 | ||||||
| chr15:66474836
|
G | A | 1 | a0001c0001t0003g0198 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.569-6919G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66474836 | ||||||
| chr15:66474902
|
C | CA | 10 | a0001c0001t0001g0231a0001c0001t0001g0337a0001c0001t0006g0002others(7): Show | 10 | HG00280.hp2 HG00639.hp1 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.569-6837dupA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66474902 | |||||
| chr15:66474902
|
CA | C | 196 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(193): Show | 196 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.569-6837delA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66474902 | |||||
| chr15:66474996
|
C | T | 1 | a0001c0003t0001g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.569-6759C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66474996 | ||||||
| chr15:66475181
|
A | G | 8 | a0001c0001t0001g0221a0001c0001t0002g0065a0001c0001t0002g0117others(5): Show | 8 | HG01255.hp2 HG02109.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.569-6574A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66475181 | ||||||
| chr15:66475518
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.569-6237G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66475518 | ||||||
| chr15:66475530
|
C | G | 20 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(17): Show | 20 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.569-6225C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66475530 | ||||||
| chr15:66475642
|
G | A | 7 | a0001c0001t0001g0252a0001c0001t0001g0259a0001c0001t0001g0260others(4): Show | 7 | HG01256.hp1 HG01346.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.569-6113G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66475642 | ||||||
| chr15:66475669
|
C | T | 7 | a0001c0001t0002g0065a0001c0001t0002g0117a0001c0001t0002g0120others(4): Show | 7 | HG01255.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.569-6086C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66475669 | ||||||
| chr15:66475707
|
G | C | 1 | a0001c0001t0001g0001 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.569-6048G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66475707 | ||||||
| chr15:66475743
|
C | T | 1 | a0001c0001t0001g0346 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.569-6012C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66475743 | ||||||
| chr15:66476027
|
C | G | 4 | a0001c0001t0001g0010a0001c0001t0001g0327a0001c0001t0001g0332others(1): Show | 4 | HG02109.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-5728C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66476027 | ||||||
| chr15:66476037
|
C | T | 1 | a0001c0001t0001g0337 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.569-5718C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66476037 | ||||||
| chr15:66476177
|
G | A | 2 | a0001c0001t0001g0339a0001c0001t0001g0340 | 2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.569-5578G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66476177 | ||||||
| chr15:66476265
|
A | C | 1 | a0001c0001t0005g0160 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.569-5490A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66476265 | ||||||
| chr15:66476280
|
T | C | 3 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0136 | 3 | NA18956.hp1 NA18971.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.569-5475T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66476280 | ||||||
| chr15:66476372
|
T | C | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | HG00735.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.569-5383T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66476372 | ||||||
| chr15:66476471
|
G | A | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.569-5284G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66476471 | ||||||
| chr15:66476516
|
C | G | 1 | a0001c0001t0001g0034 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.569-5239C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66476516 | ||||||
| chr15:66476565
|
G | A | 5 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.569-5190G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66476565 | ||||||
| chr15:66476664
|
A | G | 54 | a0001c0001t0001g0010a0001c0001t0001g0091a0001c0001t0001g0101others(51): Show | 54 | HG00280.hp2 HG00639.hp1 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.569-5091A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66476664 | ||||||
| chr15:66476691
|
G | A | 51 | a0001c0001t0003g0162a0001c0001t0003g0164a0001c0001t0003g0165others(48): Show | 51 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.569-5064G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66476691 | ||||||
| chr15:66476846
|
A | G | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-4909A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66476846 | ||||||
| chr15:66476968
|
G | T | 1 | a0001c0001t0002g0061 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.569-4787G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66476968 | ||||||
| chr15:66477002
|
A | G | 1 | a0001c0001t0001g0282 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.569-4753A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66477002 | ||||||
| chr15:66477027
|
C | T | 26 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(23): Show | 26 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.569-4728C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66477027 | ||||||
| chr15:66477145
|
G | C | 2 | a0001c0001t0002g0076a0001c0001t0002g0086 | 2 | NA19002.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.569-4610G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66477145 | ||||||
| chr15:66477256
|
T | C | 2 | a0001c0001t0001g0135a0001c0001t0001g0137 | 2 | NA18968.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.569-4499T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66477256 | ||||||
| chr15:66477275
|
G | A | 26 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(23): Show | 26 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.569-4480G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66477275 | ||||||
| chr15:66477358
|
G | A | 1 | a0001c0001t0003g0192 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.569-4397G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66477358 | ||||||
| chr15:66477567
|
C | T | 38 | a0001c0001t0001g0010a0001c0001t0001g0326a0001c0001t0001g0327others(35): Show | 38 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.569-4188C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66477567 | ||||||
| chr15:66477591
|
C | G | 207 | a0001c0001t0001g0010a0001c0001t0001g0091a0001c0001t0001g0101others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.569-4164C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66477591 | ||||||
| chr15:66477710
|
G | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(78): Show | 81 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.569-4045G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66477710 | ||||||
| chr15:66477716
|
T | A | 1 | a0001c0001t0001g0237 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.569-4039T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66477716 | ||||||
| chr15:66477724
|
G | A | 1 | a0001c0001t0001g0300 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.569-4031G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66477724 | ||||||
| chr15:66477825
|
C | T | 62 | a0001c0001t0001g0232a0001c0001t0002g0011a0001c0001t0002g0047others(59): Show | 62 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.569-3930C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66477825 | ||||||
| chr15:66477826
|
G | A | 51 | a0001c0001t0003g0162a0001c0001t0003g0164a0001c0001t0003g0165others(48): Show | 51 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.569-3929G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66477826 | ||||||
| chr15:66478002
|
C | T | 5 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.569-3753C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66478002 | ||||||
| chr15:66478164
|
C | T | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.569-3591C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66478164 | ||||||
| chr15:66478238
|
T | TTA | 4 | a0001c0001t0001g0331a0001c0001t0001g0333a0001c0001t0001g0339others(1): Show | 4 | HG02615.hp1 HG03453.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-3504_569-3503d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478238 | |||||
| chr15:66478253
|
A | T | 46 | a0001c0001t0001g0010a0001c0001t0001g0091a0001c0001t0001g0101others(43): Show | 46 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(43): Show |
intron_variant | MODIFIER | c.569-3502A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66478253 | ||||||
| chr15:66478276
|
CAT | C | 46 | a0001c0001t0001g0010a0001c0001t0001g0091a0001c0001t0001g0101others(43): Show | 46 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(43): Show |
intron_variant | MODIFIER | c.569-3467_569-3466d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478276 | |||||
| chr15:66478276
|
CATAT | C | 3 | a0001c0001t0002g0057a0001c0001t0002g0058a0001c0001t0002g0059 | 3 | NA18946.hp2 NA19056.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.569-3469_569-3466d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478276 | |||||
| chr15:66478288
|
T | C | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-3467T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66478288 | ||||||
| chr15:66478313
|
GTA | G | 19 | a0001c0001t0004g0016a0001c0001t0004g0017a0001c0001t0004g0018others(16): Show | 19 | HG00423.hp1 HG03927.hp2 NA18941.hp1 others(16): Show |
intron_variant | MODIFIER | c.569-3432_569-3431d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478313 | |||||
| chr15:66478326
|
TTATATAT others(18): Show |
T | 5 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.569-3391_569-3367d others(27): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478326 | |||||
| chr15:66478364
|
CAT | C | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-3386_569-3385d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478364 | |||||
| chr15:66478392
|
A | ATG | 50 | a0001c0001t0001g0091a0001c0001t0001g0101a0001c0001t0001g0102others(47): Show | 50 | HG00280.hp2 HG00639.hp1 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.569-3355_569-3354d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478392 | |||||
| chr15:66478400
|
G | GTGTA | 4 | a0001c0001t0001g0010a0001c0001t0001g0327a0001c0001t0001g0332others(1): Show | 4 | HG02109.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-3354_569-3353i others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478400 | |||||
| chr15:66478400
|
GTA | G | 6 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(3): Show | 6 | HG00738.hp2 HG01106.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.569-3342_569-3341d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478400 | |||||
| chr15:66478402
|
A | ATATATAT others(33): Show |
3 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0325 | 3 | HG02055.hp1 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.569-3338_569-3299d others(42): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478402 | |||||
| chr15:66478402
|
A | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(45): Show | 48 | HG00735.hp1 HG00735.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.569-3353A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66478402 | ||||||
| chr15:66478413
|
T | C | 17 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(14): Show | 17 | HG01069.hp2 HG01071.hp2 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.569-3342T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66478413 | ||||||
| chr15:66478417
|
C | CACAGGTA others(29): Show |
68 | a0001c0001t0001g0216a0001c0001t0001g0220a0001c0001t0001g0221others(65): Show | 68 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.569-3320_569-3285d others(38): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478417 | |||||
| chr15:66478417
|
C | CACAGGTA others(65): Show |
5 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0233others(2): Show | 5 | HG02145.hp1 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.569-3285_569-3284i others(74): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478417 | |||||
| chr15:66478417
|
C | CAGGTATA others(27): Show |
16 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(13): Show | 16 | HG01069.hp2 HG01071.hp2 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.569-3337_569-3336i others(36): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478417 | |||||
| chr15:66478422
|
GTATATAT others(33): Show |
G | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-3318_569-3279d others(42): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478422 | |||||
| chr15:66478433
|
T | C | 1 | a0001c0001t0001g0139 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.569-3322T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66478433 | ||||||
| chr15:66478458
|
G | GTA | 7 | a0001c0001t0001g0224a0001c0001t0001g0337a0001c0001t0003g0173others(4): Show | 7 | HG00423.hp1 HG00558.hp1 NA18522.hp2 others(4): Show |
intron_variant | MODIFIER | c.569-3282_569-3281d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478458 | |||||
| chr15:66478506
|
A | AT | 7 | a0001c0001t0001g0137a0001c0001t0003g0180a0001c0001t0003g0181others(4): Show | 7 | HG00099.hp1 HG02602.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.569-3239dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478506 | |||||
| chr15:66478506
|
A | T | 3 | a0001c0001t0001g0254a0001c0001t0001g0307a0001c0003t0001g0155 | 3 | HG00639.hp2 HG01081.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.569-3249A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66478506 | ||||||
| chr15:66478507
|
T | TA | 6 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0124others(3): Show | 6 | HG01123.hp1 NA18956.hp1 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.569-3248_569-3247i others(3): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66478507 | ||||||
| chr15:66478508
|
T | A | 81 | a0001c0001t0001g0010a0001c0001t0001g0031a0001c0001t0001g0032others(78): Show | 81 | HG00609.hp2 HG00642.hp2 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.569-3247T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66478508 | ||||||
| chr15:66478510
|
T | A | 1 | a0001c0001t0001g0226 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.569-3245T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66478510 | ||||||
| chr15:66478521
|
CA | C | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-3232delA | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478521 | |||||
| chr15:66478534
|
CTT | C | 31 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(28): Show | 31 | HG00609.hp2 HG00642.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.569-3219_569-3218d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 66478534 | |||||
| chr15:66478868
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.569-2887C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66478868 | ||||||
| chr15:66478907
|
C | T | 1 | a0001c0001t0013g0351 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.569-2848C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66478907 | ||||||
| chr15:66479065
|
A | G | 2 | a0001c0001t0002g0072a0001c0001t0002g0099 | 2 | NA18972.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.569-2690A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66479065 | ||||||
| chr15:66479298
|
A | T | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.569-2457A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66479298 | ||||||
| chr15:66479427
|
A | G | 1 | a0001c0001t0003g0211 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.569-2328A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66479427 | ||||||
| chr15:66479504
|
G | A | 11 | a0001c0001t0003g0200a0001c0001t0005g0157a0001c0001t0005g0158others(8): Show | 11 | HG00280.hp1 HG00438.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.569-2251G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66479504 | ||||||
| chr15:66479669
|
C | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(81): Show | 84 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.569-2086C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66479669 | ||||||
| chr15:66479758
|
G | A | 6 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0124others(3): Show | 6 | NA18956.hp1 NA18968.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.569-1997G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66479758 | ||||||
| chr15:66479909
|
T | C | 2 | a0001c0001t0005g0240a0001c0001t0005g0243 | 2 | HG00438.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.569-1846T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66479909 | ||||||
| chr15:66480142
|
G | A | 13 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0292others(10): Show | 13 | HG00438.hp1 HG00609.hp1 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.569-1613G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66480142 | ||||||
| chr15:66480220
|
A | C | 1 | a0001c0001t0003g0200 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.569-1535A>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66480220 | ||||||
| chr15:66480234
|
G | A | 2 | a0001c0001t0001g0343a0001c0001t0011g0265 | 2 | HG02040.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.569-1521G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66480234 | ||||||
| chr15:66480240
|
C | T | 1 | a0001c0001t0002g0069 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.569-1515C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66480240 | ||||||
| chr15:66480383
|
C | T | 16 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(13): Show | 16 | HG01069.hp2 HG01071.hp2 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.569-1372C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66480383 | ||||||
| chr15:66480480
|
T | C | 85 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(82): Show | 85 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.569-1275T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66480480 | ||||||
| chr15:66480514
|
G | A | 4 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(1): Show | 4 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.569-1241G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66480514 | ||||||
| chr15:66480521
|
C | G | 371 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(368): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.569-1234C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66480521 | ||||||
| chr15:66480580
|
T | A | 3 | a0001c0001t0003g0166a0001c0001t0003g0190a0001c0001t0003g0191 | 3 | HG00738.hp1 HG01516.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.569-1175T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66480580 | ||||||
| chr15:66480630
|
G | A | 2 | a0001c0001t0001g0352a0001c0001t0001g0353 | 2 | HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.569-1125G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66480630 | ||||||
| chr15:66480857
|
C | G | 39 | a0001c0001t0001g0010a0001c0001t0001g0326a0001c0001t0001g0327others(36): Show | 39 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.569-898C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66480857 | ||||||
| chr15:66480939
|
A | T | 1 | a0001c0001t0006g0006 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.569-816A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66480939 | ||||||
| chr15:66481131
|
G | A | 1 | a0001c0001t0003g0192 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.569-624G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66481131 | ||||||
| chr15:66481213
|
T | C | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.569-542T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66481213 | ||||||
| chr15:66481344
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.569-411A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66481344 | ||||||
| chr15:66481395
|
C | A | 26 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(23): Show | 26 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.569-360C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66481395 | ||||||
| chr15:66481414
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.569-341G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66481414 | ||||||
| chr15:66481440
|
C | T | 1 | a0001c0001t0001g0300 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.569-315C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66481440 | ||||||
| chr15:66481637
|
G | A | 51 | a0001c0001t0003g0162a0001c0001t0003g0164a0001c0001t0003g0165others(48): Show | 51 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.569-118G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66481637 | ||||||
| chr15:66481676
|
T | A | 1 | a0001c0001t0001g0353 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.569-79T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | chr15 | 66481676 | ||||||
| chr15:66481929
|
G | C | 6 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0124others(3): Show | 6 | NA18956.hp1 NA18968.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.693+50G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66481929 | ||||||
| chr15:66482113
|
C | A | 4 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0233others(1): Show | 4 | HG02145.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+234C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66482113 | ||||||
| chr15:66482154
|
T | A | 1 | a0001c0001t0001g0337 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.693+275T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66482154 | ||||||
| chr15:66482221
|
A | G | 331 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(328): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.693+342A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66482221 | ||||||
| chr15:66482225
|
C | T | 1 | a0001c0001t0001g0340 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.693+346C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66482225 | ||||||
| chr15:66482278
|
C | T | 1 | a0001c0001t0001g0135 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.693+399C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66482278 | ||||||
| chr15:66482479
|
G | T | 1 | a0001c0002t0001g0311 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.693+600G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66482479 | ||||||
| chr15:66482628
|
C | T | 2 | a0001c0001t0001g0339a0001c0001t0001g0340 | 2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.693+749C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66482628 | ||||||
| chr15:66482759
|
T | G | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.693+880T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66482759 | ||||||
| chr15:66482825
|
C | T | 7 | a0001c0001t0001g0091a0001c0001t0001g0101a0001c0001t0001g0102others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.693+946C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66482825 | ||||||
| chr15:66482873
|
G | GGCGGGGA others(10): Show |
2 | a0001c0001t0001g0232a0001c0001t0002g0089 | 2 | HG02280.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.693+998_693+1014du others(18): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 66482873 | |||||
| chr15:66482911
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.693+1032G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66482911 | ||||||
| chr15:66482979
|
C | T | 1 | a0001c0001t0006g0009 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.693+1100C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66482979 | ||||||
| chr15:66483175
|
G | C | 3 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0325 | 3 | HG02055.hp1 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.693+1296G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66483175 | ||||||
| chr15:66483250
|
G | C | 5 | a0001c0001t0001g0326a0001c0001t0001g0328a0001c0001t0001g0329others(2): Show | 5 | HG02257.hp2 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.693+1371G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66483250 | ||||||
| chr15:66483555
|
T | C | 1 | a0001c0003t0001g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.694-1435T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66483555 | ||||||
| chr15:66483748
|
C | CT | 12 | a0001c0001t0001g0109a0001c0001t0001g0127a0001c0001t0001g0152others(9): Show | 12 | HG01109.hp1 HG01891.hp1 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.694-1225dupT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 66483748 | |||||
| chr15:66483748
|
C | CTTT | 46 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(43): Show | 46 | HG00735.hp1 HG00735.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.694-1227_694-1225d others(5): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 66483748 | |||||
| chr15:66483748
|
C | CTTTT | 25 | a0001c0001t0001g0001a0001c0001t0001g0259a0001c0001t0001g0275others(22): Show | 25 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.694-1228_694-1225d others(6): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 66483748 | |||||
| chr15:66483899
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.694-1091C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66483899 | ||||||
| chr15:66483908
|
C | T | 50 | a0001c0001t0003g0162a0001c0001t0003g0164a0001c0001t0003g0165others(47): Show | 50 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.694-1082C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66483908 | ||||||
| chr15:66483921
|
TG | T | 3 | a0001c0001t0001g0250a0001c0001t0001g0253a0001c0001t0001g0284 | 3 | HG01891.hp1 HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.694-1068delG | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66483921 | ||||||
| chr15:66483997
|
C | T | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.694-993C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66483997 | ||||||
| chr15:66484102
|
A | G | 325 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(322): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.694-888A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66484102 | ||||||
| chr15:66484139
|
A | AC | 47 | a0001c0001t0001g0010a0001c0001t0001g0115a0001c0001t0001g0156others(44): Show | 47 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.694-842dupC | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 66484139 | |||||
| chr15:66484142
|
C | A | 62 | a0001c0001t0001g0228a0001c0001t0001g0232a0001c0001t0002g0011others(59): Show | 62 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.694-848C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66484142 | ||||||
| chr15:66484142
|
C | T | 1 | a0001c0001t0003g0169 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.694-848C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66484142 | ||||||
| chr15:66484146
|
C | A | 1 | a0001c0001t0001g0028 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.694-844C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66484146 | ||||||
| chr15:66484146
|
C | G | 1 | a0001c0001t0001g0298 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.694-844C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66484146 | ||||||
| chr15:66484291
|
G | T | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.694-699G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66484291 | ||||||
| chr15:66484316
|
T | C | 2 | a0001c0001t0007g0096a0001c0001t0007g0114 | 2 | HG01255.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.694-674T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66484316 | ||||||
| chr15:66484423
|
C | T | 1 | a0001c0001t0002g0064 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.694-567C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66484423 | ||||||
| chr15:66484444
|
C | T | 9 | a0001c0001t0001g0091a0001c0001t0001g0101a0001c0001t0001g0102others(6): Show | 9 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.694-546C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66484444 | ||||||
| chr15:66484501
|
G | C | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.694-489G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66484501 | ||||||
| chr15:66484668
|
G | A | 2 | a0001c0001t0001g0220a0001c0001t0001g0237 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.694-322G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66484668 | ||||||
| chr15:66484681
|
TGGCCAAG others(3): Show |
T | 36 | a0001c0001t0001g0010a0001c0001t0001g0326a0001c0001t0001g0327others(33): Show | 36 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.694-306_694-297del others(10): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 66484681 | |||||
| chr15:66484685
|
C | A | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.694-305C>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66484685 | ||||||
| chr15:66484842
|
G | C | 1 | a0001c0001t0001g0340 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.694-148G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | chr15 | 66484842 | ||||||
| chr15:66484977
|
G | GTC | 7 | a0001c0001t0001g0091a0001c0001t0001g0101a0001c0001t0001g0102others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.694-8_694-7dupTC | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 66484977 | |||||
| chr15:66485252
|
G | A | 1 | a0001c0001t0001g0338 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.895+61G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66485252 | ||||||
| chr15:66485253
|
G | A | 1 | a0001c0001t0001g0338 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.895+62G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66485253 | ||||||
| chr15:66485342
|
G | A | 5 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.895+151G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66485342 | ||||||
| chr15:66485372
|
A | G | 7 | a0001c0001t0001g0091a0001c0001t0001g0101a0001c0001t0001g0102others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.895+181A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66485372 | ||||||
| chr15:66485590
|
G | A | 1 | a0001c0001t0002g0048 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.895+399G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66485590 | ||||||
| chr15:66485622
|
A | G | 37 | a0001c0001t0001g0010a0001c0001t0001g0326a0001c0001t0001g0327others(34): Show | 37 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.895+431A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66485622 | ||||||
| chr15:66485828
|
C | T | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.895+637C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66485828 | ||||||
| chr15:66485904
|
T | G | 2 | a0001c0001t0001g0303a0001c0001t0001g0305 | 2 | HG01952.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.895+713T>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66485904 | ||||||
| chr15:66486047
|
C | T | 1 | a0001c0001t0003g0182 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.895+856C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66486047 | ||||||
| chr15:66486073
|
A | T | 6 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0174others(3): Show | 6 | HG00558.hp1 HG00673.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.895+882A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66486073 | ||||||
| chr15:66486143
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.895+952C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66486143 | ||||||
| chr15:66486279
|
C | T | 53 | a0001c0001t0001g0010a0001c0001t0001g0091a0001c0001t0001g0101others(50): Show | 53 | HG00280.hp2 HG00639.hp1 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.896-949C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66486279 | ||||||
| chr15:66486450
|
T | A | 7 | a0001c0001t0001g0091a0001c0001t0001g0101a0001c0001t0001g0102others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.896-778T>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66486450 | ||||||
| chr15:66486484
|
G | A | 4 | a0001c0001t0001g0010a0001c0001t0001g0327a0001c0001t0001g0332others(1): Show | 4 | HG02109.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.896-744G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66486484 | ||||||
| chr15:66486488
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.896-740A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66486488 | ||||||
| chr15:66486700
|
A | T | 2 | a0001c0001t0001g0339a0001c0001t0001g0340 | 2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.896-528A>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66486700 | ||||||
| chr15:66486732
|
G | A | 1 | a0001c0001t0001g0338 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.896-496G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66486732 | ||||||
| chr15:66486829
|
A | G | 333 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(330): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.896-399A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66486829 | ||||||
| chr15:66486937
|
G | C | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.896-291G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66486937 | ||||||
| chr15:66487115
|
G | A | 1 | a0001c0001t0002g0049 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.896-113G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 7/10 | chr15 | 66487115 | ||||||
| chr15:66487360
|
C | T | 27 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(24): Show | 27 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.960+68C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 8/10 | chr15 | 66487360 | ||||||
| chr15:66487506
|
G | T | 1 | a0001c0001t0001g0245 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.960+214G>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 8/10 | chr15 | 66487506 | ||||||
| chr15:66487739
|
T | C | 27 | a0001c0001t0001g0107a0001c0001t0001g0342a0001c0001t0001g0343others(24): Show | 27 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.960+447T>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 8/10 | chr15 | 66487739 | ||||||
| chr15:66487890
|
G | A | 1 | a0001c0001t0001g0293 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.960+598G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 8/10 | chr15 | 66487890 | ||||||
| chr15:66488112
|
GT | G | 25 | a0001c0001t0001g0342a0001c0001t0001g0343a0001c0001t0001g0344others(22): Show | 25 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.960+822delT | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 66488112 | |||||
| chr15:66488126
|
G | A | 5 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 5 | HG02486.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.960+834G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 8/10 | chr15 | 66488126 | ||||||
| chr15:66488360
|
G | A | 30 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0118others(27): Show | 30 | HG00609.hp2 HG00642.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.961-855G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 8/10 | chr15 | 66488360 | ||||||
| chr15:66488413
|
C | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(81): Show | 84 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.961-802C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 8/10 | chr15 | 66488413 | ||||||
| chr15:66488951
|
A | G | 1 | a0001c0001t0001g0141 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.961-264A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 8/10 | chr15 | 66488951 | ||||||
| chr15:66488960
|
CAAGT | C | 8 | a0001c0001t0006g0002a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.961-254_961-251del others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 8/10 | chr15 | 66488960 | ||||||
| chr15:66489023
|
A | G | 2 | a0001c0001t0003g0165a0001c0001t0003g0202 | 2 | NA18940.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.961-192A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 8/10 | chr15 | 66489023 | ||||||
| chr15:66489499
|
G | C | 2 | a0001c0001t0001g0339a0001c0001t0001g0340 | 2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1023-219G>C | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 9/10 | chr15 | 66489499 | ||||||
| chr15:66489516
|
AC | A | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG03041.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1023-201delC | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 9/10 | chr15 | 66489516 | ||||||
| chr15:66489675
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1023-43C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 9/10 | chr15 | 66489675 | ||||||
| chr15:66489710
|
C | T | 26 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0212others(23): Show | 26 | HG01069.hp2 HG01071.hp2 HG01123.hp1 others(23): Show |
splice_region_variant&intron_variant | LOW | c.1023-8C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 9/10 | chr15 | 66489710 | ||||||
| chr15:66489922
|
C | G | 1 | a0001c0001t0001g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1068+159C>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 10/10 | chr15 | 66489922 | ||||||
| chr15:66490090
|
CAG | C | 6 | a0001c0001t0001g0342a0001c0001t0001g0343a0001c0001t0001g0344others(3): Show | 6 | HG01884.hp2 HG02258.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1068+330_1068+331d others(4): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 66490090 | |||||
| chr15:66490103
|
C | T | 3 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0002g0060 | 3 | NA18946.hp1 NA18949.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1068+340C>T | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 10/10 | chr15 | 66490103 | ||||||
| chr15:66490132
|
A | G | 2 | a0001c0001t0001g0344a0001c0001t0001g0366 | 2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1068+369A>G | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 10/10 | chr15 | 66490132 | ||||||
| chr15:66490183
|
G | A | 1 | a0001c0003t0001g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1069-319G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 10/10 | chr15 | 66490183 | ||||||
| chr15:66490239
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1069-263G>A | MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 10/10 | chr15 | 66490239 |