Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 5599 |
|---|---|
| ensemblid | ENSG00000107643.17 |
| hgncid | 6881 |
| symbol | MAPK8 |
| name | mitogen-activated protein kinase 8 |
| refseq_nuc | NM_001323329.2 |
| refseq_prot | NP_001310258.1 |
| ensembl_nuc | ENST00000374189.6 |
| ensembl_prot | ENSP00000363304.1 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 48306677 |
| end | 48439360 |
| strand | + |
| ver | v1.2 |
| region | chr10:48306677-48439360 |
| region5000 | chr10:48301677-48444360 |
| regionname0 | MAPK8_chr10_48306677_48439360 |
| regionname5000 | MAPK8_chr10_48301677_48444360 |
| 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 | 427 | 305 | 92 | 50 | 127 | 10 | 24 | 93 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0002 | 0/0 | 427 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| 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 | 1284 | 302 | 92 | 49 | 125 | 10 | 24 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| c0002 | 0/0 | 1284 | 2 | 0 | 0 | 2 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| c0003 | 0/0 | 1284 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| c0004 | 0/0 | 1284 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 4526 | 102 | 19 | 17 | 58 | 2 | 6 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| t0002 | 0/0 | 4526 | 49 | 2 | 10 | 27 | 4 | 6 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| t0003 | 0/0 | 4526 | 23 | 22 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| t0004 | 0/0 | 4524 | 23 | 7 | 3 | 11 | 1 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| t0005 | 0/0 | 4526 | 21 | 0 | 0 | 20 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| t0006 | 0/0 | 4527 | 21 | 2 | 12 | 2 | 2 | 3 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| t0007 | 1/0 | 4526 | 17 | 12 | 1 | 0 | 0 | 3 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| t0008 | 0/0 | 4526 | 5 | 5 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| t0009 | 0/0 | 4526 | 5 | 4 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| t0010 | 0/0 | 4526 | 5 | 3 | 2 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| t0011 | 0/0 | 4526 | 4 | 4 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| t0012 | 0/0 | 4526 | 3 | 0 | 0 | 3 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| t0013 | 0/0 | 4526 | 2 | 1 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| t0014 | 0/0 | 4526 | 2 | 0 | 0 | 2 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| t0015 | 0/0 | 4526 | 2 | 0 | 0 | 0 | 0 | 2 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| t0016 | 0/0 | 4526 | 2 | 2 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| t0017 | 0/0 | 4526 | 2 | 0 | 0 | 2 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| t0018 | 0/0 | 4526 | 2 | 1 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| t0019 | 0/0 | 4526 | 2 | 2 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| t0020 | 0/1 | 4526 | 2 | 0 | 0 | 0 | 1 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| t0021 | 0/0 | 4526 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| t0022 | 0/0 | 4526 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| t0023 | 0/0 | 4526 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| t0024 | 0/0 | 4526 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| t0025 | 0/0 | 4526 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| t0026 | 0/0 | 4526 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| t0027 | 0/0 | 4526 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| t0028 | 0/0 | 4526 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| t0029 | 0/0 | 4526 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| t0030 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| t0031 | 0/0 | 4526 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| t0032 | 0/0 | 4526 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0073 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0235 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| 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 | 1284 | 302 | 92 | 49 | 125 | 10 | 24 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0002 | 0/0 | 1284 | 2 | 0 | 0 | 2 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0004 | 0/0 | 1284 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0002c0003 | 0/0 | 1284 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5809 | 101 | 19 | 16 | 58 | 2 | 6 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0001t0002 | 0/0 | 5809 | 49 | 2 | 10 | 27 | 4 | 6 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0001t0003 | 0/0 | 5809 | 23 | 22 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0001t0004 | 0/0 | 5807 | 22 | 7 | 3 | 10 | 1 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0001t0005 | 0/0 | 5809 | 21 | 0 | 0 | 20 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0001t0006 | 0/0 | 5810 | 21 | 2 | 12 | 2 | 2 | 3 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0001t0007 | 1/0 | 5809 | 17 | 12 | 1 | 0 | 0 | 3 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0001t0008 | 0/0 | 5809 | 5 | 5 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0001t0009 | 0/0 | 5809 | 5 | 4 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0001t0010 | 0/0 | 5809 | 5 | 3 | 2 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0001t0011 | 0/0 | 5809 | 4 | 4 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0001t0012 | 0/0 | 5809 | 3 | 0 | 0 | 3 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0001t0013 | 0/0 | 5809 | 2 | 1 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0001t0014 | 0/0 | 5809 | 2 | 0 | 0 | 2 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0001t0015 | 0/0 | 5809 | 2 | 0 | 0 | 0 | 0 | 2 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0001t0016 | 0/0 | 5809 | 2 | 2 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0001t0018 | 0/0 | 5809 | 2 | 1 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0001t0019 | 0/0 | 5809 | 2 | 2 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0001t0020 | 0/1 | 5809 | 2 | 0 | 0 | 0 | 1 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0001t0021 | 0/0 | 5809 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0001t0022 | 0/0 | 5809 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0001t0023 | 0/0 | 5809 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0001t0024 | 0/0 | 5809 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0001t0025 | 0/0 | 5809 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0001t0026 | 0/0 | 5809 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0001t0027 | 0/0 | 5809 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0001t0028 | 0/0 | 5809 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0001t0029 | 0/0 | 5809 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0001t0030 | 0/0 | 5807 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0001t0031 | 0/0 | 5809 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0001t0032 | 0/0 | 5809 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0002t0017 | 0/0 | 5809 | 2 | 0 | 0 | 2 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0001c0004t0001 | 0/0 | 5809 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| a0002c0003t0004 | 0/0 | 5807 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | copy fasta | chr10 | 48301677 | 48444360 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0004g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0005g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0005g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0005g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0005g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0005g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0005g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0005g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0005g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0005g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0005g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0005g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0005g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0005g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0006g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0006g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0006g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0006g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0006g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0006g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0006g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0006g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0006g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0006g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0006g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0006g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0006g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0006g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0006g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0006g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0006g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0006g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0006g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0006g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0007g0073 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0007g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0007g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0007g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0007g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0007g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0007g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0007g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0007g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0007g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0007g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0007g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0007g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0007g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0007g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0007g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0007g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0008g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0008g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0008g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0008g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0008g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0009g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0009g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0009g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0009g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0009g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0010g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0010g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0010g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0010g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0010g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0011g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0011g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0011g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0011g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0012g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0012g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0012g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0013g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0013g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0014g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0014g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0015g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0015g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0016g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0016g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0018g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0018g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0019g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0019g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0020g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0020g0235 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0021g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0022g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0023g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0024g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0025g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0026g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0027g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0028g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0029g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0030g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0031g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0001t0032g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0002t0017g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0002t0017g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0001c0004t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| a0002c0003t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0152 | EUR | GBR | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0223 | EUR | GBR | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0043 | EUR | FIN | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG00280 | hp2 | a0001 | c0001 | t0020 | g0222 | EUR | FIN | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | CHS | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | CHS | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | CHS | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG00597 | hp1 | a0001 | c0001 | t0005 | g0031 | EAS | CHS | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | CHS | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0149 | EAS | CHS | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0099 | AMR | PUR | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0117 | AMR | PUR | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0115 | AMR | PUR | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01099 | hp2 | a0001 | c0001 | t0006 | g0262 | AMR | PUR | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01106 | hp2 | a0001 | c0001 | t0006 | g0266 | AMR | PUR | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01109 | hp2 | a0001 | c0001 | t0009 | g0233 | AMR | PUR | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01167 | hp1 | a0001 | c0001 | t0007 | g0295 | AMR | PUR | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01168 | hp1 | a0001 | c0001 | t0006 | g0253 | AMR | PUR | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01168 | hp2 | a0001 | c0001 | t0013 | g0124 | AMR | PUR | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01255 | hp1 | a0001 | c0001 | t0006 | g0261 | AMR | CLM | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0061 | AMR | CLM | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01256 | hp1 | a0001 | c0001 | t0032 | g0161 | AMR | CLM | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01256 | hp2 | a0001 | c0001 | t0006 | g0086 | AMR | CLM | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01257 | hp1 | a0001 | c0001 | t0006 | g0256 | AMR | CLM | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01261 | hp1 | a0001 | c0001 | t0006 | g0257 | AMR | CLM | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | CLM | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01346 | hp1 | a0001 | c0001 | t0006 | g0264 | AMR | CLM | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | CLM | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | CLM | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0054 | EUR | IBS | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | IBS | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0049 | EUR | IBS | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01516 | hp2 | a0001 | c0001 | t0006 | g0250 | EUR | IBS | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01517 | hp1 | a0001 | c0001 | t0006 | g0254 | EUR | IBS | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0053 | EUR | IBS | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01884 | hp1 | a0001 | c0001 | t0009 | g0180 | AFR | ACB | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01884 | hp2 | a0001 | c0001 | t0011 | g0007 | AFR | ACB | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01891 | hp2 | a0001 | c0001 | t0007 | g0091 | AFR | ACB | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | PEL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01943 | hp1 | a0001 | c0001 | t0006 | g0258 | AMR | PEL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01975 | hp2 | a0001 | c0001 | t0006 | g0259 | AMR | PEL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01978 | hp1 | a0001 | c0001 | t0010 | g0220 | AMR | PEL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01978 | hp2 | a0001 | c0001 | t0006 | g0265 | AMR | PEL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01981 | hp1 | a0001 | c0004 | t0001 | g0171 | AMR | PEL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01993 | hp2 | a0001 | c0001 | t0006 | g0255 | AMR | PEL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | KHV | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | KHV | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0110 | AFR | ACB | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02055 | hp2 | a0001 | c0001 | t0019 | g0282 | AFR | ACB | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02071 | hp1 | a0001 | c0001 | t0006 | g0263 | EAS | KHV | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0158 | EAS | KHV | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | KHV | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02129 | hp2 | a0001 | c0001 | t0006 | g0267 | EAS | KHV | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | KHV | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02145 | hp1 | a0001 | c0001 | t0029 | g0107 | AFR | ACB | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02145 | hp2 | a0001 | c0001 | t0009 | g0196 | AFR | ACB | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02155 | hp1 | a0001 | c0001 | t0005 | g0080 | EAS | CDX | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | CDX | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0151 | EAS | CDX | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02165 | hp2 | a0001 | c0002 | t0017 | g0014 | EAS | CDX | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02257 | hp1 | a0001 | c0001 | t0019 | g0283 | AFR | ACB | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02257 | hp2 | a0001 | c0001 | t0016 | g0270 | AFR | ACB | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0109 | AFR | ACB | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02258 | hp2 | a0001 | c0001 | t0011 | g0004 | AFR | ACB | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0111 | AFR | ACB | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02293 | hp2 | a0001 | c0001 | t0004 | g0154 | AMR | PEL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0112 | AFR | ACB | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0159 | AFR | ACB | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0302 | EAS | KHV | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02602 | hp2 | a0001 | c0001 | t0015 | g0121 | SAS | PJL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0300 | AFR | GWD | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0285 | AFR | GWD | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0009 | AFR | GWD | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0104 | AFR | GWD | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02698 | hp1 | a0001 | c0001 | t0006 | g0252 | SAS | PJL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0048 | SAS | PJL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0286 | AFR | GWD | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02717 | hp2 | a0001 | c0001 | t0009 | g0231 | AFR | GWD | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02723 | hp1 | a0001 | c0001 | t0021 | g0134 | AFR | GWD | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0098 | AFR | GWD | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0103 | AFR | GWD | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02818 | hp1 | a0001 | c0001 | t0009 | g0232 | AFR | GWD | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0087 | AFR | GWD | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0101 | AFR | GWD | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02886 | hp2 | a0001 | c0001 | t0030 | g0272 | AFR | GWD | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02895 | hp2 | a0001 | c0001 | t0008 | g0011 | AFR | GWD | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0147 | AFR | GWD | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0296 | AFR | GWD | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02897 | hp1 | a0001 | c0001 | t0008 | g0010 | AFR | GWD | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0144 | AFR | GWD | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02965 | hp1 | a0001 | c0001 | t0010 | g0229 | AFR | ESN | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02965 | hp2 | a0001 | c0001 | t0025 | g0114 | AFR | ESN | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02976 | hp1 | a0001 | c0001 | t0018 | g0095 | AFR | ESN | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0143 | AFR | GWD | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0097 | AFR | GWD | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0280 | AFR | MSL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | MSL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0094 | AFR | ESN | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0287 | AFR | ESN | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0281 | AFR | ESN | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0100 | AFR | MSL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03209 | hp2 | a0001 | c0001 | t0011 | g0006 | AFR | MSL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0145 | AFR | MSL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03225 | hp2 | a0001 | c0001 | t0010 | g0227 | AFR | MSL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03453 | hp1 | a0001 | c0001 | t0008 | g0012 | AFR | MSL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0298 | AFR | MSL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0284 | AFR | MSL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03491 | hp2 | a0001 | c0001 | t0006 | g0251 | SAS | PJL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0108 | AFR | ESN | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0294 | AFR | ESN | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0088 | AFR | GWD | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03540 | hp2 | a0001 | c0001 | t0008 | g0008 | AFR | GWD | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03669 | hp2 | a0001 | c0001 | t0006 | g0288 | SAS | PJL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | STU | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03688 | hp2 | a0001 | c0001 | t0007 | g0092 | SAS | STU | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | BEB | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03831 | hp2 | a0001 | c0001 | t0007 | g0093 | SAS | BEB | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03927 | hp1 | a0001 | c0001 | t0022 | g0133 | SAS | BEB | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0064 | SAS | STU | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG04115 | hp2 | a0001 | c0001 | t0024 | g0125 | SAS | STU | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG04184 | hp1 | a0001 | c0001 | t0005 | g0070 | SAS | BEB | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0156 | SAS | BEB | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | STU | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG04228 | hp2 | a0001 | c0001 | t0007 | g0085 | SAS | STU | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0297 | AFR | YRI | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0105 | AFR | YRI | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | CHB | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CHB | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | CHB | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18747 | hp2 | a0001 | c0001 | t0014 | g0182 | EAS | CHB | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | YRI | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18906 | hp2 | a0001 | c0001 | t0028 | g0106 | AFR | YRI | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0155 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0148 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18957 | hp1 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18959 | hp2 | a0001 | c0001 | t0005 | g0026 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18960 | hp1 | a0001 | c0001 | t0005 | g0078 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18961 | hp1 | a0001 | c0001 | t0005 | g0019 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18970 | hp1 | a0001 | c0001 | t0005 | g0039 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18972 | hp1 | a0001 | c0001 | t0027 | g0025 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18975 | hp1 | a0001 | c0001 | t0005 | g0081 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18979 | hp1 | a0002 | c0003 | t0004 | g0157 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18981 | hp2 | a0001 | c0001 | t0005 | g0057 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18987 | hp1 | a0001 | c0002 | t0017 | g0015 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18988 | hp1 | a0001 | c0001 | t0005 | g0040 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0153 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18993 | hp1 | a0001 | c0001 | t0005 | g0079 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18994 | hp2 | a0001 | c0001 | t0005 | g0077 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18998 | hp1 | a0001 | c0001 | t0012 | g0066 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19009 | hp2 | a0001 | c0001 | t0005 | g0030 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19010 | hp1 | a0001 | c0001 | t0005 | g0017 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | LWK | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0102 | AFR | LWK | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19043 | hp1 | a0001 | c0001 | t0010 | g0228 | AFR | LWK | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0160 | AFR | LWK | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0150 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19058 | hp1 | a0001 | c0001 | t0005 | g0018 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19060 | hp2 | a0001 | c0001 | t0005 | g0038 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19062 | hp1 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19066 | hp1 | a0001 | c0001 | t0012 | g0067 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19066 | hp2 | a0001 | c0001 | t0031 | g0210 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19067 | hp2 | a0001 | c0001 | t0005 | g0082 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19079 | hp1 | a0001 | c0001 | t0012 | g0068 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19080 | hp1 | a0001 | c0001 | t0014 | g0214 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19080 | hp2 | a0001 | c0001 | t0005 | g0023 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19081 | hp2 | a0001 | c0001 | t0026 | g0035 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0299 | AFR | YRI | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA19240 | hp2 | a0001 | c0001 | t0011 | g0005 | AFR | YRI | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | ASW | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA20129 | hp2 | a0001 | c0001 | t0023 | g0176 | AFR | ASW | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | GIH | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA20905 | hp2 | a0001 | c0001 | t0015 | g0234 | SAS | GIH | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01123 | hp1 | a0001 | c0001 | t0018 | g0096 | AMR | CLM | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG01123 | hp2 | a0001 | c0001 | t0010 | g0221 | AMR | CLM | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0293 | AFR | ACB | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02486 | hp1 | a0001 | c0001 | t0013 | g0118 | AFR | ACB | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0146 | AFR | ACB | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0116 | AFR | ACB | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0113 | AFR | MSL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0279 | AFR | MSL | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0089 | AFR | USA | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | USA | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0260 | AFR | USA | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA20300 | hp2 | a0001 | c0001 | t0016 | g0269 | AFR | USA | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA21309 | hp1 | a0001 | c0001 | t0007 | g0090 | AFR | LWK | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | LWK | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0020 | g0235 | REF | REF | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0007 | g0073 | REF | REF | MAPK8_chr10_48301677_48444360 | MAPK8 | chr10 | 48301677 | 48444360 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:48426004
|
T | C | 1 | a0002 | 1 | NA18979.hp1 | missense_variant | MODERATE | c.805T>C | p.Tyr269His | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 8/12 | 999/5809 | 805/1284 | 269/427 | chr10 | 48426004 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:48409917
|
C | T | 1 | a0001c0002 | 2 | HG02165.hp2 NA18987.hp1 |
synonymous_variant | LOW | c.291C>T | p.Ser97Ser | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 4/12 | 485/5809 | 291/1284 | 97/427 | chr10 | 48409917 | ||
| chr10:48434924
|
G | A | 1 | a0001c0004 | 1 | HG01981.hp1 | synonymous_variant | LOW | c.1179G>A | p.Ser393Ser | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 1373/5809 | 1179/1284 | 393/427 | chr10 | 48434924 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:48306708
|
C | G | 2 | a0001c0001t0010a0001c0001t0032 | 6 | HG01123.hp2 HG01256.hp1 HG01978.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-163C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/12 | 94953 | chr10 | 48306708 | |||||
| chr10:48306712
|
G | A | 1 | a0001c0001t0008 | 5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-159G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/12 | 94949 | chr10 | 48306712 | |||||
| chr10:48306770
|
G | T | 1 | a0001c0001t0031 | 1 | NA19066.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-101G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/12 | chr10 | 48306770 | ||||||
| chr10:48435045
|
G | A | 1 | a0001c0001t0021 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*16G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 16 | chr10 | 48435045 | |||||
| chr10:48435183
|
A | G | 1 | a0001c0001t0020 | 2 | HG00280.hp2 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*154A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 154 | chr10 | 48435183 | |||||
| chr10:48435239
|
A | AT | 1 | a0001c0001t0006 | 21 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*218dupT | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 219 | INFO_REALIGN_3_PRIME | chr10 | 48435239 | ||||
| chr10:48435316
|
T | A | 1 | a0001c0001t0032 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*287T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 287 | chr10 | 48435316 | |||||
| chr10:48435464
|
TAC | T | 3 | a0001c0001t0004a0001c0001t0030a0002c0003t0004 | 24 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*436_*437delAC | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 436 | chr10 | 48435464 | |||||
| chr10:48435527
|
T | G | 14 | a0001c0001t0001a0001c0001t0009a0001c0001t0010others(11): Show | 126 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*498T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 498 | chr10 | 48435527 | |||||
| chr10:48436144
|
A | G | 1 | a0001c0001t0019 | 2 | HG02055.hp2 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1115A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 1115 | chr10 | 48436144 | |||||
| chr10:48436150
|
C | T | 1 | a0001c0001t0024 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1121C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 1121 | chr10 | 48436150 | |||||
| chr10:48436250
|
A | G | 1 | a0001c0001t0011 | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1221A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 1221 | chr10 | 48436250 | |||||
| chr10:48436255
|
A | G | 2 | a0001c0001t0028a0001c0001t0029 | 2 | HG02145.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1226A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 1226 | chr10 | 48436255 | |||||
| chr10:48436298
|
A | G | 2 | a0001c0001t0005a0001c0001t0027 | 22 | HG00597.hp1 HG02155.hp1 HG04184.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1269A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 1269 | chr10 | 48436298 | |||||
| chr10:48436373
|
T | C | 19 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(16): Show | 163 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*1344T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 1344 | chr10 | 48436373 | |||||
| chr10:48436385
|
T | A | 1 | a0001c0001t0025 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1356T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 1356 | chr10 | 48436385 | |||||
| chr10:48436427
|
C | T | 1 | a0001c0001t0018 | 2 | HG01123.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1398C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 1398 | chr10 | 48436427 | |||||
| chr10:48436443
|
C | T | 1 | a0001c0001t0011 | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1414C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 1414 | chr10 | 48436443 | |||||
| chr10:48436659
|
A | C | 2 | a0001c0001t0011a0001c0002t0017 | 6 | HG01884.hp2 HG02165.hp2 HG02258.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1630A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 1630 | chr10 | 48436659 | |||||
| chr10:48437069
|
G | A | 1 | a0001c0001t0027 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2040G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 2040 | chr10 | 48437069 | |||||
| chr10:48437165
|
C | G | 1 | a0001c0001t0012 | 3 | NA18998.hp1 NA19066.hp1 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2136C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 2136 | chr10 | 48437165 | |||||
| chr10:48437486
|
G | C | 1 | a0001c0001t0013 | 2 | HG01168.hp2 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2457G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 2457 | chr10 | 48437486 | |||||
| chr10:48437612
|
T | G | 1 | a0001c0001t0014 | 2 | NA18747.hp2 NA19080.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2583T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 2583 | chr10 | 48437612 | |||||
| chr10:48437714
|
T | G | 1 | a0001c0001t0016 | 2 | HG02257.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2685T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 2685 | chr10 | 48437714 | |||||
| chr10:48438309
|
T | C | 1 | a0001c0001t0031 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3280T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 3280 | chr10 | 48438309 | |||||
| chr10:48438328
|
A | G | 1 | a0001c0001t0009 | 5 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3299A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 3299 | chr10 | 48438328 | |||||
| chr10:48438394
|
A | G | 1 | a0001c0001t0030 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3365A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 3365 | chr10 | 48438394 | |||||
| chr10:48438727
|
A | G | 1 | a0001c0001t0011 | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3698A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 3698 | chr10 | 48438727 | |||||
| chr10:48438804
|
A | G | 1 | a0001c0001t0023 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3775A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 3775 | chr10 | 48438804 | |||||
| chr10:48438872
|
G | A | 1 | a0001c0001t0026 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3843G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 3843 | chr10 | 48438872 | |||||
| chr10:48438961
|
T | C | 1 | a0001c0001t0028 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3932T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 3932 | chr10 | 48438961 | |||||
| chr10:48439026
|
C | G | 1 | a0001c0001t0018 | 2 | HG01123.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3997C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 3997 | chr10 | 48439026 | |||||
| chr10:48439079
|
C | T | 2 | a0001c0001t0015a0001c0001t0024 | 3 | HG02602.hp2 HG04115.hp2 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4050C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 4050 | chr10 | 48439079 | |||||
| chr10:48439224
|
T | A | 6 | a0001c0001t0002a0001c0001t0005a0001c0001t0012others(3): Show | 77 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*4195T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 4195 | chr10 | 48439224 | |||||
| chr10:48439302
|
T | G | 1 | a0001c0001t0022 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4273T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 12/12 | 4273 | chr10 | 48439302 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:48306865
|
C | T | 1 | a0001c0001t0001g0303 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-50+44C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48306865 | ||||||
| chr10:48306907
|
TCTC | T | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+90_-50+92delCT others(1): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48306907 | |||||
| chr10:48306938
|
G | GGGGCGGG others(5): Show |
1 | a0001c0001t0004g0302 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-50+119_-50+130dup others(12): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48306938 | |||||
| chr10:48307021
|
G | A | 5 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0010others(2): Show | 5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+200G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48307021 | ||||||
| chr10:48307039
|
C | T | 8 | a0001c0001t0001g0301a0001c0001t0007g0294a0001c0001t0007g0295others(5): Show | 8 | HG01167.hp1 HG02622.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-50+218C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48307039 | ||||||
| chr10:48307041
|
G | T | 6 | a0001c0001t0003g0293a0001c0001t0008g0008a0001c0001t0008g0009others(3): Show | 6 | HG02109.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+220G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48307041 | ||||||
| chr10:48307143
|
G | C | 1 | a0001c0001t0002g0013 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-50+322G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48307143 | ||||||
| chr10:48307183
|
C | G | 2 | a0001c0001t0001g0291a0001c0001t0001g0292 | 2 | NA18953.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-50+362C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48307183 | ||||||
| chr10:48307186
|
A | G | 1 | a0001c0001t0001g0289 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-50+365A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48307186 | ||||||
| chr10:48307186
|
A | T | 1 | a0001c0001t0002g0290 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-50+365A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48307186 | ||||||
| chr10:48307358
|
C | T | 1 | a0001c0001t0006g0288 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-50+537C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48307358 | ||||||
| chr10:48307485
|
G | T | 1 | a0001c0001t0003g0287 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-50+664G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48307485 | ||||||
| chr10:48307503
|
T | C | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+682T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48307503 | ||||||
| chr10:48307514
|
A | G | 1 | a0001c0001t0003g0286 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-50+693A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48307514 | ||||||
| chr10:48307634
|
T | C | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp2 HG02165.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+813T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48307634 | ||||||
| chr10:48307693
|
A | G | 7 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(4): Show | 7 | HG02055.hp2 HG02257.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50+872A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48307693 | ||||||
| chr10:48307710
|
C | T | 230 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.-50+889C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48307710 | ||||||
| chr10:48307836
|
T | G | 1 | a0001c0001t0007g0085 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-50+1015T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48307836 | ||||||
| chr10:48308002
|
A | G | 3 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0278 | 3 | HG02523.hp2 NA18975.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-50+1181A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48308002 | ||||||
| chr10:48308104
|
C | G | 1 | a0001c0001t0001g0275 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-50+1283C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48308104 | ||||||
| chr10:48308214
|
A | G | 1 | a0001c0001t0002g0274 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-50+1393A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48308214 | ||||||
| chr10:48308951
|
T | C | 1 | a0001c0001t0007g0085 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-50+2130T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48308951 | ||||||
| chr10:48308963
|
T | C | 1 | a0001c0001t0006g0086 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-50+2142T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48308963 | ||||||
| chr10:48309203
|
A | G | 1 | a0001c0001t0001g0273 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-50+2382A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48309203 | ||||||
| chr10:48309269
|
C | G | 1 | a0001c0001t0030g0272 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-50+2448C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48309269 | ||||||
| chr10:48309322
|
C | T | 1 | a0001c0001t0001g0271 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-50+2501C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48309322 | ||||||
| chr10:48309346
|
CT | C | 17 | a0001c0001t0001g0301a0001c0001t0007g0085a0001c0001t0007g0087others(14): Show | 17 | HG01167.hp1 HG01891.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.-50+2527delT | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48309346 | |||||
| chr10:48309392
|
G | A | 2 | a0001c0001t0018g0095a0001c0001t0018g0096 | 2 | HG01123.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-50+2571G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48309392 | ||||||
| chr10:48309556
|
A | G | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+2735A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48309556 | ||||||
| chr10:48309565
|
A | G | 2 | a0001c0001t0016g0269a0001c0001t0016g0270 | 2 | HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-50+2744A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48309565 | ||||||
| chr10:48309583
|
A | G | 21 | a0001c0001t0001g0268a0001c0001t0006g0086a0001c0001t0006g0250others(18): Show | 21 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.-50+2762A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48309583 | ||||||
| chr10:48309604
|
G | A | 19 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(16): Show | 19 | HG00735.hp2 HG02055.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-50+2783G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48309604 | ||||||
| chr10:48309714
|
G | C | 3 | a0001c0001t0004g0115a0001c0001t0004g0116a0001c0001t0004g0117 | 3 | HG01069.hp1 HG01099.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-50+2893G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48309714 | ||||||
| chr10:48309968
|
G | A | 17 | a0001c0001t0001g0301a0001c0001t0007g0085a0001c0001t0007g0087others(14): Show | 17 | HG01167.hp1 HG01891.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.-50+3147G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48309968 | ||||||
| chr10:48310087
|
G | A | 9 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(6): Show | 9 | HG01070.hp2 HG01167.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.-50+3266G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48310087 | ||||||
| chr10:48310320
|
G | A | 10 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(7): Show | 10 | HG01891.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-50+3499G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48310320 | ||||||
| chr10:48310338
|
A | G | 1 | a0001c0001t0003g0286 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-50+3517A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48310338 | ||||||
| chr10:48310353
|
G | T | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-50+3532G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48310353 | ||||||
| chr10:48310729
|
T | TTG | 11 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(8): Show | 11 | HG00609.hp1 HG00741.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.-50+3932_-50+3933d others(4): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48310729 | |||||
| chr10:48310729
|
T | TTGTG | 6 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0246others(3): Show | 6 | HG00408.hp1 HG00408.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50+3930_-50+3933d others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48310729 | |||||
| chr10:48310729
|
TTG | T | 73 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(70): Show | 74 | HG00099.hp1 HG00609.hp2 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.-50+3932_-50+3933d others(4): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48310729 | |||||
| chr10:48310729
|
TTGTG | T | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+3930_-50+3933d others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48310729 | |||||
| chr10:48310729
|
TTGTGTG | T | 6 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG00544.hp2 NA18942.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+3928_-50+3933d others(8): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48310729 | |||||
| chr10:48310751
|
GTGTA | G | 3 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0025g0114 | 3 | HG02451.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-50+3934_-50+3937d others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48310751 | |||||
| chr10:48310774
|
C | T | 199 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(196): Show | 199 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.-50+3953C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48310774 | ||||||
| chr10:48310782
|
GAGAC | G | 16 | a0001c0001t0007g0085a0001c0001t0007g0087a0001c0001t0007g0088others(13): Show | 16 | HG01167.hp1 HG01891.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.-50+3965_-50+3968d others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48310782 | |||||
| chr10:48310826
|
T | C | 1 | a0001c0001t0032g0161 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-50+4005T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48310826 | ||||||
| chr10:48310990
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-50+4169G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48310990 | ||||||
| chr10:48311008
|
T | TCTAA | 222 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(219): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.-50+4190_-50+4193d others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48311008 | |||||
| chr10:48311039
|
A | G | 4 | a0001c0001t0003g0284a0001c0001t0003g0285a0001c0001t0019g0282others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+4218A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48311039 | ||||||
| chr10:48311153
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-50+4332G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48311153 | ||||||
| chr10:48311212
|
T | C | 127 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(124): Show | 127 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.-50+4391T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48311212 | ||||||
| chr10:48311223
|
G | T | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-50+4402G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48311223 | ||||||
| chr10:48311281
|
A | G | 3 | a0001c0001t0003g0286a0001c0001t0018g0095a0001c0001t0018g0096 | 3 | HG01123.hp1 HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-50+4460A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48311281 | ||||||
| chr10:48311453
|
A | G | 1 | a0001c0001t0003g0286 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-50+4632A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48311453 | ||||||
| chr10:48311487
|
C | T | 28 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(25): Show | 28 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.-50+4666C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48311487 | ||||||
| chr10:48311559
|
G | A | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG02615.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-50+4738G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48311559 | ||||||
| chr10:48311656
|
G | C | 1 | a0001c0001t0001g0239 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-50+4835G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48311656 | ||||||
| chr10:48311879
|
G | A | 1 | a0001c0001t0003g0097 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-50+5058G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48311879 | ||||||
| chr10:48311904
|
A | G | 51 | a0001c0001t0001g0268a0001c0001t0003g0097a0001c0001t0003g0098others(48): Show | 51 | HG00735.hp2 HG01099.hp2 HG01106.hp2 others(48): Show |
intron_variant | MODIFIER | c.-50+5083A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48311904 | ||||||
| chr10:48311960
|
A | G | 230 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.-50+5139A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48311960 | ||||||
| chr10:48312124
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-50+5303G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48312124 | ||||||
| chr10:48312133
|
C | T | 1 | a0001c0001t0002g0083 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-50+5312C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48312133 | ||||||
| chr10:48312154
|
A | T | 23 | a0001c0001t0004g0003a0001c0001t0004g0115a0001c0001t0004g0116others(20): Show | 24 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.-50+5333A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48312154 | ||||||
| chr10:48312227
|
A | G | 20 | a0001c0001t0006g0086a0001c0001t0006g0250a0001c0001t0006g0251others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.-50+5406A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48312227 | ||||||
| chr10:48312505
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-50+5684G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48312505 | ||||||
| chr10:48312674
|
A | G | 1 | a0001c0001t0003g0102 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-50+5853A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48312674 | ||||||
| chr10:48312722
|
G | A | 1 | a0001c0001t0007g0294 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-50+5901G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48312722 | ||||||
| chr10:48312766
|
G | C | 6 | a0001c0001t0003g0293a0001c0001t0008g0008a0001c0001t0008g0009others(3): Show | 6 | HG02109.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+5945G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48312766 | ||||||
| chr10:48312839
|
A | G | 2 | a0001c0001t0016g0269a0001c0001t0016g0270 | 2 | HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-50+6018A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48312839 | ||||||
| chr10:48312879
|
A | G | 6 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0005g0079others(3): Show | 6 | HG02155.hp1 NA18960.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50+6058A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48312879 | ||||||
| chr10:48312981
|
T | C | 3 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281 | 3 | HG03098.hp1 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-50+6160T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48312981 | ||||||
| chr10:48313006
|
G | C | 1 | a0001c0001t0001g0166 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-50+6185G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48313006 | ||||||
| chr10:48313042
|
G | A | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+6221G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48313042 | ||||||
| chr10:48313118
|
C | A | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+6297C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48313118 | ||||||
| chr10:48313170
|
C | T | 1 | a0001c0001t0021g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-50+6349C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48313170 | ||||||
| chr10:48313180
|
C | T | 4 | a0001c0001t0002g0074a0001c0001t0002g0075a0001c0001t0002g0076others(1): Show | 4 | HG02027.hp2 HG02132.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+6359C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48313180 | ||||||
| chr10:48313262
|
G | A | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-50+6441G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48313262 | ||||||
| chr10:48313421
|
GT | G | 302 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(299): Show | 305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.-50+6601delT | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48313421 | ||||||
| chr10:48313455
|
A | C | 2 | a0001c0001t0001g0238a0001c0001t0001g0268 | 2 | HG01175.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.-50+6634A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48313455 | ||||||
| chr10:48313516
|
T | C | 12 | a0001c0001t0007g0087a0001c0001t0007g0088a0001c0001t0007g0089others(9): Show | 12 | HG01167.hp1 HG01891.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-50+6695T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48313516 | ||||||
| chr10:48313541
|
CT | C | 50 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(47): Show | 50 | HG00735.hp2 HG01099.hp2 HG01106.hp2 others(47): Show |
intron_variant | MODIFIER | c.-50+6721delT | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48313541 | ||||||
| chr10:48313560
|
A | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | NA18612.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-50+6739A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48313560 | ||||||
| chr10:48313571
|
C | T | 23 | a0001c0001t0004g0003a0001c0001t0004g0115a0001c0001t0004g0116others(20): Show | 24 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.-50+6750C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48313571 | ||||||
| chr10:48313820
|
A | G | 143 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(140): Show | 143 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.-50+6999A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48313820 | ||||||
| chr10:48313847
|
C | T | 1 | a0001c0001t0020g0235 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-50+7026C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48313847 | ||||||
| chr10:48313955
|
C | T | 7 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(4): Show | 7 | HG02055.hp2 HG02257.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50+7134C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48313955 | ||||||
| chr10:48313983
|
TGA | T | 23 | a0001c0001t0004g0003a0001c0001t0004g0115a0001c0001t0004g0116others(20): Show | 24 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.-50+7167_-50+7168d others(4): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48313983 | |||||
| chr10:48314386
|
T | A | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+7565T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48314386 | ||||||
| chr10:48314401
|
A | G | 28 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(25): Show | 28 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.-50+7580A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48314401 | ||||||
| chr10:48314542
|
A | G | 1 | a0001c0001t0015g0234 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-50+7721A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48314542 | ||||||
| chr10:48314769
|
T | A | 7 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(4): Show | 7 | HG02055.hp2 HG02257.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50+7948T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48314769 | ||||||
| chr10:48315135
|
A | C | 3 | a0001c0001t0009g0231a0001c0001t0009g0232a0001c0001t0009g0233 | 3 | HG01109.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-50+8314A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48315135 | ||||||
| chr10:48315135
|
A | G | 1 | a0001c0001t0002g0072 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-50+8314A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48315135 | ||||||
| chr10:48315359
|
C | T | 1 | a0001c0001t0002g0071 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-50+8538C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48315359 | ||||||
| chr10:48315394
|
C | T | 2 | a0001c0001t0016g0269a0001c0001t0016g0270 | 2 | HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-50+8573C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48315394 | ||||||
| chr10:48315423
|
A | C | 230 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.-50+8602A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48315423 | ||||||
| chr10:48315550
|
T | C | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-50+8729T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48315550 | ||||||
| chr10:48315601
|
G | GT | 139 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(136): Show | 139 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.-50+8793dupT | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48315601 | |||||
| chr10:48315619
|
G | A | 3 | a0001c0001t0003g0286a0001c0001t0018g0095a0001c0001t0018g0096 | 3 | HG01123.hp1 HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-50+8798G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48315619 | ||||||
| chr10:48315702
|
C | T | 222 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(219): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.-50+8881C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48315702 | ||||||
| chr10:48316091
|
A | G | 1 | a0001c0001t0018g0096 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-50+9270A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48316091 | ||||||
| chr10:48316300
|
C | A | 230 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.-50+9479C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48316300 | ||||||
| chr10:48316463
|
T | C | 28 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(25): Show | 28 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.-50+9642T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48316463 | ||||||
| chr10:48316517
|
C | T | 1 | a0001c0001t0004g0117 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-50+9696C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48316517 | ||||||
| chr10:48316625
|
A | G | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-50+9804A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48316625 | ||||||
| chr10:48316672
|
G | A | 127 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(124): Show | 127 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.-50+9851G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48316672 | ||||||
| chr10:48316730
|
T | A | 9 | a0001c0001t0003g0103a0001c0001t0003g0104a0001c0001t0003g0105others(6): Show | 9 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-50+9909T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48316730 | ||||||
| chr10:48316782
|
G | C | 18 | a0001c0001t0004g0003a0001c0001t0004g0143a0001c0001t0004g0144others(15): Show | 19 | HG00099.hp1 HG00609.hp2 HG02071.hp2 others(16): Show |
intron_variant | MODIFIER | c.-50+9961G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48316782 | ||||||
| chr10:48316904
|
C | T | 2 | a0001c0001t0003g0284a0001c0001t0003g0285 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-50+10083C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48316904 | ||||||
| chr10:48316937
|
A | T | 1 | a0001c0001t0007g0091 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-50+10116A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48316937 | ||||||
| chr10:48317398
|
C | CAT | 161 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(158): Show | 161 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.-50+10577_-50+1057 others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48317398 | ||||||
| chr10:48317412
|
C | T | 1 | a0001c0001t0005g0070 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-50+10591C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48317412 | ||||||
| chr10:48317504
|
T | G | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-50+10683T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48317504 | ||||||
| chr10:48317552
|
G | A | 15 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(12): Show | 15 | HG00735.hp2 HG02055.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-50+10731G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48317552 | ||||||
| chr10:48317679
|
G | T | 2 | a0001c0001t0018g0095a0001c0001t0018g0096 | 2 | HG01123.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-50+10858G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48317679 | ||||||
| chr10:48317822
|
C | T | 13 | a0001c0001t0004g0003a0001c0001t0004g0148a0001c0001t0004g0149others(10): Show | 14 | HG00099.hp1 HG00609.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.-50+11001C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48317822 | ||||||
| chr10:48317998
|
A | C | 1 | a0001c0001t0002g0069 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-50+11177A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48317998 | ||||||
| chr10:48318062
|
C | T | 1 | a0001c0001t0002g0069 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-50+11241C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48318062 | ||||||
| chr10:48318127
|
A | G | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01123.hp1 HG01884.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+11306A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48318127 | ||||||
| chr10:48318437
|
A | G | 29 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(26): Show | 29 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.-50+11616A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48318437 | ||||||
| chr10:48318496
|
A | G | 1 | a0001c0001t0003g0102 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-50+11675A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48318496 | ||||||
| chr10:48318906
|
G | A | 23 | a0001c0001t0004g0003a0001c0001t0004g0115a0001c0001t0004g0116others(20): Show | 24 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.-50+12085G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48318906 | ||||||
| chr10:48319029
|
G | A | 22 | a0001c0001t0004g0003a0001c0001t0004g0115a0001c0001t0004g0116others(19): Show | 23 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.-50+12208G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48319029 | ||||||
| chr10:48319070
|
T | C | 26 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(23): Show | 26 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.-50+12249T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48319070 | ||||||
| chr10:48319163
|
C | T | 231 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(228): Show | 232 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.-50+12342C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48319163 | ||||||
| chr10:48319213
|
A | G | 1 | a0001c0001t0001g0230 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-50+12392A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48319213 | ||||||
| chr10:48319302
|
T | C | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+12481T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48319302 | ||||||
| chr10:48319305
|
A | G | 3 | a0001c0001t0010g0227a0001c0001t0010g0228a0001c0001t0010g0229 | 3 | HG02965.hp1 HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-50+12484A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48319305 | ||||||
| chr10:48319308
|
A | G | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+12487A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48319308 | ||||||
| chr10:48319430
|
C | T | 1 | a0001c0001t0003g0285 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-50+12609C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48319430 | ||||||
| chr10:48319493
|
C | T | 5 | a0001c0001t0004g0143a0001c0001t0004g0144a0001c0001t0004g0145others(2): Show | 5 | HG02486.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-50+12672C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48319493 | ||||||
| chr10:48319515
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-50+12694C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48319515 | ||||||
| chr10:48319551
|
G | A | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-50+12730G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48319551 | ||||||
| chr10:48319552
|
T | A | 9 | a0001c0001t0003g0103a0001c0001t0003g0104a0001c0001t0003g0105others(6): Show | 9 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-50+12731T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48319552 | ||||||
| chr10:48319563
|
C | G | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+12742C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48319563 | ||||||
| chr10:48319565
|
C | T | 13 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(10): Show | 13 | HG00099.hp2 HG00280.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.-50+12744C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48319565 | ||||||
| chr10:48319675
|
A | G | 1 | a0001c0001t0003g0286 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-50+12854A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48319675 | ||||||
| chr10:48319831
|
C | T | 2 | a0001c0001t0016g0269a0001c0001t0016g0270 | 2 | HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-50+13010C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48319831 | ||||||
| chr10:48319978
|
G | A | 16 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(13): Show | 16 | HG01070.hp2 HG01167.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.-50+13157G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48319978 | ||||||
| chr10:48320042
|
C | T | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+13221C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48320042 | ||||||
| chr10:48320076
|
C | T | 3 | a0001c0001t0012g0066a0001c0001t0012g0067a0001c0001t0012g0068 | 3 | NA18998.hp1 NA19066.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-50+13255C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48320076 | ||||||
| chr10:48320157
|
C | T | 1 | a0001c0001t0022g0133 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-50+13336C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48320157 | ||||||
| chr10:48320211
|
C | CT | 27 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0002g0059others(24): Show | 27 | HG00741.hp1 HG01175.hp1 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.-50+13422dupT | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48320211 | |||||
| chr10:48320211
|
C | CTT | 13 | a0001c0001t0003g0286a0001c0001t0006g0086a0001c0001t0006g0253others(10): Show | 13 | HG01099.hp2 HG01168.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.-50+13421_-50+1342 others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48320211 | |||||
| chr10:48320211
|
C | CTTT | 6 | a0001c0001t0001g0175a0001c0001t0003g0284a0001c0001t0006g0263others(3): Show | 6 | HG01346.hp1 HG01978.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50+13420_-50+1342 others(7): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48320211 | |||||
| chr10:48320211
|
C | CTTTT | 14 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0136others(11): Show | 14 | HG00597.hp2 HG01106.hp2 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.-50+13419_-50+1342 others(8): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48320211 | |||||
| chr10:48320211
|
C | CTTTTT | 55 | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0131others(52): Show | 55 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.-50+13418_-50+1342 others(9): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48320211 | |||||
| chr10:48320211
|
C | CTTTTTT | 48 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(45): Show | 48 | HG00423.hp2 HG00741.hp2 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.-50+13417_-50+1342 others(10): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48320211 | |||||
| chr10:48320211
|
C | CTTTTTTT | 7 | a0001c0001t0001g0126a0001c0001t0001g0141a0001c0001t0001g0142others(4): Show | 7 | HG02109.hp2 HG02615.hp2 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50+13416_-50+1342 others(11): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48320211 | |||||
| chr10:48320211
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0003g0100 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-50+13411_-50+1342 others(16): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48320211 | |||||
| chr10:48320211
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0003g0097 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-50+13403_-50+1342 others(24): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48320211 | |||||
| chr10:48320211
|
CT | C | 35 | a0001c0001t0002g0001a0001c0001t0002g0022a0001c0001t0002g0024others(32): Show | 36 | HG00597.hp1 HG01069.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.-50+13422delT | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48320211 | |||||
| chr10:48320211
|
CTT | C | 6 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0011g0004others(3): Show | 6 | HG01884.hp2 HG02258.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50+13421_-50+1342 others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48320211 | |||||
| chr10:48320211
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0006g0159 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+13412_-50+1342 others(15): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48320211 | |||||
| chr10:48320211
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0004g0302 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-50+13411_-50+1342 others(16): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48320211 | |||||
| chr10:48320211
|
CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0003g0101a0001c0001t0003g0285 | 2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-50+13410_-50+1342 others(17): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48320211 | |||||
| chr10:48320211
|
CTTTTTTT others(7): Show |
C | 9 | a0001c0001t0003g0103a0001c0001t0003g0104a0001c0001t0003g0105others(6): Show | 9 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-50+13409_-50+1342 others(18): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48320211 | |||||
| chr10:48320211
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0001g0173 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-50+13408_-50+1342 others(19): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48320211 | |||||
| chr10:48320243
|
T | A | 1 | a0001c0001t0003g0101 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-50+13422T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48320243 | ||||||
| chr10:48320244
|
A | T | 1 | a0001c0001t0002g0065 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-50+13423A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48320244 | ||||||
| chr10:48320598
|
C | T | 2 | a0001c0001t0003g0109a0001c0001t0003g0110 | 2 | HG02055.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-50+13777C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48320598 | ||||||
| chr10:48320860
|
A | G | 26 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(23): Show | 26 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.-50+14039A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48320860 | ||||||
| chr10:48320917
|
G | A | 1 | a0001c0001t0002g0059 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-50+14096G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48320917 | ||||||
| chr10:48321036
|
T | C | 2 | a0001c0001t0003g0284a0001c0001t0003g0285 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-50+14215T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48321036 | ||||||
| chr10:48321089
|
G | GT | 138 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0126others(135): Show | 138 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.-50+14291dupT | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48321089 | |||||
| chr10:48321089
|
G | GTT | 23 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0142others(20): Show | 23 | HG01891.hp1 HG01978.hp1 HG01981.hp1 others(20): Show |
intron_variant | MODIFIER | c.-50+14290_-50+1429 others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48321089 | |||||
| chr10:48321092
|
T | TG | 5 | a0001c0001t0001g0179a0001c0001t0001g0202a0001c0001t0001g0276others(2): Show | 5 | HG00423.hp2 HG02129.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.-50+14271_-50+1427 others(5): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48321092 | ||||||
| chr10:48321350
|
T | C | 26 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(23): Show | 26 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.-50+14529T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48321350 | ||||||
| chr10:48321377
|
T | C | 220 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.-50+14556T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48321377 | ||||||
| chr10:48321412
|
C | G | 1 | a0001c0001t0010g0220 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-50+14591C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48321412 | ||||||
| chr10:48321664
|
C | T | 20 | a0001c0001t0006g0086a0001c0001t0006g0250a0001c0001t0006g0251others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.-50+14843C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48321664 | ||||||
| chr10:48321691
|
G | A | 5 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0010others(2): Show | 5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+14870G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48321691 | ||||||
| chr10:48321718
|
T | A | 2 | a0001c0001t0020g0222a0001c0001t0020g0235 | 2 | HG00280.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-50+14897T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48321718 | ||||||
| chr10:48321861
|
C | A | 8 | a0001c0001t0002g0013a0001c0001t0002g0032a0001c0001t0002g0033others(5): Show | 8 | NA18941.hp2 NA18948.hp1 NA18949.hp2 others(5): Show |
intron_variant | MODIFIER | c.-50+15040C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48321861 | ||||||
| chr10:48321874
|
G | A | 3 | a0001c0001t0003g0287a0001c0001t0016g0269a0001c0001t0016g0270 | 3 | HG02257.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-50+15053G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48321874 | ||||||
| chr10:48322028
|
C | A | 1 | a0001c0001t0002g0036 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-50+15207C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48322028 | ||||||
| chr10:48322150
|
A | G | 18 | a0001c0001t0004g0003a0001c0001t0004g0143a0001c0001t0004g0144others(15): Show | 19 | HG00099.hp1 HG00609.hp2 HG02071.hp2 others(16): Show |
intron_variant | MODIFIER | c.-50+15329A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48322150 | ||||||
| chr10:48322315
|
T | TA | 97 | a0001c0001t0002g0062a0001c0001t0003g0097a0001c0001t0003g0098others(94): Show | 98 | HG00099.hp1 HG00609.hp2 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.-50+15505dupA | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48322315 | |||||
| chr10:48322315
|
T | TAA | 126 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(123): Show | 126 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.-50+15504_-50+1550 others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48322315 | |||||
| chr10:48322405
|
G | A | 1 | a0001c0001t0003g0285 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-50+15584G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48322405 | ||||||
| chr10:48322542
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-50+15721A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48322542 | ||||||
| chr10:48322547
|
G | T | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+15726G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48322547 | ||||||
| chr10:48322568
|
A | G | 3 | a0001c0001t0004g0115a0001c0001t0004g0116a0001c0001t0004g0117 | 3 | HG01069.hp1 HG01099.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-50+15747A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48322568 | ||||||
| chr10:48322624
|
G | GCCCCACA others(3): Show |
2 | a0001c0001t0018g0095a0001c0001t0018g0096 | 2 | HG01123.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-50+15810_-50+1581 others(14): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48322624 | |||||
| chr10:48322628
|
C | T | 1 | a0001c0001t0006g0262 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-50+15807C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48322628 | ||||||
| chr10:48322643
|
T | C | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp2 HG02165.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+15822T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48322643 | ||||||
| chr10:48322677
|
A | G | 1 | a0001c0001t0003g0286 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-50+15856A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48322677 | ||||||
| chr10:48323263
|
C | T | 11 | a0001c0001t0006g0086a0001c0001t0006g0256a0001c0001t0006g0257others(8): Show | 11 | HG01099.hp2 HG01106.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.-50+16442C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48323263 | ||||||
| chr10:48323367
|
A | C | 1 | a0001c0001t0003g0293 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-50+16546A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48323367 | ||||||
| chr10:48323442
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-50+16621T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48323442 | ||||||
| chr10:48323515
|
A | G | 1 | a0001c0001t0005g0030 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-50+16694A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48323515 | ||||||
| chr10:48323540
|
A | T | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0004t0001g0171 | 3 | HG01515.hp2 HG01981.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.-50+16719A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48323540 | ||||||
| chr10:48323656
|
A | C | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+16835A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48323656 | ||||||
| chr10:48323680
|
A | G | 1 | a0001c0001t0022g0133 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-50+16859A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48323680 | ||||||
| chr10:48323820
|
A | T | 1 | a0001c0001t0012g0068 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-50+16999A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48323820 | ||||||
| chr10:48323864
|
A | G | 1 | a0001c0001t0004g0154 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-50+17043A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48323864 | ||||||
| chr10:48324054
|
C | A | 1 | a0001c0001t0024g0125 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-50+17233C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48324054 | ||||||
| chr10:48324250
|
A | G | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+17429A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48324250 | ||||||
| chr10:48324472
|
G | A | 20 | a0001c0001t0006g0086a0001c0001t0006g0250a0001c0001t0006g0251others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.-50+17651G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48324472 | ||||||
| chr10:48324502
|
A | ATTTTTTT others(5): Show |
2 | a0001c0001t0011g0004a0001c0001t0011g0005 | 2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-50+17681_-50+1768 others(16): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48324502 | ||||||
| chr10:48324502
|
A | ATTTTTTT others(6): Show |
2 | a0001c0001t0011g0006a0001c0001t0011g0007 | 2 | HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-50+17681_-50+1768 others(17): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48324502 | ||||||
| chr10:48324503
|
G | GT | 122 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(119): Show | 122 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.-50+17699dupT | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48324503 | |||||
| chr10:48324503
|
G | GTT | 6 | a0001c0001t0001g0183a0001c0001t0001g0217a0001c0001t0009g0233others(3): Show | 6 | HG01109.hp2 HG01168.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+17698_-50+1769 others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48324503 | |||||
| chr10:48324503
|
G | GTTTTTTT others(2): Show |
15 | a0001c0001t0007g0088a0001c0001t0007g0089a0001c0001t0007g0090others(12): Show | 15 | HG01167.hp1 HG02622.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.-50+17691_-50+1769 others(13): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48324503 | |||||
| chr10:48324503
|
G | GTTTTTTT others(3): Show |
3 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0294 | 3 | HG01891.hp2 HG03516.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-50+17690_-50+1769 others(14): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48324503 | |||||
| chr10:48324503
|
G | GTTTTTTT others(4): Show |
4 | a0001c0001t0007g0085a0001c0001t0007g0093a0001c0001t0019g0282others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+17689_-50+1769 others(15): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48324503 | |||||
| chr10:48324503
|
G | GTTTTTTT others(5): Show |
1 | a0001c0001t0003g0103 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-50+17688_-50+1769 others(16): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48324503 | |||||
| chr10:48324503
|
G | GTTTTTTT others(6): Show |
4 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0003g0109others(1): Show | 4 | HG02258.hp1 HG02647.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+17687_-50+1769 others(17): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48324503 | |||||
| chr10:48324503
|
G | GTTTTTTT others(19): Show |
2 | a0001c0001t0006g0250a0001c0001t0006g0251 | 2 | HG01516.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.-50+17695_-50+1769 others(30): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48324503 | |||||
| chr10:48324503
|
G | GTTTTTTT others(20): Show |
15 | a0001c0001t0006g0086a0001c0001t0006g0252a0001c0001t0006g0253others(12): Show | 15 | HG01099.hp2 HG01168.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.-50+17695_-50+1769 others(31): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48324503 | |||||
| chr10:48324503
|
G | GTTTTTTT others(21): Show |
3 | a0001c0001t0006g0265a0001c0001t0006g0266a0001c0001t0006g0288 | 3 | HG01106.hp2 HG01978.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-50+17695_-50+1769 others(32): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48324503 | |||||
| chr10:48324503
|
G | GTTTTTTT others(7): Show |
13 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(10): Show | 13 | HG00735.hp2 HG01123.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.-50+17686_-50+1769 others(18): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48324503 | |||||
| chr10:48324503
|
G | GTTTTTTT others(8): Show |
15 | a0001c0001t0003g0101a0001c0001t0003g0102a0001c0001t0003g0112others(12): Show | 15 | HG01069.hp1 HG01099.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-50+17685_-50+1769 others(19): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48324503 | |||||
| chr10:48324503
|
G | GTTTTTTT others(9): Show |
10 | a0001c0001t0004g0003a0001c0001t0004g0149a0001c0001t0004g0150others(7): Show | 11 | HG00099.hp1 HG00609.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.-50+17684_-50+1769 others(20): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48324503 | |||||
| chr10:48324503
|
G | GTTTTTTT others(10): Show |
3 | a0001c0001t0004g0153a0001c0001t0004g0158a0001c0002t0017g0015 | 3 | HG02071.hp2 NA18987.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-50+17683_-50+1769 others(21): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48324503 | |||||
| chr10:48324503
|
G | GTTTTTTT others(16): Show |
2 | a0001c0001t0003g0279a0001c0001t0003g0281 | 2 | HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-50+17699_-50+1770 others(27): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48324503 | |||||
| chr10:48324503
|
G | GTTTTTTT others(17): Show |
1 | a0001c0001t0003g0280 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-50+17699_-50+1770 others(28): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48324503 | |||||
| chr10:48324503
|
G | T | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+17682G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48324503 | ||||||
| chr10:48324578
|
C | G | 35 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(32): Show | 35 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.-50+17757C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48324578 | ||||||
| chr10:48324582
|
A | G | 1 | a0001c0004t0001g0171 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-50+17761A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48324582 | ||||||
| chr10:48324684
|
GT | G | 220 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.-50+17872delT | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48324684 | |||||
| chr10:48324714
|
C | T | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+17893C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48324714 | ||||||
| chr10:48324916
|
A | C | 1 | a0001c0001t0001g0291 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-50+18095A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48324916 | ||||||
| chr10:48324956
|
T | TTTTTTTG others(6): Show |
226 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(223): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.-50+18147_-50+1814 others(17): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48324956 | |||||
| chr10:48324956
|
T | TTTTTTTT others(6): Show |
1 | a0001c0001t0016g0269 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-50+18141_-50+1814 others(17): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48324956 | |||||
| chr10:48324956
|
T | TTTTTTTT others(7): Show |
1 | a0001c0001t0016g0270 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-50+18141_-50+1814 others(18): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48324956 | |||||
| chr10:48324983
|
C | CT | 14 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(11): Show | 14 | HG01167.hp1 HG02622.hp1 HG02818.hp2 others(11): Show |
intron_variant | MODIFIER | c.-50+18172dupT | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48324983 | |||||
| chr10:48325101
|
G | A | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+18280G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48325101 | ||||||
| chr10:48325151
|
T | C | 4 | a0001c0001t0002g0074a0001c0001t0002g0075a0001c0001t0002g0076others(1): Show | 4 | HG02027.hp2 HG02132.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+18330T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48325151 | ||||||
| chr10:48325330
|
C | T | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+18509C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48325330 | ||||||
| chr10:48325528
|
C | T | 1 | a0001c0001t0007g0091 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-50+18707C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48325528 | ||||||
| chr10:48325617
|
C | T | 5 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0010others(2): Show | 5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+18796C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48325617 | ||||||
| chr10:48325618
|
G | A | 1 | a0001c0001t0003g0286 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-50+18797G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48325618 | ||||||
| chr10:48325627
|
C | T | 7 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(4): Show | 7 | NA18969.hp2 NA18972.hp2 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50+18806C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48325627 | ||||||
| chr10:48325702
|
T | G | 3 | a0001c0001t0004g0115a0001c0001t0004g0116a0001c0001t0004g0117 | 3 | HG01069.hp1 HG01099.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-50+18881T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48325702 | ||||||
| chr10:48325706
|
T | TTTTTAGC others(3): Show |
1 | a0001c0001t0026g0035 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-50+18887_-50+1889 others(14): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48325706 | |||||
| chr10:48325785
|
A | G | 1 | a0001c0001t0006g0159 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+18964A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48325785 | ||||||
| chr10:48325815
|
T | C | 1 | a0001c0001t0001g0241 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-50+18994T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48325815 | ||||||
| chr10:48325876
|
T | C | 3 | a0001c0001t0003g0286a0001c0001t0018g0095a0001c0001t0018g0096 | 3 | HG01123.hp1 HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-50+19055T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48325876 | ||||||
| chr10:48326119
|
T | C | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-50+19298T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48326119 | ||||||
| chr10:48326187
|
G | A | 2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | HG00741.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-50+19366G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48326187 | ||||||
| chr10:48326256
|
T | A | 1 | a0001c0001t0003g0285 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-50+19435T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48326256 | ||||||
| chr10:48326271
|
T | A | 2 | a0001c0001t0001g0188a0001c0001t0001g0207 | 2 | NA19058.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-50+19450T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48326271 | ||||||
| chr10:48326410
|
T | C | 1 | a0001c0001t0003g0280 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-50+19589T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48326410 | ||||||
| chr10:48326643
|
G | T | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-50+19822G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48326643 | ||||||
| chr10:48326762
|
C | T | 1 | a0001c0001t0006g0159 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+19941C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48326762 | ||||||
| chr10:48326837
|
C | T | 3 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0025g0114 | 3 | HG02451.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-50+20016C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48326837 | ||||||
| chr10:48326939
|
T | G | 1 | a0001c0001t0006g0159 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+20118T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48326939 | ||||||
| chr10:48327034
|
T | C | 2 | a0001c0001t0018g0095a0001c0001t0018g0096 | 2 | HG01123.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-50+20213T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48327034 | ||||||
| chr10:48327044
|
G | A | 3 | a0001c0001t0006g0250a0001c0001t0006g0253a0001c0001t0006g0254 | 3 | HG01168.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-50+20223G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48327044 | ||||||
| chr10:48327100
|
TATG | T | 5 | a0001c0001t0002g0013a0001c0001t0002g0033a0001c0001t0002g0034others(2): Show | 5 | NA18941.hp2 NA18948.hp1 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.-50+20283_-50+2028 others(7): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48327100 | |||||
| chr10:48327156
|
G | C | 1 | a0001c0001t0006g0159 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+20335G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48327156 | ||||||
| chr10:48327157
|
G | A | 1 | a0001c0001t0009g0196 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-50+20336G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48327157 | ||||||
| chr10:48327244
|
A | G | 1 | a0001c0001t0003g0286 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-50+20423A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48327244 | ||||||
| chr10:48327571
|
T | G | 1 | a0001c0001t0002g0013 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-50+20750T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48327571 | ||||||
| chr10:48327612
|
A | G | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+20791A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48327612 | ||||||
| chr10:48327664
|
T | C | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+20843T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48327664 | ||||||
| chr10:48327699
|
A | G | 16 | a0001c0001t0007g0085a0001c0001t0007g0087a0001c0001t0007g0088others(13): Show | 16 | HG01167.hp1 HG01891.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.-50+20878A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48327699 | ||||||
| chr10:48327964
|
A | G | 1 | a0001c0001t0010g0220 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-50+21143A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48327964 | ||||||
| chr10:48328039
|
CAA | C | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+21220_-50+2122 others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48328039 | |||||
| chr10:48328300
|
CT | C | 34 | a0001c0001t0003g0103a0001c0001t0003g0104a0001c0001t0003g0105others(31): Show | 35 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.-50+21491delT | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48328300 | |||||
| chr10:48328383
|
G | C | 2 | a0001c0001t0018g0095a0001c0001t0018g0096 | 2 | HG01123.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-50+21562G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48328383 | ||||||
| chr10:48328387
|
T | TA | 7 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(4): Show | 7 | HG00735.hp2 HG02280.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50+21567dupA | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48328387 | |||||
| chr10:48328556
|
T | A | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp2 HG02165.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+21735T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48328556 | ||||||
| chr10:48328604
|
T | G | 127 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(124): Show | 127 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.-50+21783T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48328604 | ||||||
| chr10:48328646
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-50+21825A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48328646 | ||||||
| chr10:48328650
|
C | G | 1 | a0001c0001t0001g0122 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-50+21829C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48328650 | ||||||
| chr10:48328832
|
T | C | 20 | a0001c0001t0006g0086a0001c0001t0006g0250a0001c0001t0006g0251others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.-50+22011T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48328832 | ||||||
| chr10:48328926
|
G | T | 1 | a0001c0001t0011g0005 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-50+22105G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48328926 | ||||||
| chr10:48328949
|
GTTTCA | G | 22 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(19): Show | 22 | HG00735.hp2 HG01123.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.-50+22131_-50+2213 others(9): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48328949 | |||||
| chr10:48328956
|
T | A | 2 | a0001c0001t0004g0144a0001c0001t0004g0147 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-50+22135T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48328956 | ||||||
| chr10:48329031
|
A | C | 1 | a0001c0001t0001g0141 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-50+22210A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48329031 | ||||||
| chr10:48329152
|
C | T | 1 | a0001c0001t0020g0235 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-50+22331C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48329152 | ||||||
| chr10:48329391
|
C | G | 2 | a0001c0001t0019g0282a0001c0001t0019g0283 | 2 | HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.-50+22570C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48329391 | ||||||
| chr10:48329393
|
A | G | 1 | a0001c0001t0001g0247 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-50+22572A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48329393 | ||||||
| chr10:48329458
|
T | A | 1 | a0001c0001t0003g0097 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-50+22637T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48329458 | ||||||
| chr10:48329508
|
C | CT | 123 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(120): Show | 123 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.-50+22696dupT | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48329508 | |||||
| chr10:48329516
|
T | A | 20 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(17): Show | 20 | HG00735.hp2 HG02055.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.-50+22695T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48329516 | ||||||
| chr10:48329517
|
T | A | 23 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(20): Show | 23 | HG00735.hp2 HG02055.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.-50+22696T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48329517 | ||||||
| chr10:48329518
|
A | T | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-50+22697A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48329518 | ||||||
| chr10:48329781
|
T | C | 1 | a0001c0001t0010g0221 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-50+22960T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48329781 | ||||||
| chr10:48329890
|
T | A | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-50+23069T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48329890 | ||||||
| chr10:48329943
|
T | C | 1 | a0001c0001t0018g0096 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-50+23122T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48329943 | ||||||
| chr10:48329957
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-50+23136C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48329957 | ||||||
| chr10:48329992
|
T | A | 1 | a0001c0001t0021g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-50+23171T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48329992 | ||||||
| chr10:48330043
|
T | C | 20 | a0001c0001t0006g0086a0001c0001t0006g0250a0001c0001t0006g0251others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.-50+23222T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48330043 | ||||||
| chr10:48330106
|
A | G | 23 | a0001c0001t0004g0003a0001c0001t0004g0115a0001c0001t0004g0116others(20): Show | 24 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.-50+23285A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48330106 | ||||||
| chr10:48330257
|
A | G | 7 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(4): Show | 7 | HG00735.hp2 HG02280.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50+23436A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48330257 | ||||||
| chr10:48330392
|
T | C | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG00099.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.-50+23571T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48330392 | ||||||
| chr10:48330415
|
T | C | 2 | a0001c0001t0016g0269a0001c0001t0016g0270 | 2 | HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-50+23594T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48330415 | ||||||
| chr10:48330501
|
A | C | 2 | a0001c0001t0002g0053a0001c0001t0002g0054 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-50+23680A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48330501 | ||||||
| chr10:48330555
|
G | A | 2 | a0001c0001t0004g0144a0001c0001t0004g0147 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-50+23734G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48330555 | ||||||
| chr10:48330565
|
A | G | 128 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(125): Show | 128 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.-50+23744A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48330565 | ||||||
| chr10:48330751
|
G | A | 1 | a0001c0001t0010g0220 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-50+23930G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48330751 | ||||||
| chr10:48330860
|
C | G | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-50+24039C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48330860 | ||||||
| chr10:48331093
|
C | T | 1 | a0001c0001t0004g0154 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-50+24272C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48331093 | ||||||
| chr10:48331197
|
G | A | 220 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.-50+24376G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48331197 | ||||||
| chr10:48331247
|
G | A | 2 | a0001c0001t0018g0095a0001c0001t0018g0096 | 2 | HG01123.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-50+24426G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48331247 | ||||||
| chr10:48331274
|
C | G | 1 | a0001c0001t0006g0159 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+24453C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48331274 | ||||||
| chr10:48331337
|
C | G | 22 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(19): Show | 22 | HG00735.hp2 HG01123.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.-50+24516C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48331337 | ||||||
| chr10:48331356
|
A | T | 1 | a0001c0001t0004g0146 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-50+24535A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48331356 | ||||||
| chr10:48331392
|
T | C | 1 | a0001c0001t0006g0256 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-50+24571T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48331392 | ||||||
| chr10:48331661
|
C | T | 2 | a0001c0001t0004g0152a0001c0001t0004g0154 | 2 | HG00099.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.-50+24840C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48331661 | ||||||
| chr10:48331669
|
C | T | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+24848C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48331669 | ||||||
| chr10:48332101
|
G | C | 1 | a0001c0001t0004g0160 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-50+25280G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48332101 | ||||||
| chr10:48332207
|
A | G | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+25386A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48332207 | ||||||
| chr10:48332336
|
C | T | 1 | a0001c0001t0006g0261 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-50+25515C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48332336 | ||||||
| chr10:48332411
|
G | A | 2 | a0001c0001t0016g0269a0001c0001t0016g0270 | 2 | HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-50+25590G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48332411 | ||||||
| chr10:48332418
|
C | G | 4 | a0001c0001t0002g0051a0001c0001t0002g0052a0001c0001t0002g0058others(1): Show | 4 | HG00544.hp1 HG00609.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+25597C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48332418 | ||||||
| chr10:48332461
|
A | C | 1 | a0001c0001t0004g0160 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-50+25640A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48332461 | ||||||
| chr10:48332484
|
A | T | 8 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(5): Show | 8 | NA18950.hp2 NA18960.hp2 NA18987.hp2 others(5): Show |
intron_variant | MODIFIER | c.-50+25663A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48332484 | ||||||
| chr10:48332547
|
T | C | 226 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(223): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.-50+25726T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48332547 | ||||||
| chr10:48332666
|
A | G | 7 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(4): Show | 7 | HG00408.hp1 HG00544.hp2 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50+25845A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48332666 | ||||||
| chr10:48332768
|
T | C | 3 | a0001c0001t0001g0174a0001c0001t0001g0203a0001c0001t0001g0217 | 3 | HG01346.hp2 HG01934.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.-50+25947T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48332768 | ||||||
| chr10:48332807
|
T | A | 20 | a0001c0001t0006g0086a0001c0001t0006g0250a0001c0001t0006g0251others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.-50+25986T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48332807 | ||||||
| chr10:48332825
|
A | G | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp2 HG02165.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+26004A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48332825 | ||||||
| chr10:48332897
|
A | G | 144 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(141): Show | 144 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.-50+26076A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48332897 | ||||||
| chr10:48332919
|
G | C | 1 | a0001c0001t0003g0286 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-50+26098G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48332919 | ||||||
| chr10:48332984
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-50+26163G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48332984 | ||||||
| chr10:48333013
|
T | C | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp2 HG02165.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+26192T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48333013 | ||||||
| chr10:48333021
|
C | T | 3 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281 | 3 | HG03098.hp1 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-50+26200C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48333021 | ||||||
| chr10:48333048
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-50+26227C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48333048 | ||||||
| chr10:48333321
|
G | A | 3 | a0001c0001t0001g0119a0001c0001t0015g0121a0001c0001t0024g0125 | 3 | HG02602.hp2 HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-50+26500G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48333321 | ||||||
| chr10:48333376
|
G | A | 127 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(124): Show | 127 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.-50+26555G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48333376 | ||||||
| chr10:48333501
|
A | G | 7 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(4): Show | 7 | HG00735.hp2 HG02280.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50+26680A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48333501 | ||||||
| chr10:48333604
|
C | A | 3 | a0001c0001t0001g0137a0001c0001t0001g0139a0001c0001t0001g0249 | 3 | HG00408.hp1 NA18942.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-50+26783C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48333604 | ||||||
| chr10:48333634
|
C | A | 2 | a0001c0001t0019g0282a0001c0001t0019g0283 | 2 | HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.-50+26813C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48333634 | ||||||
| chr10:48333654
|
G | A | 19 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(16): Show | 19 | HG00735.hp2 HG02055.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-50+26833G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48333654 | ||||||
| chr10:48333937
|
G | T | 127 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(124): Show | 127 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.-50+27116G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48333937 | ||||||
| chr10:48333938
|
C | T | 127 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(124): Show | 127 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.-50+27117C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48333938 | ||||||
| chr10:48333944
|
C | T | 5 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0010others(2): Show | 5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+27123C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48333944 | ||||||
| chr10:48333995
|
C | G | 2 | a0001c0001t0016g0269a0001c0001t0016g0270 | 2 | HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-50+27174C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48333995 | ||||||
| chr10:48334337
|
C | T | 127 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(124): Show | 127 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.-50+27516C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48334337 | ||||||
| chr10:48334412
|
T | G | 1 | a0001c0001t0018g0096 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-50+27591T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48334412 | ||||||
| chr10:48334442
|
C | T | 3 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0025g0114 | 3 | HG02451.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-50+27621C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48334442 | ||||||
| chr10:48334690
|
A | C | 143 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(140): Show | 143 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.-50+27869A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48334690 | ||||||
| chr10:48334888
|
T | C | 2 | a0001c0001t0007g0296a0001c0001t0007g0300 | 2 | HG02622.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-50+28067T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48334888 | ||||||
| chr10:48335011
|
C | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0206 | 2 | HG01993.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.-50+28190C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48335011 | ||||||
| chr10:48335109
|
T | C | 20 | a0001c0001t0002g0037a0001c0001t0003g0097a0001c0001t0003g0098others(17): Show | 20 | HG00735.hp2 HG02055.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.-50+28288T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48335109 | ||||||
| chr10:48335451
|
C | G | 10 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(7): Show | 10 | HG01891.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-50+28630C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48335451 | ||||||
| chr10:48335557
|
A | G | 6 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(3): Show | 6 | HG02622.hp2 HG02630.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+28736A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48335557 | ||||||
| chr10:48335591
|
G | A | 21 | a0001c0001t0006g0086a0001c0001t0006g0159a0001c0001t0006g0250others(18): Show | 21 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.-50+28770G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48335591 | ||||||
| chr10:48335773
|
C | T | 1 | a0001c0001t0006g0159 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+28952C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48335773 | ||||||
| chr10:48336094
|
G | A | 23 | a0001c0001t0004g0003a0001c0001t0004g0115a0001c0001t0004g0116others(20): Show | 24 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.-50+29273G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48336094 | ||||||
| chr10:48336212
|
A | G | 1 | a0001c0001t0002g0029 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-50+29391A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48336212 | ||||||
| chr10:48336364
|
A | T | 1 | a0001c0001t0028g0106 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-50+29543A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48336364 | ||||||
| chr10:48336653
|
CTT | C | 16 | a0001c0001t0007g0085a0001c0001t0007g0087a0001c0001t0007g0088others(13): Show | 16 | HG01167.hp1 HG01891.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.-50+29836_-50+2983 others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48336653 | |||||
| chr10:48336733
|
G | C | 1 | a0001c0001t0030g0272 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-50+29912G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48336733 | ||||||
| chr10:48336887
|
G | GCATT | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+30067_-50+3007 others(8): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48336887 | |||||
| chr10:48336983
|
A | G | 1 | a0001c0001t0007g0091 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-50+30162A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48336983 | ||||||
| chr10:48337070
|
G | A | 1 | a0001c0001t0005g0017 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-50+30249G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48337070 | ||||||
| chr10:48337091
|
G | A | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-50+30270G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48337091 | ||||||
| chr10:48337132
|
G | A | 20 | a0001c0001t0006g0086a0001c0001t0006g0250a0001c0001t0006g0251others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.-50+30311G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48337132 | ||||||
| chr10:48337230
|
T | C | 23 | a0001c0001t0004g0003a0001c0001t0004g0115a0001c0001t0004g0116others(20): Show | 24 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.-50+30409T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48337230 | ||||||
| chr10:48337395
|
A | AT | 230 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.-50+30582dupT | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48337395 | |||||
| chr10:48337750
|
A | G | 230 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.-50+30929A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48337750 | ||||||
| chr10:48337769
|
T | C | 1 | a0001c0001t0026g0035 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-50+30948T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48337769 | ||||||
| chr10:48337908
|
AAATCCTG | A | 20 | a0001c0001t0006g0086a0001c0001t0006g0250a0001c0001t0006g0251others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.-50+31090_-50+3109 others(11): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48337908 | |||||
| chr10:48337937
|
A | G | 1 | a0001c0001t0025g0114 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-50+31116A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48337937 | ||||||
| chr10:48337977
|
C | G | 3 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0025g0114 | 3 | HG02451.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-50+31156C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48337977 | ||||||
| chr10:48338087
|
A | C | 7 | a0001c0001t0002g0002a0001c0001t0002g0037a0001c0001t0002g0047others(4): Show | 8 | HG01070.hp1 HG01071.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.-50+31266A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48338087 | ||||||
| chr10:48338089
|
C | T | 2 | a0001c0001t0003g0284a0001c0001t0003g0285 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-50+31268C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48338089 | ||||||
| chr10:48338152
|
A | G | 1 | a0001c0001t0003g0293 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-50+31331A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48338152 | ||||||
| chr10:48338157
|
CAG | C | 26 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(23): Show | 26 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.-50+31338_-50+3133 others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48338157 | |||||
| chr10:48338199
|
A | G | 1 | a0001c0001t0007g0094 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-50+31378A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48338199 | ||||||
| chr10:48338302
|
T | C | 128 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(125): Show | 128 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.-50+31481T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48338302 | ||||||
| chr10:48338409
|
AG | A | 19 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(16): Show | 19 | HG00735.hp2 HG02055.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-50+31590delG | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48338409 | |||||
| chr10:48338584
|
A | G | 7 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(4): Show | 7 | HG00735.hp2 HG02280.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50+31763A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48338584 | ||||||
| chr10:48338690
|
G | C | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+31869G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48338690 | ||||||
| chr10:48338701
|
G | A | 2 | a0001c0001t0002g0037a0001c0001t0002g0047 | 2 | HG01261.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-50+31880G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48338701 | ||||||
| chr10:48338704
|
C | A | 1 | a0001c0001t0002g0058 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-50+31883C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48338704 | ||||||
| chr10:48338789
|
G | T | 1 | a0001c0001t0014g0214 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-50+31968G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48338789 | ||||||
| chr10:48338819
|
A | G | 3 | a0001c0001t0001g0225a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | HG01106.hp1 NA18612.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-50+31998A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48338819 | ||||||
| chr10:48338822
|
GAC | G | 15 | a0001c0001t0007g0085a0001c0001t0007g0087a0001c0001t0007g0088others(12): Show | 15 | HG01167.hp1 HG01891.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.-50+32009_-50+3201 others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48338822 | |||||
| chr10:48338847
|
C | T | 1 | a0001c0001t0001g0237 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-50+32026C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48338847 | ||||||
| chr10:48339085
|
A | T | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+32264A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48339085 | ||||||
| chr10:48339111
|
T | A | 226 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(223): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.-50+32290T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48339111 | ||||||
| chr10:48339131
|
C | T | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-50+32310C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48339131 | ||||||
| chr10:48339290
|
C | T | 1 | a0001c0001t0016g0269 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-50+32469C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48339290 | ||||||
| chr10:48339332
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-50+32511G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48339332 | ||||||
| chr10:48339504
|
T | C | 3 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0025g0114 | 3 | HG02451.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-50+32683T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48339504 | ||||||
| chr10:48339510
|
G | A | 1 | a0001c0001t0018g0096 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-50+32689G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48339510 | ||||||
| chr10:48339727
|
G | A | 7 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(4): Show | 7 | HG00735.hp2 HG02280.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50+32906G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48339727 | ||||||
| chr10:48339808
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-50+32987A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48339808 | ||||||
| chr10:48339986
|
T | G | 1 | a0001c0001t0007g0094 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-50+33165T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48339986 | ||||||
| chr10:48340180
|
G | C | 3 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281 | 3 | HG03098.hp1 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-50+33359G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48340180 | ||||||
| chr10:48340219
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-50+33398A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48340219 | ||||||
| chr10:48340235
|
T | C | 2 | a0001c0001t0016g0269a0001c0001t0016g0270 | 2 | HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-50+33414T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48340235 | ||||||
| chr10:48340497
|
A | T | 1 | a0001c0001t0002g0032 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-50+33676A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48340497 | ||||||
| chr10:48340515
|
C | G | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+33694C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48340515 | ||||||
| chr10:48340527
|
CT | C | 9 | a0001c0001t0003g0286a0001c0001t0003g0293a0001c0001t0008g0008others(6): Show | 9 | HG01123.hp1 HG02109.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-50+33707delT | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48340527 | ||||||
| chr10:48340831
|
C | G | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-50+34010C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48340831 | ||||||
| chr10:48340855
|
G | C | 127 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(124): Show | 127 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.-50+34034G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48340855 | ||||||
| chr10:48340858
|
A | T | 1 | a0001c0001t0001g0243 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-50+34037A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48340858 | ||||||
| chr10:48341085
|
A | G | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-50+34264A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48341085 | ||||||
| chr10:48341103
|
A | G | 1 | a0001c0001t0004g0160 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-50+34282A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48341103 | ||||||
| chr10:48341197
|
C | T | 16 | a0001c0001t0007g0085a0001c0001t0007g0087a0001c0001t0007g0088others(13): Show | 16 | HG01167.hp1 HG01891.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.-50+34376C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48341197 | ||||||
| chr10:48341211
|
G | A | 143 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(140): Show | 143 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.-50+34390G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48341211 | ||||||
| chr10:48341360
|
A | G | 143 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(140): Show | 143 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.-50+34539A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48341360 | ||||||
| chr10:48341415
|
C | T | 1 | a0001c0001t0032g0161 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-50+34594C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48341415 | ||||||
| chr10:48341417
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-50+34596C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48341417 | ||||||
| chr10:48341500
|
A | G | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp2 HG02165.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+34679A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48341500 | ||||||
| chr10:48341607
|
T | A | 19 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(16): Show | 19 | HG00735.hp2 HG02055.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-50+34786T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48341607 | ||||||
| chr10:48341610
|
G | A | 3 | a0001c0001t0010g0227a0001c0001t0018g0095a0001c0001t0018g0096 | 3 | HG01123.hp1 HG02976.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-50+34789G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48341610 | ||||||
| chr10:48341653
|
G | A | 1 | a0001c0001t0016g0270 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-50+34832G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48341653 | ||||||
| chr10:48341915
|
A | G | 2 | a0001c0001t0018g0095a0001c0001t0018g0096 | 2 | HG01123.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-50+35094A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48341915 | ||||||
| chr10:48342066
|
A | G | 2 | a0001c0001t0016g0269a0001c0001t0016g0270 | 2 | HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-50+35245A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48342066 | ||||||
| chr10:48342083
|
G | A | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+35262G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48342083 | ||||||
| chr10:48342085
|
A | T | 19 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(16): Show | 19 | HG00735.hp2 HG02055.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-50+35264A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48342085 | ||||||
| chr10:48342162
|
G | C | 4 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0020others(1): Show | 4 | NA18961.hp1 NA18983.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+35341G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48342162 | ||||||
| chr10:48342200
|
C | T | 9 | a0001c0001t0003g0103a0001c0001t0003g0104a0001c0001t0003g0105others(6): Show | 9 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-50+35379C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48342200 | ||||||
| chr10:48342294
|
A | G | 2 | a0001c0001t0019g0282a0001c0001t0019g0283 | 2 | HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.-50+35473A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48342294 | ||||||
| chr10:48342596
|
A | G | 1 | a0001c0001t0021g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-50+35775A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48342596 | ||||||
| chr10:48342651
|
A | T | 143 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(140): Show | 143 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.-50+35830A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48342651 | ||||||
| chr10:48342697
|
A | C | 13 | a0001c0001t0004g0003a0001c0001t0004g0148a0001c0001t0004g0149others(10): Show | 14 | HG00099.hp1 HG00609.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.-50+35876A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48342697 | ||||||
| chr10:48342731
|
G | A | 1 | a0001c0001t0002g0056 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-50+35910G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48342731 | ||||||
| chr10:48342892
|
G | C | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+36071G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48342892 | ||||||
| chr10:48342942
|
A | G | 9 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(6): Show | 9 | HG01070.hp2 HG01167.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.-50+36121A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48342942 | ||||||
| chr10:48343517
|
A | G | 219 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.-50+36696A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48343517 | ||||||
| chr10:48343531
|
A | G | 2 | a0001c0001t0018g0095a0001c0001t0018g0096 | 2 | HG01123.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-50+36710A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48343531 | ||||||
| chr10:48343552
|
A | G | 28 | a0001c0001t0004g0003a0001c0001t0004g0115a0001c0001t0004g0116others(25): Show | 29 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.-50+36731A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48343552 | ||||||
| chr10:48343615
|
T | A | 219 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.-50+36794T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48343615 | ||||||
| chr10:48343641
|
G | A | 1 | a0001c0001t0009g0231 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-50+36820G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48343641 | ||||||
| chr10:48343660
|
A | T | 22 | a0001c0001t0004g0003a0001c0001t0004g0115a0001c0001t0004g0116others(19): Show | 23 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.-50+36839A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48343660 | ||||||
| chr10:48343708
|
T | C | 2 | a0001c0001t0003g0284a0001c0001t0003g0285 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-50+36887T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48343708 | ||||||
| chr10:48343736
|
A | G | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+36915A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48343736 | ||||||
| chr10:48343741
|
T | C | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp2 HG02165.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+36920T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48343741 | ||||||
| chr10:48344075
|
A | T | 1 | a0001c0001t0006g0262 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-50+37254A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48344075 | ||||||
| chr10:48344175
|
A | G | 219 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.-50+37354A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48344175 | ||||||
| chr10:48344380
|
G | T | 1 | a0001c0001t0002g0084 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-50+37559G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48344380 | ||||||
| chr10:48344407
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-50+37586C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48344407 | ||||||
| chr10:48344761
|
G | T | 2 | a0001c0001t0001g0119a0001c0001t0015g0121 | 2 | HG02602.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-50+37940G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48344761 | ||||||
| chr10:48344801
|
A | G | 1 | a0001c0001t0004g0143 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-50+37980A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48344801 | ||||||
| chr10:48345000
|
T | A | 1 | a0001c0001t0019g0283 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-50+38179T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48345000 | ||||||
| chr10:48345074
|
C | T | 1 | a0001c0001t0006g0252 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-50+38253C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48345074 | ||||||
| chr10:48345172
|
G | A | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-50+38351G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48345172 | ||||||
| chr10:48345492
|
T | A | 2 | a0001c0001t0007g0085a0001c0001t0007g0092 | 2 | HG03688.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-50+38671T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48345492 | ||||||
| chr10:48345644
|
A | G | 1 | a0001c0001t0001g0191 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-50+38823A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48345644 | ||||||
| chr10:48345724
|
C | T | 2 | a0001c0001t0004g0145a0001c0001t0004g0146 | 2 | HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-50+38903C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48345724 | ||||||
| chr10:48345945
|
A | C | 21 | a0001c0001t0004g0003a0001c0001t0004g0115a0001c0001t0004g0116others(18): Show | 22 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.-50+39124A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48345945 | ||||||
| chr10:48346062
|
G | A | 1 | a0001c0001t0007g0091 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-50+39241G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48346062 | ||||||
| chr10:48346082
|
G | T | 229 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(226): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.-50+39261G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48346082 | ||||||
| chr10:48346148
|
G | A | 2 | a0001c0001t0009g0180a0001c0001t0009g0196 | 2 | HG01884.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.-50+39327G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48346148 | ||||||
| chr10:48346372
|
G | A | 2 | a0001c0001t0001g0184a0001c0001t0001g0205 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-50+39551G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48346372 | ||||||
| chr10:48346468
|
G | A | 1 | a0001c0001t0006g0251 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-50+39647G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48346468 | ||||||
| chr10:48346499
|
T | C | 3 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281 | 3 | HG03098.hp1 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-50+39678T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48346499 | ||||||
| chr10:48346549
|
A | G | 211 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(208): Show | 212 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.-50+39728A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48346549 | ||||||
| chr10:48346551
|
G | T | 3 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281 | 3 | HG03098.hp1 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-50+39730G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48346551 | ||||||
| chr10:48346554
|
G | T | 1 | a0001c0001t0001g0247 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-50+39733G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48346554 | ||||||
| chr10:48346565
|
C | T | 127 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(124): Show | 127 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.-50+39744C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48346565 | ||||||
| chr10:48346639
|
C | G | 2 | a0001c0001t0004g0144a0001c0001t0004g0147 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-50+39818C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48346639 | ||||||
| chr10:48346641
|
A | G | 225 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(222): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.-50+39820A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48346641 | ||||||
| chr10:48346815
|
TTCTCTGT others(10): Show |
T | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG02615.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-50+40018_-50+4003 others(21): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48346815 | |||||
| chr10:48346831
|
C | T | 2 | a0001c0001t0003g0284a0001c0001t0003g0285 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-50+40010C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48346831 | ||||||
| chr10:48346875
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-50+40054A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48346875 | ||||||
| chr10:48347016
|
C | T | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+40195C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48347016 | ||||||
| chr10:48347018
|
C | T | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-50+40197C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48347018 | ||||||
| chr10:48347100
|
G | A | 1 | a0001c0001t0018g0095 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-50+40279G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48347100 | ||||||
| chr10:48347105
|
C | T | 16 | a0001c0001t0007g0085a0001c0001t0007g0087a0001c0001t0007g0088others(13): Show | 16 | HG01167.hp1 HG01891.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.-50+40284C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48347105 | ||||||
| chr10:48347106
|
G | T | 7 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(4): Show | 7 | HG00735.hp2 HG02280.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50+40285G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48347106 | ||||||
| chr10:48347268
|
A | G | 1 | a0001c0001t0022g0133 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-50+40447A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48347268 | ||||||
| chr10:48347291
|
A | G | 1 | a0001c0001t0006g0263 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-50+40470A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48347291 | ||||||
| chr10:48347404
|
T | C | 7 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(4): Show | 7 | HG00735.hp2 HG02280.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50+40583T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48347404 | ||||||
| chr10:48347505
|
G | A | 1 | a0001c0001t0002g0083 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-50+40684G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48347505 | ||||||
| chr10:48347512
|
A | G | 1 | a0001c0001t0003g0097 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-50+40691A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48347512 | ||||||
| chr10:48347745
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-50+40924G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48347745 | ||||||
| chr10:48347950
|
C | G | 2 | a0001c0001t0003g0284a0001c0001t0003g0285 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-50+41129C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48347950 | ||||||
| chr10:48348196
|
A | C | 2 | a0001c0001t0004g0145a0001c0001t0004g0146 | 2 | HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-50+41375A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48348196 | ||||||
| chr10:48348199
|
A | C | 16 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(13): Show | 16 | HG00735.hp2 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-50+41378A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48348199 | ||||||
| chr10:48348199
|
A | T | 3 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0025g0114 | 3 | HG02451.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-50+41378A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48348199 | ||||||
| chr10:48348241
|
T | G | 3 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0025g0114 | 3 | HG02451.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-50+41420T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48348241 | ||||||
| chr10:48348325
|
C | T | 1 | a0001c0001t0003g0099 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-50+41504C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48348325 | ||||||
| chr10:48348326
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-50+41505G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48348326 | ||||||
| chr10:48348342
|
A | G | 1 | a0001c0001t0006g0159 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-50+41521A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48348342 | ||||||
| chr10:48348362
|
CTTTTGCT others(21): Show |
C | 1 | a0001c0001t0006g0253 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-50+41542_-50+4156 others(32): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48348362 | ||||||
| chr10:48348591
|
A | G | 5 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0010others(2): Show | 5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+41770A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48348591 | ||||||
| chr10:48348646
|
C | G | 2 | a0001c0001t0001g0173a0001c0001t0023g0176 | 2 | HG03130.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-50+41825C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48348646 | ||||||
| chr10:48348791
|
T | C | 1 | a0001c0001t0006g0255 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-50+41970T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48348791 | ||||||
| chr10:48348822
|
A | G | 127 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(124): Show | 127 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.-50+42001A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48348822 | ||||||
| chr10:48348950
|
CA | C | 160 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0123others(157): Show | 160 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.-50+42143delA | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48348950 | |||||
| chr10:48349052
|
G | A | 2 | a0001c0001t0001g0184a0001c0001t0001g0205 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-50+42231G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48349052 | ||||||
| chr10:48349067
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-50+42246A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48349067 | ||||||
| chr10:48349179
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-50+42358G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48349179 | ||||||
| chr10:48349205
|
T | C | 23 | a0001c0001t0004g0003a0001c0001t0004g0115a0001c0001t0004g0116others(20): Show | 24 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.-50+42384T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48349205 | ||||||
| chr10:48349480
|
A | T | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-50+42659A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48349480 | ||||||
| chr10:48349725
|
C | T | 127 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(124): Show | 127 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.-50+42904C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48349725 | ||||||
| chr10:48349803
|
A | C | 13 | a0001c0001t0007g0087a0001c0001t0007g0088a0001c0001t0007g0089others(10): Show | 13 | HG01167.hp1 HG01891.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-50+42982A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48349803 | ||||||
| chr10:48349894
|
A | G | 9 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(6): Show | 9 | HG01891.hp1 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-50+43073A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48349894 | ||||||
| chr10:48349900
|
A | T | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+43079A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48349900 | ||||||
| chr10:48349925
|
T | C | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-50+43104T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48349925 | ||||||
| chr10:48350044
|
A | G | 5 | a0001c0001t0009g0180a0001c0001t0009g0196a0001c0001t0009g0231others(2): Show | 5 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.-50+43223A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48350044 | ||||||
| chr10:48350130
|
C | T | 1 | a0001c0001t0030g0272 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-50+43309C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48350130 | ||||||
| chr10:48350272
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-50+43451G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48350272 | ||||||
| chr10:48350771
|
A | G | 1 | a0001c0001t0007g0092 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-50+43950A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48350771 | ||||||
| chr10:48350918
|
G | A | 3 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0025g0114 | 3 | HG02451.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-50+44097G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48350918 | ||||||
| chr10:48350930
|
A | G | 2 | a0001c0001t0016g0269a0001c0001t0016g0270 | 2 | HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-50+44109A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48350930 | ||||||
| chr10:48350988
|
A | G | 226 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(223): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.-50+44167A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48350988 | ||||||
| chr10:48351210
|
C | G | 1 | a0001c0001t0022g0133 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-50+44389C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48351210 | ||||||
| chr10:48351272
|
A | AT | 12 | a0001c0001t0002g0034a0001c0001t0002g0047a0001c0001t0003g0285others(9): Show | 12 | HG01123.hp1 HG01261.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-50+44469dupT | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48351272 | |||||
| chr10:48351272
|
A | ATT | 73 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(70): Show | 74 | HG00099.hp1 HG00609.hp2 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.-50+44468_-50+4446 others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48351272 | |||||
| chr10:48351272
|
A | ATTT | 21 | a0001c0001t0001g0163a0001c0001t0003g0284a0001c0001t0003g0286others(18): Show | 21 | HG01167.hp1 HG01891.hp2 HG02622.hp1 others(18): Show |
intron_variant | MODIFIER | c.-50+44467_-50+4446 others(7): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48351272 | |||||
| chr10:48351272
|
A | ATTTT | 105 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(102): Show | 105 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.-50+44466_-50+4446 others(8): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48351272 | |||||
| chr10:48351272
|
A | ATTTTT | 21 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0136others(18): Show | 21 | HG01884.hp1 HG01891.hp1 HG01978.hp1 others(18): Show |
intron_variant | MODIFIER | c.-50+44465_-50+4446 others(9): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48351272 | |||||
| chr10:48351355
|
A | G | 23 | a0001c0001t0004g0003a0001c0001t0004g0115a0001c0001t0004g0116others(20): Show | 24 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.-50+44534A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48351355 | ||||||
| chr10:48351490
|
A | G | 1 | a0001c0001t0007g0295 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-50+44669A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48351490 | ||||||
| chr10:48351506
|
C | T | 1 | a0001c0001t0030g0272 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-50+44685C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48351506 | ||||||
| chr10:48351582
|
A | T | 5 | a0001c0001t0002g0059a0001c0001t0011g0004a0001c0001t0011g0005others(2): Show | 5 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-50+44761A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48351582 | ||||||
| chr10:48351614
|
A | C | 1 | a0001c0001t0002g0002 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-50+44793A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48351614 | ||||||
| chr10:48352034
|
A | G | 3 | a0001c0001t0012g0066a0001c0001t0012g0067a0001c0001t0012g0068 | 3 | NA18998.hp1 NA19066.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-50+45213A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48352034 | ||||||
| chr10:48352111
|
A | C | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+45290A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48352111 | ||||||
| chr10:48352415
|
A | T | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+45594A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48352415 | ||||||
| chr10:48352464
|
T | G | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp2 HG02165.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+45643T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48352464 | ||||||
| chr10:48352685
|
C | A | 20 | a0001c0001t0006g0086a0001c0001t0006g0250a0001c0001t0006g0251others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.-50+45864C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48352685 | ||||||
| chr10:48352841
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-50+46020C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48352841 | ||||||
| chr10:48352884
|
C | G | 1 | a0001c0001t0003g0286 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-50+46063C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48352884 | ||||||
| chr10:48352959
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-50+46138C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48352959 | ||||||
| chr10:48353003
|
T | TA | 11 | a0001c0001t0001g0129a0001c0001t0001g0191a0001c0001t0003g0286others(8): Show | 11 | HG02165.hp2 HG02486.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.-50+46191dupA | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48353003 | |||||
| chr10:48353052
|
G | A | 5 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0010others(2): Show | 5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+46231G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48353052 | ||||||
| chr10:48353071
|
A | G | 5 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(2): Show | 5 | HG02630.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-50+46250A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48353071 | ||||||
| chr10:48353198
|
A | C | 1 | a0001c0004t0001g0171 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-50+46377A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48353198 | ||||||
| chr10:48353201
|
T | A | 1 | a0001c0004t0001g0171 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-50+46380T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48353201 | ||||||
| chr10:48353325
|
A | G | 1 | a0001c0001t0002g0060 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-50+46504A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48353325 | ||||||
| chr10:48353366
|
T | C | 1 | a0001c0001t0002g0022 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-50+46545T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48353366 | ||||||
| chr10:48353649
|
A | T | 1 | a0001c0001t0002g0052 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-50+46828A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48353649 | ||||||
| chr10:48353671
|
A | G | 2 | a0001c0001t0001g0173a0001c0001t0011g0007 | 2 | HG01884.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-50+46850A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48353671 | ||||||
| chr10:48353747
|
A | C | 3 | a0001c0001t0006g0250a0001c0001t0006g0253a0001c0001t0006g0254 | 3 | HG01168.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-50+46926A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48353747 | ||||||
| chr10:48353875
|
T | C | 1 | a0001c0001t0007g0091 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-50+47054T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48353875 | ||||||
| chr10:48354094
|
G | T | 1 | a0001c0001t0007g0298 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-50+47273G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48354094 | ||||||
| chr10:48354155
|
TAA | T | 9 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(6): Show | 9 | HG01891.hp1 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-50+47342_-50+4734 others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48354155 | |||||
| chr10:48354164
|
A | T | 1 | a0001c0001t0002g0034 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-50+47343A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48354164 | ||||||
| chr10:48354165
|
T | A | 11 | a0001c0001t0003g0103a0001c0001t0003g0104a0001c0001t0003g0105others(8): Show | 11 | HG01123.hp1 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-50+47344T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48354165 | ||||||
| chr10:48354171
|
T | A | 1 | a0001c0001t0004g0160 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-50+47350T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48354171 | ||||||
| chr10:48354205
|
C | A | 4 | a0001c0001t0001g0120a0001c0001t0001g0126a0001c0001t0013g0118others(1): Show | 4 | HG01070.hp2 HG01168.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+47384C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48354205 | ||||||
| chr10:48354334
|
G | A | 1 | a0001c0001t0001g0239 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-49-47278G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48354334 | ||||||
| chr10:48354375
|
G | A | 23 | a0001c0001t0004g0003a0001c0001t0004g0115a0001c0001t0004g0116others(20): Show | 24 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.-49-47237G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48354375 | ||||||
| chr10:48354393
|
G | A | 4 | a0001c0001t0001g0239a0001c0001t0001g0246a0001c0001t0001g0247others(1): Show | 4 | HG00408.hp2 HG02040.hp1 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-47219G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48354393 | ||||||
| chr10:48354424
|
A | C | 1 | a0001c0001t0006g0255 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-49-47188A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48354424 | ||||||
| chr10:48354531
|
A | T | 142 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(139): Show | 142 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-49-47081A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48354531 | ||||||
| chr10:48354702
|
A | C | 6 | a0001c0001t0003g0293a0001c0001t0008g0008a0001c0001t0008g0009others(3): Show | 6 | HG02109.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49-46910A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48354702 | ||||||
| chr10:48354729
|
A | AT | 23 | a0001c0001t0004g0003a0001c0001t0004g0115a0001c0001t0004g0116others(20): Show | 24 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.-49-46879dupT | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48354729 | |||||
| chr10:48354793
|
T | TA | 15 | a0001c0001t0007g0087a0001c0001t0007g0088a0001c0001t0007g0089others(12): Show | 15 | HG01167.hp1 HG01891.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.-49-46809dupA | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48354793 | |||||
| chr10:48354804
|
C | A | 197 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(194): Show | 197 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.-49-46808C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48354804 | ||||||
| chr10:48354860
|
G | A | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-46752G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48354860 | ||||||
| chr10:48355147
|
C | A | 31 | a0001c0001t0002g0001a0001c0001t0002g0022a0001c0001t0002g0024others(28): Show | 32 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.-49-46465C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48355147 | ||||||
| chr10:48355177
|
T | C | 5 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(2): Show | 5 | HG02630.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-46435T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48355177 | ||||||
| chr10:48355247
|
C | T | 126 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(123): Show | 126 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.-49-46365C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48355247 | ||||||
| chr10:48355273
|
G | T | 1 | a0001c0001t0001g0191 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-49-46339G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48355273 | ||||||
| chr10:48355329
|
G | T | 3 | a0001c0001t0003g0286a0001c0001t0018g0095a0001c0001t0018g0096 | 3 | HG01123.hp1 HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-49-46283G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48355329 | ||||||
| chr10:48355425
|
C | T | 21 | a0001c0001t0001g0206a0001c0001t0006g0086a0001c0001t0006g0250others(18): Show | 21 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.-49-46187C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48355425 | ||||||
| chr10:48355508
|
C | CA | 20 | a0001c0001t0001g0120a0001c0001t0002g0033a0001c0001t0003g0097others(17): Show | 20 | HG00735.hp2 HG01070.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-49-46087dupA | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48355508 | |||||
| chr10:48355508
|
C | CAA | 139 | a0001c0001t0001g0119a0001c0001t0001g0122a0001c0001t0001g0123others(136): Show | 139 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.-49-46088_-49-4608 others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48355508 | |||||
| chr10:48355890
|
A | G | 22 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(19): Show | 22 | HG00735.hp2 HG01123.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.-49-45722A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48355890 | ||||||
| chr10:48355915
|
G | A | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-49-45697G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48355915 | ||||||
| chr10:48356077
|
G | GT | 127 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(124): Show | 127 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.-49-45534dupT | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48356077 | |||||
| chr10:48356100
|
A | G | 1 | a0001c0001t0006g0255 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-49-45512A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48356100 | ||||||
| chr10:48356176
|
A | G | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-49-45436A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48356176 | ||||||
| chr10:48356198
|
G | A | 1 | a0001c0001t0010g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-49-45414G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48356198 | ||||||
| chr10:48356443
|
G | A | 1 | a0001c0004t0001g0171 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-49-45169G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48356443 | ||||||
| chr10:48356473
|
A | T | 1 | a0001c0001t0001g0242 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-49-45139A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48356473 | ||||||
| chr10:48356534
|
A | T | 1 | a0001c0001t0007g0295 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-49-45078A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48356534 | ||||||
| chr10:48356556
|
A | G | 1 | a0001c0001t0007g0089 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-49-45056A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48356556 | ||||||
| chr10:48356645
|
C | A | 1 | a0001c0001t0001g0130 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-49-44967C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48356645 | ||||||
| chr10:48356670
|
C | T | 1 | a0001c0001t0030g0272 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-49-44942C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48356670 | ||||||
| chr10:48356805
|
A | G | 19 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(16): Show | 19 | HG00735.hp2 HG02055.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-49-44807A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48356805 | ||||||
| chr10:48356841
|
C | CA | 7 | a0001c0001t0001g0247a0001c0001t0002g0016a0001c0001t0002g0058others(4): Show | 7 | HG02040.hp1 HG02109.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49-44732dupA | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48356841 | |||||
| chr10:48356841
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0002g0059 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-49-44742_-49-4473 others(15): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48356841 | |||||
| chr10:48356841
|
C | CAAAAAAA others(6): Show |
2 | a0001c0001t0002g0060a0001c0001t0026g0035 | 2 | HG02602.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-49-44744_-49-4473 others(17): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48356841 | |||||
| chr10:48356841
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0002g0034 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-49-44745_-49-4473 others(18): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48356841 | |||||
| chr10:48356841
|
CA | C | 24 | a0001c0001t0001g0126a0001c0001t0001g0130a0001c0001t0001g0132others(21): Show | 25 | HG00609.hp1 HG02109.hp2 HG02155.hp1 others(22): Show |
intron_variant | MODIFIER | c.-49-44732delA | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48356841 | |||||
| chr10:48356841
|
CAA | C | 32 | a0001c0001t0001g0129a0001c0001t0001g0138a0001c0001t0001g0139others(29): Show | 32 | HG00408.hp1 HG00544.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.-49-44733_-49-4473 others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48356841 | |||||
| chr10:48356841
|
CAAA | C | 32 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(29): Show | 32 | HG00423.hp2 HG01070.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.-49-44734_-49-4473 others(7): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48356841 | |||||
| chr10:48356841
|
CAAAA | C | 41 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0163others(38): Show | 41 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.-49-44735_-49-4473 others(8): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48356841 | |||||
| chr10:48356841
|
CAAAAAAA others(3): Show |
C | 6 | a0001c0001t0001g0213a0001c0001t0002g0053a0001c0001t0002g0054others(3): Show | 6 | HG01515.hp1 HG01517.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.-49-44741_-49-4473 others(14): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48356841 | |||||
| chr10:48356841
|
CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0002g0052a0001c0001t0016g0269a0001c0001t0016g0270 | 3 | HG00544.hp1 HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-49-44743_-49-4473 others(16): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48356841 | |||||
| chr10:48356841
|
CAAAAAAA others(6): Show |
C | 3 | a0001c0001t0003g0286a0001c0001t0018g0095a0001c0001t0018g0096 | 3 | HG01123.hp1 HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-49-44744_-49-4473 others(17): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48356841 | |||||
| chr10:48356841
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0002g0028 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-49-44745_-49-4473 others(18): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48356841 | |||||
| chr10:48356841
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0239 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-49-44746_-49-4473 others(19): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48356841 | |||||
| chr10:48356841
|
CAAAAAAA others(9): Show |
C | 4 | a0001c0001t0004g0143a0001c0001t0004g0156a0001c0001t0004g0160others(1): Show | 4 | HG03041.hp1 HG04184.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-44747_-49-4473 others(20): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48356841 | |||||
| chr10:48356841
|
CAAAAAAA others(10): Show |
C | 39 | a0001c0001t0004g0003a0001c0001t0004g0115a0001c0001t0004g0116others(36): Show | 40 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.-49-44748_-49-4473 others(21): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48356841 | |||||
| chr10:48356841
|
CAAAAAAA others(11): Show |
C | 24 | a0001c0001t0002g0072a0001c0001t0003g0279a0001c0001t0003g0280others(21): Show | 24 | HG00735.hp1 HG01106.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.-49-44749_-49-4473 others(22): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48356841 | |||||
| chr10:48356841
|
CAAAAAAA others(12): Show |
C | 1 | a0001c0001t0006g0262 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-49-44750_-49-4473 others(23): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48356841 | |||||
| chr10:48356841
|
CAAAAAAA others(13): Show |
C | 5 | a0001c0001t0001g0237a0001c0001t0003g0097a0001c0001t0003g0100others(2): Show | 5 | HG02258.hp1 HG02451.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-44751_-49-4473 others(24): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48356841 | |||||
| chr10:48356841
|
CAAAAAAA others(14): Show |
C | 16 | a0001c0001t0003g0098a0001c0001t0003g0099a0001c0001t0003g0101others(13): Show | 16 | HG00735.hp2 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-49-44752_-49-4473 others(25): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48356841 | |||||
| chr10:48356899
|
C | CA | 15 | a0001c0001t0001g0162a0001c0001t0001g0169a0001c0001t0001g0197others(12): Show | 15 | HG00735.hp2 HG02165.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.-49-44694dupA | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48356899 | |||||
| chr10:48356899
|
CA | C | 31 | a0001c0001t0001g0127a0001c0001t0001g0183a0001c0001t0003g0279others(28): Show | 31 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.-49-44694delA | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48356899 | |||||
| chr10:48357002
|
TG | T | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0170others(1): Show | 4 | HG02559.hp2 HG02615.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-44609delG | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48357002 | ||||||
| chr10:48357023
|
G | C | 1 | a0001c0001t0002g0036 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-49-44589G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48357023 | ||||||
| chr10:48357188
|
C | G | 20 | a0001c0001t0006g0086a0001c0001t0006g0250a0001c0001t0006g0251others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.-49-44424C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48357188 | ||||||
| chr10:48357357
|
G | A | 7 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(4): Show | 7 | HG00735.hp2 HG02280.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49-44255G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48357357 | ||||||
| chr10:48357709
|
T | A | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp2 HG02165.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49-43903T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48357709 | ||||||
| chr10:48357845
|
C | T | 16 | a0001c0001t0002g0045a0001c0001t0004g0145a0001c0001t0004g0146others(13): Show | 16 | HG01167.hp1 HG01891.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.-49-43767C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48357845 | ||||||
| chr10:48357943
|
T | G | 220 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.-49-43669T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48357943 | ||||||
| chr10:48358116
|
T | C | 1 | a0001c0001t0011g0005 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-49-43496T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48358116 | ||||||
| chr10:48358342
|
A | C | 2 | a0001c0001t0016g0269a0001c0001t0016g0270 | 2 | HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-49-43270A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48358342 | ||||||
| chr10:48358345
|
A | G | 2 | a0001c0001t0005g0027a0001c0001t0005g0031 | 2 | HG00597.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.-49-43267A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48358345 | ||||||
| chr10:48358933
|
G | A | 26 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(23): Show | 26 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.-49-42679G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48358933 | ||||||
| chr10:48359516
|
T | C | 9 | a0001c0001t0003g0103a0001c0001t0003g0104a0001c0001t0003g0105others(6): Show | 9 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-49-42096T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48359516 | ||||||
| chr10:48359746
|
G | A | 21 | a0001c0001t0006g0086a0001c0001t0006g0159a0001c0001t0006g0250others(18): Show | 21 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.-49-41866G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48359746 | ||||||
| chr10:48359748
|
A | G | 5 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0010others(2): Show | 5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49-41864A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48359748 | ||||||
| chr10:48359946
|
G | A | 16 | a0001c0001t0007g0085a0001c0001t0007g0087a0001c0001t0007g0088others(13): Show | 16 | HG01167.hp1 HG01891.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.-49-41666G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48359946 | ||||||
| chr10:48359993
|
A | G | 1 | a0001c0001t0005g0031 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-49-41619A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48359993 | ||||||
| chr10:48360012
|
T | C | 1 | a0001c0001t0004g0116 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-49-41600T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48360012 | ||||||
| chr10:48360021
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-49-41591A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48360021 | ||||||
| chr10:48360035
|
C | T | 142 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(139): Show | 142 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-49-41577C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48360035 | ||||||
| chr10:48360143
|
G | C | 3 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0025g0114 | 3 | HG02451.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-49-41469G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48360143 | ||||||
| chr10:48360236
|
A | C | 2 | a0001c0001t0006g0250a0001c0001t0006g0254 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-49-41376A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48360236 | ||||||
| chr10:48360341
|
A | G | 7 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(4): Show | 7 | HG00735.hp2 HG02280.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49-41271A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48360341 | ||||||
| chr10:48360346
|
A | G | 3 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0025g0114 | 3 | HG02451.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-49-41266A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48360346 | ||||||
| chr10:48360374
|
G | T | 1 | a0001c0001t0006g0264 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-49-41238G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48360374 | ||||||
| chr10:48360849
|
T | C | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-40763T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48360849 | ||||||
| chr10:48361078
|
G | A | 3 | a0001c0001t0007g0085a0001c0001t0007g0092a0001c0001t0007g0093 | 3 | HG03688.hp2 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-49-40534G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48361078 | ||||||
| chr10:48361571
|
T | G | 1 | a0001c0001t0008g0012 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-49-40041T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48361571 | ||||||
| chr10:48361687
|
C | T | 18 | a0001c0001t0004g0003a0001c0001t0004g0143a0001c0001t0004g0144others(15): Show | 19 | HG00099.hp1 HG00609.hp2 HG02071.hp2 others(16): Show |
intron_variant | MODIFIER | c.-49-39925C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48361687 | ||||||
| chr10:48361745
|
G | C | 145 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(142): Show | 145 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.-49-39867G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48361745 | ||||||
| chr10:48361745
|
G | T | 26 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(23): Show | 26 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.-49-39867G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48361745 | ||||||
| chr10:48362018
|
T | G | 1 | a0001c0001t0001g0273 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-49-39594T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48362018 | ||||||
| chr10:48362085
|
C | T | 1 | a0001c0001t0007g0089 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-49-39527C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48362085 | ||||||
| chr10:48362176
|
T | G | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-39436T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48362176 | ||||||
| chr10:48362323
|
A | G | 5 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0010others(2): Show | 5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49-39289A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48362323 | ||||||
| chr10:48362361
|
C | G | 5 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(2): Show | 5 | HG02630.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-39251C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48362361 | ||||||
| chr10:48362502
|
G | A | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-49-39110G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48362502 | ||||||
| chr10:48362559
|
G | A | 9 | a0001c0001t0003g0103a0001c0001t0003g0104a0001c0001t0003g0105others(6): Show | 9 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-49-39053G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48362559 | ||||||
| chr10:48362737
|
G | GT | 7 | a0001c0001t0002g0056a0001c0001t0002g0069a0001c0001t0005g0026others(4): Show | 7 | HG01934.hp1 HG02055.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-49-38855dupT | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48362737 | |||||
| chr10:48362737
|
GT | G | 197 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(194): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.-49-38855delT | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48362737 | |||||
| chr10:48362801
|
C | T | 27 | a0001c0001t0001g0206a0001c0001t0003g0279a0001c0001t0003g0280others(24): Show | 27 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.-49-38811C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48362801 | ||||||
| chr10:48362933
|
G | T | 27 | a0001c0001t0001g0206a0001c0001t0003g0279a0001c0001t0003g0280others(24): Show | 27 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.-49-38679G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48362933 | ||||||
| chr10:48362960
|
C | G | 1 | a0001c0001t0030g0272 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-49-38652C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48362960 | ||||||
| chr10:48362966
|
C | T | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0004t0001g0171 | 3 | HG01515.hp2 HG01981.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.-49-38646C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48362966 | ||||||
| chr10:48363048
|
T | C | 1 | a0001c0001t0007g0088 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-49-38564T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48363048 | ||||||
| chr10:48363067
|
C | T | 2 | a0001c0001t0018g0095a0001c0001t0018g0096 | 2 | HG01123.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-49-38545C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48363067 | ||||||
| chr10:48363142
|
G | A | 29 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(26): Show | 29 | HG00099.hp2 HG00280.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.-49-38470G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48363142 | ||||||
| chr10:48363160
|
G | A | 19 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(16): Show | 19 | HG00735.hp2 HG02055.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-49-38452G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48363160 | ||||||
| chr10:48363307
|
C | A | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0004t0001g0171 | 3 | HG01515.hp2 HG01981.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.-49-38305C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48363307 | ||||||
| chr10:48363380
|
C | T | 220 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.-49-38232C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48363380 | ||||||
| chr10:48363463
|
A | G | 21 | a0001c0001t0001g0206a0001c0001t0006g0086a0001c0001t0006g0250others(18): Show | 21 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.-49-38149A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48363463 | ||||||
| chr10:48363649
|
A | G | 2 | a0001c0001t0016g0269a0001c0001t0016g0270 | 2 | HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-49-37963A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48363649 | ||||||
| chr10:48363677
|
A | T | 15 | a0001c0001t0007g0087a0001c0001t0007g0088a0001c0001t0007g0089others(12): Show | 15 | HG01167.hp1 HG01891.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.-49-37935A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48363677 | ||||||
| chr10:48363925
|
A | G | 2 | a0001c0001t0016g0269a0001c0001t0016g0270 | 2 | HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-49-37687A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48363925 | ||||||
| chr10:48364023
|
C | A | 1 | a0001c0001t0001g0162 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-49-37589C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48364023 | ||||||
| chr10:48364055
|
A | T | 1 | a0001c0002t0017g0014 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-49-37557A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48364055 | ||||||
| chr10:48364092
|
C | T | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-49-37520C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48364092 | ||||||
| chr10:48364169
|
A | C | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-37443A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48364169 | ||||||
| chr10:48364333
|
A | G | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-49-37279A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48364333 | ||||||
| chr10:48364347
|
T | C | 1 | a0001c0001t0006g0252 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-49-37265T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48364347 | ||||||
| chr10:48364515
|
A | C | 6 | a0001c0001t0003g0293a0001c0001t0008g0008a0001c0001t0008g0009others(3): Show | 6 | HG02109.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49-37097A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48364515 | ||||||
| chr10:48364552
|
C | T | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0170others(1): Show | 4 | HG02559.hp2 HG02615.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-37060C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48364552 | ||||||
| chr10:48364793
|
A | C | 1 | a0001c0001t0001g0165 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-49-36819A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48364793 | ||||||
| chr10:48364863
|
C | T | 1 | a0001c0001t0001g0271 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-49-36749C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48364863 | ||||||
| chr10:48364900
|
C | T | 1 | a0001c0001t0010g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-49-36712C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48364900 | ||||||
| chr10:48364923
|
A | C | 1 | a0001c0001t0030g0272 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-49-36689A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48364923 | ||||||
| chr10:48365177
|
G | A | 9 | a0001c0001t0003g0103a0001c0001t0003g0104a0001c0001t0003g0105others(6): Show | 9 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-49-36435G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48365177 | ||||||
| chr10:48365228
|
T | G | 1 | a0001c0001t0003g0286 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-49-36384T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48365228 | ||||||
| chr10:48365470
|
G | A | 1 | a0001c0001t0002g0072 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-49-36142G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48365470 | ||||||
| chr10:48365547
|
G | A | 21 | a0001c0001t0001g0206a0001c0001t0006g0086a0001c0001t0006g0250others(18): Show | 21 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.-49-36065G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48365547 | ||||||
| chr10:48365833
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-49-35779G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48365833 | ||||||
| chr10:48366165
|
A | AT | 6 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0126others(3): Show | 6 | HG01070.hp2 HG01168.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49-35439dupT | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48366165 | |||||
| chr10:48366268
|
C | A | 1 | a0001c0001t0004g0153 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-49-35344C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48366268 | ||||||
| chr10:48366279
|
C | G | 3 | a0001c0001t0004g0115a0001c0001t0004g0116a0001c0001t0004g0117 | 3 | HG01069.hp1 HG01099.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-49-35333C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48366279 | ||||||
| chr10:48366378
|
G | A | 1 | a0001c0001t0004g0153 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-49-35234G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48366378 | ||||||
| chr10:48366429
|
G | T | 1 | a0001c0002t0017g0014 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-49-35183G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48366429 | ||||||
| chr10:48366529
|
T | A | 7 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(4): Show | 7 | HG00735.hp2 HG02280.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49-35083T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48366529 | ||||||
| chr10:48366532
|
G | A | 1 | a0001c0001t0004g0152 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-49-35080G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48366532 | ||||||
| chr10:48366725
|
G | A | 220 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.-49-34887G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48366725 | ||||||
| chr10:48366783
|
A | T | 3 | a0001c0001t0003g0286a0001c0001t0018g0095a0001c0001t0018g0096 | 3 | HG01123.hp1 HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-49-34829A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48366783 | ||||||
| chr10:48366819
|
A | G | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-49-34793A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48366819 | ||||||
| chr10:48366878
|
T | A | 1 | a0001c0001t0007g0093 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-49-34734T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48366878 | ||||||
| chr10:48366878
|
TA | T | 7 | a0001c0001t0001g0137a0001c0001t0001g0230a0001c0001t0002g0054others(4): Show | 7 | HG01515.hp1 HG01884.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49-34722delA | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48366878 | |||||
| chr10:48366879
|
A | T | 1 | a0001c0001t0005g0078 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-49-34733A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48366879 | ||||||
| chr10:48367117
|
C | T | 1 | a0001c0001t0012g0066 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-49-34495C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48367117 | ||||||
| chr10:48367238
|
C | T | 13 | a0001c0001t0002g0002a0001c0001t0002g0037a0001c0001t0002g0047others(10): Show | 14 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.-49-34374C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48367238 | ||||||
| chr10:48367252
|
G | C | 1 | a0001c0001t0002g0274 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-49-34360G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48367252 | ||||||
| chr10:48367266
|
T | C | 23 | a0001c0001t0004g0003a0001c0001t0004g0115a0001c0001t0004g0116others(20): Show | 24 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.-49-34346T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48367266 | ||||||
| chr10:48367362
|
G | T | 2 | a0001c0001t0018g0095a0001c0001t0018g0096 | 2 | HG01123.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-49-34250G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48367362 | ||||||
| chr10:48367374
|
AAAAT | A | 17 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(14): Show | 17 | HG00735.hp2 HG02145.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-49-34212_-49-3420 others(8): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48367374 | |||||
| chr10:48367374
|
AAAATAAA others(1): Show |
A | 7 | a0001c0001t0001g0169a0001c0001t0003g0103a0001c0001t0003g0104others(4): Show | 7 | HG02055.hp1 HG02258.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49-34216_-49-3420 others(12): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48367374 | |||||
| chr10:48367374
|
AAAATAAA others(5): Show |
A | 11 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(8): Show | 11 | HG01891.hp1 HG02622.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.-49-34220_-49-3420 others(16): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48367374 | |||||
| chr10:48367453
|
G | T | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-34159G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48367453 | ||||||
| chr10:48367498
|
A | G | 2 | a0001c0001t0010g0227a0001c0001t0010g0229 | 2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-49-34114A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48367498 | ||||||
| chr10:48367545
|
A | G | 9 | a0001c0001t0003g0103a0001c0001t0003g0104a0001c0001t0003g0105others(6): Show | 9 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-49-34067A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48367545 | ||||||
| chr10:48367656
|
A | G | 1 | a0001c0001t0002g0002 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-49-33956A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48367656 | ||||||
| chr10:48367836
|
A | G | 2 | a0001c0001t0005g0070a0001c0001t0027g0025 | 2 | HG04184.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.-49-33776A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48367836 | ||||||
| chr10:48367950
|
G | A | 1 | a0001c0001t0026g0035 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-49-33662G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48367950 | ||||||
| chr10:48367950
|
G | C | 143 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(140): Show | 143 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.-49-33662G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48367950 | ||||||
| chr10:48367968
|
T | C | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG02615.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-49-33644T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48367968 | ||||||
| chr10:48367973
|
C | T | 5 | a0001c0001t0009g0180a0001c0001t0009g0196a0001c0001t0009g0231others(2): Show | 5 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-33639C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48367973 | ||||||
| chr10:48368298
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-49-33314A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48368298 | ||||||
| chr10:48368411
|
C | T | 16 | a0001c0001t0007g0085a0001c0001t0007g0087a0001c0001t0007g0088others(13): Show | 16 | HG01167.hp1 HG01891.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.-49-33201C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48368411 | ||||||
| chr10:48368577
|
T | C | 2 | a0001c0001t0001g0139a0001c0001t0001g0249 | 2 | HG00408.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-49-33035T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48368577 | ||||||
| chr10:48368689
|
T | C | 1 | a0001c0001t0030g0272 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-49-32923T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48368689 | ||||||
| chr10:48368835
|
G | T | 220 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.-49-32777G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48368835 | ||||||
| chr10:48368911
|
A | G | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-32701A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48368911 | ||||||
| chr10:48368978
|
G | T | 7 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(4): Show | 7 | HG00735.hp2 HG02280.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49-32634G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48368978 | ||||||
| chr10:48369069
|
A | C | 1 | a0001c0001t0003g0293 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-49-32543A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48369069 | ||||||
| chr10:48369284
|
T | A | 1 | a0001c0001t0007g0090 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-49-32328T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48369284 | ||||||
| chr10:48369508
|
TAGACCCT others(4): Show |
T | 1 | a0001c0001t0002g0075 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-49-32103_-49-3209 others(15): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48369508 | ||||||
| chr10:48369782
|
C | T | 5 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0010others(2): Show | 5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49-31830C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48369782 | ||||||
| chr10:48369867
|
T | C | 16 | a0001c0001t0007g0085a0001c0001t0007g0087a0001c0001t0007g0088others(13): Show | 16 | HG01167.hp1 HG01891.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.-49-31745T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48369867 | ||||||
| chr10:48369920
|
G | A | 9 | a0001c0001t0003g0103a0001c0001t0003g0104a0001c0001t0003g0105others(6): Show | 9 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-49-31692G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48369920 | ||||||
| chr10:48369993
|
G | A | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-49-31619G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48369993 | ||||||
| chr10:48370233
|
A | C | 1 | a0001c0001t0003g0286 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-49-31379A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48370233 | ||||||
| chr10:48370251
|
G | A | 1 | a0001c0001t0003g0293 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-49-31361G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48370251 | ||||||
| chr10:48370254
|
G | A | 1 | a0001c0001t0005g0019 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-49-31358G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48370254 | ||||||
| chr10:48370308
|
A | G | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-31304A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48370308 | ||||||
| chr10:48370444
|
A | C | 143 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(140): Show | 143 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.-49-31168A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48370444 | ||||||
| chr10:48370470
|
G | A | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-49-31142G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48370470 | ||||||
| chr10:48370496
|
A | G | 19 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(16): Show | 19 | HG00735.hp2 HG02055.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-49-31116A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48370496 | ||||||
| chr10:48370587
|
C | G | 220 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.-49-31025C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48370587 | ||||||
| chr10:48370593
|
C | T | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-31019C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48370593 | ||||||
| chr10:48370986
|
T | C | 1 | a0001c0001t0001g0273 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-49-30626T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48370986 | ||||||
| chr10:48371056
|
G | A | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0170others(1): Show | 4 | HG02559.hp2 HG02615.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-30556G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48371056 | ||||||
| chr10:48371339
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-49-30273C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48371339 | ||||||
| chr10:48371475
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-49-30137G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48371475 | ||||||
| chr10:48371556
|
A | G | 1 | a0001c0001t0003g0101 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-49-30056A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48371556 | ||||||
| chr10:48371713
|
A | T | 220 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.-49-29899A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48371713 | ||||||
| chr10:48371800
|
A | G | 1 | a0001c0001t0001g0212 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-49-29812A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48371800 | ||||||
| chr10:48372038
|
C | G | 1 | a0001c0001t0001g0183 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-49-29574C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48372038 | ||||||
| chr10:48372080
|
T | C | 8 | a0001c0001t0002g0013a0001c0001t0002g0032a0001c0001t0002g0033others(5): Show | 8 | NA18941.hp2 NA18948.hp1 NA18949.hp2 others(5): Show |
intron_variant | MODIFIER | c.-49-29532T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48372080 | ||||||
| chr10:48372249
|
G | A | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp2 HG02165.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49-29363G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48372249 | ||||||
| chr10:48372432
|
A | G | 1 | a0001c0001t0006g0159 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-29180A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48372432 | ||||||
| chr10:48372511
|
C | A | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-29101C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48372511 | ||||||
| chr10:48372591
|
T | C | 5 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0010others(2): Show | 5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49-29021T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48372591 | ||||||
| chr10:48372880
|
G | A | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-28732G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48372880 | ||||||
| chr10:48373128
|
G | T | 2 | a0001c0001t0001g0242a0001c0001t0001g0268 | 2 | HG01975.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.-49-28484G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48373128 | ||||||
| chr10:48373346
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-49-28266A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48373346 | ||||||
| chr10:48373372
|
T | A | 230 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.-49-28240T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48373372 | ||||||
| chr10:48373507
|
G | A | 21 | a0001c0001t0001g0206a0001c0001t0006g0086a0001c0001t0006g0250others(18): Show | 21 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.-49-28105G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48373507 | ||||||
| chr10:48373571
|
C | CA | 114 | a0001c0001t0001g0119a0001c0001t0001g0122a0001c0001t0001g0123others(111): Show | 114 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.-49-28014dupA | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48373571 | |||||
| chr10:48373571
|
C | CAA | 28 | a0001c0001t0001g0126a0001c0001t0001g0130a0001c0001t0001g0131others(25): Show | 28 | HG00423.hp2 HG01109.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.-49-28015_-49-2801 others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48373571 | |||||
| chr10:48373571
|
C | CAAA | 10 | a0001c0001t0001g0226a0001c0001t0006g0159a0001c0001t0006g0251others(7): Show | 10 | HG02145.hp2 HG02451.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.-49-28016_-49-2801 others(7): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48373571 | |||||
| chr10:48373571
|
C | CAAAA | 17 | a0001c0001t0001g0206a0001c0001t0006g0250a0001c0001t0006g0252others(14): Show | 17 | HG01099.hp2 HG01106.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.-49-28017_-49-2801 others(8): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48373571 | |||||
| chr10:48373571
|
C | CAAAAA | 6 | a0001c0001t0001g0292a0001c0001t0006g0086a0001c0001t0006g0253others(3): Show | 6 | HG01168.hp1 HG01255.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49-28018_-49-2801 others(9): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48373571 | |||||
| chr10:48373571
|
C | CAAAAAAA others(2): Show |
6 | a0001c0001t0003g0112a0001c0001t0003g0285a0001c0001t0007g0085others(3): Show | 6 | HG01167.hp1 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-49-28022_-49-2801 others(13): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48373571 | |||||
| chr10:48373571
|
C | CAAAAAAA others(3): Show |
9 | a0001c0001t0003g0104a0001c0001t0007g0087a0001c0001t0007g0088others(6): Show | 9 | HG02622.hp1 HG02647.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-49-28023_-49-2801 others(14): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48373571 | |||||
| chr10:48373571
|
C | CAAAAAAA others(4): Show |
10 | a0001c0001t0003g0103a0001c0001t0003g0105a0001c0001t0003g0109others(7): Show | 10 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-49-28024_-49-2801 others(15): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48373571 | |||||
| chr10:48373571
|
C | CAAAAAAA others(5): Show |
3 | a0001c0001t0003g0108a0001c0001t0003g0279a0001c0001t0003g0280 | 3 | HG03098.hp1 HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-49-28025_-49-2801 others(16): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48373571 | |||||
| chr10:48373571
|
CA | C | 6 | a0001c0001t0002g0028a0001c0001t0002g0029a0001c0001t0002g0041others(3): Show | 6 | HG00423.hp1 HG00558.hp1 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49-28014delA | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48373571 | |||||
| chr10:48373571
|
CAAAAAAA others(2): Show |
C | 9 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(6): Show | 9 | HG00735.hp2 HG01069.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.-49-28022_-49-2801 others(13): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48373571 | |||||
| chr10:48373571
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0025g0114 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-49-28023_-49-2801 others(14): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48373571 | |||||
| chr10:48373571
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0003g0286 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-49-28026_-49-2801 others(17): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48373571 | |||||
| chr10:48373615
|
T | C | 3 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281 | 3 | HG03098.hp1 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-49-27997T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48373615 | ||||||
| chr10:48373736
|
G | A | 5 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0010others(2): Show | 5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49-27876G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48373736 | ||||||
| chr10:48373862
|
A | G | 1 | a0001c0001t0002g0045 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-49-27750A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48373862 | ||||||
| chr10:48373892
|
G | A | 1 | a0001c0001t0001g0291 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-49-27720G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48373892 | ||||||
| chr10:48373944
|
C | T | 2 | a0001c0001t0001g0215a0001c0001t0006g0251 | 2 | HG03491.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.-49-27668C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48373944 | ||||||
| chr10:48374085
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-49-27527G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48374085 | ||||||
| chr10:48374150
|
A | T | 220 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.-49-27462A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48374150 | ||||||
| chr10:48374257
|
A | T | 3 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281 | 3 | HG03098.hp1 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-49-27355A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48374257 | ||||||
| chr10:48374307
|
G | A | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-49-27305G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48374307 | ||||||
| chr10:48374336
|
A | G | 1 | a0001c0001t0001g0211 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-49-27276A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48374336 | ||||||
| chr10:48374556
|
A | G | 127 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(124): Show | 127 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.-49-27056A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48374556 | ||||||
| chr10:48374589
|
A | G | 230 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.-49-27023A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48374589 | ||||||
| chr10:48374774
|
A | G | 4 | a0001c0001t0004g0115a0001c0001t0004g0116a0001c0001t0004g0117others(1): Show | 4 | HG01069.hp1 HG01099.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-26838A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48374774 | ||||||
| chr10:48374887
|
A | G | 18 | a0001c0001t0004g0003a0001c0001t0004g0143a0001c0001t0004g0144others(15): Show | 19 | HG00099.hp1 HG00609.hp2 HG02071.hp2 others(16): Show |
intron_variant | MODIFIER | c.-49-26725A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48374887 | ||||||
| chr10:48374998
|
C | T | 1 | a0001c0001t0004g0116 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-49-26614C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48374998 | ||||||
| chr10:48375030
|
C | G | 1 | a0001c0001t0001g0202 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-49-26582C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48375030 | ||||||
| chr10:48375053
|
CT | C | 9 | a0001c0001t0003g0103a0001c0001t0003g0104a0001c0001t0003g0105others(6): Show | 9 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-49-26557delT | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48375053 | |||||
| chr10:48375152
|
G | C | 8 | a0001c0001t0004g0003a0001c0001t0004g0148a0001c0001t0004g0149others(5): Show | 9 | HG00609.hp2 HG02165.hp1 NA18945.hp1 others(6): Show |
intron_variant | MODIFIER | c.-49-26460G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48375152 | ||||||
| chr10:48375156
|
A | G | 1 | a0001c0001t0003g0286 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-49-26456A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48375156 | ||||||
| chr10:48375191
|
C | A | 146 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(143): Show | 146 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.-49-26421C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48375191 | ||||||
| chr10:48375192
|
C | T | 5 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(2): Show | 5 | HG02630.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-26420C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48375192 | ||||||
| chr10:48375313
|
T | C | 220 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.-49-26299T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48375313 | ||||||
| chr10:48375412
|
A | G | 1 | a0001c0001t0003g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-49-26200A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48375412 | ||||||
| chr10:48375413
|
T | G | 2 | a0001c0001t0019g0282a0001c0001t0019g0283 | 2 | HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.-49-26199T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48375413 | ||||||
| chr10:48375430
|
G | A | 2 | a0001c0001t0002g0074a0001c0001t0002g0075 | 2 | NA18952.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.-49-26182G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48375430 | ||||||
| chr10:48375501
|
C | T | 9 | a0001c0001t0003g0103a0001c0001t0003g0104a0001c0001t0003g0105others(6): Show | 9 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-49-26111C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48375501 | ||||||
| chr10:48375506
|
C | CA | 302 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(299): Show | 305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.-49-26103dupA | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48375506 | |||||
| chr10:48375786
|
T | A | 2 | a0001c0001t0002g0041a0001c0001t0002g0290 | 2 | HG00423.hp1 HG00558.hp1 |
intron_variant | MODIFIER | c.-49-25826T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48375786 | ||||||
| chr10:48376395
|
G | A | 197 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(194): Show | 197 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.-49-25217G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48376395 | ||||||
| chr10:48376425
|
CTA | C | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-25185_-49-2518 others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48376425 | |||||
| chr10:48376451
|
A | G | 9 | a0001c0001t0003g0103a0001c0001t0003g0104a0001c0001t0003g0105others(6): Show | 9 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-49-25161A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48376451 | ||||||
| chr10:48376477
|
C | A | 13 | a0001c0001t0004g0003a0001c0001t0004g0148a0001c0001t0004g0149others(10): Show | 14 | HG00099.hp1 HG00609.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.-49-25135C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48376477 | ||||||
| chr10:48376569
|
G | A | 2 | a0001c0001t0019g0282a0001c0001t0019g0283 | 2 | HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.-49-25043G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48376569 | ||||||
| chr10:48376752
|
C | G | 1 | a0001c0001t0001g0138 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-49-24860C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48376752 | ||||||
| chr10:48376768
|
G | C | 1 | a0001c0001t0012g0067 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-49-24844G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48376768 | ||||||
| chr10:48376772
|
G | A | 9 | a0001c0001t0003g0103a0001c0001t0003g0104a0001c0001t0003g0105others(6): Show | 9 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-49-24840G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48376772 | ||||||
| chr10:48376915
|
C | T | 2 | a0001c0001t0002g0074a0001c0001t0002g0075 | 2 | NA18952.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.-49-24697C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48376915 | ||||||
| chr10:48377037
|
A | G | 220 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.-49-24575A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48377037 | ||||||
| chr10:48377071
|
A | G | 2 | a0001c0001t0002g0016a0001c0001t0002g0060 | 2 | HG02602.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-49-24541A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48377071 | ||||||
| chr10:48377165
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-49-24447A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48377165 | ||||||
| chr10:48377360
|
T | TA | 208 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(205): Show | 209 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.-49-24242dupA | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48377360 | |||||
| chr10:48377387
|
G | A | 230 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.-49-24225G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48377387 | ||||||
| chr10:48377503
|
G | A | 1 | a0001c0001t0002g0033 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-49-24109G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48377503 | ||||||
| chr10:48377524
|
G | T | 19 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(16): Show | 19 | HG00735.hp2 HG02055.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-49-24088G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48377524 | ||||||
| chr10:48377526
|
G | A | 19 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(16): Show | 19 | HG00735.hp2 HG02055.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-49-24086G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48377526 | ||||||
| chr10:48377835
|
T | C | 5 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0010others(2): Show | 5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49-23777T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48377835 | ||||||
| chr10:48377869
|
A | G | 7 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(4): Show | 7 | HG00735.hp2 HG02280.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49-23743A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48377869 | ||||||
| chr10:48378421
|
AG | A | 197 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(194): Show | 197 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.-49-23190delG | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48378421 | ||||||
| chr10:48378576
|
G | T | 1 | a0001c0001t0001g0120 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-49-23036G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48378576 | ||||||
| chr10:48378614
|
G | C | 2 | a0001c0001t0004g0145a0001c0001t0004g0146 | 2 | HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-49-22998G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48378614 | ||||||
| chr10:48378792
|
A | G | 10 | a0001c0001t0002g0002a0001c0001t0002g0037a0001c0001t0002g0047others(7): Show | 11 | HG01070.hp1 HG01071.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-49-22820A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48378792 | ||||||
| chr10:48378841
|
T | C | 23 | a0001c0001t0004g0003a0001c0001t0004g0115a0001c0001t0004g0116others(20): Show | 24 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.-49-22771T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48378841 | ||||||
| chr10:48378886
|
G | A | 26 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(23): Show | 26 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.-49-22726G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48378886 | ||||||
| chr10:48379077
|
G | A | 2 | a0001c0001t0008g0010a0001c0001t0008g0011 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-49-22535G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48379077 | ||||||
| chr10:48379418
|
G | A | 3 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0025g0114 | 3 | HG02451.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-49-22194G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48379418 | ||||||
| chr10:48379432
|
C | T | 1 | a0001c0001t0003g0286 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-49-22180C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48379432 | ||||||
| chr10:48379938
|
T | TA | 116 | a0001c0001t0001g0119a0001c0001t0001g0122a0001c0001t0001g0123others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.-49-21653dupA | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48379938 | |||||
| chr10:48379938
|
T | TAA | 33 | a0001c0001t0001g0178a0001c0001t0001g0193a0001c0001t0001g0213others(30): Show | 34 | HG00597.hp2 HG00609.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.-49-21654_-49-2165 others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48379938 | |||||
| chr10:48379938
|
T | TAAA | 12 | a0001c0001t0007g0087a0001c0001t0007g0088a0001c0001t0007g0089others(9): Show | 12 | HG01891.hp2 HG02622.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.-49-21655_-49-2165 others(7): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48379938 | |||||
| chr10:48379938
|
TA | T | 9 | a0001c0001t0002g0054a0001c0001t0003g0097a0001c0001t0003g0098others(6): Show | 9 | HG00735.hp2 HG01515.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-49-21653delA | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48379938 | |||||
| chr10:48379952
|
A | C | 1 | a0001c0001t0002g0052 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-49-21660A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48379952 | ||||||
| chr10:48379991
|
C | G | 1 | a0001c0001t0001g0211 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-49-21621C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48379991 | ||||||
| chr10:48380071
|
G | A | 1 | a0001c0001t0002g0036 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-49-21541G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48380071 | ||||||
| chr10:48380076
|
T | C | 1 | a0001c0001t0006g0262 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-49-21536T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48380076 | ||||||
| chr10:48380098
|
C | T | 1 | a0001c0001t0006g0159 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-21514C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48380098 | ||||||
| chr10:48380116
|
C | T | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp2 HG02165.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49-21496C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48380116 | ||||||
| chr10:48380143
|
G | A | 1 | a0001c0001t0004g0116 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-49-21469G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48380143 | ||||||
| chr10:48380174
|
G | A | 3 | a0001c0001t0004g0115a0001c0001t0004g0116a0001c0001t0004g0117 | 3 | HG01069.hp1 HG01099.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-49-21438G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48380174 | ||||||
| chr10:48380428
|
A | G | 9 | a0001c0001t0003g0293a0001c0001t0006g0159a0001c0001t0008g0008others(6): Show | 9 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-49-21184A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48380428 | ||||||
| chr10:48380633
|
T | C | 3 | a0001c0001t0004g0115a0001c0001t0004g0116a0001c0001t0004g0117 | 3 | HG01069.hp1 HG01099.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-49-20979T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48380633 | ||||||
| chr10:48380754
|
G | A | 1 | a0001c0001t0007g0091 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-49-20858G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48380754 | ||||||
| chr10:48380783
|
G | C | 1 | a0001c0001t0002g0046 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-49-20829G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48380783 | ||||||
| chr10:48380809
|
G | A | 16 | a0001c0001t0007g0085a0001c0001t0007g0087a0001c0001t0007g0088others(13): Show | 16 | HG01167.hp1 HG01891.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.-49-20803G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48380809 | ||||||
| chr10:48380857
|
G | A | 8 | a0001c0001t0005g0017a0001c0001t0005g0023a0001c0001t0005g0026others(5): Show | 8 | NA18959.hp2 NA18970.hp1 NA18981.hp2 others(5): Show |
intron_variant | MODIFIER | c.-49-20755G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48380857 | ||||||
| chr10:48381111
|
C | T | 4 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0020others(1): Show | 4 | NA18961.hp1 NA18983.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-20501C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48381111 | ||||||
| chr10:48381192
|
T | G | 16 | a0001c0001t0007g0085a0001c0001t0007g0087a0001c0001t0007g0088others(13): Show | 16 | HG01167.hp1 HG01891.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.-49-20420T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48381192 | ||||||
| chr10:48381314
|
A | G | 1 | a0001c0001t0003g0293 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-49-20298A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48381314 | ||||||
| chr10:48381363
|
C | G | 2 | a0001c0001t0001g0186a0001c0001t0001g0204 | 2 | HG02080.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.-49-20249C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48381363 | ||||||
| chr10:48381430
|
AGT | A | 26 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(23): Show | 26 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.-49-20179_-49-2017 others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48381430 | |||||
| chr10:48381581
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-49-20031T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48381581 | ||||||
| chr10:48381789
|
A | G | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp2 HG02165.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49-19823A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48381789 | ||||||
| chr10:48381822
|
A | G | 1 | a0001c0001t0004g0151 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-49-19790A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48381822 | ||||||
| chr10:48381831
|
A | C | 9 | a0001c0001t0003g0103a0001c0001t0003g0104a0001c0001t0003g0105others(6): Show | 9 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-49-19781A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48381831 | ||||||
| chr10:48381878
|
G | T | 1 | a0001c0001t0001g0292 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-49-19734G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48381878 | ||||||
| chr10:48381917
|
C | T | 1 | a0001c0001t0009g0196 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-49-19695C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48381917 | ||||||
| chr10:48382713
|
G | C | 16 | a0001c0001t0007g0085a0001c0001t0007g0087a0001c0001t0007g0088others(13): Show | 16 | HG01167.hp1 HG01891.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.-49-18899G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48382713 | ||||||
| chr10:48382728
|
G | A | 1 | a0001c0001t0001g0277 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-49-18884G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48382728 | ||||||
| chr10:48382740
|
C | CA | 7 | a0001c0001t0002g0084a0001c0001t0011g0004a0001c0001t0011g0005others(4): Show | 7 | HG00609.hp1 HG01884.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49-18862dupA | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48382740 | |||||
| chr10:48382888
|
GTATATAT others(27): Show |
G | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-49-18694_-49-1866 others(38): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48382888 | |||||
| chr10:48382898
|
A | G | 2 | a0001c0001t0016g0269a0001c0001t0016g0270 | 2 | HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-49-18714A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48382898 | ||||||
| chr10:48382904
|
GTGTATAT others(7): Show |
G | 2 | a0001c0001t0004g0144a0001c0001t0004g0147 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-49-18693_-49-1868 others(18): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48382904 | |||||
| chr10:48382908
|
A | G | 128 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(125): Show | 128 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.-49-18704A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48382908 | ||||||
| chr10:48382922
|
A | G | 2 | a0001c0001t0002g0028a0001c0001t0004g0160 | 2 | HG02040.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-49-18690A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48382922 | ||||||
| chr10:48382940
|
G | GTA | 125 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(122): Show | 125 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.-49-18662_-49-1866 others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48382940 | |||||
| chr10:48383413
|
G | A | 143 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(140): Show | 143 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.-49-18199G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48383413 | ||||||
| chr10:48383494
|
A | G | 23 | a0001c0001t0004g0003a0001c0001t0004g0115a0001c0001t0004g0116others(20): Show | 24 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.-49-18118A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48383494 | ||||||
| chr10:48383675
|
C | T | 142 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(139): Show | 142 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-49-17937C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48383675 | ||||||
| chr10:48383722
|
A | G | 1 | a0001c0001t0004g0156 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-49-17890A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48383722 | ||||||
| chr10:48383909
|
A | T | 2 | a0001c0001t0002g0016a0001c0001t0002g0060 | 2 | HG02602.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-49-17703A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48383909 | ||||||
| chr10:48383972
|
C | G | 1 | a0001c0001t0002g0047 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-49-17640C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48383972 | ||||||
| chr10:48384151
|
G | C | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp2 HG02165.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49-17461G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48384151 | ||||||
| chr10:48384155
|
G | A | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG01943.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.-49-17457G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48384155 | ||||||
| chr10:48384508
|
A | G | 5 | a0001c0001t0001g0174a0001c0001t0001g0197a0001c0001t0001g0203others(2): Show | 5 | HG01346.hp2 HG01934.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-17104A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48384508 | ||||||
| chr10:48384518
|
G | A | 16 | a0001c0001t0007g0085a0001c0001t0007g0087a0001c0001t0007g0088others(13): Show | 16 | HG01167.hp1 HG01891.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.-49-17094G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48384518 | ||||||
| chr10:48384560
|
A | C | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp2 HG02165.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49-17052A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48384560 | ||||||
| chr10:48384709
|
A | T | 5 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(2): Show | 5 | HG02630.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-16903A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48384709 | ||||||
| chr10:48384765
|
T | G | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-16847T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48384765 | ||||||
| chr10:48384925
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-49-16687C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48384925 | ||||||
| chr10:48384985
|
G | GA | 27 | a0001c0001t0001g0206a0001c0001t0003g0279a0001c0001t0003g0280others(24): Show | 27 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.-49-16620dupA | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48384985 | |||||
| chr10:48384989
|
AAAAG | A | 16 | a0001c0001t0007g0085a0001c0001t0007g0087a0001c0001t0007g0088others(13): Show | 16 | HG01167.hp1 HG01891.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.-49-16622_-49-1661 others(8): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48384989 | ||||||
| chr10:48385068
|
G | C | 1 | a0001c0001t0003g0293 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-49-16544G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48385068 | ||||||
| chr10:48385080
|
C | G | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-49-16532C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48385080 | ||||||
| chr10:48385097
|
A | G | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-16515A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48385097 | ||||||
| chr10:48385272
|
G | A | 2 | a0001c0001t0016g0269a0001c0001t0016g0270 | 2 | HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-49-16340G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48385272 | ||||||
| chr10:48385334
|
C | T | 1 | a0001c0001t0002g0052 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-49-16278C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48385334 | ||||||
| chr10:48385385
|
A | C | 5 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0010others(2): Show | 5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49-16227A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48385385 | ||||||
| chr10:48385554
|
A | G | 16 | a0001c0001t0007g0085a0001c0001t0007g0087a0001c0001t0007g0088others(13): Show | 16 | HG01167.hp1 HG01891.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.-49-16058A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48385554 | ||||||
| chr10:48385613
|
G | GT | 11 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0003g0103others(8): Show | 11 | HG00741.hp2 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-49-15989dupT | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48385613 | |||||
| chr10:48385713
|
A | G | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp2 HG02165.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49-15899A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48385713 | ||||||
| chr10:48385796
|
A | T | 1 | a0001c0001t0018g0096 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-49-15816A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48385796 | ||||||
| chr10:48386098
|
C | A | 23 | a0001c0001t0004g0003a0001c0001t0004g0115a0001c0001t0004g0116others(20): Show | 24 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.-49-15514C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48386098 | ||||||
| chr10:48386197
|
A | C | 127 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(124): Show | 127 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.-49-15415A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48386197 | ||||||
| chr10:48386221
|
C | T | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-15391C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48386221 | ||||||
| chr10:48386620
|
A | G | 2 | a0001c0001t0016g0269a0001c0001t0016g0270 | 2 | HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-49-14992A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48386620 | ||||||
| chr10:48386649
|
A | G | 2 | a0001c0001t0019g0282a0001c0001t0019g0283 | 2 | HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.-49-14963A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48386649 | ||||||
| chr10:48386650
|
T | C | 1 | a0001c0001t0001g0275 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-49-14962T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48386650 | ||||||
| chr10:48386765
|
G | A | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-14847G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48386765 | ||||||
| chr10:48386797
|
C | T | 1 | a0001c0001t0003g0108 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-49-14815C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48386797 | ||||||
| chr10:48386830
|
A | G | 1 | a0001c0001t0001g0246 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-49-14782A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48386830 | ||||||
| chr10:48386868
|
G | A | 23 | a0001c0001t0004g0003a0001c0001t0004g0115a0001c0001t0004g0116others(20): Show | 24 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.-49-14744G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48386868 | ||||||
| chr10:48387001
|
G | T | 2 | a0001c0001t0004g0144a0001c0001t0004g0147 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-49-14611G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48387001 | ||||||
| chr10:48387004
|
A | T | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-49-14608A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48387004 | ||||||
| chr10:48387109
|
G | T | 26 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(23): Show | 26 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.-49-14503G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48387109 | ||||||
| chr10:48387137
|
A | G | 1 | a0001c0001t0004g0158 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-49-14475A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48387137 | ||||||
| chr10:48387182
|
C | T | 3 | a0001c0001t0007g0085a0001c0001t0007g0092a0001c0001t0007g0093 | 3 | HG03688.hp2 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-49-14430C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48387182 | ||||||
| chr10:48387821
|
A | G | 27 | a0001c0001t0001g0206a0001c0001t0003g0279a0001c0001t0003g0280others(24): Show | 27 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.-49-13791A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48387821 | ||||||
| chr10:48387884
|
TG | T | 16 | a0001c0001t0007g0085a0001c0001t0007g0087a0001c0001t0007g0088others(13): Show | 16 | HG01167.hp1 HG01891.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.-49-13727delG | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48387884 | ||||||
| chr10:48388012
|
C | T | 1 | a0001c0001t0014g0182 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-49-13600C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48388012 | ||||||
| chr10:48388525
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-49-13087G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48388525 | ||||||
| chr10:48388800
|
A | G | 1 | a0001c0001t0003g0293 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-49-12812A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48388800 | ||||||
| chr10:48388850
|
A | G | 2 | a0001c0001t0004g0145a0001c0001t0004g0146 | 2 | HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-49-12762A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48388850 | ||||||
| chr10:48388961
|
T | G | 16 | a0001c0001t0007g0085a0001c0001t0007g0087a0001c0001t0007g0088others(13): Show | 16 | HG01167.hp1 HG01891.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.-49-12651T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48388961 | ||||||
| chr10:48389114
|
G | A | 300 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(297): Show | 303 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.-49-12498G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48389114 | ||||||
| chr10:48389361
|
C | T | 1 | a0001c0001t0002g0029 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-49-12251C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48389361 | ||||||
| chr10:48389420
|
G | A | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-49-12192G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48389420 | ||||||
| chr10:48389591
|
G | T | 1 | a0001c0001t0001g0225 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-49-12021G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48389591 | ||||||
| chr10:48389707
|
G | T | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-49-11905G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48389707 | ||||||
| chr10:48389709
|
A | G | 5 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0010others(2): Show | 5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49-11903A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48389709 | ||||||
| chr10:48389889
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-49-11723G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48389889 | ||||||
| chr10:48390101
|
A | G | 2 | a0001c0001t0018g0095a0001c0001t0018g0096 | 2 | HG01123.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-49-11511A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48390101 | ||||||
| chr10:48390457
|
T | C | 1 | a0001c0001t0004g0160 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-49-11155T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48390457 | ||||||
| chr10:48390694
|
T | C | 1 | a0001c0001t0004g0116 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-49-10918T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48390694 | ||||||
| chr10:48390781
|
C | T | 2 | a0001c0001t0016g0269a0001c0001t0016g0270 | 2 | HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-49-10831C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48390781 | ||||||
| chr10:48390840
|
A | G | 7 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(4): Show | 7 | HG00408.hp1 HG00544.hp2 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49-10772A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48390840 | ||||||
| chr10:48390902
|
C | T | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-49-10710C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48390902 | ||||||
| chr10:48390904
|
A | G | 49 | a0001c0001t0001g0206a0001c0001t0003g0097a0001c0001t0003g0098others(46): Show | 49 | HG00735.hp2 HG01099.hp2 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.-49-10708A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48390904 | ||||||
| chr10:48391683
|
A | G | 2 | a0001c0001t0002g0042a0001c0001t0002g0046 | 2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-49-9929A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48391683 | ||||||
| chr10:48391686
|
A | G | 21 | a0001c0001t0001g0206a0001c0001t0006g0086a0001c0001t0006g0250others(18): Show | 21 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.-49-9926A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48391686 | ||||||
| chr10:48391990
|
G | A | 1 | a0001c0001t0030g0272 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-49-9622G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48391990 | ||||||
| chr10:48392348
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-49-9264A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48392348 | ||||||
| chr10:48392388
|
C | T | 1 | a0001c0001t0003g0286 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-49-9224C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48392388 | ||||||
| chr10:48392446
|
A | G | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-49-9166A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48392446 | ||||||
| chr10:48392692
|
G | A | 1 | a0001c0001t0002g0034 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-49-8920G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48392692 | ||||||
| chr10:48392695
|
A | ATAAAGGA others(13): Show |
1 | a0001c0001t0002g0034 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-49-8917_-49-8916i others(22): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48392695 | ||||||
| chr10:48392747
|
A | G | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-49-8865A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48392747 | ||||||
| chr10:48392759
|
C | A | 230 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.-49-8853C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48392759 | ||||||
| chr10:48392846
|
G | A | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-8766G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48392846 | ||||||
| chr10:48392911
|
G | A | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-8701G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48392911 | ||||||
| chr10:48393312
|
C | A | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-49-8300C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48393312 | ||||||
| chr10:48393324
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-49-8288C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48393324 | ||||||
| chr10:48393353
|
A | T | 197 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(194): Show | 197 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.-49-8259A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48393353 | ||||||
| chr10:48393398
|
C | G | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-49-8214C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48393398 | ||||||
| chr10:48393447
|
T | C | 1 | a0001c0001t0001g0204 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-49-8165T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48393447 | ||||||
| chr10:48393653
|
T | A | 2 | a0001c0001t0015g0121a0001c0001t0015g0234 | 2 | HG02602.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-49-7959T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48393653 | ||||||
| chr10:48393793
|
T | G | 1 | a0001c0001t0003g0286 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-49-7819T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48393793 | ||||||
| chr10:48393941
|
G | A | 1 | a0001c0001t0010g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-49-7671G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48393941 | ||||||
| chr10:48394150
|
C | A | 2 | a0001c0001t0019g0282a0001c0001t0019g0283 | 2 | HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.-49-7462C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48394150 | ||||||
| chr10:48394258
|
TG | T | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp2 HG02165.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49-7353delG | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48394258 | ||||||
| chr10:48394311
|
C | A | 5 | a0001c0001t0002g0036a0001c0001t0002g0056a0001c0001t0002g0063others(2): Show | 5 | HG00741.hp1 HG01175.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-7301C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48394311 | ||||||
| chr10:48394314
|
G | A | 19 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(16): Show | 19 | HG00735.hp2 HG02055.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-49-7298G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48394314 | ||||||
| chr10:48394438
|
A | G | 7 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(4): Show | 7 | HG00408.hp1 HG00544.hp2 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49-7174A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48394438 | ||||||
| chr10:48394450
|
A | G | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-49-7162A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48394450 | ||||||
| chr10:48394683
|
C | T | 23 | a0001c0001t0004g0003a0001c0001t0004g0115a0001c0001t0004g0116others(20): Show | 24 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.-49-6929C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48394683 | ||||||
| chr10:48394700
|
C | T | 1 | a0001c0001t0003g0293 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-49-6912C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48394700 | ||||||
| chr10:48394831
|
ATGAATAA others(21): Show |
A | 2 | a0001c0001t0016g0269a0001c0001t0016g0270 | 2 | HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-49-6779_-49-6752d others(30): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48394831 | |||||
| chr10:48394871
|
T | A | 2 | a0001c0001t0016g0269a0001c0001t0016g0270 | 2 | HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-49-6741T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48394871 | ||||||
| chr10:48394939
|
A | G | 49 | a0001c0001t0001g0206a0001c0001t0003g0097a0001c0001t0003g0098others(46): Show | 49 | HG00735.hp2 HG01099.hp2 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.-49-6673A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48394939 | ||||||
| chr10:48394996
|
G | A | 16 | a0001c0001t0007g0085a0001c0001t0007g0087a0001c0001t0007g0088others(13): Show | 16 | HG01167.hp1 HG01891.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.-49-6616G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48394996 | ||||||
| chr10:48395164
|
C | G | 3 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281 | 3 | HG03098.hp1 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-49-6448C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48395164 | ||||||
| chr10:48395356
|
A | G | 2 | a0001c0001t0018g0095a0001c0001t0018g0096 | 2 | HG01123.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-49-6256A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48395356 | ||||||
| chr10:48395390
|
G | A | 2 | a0001c0001t0018g0095a0001c0001t0018g0096 | 2 | HG01123.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-49-6222G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48395390 | ||||||
| chr10:48395441
|
A | G | 3 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281 | 3 | HG03098.hp1 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-49-6171A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48395441 | ||||||
| chr10:48395550
|
C | G | 1 | a0001c0001t0001g0129 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-49-6062C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48395550 | ||||||
| chr10:48395577
|
A | C | 1 | a0001c0001t0006g0159 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-6035A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48395577 | ||||||
| chr10:48395738
|
C | T | 2 | a0001c0001t0001g0127a0001c0001t0002g0042 | 2 | HG04228.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-49-5874C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48395738 | ||||||
| chr10:48395739
|
G | T | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-5873G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48395739 | ||||||
| chr10:48395799
|
C | G | 19 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(16): Show | 19 | HG00735.hp2 HG02055.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-49-5813C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48395799 | ||||||
| chr10:48395879
|
G | C | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-5733G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48395879 | ||||||
| chr10:48395948
|
C | T | 1 | a0001c0001t0018g0096 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-49-5664C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48395948 | ||||||
| chr10:48396125
|
T | C | 1 | a0001c0001t0006g0255 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-49-5487T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48396125 | ||||||
| chr10:48396281
|
G | C | 1 | a0001c0001t0023g0176 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-49-5331G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48396281 | ||||||
| chr10:48396293
|
G | C | 1 | a0001c0001t0002g0029 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-49-5319G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48396293 | ||||||
| chr10:48396317
|
T | C | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-5295T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48396317 | ||||||
| chr10:48396325
|
A | G | 7 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(4): Show | 7 | HG00735.hp2 HG02280.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49-5287A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48396325 | ||||||
| chr10:48396667
|
G | A | 230 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.-49-4945G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48396667 | ||||||
| chr10:48396701
|
C | G | 3 | a0001c0001t0007g0085a0001c0001t0007g0092a0001c0001t0007g0093 | 3 | HG03688.hp2 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-49-4911C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48396701 | ||||||
| chr10:48396891
|
C | G | 1 | a0001c0001t0005g0078 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-49-4721C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48396891 | ||||||
| chr10:48397096
|
T | C | 197 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(194): Show | 197 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.-49-4516T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48397096 | ||||||
| chr10:48397200
|
A | C | 4 | a0001c0001t0002g0002a0001c0001t0002g0037a0001c0001t0002g0047others(1): Show | 5 | HG01070.hp1 HG01071.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-4412A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48397200 | ||||||
| chr10:48397485
|
T | C | 26 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(23): Show | 26 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.-49-4127T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48397485 | ||||||
| chr10:48397713
|
C | T | 13 | a0001c0001t0004g0003a0001c0001t0004g0148a0001c0001t0004g0149others(10): Show | 14 | HG00099.hp1 HG00609.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.-49-3899C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48397713 | ||||||
| chr10:48397747
|
C | T | 34 | a0001c0001t0002g0001a0001c0001t0002g0022a0001c0001t0002g0024others(31): Show | 35 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.-49-3865C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48397747 | ||||||
| chr10:48397806
|
G | A | 2 | a0001c0001t0016g0269a0001c0001t0016g0270 | 2 | HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-49-3806G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48397806 | ||||||
| chr10:48397827
|
G | A | 1 | a0001c0001t0006g0260 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-49-3785G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48397827 | ||||||
| chr10:48397940
|
A | G | 1 | a0001c0001t0003g0293 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-49-3672A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48397940 | ||||||
| chr10:48398012
|
A | G | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-49-3600A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48398012 | ||||||
| chr10:48398028
|
T | G | 20 | a0001c0001t0006g0086a0001c0001t0006g0250a0001c0001t0006g0251others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.-49-3584T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48398028 | ||||||
| chr10:48398067
|
A | G | 1 | a0001c0001t0002g0034 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-49-3545A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48398067 | ||||||
| chr10:48398087
|
G | C | 1 | a0001c0001t0002g0032 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-49-3525G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48398087 | ||||||
| chr10:48398240
|
T | A | 1 | a0001c0001t0007g0295 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-49-3372T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48398240 | ||||||
| chr10:48398342
|
A | T | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-49-3270A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48398342 | ||||||
| chr10:48398414
|
C | T | 1 | a0001c0001t0002g0069 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-49-3198C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48398414 | ||||||
| chr10:48398486
|
T | C | 48 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(45): Show | 48 | HG00735.hp2 HG01099.hp2 HG01106.hp2 others(45): Show |
intron_variant | MODIFIER | c.-49-3126T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48398486 | ||||||
| chr10:48398565
|
A | G | 1 | a0001c0001t0024g0125 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-49-3047A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48398565 | ||||||
| chr10:48398603
|
A | G | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-3009A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48398603 | ||||||
| chr10:48398867
|
G | A | 20 | a0001c0001t0006g0086a0001c0001t0006g0250a0001c0001t0006g0251others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.-49-2745G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48398867 | ||||||
| chr10:48398937
|
C | T | 2 | a0001c0001t0008g0010a0001c0001t0008g0011 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-49-2675C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48398937 | ||||||
| chr10:48399026
|
A | G | 3 | a0001c0001t0007g0085a0001c0001t0007g0092a0001c0001t0007g0093 | 3 | HG03688.hp2 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-49-2586A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48399026 | ||||||
| chr10:48399241
|
A | G | 2 | a0001c0001t0018g0095a0001c0001t0018g0096 | 2 | HG01123.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-49-2371A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48399241 | ||||||
| chr10:48399397
|
A | G | 16 | a0001c0001t0007g0085a0001c0001t0007g0087a0001c0001t0007g0088others(13): Show | 16 | HG01167.hp1 HG01891.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.-49-2215A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48399397 | ||||||
| chr10:48399707
|
G | A | 5 | a0001c0001t0002g0036a0001c0001t0002g0056a0001c0001t0002g0063others(2): Show | 5 | HG00741.hp1 HG01175.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-1905G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48399707 | ||||||
| chr10:48399721
|
C | T | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-1891C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48399721 | ||||||
| chr10:48399805
|
T | C | 1 | a0001c0001t0003g0097 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-49-1807T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48399805 | ||||||
| chr10:48399856
|
C | G | 2 | a0001c0001t0013g0118a0001c0001t0013g0124 | 2 | HG01168.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-49-1756C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48399856 | ||||||
| chr10:48400126
|
T | G | 2 | a0001c0001t0018g0095a0001c0001t0018g0096 | 2 | HG01123.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-49-1486T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48400126 | ||||||
| chr10:48400595
|
G | A | 105 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(102): Show | 108 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.-49-1017G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48400595 | ||||||
| chr10:48400747
|
C | T | 21 | a0001c0001t0006g0086a0001c0001t0006g0159a0001c0001t0006g0250others(18): Show | 21 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.-49-865C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48400747 | ||||||
| chr10:48400754
|
T | C | 1 | a0001c0001t0006g0159 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-49-858T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48400754 | ||||||
| chr10:48400799
|
C | G | 3 | a0001c0001t0002g0028a0001c0001t0002g0041a0001c0001t0002g0290 | 3 | HG00423.hp1 HG00558.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.-49-813C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48400799 | ||||||
| chr10:48400968
|
GC | G | 159 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(156): Show | 162 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.-49-642delC | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 48400968 | |||||
| chr10:48400986
|
C | G | 19 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(16): Show | 19 | HG00735.hp2 HG02055.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-49-626C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48400986 | ||||||
| chr10:48401135
|
A | G | 21 | a0001c0001t0006g0086a0001c0001t0006g0159a0001c0001t0006g0250others(18): Show | 21 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.-49-477A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48401135 | ||||||
| chr10:48401203
|
A | G | 1 | a0001c0001t0004g0156 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-49-409A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48401203 | ||||||
| chr10:48401242
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-49-370T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48401242 | ||||||
| chr10:48401421
|
A | T | 6 | a0001c0001t0003g0293a0001c0001t0008g0008a0001c0001t0008g0009others(3): Show | 6 | HG02109.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49-191A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48401421 | ||||||
| chr10:48401462
|
C | A | 1 | a0001c0001t0001g0119 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-49-150C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48401462 | ||||||
| chr10:48401535
|
C | A | 286 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(283): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.-49-77C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 1/11 | chr10 | 48401535 | ||||||
| chr10:48401849
|
T | G | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.122+67T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48401849 | ||||||
| chr10:48401985
|
A | G | 1 | a0001c0001t0006g0252 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.122+203A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48401985 | ||||||
| chr10:48401992
|
A | G | 1 | a0001c0001t0007g0094 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.122+210A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48401992 | ||||||
| chr10:48402156
|
T | A | 9 | a0001c0001t0003g0103a0001c0001t0003g0104a0001c0001t0003g0105others(6): Show | 9 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.122+374T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48402156 | ||||||
| chr10:48402303
|
T | G | 1 | a0001c0001t0001g0128 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.122+521T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48402303 | ||||||
| chr10:48402328
|
A | G | 19 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(16): Show | 19 | HG00735.hp2 HG02055.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.122+546A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48402328 | ||||||
| chr10:48402383
|
G | C | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp2 HG02165.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.122+601G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48402383 | ||||||
| chr10:48402414
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.122+632G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48402414 | ||||||
| chr10:48402728
|
A | G | 1 | a0001c0001t0004g0143 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.122+946A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48402728 | ||||||
| chr10:48402797
|
A | G | 1 | a0001c0001t0002g0034 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.122+1015A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48402797 | ||||||
| chr10:48403097
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.122+1315G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48403097 | ||||||
| chr10:48403168
|
A | C | 2 | a0001c0001t0003g0284a0001c0001t0003g0285 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.122+1386A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48403168 | ||||||
| chr10:48403188
|
G | T | 1 | a0001c0001t0001g0179 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.122+1406G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48403188 | ||||||
| chr10:48403193
|
C | A | 127 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(124): Show | 127 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.122+1411C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48403193 | ||||||
| chr10:48403197
|
C | T | 4 | a0001c0001t0001g0174a0001c0001t0001g0203a0001c0001t0001g0213others(1): Show | 4 | HG01346.hp2 HG01934.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.122+1415C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48403197 | ||||||
| chr10:48403273
|
C | T | 2 | a0001c0001t0003g0284a0001c0001t0003g0285 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.122+1491C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48403273 | ||||||
| chr10:48403426
|
C | T | 2 | a0001c0001t0018g0095a0001c0001t0018g0096 | 2 | HG01123.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.123-1426C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48403426 | ||||||
| chr10:48403453
|
G | A | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.123-1399G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48403453 | ||||||
| chr10:48403456
|
T | TA | 11 | a0001c0001t0001g0178a0001c0001t0001g0225a0001c0001t0001g0238others(8): Show | 11 | HG00597.hp2 HG01106.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.123-1380dupA | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 48403456 | |||||
| chr10:48403727
|
GTTTTTTG others(8): Show |
G | 1 | a0001c0001t0001g0211 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.123-1111_123-1097d others(17): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 48403727 | |||||
| chr10:48403734
|
GTTTTTTG others(9): Show |
G | 1 | a0001c0001t0003g0100 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.123-1103_123-1088d others(18): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 48403734 | |||||
| chr10:48403749
|
GTTTT | G | 9 | a0001c0001t0003g0103a0001c0001t0003g0104a0001c0001t0003g0105others(6): Show | 9 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.123-1099_123-1096d others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 48403749 | |||||
| chr10:48403809
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.123-1043C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48403809 | ||||||
| chr10:48403817
|
T | C | 159 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(156): Show | 162 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.123-1035T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48403817 | ||||||
| chr10:48403844
|
G | C | 23 | a0001c0001t0004g0003a0001c0001t0004g0115a0001c0001t0004g0116others(20): Show | 24 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.123-1008G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48403844 | ||||||
| chr10:48403876
|
G | A | 1 | a0001c0001t0003g0284 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.123-976G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48403876 | ||||||
| chr10:48403917
|
T | TGTGTG | 4 | a0001c0001t0001g0142a0001c0001t0001g0166a0001c0001t0001g0219others(1): Show | 4 | HG02071.hp2 HG03927.hp2 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.123-935_123-934ins others(5): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48403917 | ||||||
| chr10:48403917
|
T | TTG | 26 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(23): Show | 27 | HG00609.hp1 HG01175.hp2 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.123-895_123-894dup others(2): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 48403917 | |||||
| chr10:48403917
|
T | TTGTG | 72 | a0001c0001t0001g0119a0001c0001t0001g0128a0001c0001t0001g0137others(69): Show | 72 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.123-897_123-894dup others(4): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 48403917 | |||||
| chr10:48403917
|
T | TTGTGTG | 35 | a0001c0001t0001g0120a0001c0001t0001g0122a0001c0001t0001g0123others(32): Show | 35 | HG00280.hp2 HG01070.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.123-899_123-894dup others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 48403917 | |||||
| chr10:48403917
|
T | TTGTGTGT others(1): Show |
20 | a0001c0001t0001g0126a0001c0001t0001g0173a0001c0001t0001g0188others(17): Show | 20 | HG00099.hp2 HG00735.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.123-901_123-894dup others(8): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 48403917 | |||||
| chr10:48403917
|
T | TTGTGTGT others(3): Show |
6 | a0001c0001t0001g0197a0001c0001t0003g0098a0001c0001t0010g0221others(3): Show | 6 | HG01123.hp2 HG01256.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.123-903_123-894dup others(10): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 48403917 | |||||
| chr10:48403917
|
T | TTGTGTGT others(5): Show |
4 | a0001c0001t0003g0102a0001c0001t0009g0180a0001c0001t0009g0196others(1): Show | 4 | HG01884.hp1 HG02145.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.123-905_123-894dup others(12): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 48403917 | |||||
| chr10:48403917
|
T | TTGTGTGT others(7): Show |
3 | a0001c0001t0001g0248a0001c0001t0003g0101a0001c0001t0003g0113 | 3 | HG00408.hp2 HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.123-907_123-894dup others(14): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 48403917 | |||||
| chr10:48403917
|
T | TTGTGTGT others(9): Show |
2 | a0001c0001t0001g0177a0001c0001t0003g0097 | 2 | HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.123-909_123-894dup others(16): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 48403917 | |||||
| chr10:48403917
|
T | TTGTGTGT others(11): Show |
1 | a0001c0001t0001g0175 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.123-911_123-894dup others(18): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 48403917 | |||||
| chr10:48403917
|
T | TTGTGTGT others(17): Show |
1 | a0001c0001t0003g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.123-917_123-894dup others(24): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 48403917 | |||||
| chr10:48403917
|
TTG | T | 37 | a0001c0001t0002g0013a0001c0001t0002g0032a0001c0001t0002g0033others(34): Show | 38 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.123-895_123-894del others(2): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 48403917 | |||||
| chr10:48403917
|
TTGTGTGT others(3): Show |
T | 3 | a0001c0001t0007g0085a0001c0001t0007g0092a0001c0001t0007g0093 | 3 | HG03688.hp2 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.123-903_123-894del others(10): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 48403917 | |||||
| chr10:48403971
|
G | C | 127 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(124): Show | 127 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.123-881G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48403971 | ||||||
| chr10:48404074
|
C | T | 1 | a0001c0001t0001g0292 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.123-778C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48404074 | ||||||
| chr10:48404114
|
A | G | 2 | a0001c0001t0018g0095a0001c0001t0018g0096 | 2 | HG01123.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.123-738A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48404114 | ||||||
| chr10:48404173
|
C | CT | 6 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0006g0159others(3): Show | 6 | HG02165.hp2 HG02451.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.123-666dupT | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 48404173 | |||||
| chr10:48404173
|
C | CTT | 20 | a0001c0001t0004g0003a0001c0001t0004g0115a0001c0001t0004g0116others(17): Show | 21 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.123-667_123-666dup others(2): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 48404173 | |||||
| chr10:48404211
|
C | T | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.123-641C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48404211 | ||||||
| chr10:48404212
|
G | A | 3 | a0001c0001t0004g0115a0001c0001t0004g0116a0001c0001t0004g0117 | 3 | HG01069.hp1 HG01099.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.123-640G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48404212 | ||||||
| chr10:48404219
|
C | T | 1 | a0001c0001t0001g0211 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.123-633C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48404219 | ||||||
| chr10:48404309
|
A | G | 2 | a0001c0001t0003g0284a0001c0001t0003g0285 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.123-543A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48404309 | ||||||
| chr10:48404370
|
A | C | 5 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(2): Show | 5 | HG02630.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-482A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48404370 | ||||||
| chr10:48404435
|
C | T | 82 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(79): Show | 84 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.123-417C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48404435 | ||||||
| chr10:48404458
|
G | A | 1 | a0001c0001t0003g0279 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.123-394G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48404458 | ||||||
| chr10:48404529
|
C | G | 72 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(69): Show | 74 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.123-323C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48404529 | ||||||
| chr10:48404575
|
T | G | 2 | a0001c0001t0001g0162a0001c0001t0001g0218 | 2 | NA18949.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.123-277T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48404575 | ||||||
| chr10:48404619
|
C | T | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG02615.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.123-233C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48404619 | ||||||
| chr10:48404673
|
T | G | 36 | a0001c0001t0001g0119a0001c0001t0001g0137a0001c0001t0001g0138others(33): Show | 36 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.123-179T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48404673 | ||||||
| chr10:48404751
|
G | A | 3 | a0001c0001t0003g0286a0001c0001t0018g0095a0001c0001t0018g0096 | 3 | HG01123.hp1 HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.123-101G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48404751 | ||||||
| chr10:48404801
|
A | C | 20 | a0001c0001t0006g0086a0001c0001t0006g0250a0001c0001t0006g0251others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.123-51A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 2/11 | chr10 | 48404801 | ||||||
| chr10:48405106
|
G | GAT | 165 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(162): Show | 167 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.252+146_252+147dup others(2): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 48405106 | |||||
| chr10:48405106
|
G | GATAT | 22 | a0001c0001t0001g0137a0001c0001t0001g0141a0001c0001t0001g0142others(19): Show | 22 | HG00544.hp1 HG01175.hp2 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.252+144_252+147dup others(4): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 48405106 | |||||
| chr10:48405106
|
G | GATATAT | 14 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(11): Show | 14 | HG00099.hp2 HG00280.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.252+142_252+147dup others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 48405106 | |||||
| chr10:48405106
|
G | GATATATA others(3): Show |
5 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0010others(2): Show | 5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+138_252+147dup others(10): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 48405106 | |||||
| chr10:48405106
|
GAT | G | 7 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(4): Show | 7 | HG01069.hp1 HG02165.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.252+146_252+147del others(2): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 48405106 | |||||
| chr10:48405121
|
A | ATG | 20 | a0001c0001t0004g0003a0001c0001t0004g0115a0001c0001t0004g0143others(17): Show | 21 | HG00099.hp1 HG00609.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.252+141_252+142ins others(2): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 48405121 | |||||
| chr10:48405121
|
A | G | 2 | a0001c0001t0004g0116a0001c0001t0004g0117 | 2 | HG01069.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.252+140A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48405121 | ||||||
| chr10:48405295
|
C | T | 1 | a0001c0001t0002g0033 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.252+314C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48405295 | ||||||
| chr10:48405523
|
T | C | 1 | a0001c0001t0004g0156 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.252+542T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48405523 | ||||||
| chr10:48405754
|
G | A | 13 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(10): Show | 13 | HG01891.hp1 HG02622.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.252+773G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48405754 | ||||||
| chr10:48405892
|
GA | G | 291 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(288): Show | 294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.252+920delA | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 48405892 | |||||
| chr10:48406132
|
G | C | 9 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(6): Show | 9 | HG01891.hp1 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.252+1151G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48406132 | ||||||
| chr10:48406234
|
G | A | 127 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(124): Show | 127 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.252+1253G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48406234 | ||||||
| chr10:48406348
|
G | A | 159 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(156): Show | 162 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.252+1367G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48406348 | ||||||
| chr10:48406394
|
G | A | 2 | a0001c0001t0018g0095a0001c0001t0018g0096 | 2 | HG01123.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.252+1413G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48406394 | ||||||
| chr10:48406435
|
A | G | 1 | a0001c0001t0003g0293 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.252+1454A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48406435 | ||||||
| chr10:48406644
|
C | T | 20 | a0001c0001t0006g0086a0001c0001t0006g0250a0001c0001t0006g0251others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.252+1663C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48406644 | ||||||
| chr10:48406865
|
G | A | 1 | a0001c0001t0002g0048 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.252+1884G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48406865 | ||||||
| chr10:48406948
|
C | T | 3 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0025g0114 | 3 | HG02451.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.252+1967C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48406948 | ||||||
| chr10:48406977
|
C | G | 1 | a0001c0001t0001g0241 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.252+1996C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48406977 | ||||||
| chr10:48407049
|
G | A | 1 | a0001c0001t0001g0166 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.252+2068G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48407049 | ||||||
| chr10:48407112
|
A | G | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+2131A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48407112 | ||||||
| chr10:48407133
|
T | C | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.252+2152T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48407133 | ||||||
| chr10:48407302
|
T | A | 1 | a0001c0001t0005g0038 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.252+2321T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48407302 | ||||||
| chr10:48407313
|
A | G | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+2332A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48407313 | ||||||
| chr10:48407389
|
A | G | 5 | a0001c0001t0009g0180a0001c0001t0009g0196a0001c0001t0009g0231others(2): Show | 5 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.252+2408A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48407389 | ||||||
| chr10:48407588
|
C | A | 1 | a0001c0001t0003g0097 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.253-2291C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48407588 | ||||||
| chr10:48407683
|
T | TA | 3 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0025g0114 | 3 | HG02451.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.253-2195dupA | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr10 | 48407683 | |||||
| chr10:48407690
|
G | A | 1 | a0001c0001t0005g0038 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.253-2189G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48407690 | ||||||
| chr10:48407718
|
A | G | 159 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(156): Show | 162 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.253-2161A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48407718 | ||||||
| chr10:48407939
|
G | T | 23 | a0001c0001t0004g0003a0001c0001t0004g0115a0001c0001t0004g0116others(20): Show | 24 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.253-1940G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48407939 | ||||||
| chr10:48407950
|
A | G | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.253-1929A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48407950 | ||||||
| chr10:48408023
|
A | C | 26 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(23): Show | 26 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.253-1856A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48408023 | ||||||
| chr10:48408082
|
G | C | 1 | a0001c0001t0001g0240 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.253-1797G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48408082 | ||||||
| chr10:48408308
|
A | G | 2 | a0001c0001t0019g0282a0001c0001t0019g0283 | 2 | HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.253-1571A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48408308 | ||||||
| chr10:48408371
|
G | A | 1 | a0001c0001t0003g0286 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.253-1508G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48408371 | ||||||
| chr10:48408458
|
A | T | 1 | a0001c0001t0003g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.253-1421A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48408458 | ||||||
| chr10:48408947
|
C | T | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.253-932C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48408947 | ||||||
| chr10:48408949
|
T | C | 3 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281 | 3 | HG03098.hp1 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.253-930T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48408949 | ||||||
| chr10:48408975
|
C | T | 1 | a0001c0001t0026g0035 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.253-904C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48408975 | ||||||
| chr10:48408980
|
A | G | 1 | a0001c0001t0010g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.253-899A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48408980 | ||||||
| chr10:48408986
|
G | A | 2 | a0001c0001t0018g0095a0001c0001t0018g0096 | 2 | HG01123.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.253-893G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48408986 | ||||||
| chr10:48408989
|
C | A | 1 | a0001c0001t0001g0206 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.253-890C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48408989 | ||||||
| chr10:48409054
|
T | C | 1 | a0001c0001t0004g0154 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.253-825T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48409054 | ||||||
| chr10:48409077
|
T | C | 2 | a0001c0001t0019g0282a0001c0001t0019g0283 | 2 | HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.253-802T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48409077 | ||||||
| chr10:48409142
|
A | G | 1 | a0001c0001t0003g0110 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.253-737A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48409142 | ||||||
| chr10:48409280
|
T | C | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp2 HG02165.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.253-599T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48409280 | ||||||
| chr10:48409365
|
T | C | 1 | a0001c0001t0003g0287 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.253-514T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48409365 | ||||||
| chr10:48409385
|
T | C | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.253-494T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48409385 | ||||||
| chr10:48409444
|
T | A | 1 | a0001c0001t0025g0114 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.253-435T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48409444 | ||||||
| chr10:48409799
|
T | A | 26 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(23): Show | 26 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.253-80T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48409799 | ||||||
| chr10:48409858
|
G | A | 2 | a0001c0001t0003g0112a0001c0001t0003g0113 | 2 | HG02451.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.253-21G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 3/11 | chr10 | 48409858 | ||||||
| chr10:48409974
|
A | G | 20 | a0001c0001t0006g0086a0001c0001t0006g0250a0001c0001t0006g0251others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.311+37A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 4/11 | chr10 | 48409974 | ||||||
| chr10:48410188
|
G | A | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp2 HG02165.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.450+20G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48410188 | ||||||
| chr10:48410302
|
T | C | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.450+134T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48410302 | ||||||
| chr10:48410309
|
T | G | 23 | a0001c0001t0004g0003a0001c0001t0004g0115a0001c0001t0004g0116others(20): Show | 24 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.450+141T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48410309 | ||||||
| chr10:48410586
|
G | A | 1 | a0001c0001t0004g0302 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.450+418G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48410586 | ||||||
| chr10:48410637
|
C | A | 23 | a0001c0001t0004g0003a0001c0001t0004g0115a0001c0001t0004g0116others(20): Show | 24 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.450+469C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48410637 | ||||||
| chr10:48410736
|
A | C | 82 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(79): Show | 84 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.450+568A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48410736 | ||||||
| chr10:48410751
|
G | T | 1 | a0001c0001t0004g0115 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.450+583G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48410751 | ||||||
| chr10:48410939
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.450+771G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48410939 | ||||||
| chr10:48410979
|
T | C | 1 | a0001c0001t0001g0213 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.450+811T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48410979 | ||||||
| chr10:48410996
|
T | G | 1 | a0001c0001t0001g0129 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.450+828T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48410996 | ||||||
| chr10:48411160
|
C | T | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+992C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48411160 | ||||||
| chr10:48411513
|
G | T | 1 | a0001c0001t0001g0268 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.450+1345G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48411513 | ||||||
| chr10:48411530
|
T | C | 1 | a0001c0001t0005g0080 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.450+1362T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48411530 | ||||||
| chr10:48411550
|
G | A | 1 | a0001c0001t0005g0079 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.450+1382G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48411550 | ||||||
| chr10:48411723
|
A | G | 22 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(19): Show | 22 | HG00735.hp2 HG01123.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.450+1555A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48411723 | ||||||
| chr10:48411736
|
A | G | 1 | a0001c0001t0007g0297 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.450+1568A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48411736 | ||||||
| chr10:48411750
|
G | A | 82 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(79): Show | 84 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.450+1582G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48411750 | ||||||
| chr10:48411767
|
T | G | 3 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0289 | 3 | NA18945.hp2 NA18988.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.450+1599T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48411767 | ||||||
| chr10:48411860
|
TTCCCC | T | 7 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(4): Show | 7 | HG00735.hp2 HG02280.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.450+1712_450+1716d others(7): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48411860 | |||||
| chr10:48411926
|
C | T | 1 | a0001c0001t0003g0099 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.450+1758C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48411926 | ||||||
| chr10:48411946
|
A | G | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp2 HG02165.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.450+1778A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48411946 | ||||||
| chr10:48411960
|
G | A | 2 | a0001c0001t0018g0095a0001c0001t0018g0096 | 2 | HG01123.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.450+1792G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48411960 | ||||||
| chr10:48412091
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.450+1923C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48412091 | ||||||
| chr10:48412092
|
C | T | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.450+1924C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48412092 | ||||||
| chr10:48412148
|
T | C | 1 | a0001c0001t0001g0185 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.450+1980T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48412148 | ||||||
| chr10:48412195
|
C | T | 1 | a0001c0001t0006g0255 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.450+2027C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48412195 | ||||||
| chr10:48412224
|
A | G | 159 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(156): Show | 162 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.450+2056A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48412224 | ||||||
| chr10:48412290
|
C | T | 1 | a0001c0001t0003g0293 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.450+2122C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48412290 | ||||||
| chr10:48412385
|
C | T | 1 | a0001c0001t0006g0263 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.450+2217C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48412385 | ||||||
| chr10:48412426
|
G | A | 2 | a0001c0001t0018g0095a0001c0001t0018g0096 | 2 | HG01123.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.450+2258G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48412426 | ||||||
| chr10:48412522
|
C | T | 19 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(16): Show | 19 | HG00735.hp2 HG02055.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.450+2354C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48412522 | ||||||
| chr10:48412839
|
G | T | 1 | a0001c0001t0022g0133 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.450+2671G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48412839 | ||||||
| chr10:48413089
|
C | T | 1 | a0001c0001t0003g0286 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.450+2921C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48413089 | ||||||
| chr10:48413102
|
T | C | 1 | a0001c0001t0001g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.450+2934T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48413102 | ||||||
| chr10:48413144
|
A | C | 7 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(4): Show | 7 | HG00735.hp2 HG02280.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.450+2976A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48413144 | ||||||
| chr10:48413201
|
A | G | 5 | a0001c0001t0002g0001a0001c0001t0002g0022a0001c0001t0002g0024others(2): Show | 6 | NA18612.hp1 NA19001.hp1 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.450+3033A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48413201 | ||||||
| chr10:48413225
|
CTT | C | 6 | a0001c0001t0003g0293a0001c0001t0008g0008a0001c0001t0008g0009others(3): Show | 6 | HG02109.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.450+3060_450+3061d others(4): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48413225 | |||||
| chr10:48413241
|
C | CTATGAA | 3 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281 | 3 | HG03098.hp1 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.450+3074_450+3079d others(8): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48413241 | |||||
| chr10:48413243
|
A | G | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+3075A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48413243 | ||||||
| chr10:48413278
|
T | G | 3 | a0001c0001t0007g0085a0001c0001t0007g0092a0001c0001t0007g0093 | 3 | HG03688.hp2 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.450+3110T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48413278 | ||||||
| chr10:48413293
|
T | C | 3 | a0001c0001t0007g0085a0001c0001t0007g0092a0001c0001t0007g0093 | 3 | HG03688.hp2 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.450+3125T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48413293 | ||||||
| chr10:48413328
|
A | G | 1 | a0001c0001t0030g0272 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.450+3160A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48413328 | ||||||
| chr10:48413395
|
A | T | 1 | a0001c0001t0001g0169 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.450+3227A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48413395 | ||||||
| chr10:48413517
|
T | G | 74 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(71): Show | 76 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.450+3349T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48413517 | ||||||
| chr10:48413540
|
C | T | 82 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(79): Show | 84 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.450+3372C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48413540 | ||||||
| chr10:48413815
|
T | TTA | 46 | a0001c0001t0001g0138a0001c0001t0001g0141a0001c0001t0001g0168others(43): Show | 46 | HG00544.hp2 HG01433.hp1 HG01433.hp2 others(43): Show |
intron_variant | MODIFIER | c.450+3691_450+3692d others(4): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48413815 | |||||
| chr10:48413815
|
T | TTATA | 44 | a0001c0001t0001g0122a0001c0001t0001g0128a0001c0001t0001g0132others(41): Show | 45 | HG00609.hp2 HG00735.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.450+3689_450+3692d others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48413815 | |||||
| chr10:48413815
|
T | TTATATA | 49 | a0001c0001t0001g0120a0001c0001t0001g0129a0001c0001t0001g0130others(46): Show | 49 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.450+3687_450+3692d others(8): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48413815 | |||||
| chr10:48413815
|
T | TTATATAT others(1): Show |
28 | a0001c0001t0001g0137a0001c0001t0001g0165a0001c0001t0001g0178others(25): Show | 28 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.450+3685_450+3692d others(10): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48413815 | |||||
| chr10:48413815
|
T | TTATATAT others(3): Show |
27 | a0001c0001t0001g0127a0001c0001t0001g0131a0001c0001t0001g0135others(24): Show | 28 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(25): Show |
intron_variant | MODIFIER | c.450+3683_450+3692d others(12): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48413815 | |||||
| chr10:48413815
|
T | TTATATAT others(5): Show |
15 | a0001c0001t0001g0139a0001c0001t0001g0212a0001c0001t0001g0244others(12): Show | 15 | HG01884.hp1 HG02809.hp2 HG03471.hp1 others(12): Show |
intron_variant | MODIFIER | c.450+3681_450+3692d others(14): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48413815 | |||||
| chr10:48413815
|
T | TTATATAT others(7): Show |
6 | a0001c0001t0001g0277a0001c0001t0002g0034a0001c0001t0002g0045others(3): Show | 6 | HG01934.hp1 HG02080.hp1 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.450+3679_450+3692d others(16): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48413815 | |||||
| chr10:48413815
|
T | TTATATAT others(9): Show |
2 | a0001c0001t0005g0020a0001c0001t0026g0035 | 2 | NA18983.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.450+3677_450+3692d others(18): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48413815 | |||||
| chr10:48413815
|
T | TTATATAT others(11): Show |
1 | a0001c0001t0001g0301 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.450+3675_450+3692d others(20): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48413815 | |||||
| chr10:48413815
|
T | TTATATAT others(13): Show |
1 | a0001c0001t0001g0278 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.450+3673_450+3692d others(22): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48413815 | |||||
| chr10:48413815
|
T | TTTTATAT others(3): Show |
2 | a0001c0001t0011g0006a0001c0001t0011g0007 | 2 | HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.450+3648_450+3649i others(12): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48413815 | |||||
| chr10:48413815
|
T | TTTTATAT others(9): Show |
1 | a0001c0001t0011g0004 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.450+3648_450+3649i others(18): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48413815 | |||||
| chr10:48413815
|
TTA | T | 14 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0184others(11): Show | 14 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.450+3691_450+3692d others(4): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48413815 | |||||
| chr10:48413815
|
TTATA | T | 5 | a0001c0001t0001g0123a0001c0001t0001g0126a0001c0001t0002g0002others(2): Show | 6 | HG01070.hp1 HG01071.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.450+3689_450+3692d others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48413815 | |||||
| chr10:48413815
|
TTATATAT others(3): Show |
T | 3 | a0001c0001t0001g0166a0001c0001t0002g0075a0001c0004t0001g0171 | 3 | HG01981.hp1 NA18961.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.450+3683_450+3692d others(12): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48413815 | |||||
| chr10:48413815
|
TTATATAT others(5): Show |
T | 2 | a0001c0001t0001g0167a0001c0001t0006g0159 | 2 | HG02451.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.450+3681_450+3692d others(14): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48413815 | |||||
| chr10:48413815
|
TTATATAT others(7): Show |
T | 1 | a0001c0001t0001g0119 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.450+3679_450+3692d others(16): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48413815 | |||||
| chr10:48413815
|
TTATATAT others(9): Show |
T | 1 | a0001c0001t0030g0272 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.450+3677_450+3692d others(18): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48413815 | |||||
| chr10:48413815
|
TTATATAT others(11): Show |
T | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG01943.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.450+3675_450+3692d others(20): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48413815 | |||||
| chr10:48413815
|
TTATATAT others(13): Show |
T | 1 | a0001c0001t0001g0246 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.450+3673_450+3692d others(22): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48413815 | |||||
| chr10:48413815
|
TTATATAT others(15): Show |
T | 21 | a0001c0001t0003g0284a0001c0001t0006g0086a0001c0001t0006g0250others(18): Show | 21 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.450+3671_450+3692d others(24): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48413815 | |||||
| chr10:48413815
|
TTATATAT others(21): Show |
T | 5 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0010others(2): Show | 5 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.450+3665_450+3692d others(30): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48413815 | |||||
| chr10:48413815
|
TTATATAT others(23): Show |
T | 3 | a0001c0001t0003g0286a0001c0001t0018g0095a0001c0001t0018g0096 | 3 | HG01123.hp1 HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.450+3663_450+3692d others(32): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48413815 | |||||
| chr10:48413857
|
A | G | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+3689A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48413857 | ||||||
| chr10:48413858
|
T | TATATATA others(32): Show |
2 | a0001c0001t0015g0121a0001c0001t0024g0125 | 2 | HG02602.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.450+3692_450+3693i others(41): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48413858 | |||||
| chr10:48413858
|
T | TATATATA others(28): Show |
1 | a0001c0001t0015g0234 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.450+3692_450+3693i others(37): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48413858 | |||||
| chr10:48413933
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.450+3765A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48413933 | ||||||
| chr10:48413991
|
G | A | 2 | a0001c0001t0002g0074a0001c0001t0002g0075 | 2 | NA18952.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.450+3823G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48413991 | ||||||
| chr10:48414271
|
A | G | 1 | a0001c0002t0017g0014 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.450+4103A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48414271 | ||||||
| chr10:48414307
|
A | G | 2 | a0001c0001t0003g0097a0001c0001t0003g0100 | 2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.450+4139A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48414307 | ||||||
| chr10:48414343
|
A | G | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+4175A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48414343 | ||||||
| chr10:48414373
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.450+4205G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48414373 | ||||||
| chr10:48414448
|
A | AT | 132 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(129): Show | 132 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.450+4297dupT | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48414448 | |||||
| chr10:48414448
|
A | ATT | 123 | a0001c0001t0001g0218a0001c0001t0001g0243a0001c0001t0001g0289others(120): Show | 126 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.450+4296_450+4297d others(4): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48414448 | |||||
| chr10:48414448
|
A | ATTT | 18 | a0001c0001t0002g0049a0001c0001t0002g0076a0001c0001t0003g0103others(15): Show | 18 | HG01516.hp1 HG02027.hp2 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.450+4295_450+4297d others(5): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48414448 | |||||
| chr10:48414448
|
A | ATTTT | 15 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(12): Show | 15 | HG00735.hp2 HG01884.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.450+4294_450+4297d others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48414448 | |||||
| chr10:48414514
|
G | A | 25 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(22): Show | 25 | HG00735.hp2 HG01884.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.450+4346G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48414514 | ||||||
| chr10:48414568
|
A | AT | 28 | a0001c0001t0001g0130a0001c0001t0001g0142a0001c0001t0001g0162others(25): Show | 28 | HG00280.hp2 HG01175.hp2 HG01515.hp2 others(25): Show |
intron_variant | MODIFIER | c.450+4426dupT | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48414568 | |||||
| chr10:48414568
|
AT | A | 87 | a0001c0001t0001g0123a0001c0001t0001g0163a0001c0001t0001g0165others(84): Show | 89 | HG00280.hp1 HG00544.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.450+4426delT | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48414568 | |||||
| chr10:48414568
|
ATT | A | 24 | a0001c0001t0002g0060a0001c0001t0003g0100a0001c0001t0003g0112others(21): Show | 24 | HG01069.hp1 HG01099.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.450+4425_450+4426d others(4): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48414568 | |||||
| chr10:48414568
|
ATTT | A | 46 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(43): Show | 47 | HG00099.hp1 HG00609.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.450+4424_450+4426d others(5): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48414568 | |||||
| chr10:48414609
|
G | C | 2 | a0001c0001t0002g0043a0001c0001t0002g0044 | 2 | HG00280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.450+4441G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48414609 | ||||||
| chr10:48414688
|
A | G | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.450+4520A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48414688 | ||||||
| chr10:48414773
|
G | T | 1 | a0001c0001t0006g0251 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.450+4605G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48414773 | ||||||
| chr10:48414782
|
A | G | 2 | a0001c0001t0019g0282a0001c0001t0019g0283 | 2 | HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.450+4614A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48414782 | ||||||
| chr10:48414874
|
G | T | 23 | a0001c0001t0004g0003a0001c0001t0004g0115a0001c0001t0004g0116others(20): Show | 24 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.450+4706G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48414874 | ||||||
| chr10:48414936
|
T | G | 1 | a0001c0001t0005g0038 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.450+4768T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48414936 | ||||||
| chr10:48414981
|
G | T | 159 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(156): Show | 162 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.450+4813G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48414981 | ||||||
| chr10:48415032
|
T | TCA | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+4864_450+4865i others(4): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48415032 | ||||||
| chr10:48415034
|
T | TAA | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+4867_450+4868d others(4): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48415034 | |||||
| chr10:48415104
|
A | G | 1 | a0001c0001t0001g0273 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.450+4936A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48415104 | ||||||
| chr10:48415197
|
C | G | 1 | a0001c0001t0002g0048 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.451-4958C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48415197 | ||||||
| chr10:48415230
|
A | C | 1 | a0001c0001t0001g0208 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.451-4925A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48415230 | ||||||
| chr10:48415318
|
G | C | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-4837G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48415318 | ||||||
| chr10:48415410
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.451-4745A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48415410 | ||||||
| chr10:48415414
|
A | G | 4 | a0001c0001t0003g0286a0001c0001t0006g0159a0001c0001t0018g0095others(1): Show | 4 | HG01123.hp1 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.451-4741A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48415414 | ||||||
| chr10:48415495
|
T | C | 1 | a0001c0001t0002g0016 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.451-4660T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48415495 | ||||||
| chr10:48415506
|
G | C | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-4649G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48415506 | ||||||
| chr10:48415569
|
G | A | 1 | a0001c0001t0004g0115 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.451-4586G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48415569 | ||||||
| chr10:48415634
|
T | C | 286 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(283): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.451-4521T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48415634 | ||||||
| chr10:48415723
|
C | T | 1 | a0001c0001t0003g0280 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.451-4432C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48415723 | ||||||
| chr10:48415953
|
C | G | 2 | a0001c0001t0015g0121a0001c0001t0015g0234 | 2 | HG02602.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.451-4202C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48415953 | ||||||
| chr10:48416024
|
G | A | 13 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(10): Show | 13 | HG01891.hp1 HG02622.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.451-4131G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48416024 | ||||||
| chr10:48416312
|
T | C | 2 | a0001c0001t0018g0095a0001c0001t0018g0096 | 2 | HG01123.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.451-3843T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48416312 | ||||||
| chr10:48416384
|
C | T | 1 | a0001c0001t0003g0100 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.451-3771C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48416384 | ||||||
| chr10:48416499
|
G | A | 1 | a0001c0001t0002g0048 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.451-3656G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48416499 | ||||||
| chr10:48416666
|
T | C | 3 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281 | 3 | HG03098.hp1 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.451-3489T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48416666 | ||||||
| chr10:48416701
|
T | C | 1 | a0001c0001t0003g0098 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.451-3454T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48416701 | ||||||
| chr10:48416931
|
C | T | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.451-3224C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48416931 | ||||||
| chr10:48416933
|
T | G | 1 | a0001c0001t0001g0200 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.451-3222T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48416933 | ||||||
| chr10:48416976
|
A | G | 1 | a0001c0001t0028g0106 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.451-3179A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48416976 | ||||||
| chr10:48416986
|
G | C | 3 | a0001c0001t0004g0115a0001c0001t0004g0116a0001c0001t0004g0117 | 3 | HG01069.hp1 HG01099.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.451-3169G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48416986 | ||||||
| chr10:48417161
|
G | T | 5 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(2): Show | 5 | HG02630.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.451-2994G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48417161 | ||||||
| chr10:48417396
|
T | A | 1 | a0001c0001t0001g0126 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.451-2759T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48417396 | ||||||
| chr10:48417442
|
A | G | 1 | a0001c0001t0032g0161 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.451-2713A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48417442 | ||||||
| chr10:48417540
|
G | A | 159 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(156): Show | 162 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.451-2615G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48417540 | ||||||
| chr10:48417737
|
A | G | 290 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(287): Show | 293 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.451-2418A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48417737 | ||||||
| chr10:48417838
|
C | T | 1 | a0001c0001t0020g0235 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.451-2317C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48417838 | ||||||
| chr10:48418113
|
A | G | 3 | a0001c0001t0007g0085a0001c0001t0007g0092a0001c0001t0007g0093 | 3 | HG03688.hp2 HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.451-2042A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48418113 | ||||||
| chr10:48418237
|
G | C | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-1918G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48418237 | ||||||
| chr10:48418325
|
G | A | 82 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(79): Show | 84 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.451-1830G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48418325 | ||||||
| chr10:48418437
|
TTGTGGAC others(2): Show |
T | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-1715_451-1707d others(11): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48418437 | |||||
| chr10:48418580
|
A | G | 1 | a0001c0001t0029g0107 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.451-1575A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48418580 | ||||||
| chr10:48418728
|
A | G | 2 | a0001c0001t0016g0269a0001c0001t0016g0270 | 2 | HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.451-1427A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48418728 | ||||||
| chr10:48418904
|
T | C | 1 | a0001c0001t0003g0285 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.451-1251T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48418904 | ||||||
| chr10:48419127
|
A | G | 1 | a0001c0001t0002g0032 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.451-1028A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48419127 | ||||||
| chr10:48419248
|
T | C | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-907T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48419248 | ||||||
| chr10:48419268
|
C | T | 1 | a0001c0001t0004g0156 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.451-887C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48419268 | ||||||
| chr10:48419355
|
C | A | 99 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(96): Show | 102 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.451-800C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48419355 | ||||||
| chr10:48419403
|
A | G | 2 | a0001c0001t0003g0097a0001c0001t0003g0100 | 2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.451-752A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48419403 | ||||||
| chr10:48419416
|
T | G | 2 | a0001c0001t0004g0145a0001c0001t0004g0146 | 2 | HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.451-739T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48419416 | ||||||
| chr10:48419489
|
A | C | 2 | a0001c0001t0001g0194a0001c0001t0001g0216 | 2 | NA18998.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.451-666A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48419489 | ||||||
| chr10:48419502
|
CAGT | C | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-648_451-646del others(3): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 48419502 | |||||
| chr10:48419869
|
T | G | 77 | a0001c0001t0001g0119a0001c0001t0001g0137a0001c0001t0001g0138others(74): Show | 77 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.451-286T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48419869 | ||||||
| chr10:48419947
|
T | C | 1 | a0001c0001t0001g0303 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.451-208T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48419947 | ||||||
| chr10:48419966
|
T | C | 8 | a0001c0001t0004g0003a0001c0001t0004g0148a0001c0001t0004g0149others(5): Show | 9 | HG00609.hp2 HG02165.hp1 NA18945.hp1 others(6): Show |
intron_variant | MODIFIER | c.451-189T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48419966 | ||||||
| chr10:48420103
|
A | G | 1 | a0001c0001t0001g0219 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.451-52A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48420103 | ||||||
| chr10:48420114
|
A | G | 1 | a0001c0001t0001g0239 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.451-41A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 5/11 | chr10 | 48420114 | ||||||
| chr10:48420380
|
G | T | 9 | a0001c0001t0003g0103a0001c0001t0003g0104a0001c0001t0003g0105others(6): Show | 9 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.616+60G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | chr10 | 48420380 | ||||||
| chr10:48420523
|
G | A | 4 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0002t0017g0014others(1): Show | 4 | HG01433.hp1 HG01516.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.616+203G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | chr10 | 48420523 | ||||||
| chr10:48420709
|
A | G | 10 | a0001c0001t0003g0103a0001c0001t0003g0104a0001c0001t0003g0105others(7): Show | 10 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.616+389A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | chr10 | 48420709 | ||||||
| chr10:48420873
|
T | C | 1 | a0001c0001t0006g0258 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.616+553T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | chr10 | 48420873 | ||||||
| chr10:48421010
|
A | T | 1 | a0001c0001t0003g0285 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.616+690A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | chr10 | 48421010 | ||||||
| chr10:48421238
|
T | A | 3 | a0001c0001t0009g0231a0001c0001t0009g0232a0001c0001t0009g0233 | 3 | HG01109.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.616+918T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | chr10 | 48421238 | ||||||
| chr10:48421294
|
T | C | 1 | a0001c0001t0006g0288 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.616+974T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | chr10 | 48421294 | ||||||
| chr10:48421339
|
G | C | 1 | a0001c0001t0001g0211 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.616+1019G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | chr10 | 48421339 | ||||||
| chr10:48421405
|
T | G | 7 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(4): Show | 7 | HG00735.hp2 HG02280.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.616+1085T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | chr10 | 48421405 | ||||||
| chr10:48421701
|
A | G | 1 | a0001c0001t0002g0084 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.616+1381A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | chr10 | 48421701 | ||||||
| chr10:48421703
|
G | A | 127 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(124): Show | 127 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.616+1383G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | chr10 | 48421703 | ||||||
| chr10:48421963
|
G | A | 1 | a0001c0001t0001g0137 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.616+1643G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | chr10 | 48421963 | ||||||
| chr10:48422005
|
T | TTTTA | 3 | a0001c0001t0004g0117a0001c0001t0004g0143a0001c0001t0004g0151 | 3 | HG01069.hp1 HG02165.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.616+1685_616+1686i others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | chr10 | 48422005 | ||||||
| chr10:48422005
|
T | TTTTATTT others(1): Show |
3 | a0001c0001t0004g0115a0001c0001t0004g0116a0001c0001t0004g0160 | 3 | HG01099.hp1 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.616+1685_616+1686i others(10): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | chr10 | 48422005 | ||||||
| chr10:48422006
|
C | CTTAT | 78 | a0001c0001t0001g0119a0001c0001t0001g0122a0001c0001t0001g0129others(75): Show | 78 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.616+1725_616+1728d others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr10 | 48422006 | |||||
| chr10:48422006
|
C | CTTATTTA others(1): Show |
66 | a0001c0001t0001g0120a0001c0001t0001g0127a0001c0001t0001g0128others(63): Show | 66 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.616+1721_616+1728d others(10): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr10 | 48422006 | |||||
| chr10:48422006
|
C | CTTATTTA others(5): Show |
2 | a0001c0001t0001g0130a0001c0001t0006g0255 | 2 | HG01993.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.616+1717_616+1728d others(14): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr10 | 48422006 | |||||
| chr10:48422006
|
C | T | 21 | a0001c0001t0004g0003a0001c0001t0004g0115a0001c0001t0004g0116others(18): Show | 22 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.616+1686C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | chr10 | 48422006 | ||||||
| chr10:48422006
|
CTTAT | C | 13 | a0001c0001t0001g0126a0001c0001t0001g0165a0001c0001t0001g0184others(10): Show | 13 | HG00280.hp1 HG00609.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.616+1725_616+1728d others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr10 | 48422006 | |||||
| chr10:48422006
|
CTTATTTA others(1): Show |
C | 81 | a0001c0001t0001g0123a0001c0001t0001g0223a0001c0001t0001g0224others(78): Show | 83 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.616+1721_616+1728d others(10): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr10 | 48422006 | |||||
| chr10:48422006
|
CTTATTTA others(5): Show |
C | 2 | a0001c0001t0016g0269a0001c0001t0016g0270 | 2 | HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.616+1717_616+1728d others(14): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr10 | 48422006 | |||||
| chr10:48422006
|
CTTATTTA others(9): Show |
C | 1 | a0001c0001t0006g0159 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.616+1713_616+1728d others(18): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr10 | 48422006 | |||||
| chr10:48422064
|
A | G | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp2 HG02165.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.616+1744A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | chr10 | 48422064 | ||||||
| chr10:48422191
|
C | G | 1 | a0001c0001t0003g0112 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.616+1871C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | chr10 | 48422191 | ||||||
| chr10:48422395
|
T | C | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.617-1693T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | chr10 | 48422395 | ||||||
| chr10:48422453
|
C | A | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.617-1635C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | chr10 | 48422453 | ||||||
| chr10:48422844
|
G | A | 72 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(69): Show | 74 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.617-1244G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | chr10 | 48422844 | ||||||
| chr10:48423008
|
T | G | 1 | a0001c0001t0007g0091 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.617-1080T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | chr10 | 48423008 | ||||||
| chr10:48423500
|
T | C | 1 | a0001c0001t0005g0026 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.617-588T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | chr10 | 48423500 | ||||||
| chr10:48423521
|
G | A | 21 | a0001c0001t0006g0086a0001c0001t0006g0159a0001c0001t0006g0250others(18): Show | 21 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.617-567G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | chr10 | 48423521 | ||||||
| chr10:48423545
|
A | G | 5 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(2): Show | 5 | HG02630.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.617-543A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | chr10 | 48423545 | ||||||
| chr10:48423870
|
AG | A | 3 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281 | 3 | HG03098.hp1 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.617-217delG | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | chr10 | 48423870 | ||||||
| chr10:48423934
|
T | A | 1 | a0001c0001t0003g0286 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.617-154T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | chr10 | 48423934 | ||||||
| chr10:48423972
|
A | G | 1 | a0001c0001t0006g0159 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.617-116A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 6/11 | chr10 | 48423972 | ||||||
| chr10:48424193
|
A | G | 1 | a0001c0001t0001g0211 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.688+34A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 7/11 | chr10 | 48424193 | ||||||
| chr10:48424250
|
T | A | 2 | a0001c0001t0019g0282a0001c0001t0019g0283 | 2 | HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.688+91T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 7/11 | chr10 | 48424250 | ||||||
| chr10:48424253
|
G | A | 7 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(4): Show | 7 | HG00735.hp2 HG02280.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.688+94G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 7/11 | chr10 | 48424253 | ||||||
| chr10:48424376
|
A | G | 1 | a0001c0001t0002g0060 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.688+217A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 7/11 | chr10 | 48424376 | ||||||
| chr10:48424384
|
T | C | 1 | a0001c0004t0001g0171 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.688+225T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 7/11 | chr10 | 48424384 | ||||||
| chr10:48424388
|
T | A | 3 | a0001c0001t0009g0231a0001c0001t0009g0232a0001c0001t0009g0233 | 3 | HG01109.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.688+229T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 7/11 | chr10 | 48424388 | ||||||
| chr10:48424451
|
C | A | 1 | a0001c0001t0001g0249 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.688+292C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 7/11 | chr10 | 48424451 | ||||||
| chr10:48424620
|
A | C | 1 | a0001c0001t0001g0177 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.688+461A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 7/11 | chr10 | 48424620 | ||||||
| chr10:48424657
|
G | T | 1 | a0001c0001t0007g0088 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.688+498G>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 7/11 | chr10 | 48424657 | ||||||
| chr10:48424708
|
A | T | 1 | a0001c0001t0007g0294 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.688+549A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 7/11 | chr10 | 48424708 | ||||||
| chr10:48425191
|
G | A | 2 | a0001c0001t0018g0095a0001c0001t0018g0096 | 2 | HG01123.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.689-697G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 7/11 | chr10 | 48425191 | ||||||
| chr10:48425216
|
A | G | 3 | a0001c0001t0004g0115a0001c0001t0004g0116a0001c0001t0004g0117 | 3 | HG01069.hp1 HG01099.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.689-672A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 7/11 | chr10 | 48425216 | ||||||
| chr10:48425705
|
A | C | 1 | a0001c0001t0031g0210 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.689-183A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 7/11 | chr10 | 48425705 | ||||||
| chr10:48425831
|
A | ACAAGAAT others(7): Show |
127 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(124): Show | 127 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.689-57_689-56insCA others(12): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 7/11 | chr10 | 48425831 | ||||||
| chr10:48425833
|
G | GTAA | 127 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(124): Show | 127 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.689-55_689-54insTA others(1): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 7/11 | chr10 | 48425833 | ||||||
| chr10:48425835
|
C | T | 127 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(124): Show | 127 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.689-53C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 7/11 | chr10 | 48425835 | ||||||
| chr10:48425836
|
T | G | 127 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(124): Show | 127 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.689-52T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 7/11 | chr10 | 48425836 | ||||||
| chr10:48425856
|
A | G | 1 | a0001c0001t0004g0160 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.689-32A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 7/11 | chr10 | 48425856 | ||||||
| chr10:48426136
|
G | A | 21 | a0001c0001t0006g0086a0001c0001t0006g0159a0001c0001t0006g0250others(18): Show | 21 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.871+66G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 8/11 | chr10 | 48426136 | ||||||
| chr10:48426611
|
G | A | 1 | a0001c0001t0003g0286 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.996+107G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 9/11 | chr10 | 48426611 | ||||||
| chr10:48426671
|
C | T | 1 | a0001c0001t0003g0293 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.996+167C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 9/11 | chr10 | 48426671 | ||||||
| chr10:48426770
|
A | G | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.996+266A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 9/11 | chr10 | 48426770 | ||||||
| chr10:48426825
|
G | A | 5 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(2): Show | 5 | HG02630.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.997-255G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 9/11 | chr10 | 48426825 | ||||||
| chr10:48426933
|
T | C | 1 | a0001c0001t0015g0121 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.997-147T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 9/11 | chr10 | 48426933 | ||||||
| chr10:48427016
|
A | G | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.997-64A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 9/11 | chr10 | 48427016 | ||||||
| chr10:48427029
|
T | A | 5 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0281others(2): Show | 5 | HG02630.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.997-51T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 9/11 | chr10 | 48427029 | ||||||
| chr10:48427043
|
C | T | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.997-37C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 9/11 | chr10 | 48427043 | ||||||
| chr10:48427152
|
G | A | 1 | a0001c0001t0002g0050 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1060+9G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48427152 | ||||||
| chr10:48427234
|
T | G | 21 | a0001c0001t0006g0086a0001c0001t0006g0159a0001c0001t0006g0250others(18): Show | 21 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.1060+91T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48427234 | ||||||
| chr10:48427448
|
G | A | 7 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(4): Show | 7 | HG00735.hp2 HG02280.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1060+305G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48427448 | ||||||
| chr10:48427462
|
G | A | 20 | a0001c0001t0006g0086a0001c0001t0006g0250a0001c0001t0006g0251others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.1060+319G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48427462 | ||||||
| chr10:48427513
|
T | C | 3 | a0001c0001t0003g0286a0001c0001t0018g0095a0001c0001t0018g0096 | 3 | HG01123.hp1 HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1060+370T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48427513 | ||||||
| chr10:48427735
|
A | G | 295 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(292): Show | 298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1060+592A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48427735 | ||||||
| chr10:48427738
|
C | A | 1 | a0001c0001t0001g0175 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1060+595C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48427738 | ||||||
| chr10:48427825
|
C | A | 2 | a0001c0001t0016g0269a0001c0001t0016g0270 | 2 | HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1060+682C>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48427825 | ||||||
| chr10:48427883
|
A | G | 1 | a0001c0001t0001g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1060+740A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48427883 | ||||||
| chr10:48427928
|
T | C | 1 | a0001c0001t0001g0223 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1060+785T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48427928 | ||||||
| chr10:48427938
|
T | A | 7 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(4): Show | 7 | HG00735.hp2 HG02280.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1060+795T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48427938 | ||||||
| chr10:48428097
|
A | G | 3 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0025g0114 | 3 | HG02451.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1060+954A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48428097 | ||||||
| chr10:48428163
|
A | G | 2 | a0001c0001t0002g0074a0001c0001t0002g0075 | 2 | NA18952.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.1060+1020A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48428163 | ||||||
| chr10:48428214
|
A | G | 7 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(4): Show | 7 | HG00735.hp2 HG02280.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1060+1071A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48428214 | ||||||
| chr10:48428324
|
T | G | 6 | a0001c0001t0003g0293a0001c0001t0008g0008a0001c0001t0008g0009others(3): Show | 6 | HG02109.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1060+1181T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48428324 | ||||||
| chr10:48428396
|
G | A | 3 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0025g0114 | 3 | HG02451.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1060+1253G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48428396 | ||||||
| chr10:48428464
|
A | G | 290 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(287): Show | 293 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.1060+1321A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48428464 | ||||||
| chr10:48428571
|
T | C | 9 | a0001c0001t0003g0103a0001c0001t0003g0104a0001c0001t0003g0105others(6): Show | 9 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1060+1428T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48428571 | ||||||
| chr10:48428599
|
A | G | 7 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(4): Show | 7 | HG00735.hp2 HG02280.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1060+1456A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48428599 | ||||||
| chr10:48428707
|
T | C | 3 | a0001c0001t0009g0231a0001c0001t0009g0232a0001c0001t0009g0233 | 3 | HG01109.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1060+1564T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48428707 | ||||||
| chr10:48428770
|
G | A | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1060+1627G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48428770 | ||||||
| chr10:48428860
|
C | G | 6 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(3): Show | 6 | HG01884.hp2 HG02165.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1060+1717C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48428860 | ||||||
| chr10:48428993
|
G | GT | 100 | a0001c0001t0001g0167a0001c0001t0001g0226a0001c0001t0002g0001others(97): Show | 103 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1060+1862dupT | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 48428993 | |||||
| chr10:48428993
|
G | GTT | 8 | a0001c0001t0003g0293a0001c0001t0004g0145a0001c0001t0004g0146others(5): Show | 8 | HG02109.hp1 HG02486.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1060+1861_1060+186 others(6): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 48428993 | |||||
| chr10:48429114
|
C | T | 1 | a0001c0001t0001g0185 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1060+1971C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48429114 | ||||||
| chr10:48429115
|
G | A | 1 | a0001c0001t0006g0159 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1060+1972G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48429115 | ||||||
| chr10:48429136
|
A | G | 21 | a0001c0001t0006g0086a0001c0001t0006g0159a0001c0001t0006g0250others(18): Show | 21 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.1060+1993A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48429136 | ||||||
| chr10:48429140
|
T | A | 1 | a0001c0001t0002g0034 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1060+1997T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48429140 | ||||||
| chr10:48429244
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1061-1949G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48429244 | ||||||
| chr10:48429301
|
A | G | 2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | HG00741.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1061-1892A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48429301 | ||||||
| chr10:48429371
|
T | C | 1 | a0001c0001t0001g0216 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1061-1822T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48429371 | ||||||
| chr10:48429381
|
A | C | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.1061-1812A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48429381 | ||||||
| chr10:48429496
|
G | A | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1061-1697G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48429496 | ||||||
| chr10:48429699
|
GCTTT | G | 23 | a0001c0001t0004g0003a0001c0001t0004g0115a0001c0001t0004g0116others(20): Show | 24 | HG00099.hp1 HG00609.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.1061-1491_1061-148 others(8): Show |
MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 48429699 | |||||
| chr10:48429922
|
G | C | 1 | a0001c0001t0006g0262 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1061-1271G>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48429922 | ||||||
| chr10:48430016
|
G | A | 1 | a0001c0001t0001g0291 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1061-1177G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48430016 | ||||||
| chr10:48430096
|
T | C | 1 | a0001c0001t0001g0189 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1061-1097T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48430096 | ||||||
| chr10:48430101
|
T | G | 1 | a0001c0001t0005g0080 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1061-1092T>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48430101 | ||||||
| chr10:48430218
|
C | T | 1 | a0001c0001t0005g0080 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1061-975C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48430218 | ||||||
| chr10:48430317
|
T | C | 286 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(283): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1061-876T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48430317 | ||||||
| chr10:48430387
|
C | T | 1 | a0001c0001t0006g0252 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1061-806C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48430387 | ||||||
| chr10:48430428
|
A | G | 3 | a0001c0001t0003g0112a0001c0001t0003g0113a0001c0001t0025g0114 | 3 | HG02451.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1061-765A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48430428 | ||||||
| chr10:48430467
|
A | G | 19 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(16): Show | 19 | HG00735.hp2 HG02055.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.1061-726A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48430467 | ||||||
| chr10:48430621
|
C | G | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1061-572C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48430621 | ||||||
| chr10:48431054
|
C | T | 2 | a0001c0002t0017g0014a0001c0002t0017g0015 | 2 | HG02165.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.1061-139C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 10/11 | chr10 | 48431054 | ||||||
| chr10:48431804
|
T | C | 1 | a0001c0001t0006g0159 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1138+534T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 11/11 | chr10 | 48431804 | ||||||
| chr10:48432008
|
A | C | 73 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(70): Show | 75 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.1138+738A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 11/11 | chr10 | 48432008 | ||||||
| chr10:48432079
|
C | T | 1 | a0001c0001t0030g0272 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1138+809C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 11/11 | chr10 | 48432079 | ||||||
| chr10:48432250
|
G | A | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1138+980G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 11/11 | chr10 | 48432250 | ||||||
| chr10:48432679
|
T | A | 1 | a0001c0001t0006g0259 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1138+1409T>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 11/11 | chr10 | 48432679 | ||||||
| chr10:48432779
|
C | G | 1 | a0001c0001t0002g0064 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1138+1509C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 11/11 | chr10 | 48432779 | ||||||
| chr10:48432894
|
T | C | 1 | a0001c0001t0003g0286 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1138+1624T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 11/11 | chr10 | 48432894 | ||||||
| chr10:48433116
|
T | C | 286 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(283): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1139-1768T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 11/11 | chr10 | 48433116 | ||||||
| chr10:48433138
|
A | G | 20 | a0001c0001t0006g0086a0001c0001t0006g0250a0001c0001t0006g0251others(17): Show | 20 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.1139-1746A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 11/11 | chr10 | 48433138 | ||||||
| chr10:48433190
|
C | G | 1 | a0001c0001t0004g0150 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1139-1694C>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 11/11 | chr10 | 48433190 | ||||||
| chr10:48433206
|
C | T | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1139-1678C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 11/11 | chr10 | 48433206 | ||||||
| chr10:48433289
|
A | C | 127 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(124): Show | 127 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.1139-1595A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 11/11 | chr10 | 48433289 | ||||||
| chr10:48433376
|
A | C | 1 | a0001c0001t0002g0084 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1139-1508A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 11/11 | chr10 | 48433376 | ||||||
| chr10:48433413
|
T | C | 1 | a0001c0001t0004g0160 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1139-1471T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 11/11 | chr10 | 48433413 | ||||||
| chr10:48433688
|
T | C | 7 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(4): Show | 7 | HG00735.hp2 HG02280.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1139-1196T>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 11/11 | chr10 | 48433688 | ||||||
| chr10:48433807
|
G | A | 1 | a0001c0001t0021g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1139-1077G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 11/11 | chr10 | 48433807 | ||||||
| chr10:48434007
|
A | G | 1 | a0001c0001t0003g0293 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1139-877A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 11/11 | chr10 | 48434007 | ||||||
| chr10:48434103
|
G | A | 153 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(150): Show | 156 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.1139-781G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 11/11 | chr10 | 48434103 | ||||||
| chr10:48434167
|
A | T | 153 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(150): Show | 156 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.1139-717A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 11/11 | chr10 | 48434167 | ||||||
| chr10:48434183
|
A | T | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1139-701A>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 11/11 | chr10 | 48434183 | ||||||
| chr10:48434441
|
G | A | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1139-443G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 11/11 | chr10 | 48434441 | ||||||
| chr10:48434519
|
G | A | 11 | a0001c0001t0006g0086a0001c0001t0006g0256a0001c0001t0006g0257others(8): Show | 11 | HG01099.hp2 HG01106.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.1139-365G>A | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 11/11 | chr10 | 48434519 | ||||||
| chr10:48434548
|
A | C | 127 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0122others(124): Show | 127 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.1139-336A>C | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 11/11 | chr10 | 48434548 | ||||||
| chr10:48434669
|
A | G | 4 | a0001c0001t0011g0004a0001c0001t0011g0005a0001c0001t0011g0006others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1139-215A>G | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 11/11 | chr10 | 48434669 | ||||||
| chr10:48434810
|
C | T | 1 | a0001c0001t0006g0255 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1139-74C>T | MAPK8 | ENSG00000107643.17 | transcript | ENST00000374189.6 | protein_coding | 11/11 | chr10 | 48434810 |