Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 6416 |
|---|---|
| ensemblid | ENSG00000065559.15 |
| hgncid | 6844 |
| symbol | MAP2K4 |
| name | mitogen-activated protein kinase kinase 4 |
| refseq_nuc | NM_003010.4 |
| refseq_prot | NP_003001.1 |
| ensembl_nuc | ENST00000353533.10 |
| ensembl_prot | ENSP00000262445.5 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 12020877 |
| end | 12143828 |
| strand | + |
| ver | v1.2 |
| region | chr17:12020877-12143828 |
| region5000 | chr17:12015877-12148828 |
| regionname0 | MAP2K4_chr17_12020877_12143828 |
| regionname5000 | MAP2K4_chr17_12015877_12148828 |
| 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 | 399 | 321 | 90 | 45 | 140 | 12 | 32 | 102 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| a0002 | 0/0 | 399 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| 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 | 1200 | 317 | 88 | 45 | 138 | 12 | 32 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| c0002 | 0/0 | 1200 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| c0003 | 0/0 | 1200 | 2 | 2 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| c0004 | 0/0 | 1200 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 2579 | 198 | 74 | 28 | 65 | 10 | 20 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| t0002 | 0/0 | 2579 | 61 | 8 | 14 | 28 | 1 | 10 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| t0003 | 0/0 | 2579 | 18 | 0 | 0 | 18 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| t0004 | 0/0 | 2580 | 18 | 3 | 0 | 15 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| t0005 | 0/0 | 2579 | 5 | 0 | 0 | 5 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| t0006 | 0/0 | 2579 | 4 | 0 | 0 | 4 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| t0007 | 0/0 | 2579 | 3 | 3 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| t0008 | 0/0 | 2579 | 3 | 0 | 0 | 3 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| t0009 | 0/0 | 2579 | 2 | 0 | 0 | 0 | 0 | 2 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| t0010 | 0/1 | 2579 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| t0011 | 0/0 | 2579 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| t0012 | 0/0 | 2579 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| t0013 | 0/0 | 2579 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| t0014 | 0/0 | 2579 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| t0015 | 0/0 | 2579 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| t0016 | 0/0 | 2579 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| t0017 | 0/0 | 2579 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| t0018 | 0/0 | 2579 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| t0019 | 0/0 | 2579 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| 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 | 0 | 0 | 2 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0025 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0205 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| 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 | 1200 | 317 | 88 | 45 | 138 | 12 | 32 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| a0001c0002 | 0/0 | 1200 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| a0001c0003 | 0/0 | 1200 | 2 | 2 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| a0002c0004 | 0/0 | 1200 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3778 | 197 | 73 | 28 | 65 | 10 | 20 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| a0001c0001t0002 | 0/0 | 3778 | 60 | 7 | 14 | 28 | 1 | 10 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| a0001c0001t0003 | 0/0 | 3778 | 16 | 0 | 0 | 16 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| a0001c0001t0004 | 0/0 | 3779 | 18 | 3 | 0 | 15 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| a0001c0001t0005 | 0/0 | 3778 | 5 | 0 | 0 | 5 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| a0001c0001t0006 | 0/0 | 3778 | 4 | 0 | 0 | 4 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| a0001c0001t0007 | 0/0 | 3778 | 3 | 3 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| a0001c0001t0008 | 0/0 | 3778 | 3 | 0 | 0 | 3 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| a0001c0001t0009 | 0/0 | 3778 | 2 | 0 | 0 | 0 | 0 | 2 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| a0001c0001t0010 | 0/1 | 3778 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| a0001c0001t0011 | 0/0 | 3778 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| a0001c0001t0013 | 0/0 | 3778 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| a0001c0001t0014 | 0/0 | 3778 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| a0001c0001t0015 | 0/0 | 3778 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| a0001c0001t0016 | 0/0 | 3778 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| a0001c0001t0017 | 0/0 | 3778 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| a0001c0001t0018 | 0/0 | 3778 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| a0001c0001t0019 | 0/0 | 3778 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| a0001c0002t0003 | 0/0 | 3778 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| a0001c0003t0001 | 0/0 | 3778 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| a0001c0003t0002 | 0/0 | 3778 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| a0002c0004t0012 | 0/0 | 3778 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | copy fasta | chr17 | 12015877 | 12148828 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0025 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0005g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0005g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0006g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0006g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0006g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0006g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0007g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0007g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0007g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0008g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0008g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0008g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0009g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0010g0205 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0011g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0013g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0014g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0015g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0016g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0017g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0018g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0001t0019g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0003t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0001c0003t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| a0002c0004t0012g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0184 | EUR | GBR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0048 | EUR | GBR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0109 | EUR | FIN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0293 | EUR | FIN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | CHS | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | CHS | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | CHS | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00597 | hp2 | a0001 | c0002 | t0003 | g0052 | EAS | CHS | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | CHS | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00609 | hp2 | a0001 | c0001 | t0006 | g0095 | EAS | CHS | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0261 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0267 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00673 | hp1 | a0001 | c0001 | t0005 | g0306 | EAS | CHS | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0156 | EAS | CHS | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0264 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0269 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01243 | hp1 | a0001 | c0001 | t0013 | g0005 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01243 | hp2 | a0002 | c0004 | t0012 | g0028 | AMR | PUR | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0258 | AMR | CLM | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0319 | AMR | CLM | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | CLM | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | IBS | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | IBS | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0064 | EUR | IBS | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0152 | EUR | IBS | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01884 | hp1 | a0001 | c0001 | t0007 | g0026 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0175 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0268 | AMR | PEL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0316 | AMR | PEL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0039 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02083 | hp2 | a0001 | c0001 | t0005 | g0197 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0304 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0290 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02145 | hp2 | a0001 | c0001 | t0011 | g0017 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CDX | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | CDX | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CDX | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CDX | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02273 | hp1 | a0001 | c0001 | t0015 | g0217 | AMR | PEL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02273 | hp2 | a0001 | c0001 | t0016 | g0235 | AMR | PEL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0270 | AMR | PEL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02572 | hp1 | a0001 | c0003 | t0002 | g0280 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0266 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0260 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0120 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0253 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0165 | AFR | ESN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0252 | AFR | ESN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | ESN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ESN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ESN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0250 | AFR | ESN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ESN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0073 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0318 | AFR | MSL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03490 | hp1 | a0001 | c0001 | t0009 | g0001 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03492 | hp2 | a0001 | c0001 | t0009 | g0001 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ESN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0275 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0257 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0265 | SAS | BEB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | STU | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | STU | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0119 | SAS | STU | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | STU | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0259 | SAS | STU | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | STU | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | YRI | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | YRI | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18612 | hp1 | a0001 | c0002 | t0003 | g0085 | EAS | CHB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | CHB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | CHB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | YRI | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18906 | hp2 | a0001 | c0001 | t0018 | g0047 | AFR | YRI | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0305 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18950 | hp1 | a0001 | c0001 | t0005 | g0196 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0289 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18967 | hp2 | a0001 | c0001 | t0006 | g0112 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18972 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18980 | hp1 | a0001 | c0001 | t0005 | g0201 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18990 | hp1 | a0001 | c0001 | t0008 | g0191 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18992 | hp1 | a0001 | c0001 | t0019 | g0295 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0231 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18997 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18997 | hp2 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19006 | hp1 | a0001 | c0001 | t0005 | g0186 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19006 | hp2 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | LWK | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0224 | AFR | LWK | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | LWK | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19054 | hp2 | a0001 | c0001 | t0008 | g0192 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19060 | hp1 | a0001 | c0001 | t0006 | g0116 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19066 | hp2 | a0001 | c0001 | t0006 | g0127 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19075 | hp1 | a0001 | c0001 | t0014 | g0091 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19084 | hp2 | a0001 | c0001 | t0008 | g0189 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ASW | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ASW | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA20752 | hp1 | a0001 | c0001 | t0017 | g0078 | EUR | TSI | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0204 | EUR | TSI | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0271 | EUR | TSI | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0093 | EUR | TSI | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | CLM | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0279 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0249 | AFR | ACB | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | MSL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | USA | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | USA | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0263 | AFR | USA | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | USA | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | LWK | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | LWK | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0010 | g0205 | REF | REF | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0025 | REF | REF | MAP2K4_chr17_12015877_12148828 | MAP2K4 | chr17 | 12015877 | 12148828 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:12054976
|
T | C | 1 | a0002 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.203T>C | p.Val68Ala | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/11 | 213/3778 | 203/1200 | 68/399 | chr17 | 12054976 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:12020949
|
C | T | 1 | a0001c0003 | 2 | HG02559.hp1 HG02572.hp1 |
synonymous_variant | LOW | c.63C>T | p.Pro21Pro | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/11 | 73/3778 | 63/1200 | 21/399 | chr17 | 12020949 | ||
| chr17:12139845
|
G | A | 1 | a0001c0002 | 2 | HG00597.hp2 NA18612.hp1 |
synonymous_variant | LOW | c.1047G>A | p.Thr349Thr | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/11 | 1057/3778 | 1047/1200 | 349/399 | chr17 | 12139845 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:12141709
|
A | G | 1 | a0001c0001t0008 | 3 | NA18990.hp1 NA19054.hp2 NA19084.hp2 |
3_prime_UTR_variant | MODIFIER | c.*449A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 449 | chr17 | 12141709 | |||||
| chr17:12141814
|
T | C | 1 | a0001c0001t0010 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*554T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 554 | chr17 | 12141814 | |||||
| chr17:12141976
|
A | G | 1 | a0001c0001t0006 | 4 | HG00609.hp2 NA18967.hp2 NA19060.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*716A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 716 | chr17 | 12141976 | |||||
| chr17:12141985
|
T | TG | 1 | a0001c0001t0004 | 18 | HG00673.hp2 HG01891.hp2 HG02040.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*728dupG | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 729 | INFO_REALIGN_3_PRIME | chr17 | 12141985 | ||||
| chr17:12142026
|
G | C | 1 | a0001c0001t0011 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*766G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 766 | chr17 | 12142026 | |||||
| chr17:12142057
|
G | A | 1 | a0001c0001t0005 | 5 | HG00673.hp1 HG02083.hp2 NA18950.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*797G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 797 | chr17 | 12142057 | |||||
| chr17:12142214
|
C | G | 1 | a0001c0001t0019 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*954C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 954 | chr17 | 12142214 | |||||
| chr17:12142359
|
G | A | 1 | a0002c0004t0012 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1099G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 1099 | chr17 | 12142359 | |||||
| chr17:12142434
|
A | G | 1 | a0001c0001t0018 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1174A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 1174 | chr17 | 12142434 | |||||
| chr17:12142446
|
C | T | 1 | a0001c0001t0017 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1186C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 1186 | chr17 | 12142446 | |||||
| chr17:12142588
|
G | A | 3 | a0001c0001t0002a0001c0001t0019a0001c0003t0002 | 62 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1328G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 1328 | chr17 | 12142588 | |||||
| chr17:12142692
|
A | G | 1 | a0001c0001t0007 | 3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1432A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 1432 | chr17 | 12142692 | |||||
| chr17:12142857
|
A | G | 1 | a0001c0001t0009 | 2 | HG03490.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1597A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 1597 | chr17 | 12142857 | |||||
| chr17:12142989
|
T | C | 1 | a0001c0001t0013 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1729T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 1729 | chr17 | 12142989 | |||||
| chr17:12143300
|
C | G | 1 | a0001c0001t0016 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2040C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 2040 | chr17 | 12143300 | |||||
| chr17:12143355
|
A | G | 1 | a0001c0001t0015 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2095A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 2095 | chr17 | 12143355 | |||||
| chr17:12143574
|
A | G | 2 | a0001c0001t0003a0001c0002t0003 | 18 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2314A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 2314 | chr17 | 12143574 | |||||
| chr17:12143635
|
T | C | 1 | a0001c0001t0014 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2375T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 2375 | chr17 | 12143635 | |||||
| chr17:12143663
|
C | T | 1 | a0002c0004t0012 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2403C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 11/11 | 2403 | chr17 | 12143663 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:12021118
|
T | C | 20 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(17): Show | 20 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.115+117T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12021118 | ||||||
| chr17:12021154
|
C | T | 66 | a0001c0001t0001g0256a0001c0001t0001g0272a0001c0001t0001g0273others(63): Show | 66 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.115+153C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12021154 | ||||||
| chr17:12021167
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.115+166G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12021167 | ||||||
| chr17:12021257
|
A | C | 318 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(315): Show | 321 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.115+256A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12021257 | ||||||
| chr17:12021278
|
T | C | 1 | a0001c0001t0007g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.115+277T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12021278 | ||||||
| chr17:12021285
|
C | G | 2 | a0001c0001t0002g0252a0001c0001t0002g0253 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.115+284C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12021285 | ||||||
| chr17:12021322
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.115+321C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12021322 | ||||||
| chr17:12021370
|
T | C | 1 | a0001c0001t0004g0027 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.115+369T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12021370 | ||||||
| chr17:12021407
|
G | A | 2 | a0001c0001t0007g0026a0002c0004t0012g0028 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.115+406G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12021407 | ||||||
| chr17:12021619
|
G | T | 2 | a0001c0001t0007g0249a0001c0001t0007g0250 | 2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.115+618G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12021619 | ||||||
| chr17:12021708
|
T | A | 1 | a0001c0001t0007g0249 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.115+707T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12021708 | ||||||
| chr17:12021734
|
G | GA | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0024others(132): Show | 138 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.115+754dupA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12021734 | |||||
| chr17:12021734
|
G | GAA | 7 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0256others(4): Show | 7 | HG01884.hp1 HG02027.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.115+753_115+754dup others(2): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12021734 | |||||
| chr17:12021734
|
GA | G | 7 | a0001c0001t0001g0023a0001c0001t0001g0240a0001c0001t0001g0241others(4): Show | 7 | HG01256.hp2 HG02818.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+754delA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12021734 | |||||
| chr17:12021753
|
A | G | 5 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(2): Show | 5 | HG02647.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+752A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12021753 | ||||||
| chr17:12021841
|
C | T | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG01934.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.115+840C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12021841 | ||||||
| chr17:12022019
|
T | C | 16 | a0001c0001t0002g0257a0001c0001t0002g0258a0001c0001t0002g0259others(13): Show | 16 | HG00639.hp2 HG00642.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.115+1018T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12022019 | ||||||
| chr17:12022275
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.115+1274A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12022275 | ||||||
| chr17:12022725
|
T | C | 1 | a0001c0001t0003g0032 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.115+1724T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12022725 | ||||||
| chr17:12022737
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.115+1736G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12022737 | ||||||
| chr17:12022796
|
G | C | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | NA18747.hp2 NA18955.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.115+1795G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12022796 | ||||||
| chr17:12022834
|
A | G | 1 | a0001c0001t0001g0237 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.115+1833A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12022834 | ||||||
| chr17:12022871
|
C | T | 1 | a0001c0001t0002g0315 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.115+1870C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12022871 | ||||||
| chr17:12022893
|
C | G | 2 | a0001c0001t0007g0249a0001c0001t0007g0250 | 2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.115+1892C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12022893 | ||||||
| chr17:12023266
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.115+2265G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12023266 | ||||||
| chr17:12023296
|
T | G | 1 | a0001c0001t0001g0029 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.115+2295T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12023296 | ||||||
| chr17:12023516
|
C | G | 19 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.115+2515C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12023516 | ||||||
| chr17:12023521
|
C | G | 2 | a0001c0001t0001g0236a0001c0001t0016g0235 | 2 | HG00639.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.115+2520C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12023521 | ||||||
| chr17:12023620
|
G | A | 19 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.115+2619G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12023620 | ||||||
| chr17:12023719
|
A | G | 2 | a0001c0001t0007g0026a0002c0004t0012g0028 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.115+2718A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12023719 | ||||||
| chr17:12023785
|
G | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0240 | 2 | HG01255.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.115+2784G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12023785 | ||||||
| chr17:12023848
|
G | A | 2 | a0001c0001t0007g0026a0002c0004t0012g0028 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.115+2847G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12023848 | ||||||
| chr17:12023857
|
G | C | 1 | a0001c0001t0001g0272 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.115+2856G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12023857 | ||||||
| chr17:12023997
|
A | C | 1 | a0001c0001t0001g0314 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.115+2996A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12023997 | ||||||
| chr17:12024140
|
A | G | 62 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(59): Show | 65 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.115+3139A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12024140 | ||||||
| chr17:12024318
|
C | T | 60 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(57): Show | 63 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.115+3317C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12024318 | ||||||
| chr17:12024421
|
A | T | 1 | a0001c0001t0001g0099 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.115+3420A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12024421 | ||||||
| chr17:12024448
|
A | G | 1 | a0001c0001t0002g0313 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.115+3447A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12024448 | ||||||
| chr17:12024449
|
T | C | 2 | a0001c0001t0007g0026a0002c0004t0012g0028 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.115+3448T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12024449 | ||||||
| chr17:12024748
|
G | A | 1 | a0001c0001t0001g0241 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.115+3747G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12024748 | ||||||
| chr17:12024977
|
G | T | 37 | a0001c0001t0001g0256a0001c0001t0001g0272a0001c0001t0001g0288others(34): Show | 37 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.115+3976G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12024977 | ||||||
| chr17:12025018
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.115+4017A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12025018 | ||||||
| chr17:12025231
|
C | A | 2 | a0001c0001t0007g0026a0002c0004t0012g0028 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.115+4230C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12025231 | ||||||
| chr17:12025550
|
T | C | 2 | a0001c0001t0002g0107a0001c0001t0002g0108 | 2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.115+4549T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12025550 | ||||||
| chr17:12025629
|
T | G | 2 | a0001c0001t0007g0026a0002c0004t0012g0028 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.115+4628T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12025629 | ||||||
| chr17:12025712
|
G | A | 41 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(38): Show | 41 | HG00280.hp1 HG00558.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.115+4711G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12025712 | ||||||
| chr17:12025870
|
CTAAT | C | 3 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099 | 3 | HG01106.hp2 HG03710.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.115+4872_115+4875d others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12025870 | |||||
| chr17:12026305
|
T | C | 1 | a0001c0001t0001g0031 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.115+5304T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12026305 | ||||||
| chr17:12026408
|
G | A | 6 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(3): Show | 6 | HG01243.hp1 HG02647.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.115+5407G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12026408 | ||||||
| chr17:12026738
|
G | A | 1 | a0001c0001t0007g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.115+5737G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12026738 | ||||||
| chr17:12026956
|
T | G | 1 | a0001c0001t0007g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.115+5955T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12026956 | ||||||
| chr17:12027467
|
A | T | 66 | a0001c0001t0001g0256a0001c0001t0001g0272a0001c0001t0001g0273others(63): Show | 66 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.115+6466A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12027467 | ||||||
| chr17:12027484
|
T | TAC | 3 | a0001c0001t0007g0026a0001c0001t0007g0249a0001c0001t0007g0250 | 3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.115+6497_115+6498d others(4): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12027484 | |||||
| chr17:12027664
|
T | G | 16 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(13): Show | 16 | HG00673.hp2 HG00733.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.115+6663T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12027664 | ||||||
| chr17:12027777
|
G | A | 2 | a0001c0001t0002g0285a0001c0001t0002g0286 | 2 | NA18986.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.115+6776G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12027777 | ||||||
| chr17:12027824
|
A | T | 1 | a0001c0001t0001g0272 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.115+6823A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12027824 | ||||||
| chr17:12028084
|
A | G | 1 | a0001c0001t0007g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.115+7083A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12028084 | ||||||
| chr17:12028132
|
A | G | 2 | a0001c0001t0002g0252a0001c0001t0002g0253 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.115+7131A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12028132 | ||||||
| chr17:12028725
|
G | C | 1 | a0001c0001t0007g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.115+7724G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12028725 | ||||||
| chr17:12028911
|
A | G | 1 | a0001c0001t0002g0319 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.115+7910A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12028911 | ||||||
| chr17:12028922
|
A | G | 1 | a0001c0001t0001g0141 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.115+7921A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12028922 | ||||||
| chr17:12029043
|
C | T | 1 | a0001c0001t0007g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.115+8042C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12029043 | ||||||
| chr17:12029087
|
C | T | 5 | a0001c0001t0001g0022a0001c0001t0001g0281a0001c0001t0001g0282others(2): Show | 5 | HG02055.hp2 HG02647.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+8086C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12029087 | ||||||
| chr17:12029173
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.115+8172G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12029173 | ||||||
| chr17:12029200
|
C | T | 121 | a0001c0001t0001g0023a0001c0001t0001g0046a0001c0001t0001g0102others(118): Show | 121 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.115+8199C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12029200 | ||||||
| chr17:12029213
|
T | TA | 6 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(3): Show | 6 | HG01243.hp1 HG02647.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.115+8213dupA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12029213 | |||||
| chr17:12029278
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.115+8277G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12029278 | ||||||
| chr17:12029419
|
A | C | 2 | a0001c0003t0001g0279a0001c0003t0002g0280 | 2 | HG02559.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.115+8418A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12029419 | ||||||
| chr17:12029681
|
A | G | 26 | a0001c0001t0001g0256a0001c0001t0001g0294a0001c0001t0002g0254others(23): Show | 26 | HG00544.hp1 HG00597.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.115+8680A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12029681 | ||||||
| chr17:12029732
|
C | A | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG00733.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.115+8731C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12029732 | ||||||
| chr17:12030096
|
C | A | 1 | a0001c0001t0001g0157 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.115+9095C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12030096 | ||||||
| chr17:12030255
|
A | G | 1 | a0001c0001t0001g0272 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.115+9254A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12030255 | ||||||
| chr17:12030315
|
C | T | 5 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0243others(2): Show | 5 | HG02083.hp1 NA18982.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.115+9314C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12030315 | ||||||
| chr17:12030336
|
A | G | 66 | a0001c0001t0001g0256a0001c0001t0001g0272a0001c0001t0001g0273others(63): Show | 66 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.115+9335A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12030336 | ||||||
| chr17:12030405
|
A | T | 1 | a0001c0001t0001g0140 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.115+9404A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12030405 | ||||||
| chr17:12030563
|
A | G | 1 | a0001c0001t0002g0318 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.115+9562A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12030563 | ||||||
| chr17:12030657
|
A | T | 197 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(194): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.115+9656A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12030657 | ||||||
| chr17:12031024
|
T | A | 2 | a0001c0001t0002g0252a0001c0001t0002g0253 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.115+10023T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12031024 | ||||||
| chr17:12031231
|
T | C | 1 | a0001c0001t0001g0281 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.115+10230T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12031231 | ||||||
| chr17:12031304
|
T | G | 1 | a0001c0001t0001g0046 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.115+10303T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12031304 | ||||||
| chr17:12031375
|
G | A | 2 | a0001c0001t0002g0233a0001c0001t0018g0047 | 2 | NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.115+10374G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12031375 | ||||||
| chr17:12031421
|
A | G | 1 | a0001c0001t0002g0228 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.115+10420A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12031421 | ||||||
| chr17:12031444
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.115+10443G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12031444 | ||||||
| chr17:12031533
|
C | T | 2 | a0001c0001t0002g0233a0001c0001t0018g0047 | 2 | NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.115+10532C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12031533 | ||||||
| chr17:12031701
|
C | T | 19 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.115+10700C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12031701 | ||||||
| chr17:12031709
|
T | C | 6 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(3): Show | 6 | HG01071.hp2 HG01346.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.115+10708T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12031709 | ||||||
| chr17:12031728
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.115+10727G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12031728 | ||||||
| chr17:12031800
|
T | C | 6 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(3): Show | 6 | HG01243.hp1 HG02647.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.115+10799T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12031800 | ||||||
| chr17:12032579
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.115+11578A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12032579 | ||||||
| chr17:12032604
|
A | G | 4 | a0001c0001t0001g0034a0001c0001t0001g0101a0001c0001t0001g0176others(1): Show | 4 | HG01192.hp1 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.115+11603A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12032604 | ||||||
| chr17:12032715
|
A | C | 13 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(10): Show | 13 | HG02040.hp2 HG02818.hp1 NA18945.hp1 others(10): Show |
intron_variant | MODIFIER | c.115+11714A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12032715 | ||||||
| chr17:12032975
|
G | A | 1 | a0001c0001t0007g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.115+11974G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12032975 | ||||||
| chr17:12033196
|
A | G | 1 | a0001c0001t0002g0312 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.115+12195A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12033196 | ||||||
| chr17:12033337
|
C | CA | 66 | a0001c0001t0001g0256a0001c0001t0001g0272a0001c0001t0001g0273others(63): Show | 66 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.115+12344dupA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12033337 | |||||
| chr17:12033513
|
A | G | 13 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(10): Show | 13 | HG02040.hp2 HG02818.hp1 NA18945.hp1 others(10): Show |
intron_variant | MODIFIER | c.115+12512A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12033513 | ||||||
| chr17:12033635
|
T | C | 1 | a0001c0001t0002g0258 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.115+12634T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12033635 | ||||||
| chr17:12033815
|
T | C | 1 | a0001c0001t0007g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.115+12814T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12033815 | ||||||
| chr17:12033831
|
G | A | 1 | a0001c0001t0001g0035 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.115+12830G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12033831 | ||||||
| chr17:12033961
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.115+12960A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12033961 | ||||||
| chr17:12034128
|
C | A | 28 | a0001c0001t0001g0046a0001c0001t0001g0105a0001c0001t0001g0178others(25): Show | 28 | HG00099.hp1 HG01071.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.115+13127C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12034128 | ||||||
| chr17:12034256
|
C | T | 1 | a0001c0001t0007g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.115+13255C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12034256 | ||||||
| chr17:12034358
|
A | G | 4 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG02055.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+13357A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12034358 | ||||||
| chr17:12034593
|
C | T | 4 | a0001c0001t0001g0034a0001c0001t0001g0101a0001c0001t0001g0176others(1): Show | 4 | HG01192.hp1 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.115+13592C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12034593 | ||||||
| chr17:12034614
|
G | T | 1 | a0001c0001t0004g0175 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.115+13613G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12034614 | ||||||
| chr17:12034641
|
A | G | 1 | a0001c0001t0007g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.115+13640A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12034641 | ||||||
| chr17:12034770
|
T | G | 1 | a0001c0001t0007g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.115+13769T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12034770 | ||||||
| chr17:12034790
|
C | T | 1 | a0001c0001t0013g0005 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.115+13789C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12034790 | ||||||
| chr17:12034978
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.115+13977G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12034978 | ||||||
| chr17:12035227
|
T | C | 4 | a0001c0001t0001g0034a0001c0001t0001g0101a0001c0001t0001g0176others(1): Show | 4 | HG01192.hp1 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.115+14226T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12035227 | ||||||
| chr17:12035243
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.115+14242C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12035243 | ||||||
| chr17:12035246
|
G | A | 6 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(3): Show | 6 | HG01243.hp1 HG02647.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.115+14245G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12035246 | ||||||
| chr17:12035377
|
C | T | 2 | a0001c0001t0007g0249a0001c0001t0007g0250 | 2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.115+14376C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12035377 | ||||||
| chr17:12035469
|
T | A | 58 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(55): Show | 61 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.115+14468T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12035469 | ||||||
| chr17:12035511
|
C | T | 2 | a0001c0001t0001g0137a0001c0001t0001g0242 | 2 | NA19010.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.115+14510C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12035511 | ||||||
| chr17:12036346
|
A | T | 1 | a0001c0001t0001g0227 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.115+15345A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12036346 | ||||||
| chr17:12036564
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.115+15563C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12036564 | ||||||
| chr17:12036676
|
T | A | 1 | a0001c0001t0002g0233 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.115+15675T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12036676 | ||||||
| chr17:12036706
|
AT | A | 123 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0096others(120): Show | 123 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.115+15718delT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12036706 | |||||
| chr17:12036903
|
C | CT | 135 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(132): Show | 135 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.115+15910dupT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12036903 | |||||
| chr17:12036979
|
A | G | 1 | a0001c0001t0007g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.115+15978A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12036979 | ||||||
| chr17:12037251
|
G | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0049a0001c0001t0001g0094 | 4 | NA18955.hp1 NA18984.hp2 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.115+16250G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12037251 | ||||||
| chr17:12037572
|
A | G | 17 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(14): Show | 17 | HG02040.hp2 HG02818.hp1 NA18945.hp1 others(14): Show |
intron_variant | MODIFIER | c.115+16571A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12037572 | ||||||
| chr17:12037630
|
T | TTA | 122 | a0001c0001t0001g0046a0001c0001t0001g0096a0001c0001t0001g0102others(119): Show | 122 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.115+16638_115+1663 others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12037630 | |||||
| chr17:12037705
|
A | G | 1 | a0001c0001t0007g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.115+16704A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12037705 | ||||||
| chr17:12037843
|
C | G | 6 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(3): Show | 6 | HG01243.hp1 HG02647.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.115+16842C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12037843 | ||||||
| chr17:12037916
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.115+16915G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12037916 | ||||||
| chr17:12038166
|
C | T | 122 | a0001c0001t0001g0046a0001c0001t0001g0096a0001c0001t0001g0102others(119): Show | 122 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.116-16723C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12038166 | ||||||
| chr17:12038177
|
A | T | 122 | a0001c0001t0001g0046a0001c0001t0001g0096a0001c0001t0001g0102others(119): Show | 122 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.116-16712A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12038177 | ||||||
| chr17:12038358
|
T | C | 65 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(62): Show | 68 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.116-16531T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12038358 | ||||||
| chr17:12038396
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.116-16493G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12038396 | ||||||
| chr17:12038421
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.116-16468C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12038421 | ||||||
| chr17:12038462
|
G | C | 2 | a0001c0001t0001g0110a0001c0001t0001g0141 | 2 | NA18945.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.116-16427G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12038462 | ||||||
| chr17:12038586
|
A | T | 1 | a0001c0001t0001g0203 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.116-16303A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12038586 | ||||||
| chr17:12038756
|
A | G | 1 | a0001c0001t0004g0156 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.116-16133A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12038756 | ||||||
| chr17:12039095
|
G | A | 6 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(3): Show | 6 | HG01243.hp1 HG02647.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.116-15794G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12039095 | ||||||
| chr17:12039218
|
A | C | 1 | a0001c0001t0001g0184 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.116-15671A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12039218 | ||||||
| chr17:12039521
|
A | C | 1 | a0001c0001t0001g0093 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.116-15368A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12039521 | ||||||
| chr17:12039567
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.116-15322A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12039567 | ||||||
| chr17:12039622
|
A | G | 1 | a0001c0001t0001g0273 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.116-15267A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12039622 | ||||||
| chr17:12039671
|
A | G | 11 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220others(8): Show | 11 | HG01934.hp1 HG02145.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.116-15218A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12039671 | ||||||
| chr17:12040004
|
C | T | 1 | a0001c0001t0018g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.116-14885C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12040004 | ||||||
| chr17:12040144
|
C | T | 6 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(3): Show | 6 | NA18967.hp1 NA19002.hp2 NA19054.hp1 others(3): Show |
intron_variant | MODIFIER | c.116-14745C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12040144 | ||||||
| chr17:12040294
|
GC | G | 66 | a0001c0001t0001g0256a0001c0001t0001g0272a0001c0001t0001g0273others(63): Show | 66 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.116-14594delC | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12040294 | ||||||
| chr17:12040384
|
C | T | 23 | a0001c0001t0001g0096a0001c0001t0001g0106a0001c0001t0001g0206others(20): Show | 23 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.116-14505C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12040384 | ||||||
| chr17:12040423
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.116-14466A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12040423 | ||||||
| chr17:12040802
|
T | C | 1 | a0001c0001t0001g0274 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.116-14087T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12040802 | ||||||
| chr17:12040949
|
T | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | NA18747.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.116-13940T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12040949 | ||||||
| chr17:12041173
|
A | G | 8 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(5): Show | 8 | HG02451.hp2 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.116-13716A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12041173 | ||||||
| chr17:12041656
|
G | GA | 14 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(11): Show | 14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.116-13225dupA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12041656 | |||||
| chr17:12041828
|
A | AAAGAACT others(6): Show |
1 | a0001c0001t0001g0035 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.116-13060_116-1304 others(17): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12041828 | |||||
| chr17:12041906
|
C | T | 97 | a0001c0001t0001g0046a0001c0001t0001g0102a0001c0001t0001g0103others(94): Show | 97 | HG00099.hp1 HG00280.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.116-12983C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12041906 | ||||||
| chr17:12042048
|
G | A | 3 | a0001c0001t0007g0026a0001c0001t0007g0249a0001c0001t0007g0250 | 3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.116-12841G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12042048 | ||||||
| chr17:12042167
|
C | CA | 85 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0035others(82): Show | 85 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.116-12699dupA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12042167 | |||||
| chr17:12042167
|
C | CAA | 123 | a0001c0001t0001g0031a0001c0001t0001g0046a0001c0001t0001g0049others(120): Show | 123 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.116-12700_116-1269 others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12042167 | |||||
| chr17:12042167
|
C | CAAA | 51 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(48): Show | 54 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.116-12701_116-1269 others(7): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12042167 | |||||
| chr17:12042167
|
C | CAAAA | 9 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0001g0054others(6): Show | 9 | HG00597.hp2 HG01256.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.116-12702_116-1269 others(8): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12042167 | |||||
| chr17:12042226
|
C | T | 3 | a0001c0001t0007g0026a0001c0001t0007g0249a0001c0001t0007g0250 | 3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.116-12663C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12042226 | ||||||
| chr17:12042330
|
T | C | 1 | a0001c0001t0002g0057 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.116-12559T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12042330 | ||||||
| chr17:12042465
|
G | T | 58 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(55): Show | 61 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.116-12424G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12042465 | ||||||
| chr17:12042579
|
C | T | 1 | a0001c0001t0018g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.116-12310C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12042579 | ||||||
| chr17:12042580
|
G | A | 1 | a0001c0001t0013g0005 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.116-12309G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12042580 | ||||||
| chr17:12042621
|
G | A | 318 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(315): Show | 321 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.116-12268G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12042621 | ||||||
| chr17:12042643
|
A | AAAAC | 266 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(263): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.116-12234_116-1223 others(8): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12042643 | |||||
| chr17:12042659
|
A | T | 1 | a0001c0001t0001g0035 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.116-12230A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12042659 | ||||||
| chr17:12042852
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.116-12037C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12042852 | ||||||
| chr17:12043189
|
A | G | 58 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(55): Show | 61 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.116-11700A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12043189 | ||||||
| chr17:12043193
|
C | A | 1 | a0001c0001t0001g0114 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.116-11696C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12043193 | ||||||
| chr17:12043239
|
T | G | 4 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220others(1): Show | 4 | HG02145.hp1 HG02895.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.116-11650T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12043239 | ||||||
| chr17:12043277
|
A | G | 1 | a0001c0001t0001g0243 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.116-11612A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12043277 | ||||||
| chr17:12043315
|
A | C | 130 | a0001c0001t0001g0046a0001c0001t0001g0096a0001c0001t0001g0102others(127): Show | 130 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.116-11574A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12043315 | ||||||
| chr17:12043442
|
T | G | 1 | a0001c0001t0001g0035 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.116-11447T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12043442 | ||||||
| chr17:12043448
|
G | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0240 | 2 | HG01255.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.116-11441G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12043448 | ||||||
| chr17:12043609
|
G | A | 1 | a0001c0001t0002g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.116-11280G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12043609 | ||||||
| chr17:12043757
|
T | G | 58 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(55): Show | 61 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.116-11132T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12043757 | ||||||
| chr17:12043919
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0101 | 2 | HG01192.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.116-10970G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12043919 | ||||||
| chr17:12044061
|
C | G | 64 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(61): Show | 67 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.116-10828C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12044061 | ||||||
| chr17:12044293
|
G | A | 6 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(3): Show | 6 | HG01243.hp1 HG02647.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.116-10596G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12044293 | ||||||
| chr17:12044386
|
A | G | 14 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(11): Show | 14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.116-10503A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12044386 | ||||||
| chr17:12044616
|
T | C | 19 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.116-10273T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12044616 | ||||||
| chr17:12044826
|
T | G | 1 | a0001c0001t0002g0260 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.116-10063T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12044826 | ||||||
| chr17:12044829
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.116-10060C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12044829 | ||||||
| chr17:12045357
|
ATGTGATG others(7): Show |
A | 1 | a0001c0001t0007g0250 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.116-9527_116-9514d others(16): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12045357 | |||||
| chr17:12045581
|
T | A | 1 | a0001c0001t0002g0108 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.116-9308T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12045581 | ||||||
| chr17:12045644
|
T | G | 293 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(290): Show | 296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.116-9245T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12045644 | ||||||
| chr17:12045808
|
A | G | 1 | a0001c0001t0001g0273 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.116-9081A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12045808 | ||||||
| chr17:12045910
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.116-8979G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12045910 | ||||||
| chr17:12046119
|
T | A | 293 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(290): Show | 296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.116-8770T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12046119 | ||||||
| chr17:12046158
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.116-8731G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12046158 | ||||||
| chr17:12046335
|
G | A | 1 | a0001c0001t0002g0261 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.116-8554G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12046335 | ||||||
| chr17:12046344
|
C | T | 1 | a0001c0001t0018g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.116-8545C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12046344 | ||||||
| chr17:12046440
|
T | A | 1 | a0001c0001t0018g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.116-8449T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12046440 | ||||||
| chr17:12046497
|
A | T | 1 | a0001c0001t0001g0035 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.116-8392A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12046497 | ||||||
| chr17:12046672
|
T | C | 14 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(11): Show | 14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.116-8217T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12046672 | ||||||
| chr17:12046899
|
C | A | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(15): Show | 18 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.116-7990C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12046899 | ||||||
| chr17:12046960
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.116-7929G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12046960 | ||||||
| chr17:12047017
|
T | C | 6 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(3): Show | 6 | HG01243.hp1 HG02647.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.116-7872T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12047017 | ||||||
| chr17:12047061
|
G | A | 64 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(61): Show | 67 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.116-7828G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12047061 | ||||||
| chr17:12047063
|
C | T | 1 | a0001c0001t0002g0311 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.116-7826C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12047063 | ||||||
| chr17:12047065
|
C | T | 298 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(295): Show | 301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.116-7824C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12047065 | ||||||
| chr17:12047112
|
G | A | 1 | a0001c0001t0001g0203 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.116-7777G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12047112 | ||||||
| chr17:12047137
|
C | G | 58 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(55): Show | 61 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.116-7752C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12047137 | ||||||
| chr17:12047183
|
T | C | 293 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(290): Show | 296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.116-7706T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12047183 | ||||||
| chr17:12047267
|
T | C | 1 | a0001c0001t0013g0005 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.116-7622T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12047267 | ||||||
| chr17:12047606
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.116-7283A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12047606 | ||||||
| chr17:12047726
|
T | C | 1 | a0001c0001t0018g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.116-7163T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12047726 | ||||||
| chr17:12047831
|
TTATCACA others(4): Show |
T | 1 | a0001c0001t0001g0035 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.116-7055_116-7045d others(13): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12047831 | |||||
| chr17:12048105
|
C | T | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG00733.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.116-6784C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12048105 | ||||||
| chr17:12048445
|
A | T | 1 | a0001c0001t0001g0131 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.116-6444A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12048445 | ||||||
| chr17:12048497
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.116-6392T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12048497 | ||||||
| chr17:12048545
|
G | C | 1 | a0001c0001t0018g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.116-6344G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12048545 | ||||||
| chr17:12048671
|
T | G | 1 | a0001c0001t0002g0262 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.116-6218T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12048671 | ||||||
| chr17:12048678
|
C | T | 61 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(58): Show | 64 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.116-6211C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12048678 | ||||||
| chr17:12048692
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.116-6197T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12048692 | ||||||
| chr17:12048894
|
T | G | 1 | a0001c0001t0001g0051 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.116-5995T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12048894 | ||||||
| chr17:12048998
|
C | T | 54 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(51): Show | 57 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.116-5891C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12048998 | ||||||
| chr17:12049084
|
A | G | 5 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(2): Show | 5 | NA18967.hp1 NA19002.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.116-5805A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12049084 | ||||||
| chr17:12049124
|
C | G | 4 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG02055.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-5765C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12049124 | ||||||
| chr17:12049150
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.116-5739A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12049150 | ||||||
| chr17:12049444
|
T | G | 1 | a0001c0001t0001g0140 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.116-5445T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12049444 | ||||||
| chr17:12049553
|
A | G | 14 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(11): Show | 14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.116-5336A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12049553 | ||||||
| chr17:12049639
|
A | G | 1 | a0001c0001t0001g0277 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.116-5250A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12049639 | ||||||
| chr17:12049791
|
A | G | 6 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(3): Show | 6 | HG01243.hp1 HG02647.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.116-5098A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12049791 | ||||||
| chr17:12050146
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.116-4743C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12050146 | ||||||
| chr17:12050190
|
G | A | 198 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(195): Show | 201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.116-4699G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12050190 | ||||||
| chr17:12050586
|
TGTATTGA others(15): Show |
T | 5 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(2): Show | 5 | HG02647.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.116-4302_116-4281d others(24): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12050586 | ||||||
| chr17:12050609
|
C | T | 5 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(2): Show | 5 | HG02647.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.116-4280C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12050609 | ||||||
| chr17:12050623
|
GT | G | 5 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(2): Show | 5 | HG02647.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.116-4261delT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 12050623 | |||||
| chr17:12050744
|
T | C | 1 | a0001c0001t0014g0091 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.116-4145T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12050744 | ||||||
| chr17:12050918
|
C | G | 1 | a0001c0001t0001g0129 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.116-3971C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12050918 | ||||||
| chr17:12050971
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.116-3918G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12050971 | ||||||
| chr17:12051120
|
C | G | 2 | a0001c0001t0001g0100a0001c0001t0001g0158 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.116-3769C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12051120 | ||||||
| chr17:12051313
|
A | G | 6 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(3): Show | 6 | HG01243.hp1 HG02647.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.116-3576A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12051313 | ||||||
| chr17:12051515
|
A | G | 6 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(3): Show | 6 | NA18967.hp1 NA19002.hp2 NA19054.hp1 others(3): Show |
intron_variant | MODIFIER | c.116-3374A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12051515 | ||||||
| chr17:12051518
|
T | G | 1 | a0001c0001t0001g0314 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.116-3371T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12051518 | ||||||
| chr17:12051602
|
G | C | 2 | a0001c0003t0001g0279a0001c0003t0002g0280 | 2 | HG02559.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.116-3287G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12051602 | ||||||
| chr17:12051908
|
G | A | 1 | a0001c0001t0009g0001 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.116-2981G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12051908 | ||||||
| chr17:12051925
|
T | A | 5 | a0001c0001t0001g0034a0001c0001t0001g0101a0001c0001t0001g0157others(2): Show | 5 | HG01192.hp1 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.116-2964T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12051925 | ||||||
| chr17:12051926
|
A | T | 1 | a0001c0001t0002g0310 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.116-2963A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12051926 | ||||||
| chr17:12051983
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.116-2906A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12051983 | ||||||
| chr17:12052215
|
C | G | 8 | a0001c0001t0002g0255a0001c0001t0002g0303a0001c0001t0002g0307others(5): Show | 8 | HG00544.hp1 HG00673.hp1 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.116-2674C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12052215 | ||||||
| chr17:12052296
|
C | G | 272 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0024others(269): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.116-2593C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12052296 | ||||||
| chr17:12052384
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.116-2505A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12052384 | ||||||
| chr17:12052494
|
T | G | 2 | a0001c0002t0003g0052a0001c0002t0003g0085 | 2 | HG00597.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.116-2395T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12052494 | ||||||
| chr17:12052610
|
G | A | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.116-2279G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12052610 | ||||||
| chr17:12052817
|
G | A | 4 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(1): Show | 4 | HG01258.hp2 HG01261.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-2072G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12052817 | ||||||
| chr17:12053359
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.116-1530G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12053359 | ||||||
| chr17:12053675
|
T | C | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.116-1214T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12053675 | ||||||
| chr17:12053745
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.116-1144G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12053745 | ||||||
| chr17:12053807
|
G | A | 1 | a0001c0001t0004g0175 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.116-1082G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12053807 | ||||||
| chr17:12053945
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.116-944A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12053945 | ||||||
| chr17:12054299
|
C | T | 1 | a0001c0001t0002g0228 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.116-590C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12054299 | ||||||
| chr17:12054382
|
A | G | 58 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(55): Show | 61 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.116-507A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12054382 | ||||||
| chr17:12054430
|
C | T | 2 | a0001c0001t0001g0276a0002c0004t0012g0028 | 2 | HG01243.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.116-459C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12054430 | ||||||
| chr17:12054736
|
A | G | 266 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(263): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.116-153A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | chr17 | 12054736 | ||||||
| chr17:12055224
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG02486.hp2 HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.218+233G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12055224 | ||||||
| chr17:12055299
|
G | A | 1 | a0001c0001t0001g0288 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.218+308G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12055299 | ||||||
| chr17:12055354
|
T | C | 67 | a0001c0001t0001g0256a0001c0001t0001g0272a0001c0001t0001g0273others(64): Show | 67 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.218+363T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12055354 | ||||||
| chr17:12056298
|
A | T | 1 | a0001c0001t0001g0202 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.218+1307A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12056298 | ||||||
| chr17:12056326
|
C | CT | 61 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(58): Show | 64 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.218+1336dupT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12056326 | |||||
| chr17:12056398
|
A | C | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.218+1407A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12056398 | ||||||
| chr17:12056434
|
G | A | 1 | a0001c0001t0002g0263 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.218+1443G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12056434 | ||||||
| chr17:12056502
|
C | T | 123 | a0001c0001t0001g0046a0001c0001t0001g0096a0001c0001t0001g0102others(120): Show | 123 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.218+1511C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12056502 | ||||||
| chr17:12056666
|
A | G | 1 | a0001c0001t0002g0228 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.218+1675A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12056666 | ||||||
| chr17:12056774
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.218+1783T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12056774 | ||||||
| chr17:12056907
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.218+1916A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12056907 | ||||||
| chr17:12056918
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.218+1927C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12056918 | ||||||
| chr17:12056956
|
A | G | 1 | a0001c0001t0001g0050 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.218+1965A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12056956 | ||||||
| chr17:12057159
|
A | G | 1 | a0001c0001t0018g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.218+2168A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12057159 | ||||||
| chr17:12057332
|
A | G | 61 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(58): Show | 64 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.218+2341A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12057332 | ||||||
| chr17:12057501
|
G | T | 1 | a0001c0001t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.218+2510G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12057501 | ||||||
| chr17:12057684
|
C | T | 20 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(17): Show | 20 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.218+2693C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12057684 | ||||||
| chr17:12057726
|
G | C | 4 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0003g0033others(1): Show | 4 | HG00673.hp2 HG02129.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+2735G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12057726 | ||||||
| chr17:12058076
|
C | G | 1 | a0001c0001t0001g0143 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.218+3085C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12058076 | ||||||
| chr17:12058227
|
C | CT | 13 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(10): Show | 13 | HG00558.hp2 HG00642.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.218+3255dupT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12058227 | |||||
| chr17:12058227
|
CT | C | 29 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(26): Show | 29 | HG01081.hp2 HG01123.hp2 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.218+3255delT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12058227 | |||||
| chr17:12058227
|
CTTTTTTT | C | 14 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(11): Show | 14 | HG00733.hp2 HG00738.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.218+3249_218+3255d others(9): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12058227 | |||||
| chr17:12058701
|
G | A | 22 | a0001c0001t0001g0096a0001c0001t0001g0106a0001c0001t0001g0206others(19): Show | 22 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.218+3710G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12058701 | ||||||
| chr17:12058833
|
A | G | 1 | a0001c0001t0004g0165 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.218+3842A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12058833 | ||||||
| chr17:12058917
|
C | G | 14 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(11): Show | 14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.218+3926C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12058917 | ||||||
| chr17:12058968
|
A | T | 1 | a0001c0001t0018g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.218+3977A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12058968 | ||||||
| chr17:12059436
|
C | T | 1 | a0001c0001t0018g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.218+4445C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12059436 | ||||||
| chr17:12059684
|
C | T | 1 | a0001c0001t0018g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.218+4693C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12059684 | ||||||
| chr17:12059735
|
T | G | 1 | a0001c0001t0001g0104 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.218+4744T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12059735 | ||||||
| chr17:12059866
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.218+4875T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12059866 | ||||||
| chr17:12059894
|
G | A | 1 | a0001c0001t0008g0189 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218+4903G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12059894 | ||||||
| chr17:12059916
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.218+4925G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12059916 | ||||||
| chr17:12059942
|
T | C | 298 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(295): Show | 301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.218+4951T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12059942 | ||||||
| chr17:12060046
|
T | C | 56 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(53): Show | 59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.218+5055T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12060046 | ||||||
| chr17:12060163
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.218+5172C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12060163 | ||||||
| chr17:12060169
|
T | TA | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(3): Show | 6 | HG02055.hp1 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.218+5192dupA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12060169 | |||||
| chr17:12060169
|
TA | T | 10 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(7): Show | 10 | HG02109.hp2 HG02145.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.218+5192delA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12060169 | |||||
| chr17:12060243
|
T | C | 56 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(53): Show | 59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.218+5252T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12060243 | ||||||
| chr17:12060323
|
C | T | 3 | a0001c0001t0001g0244a0001c0001t0001g0247a0001c0001t0001g0248 | 3 | HG02970.hp2 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.218+5332C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12060323 | ||||||
| chr17:12060353
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.218+5362G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12060353 | ||||||
| chr17:12060606
|
A | G | 123 | a0001c0001t0001g0046a0001c0001t0001g0096a0001c0001t0001g0102others(120): Show | 123 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.218+5615A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12060606 | ||||||
| chr17:12060728
|
G | GGGGTGT | 41 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0048others(38): Show | 43 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.218+5738_218+5739i others(8): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12060728 | |||||
| chr17:12060728
|
G | GGGGTGTG others(5): Show |
8 | a0001c0001t0001g0003a0001c0001t0001g0049a0001c0001t0001g0075others(5): Show | 9 | HG00597.hp2 HG01934.hp2 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.218+5738_218+5739i others(14): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12060728 | |||||
| chr17:12060730
|
T | G | 1 | a0001c0001t0001g0051 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.218+5739T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12060730 | ||||||
| chr17:12060748
|
C | G | 1 | a0001c0001t0001g0051 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.218+5757C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12060748 | ||||||
| chr17:12060748
|
C | T | 54 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(51): Show | 57 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.218+5757C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12060748 | ||||||
| chr17:12060750
|
C | T | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+5759C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12060750 | ||||||
| chr17:12060753
|
G | C | 3 | a0001c0001t0007g0026a0001c0001t0007g0249a0001c0001t0007g0250 | 3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.218+5762G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12060753 | ||||||
| chr17:12060954
|
G | A | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+5963G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12060954 | ||||||
| chr17:12061477
|
T | C | 1 | a0001c0001t0013g0005 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.218+6486T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12061477 | ||||||
| chr17:12061771
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.218+6780T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12061771 | ||||||
| chr17:12061851
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.218+6860T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12061851 | ||||||
| chr17:12061896
|
G | GT | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+6914dupT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12061896 | |||||
| chr17:12061906
|
A | T | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+6915A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12061906 | ||||||
| chr17:12061927
|
C | T | 3 | a0001c0001t0002g0233a0001c0001t0002g0252a0001c0001t0002g0253 | 3 | HG02818.hp2 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.218+6936C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12061927 | ||||||
| chr17:12062035
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.218+7044G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12062035 | ||||||
| chr17:12062065
|
C | A | 2 | a0001c0002t0003g0052a0001c0002t0003g0085 | 2 | HG00597.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.218+7074C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12062065 | ||||||
| chr17:12062065
|
C | G | 14 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(11): Show | 14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.218+7074C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12062065 | ||||||
| chr17:12062066
|
C | G | 3 | a0001c0001t0007g0026a0001c0001t0007g0249a0001c0001t0007g0250 | 3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.218+7075C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12062066 | ||||||
| chr17:12062116
|
C | T | 1 | a0001c0001t0016g0235 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.218+7125C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12062116 | ||||||
| chr17:12062135
|
G | A | 123 | a0001c0001t0001g0046a0001c0001t0001g0096a0001c0001t0001g0102others(120): Show | 123 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.218+7144G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12062135 | ||||||
| chr17:12062227
|
C | T | 2 | a0001c0001t0001g0292a0001c0001t0001g0293 | 2 | HG00280.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.218+7236C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12062227 | ||||||
| chr17:12062242
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.218+7251G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12062242 | ||||||
| chr17:12062501
|
A | T | 123 | a0001c0001t0001g0046a0001c0001t0001g0096a0001c0001t0001g0102others(120): Show | 123 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.218+7510A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12062501 | ||||||
| chr17:12062568
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.218+7577A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12062568 | ||||||
| chr17:12062743
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.218+7752A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12062743 | ||||||
| chr17:12062800
|
G | A | 38 | a0001c0001t0001g0256a0001c0001t0001g0272a0001c0001t0001g0288others(35): Show | 38 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.218+7809G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12062800 | ||||||
| chr17:12063119
|
A | G | 1 | a0001c0001t0001g0132 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.218+8128A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12063119 | ||||||
| chr17:12063312
|
C | G | 219 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(216): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.218+8321C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12063312 | ||||||
| chr17:12063583
|
G | A | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+8592G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12063583 | ||||||
| chr17:12063728
|
T | C | 1 | a0001c0001t0013g0005 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.218+8737T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12063728 | ||||||
| chr17:12063739
|
G | C | 1 | a0001c0001t0006g0116 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.218+8748G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12063739 | ||||||
| chr17:12063749
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.218+8758G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12063749 | ||||||
| chr17:12063840
|
C | T | 2 | a0001c0001t0001g0149a0001c0001t0004g0156 | 2 | HG00673.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.218+8849C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12063840 | ||||||
| chr17:12063855
|
C | A | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+8864C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12063855 | ||||||
| chr17:12063904
|
G | A | 4 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(1): Show | 4 | HG00544.hp2 HG02040.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+8913G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12063904 | ||||||
| chr17:12063926
|
C | T | 2 | a0001c0001t0001g0256a0001c0001t0001g0294 | 2 | NA18949.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.218+8935C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12063926 | ||||||
| chr17:12063938
|
C | G | 2 | a0001c0001t0001g0256a0001c0001t0001g0294 | 2 | NA18949.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.218+8947C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12063938 | ||||||
| chr17:12063970
|
CA | C | 125 | a0001c0001t0001g0046a0001c0001t0001g0096a0001c0001t0001g0102others(122): Show | 125 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.218+8980delA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12063970 | ||||||
| chr17:12064001
|
A | T | 2 | a0001c0001t0002g0285a0001c0001t0002g0286 | 2 | NA18986.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.218+9010A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12064001 | ||||||
| chr17:12064017
|
G | T | 1 | a0001c0001t0001g0247 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.218+9026G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12064017 | ||||||
| chr17:12064021
|
G | GGA | 53 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(50): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.218+9051_218+9052d others(4): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12064021 | |||||
| chr17:12064023
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.218+9032A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12064023 | ||||||
| chr17:12064076
|
T | C | 2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | NA18970.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.218+9085T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12064076 | ||||||
| chr17:12064107
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.218+9116A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12064107 | ||||||
| chr17:12064185
|
A | C | 1 | a0001c0001t0001g0106 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.218+9194A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12064185 | ||||||
| chr17:12064243
|
C | T | 4 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0256others(1): Show | 4 | HG02717.hp1 NA18949.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+9252C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12064243 | ||||||
| chr17:12064269
|
G | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG00733.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.218+9278G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12064269 | ||||||
| chr17:12064336
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.218+9345C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12064336 | ||||||
| chr17:12064370
|
G | A | 54 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(51): Show | 57 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.218+9379G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12064370 | ||||||
| chr17:12064412
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.218+9421G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12064412 | ||||||
| chr17:12064812
|
G | A | 2 | a0001c0001t0002g0057a0001c0001t0002g0058 | 2 | HG01123.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.218+9821G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12064812 | ||||||
| chr17:12064883
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.218+9892G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12064883 | ||||||
| chr17:12065107
|
G | A | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+10116G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12065107 | ||||||
| chr17:12065196
|
C | A | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+10205C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12065196 | ||||||
| chr17:12065258
|
A | ATAT | 18 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(15): Show | 18 | HG00099.hp1 HG00621.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.218+10299_218+1030 others(7): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12065258 | |||||
| chr17:12065258
|
A | ATATTAT | 69 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(66): Show | 69 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.218+10296_218+1030 others(10): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12065258 | |||||
| chr17:12065258
|
A | ATATTATT others(2): Show |
97 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0018others(94): Show | 97 | HG00544.hp1 HG00609.hp2 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.218+10293_218+1030 others(13): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12065258 | |||||
| chr17:12065258
|
A | ATATTATT others(5): Show |
45 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(42): Show | 45 | HG01071.hp2 HG01123.hp1 HG01192.hp2 others(42): Show |
intron_variant | MODIFIER | c.218+10290_218+1030 others(16): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12065258 | |||||
| chr17:12065258
|
A | ATATTATT others(8): Show |
5 | a0001c0001t0001g0105a0001c0001t0001g0179a0001c0001t0001g0180others(2): Show | 5 | HG00558.hp2 HG02683.hp2 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.218+10287_218+1030 others(19): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12065258 | |||||
| chr17:12065258
|
A | ATATTATT others(11): Show |
1 | a0001c0001t0004g0036 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.218+10284_218+1030 others(22): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12065258 | |||||
| chr17:12065258
|
ATATTAT | A | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+10296_218+1030 others(10): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12065258 | |||||
| chr17:12065280
|
T | G | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+10289T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12065280 | ||||||
| chr17:12065303
|
G | GT | 73 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(70): Show | 76 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.218+10325dupT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12065303 | |||||
| chr17:12065361
|
C | T | 5 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0074others(2): Show | 5 | HG01071.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+10370C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12065361 | ||||||
| chr17:12065595
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.218+10604T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12065595 | ||||||
| chr17:12065741
|
A | G | 4 | a0001c0001t0002g0299a0001c0001t0002g0300a0001c0001t0002g0301others(1): Show | 4 | HG00597.hp1 NA18612.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+10750A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12065741 | ||||||
| chr17:12065762
|
T | A | 2 | a0001c0001t0001g0276a0002c0004t0012g0028 | 2 | HG01243.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.218+10771T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12065762 | ||||||
| chr17:12065821
|
G | T | 2 | a0001c0001t0002g0298a0001c0001t0002g0312 | 2 | NA18747.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.218+10830G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12065821 | ||||||
| chr17:12065924
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.218+10933G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12065924 | ||||||
| chr17:12065984
|
G | A | 1 | a0001c0001t0002g0265 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.218+10993G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12065984 | ||||||
| chr17:12066135
|
TC | T | 52 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(49): Show | 55 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.218+11145delC | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12066135 | ||||||
| chr17:12066136
|
C | CT | 15 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(12): Show | 15 | HG01106.hp1 HG02040.hp2 HG02523.hp2 others(12): Show |
intron_variant | MODIFIER | c.218+11158dupT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12066136 | |||||
| chr17:12066136
|
CT | C | 20 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(17): Show | 20 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.218+11158delT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12066136 | |||||
| chr17:12066279
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.218+11288A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12066279 | ||||||
| chr17:12066356
|
A | G | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+11365A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12066356 | ||||||
| chr17:12066491
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.218+11500A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12066491 | ||||||
| chr17:12066530
|
T | C | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+11539T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12066530 | ||||||
| chr17:12066669
|
T | C | 1 | a0001c0001t0002g0108 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.218+11678T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12066669 | ||||||
| chr17:12066687
|
C | T | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+11696C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12066687 | ||||||
| chr17:12066712
|
C | T | 14 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(11): Show | 14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.218+11721C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12066712 | ||||||
| chr17:12066782
|
C | T | 1 | a0001c0001t0004g0231 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.218+11791C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12066782 | ||||||
| chr17:12066789
|
A | C | 14 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(11): Show | 14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.218+11798A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12066789 | ||||||
| chr17:12066839
|
G | A | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG01346.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.218+11848G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12066839 | ||||||
| chr17:12066879
|
C | T | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0073 | 3 | HG00642.hp1 HG01516.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.218+11888C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12066879 | ||||||
| chr17:12066967
|
G | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0049a0001c0001t0001g0051others(3): Show | 7 | HG01934.hp2 HG02300.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.218+11976G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12066967 | ||||||
| chr17:12066980
|
A | G | 1 | a0001c0001t0004g0165 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.218+11989A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12066980 | ||||||
| chr17:12067166
|
G | A | 14 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(11): Show | 14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.218+12175G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12067166 | ||||||
| chr17:12067234
|
C | G | 70 | a0001c0001t0001g0256a0001c0001t0001g0272a0001c0001t0001g0273others(67): Show | 70 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.218+12243C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12067234 | ||||||
| chr17:12067336
|
T | C | 1 | a0001c0001t0002g0263 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.218+12345T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12067336 | ||||||
| chr17:12067361
|
T | C | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+12370T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12067361 | ||||||
| chr17:12067366
|
C | T | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+12375C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12067366 | ||||||
| chr17:12067367
|
G | A | 14 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(11): Show | 14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.218+12376G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12067367 | ||||||
| chr17:12067516
|
C | T | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+12525C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12067516 | ||||||
| chr17:12067749
|
A | G | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.218+12758A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12067749 | ||||||
| chr17:12067955
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.218+12964G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12067955 | ||||||
| chr17:12067978
|
G | A | 6 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(3): Show | 6 | HG01243.hp1 HG02647.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.218+12987G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12067978 | ||||||
| chr17:12068028
|
T | G | 1 | a0001c0001t0001g0199 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.218+13037T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12068028 | ||||||
| chr17:12068123
|
A | G | 1 | a0001c0001t0001g0209 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.218+13132A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12068123 | ||||||
| chr17:12068300
|
C | G | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-13056C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12068300 | ||||||
| chr17:12068366
|
A | G | 13 | a0001c0001t0003g0002a0001c0001t0003g0032a0001c0001t0003g0055others(10): Show | 14 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.219-12990A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12068366 | ||||||
| chr17:12068458
|
A | G | 1 | a0002c0004t0012g0028 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.219-12898A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12068458 | ||||||
| chr17:12068495
|
G | A | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-12861G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12068495 | ||||||
| chr17:12068662
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.219-12694G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12068662 | ||||||
| chr17:12068678
|
C | T | 1 | a0002c0004t0012g0028 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.219-12678C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12068678 | ||||||
| chr17:12068783
|
A | ATG | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-12572_219-1257 others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12068783 | |||||
| chr17:12068785
|
T | A | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-12571T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12068785 | ||||||
| chr17:12068858
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.219-12498C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12068858 | ||||||
| chr17:12069102
|
A | G | 119 | a0001c0001t0001g0046a0001c0001t0001g0096a0001c0001t0001g0102others(116): Show | 119 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.219-12254A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12069102 | ||||||
| chr17:12069432
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.219-11924T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12069432 | ||||||
| chr17:12069449
|
C | G | 2 | a0001c0001t0002g0057a0001c0001t0002g0058 | 2 | HG01123.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.219-11907C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12069449 | ||||||
| chr17:12069573
|
A | G | 1 | a0001c0001t0001g0314 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.219-11783A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12069573 | ||||||
| chr17:12069711
|
C | T | 1 | a0001c0001t0002g0059 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.219-11645C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12069711 | ||||||
| chr17:12069729
|
G | A | 6 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0299others(3): Show | 6 | HG00597.hp1 NA18612.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-11627G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12069729 | ||||||
| chr17:12069749
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.219-11607C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12069749 | ||||||
| chr17:12069750
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.219-11606G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12069750 | ||||||
| chr17:12069890
|
C | CAT | 7 | a0001c0001t0001g0093a0001c0001t0001g0243a0001c0001t0002g0298others(4): Show | 7 | HG01361.hp2 HG01891.hp2 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.219-11405_219-1140 others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | |||||
| chr17:12069890
|
C | CATAT | 5 | a0001c0001t0001g0138a0001c0001t0001g0145a0001c0001t0002g0285others(2): Show | 5 | HG00673.hp2 HG01261.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-11407_219-1140 others(8): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | |||||
| chr17:12069890
|
CAT | C | 11 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0023others(8): Show | 11 | HG01071.hp2 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.219-11405_219-1140 others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | |||||
| chr17:12069890
|
CATAT | C | 21 | a0001c0001t0001g0020a0001c0001t0001g0149a0001c0001t0001g0161others(18): Show | 21 | HG01123.hp2 HG02109.hp2 HG02129.hp1 others(18): Show |
intron_variant | MODIFIER | c.219-11407_219-1140 others(8): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | |||||
| chr17:12069890
|
CATATAT | C | 23 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0018others(20): Show | 23 | HG00099.hp1 HG00639.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.219-11409_219-1140 others(10): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | |||||
| chr17:12069890
|
CATATATA others(1): Show |
C | 21 | a0001c0001t0001g0031a0001c0001t0001g0063a0001c0001t0001g0146others(18): Show | 21 | HG01361.hp1 HG01934.hp1 HG01975.hp1 others(18): Show |
intron_variant | MODIFIER | c.219-11411_219-1140 others(12): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | |||||
| chr17:12069890
|
CATATATA others(3): Show |
C | 25 | a0001c0001t0001g0004a0001c0001t0001g0074a0001c0001t0001g0090others(22): Show | 25 | HG00544.hp2 HG00733.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.219-11413_219-1140 others(14): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | |||||
| chr17:12069890
|
CATATATA others(5): Show |
C | 17 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0024others(14): Show | 17 | HG00099.hp2 HG00544.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.219-11415_219-1140 others(16): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | |||||
| chr17:12069890
|
CATATATA others(7): Show |
C | 24 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0089others(21): Show | 24 | HG00280.hp1 HG00621.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.219-11417_219-1140 others(18): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | |||||
| chr17:12069890
|
CATATATA others(9): Show |
C | 19 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0001g0056others(16): Show | 20 | HG00609.hp1 HG01256.hp1 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.219-11419_219-1140 others(20): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | |||||
| chr17:12069890
|
CATATATA others(11): Show |
C | 44 | a0001c0001t0001g0003a0001c0001t0001g0049a0001c0001t0001g0050others(41): Show | 46 | HG00621.hp1 HG00639.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.219-11421_219-1140 others(22): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | |||||
| chr17:12069890
|
CATATATA others(13): Show |
C | 19 | a0001c0001t0001g0029a0001c0001t0001g0054a0001c0001t0001g0061others(16): Show | 19 | HG00597.hp2 HG00609.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.219-11423_219-1140 others(24): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | |||||
| chr17:12069890
|
CATATATA others(15): Show |
C | 10 | a0001c0001t0001g0081a0001c0001t0001g0106a0001c0001t0001g0139others(7): Show | 10 | HG01255.hp1 HG01255.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.219-11425_219-1140 others(26): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | |||||
| chr17:12069890
|
CATATATA others(17): Show |
C | 12 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0105others(9): Show | 12 | HG02109.hp1 HG02258.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.219-11427_219-1140 others(28): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | |||||
| chr17:12069890
|
CATATATA others(19): Show |
C | 14 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(11): Show | 14 | HG00280.hp2 HG01081.hp1 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.219-11429_219-1140 others(30): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | |||||
| chr17:12069890
|
CATATATA others(21): Show |
C | 18 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(15): Show | 18 | HG00558.hp1 HG01106.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.219-11431_219-1140 others(32): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | |||||
| chr17:12069890
|
CATATATA others(23): Show |
C | 5 | a0001c0001t0001g0244a0001c0001t0004g0042a0001c0001t0004g0043others(2): Show | 5 | HG01243.hp2 HG02572.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-11433_219-1140 others(34): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | |||||
| chr17:12069890
|
CATATATA others(25): Show |
C | 3 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0248 | 3 | HG02647.hp2 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.219-11435_219-1140 others(36): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | |||||
| chr17:12069890
|
CATATATA others(37): Show |
C | 2 | a0001c0001t0001g0126a0001c0001t0001g0131 | 2 | HG03453.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.219-11447_219-1140 others(48): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | |||||
| chr17:12069890
|
CATATATA others(39): Show |
C | 1 | a0001c0001t0001g0194 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.219-11449_219-1140 others(50): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069890 | |||||
| chr17:12069900
|
T | C | 1 | a0001c0001t0001g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.219-11456T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12069900 | ||||||
| chr17:12069907
|
A | C | 1 | a0001c0001t0002g0308 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.219-11449A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12069907 | ||||||
| chr17:12069919
|
ATATATAT others(8): Show |
A | 1 | a0001c0001t0001g0256 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.219-11436_219-1142 others(19): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12069919 | ||||||
| chr17:12069925
|
ATATATAT others(4): Show |
A | 1 | a0001c0001t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.219-11430_219-1142 others(15): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12069925 | ||||||
| chr17:12069930
|
T | C | 17 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0260others(14): Show | 17 | HG00639.hp2 HG00642.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.219-11426T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12069930 | ||||||
| chr17:12069935
|
A | C | 1 | a0001c0001t0001g0256 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.219-11421A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12069935 | ||||||
| chr17:12069935
|
ATATATAT others(8): Show |
A | 1 | a0001c0001t0001g0141 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.219-11420_219-1140 others(19): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12069935 | ||||||
| chr17:12069976
|
A | AGC | 71 | a0001c0001t0001g0256a0001c0001t0001g0272a0001c0001t0001g0273others(68): Show | 71 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.219-11379_219-1137 others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12069976 | |||||
| chr17:12070174
|
T | TA | 6 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(3): Show | 6 | HG01243.hp1 HG02647.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-11181dupA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12070174 | |||||
| chr17:12070263
|
CAT | C | 3 | a0001c0001t0001g0109a0001c0001t0001g0139a0001c0001t0001g0236 | 3 | HG00280.hp1 HG00639.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.219-11092_219-1109 others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12070263 | ||||||
| chr17:12070266
|
G | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.219-11090G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12070266 | ||||||
| chr17:12070348
|
A | G | 1 | a0001c0001t0003g0071 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.219-11008A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12070348 | ||||||
| chr17:12070559
|
G | A | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-10797G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12070559 | ||||||
| chr17:12070592
|
T | C | 1 | a0001c0001t0018g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.219-10764T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12070592 | ||||||
| chr17:12070683
|
T | C | 266 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(263): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.219-10673T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12070683 | ||||||
| chr17:12070753
|
A | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0240 | 2 | HG01255.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.219-10603A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12070753 | ||||||
| chr17:12070963
|
T | C | 1 | a0001c0001t0001g0088 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.219-10393T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12070963 | ||||||
| chr17:12070991
|
C | T | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-10365C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12070991 | ||||||
| chr17:12070992
|
C | T | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-10364C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12070992 | ||||||
| chr17:12070993
|
C | G | 14 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(11): Show | 14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.219-10363C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12070993 | ||||||
| chr17:12071166
|
C | A | 1 | a0001c0001t0002g0108 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.219-10190C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12071166 | ||||||
| chr17:12071166
|
C | G | 1 | a0001c0001t0002g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.219-10190C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12071166 | ||||||
| chr17:12071228
|
C | T | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-10128C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12071228 | ||||||
| chr17:12071257
|
A | G | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG01934.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.219-10099A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12071257 | ||||||
| chr17:12072816
|
C | T | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-8540C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12072816 | ||||||
| chr17:12072828
|
A | G | 2 | a0001c0001t0001g0276a0001c0001t0013g0005 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.219-8528A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12072828 | ||||||
| chr17:12072976
|
A | G | 1 | a0001c0001t0003g0069 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.219-8380A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12072976 | ||||||
| chr17:12073183
|
T | C | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-8173T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12073183 | ||||||
| chr17:12073191
|
A | T | 1 | a0001c0001t0001g0049 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.219-8165A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12073191 | ||||||
| chr17:12073202
|
C | G | 2 | a0001c0001t0002g0259a0001c0001t0002g0265 | 2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.219-8154C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12073202 | ||||||
| chr17:12073219
|
T | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(5): Show | 8 | HG02055.hp1 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.219-8137T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12073219 | ||||||
| chr17:12073245
|
A | G | 4 | a0001c0001t0001g0190a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | NA18966.hp1 NA18979.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.219-8111A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12073245 | ||||||
| chr17:12073635
|
T | C | 4 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(1): Show | 4 | HG02451.hp2 HG02572.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-7721T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12073635 | ||||||
| chr17:12073667
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.219-7689G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12073667 | ||||||
| chr17:12073770
|
A | AT | 103 | a0001c0001t0001g0011a0001c0001t0001g0111a0001c0001t0001g0121others(100): Show | 103 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.219-7568dupT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12073770 | |||||
| chr17:12073770
|
ATT | A | 54 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(51): Show | 57 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.219-7569_219-7568d others(4): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12073770 | |||||
| chr17:12073812
|
G | C | 51 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(48): Show | 54 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.219-7544G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12073812 | ||||||
| chr17:12073867
|
G | A | 1 | a0001c0001t0005g0186 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.219-7489G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12073867 | ||||||
| chr17:12073963
|
G | A | 72 | a0001c0001t0001g0256a0001c0001t0001g0272a0001c0001t0001g0273others(69): Show | 72 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.219-7393G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12073963 | ||||||
| chr17:12074075
|
T | C | 260 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(257): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.219-7281T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12074075 | ||||||
| chr17:12074238
|
A | G | 3 | a0001c0001t0006g0112a0001c0001t0006g0116a0001c0001t0006g0127 | 3 | NA18967.hp2 NA19060.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.219-7118A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12074238 | ||||||
| chr17:12074264
|
T | G | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG01346.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.219-7092T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12074264 | ||||||
| chr17:12074335
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.219-7021G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12074335 | ||||||
| chr17:12074509
|
A | G | 1 | a0001c0001t0002g0108 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.219-6847A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12074509 | ||||||
| chr17:12074635
|
G | A | 188 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(185): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.219-6721G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12074635 | ||||||
| chr17:12074658
|
A | G | 1 | a0001c0001t0001g0293 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.219-6698A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12074658 | ||||||
| chr17:12074667
|
G | C | 14 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(11): Show | 14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.219-6689G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12074667 | ||||||
| chr17:12074759
|
G | T | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-6597G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12074759 | ||||||
| chr17:12074770
|
G | T | 119 | a0001c0001t0001g0046a0001c0001t0001g0096a0001c0001t0001g0102others(116): Show | 119 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.219-6586G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12074770 | ||||||
| chr17:12075062
|
T | C | 2 | a0001c0001t0001g0169a0001c0001t0001g0172 | 2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.219-6294T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12075062 | ||||||
| chr17:12075077
|
T | A | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-6279T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12075077 | ||||||
| chr17:12075083
|
C | T | 1 | a0001c0001t0002g0275 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.219-6273C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12075083 | ||||||
| chr17:12075387
|
T | A | 3 | a0001c0001t0002g0261a0001c0001t0002g0266a0001c0001t0002g0271 | 3 | HG00639.hp2 HG02602.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.219-5969T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12075387 | ||||||
| chr17:12075401
|
A | G | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-5955A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12075401 | ||||||
| chr17:12075431
|
A | G | 1 | a0001c0001t0007g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.219-5925A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12075431 | ||||||
| chr17:12075551
|
G | A | 6 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0299others(3): Show | 6 | HG00597.hp1 NA18612.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-5805G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12075551 | ||||||
| chr17:12076106
|
A | G | 24 | a0001c0001t0001g0046a0001c0001t0001g0105a0001c0001t0001g0184others(21): Show | 24 | HG00099.hp1 HG02015.hp2 HG02071.hp2 others(21): Show |
intron_variant | MODIFIER | c.219-5250A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12076106 | ||||||
| chr17:12076113
|
T | A | 3 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0132 | 3 | HG00621.hp2 NA18969.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.219-5243T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12076113 | ||||||
| chr17:12076279
|
C | CTG | 42 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0103others(39): Show | 42 | HG00280.hp1 HG00544.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.219-5031_219-5030d others(4): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12076279 | |||||
| chr17:12076279
|
C | CTGTG | 88 | a0001c0001t0001g0046a0001c0001t0001g0105a0001c0001t0001g0106others(85): Show | 88 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.219-5033_219-5030d others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12076279 | |||||
| chr17:12076279
|
C | CTGTGTG | 27 | a0001c0001t0001g0012a0001c0001t0001g0096a0001c0001t0001g0115others(24): Show | 27 | HG00597.hp1 HG00642.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.219-5035_219-5030d others(8): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12076279 | |||||
| chr17:12076279
|
C | CTGTGTGT others(1): Show |
5 | a0001c0001t0001g0102a0001c0001t0001g0131a0001c0001t0001g0294others(2): Show | 5 | HG04115.hp2 NA18747.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-5037_219-5030d others(10): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12076279 | |||||
| chr17:12076279
|
C | CTGTGTGT others(3): Show |
2 | a0001c0001t0001g0104a0001c0001t0001g0184 | 2 | HG00099.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.219-5039_219-5030d others(12): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12076279 | |||||
| chr17:12076279
|
C | CTGTGTGT others(7): Show |
2 | a0001c0001t0001g0140a0001c0001t0001g0145 | 2 | HG01261.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.219-5043_219-5030d others(16): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12076279 | |||||
| chr17:12076279
|
C | CTGTGTGT others(9): Show |
1 | a0001c0001t0001g0146 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.219-5045_219-5030d others(18): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12076279 | |||||
| chr17:12076279
|
CTG | C | 66 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(63): Show | 68 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.219-5031_219-5030d others(4): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12076279 | |||||
| chr17:12076279
|
CTGTG | C | 9 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(6): Show | 9 | HG00558.hp1 HG02258.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.219-5033_219-5030d others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12076279 | |||||
| chr17:12076279
|
CTGTGTG | C | 7 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0050others(4): Show | 7 | HG00738.hp2 HG01243.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.219-5035_219-5030d others(8): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12076279 | |||||
| chr17:12076279
|
CTGTGTGT others(1): Show |
C | 7 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0244others(4): Show | 7 | HG02055.hp1 HG02647.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.219-5037_219-5030d others(10): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12076279 | |||||
| chr17:12076279
|
CTGTGTGT others(3): Show |
C | 2 | a0001c0001t0001g0014a0001c0001t0001g0022 | 2 | HG02647.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.219-5039_219-5030d others(12): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12076279 | |||||
| chr17:12076279
|
CTGTGTGT others(13): Show |
C | 1 | a0001c0001t0001g0130 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.219-5049_219-5030d others(22): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12076279 | |||||
| chr17:12076283
|
G | C | 4 | a0001c0001t0001g0034a0001c0001t0001g0101a0001c0001t0001g0176others(1): Show | 4 | HG01192.hp1 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-5073G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12076283 | ||||||
| chr17:12076388
|
A | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG02145.hp2 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-4968A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12076388 | ||||||
| chr17:12076532
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.219-4824T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12076532 | ||||||
| chr17:12076721
|
T | TC | 119 | a0001c0001t0001g0046a0001c0001t0001g0096a0001c0001t0001g0102others(116): Show | 119 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.219-4634dupC | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12076721 | |||||
| chr17:12076857
|
T | TTG | 90 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(87): Show | 90 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.219-4483_219-4482d others(4): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12076857 | |||||
| chr17:12076857
|
T | TTGTG | 56 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(53): Show | 59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.219-4485_219-4482d others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12076857 | |||||
| chr17:12076882
|
G | C | 2 | a0001c0001t0001g0292a0001c0001t0001g0293 | 2 | HG00280.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.219-4474G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12076882 | ||||||
| chr17:12076911
|
T | C | 1 | a0001c0001t0001g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.219-4445T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12076911 | ||||||
| chr17:12076954
|
G | A | 1 | a0001c0001t0013g0005 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.219-4402G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12076954 | ||||||
| chr17:12077026
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0101 | 2 | HG01192.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.219-4330G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12077026 | ||||||
| chr17:12077154
|
T | A | 3 | a0001c0001t0001g0115a0001c0001t0001g0124a0001c0001t0001g0237 | 3 | HG02165.hp2 NA18946.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.219-4202T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12077154 | ||||||
| chr17:12077206
|
G | T | 19 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.219-4150G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12077206 | ||||||
| chr17:12077486
|
A | G | 1 | a0001c0001t0001g0245 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.219-3870A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12077486 | ||||||
| chr17:12077630
|
C | G | 1 | a0001c0001t0001g0200 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.219-3726C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12077630 | ||||||
| chr17:12077761
|
C | T | 133 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(130): Show | 133 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.219-3595C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12077761 | ||||||
| chr17:12078024
|
C | T | 1 | a0001c0001t0002g0298 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.219-3332C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12078024 | ||||||
| chr17:12078046
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.219-3310G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12078046 | ||||||
| chr17:12078128
|
A | C | 14 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(11): Show | 14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.219-3228A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12078128 | ||||||
| chr17:12078129
|
G | C | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-3227G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12078129 | ||||||
| chr17:12078235
|
G | T | 3 | a0001c0001t0002g0233a0001c0001t0002g0252a0001c0001t0002g0253 | 3 | HG02818.hp2 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.219-3121G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12078235 | ||||||
| chr17:12078644
|
G | C | 266 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(263): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.219-2712G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12078644 | ||||||
| chr17:12078693
|
A | G | 1 | a0001c0001t0003g0071 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.219-2663A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12078693 | ||||||
| chr17:12078811
|
C | T | 1 | a0001c0001t0006g0095 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.219-2545C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12078811 | ||||||
| chr17:12079093
|
A | G | 1 | a0001c0001t0004g0030 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.219-2263A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12079093 | ||||||
| chr17:12079132
|
G | T | 1 | a0001c0001t0001g0276 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.219-2224G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12079132 | ||||||
| chr17:12079134
|
TTTTAGTA others(2): Show |
T | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-2208_219-2200d others(11): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 12079134 | |||||
| chr17:12079238
|
T | C | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-2118T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12079238 | ||||||
| chr17:12079524
|
C | T | 1 | a0001c0001t0003g0069 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.219-1832C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12079524 | ||||||
| chr17:12079985
|
G | C | 1 | a0001c0001t0001g0044 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.219-1371G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12079985 | ||||||
| chr17:12080237
|
A | G | 1 | a0001c0001t0001g0273 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.219-1119A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12080237 | ||||||
| chr17:12080270
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.219-1086C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12080270 | ||||||
| chr17:12080434
|
T | G | 1 | a0001c0001t0001g0109 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.219-922T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12080434 | ||||||
| chr17:12080487
|
A | G | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.219-869A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12080487 | ||||||
| chr17:12080571
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.219-785C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12080571 | ||||||
| chr17:12080734
|
C | T | 8 | a0001c0001t0002g0133a0001c0001t0002g0134a0001c0001t0002g0135others(5): Show | 8 | NA18964.hp2 NA18977.hp2 NA18979.hp2 others(5): Show |
intron_variant | MODIFIER | c.219-622C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12080734 | ||||||
| chr17:12080897
|
A | G | 5 | a0001c0001t0001g0272a0001c0001t0002g0287a0001c0001t0002g0291others(2): Show | 5 | HG02132.hp1 HG03654.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-459A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12080897 | ||||||
| chr17:12080915
|
G | C | 119 | a0001c0001t0001g0046a0001c0001t0001g0096a0001c0001t0001g0102others(116): Show | 119 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.219-441G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12080915 | ||||||
| chr17:12081022
|
C | T | 56 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(53): Show | 59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.219-334C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12081022 | ||||||
| chr17:12081039
|
A | G | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0073 | 3 | HG00642.hp1 HG01516.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.219-317A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12081039 | ||||||
| chr17:12081057
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.219-299A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | chr17 | 12081057 | ||||||
| chr17:12081710
|
A | T | 1 | a0001c0001t0002g0057 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.393+180A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12081710 | ||||||
| chr17:12081832
|
A | C | 1 | a0001c0001t0007g0249 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.393+302A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12081832 | ||||||
| chr17:12082187
|
T | C | 70 | a0001c0001t0001g0256a0001c0001t0001g0272a0001c0001t0001g0273others(67): Show | 70 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.393+657T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12082187 | ||||||
| chr17:12082226
|
G | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0021others(1): Show | 4 | HG02809.hp2 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+696G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12082226 | ||||||
| chr17:12082257
|
T | C | 119 | a0001c0001t0001g0046a0001c0001t0001g0096a0001c0001t0001g0102others(116): Show | 119 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.393+727T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12082257 | ||||||
| chr17:12082630
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.393+1100C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12082630 | ||||||
| chr17:12082635
|
C | G | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.393+1105C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12082635 | ||||||
| chr17:12082784
|
G | A | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.393+1254G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12082784 | ||||||
| chr17:12082952
|
C | G | 3 | a0001c0001t0001g0244a0001c0001t0001g0247a0001c0001t0001g0248 | 3 | HG02970.hp2 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.393+1422C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12082952 | ||||||
| chr17:12083160
|
A | C | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.393+1630A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12083160 | ||||||
| chr17:12083517
|
G | A | 2 | a0001c0001t0002g0107a0001c0001t0002g0108 | 2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.393+1987G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12083517 | ||||||
| chr17:12083672
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.393+2142A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12083672 | ||||||
| chr17:12084125
|
C | T | 1 | a0001c0001t0002g0260 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.393+2595C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12084125 | ||||||
| chr17:12084337
|
C | T | 1 | a0001c0001t0002g0310 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.393+2807C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12084337 | ||||||
| chr17:12084428
|
C | T | 1 | a0001c0001t0019g0295 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.393+2898C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12084428 | ||||||
| chr17:12084501
|
A | G | 1 | a0001c0001t0001g0216 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.393+2971A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12084501 | ||||||
| chr17:12084548
|
A | G | 5 | a0001c0001t0004g0027a0001c0001t0004g0030a0001c0001t0004g0039others(2): Show | 5 | HG02040.hp2 NA18945.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+3018A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12084548 | ||||||
| chr17:12084594
|
C | T | 70 | a0001c0001t0001g0256a0001c0001t0001g0272a0001c0001t0001g0273others(67): Show | 70 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.393+3064C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12084594 | ||||||
| chr17:12084733
|
G | A | 2 | a0001c0003t0001g0279a0001c0003t0002g0280 | 2 | HG02559.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.393+3203G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12084733 | ||||||
| chr17:12084928
|
G | GAGAA | 56 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(53): Show | 59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.393+3401_393+3402i others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12084928 | |||||
| chr17:12085494
|
C | T | 19 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.393+3964C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12085494 | ||||||
| chr17:12085599
|
G | T | 70 | a0001c0001t0001g0256a0001c0001t0001g0272a0001c0001t0001g0273others(67): Show | 70 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.393+4069G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12085599 | ||||||
| chr17:12085773
|
A | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0064 | 2 | HG01081.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.393+4243A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12085773 | ||||||
| chr17:12085850
|
T | C | 56 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(53): Show | 59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.393+4320T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12085850 | ||||||
| chr17:12086244
|
G | A | 23 | a0001c0001t0001g0096a0001c0001t0001g0106a0001c0001t0001g0182others(20): Show | 23 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.393+4714G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12086244 | ||||||
| chr17:12086446
|
A | G | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(1): Show | 4 | HG01123.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+4916A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12086446 | ||||||
| chr17:12086599
|
C | T | 5 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0019others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+5069C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12086599 | ||||||
| chr17:12086826
|
T | TTTTTG | 41 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(38): Show | 41 | HG01106.hp1 HG01243.hp1 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.393+5331_393+5335d others(7): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12086826 | |||||
| chr17:12086826
|
T | TTTTTGTT others(3): Show |
5 | a0001c0001t0001g0037a0001c0001t0002g0233a0001c0001t0002g0252others(2): Show | 5 | HG02818.hp2 HG02976.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+5326_393+5335d others(12): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12086826 | |||||
| chr17:12086826
|
TTTTTG | T | 117 | a0001c0001t0001g0046a0001c0001t0001g0096a0001c0001t0001g0102others(114): Show | 117 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.393+5331_393+5335d others(7): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12086826 | |||||
| chr17:12086826
|
TTTTTGTT others(3): Show |
T | 124 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0031others(121): Show | 127 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.393+5326_393+5335d others(12): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12086826 | |||||
| chr17:12086826
|
TTTTTGTT others(8): Show |
T | 1 | a0001c0001t0001g0024 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.393+5321_393+5335d others(17): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12086826 | |||||
| chr17:12087007
|
C | T | 1 | a0001c0001t0002g0298 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.393+5477C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12087007 | ||||||
| chr17:12087090
|
G | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG02145.hp2 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+5560G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12087090 | ||||||
| chr17:12087092
|
C | T | 1 | a0001c0001t0002g0275 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.393+5562C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12087092 | ||||||
| chr17:12087140
|
G | A | 2 | a0001c0001t0002g0298a0001c0001t0002g0312 | 2 | NA18747.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.393+5610G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12087140 | ||||||
| chr17:12087307
|
G | A | 3 | a0001c0001t0001g0244a0001c0001t0001g0247a0001c0001t0001g0248 | 3 | HG02970.hp2 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.393+5777G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12087307 | ||||||
| chr17:12087362
|
A | G | 119 | a0001c0001t0001g0046a0001c0001t0001g0096a0001c0001t0001g0102others(116): Show | 119 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.393+5832A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12087362 | ||||||
| chr17:12087502
|
T | C | 1 | a0001c0001t0002g0275 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.393+5972T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12087502 | ||||||
| chr17:12087546
|
C | T | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.393+6016C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12087546 | ||||||
| chr17:12087616
|
T | TATTA | 8 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(5): Show | 8 | HG02451.hp2 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+6105_393+6108d others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12087616 | |||||
| chr17:12087616
|
TATTA | T | 17 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0260others(14): Show | 17 | HG00639.hp2 HG00642.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.393+6105_393+6108d others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12087616 | |||||
| chr17:12087813
|
T | G | 1 | a0001c0001t0002g0315 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.393+6283T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12087813 | ||||||
| chr17:12087847
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.393+6317C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12087847 | ||||||
| chr17:12087854
|
T | C | 2 | a0001c0001t0002g0107a0001c0001t0002g0108 | 2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.393+6324T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12087854 | ||||||
| chr17:12088151
|
G | C | 6 | a0001c0001t0001g0273a0001c0001t0001g0277a0001c0001t0001g0281others(3): Show | 6 | HG02055.hp2 HG02451.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.393+6621G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088151 | ||||||
| chr17:12088445
|
T | TATATATT others(9): Show |
291 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(288): Show | 294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.393+6930_393+6931i others(18): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12088445 | |||||
| chr17:12088458
|
T | TTAAATAT others(6): Show |
2 | a0001c0001t0001g0207a0001c0001t0018g0047 | 2 | HG02040.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.393+6930_393+6931i others(15): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12088458 | |||||
| chr17:12088461
|
T | C | 56 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(53): Show | 59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.393+6931T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088461 | ||||||
| chr17:12088496
|
T | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(54): Show | 60 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.393+6966T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088496 | ||||||
| chr17:12088507
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.393+6977C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088507 | ||||||
| chr17:12088541
|
A | G | 3 | a0001c0001t0007g0026a0001c0001t0007g0249a0001c0001t0007g0250 | 3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.393+7011A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088541 | ||||||
| chr17:12088541
|
AT | A | 116 | a0001c0001t0001g0046a0001c0001t0001g0096a0001c0001t0001g0102others(113): Show | 116 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.393+7013delT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12088541 | |||||
| chr17:12088542
|
TTATATCT others(19): Show |
T | 1 | a0001c0001t0010g0205 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.393+7013_394-7007d others(28): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088542 | ||||||
| chr17:12088548
|
C | A | 118 | a0001c0001t0001g0046a0001c0001t0001g0096a0001c0001t0001g0102others(115): Show | 118 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.393+7018C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088548 | ||||||
| chr17:12088548
|
C | G | 56 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(53): Show | 59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.393+7018C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088548 | ||||||
| chr17:12088568
|
A | AAT | 195 | a0001c0001t0001g0046a0001c0001t0001g0075a0001c0001t0001g0096others(192): Show | 195 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.394-7001_394-7000d others(4): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12088568 | |||||
| chr17:12088568
|
A | AATATATA others(22): Show |
54 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(51): Show | 57 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.394-7000_394-6999i others(31): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12088568 | |||||
| chr17:12088575
|
A | T | 1 | a0001c0001t0001g0278 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.394-7000A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088575 | ||||||
| chr17:12088576
|
A | T | 15 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(12): Show | 15 | HG01106.hp1 HG02040.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.394-6999A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088576 | ||||||
| chr17:12088577
|
T | A | 15 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(12): Show | 15 | HG01106.hp1 HG02040.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.394-6998T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088577 | ||||||
| chr17:12088583
|
A | T | 15 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(12): Show | 15 | HG01106.hp1 HG02040.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.394-6992A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088583 | ||||||
| chr17:12088584
|
T | A | 15 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(12): Show | 15 | HG01106.hp1 HG02040.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.394-6991T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088584 | ||||||
| chr17:12088592
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.394-6983A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088592 | ||||||
| chr17:12088618
|
G | GATTA | 56 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(53): Show | 59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.394-6955_394-6952d others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12088618 | |||||
| chr17:12088646
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.394-6929T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088646 | ||||||
| chr17:12088778
|
A | C | 5 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0243others(2): Show | 5 | HG02083.hp1 NA18982.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-6797A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088778 | ||||||
| chr17:12088911
|
C | CT | 8 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0195others(5): Show | 8 | HG01243.hp1 HG01891.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.394-6646dupT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12088911 | |||||
| chr17:12088911
|
CT | C | 63 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(60): Show | 66 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.394-6646delT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12088911 | |||||
| chr17:12088942
|
C | T | 1 | a0001c0001t0003g0072 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.394-6633C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088942 | ||||||
| chr17:12088991
|
A | G | 9 | a0001c0001t0001g0190a0001c0001t0001g0195a0001c0001t0001g0198others(6): Show | 9 | HG02165.hp1 NA18944.hp1 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.394-6584A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12088991 | ||||||
| chr17:12089004
|
C | T | 1 | a0001c0001t0001g0242 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.394-6571C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12089004 | ||||||
| chr17:12089060
|
C | T | 1 | a0001c0001t0001g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.394-6515C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12089060 | ||||||
| chr17:12089110
|
C | A | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.394-6465C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12089110 | ||||||
| chr17:12089164
|
G | A | 1 | a0001c0001t0018g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.394-6411G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12089164 | ||||||
| chr17:12089213
|
A | G | 293 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(290): Show | 296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.394-6362A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12089213 | ||||||
| chr17:12089614
|
A | G | 1 | a0001c0001t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.394-5961A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12089614 | ||||||
| chr17:12089976
|
G | T | 1 | a0001c0001t0001g0149 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.394-5599G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12089976 | ||||||
| chr17:12089981
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.394-5594C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12089981 | ||||||
| chr17:12090051
|
A | G | 14 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(11): Show | 14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.394-5524A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12090051 | ||||||
| chr17:12090056
|
C | G | 1 | a0001c0001t0002g0319 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.394-5519C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12090056 | ||||||
| chr17:12090214
|
A | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(1): Show | 4 | HG02486.hp2 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-5361A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12090214 | ||||||
| chr17:12090472
|
A | G | 1 | a0001c0001t0001g0004 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.394-5103A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12090472 | ||||||
| chr17:12090482
|
G | T | 1 | a0001c0001t0001g0157 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.394-5093G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12090482 | ||||||
| chr17:12090555
|
G | T | 1 | a0001c0001t0001g0154 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.394-5020G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12090555 | ||||||
| chr17:12090750
|
T | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0166 | 2 | HG02258.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.394-4825T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12090750 | ||||||
| chr17:12090862
|
G | T | 56 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(53): Show | 59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.394-4713G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12090862 | ||||||
| chr17:12090887
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.394-4688C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12090887 | ||||||
| chr17:12091078
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.394-4497G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12091078 | ||||||
| chr17:12091183
|
A | G | 56 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(53): Show | 59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.394-4392A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12091183 | ||||||
| chr17:12091238
|
G | A | 1 | a0001c0001t0003g0080 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.394-4337G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12091238 | ||||||
| chr17:12091455
|
A | T | 71 | a0001c0001t0001g0256a0001c0001t0001g0272a0001c0001t0001g0273others(68): Show | 71 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.394-4120A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12091455 | ||||||
| chr17:12091553
|
C | G | 56 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(53): Show | 59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.394-4022C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12091553 | ||||||
| chr17:12091742
|
T | C | 56 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(53): Show | 59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.394-3833T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12091742 | ||||||
| chr17:12091799
|
A | G | 71 | a0001c0001t0001g0256a0001c0001t0001g0272a0001c0001t0001g0273others(68): Show | 71 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.394-3776A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12091799 | ||||||
| chr17:12092034
|
G | C | 71 | a0001c0001t0001g0256a0001c0001t0001g0272a0001c0001t0001g0273others(68): Show | 71 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.394-3541G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12092034 | ||||||
| chr17:12092078
|
A | G | 1 | a0001c0001t0004g0290 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.394-3497A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12092078 | ||||||
| chr17:12092285
|
G | A | 1 | a0001c0001t0002g0291 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.394-3290G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12092285 | ||||||
| chr17:12092684
|
C | G | 56 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(53): Show | 59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.394-2891C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12092684 | ||||||
| chr17:12092706
|
A | G | 5 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(2): Show | 5 | HG02647.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.394-2869A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12092706 | ||||||
| chr17:12092748
|
C | A | 1 | a0001c0001t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.394-2827C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12092748 | ||||||
| chr17:12092749
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.394-2826G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12092749 | ||||||
| chr17:12092793
|
G | A | 5 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(2): Show | 5 | HG02647.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.394-2782G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12092793 | ||||||
| chr17:12092801
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.394-2774C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12092801 | ||||||
| chr17:12092851
|
C | G | 1 | a0001c0001t0003g0062 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.394-2724C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12092851 | ||||||
| chr17:12092862
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.394-2713T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12092862 | ||||||
| chr17:12092918
|
C | T | 4 | a0001c0001t0001g0034a0001c0001t0001g0101a0001c0001t0001g0176others(1): Show | 4 | HG01192.hp1 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-2657C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12092918 | ||||||
| chr17:12092941
|
G | A | 1 | a0001c0001t0019g0295 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.394-2634G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12092941 | ||||||
| chr17:12092981
|
G | A | 1 | a0001c0001t0013g0005 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.394-2594G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12092981 | ||||||
| chr17:12092984
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.394-2591C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12092984 | ||||||
| chr17:12093046
|
T | C | 56 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(53): Show | 59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.394-2529T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12093046 | ||||||
| chr17:12093144
|
T | C | 1 | a0001c0001t0002g0316 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.394-2431T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12093144 | ||||||
| chr17:12093211
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.394-2364A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12093211 | ||||||
| chr17:12093317
|
A | G | 293 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(290): Show | 296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.394-2258A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12093317 | ||||||
| chr17:12093379
|
A | T | 3 | a0001c0001t0002g0057a0001c0001t0002g0058a0001c0001t0002g0059 | 3 | HG01099.hp2 HG01123.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.394-2196A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12093379 | ||||||
| chr17:12093511
|
T | A | 1 | a0001c0001t0001g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.394-2064T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12093511 | ||||||
| chr17:12093987
|
T | C | 19 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.394-1588T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12093987 | ||||||
| chr17:12094172
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.394-1403G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12094172 | ||||||
| chr17:12094311
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.394-1264C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12094311 | ||||||
| chr17:12094327
|
C | G | 1 | a0001c0001t0001g0215 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.394-1248C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12094327 | ||||||
| chr17:12094375
|
C | T | 293 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(290): Show | 296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.394-1200C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12094375 | ||||||
| chr17:12094628
|
A | G | 1 | a0001c0001t0001g0243 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.394-947A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12094628 | ||||||
| chr17:12094725
|
GGGA | G | 56 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(53): Show | 59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.394-844_394-842del others(3): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 12094725 | |||||
| chr17:12095166
|
A | C | 1 | a0001c0001t0001g0124 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.394-409A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12095166 | ||||||
| chr17:12095204
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.394-371T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12095204 | ||||||
| chr17:12095231
|
G | A | 14 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(11): Show | 14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.394-344G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | 12095231 | ||||||
| chr17:12095830
|
G | A | 266 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(263): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.513+136G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12095830 | ||||||
| chr17:12095895
|
T | TGTGTGTG others(10): Show |
1 | a0001c0001t0007g0249 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.513+201_513+202ins others(17): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12095895 | ||||||
| chr17:12095895
|
T | TTG | 26 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0001g0056others(23): Show | 26 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.513+233_513+234dup others(2): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | |||||
| chr17:12095895
|
T | TTGTG | 43 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0054others(40): Show | 45 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.513+231_513+234dup others(4): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | |||||
| chr17:12095895
|
T | TTGTGTG | 6 | a0001c0001t0001g0082a0001c0001t0001g0097a0001c0001t0001g0160others(3): Show | 6 | HG00642.hp1 HG01884.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+229_513+234dup others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | |||||
| chr17:12095895
|
T | TTGTGTGT others(1): Show |
6 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0021others(3): Show | 6 | HG02109.hp1 HG02809.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+227_513+234dup others(8): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | |||||
| chr17:12095895
|
T | TTGTGTGT others(3): Show |
1 | a0001c0001t0001g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.513+225_513+234dup others(10): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | |||||
| chr17:12095895
|
T | TTGTGTGT others(5): Show |
2 | a0001c0001t0007g0250a0001c0001t0011g0017 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.513+223_513+234dup others(12): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | |||||
| chr17:12095895
|
T | TTGTGTGT others(7): Show |
1 | a0001c0001t0007g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.513+221_513+234dup others(14): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | |||||
| chr17:12095895
|
T | TTGTGTGT others(9): Show |
2 | a0001c0001t0001g0018a0001c0001t0001g0023 | 2 | HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.513+219_513+234dup others(16): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | |||||
| chr17:12095895
|
T | TTGTGTGT others(11): Show |
2 | a0001c0001t0001g0008a0001c0001t0001g0019 | 2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.513+217_513+234dup others(18): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | |||||
| chr17:12095895
|
TTG | T | 28 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0161others(25): Show | 28 | HG01243.hp2 HG01361.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.513+233_513+234del others(2): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | |||||
| chr17:12095895
|
TTGTG | T | 59 | a0001c0001t0001g0010a0001c0001t0001g0102a0001c0001t0001g0103others(56): Show | 59 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.513+231_513+234del others(4): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | |||||
| chr17:12095895
|
TTGTGTG | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(3): Show | 6 | HG01975.hp1 HG02273.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.513+229_513+234del others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | |||||
| chr17:12095895
|
TTGTGTGT others(1): Show |
T | 9 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0049others(6): Show | 10 | HG00558.hp1 HG01934.hp2 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.513+227_513+234del others(8): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | |||||
| chr17:12095895
|
TTGTGTGT others(3): Show |
T | 10 | a0001c0001t0001g0100a0001c0001t0001g0158a0001c0001t0001g0251others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.513+225_513+234del others(10): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | |||||
| chr17:12095895
|
TTGTGTGT others(5): Show |
T | 1 | a0001c0001t0001g0272 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.513+223_513+234del others(12): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | |||||
| chr17:12095895
|
TTGTGTGT others(7): Show |
T | 1 | a0001c0001t0001g0109 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.513+221_513+234del others(14): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | |||||
| chr17:12095895
|
TTGTGTGT others(9): Show |
T | 2 | a0001c0001t0001g0006a0001c0001t0001g0223 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.513+219_513+234del others(16): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | |||||
| chr17:12095895
|
TTGTGTGT others(11): Show |
T | 1 | a0001c0001t0001g0155 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.513+217_513+234del others(18): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12095895 | |||||
| chr17:12095927
|
G | A | 1 | a0001c0001t0018g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.513+233G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12095927 | ||||||
| chr17:12095929
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.513+235A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12095929 | ||||||
| chr17:12096063
|
C | A | 1 | a0001c0001t0001g0219 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.513+369C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12096063 | ||||||
| chr17:12096067
|
T | TC | 30 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0100others(27): Show | 30 | HG00544.hp1 HG00621.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.513+394dupC | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12096067 | |||||
| chr17:12096067
|
T | TCC | 23 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0016others(20): Show | 23 | HG00639.hp2 HG01081.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.513+393_513+394dup others(2): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12096067 | |||||
| chr17:12096067
|
T | TCCCCCCC others(6): Show |
1 | a0001c0001t0001g0129 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.513+382_513+394dup others(13): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12096067 | |||||
| chr17:12096067
|
TC | T | 38 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0019others(35): Show | 38 | HG00558.hp2 HG00639.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.513+394delC | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12096067 | |||||
| chr17:12096067
|
TCC | T | 42 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0103others(39): Show | 42 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.513+393_513+394del others(2): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12096067 | |||||
| chr17:12096067
|
TCCC | T | 21 | a0001c0001t0001g0117a0001c0001t0001g0158a0001c0001t0001g0162others(18): Show | 21 | HG00280.hp2 HG01891.hp2 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.513+392_513+394del others(3): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12096067 | |||||
| chr17:12096067
|
TCCCC | T | 14 | a0001c0001t0001g0046a0001c0001t0001g0096a0001c0001t0001g0115others(11): Show | 14 | HG02015.hp2 HG02071.hp2 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.513+391_513+394del others(4): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12096067 | |||||
| chr17:12096067
|
TCCCCCCC others(1): Show |
T | 26 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0031others(23): Show | 26 | HG00597.hp2 HG00609.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.513+387_513+394del others(8): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12096067 | |||||
| chr17:12096067
|
TCCCCCCC others(2): Show |
T | 25 | a0001c0001t0001g0003a0001c0001t0001g0048a0001c0001t0001g0049others(22): Show | 27 | HG00099.hp2 HG00558.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.513+386_513+394del others(9): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12096067 | |||||
| chr17:12096067
|
TCCCCCCC others(4): Show |
T | 1 | a0001c0001t0004g0040 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.513+384_513+394del others(11): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12096067 | |||||
| chr17:12096067
|
TCCCCCCC others(5): Show |
T | 13 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(10): Show | 13 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.513+383_513+394del others(12): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12096067 | |||||
| chr17:12096067
|
TCCCCCCC others(6): Show |
T | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0107 | 3 | HG06807.hp1 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.513+382_513+394del others(13): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12096067 | |||||
| chr17:12096067
|
TCCCCCCC others(7): Show |
T | 6 | a0001c0001t0001g0276a0001c0001t0002g0233a0001c0001t0002g0252others(3): Show | 6 | HG01243.hp2 HG02615.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.513+381_513+394del others(14): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12096067 | |||||
| chr17:12096089
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.513+395G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12096089 | ||||||
| chr17:12096176
|
A | T | 1 | a0001c0001t0001g0024 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.513+482A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12096176 | ||||||
| chr17:12096380
|
A | G | 1 | a0001c0001t0017g0078 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.513+686A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12096380 | ||||||
| chr17:12096477
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.513+783C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12096477 | ||||||
| chr17:12096562
|
T | G | 1 | a0001c0001t0013g0005 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.513+868T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12096562 | ||||||
| chr17:12096784
|
A | C | 1 | a0001c0001t0001g0110 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.513+1090A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12096784 | ||||||
| chr17:12096925
|
A | G | 1 | a0001c0001t0004g0224 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.513+1231A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12096925 | ||||||
| chr17:12096956
|
T | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0022 | 3 | HG02055.hp1 HG02647.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.513+1262T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12096956 | ||||||
| chr17:12097016
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.513+1322G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12097016 | ||||||
| chr17:12097267
|
A | G | 135 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(132): Show | 135 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.513+1573A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12097267 | ||||||
| chr17:12097315
|
G | A | 195 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(192): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.513+1621G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12097315 | ||||||
| chr17:12097504
|
A | G | 3 | a0001c0001t0004g0036a0001c0001t0004g0040a0001c0001t0004g0041 | 3 | NA18971.hp1 NA18972.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.513+1810A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12097504 | ||||||
| chr17:12097730
|
A | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0148 | 2 | NA18945.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.513+2036A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12097730 | ||||||
| chr17:12097760
|
A | C | 56 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(53): Show | 59 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.513+2066A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12097760 | ||||||
| chr17:12097879
|
T | A | 1 | a0001c0001t0001g0241 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.513+2185T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12097879 | ||||||
| chr17:12098114
|
A | T | 1 | a0001c0001t0009g0001 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.513+2420A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12098114 | ||||||
| chr17:12098254
|
C | T | 1 | a0001c0001t0013g0005 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.513+2560C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12098254 | ||||||
| chr17:12098362
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0166 | 2 | HG02258.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.513+2668C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12098362 | ||||||
| chr17:12098400
|
T | C | 266 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(263): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.513+2706T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12098400 | ||||||
| chr17:12098437
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.513+2743C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12098437 | ||||||
| chr17:12098477
|
C | CA | 51 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0031others(48): Show | 53 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.513+2798dupA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12098477 | |||||
| chr17:12098709
|
A | T | 4 | a0001c0001t0005g0186a0001c0001t0005g0196a0001c0001t0005g0197others(1): Show | 4 | HG02083.hp2 NA18950.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.513+3015A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12098709 | ||||||
| chr17:12098913
|
T | A | 1 | a0001c0001t0001g0241 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.513+3219T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12098913 | ||||||
| chr17:12099102
|
T | C | 6 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(3): Show | 6 | HG02165.hp2 NA18946.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+3408T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12099102 | ||||||
| chr17:12099213
|
C | CA | 12 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0020others(9): Show | 12 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.513+3532dupA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12099213 | |||||
| chr17:12099228
|
A | C | 1 | a0001c0001t0001g0180 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.513+3534A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12099228 | ||||||
| chr17:12099318
|
A | G | 55 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(52): Show | 58 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.513+3624A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12099318 | ||||||
| chr17:12099408
|
G | A | 2 | a0001c0001t0001g0149a0001c0001t0004g0156 | 2 | HG00673.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.513+3714G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12099408 | ||||||
| chr17:12099618
|
A | G | 3 | a0001c0001t0002g0261a0001c0001t0002g0266a0001c0001t0002g0271 | 3 | HG00639.hp2 HG02602.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.513+3924A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12099618 | ||||||
| chr17:12099689
|
C | G | 1 | a0001c0001t0001g0202 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.513+3995C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12099689 | ||||||
| chr17:12099720
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.513+4026A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12099720 | ||||||
| chr17:12099724
|
A | G | 3 | a0001c0001t0007g0026a0001c0001t0007g0249a0001c0001t0007g0250 | 3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.513+4030A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12099724 | ||||||
| chr17:12099985
|
C | G | 1 | a0001c0001t0005g0197 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.513+4291C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12099985 | ||||||
| chr17:12100033
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.513+4339C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12100033 | ||||||
| chr17:12100090
|
C | G | 1 | a0001c0001t0002g0257 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.513+4396C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12100090 | ||||||
| chr17:12100191
|
A | T | 1 | a0001c0001t0001g0034 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.513+4497A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12100191 | ||||||
| chr17:12100361
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.513+4667A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12100361 | ||||||
| chr17:12100504
|
A | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG02145.hp2 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+4810A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12100504 | ||||||
| chr17:12100753
|
G | A | 1 | a0001c0001t0002g0298 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.513+5059G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12100753 | ||||||
| chr17:12100765
|
G | A | 8 | a0001c0001t0001g0034a0001c0001t0001g0101a0001c0001t0001g0157others(5): Show | 8 | HG01192.hp1 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.513+5071G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12100765 | ||||||
| chr17:12100819
|
T | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0048 | 2 | HG00099.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.513+5125T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12100819 | ||||||
| chr17:12101005
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.513+5311G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12101005 | ||||||
| chr17:12101017
|
A | G | 2 | a0001c0001t0002g0107a0001c0001t0002g0108 | 2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.513+5323A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12101017 | ||||||
| chr17:12101440
|
T | C | 1 | a0001c0001t0001g0288 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.513+5746T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12101440 | ||||||
| chr17:12101610
|
A | T | 1 | a0001c0001t0001g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.513+5916A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12101610 | ||||||
| chr17:12101700
|
T | C | 1 | a0001c0001t0001g0241 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.513+6006T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12101700 | ||||||
| chr17:12101761
|
C | T | 40 | a0001c0001t0001g0256a0001c0001t0001g0272a0001c0001t0001g0288others(37): Show | 40 | HG00544.hp1 HG00597.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.514-6029C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12101761 | ||||||
| chr17:12101780
|
T | C | 1 | a0001c0001t0001g0241 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.514-6010T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12101780 | ||||||
| chr17:12101934
|
A | G | 121 | a0001c0001t0001g0046a0001c0001t0001g0096a0001c0001t0001g0102others(118): Show | 121 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.514-5856A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12101934 | ||||||
| chr17:12101957
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.514-5833G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12101957 | ||||||
| chr17:12102335
|
A | C | 3 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099 | 3 | HG01106.hp2 HG03710.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.514-5455A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12102335 | ||||||
| chr17:12102336
|
T | A | 6 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(3): Show | 6 | HG02165.hp2 NA18946.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.514-5454T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12102336 | ||||||
| chr17:12102361
|
A | G | 1 | a0001c0001t0002g0119 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.514-5429A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12102361 | ||||||
| chr17:12102463
|
C | G | 3 | a0001c0001t0007g0026a0001c0001t0007g0249a0001c0001t0007g0250 | 3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.514-5327C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12102463 | ||||||
| chr17:12102818
|
C | G | 1 | a0001c0001t0001g0210 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.514-4972C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12102818 | ||||||
| chr17:12103039
|
T | TA | 7 | a0001c0001t0001g0013a0001c0001t0001g0063a0001c0001t0001g0097others(4): Show | 7 | HG00597.hp1 HG01081.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.514-4731dupA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12103039 | |||||
| chr17:12103039
|
TA | T | 11 | a0001c0001t0001g0148a0001c0001t0001g0245a0001c0001t0002g0134others(8): Show | 11 | HG02559.hp2 HG03139.hp1 HG03139.hp2 others(8): Show |
intron_variant | MODIFIER | c.514-4731delA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12103039 | |||||
| chr17:12103212
|
A | AT | 8 | a0001c0001t0001g0004a0001c0001t0001g0208a0001c0001t0004g0043others(5): Show | 8 | HG00544.hp2 HG01884.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.514-4561dupT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12103212 | |||||
| chr17:12103350
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.514-4440G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12103350 | ||||||
| chr17:12103398
|
G | T | 1 | a0001c0001t0001g0172 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.514-4392G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12103398 | ||||||
| chr17:12103403
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.514-4387G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12103403 | ||||||
| chr17:12103463
|
G | A | 17 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0260others(14): Show | 17 | HG00639.hp2 HG00642.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.514-4327G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12103463 | ||||||
| chr17:12103475
|
A | T | 1 | a0001c0001t0001g0031 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.514-4315A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12103475 | ||||||
| chr17:12103697
|
T | C | 3 | a0001c0001t0007g0026a0001c0001t0007g0249a0001c0001t0007g0250 | 3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.514-4093T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12103697 | ||||||
| chr17:12103720
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0022 | 3 | HG02055.hp1 HG02647.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.514-4070G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12103720 | ||||||
| chr17:12103762
|
C | T | 7 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(4): Show | 7 | HG02055.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.514-4028C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12103762 | ||||||
| chr17:12103826
|
A | G | 1 | a0001c0001t0018g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.514-3964A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12103826 | ||||||
| chr17:12104326
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.514-3464A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12104326 | ||||||
| chr17:12104516
|
C | T | 2 | a0001c0001t0001g0276a0002c0004t0012g0028 | 2 | HG01243.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.514-3274C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12104516 | ||||||
| chr17:12104565
|
A | T | 4 | a0001c0001t0001g0188a0001c0001t0001g0213a0001c0001t0002g0275others(1): Show | 4 | HG02015.hp2 HG03669.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.514-3225A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12104565 | ||||||
| chr17:12104579
|
T | G | 1 | a0001c0001t0001g0219 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.514-3211T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12104579 | ||||||
| chr17:12104621
|
T | C | 1 | a0001c0001t0003g0068 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.514-3169T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12104621 | ||||||
| chr17:12104625
|
A | G | 2 | a0001c0001t0004g0289a0001c0001t0004g0290 | 2 | HG02132.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.514-3165A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12104625 | ||||||
| chr17:12104690
|
C | T | 1 | a0001c0001t0013g0005 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.514-3100C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12104690 | ||||||
| chr17:12105376
|
C | T | 6 | a0001c0001t0001g0273a0001c0001t0001g0277a0001c0001t0001g0281others(3): Show | 6 | HG02055.hp2 HG02451.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.514-2414C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12105376 | ||||||
| chr17:12105445
|
C | T | 1 | a0001c0001t0011g0017 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.514-2345C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12105445 | ||||||
| chr17:12105542
|
T | A | 5 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(2): Show | 5 | HG02647.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.514-2248T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12105542 | ||||||
| chr17:12105548
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.514-2242T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12105548 | ||||||
| chr17:12105581
|
T | G | 1 | a0001c0001t0001g0074 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.514-2209T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12105581 | ||||||
| chr17:12106568
|
A | G | 3 | a0001c0001t0002g0233a0001c0001t0002g0252a0001c0001t0002g0253 | 3 | HG02818.hp2 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.514-1222A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12106568 | ||||||
| chr17:12106678
|
C | T | 1 | a0001c0001t0018g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.514-1112C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12106678 | ||||||
| chr17:12106686
|
A | G | 2 | a0001c0001t0001g0236a0001c0001t0016g0235 | 2 | HG00639.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.514-1104A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12106686 | ||||||
| chr17:12106888
|
T | C | 1 | a0001c0001t0018g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.514-902T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12106888 | ||||||
| chr17:12106914
|
A | G | 53 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(50): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.514-876A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12106914 | ||||||
| chr17:12106941
|
T | C | 2 | a0001c0001t0002g0107a0001c0001t0002g0108 | 2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.514-849T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12106941 | ||||||
| chr17:12106958
|
T | C | 4 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0021others(1): Show | 4 | HG02809.hp2 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.514-832T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12106958 | ||||||
| chr17:12107220
|
A | G | 3 | a0001c0001t0001g0244a0001c0001t0001g0247a0001c0001t0001g0248 | 3 | HG02970.hp2 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.514-570A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12107220 | ||||||
| chr17:12107363
|
A | G | 181 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(178): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.514-427A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12107363 | ||||||
| chr17:12107382
|
C | CT | 18 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0109others(15): Show | 18 | HG00280.hp1 HG00558.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.514-389dupT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12107382 | |||||
| chr17:12107382
|
C | CTT | 8 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0128others(5): Show | 8 | HG00609.hp2 HG00621.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.514-390_514-389dup others(2): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 12107382 | |||||
| chr17:12107488
|
A | T | 1 | a0001c0001t0002g0252 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.514-302A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12107488 | ||||||
| chr17:12107629
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.514-161T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | chr17 | 12107629 | ||||||
| chr17:12107969
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.633+60A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12107969 | ||||||
| chr17:12108089
|
C | T | 3 | a0001c0001t0002g0233a0001c0001t0002g0252a0001c0001t0002g0253 | 3 | HG02818.hp2 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.633+180C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12108089 | ||||||
| chr17:12108557
|
T | TTTGTA | 113 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(110): Show | 113 | HG00099.hp1 HG00280.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.633+648_633+649ins others(5): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12108557 | ||||||
| chr17:12108591
|
T | G | 1 | a0001c0001t0018g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.633+682T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12108591 | ||||||
| chr17:12108802
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.633+893A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12108802 | ||||||
| chr17:12108877
|
A | C | 1 | a0001c0001t0001g0022 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.633+968A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12108877 | ||||||
| chr17:12108981
|
A | C | 1 | a0001c0001t0001g0141 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.633+1072A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12108981 | ||||||
| chr17:12109215
|
G | A | 1 | a0001c0001t0002g0318 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.634-1160G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12109215 | ||||||
| chr17:12109350
|
A | G | 1 | a0001c0001t0003g0033 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.634-1025A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12109350 | ||||||
| chr17:12109379
|
A | G | 266 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(263): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.634-996A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12109379 | ||||||
| chr17:12109488
|
G | A | 1 | a0001c0001t0018g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.634-887G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12109488 | ||||||
| chr17:12109612
|
G | C | 1 | a0001c0001t0002g0133 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.634-763G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12109612 | ||||||
| chr17:12109954
|
C | A | 1 | a0001c0001t0001g0180 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.634-421C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12109954 | ||||||
| chr17:12109967
|
A | C | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG01934.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.634-408A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12109967 | ||||||
| chr17:12110042
|
G | C | 1 | a0001c0001t0003g0113 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.634-333G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12110042 | ||||||
| chr17:12110210
|
T | C | 3 | a0001c0001t0002g0233a0001c0001t0002g0252a0001c0001t0002g0253 | 3 | HG02818.hp2 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.634-165T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12110210 | ||||||
| chr17:12110291
|
C | A | 1 | a0001c0001t0002g0298 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.634-84C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12110291 | ||||||
| chr17:12110291
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.634-84C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12110291 | ||||||
| chr17:12110304
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.634-71G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12110304 | ||||||
| chr17:12110311
|
A | G | 1 | a0001c0001t0003g0113 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.634-64A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 5/10 | chr17 | 12110311 | ||||||
| chr17:12110487
|
C | T | 1 | a0001c0001t0018g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.685+61C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12110487 | ||||||
| chr17:12110776
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.685+350A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12110776 | ||||||
| chr17:12111375
|
T | C | 2 | a0001c0001t0001g0281a0001c0001t0001g0282 | 2 | HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.685+949T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12111375 | ||||||
| chr17:12111468
|
G | C | 1 | a0001c0001t0001g0031 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.685+1042G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12111468 | ||||||
| chr17:12111493
|
T | C | 6 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0243others(3): Show | 6 | HG02083.hp1 NA18945.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.685+1067T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12111493 | ||||||
| chr17:12111658
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.685+1232A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12111658 | ||||||
| chr17:12111782
|
G | T | 4 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG02055.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.685+1356G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12111782 | ||||||
| chr17:12111834
|
A | AATATGAC | 5 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(2): Show | 5 | HG02145.hp2 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.686-1399_686-1398i others(9): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12111834 | ||||||
| chr17:12111836
|
A | AGGGGTCA others(3): Show |
5 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(2): Show | 5 | HG02145.hp2 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.686-1397_686-1396i others(12): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12111836 | ||||||
| chr17:12111836
|
A | ATCACTAG others(9): Show |
1 | a0002c0004t0012g0028 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.686-1396_686-1395i others(18): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 12111836 | |||||
| chr17:12111836
|
A | ATGACTAG others(9): Show |
286 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(283): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.686-1395_686-1394i others(18): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 12111836 | |||||
| chr17:12111980
|
T | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0021others(1): Show | 4 | HG02809.hp2 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.686-1253T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12111980 | ||||||
| chr17:12111995
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.686-1238C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12111995 | ||||||
| chr17:12112053
|
C | G | 1 | a0001c0001t0001g0051 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.686-1180C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12112053 | ||||||
| chr17:12112228
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.686-1005C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12112228 | ||||||
| chr17:12112235
|
G | A | 14 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(11): Show | 14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.686-998G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12112235 | ||||||
| chr17:12112332
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.686-901G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12112332 | ||||||
| chr17:12112388
|
G | C | 1 | a0001c0001t0001g0009 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.686-845G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12112388 | ||||||
| chr17:12112409
|
G | T | 2 | a0001c0001t0001g0276a0002c0004t0012g0028 | 2 | HG01243.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.686-824G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12112409 | ||||||
| chr17:12112442
|
A | G | 1 | a0001c0001t0002g0287 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.686-791A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | chr17 | 12112442 | ||||||
| chr17:12112465
|
C | CA | 139 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(136): Show | 140 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.686-748dupA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 12112465 | |||||
| chr17:12112465
|
C | CAA | 6 | a0001c0001t0001g0179a0001c0001t0001g0239a0001c0001t0001g0273others(3): Show | 6 | HG01243.hp1 HG01934.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.686-749_686-748dup others(2): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 12112465 | |||||
| chr17:12113371
|
A | G | 2 | a0001c0001t0004g0231a0001c0001t0004g0232 | 2 | NA18995.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.813+11A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12113371 | ||||||
| chr17:12113442
|
C | T | 8 | a0001c0001t0002g0133a0001c0001t0002g0255a0001c0001t0002g0303others(5): Show | 8 | HG00544.hp1 HG00673.hp1 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.813+82C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12113442 | ||||||
| chr17:12113731
|
A | G | 2 | a0001c0001t0001g0161a0001c0001t0001g0166 | 2 | HG02258.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.813+371A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12113731 | ||||||
| chr17:12114128
|
G | C | 265 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(262): Show | 268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.813+768G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12114128 | ||||||
| chr17:12114387
|
G | GGT | 33 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(30): Show | 33 | HG01106.hp1 HG01891.hp1 HG02040.hp2 others(30): Show |
intron_variant | MODIFIER | c.813+1056_813+1057d others(4): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12114387 | |||||
| chr17:12114387
|
G | GGTGT | 8 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(5): Show | 8 | HG02055.hp1 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.813+1054_813+1057d others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12114387 | |||||
| chr17:12114387
|
G | GGTGTGTG others(5): Show |
1 | a0001c0001t0013g0005 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.813+1046_813+1057d others(14): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12114387 | |||||
| chr17:12114387
|
GGT | G | 175 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(172): Show | 177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.813+1056_813+1057d others(4): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12114387 | |||||
| chr17:12114387
|
GGTGTGTG others(7): Show |
G | 71 | a0001c0001t0001g0256a0001c0001t0001g0272a0001c0001t0001g0273others(68): Show | 71 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.813+1044_813+1057d others(16): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12114387 | |||||
| chr17:12114517
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.813+1157T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12114517 | ||||||
| chr17:12114631
|
A | G | 2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | NA18970.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.813+1271A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12114631 | ||||||
| chr17:12114672
|
G | A | 14 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(11): Show | 14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.813+1312G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12114672 | ||||||
| chr17:12114828
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.813+1468T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12114828 | ||||||
| chr17:12114872
|
G | A | 1 | a0001c0001t0002g0298 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.813+1512G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12114872 | ||||||
| chr17:12114971
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.813+1611C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12114971 | ||||||
| chr17:12115090
|
C | A | 2 | a0001c0001t0002g0107a0001c0001t0002g0108 | 2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.813+1730C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12115090 | ||||||
| chr17:12115230
|
C | T | 14 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(11): Show | 14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.813+1870C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12115230 | ||||||
| chr17:12115264
|
T | C | 1 | a0001c0001t0004g0231 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.813+1904T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12115264 | ||||||
| chr17:12115311
|
A | G | 1 | a0001c0001t0001g0129 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.813+1951A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12115311 | ||||||
| chr17:12115520
|
G | A | 8 | a0001c0001t0001g0122a0001c0001t0001g0128a0001c0001t0001g0129others(5): Show | 8 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(5): Show |
intron_variant | MODIFIER | c.813+2160G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12115520 | ||||||
| chr17:12115533
|
C | T | 1 | a0001c0001t0002g0317 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.813+2173C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12115533 | ||||||
| chr17:12115534
|
G | A | 14 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(11): Show | 14 | HG01106.hp1 HG02040.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.813+2174G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12115534 | ||||||
| chr17:12115538
|
C | T | 5 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(2): Show | 5 | HG02647.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.813+2178C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12115538 | ||||||
| chr17:12115541
|
A | AG | 318 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(315): Show | 321 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.813+2182dupG | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12115541 | |||||
| chr17:12115878
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.813+2518T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12115878 | ||||||
| chr17:12115975
|
T | G | 1 | a0001c0001t0003g0071 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.813+2615T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12115975 | ||||||
| chr17:12116076
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.813+2716C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12116076 | ||||||
| chr17:12116265
|
T | C | 3 | a0001c0001t0007g0026a0001c0001t0007g0249a0001c0001t0007g0250 | 3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.813+2905T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12116265 | ||||||
| chr17:12116438
|
TAATA | T | 4 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG02055.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.813+3082_813+3085d others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12116438 | |||||
| chr17:12116499
|
A | T | 3 | a0001c0001t0001g0288a0001c0001t0001g0292a0001c0001t0001g0293 | 3 | HG00280.hp2 HG02257.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.813+3139A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12116499 | ||||||
| chr17:12116500
|
T | A | 1 | a0001c0001t0002g0267 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.813+3140T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12116500 | ||||||
| chr17:12116553
|
AG | A | 3 | a0001c0001t0007g0026a0001c0001t0007g0249a0001c0001t0007g0250 | 3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.813+3194delG | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12116553 | ||||||
| chr17:12116557
|
G | A | 1 | a0001c0001t0002g0134 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.813+3197G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12116557 | ||||||
| chr17:12116771
|
A | G | 62 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(59): Show | 65 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.813+3411A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12116771 | ||||||
| chr17:12116773
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.813+3413G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12116773 | ||||||
| chr17:12117171
|
C | T | 65 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(62): Show | 68 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.813+3811C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12117171 | ||||||
| chr17:12117276
|
G | A | 2 | a0001c0001t0007g0249a0001c0001t0007g0250 | 2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.813+3916G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12117276 | ||||||
| chr17:12117317
|
G | A | 2 | a0001c0001t0007g0249a0001c0001t0007g0250 | 2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.813+3957G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12117317 | ||||||
| chr17:12117409
|
TA | T | 6 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(3): Show | 6 | HG02165.hp2 NA18970.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.813+4060delA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12117409 | |||||
| chr17:12117509
|
A | C | 1 | a0001c0001t0018g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.813+4149A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12117509 | ||||||
| chr17:12117597
|
AT | A | 197 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(194): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.813+4246delT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12117597 | |||||
| chr17:12117608
|
T | G | 3 | a0001c0001t0001g0141a0001c0001t0003g0033a0001c0001t0003g0080 | 3 | NA18983.hp2 NA18997.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.813+4248T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12117608 | ||||||
| chr17:12117810
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.813+4450G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12117810 | ||||||
| chr17:12117953
|
G | A | 1 | a0001c0001t0004g0165 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.813+4593G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12117953 | ||||||
| chr17:12118230
|
T | C | 83 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(80): Show | 86 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.813+4870T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12118230 | ||||||
| chr17:12118263
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.813+4903C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12118263 | ||||||
| chr17:12118348
|
G | A | 2 | a0001c0001t0002g0316a0001c0001t0014g0091 | 2 | HG01975.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.813+4988G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12118348 | ||||||
| chr17:12118447
|
G | A | 3 | a0001c0001t0007g0026a0001c0001t0007g0249a0001c0001t0007g0250 | 3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.813+5087G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12118447 | ||||||
| chr17:12118489
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.813+5129T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12118489 | ||||||
| chr17:12118779
|
A | T | 1 | a0001c0001t0001g0273 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.813+5419A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12118779 | ||||||
| chr17:12118893
|
G | A | 4 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(1): Show | 4 | HG01123.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.813+5533G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12118893 | ||||||
| chr17:12119001
|
G | A | 1 | a0001c0001t0005g0186 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.813+5641G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12119001 | ||||||
| chr17:12119249
|
T | C | 286 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(283): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.813+5889T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12119249 | ||||||
| chr17:12119265
|
A | G | 5 | a0001c0001t0003g0002a0001c0001t0003g0032a0001c0001t0003g0055others(2): Show | 6 | HG00621.hp1 NA18943.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.813+5905A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12119265 | ||||||
| chr17:12119404
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.814-5890G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12119404 | ||||||
| chr17:12119437
|
G | A | 1 | a0001c0001t0003g0070 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.814-5857G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12119437 | ||||||
| chr17:12119476
|
T | A | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.814-5818T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12119476 | ||||||
| chr17:12119559
|
A | G | 1 | a0001c0001t0004g0045 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.814-5735A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12119559 | ||||||
| chr17:12119583
|
C | A | 2 | a0001c0001t0001g0157a0001c0001t0018g0047 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.814-5711C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12119583 | ||||||
| chr17:12119588
|
A | G | 2 | a0001c0001t0001g0157a0001c0001t0018g0047 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.814-5706A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12119588 | ||||||
| chr17:12119616
|
C | T | 3 | a0001c0001t0007g0026a0001c0001t0007g0249a0001c0001t0007g0250 | 3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.814-5678C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12119616 | ||||||
| chr17:12119870
|
A | G | 1 | a0001c0001t0001g0129 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.814-5424A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12119870 | ||||||
| chr17:12120044
|
A | G | 2 | a0001c0001t0001g0274a0001c0001t0001g0278 | 2 | HG02809.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.814-5250A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12120044 | ||||||
| chr17:12120186
|
C | T | 81 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(78): Show | 84 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.814-5108C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12120186 | ||||||
| chr17:12120188
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.814-5106C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12120188 | ||||||
| chr17:12120227
|
A | G | 65 | a0001c0001t0001g0274a0001c0001t0001g0278a0001c0001t0002g0057others(62): Show | 65 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.814-5067A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12120227 | ||||||
| chr17:12120534
|
T | TC | 261 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(258): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.814-4751dupC | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12120534 | |||||
| chr17:12120738
|
T | G | 1 | a0001c0001t0001g0173 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.814-4556T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12120738 | ||||||
| chr17:12121030
|
C | G | 61 | a0001c0001t0001g0210a0001c0001t0002g0057a0001c0001t0002g0058others(58): Show | 61 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.814-4264C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12121030 | ||||||
| chr17:12121039
|
G | A | 14 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(11): Show | 14 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.814-4255G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12121039 | ||||||
| chr17:12121058
|
G | A | 6 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(3): Show | 6 | HG02165.hp2 NA18946.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.814-4236G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12121058 | ||||||
| chr17:12121166
|
A | G | 197 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(194): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.814-4128A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12121166 | ||||||
| chr17:12121169
|
T | A | 3 | a0001c0001t0007g0026a0001c0001t0007g0249a0001c0001t0007g0250 | 3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.814-4125T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12121169 | ||||||
| chr17:12121205
|
T | C | 1 | a0001c0001t0002g0300 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.814-4089T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12121205 | ||||||
| chr17:12121418
|
T | C | 4 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(1): Show | 4 | HG01106.hp2 HG02683.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.814-3876T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12121418 | ||||||
| chr17:12121532
|
G | A | 2 | a0001c0001t0002g0107a0001c0001t0002g0108 | 2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.814-3762G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12121532 | ||||||
| chr17:12121574
|
C | CA | 70 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0121others(67): Show | 70 | HG00544.hp1 HG00597.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.814-3700dupA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12121574 | |||||
| chr17:12121574
|
C | CAA | 9 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(6): Show | 9 | HG01261.hp2 HG02109.hp1 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.814-3701_814-3700d others(4): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12121574 | |||||
| chr17:12121574
|
CA | C | 74 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0031others(71): Show | 76 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.814-3700delA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12121574 | |||||
| chr17:12121574
|
CAA | C | 6 | a0001c0001t0003g0002a0001c0001t0003g0032a0001c0001t0003g0055others(3): Show | 7 | HG00621.hp1 NA18943.hp2 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.814-3701_814-3700d others(4): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12121574 | |||||
| chr17:12121687
|
T | C | 1 | a0001c0001t0002g0266 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.814-3607T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12121687 | ||||||
| chr17:12121725
|
G | T | 5 | a0001c0001t0001g0034a0001c0001t0001g0101a0001c0001t0001g0158others(2): Show | 5 | HG01192.hp1 HG02615.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.814-3569G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12121725 | ||||||
| chr17:12121735
|
G | C | 5 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(2): Show | 5 | HG02647.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.814-3559G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12121735 | ||||||
| chr17:12121892
|
G | C | 267 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.814-3402G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12121892 | ||||||
| chr17:12121944
|
T | C | 2 | a0001c0001t0001g0274a0001c0001t0001g0278 | 2 | HG02809.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.814-3350T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12121944 | ||||||
| chr17:12121958
|
G | A | 1 | a0001c0001t0002g0310 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.814-3336G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12121958 | ||||||
| chr17:12121996
|
A | G | 2 | a0001c0001t0001g0273a0001c0001t0001g0277 | 2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.814-3298A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12121996 | ||||||
| chr17:12122133
|
C | T | 6 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(3): Show | 6 | HG02165.hp2 NA18946.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.814-3161C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12122133 | ||||||
| chr17:12122556
|
T | A | 1 | a0001c0001t0019g0295 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.814-2738T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12122556 | ||||||
| chr17:12122679
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.814-2615A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12122679 | ||||||
| chr17:12122738
|
A | G | 2 | a0001c0001t0001g0098a0001c0001t0001g0099 | 2 | HG01106.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.814-2556A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12122738 | ||||||
| chr17:12122764
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.814-2530A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12122764 | ||||||
| chr17:12122790
|
A | G | 2 | a0001c0001t0002g0301a0001c0001t0002g0311 | 2 | NA18950.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.814-2504A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12122790 | ||||||
| chr17:12123033
|
T | A | 1 | a0001c0001t0004g0045 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.814-2261T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12123033 | ||||||
| chr17:12123142
|
C | T | 17 | a0001c0001t0004g0027a0001c0001t0004g0030a0001c0001t0004g0036others(14): Show | 17 | HG00673.hp2 HG01891.hp2 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.814-2152C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12123142 | ||||||
| chr17:12123201
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.814-2093G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12123201 | ||||||
| chr17:12123315
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.814-1979T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12123315 | ||||||
| chr17:12123593
|
C | CT | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.814-1693dupT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12123593 | |||||
| chr17:12123617
|
A | G | 6 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(3): Show | 6 | HG02165.hp2 NA18946.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.814-1677A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12123617 | ||||||
| chr17:12123745
|
A | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.814-1549A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12123745 | ||||||
| chr17:12123795
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.814-1499G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12123795 | ||||||
| chr17:12123891
|
G | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0019others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.814-1403G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12123891 | ||||||
| chr17:12123919
|
G | A | 1 | a0001c0001t0002g0233 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.814-1375G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12123919 | ||||||
| chr17:12124077
|
C | CA | 5 | a0001c0001t0001g0034a0001c0001t0001g0101a0001c0001t0001g0158others(2): Show | 5 | HG01192.hp1 HG02615.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.814-1208dupA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12124077 | |||||
| chr17:12124077
|
CA | C | 207 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(204): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.814-1208delA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 12124077 | |||||
| chr17:12124279
|
G | A | 5 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(2): Show | 5 | HG02647.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.814-1015G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12124279 | ||||||
| chr17:12124283
|
C | T | 6 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(3): Show | 6 | HG02165.hp2 NA18946.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.814-1011C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12124283 | ||||||
| chr17:12124367
|
T | C | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG01123.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.814-927T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12124367 | ||||||
| chr17:12124565
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.814-729T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12124565 | ||||||
| chr17:12124884
|
C | G | 1 | a0001c0001t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.814-410C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12124884 | ||||||
| chr17:12124911
|
C | A | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.814-383C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12124911 | ||||||
| chr17:12125048
|
C | G | 1 | a0001c0001t0001g0014 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.814-246C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12125048 | ||||||
| chr17:12125267
|
T | G | 1 | a0001c0001t0002g0136 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.814-27T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 7/10 | chr17 | 12125267 | ||||||
| chr17:12125473
|
A | G | 2 | a0001c0001t0001g0157a0001c0001t0018g0047 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.891+102A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12125473 | ||||||
| chr17:12125540
|
A | C | 1 | a0002c0004t0012g0028 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.891+169A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12125540 | ||||||
| chr17:12125675
|
C | T | 3 | a0001c0001t0003g0068a0001c0001t0003g0086a0001c0001t0003g0113 | 3 | HG00558.hp2 HG00609.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.891+304C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12125675 | ||||||
| chr17:12125911
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.891+540C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12125911 | ||||||
| chr17:12125950
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.891+579A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12125950 | ||||||
| chr17:12126157
|
G | A | 1 | a0001c0001t0003g0033 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.891+786G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12126157 | ||||||
| chr17:12126572
|
G | A | 1 | a0001c0001t0002g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.891+1201G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12126572 | ||||||
| chr17:12126575
|
G | A | 4 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG02055.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.891+1204G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12126575 | ||||||
| chr17:12126611
|
G | T | 1 | a0001c0001t0001g0007 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.891+1240G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12126611 | ||||||
| chr17:12126771
|
T | C | 5 | a0001c0001t0004g0039a0001c0001t0004g0156a0001c0001t0004g0289others(2): Show | 5 | HG00673.hp2 HG02040.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+1400T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12126771 | ||||||
| chr17:12126773
|
G | C | 2 | a0001c0001t0002g0136a0001c0001t0002g0308 | 2 | NA18977.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.891+1402G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12126773 | ||||||
| chr17:12126871
|
C | T | 1 | a0001c0001t0002g0275 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.891+1500C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12126871 | ||||||
| chr17:12126973
|
C | G | 2 | a0001c0001t0002g0287a0001c0001t0002g0291 | 2 | NA18966.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.891+1602C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12126973 | ||||||
| chr17:12127160
|
A | G | 1 | a0001c0003t0001g0279 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.891+1789A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12127160 | ||||||
| chr17:12127300
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.892-1839G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12127300 | ||||||
| chr17:12127333
|
G | C | 1 | a0001c0001t0001g0035 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.892-1806G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12127333 | ||||||
| chr17:12127464
|
A | C | 5 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(2): Show | 5 | HG02647.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.892-1675A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12127464 | ||||||
| chr17:12127792
|
C | T | 196 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(193): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.892-1347C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12127792 | ||||||
| chr17:12127830
|
G | A | 65 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(62): Show | 68 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.892-1309G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12127830 | ||||||
| chr17:12127847
|
CAT | C | 3 | a0001c0001t0001g0046a0001c0001t0001g0054a0001c0001t0001g0105 | 3 | HG02027.hp1 HG02071.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.892-1291_892-1290d others(4): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12127847 | ||||||
| chr17:12127884
|
G | T | 1 | a0001c0001t0002g0313 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.892-1255G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12127884 | ||||||
| chr17:12128027
|
C | T | 3 | a0001c0001t0007g0026a0001c0001t0007g0249a0001c0001t0007g0250 | 3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.892-1112C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12128027 | ||||||
| chr17:12128164
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.892-975G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12128164 | ||||||
| chr17:12128279
|
G | A | 2 | a0001c0001t0002g0059a0001c0001t0002g0264 | 2 | HG00738.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.892-860G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12128279 | ||||||
| chr17:12128323
|
C | T | 1 | a0001c0001t0018g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.892-816C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12128323 | ||||||
| chr17:12128324
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.892-815G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12128324 | ||||||
| chr17:12128346
|
G | C | 2 | a0001c0001t0001g0157a0001c0001t0018g0047 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.892-793G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12128346 | ||||||
| chr17:12128386
|
G | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(2): Show | 5 | HG02486.hp2 HG02717.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.892-753G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12128386 | ||||||
| chr17:12128457
|
T | C | 1 | a0001c0001t0001g0104 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.892-682T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12128457 | ||||||
| chr17:12128491
|
G | A | 1 | a0001c0001t0004g0042 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.892-648G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12128491 | ||||||
| chr17:12128608
|
G | C | 4 | a0001c0001t0002g0073a0001c0001t0002g0261a0001c0001t0002g0266others(1): Show | 4 | HG00639.hp2 HG02602.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.892-531G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12128608 | ||||||
| chr17:12128825
|
T | A | 1 | a0001c0001t0001g0184 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.892-314T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12128825 | ||||||
| chr17:12128870
|
G | A | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.892-269G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12128870 | ||||||
| chr17:12129030
|
A | G | 3 | a0001c0001t0007g0026a0001c0001t0007g0249a0001c0001t0007g0250 | 3 | HG01884.hp1 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.892-109A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 8/10 | chr17 | 12129030 | ||||||
| chr17:12129304
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1040+17T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12129304 | ||||||
| chr17:12129325
|
C | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0168 | 2 | HG02630.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1040+38C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12129325 | ||||||
| chr17:12129537
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1040+250T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12129537 | ||||||
| chr17:12129622
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1040+335A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12129622 | ||||||
| chr17:12129627
|
A | G | 61 | a0001c0001t0001g0210a0001c0001t0002g0057a0001c0001t0002g0058others(58): Show | 61 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.1040+340A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12129627 | ||||||
| chr17:12130382
|
T | G | 1 | a0001c0001t0005g0196 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1040+1095T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12130382 | ||||||
| chr17:12130619
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1040+1332T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12130619 | ||||||
| chr17:12130835
|
A | G | 3 | a0001c0001t0001g0274a0001c0001t0001g0278a0002c0004t0012g0028 | 3 | HG01243.hp2 HG02809.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1040+1548A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12130835 | ||||||
| chr17:12130946
|
A | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0288 | 2 | HG03239.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1040+1659A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12130946 | ||||||
| chr17:12130970
|
G | A | 1 | a0001c0001t0001g0294 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1040+1683G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12130970 | ||||||
| chr17:12131143
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1040+1856A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12131143 | ||||||
| chr17:12131200
|
G | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(2): Show | 5 | HG02486.hp2 HG02717.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1040+1913G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12131200 | ||||||
| chr17:12131209
|
T | C | 1 | a0001c0001t0005g0306 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1040+1922T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12131209 | ||||||
| chr17:12131234
|
CT | C | 122 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(119): Show | 122 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.1040+1964delT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 12131234 | |||||
| chr17:12131271
|
A | G | 1 | a0001c0001t0002g0317 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1040+1984A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12131271 | ||||||
| chr17:12131289
|
A | G | 4 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(1): Show | 4 | HG02055.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1040+2002A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12131289 | ||||||
| chr17:12131492
|
G | T | 1 | a0001c0001t0001g0242 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1040+2205G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12131492 | ||||||
| chr17:12131546
|
G | A | 2 | a0001c0001t0001g0157a0001c0001t0018g0047 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1040+2259G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12131546 | ||||||
| chr17:12131636
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1040+2349G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12131636 | ||||||
| chr17:12131959
|
G | A | 28 | a0001c0001t0002g0057a0001c0001t0002g0058a0001c0001t0002g0059others(25): Show | 28 | HG00639.hp2 HG00642.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1040+2672G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12131959 | ||||||
| chr17:12132190
|
T | A | 1 | a0001c0001t0001g0185 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1040+2903T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12132190 | ||||||
| chr17:12132351
|
A | G | 4 | a0001c0001t0001g0034a0001c0001t0001g0101a0001c0001t0001g0176others(1): Show | 4 | HG01192.hp1 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1040+3064A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12132351 | ||||||
| chr17:12132362
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1040+3075G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12132362 | ||||||
| chr17:12132436
|
C | G | 2 | a0001c0001t0002g0107a0001c0001t0002g0108 | 2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1040+3149C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12132436 | ||||||
| chr17:12132608
|
AG | A | 6 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(3): Show | 6 | HG02165.hp2 NA18946.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1040+3323delG | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 12132608 | |||||
| chr17:12132610
|
G | GA | 11 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0014others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1040+3335dupA | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 12132610 | |||||
| chr17:12132658
|
C | A | 3 | a0001c0001t0001g0034a0001c0001t0001g0101a0001c0001t0001g0176 | 3 | HG01192.hp1 HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1040+3371C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12132658 | ||||||
| chr17:12132702
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1040+3415G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12132702 | ||||||
| chr17:12132760
|
TAGAA | T | 28 | a0001c0001t0002g0057a0001c0001t0002g0058a0001c0001t0002g0059others(25): Show | 28 | HG00639.hp2 HG00642.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1040+3480_1040+348 others(8): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 12132760 | |||||
| chr17:12132776
|
T | G | 1 | a0001c0001t0018g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1040+3489T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12132776 | ||||||
| chr17:12133027
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1040+3740A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133027 | ||||||
| chr17:12133070
|
T | TTTG | 6 | a0001c0001t0001g0009a0001c0001t0001g0157a0001c0001t0001g0198others(3): Show | 6 | HG02165.hp1 HG02622.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1040+3807_1040+380 others(7): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 12133070 | |||||
| chr17:12133185
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1040+3898G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133185 | ||||||
| chr17:12133285
|
C | G | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040+3998C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133285 | ||||||
| chr17:12133328
|
C | T | 2 | a0001c0001t0003g0068a0001c0001t0003g0113 | 2 | HG00558.hp2 HG00609.hp1 |
intron_variant | MODIFIER | c.1040+4041C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133328 | ||||||
| chr17:12133343
|
G | A | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040+4056G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133343 | ||||||
| chr17:12133345
|
G | A | 3 | a0001c0001t0008g0189a0001c0001t0008g0191a0001c0001t0008g0192 | 3 | NA18990.hp1 NA19054.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1040+4058G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133345 | ||||||
| chr17:12133362
|
G | A | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040+4075G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133362 | ||||||
| chr17:12133363
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1040+4076T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133363 | ||||||
| chr17:12133430
|
T | C | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040+4143T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133430 | ||||||
| chr17:12133500
|
C | T | 1 | a0001c0001t0001g0203 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1040+4213C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133500 | ||||||
| chr17:12133554
|
C | G | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040+4267C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133554 | ||||||
| chr17:12133606
|
ATT | A | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040+4326_1040+432 others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 12133606 | |||||
| chr17:12133643
|
G | GA | 6 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(3): Show | 6 | HG02165.hp2 NA18946.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1040+4356_1040+435 others(5): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133643 | ||||||
| chr17:12133644
|
G | A | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040+4357G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133644 | ||||||
| chr17:12133647
|
G | A | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040+4360G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133647 | ||||||
| chr17:12133733
|
C | A | 1 | a0001c0001t0001g0272 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1040+4446C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133733 | ||||||
| chr17:12133771
|
C | G | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040+4484C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133771 | ||||||
| chr17:12133777
|
C | G | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040+4490C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133777 | ||||||
| chr17:12133999
|
A | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(4): Show | 7 | HG01243.hp1 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1040+4712A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12133999 | ||||||
| chr17:12134063
|
T | C | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040+4776T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134063 | ||||||
| chr17:12134084
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1040+4797A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134084 | ||||||
| chr17:12134096
|
A | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1040+4809A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134096 | ||||||
| chr17:12134108
|
G | C | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040+4821G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134108 | ||||||
| chr17:12134190
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1040+4903C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134190 | ||||||
| chr17:12134208
|
C | G | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040+4921C>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134208 | ||||||
| chr17:12134295
|
C | CCTAT | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040+5011_1040+501 others(8): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 12134295 | |||||
| chr17:12134491
|
C | T | 83 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(80): Show | 83 | HG00099.hp1 HG00280.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.1040+5204C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134491 | ||||||
| chr17:12134492
|
G | C | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1040+5205G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134492 | ||||||
| chr17:12134545
|
G | A | 1 | a0001c0001t0001g0161 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1040+5258G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134545 | ||||||
| chr17:12134599
|
T | C | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-5240T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134599 | ||||||
| chr17:12134653
|
A | G | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-5186A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134653 | ||||||
| chr17:12134701
|
G | A | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-5138G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134701 | ||||||
| chr17:12134735
|
A | G | 199 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(196): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.1041-5104A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134735 | ||||||
| chr17:12134751
|
A | C | 1 | a0001c0001t0004g0045 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1041-5088A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134751 | ||||||
| chr17:12134824
|
T | C | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-5015T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134824 | ||||||
| chr17:12134949
|
C | A | 6 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0299others(3): Show | 6 | HG00597.hp1 NA18612.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1041-4890C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134949 | ||||||
| chr17:12134969
|
T | C | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-4870T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12134969 | ||||||
| chr17:12135002
|
A | T | 1 | a0001c0001t0003g0033 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1041-4837A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12135002 | ||||||
| chr17:12135065
|
G | T | 1 | a0001c0001t0001g0140 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1041-4774G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12135065 | ||||||
| chr17:12135075
|
G | GT | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-4757dupT | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 12135075 | |||||
| chr17:12135151
|
T | G | 1 | a0001c0001t0001g0139 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1041-4688T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12135151 | ||||||
| chr17:12135158
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG00642.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1041-4681G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12135158 | ||||||
| chr17:12135198
|
C | A | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-4641C>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12135198 | ||||||
| chr17:12135258
|
T | C | 2 | a0001c0001t0001g0256a0001c0001t0001g0294 | 2 | NA18949.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1041-4581T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12135258 | ||||||
| chr17:12135327
|
G | A | 10 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(7): Show | 10 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1041-4512G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12135327 | ||||||
| chr17:12135335
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1041-4504C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12135335 | ||||||
| chr17:12135460
|
A | T | 1 | a0001c0001t0009g0001 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1041-4379A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12135460 | ||||||
| chr17:12135484
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0011g0017 | 3 | HG02145.hp2 HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1041-4355G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12135484 | ||||||
| chr17:12135491
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1041-4348C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12135491 | ||||||
| chr17:12135697
|
G | C | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-4142G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12135697 | ||||||
| chr17:12135746
|
T | C | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-4093T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12135746 | ||||||
| chr17:12135770
|
G | A | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-4069G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12135770 | ||||||
| chr17:12136103
|
C | T | 1 | a0001c0001t0003g0062 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1041-3736C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12136103 | ||||||
| chr17:12136406
|
A | G | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-3433A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12136406 | ||||||
| chr17:12136584
|
G | T | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-3255G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12136584 | ||||||
| chr17:12136650
|
G | A | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-3189G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12136650 | ||||||
| chr17:12136669
|
AAAAG | A | 104 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(101): Show | 104 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.1041-3167_1041-316 others(8): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 12136669 | |||||
| chr17:12136671
|
A | C | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-3168A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12136671 | ||||||
| chr17:12136680
|
G | T | 6 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(3): Show | 6 | HG02165.hp2 NA18946.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1041-3159G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12136680 | ||||||
| chr17:12136715
|
G | A | 5 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(2): Show | 5 | HG02647.hp2 HG02970.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1041-3124G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12136715 | ||||||
| chr17:12136754
|
G | C | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-3085G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12136754 | ||||||
| chr17:12136872
|
T | C | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-2967T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12136872 | ||||||
| chr17:12136877
|
TG | T | 5 | a0001c0001t0002g0133a0001c0001t0002g0255a0001c0001t0002g0303others(2): Show | 5 | HG00544.hp1 HG02015.hp1 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.1041-2960delG | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 12136877 | |||||
| chr17:12137438
|
T | C | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-2401T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12137438 | ||||||
| chr17:12137552
|
G | A | 1 | a0001c0001t0002g0275 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1041-2287G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12137552 | ||||||
| chr17:12137610
|
A | G | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-2229A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12137610 | ||||||
| chr17:12137734
|
A | G | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-2105A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12137734 | ||||||
| chr17:12137781
|
CAA | C | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-2056_1041-205 others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 12137781 | |||||
| chr17:12137825
|
T | C | 2 | a0001c0001t0001g0122a0001c0001t0001g0138 | 2 | NA18943.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1041-2014T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12137825 | ||||||
| chr17:12137866
|
A | AATG | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-1970_1041-196 others(7): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 12137866 | |||||
| chr17:12137871
|
TAAAC | T | 5 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(2): Show | 5 | HG02055.hp1 HG02145.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1041-1964_1041-196 others(8): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 12137871 | |||||
| chr17:12138007
|
G | A | 65 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0002g0057others(62): Show | 65 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.1041-1832G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12138007 | ||||||
| chr17:12138176
|
T | G | 1 | a0001c0001t0006g0112 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1041-1663T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12138176 | ||||||
| chr17:12138200
|
T | C | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-1639T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12138200 | ||||||
| chr17:12138231
|
A | AGGTTAGG others(16): Show |
8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-1607_1041-158 others(27): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 12138231 | |||||
| chr17:12138232
|
G | A | 4 | a0001c0001t0004g0156a0001c0001t0004g0289a0001c0001t0004g0290others(1): Show | 4 | HG00673.hp2 HG02132.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.1041-1607G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12138232 | ||||||
| chr17:12138316
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1041-1523T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12138316 | ||||||
| chr17:12138344
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0023 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1041-1495C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12138344 | ||||||
| chr17:12138447
|
ATATAT | A | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-1388_1041-138 others(9): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 12138447 | |||||
| chr17:12138471
|
G | A | 6 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(3): Show | 6 | HG02165.hp2 NA18946.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1041-1368G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12138471 | ||||||
| chr17:12138557
|
A | G | 9 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(6): Show | 9 | HG02165.hp2 HG02622.hp1 HG03486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1041-1282A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12138557 | ||||||
| chr17:12138691
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1041-1148G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12138691 | ||||||
| chr17:12138712
|
G | A | 2 | a0001c0001t0001g0204a0001c0001t0010g0205 | 2 | NA20752.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1041-1127G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12138712 | ||||||
| chr17:12138777
|
G | A | 6 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0021others(3): Show | 6 | HG01243.hp1 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1041-1062G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12138777 | ||||||
| chr17:12138791
|
A | G | 1 | a0001c0001t0002g0257 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1041-1048A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12138791 | ||||||
| chr17:12138846
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1041-993G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12138846 | ||||||
| chr17:12139050
|
T | C | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-789T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12139050 | ||||||
| chr17:12139247
|
A | G | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-592A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12139247 | ||||||
| chr17:12139307
|
T | C | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-532T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12139307 | ||||||
| chr17:12139315
|
T | C | 89 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0029others(86): Show | 92 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.1041-524T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12139315 | ||||||
| chr17:12139460
|
A | G | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-379A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12139460 | ||||||
| chr17:12139534
|
CATTT | C | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-302_1041-299d others(6): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 12139534 | |||||
| chr17:12139617
|
T | A | 65 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0002g0057others(62): Show | 65 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.1041-222T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12139617 | ||||||
| chr17:12139697
|
G | A | 1 | a0001c0001t0002g0211 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1041-142G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12139697 | ||||||
| chr17:12139738
|
G | C | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-101G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 9/10 | chr17 | 12139738 | ||||||
| chr17:12139977
|
C | T | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1086+93C>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12139977 | ||||||
| chr17:12139995
|
A | C | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1086+111A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12139995 | ||||||
| chr17:12140136
|
A | T | 6 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(3): Show | 6 | HG02165.hp2 NA18946.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1086+252A>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12140136 | ||||||
| chr17:12140162
|
A | C | 1 | a0001c0001t0001g0140 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1086+278A>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12140162 | ||||||
| chr17:12140214
|
A | AG | 289 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(286): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.1086+330_1086+331i others(3): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12140214 | ||||||
| chr17:12140256
|
G | A | 270 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(267): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1086+372G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12140256 | ||||||
| chr17:12140301
|
A | G | 1 | a0001c0001t0002g0108 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1086+417A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12140301 | ||||||
| chr17:12140338
|
G | A | 2 | a0001c0001t0001g0100a0001c0001t0001g0251 | 2 | HG02886.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1086+454G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12140338 | ||||||
| chr17:12140342
|
T | A | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1086+458T>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12140342 | ||||||
| chr17:12140460
|
A | G | 63 | a0001c0001t0001g0105a0001c0001t0002g0057a0001c0001t0002g0058others(60): Show | 63 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1086+576A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12140460 | ||||||
| chr17:12140532
|
G | A | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1087-615G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12140532 | ||||||
| chr17:12140772
|
T | C | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1087-375T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12140772 | ||||||
| chr17:12140810
|
G | T | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1087-337G>T | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12140810 | ||||||
| chr17:12140832
|
G | C | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1087-315G>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12140832 | ||||||
| chr17:12140865
|
T | G | 1 | a0001c0001t0001g0227 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1087-282T>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12140865 | ||||||
| chr17:12140892
|
G | A | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1087-255G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12140892 | ||||||
| chr17:12140928
|
G | A | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1087-219G>A | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12140928 | ||||||
| chr17:12141036
|
T | C | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(5): Show | 8 | HG02165.hp2 HG02622.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.1087-111T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12141036 | ||||||
| chr17:12141066
|
T | C | 4 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220others(1): Show | 4 | HG02145.hp1 HG02895.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1087-81T>C | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12141066 | ||||||
| chr17:12141067
|
A | G | 1 | a0001c0001t0001g0288 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1087-80A>G | MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 10/10 | chr17 | 12141067 |